2023

Tregidgo, H.F.J., Soskic, S., Althonayan, J., Maffei, C., Leemput, K.V., Golland, P., ...Paz-Alonso, P.M. (2023). Accurate Bayesian segmentation of thalamic nuclei using diffusion MRI and an improved histological atlas. NeuroImage, doi:10.1016/j.neuroimage.2023.120129
Jiskoot, L.C., Russell, L.L., Greaves, C.V., van Schaik, E., van den Berg, E., Poos, J.M., ...Pijnenburg, Y.A.L. (2023). Addition of the FTD Module to the Neuropsychiatric Inventory improves classification of frontotemporal dementia spectrum disorders. Journal of Neurology, doi:10.1007/s00415-023-11596-3
Bussy, A., Levy, J.P., Best, T., Patel, R., Cupo, L., Van Langenhove, T., ...Remes, A.M. (2023). Cerebellar and subcortical atrophy contribute to psychiatric symptoms in frontotemporal dementia. Human Brain Mapping, doi:10.1002/hbm.26220
Tse, N.Y., Bocchetta, M., Todd, E.G., Devenney, E.M., Tu, S., Caga, J., ...Kiernan, M.C. (2023). Distinct hypothalamic involvement in the amyotrophic lateral sclerosis-frontotemporal dementia spectrum. NeuroImage: Clinical, 37 103281. doi:10.1016/j.nicl.2022.103281
Tregidgo, H.F.J., Soskic, S., Olchanyi, M.D., Althonayan, J., Billot, B., Maffei, C., ...Bocchetta, M. (2023). Domain-agnostic segmentation of thalamic nuclei from joint structural and diffusion MRI.
Premi, E., Pengo, M., Mattioli, I., Cantoni, V., Dukart, J., Gasparotti, R., ...Todd, E.G. (2023). Early neurotransmitters changes in prodromal frontotemporal dementia: A GENFI study. Neurobiology of Disease, doi:10.1016/j.nbd.2023.106068
Samra, K., MacDougall, A.M., Bouzigues, A., Bocchetta, M., Cash, D.M., Greaves, C.V., ...Seelaar, H. (2023). Genetic forms of primary progressive aphasia within the GENetic Frontotemporal dementia Initiative (GENFI) cohort: comparison with sporadic primary progressive aphasia. Brain Communications, 5 (2), doi:10.1093/braincomms/fcad036
Cullinane, P.W., Fumi, R., Theilmann Jensen, M., Jabbari, E., Warner, T.T., Revesz, T., ...Jaunmuktane, Z. (2023). MAPT-Associated Familial Progressive Supranuclear Palsy with Typical Corticobasal Degeneration Neuropathology: A Clinicopathological Report. Movement Disorders Clinical Practice, doi:10.1002/mdc3.13706
Seddighi, S., Qi, Y., Brown, A.-.L., Wilkins, O., Bereda, C., Belair, C., ...Khandeshi, A. (2023). Mis-spliced transcripts generatede novoproteins in TDP-43-related ALS/FTD.
Meda, F.J., Knowles, K., Swift, I.J., Sogorb-Esteve, A., Rohrer, J.D., Dittrich, A., ...Blennow, K. (2023). Neurofilament light oligomers in neurodegenerative diseases: quantification by homogeneous immunoassay in cerebrospinal fluid. BMJ Neurology Open, 5 (1), doi:10.1136/bmjno-2022-000395
Samra, K., Macdougall, A., Peakman, G., Bouzigues, A., Bocchetta, M., Cash, D.M., ...Jiskoot, L.C. (2023). Neuropsychiatric symptoms in genetic frontotemporal dementia: developing a new module for Clinical Rating Scales. Journal of Neurology, Neurosurgery and Psychiatry, doi:10.1136/jnnp-2022-330152
Street, D., Jabbari, E., Costantini, A., Jones, P.S., Holland, N., Rittman, T., ...Guo, T. (2023). Progression of atypical parkinsonian syndromes: PROSPECT-M-UK study implications for clinical trials. Brain, doi:10.1093/brain/awad105
Mok, T.H., Nihat, A., Majbour, N., Sequeira, D., Holm-Mercer, L., Coysh, T., ...Orrù, C.D. (2023). Seed amplification and neurodegeneration marker trajectories in individuals at risk of prion disease. Brain, doi:10.1093/brain/awad101
Bocchetta, M., Todd, E.G., Bouzigues, A., Cash, D.M., Nicholas, J.M., Convery, R.S., ...Iglesias, J.E. (2023). Structural MRI predicts clinical progression in presymptomatic genetic frontotemporal dementia: findings from the GENetic Frontotemporal dementia Initiative (GENFI) cohort. Brain Communications, doi:10.1093/braincomms/fcad061
Hardy, C.J., Taylor-Rubin, C., Taylor, B., Harding, E., Gonzalez, A.S., Jiang, J., ...Walker, F. (2023). Symptom-led staging for primary progressive aphasia..
Chokesuwattanaskul, A., Jiang, H., Bond, R.L., Jimenez, D.A., Russell, L.L., Sivasathiaseelan, H., ...van Leeuwen, J.E.P. (2023). The architecture of abnormal reward behaviour in dementia: multimodal hedonic phenotypes and brain substrate. Brain Communications, 5 (2), doi:10.1093/braincomms/fcad027
Jiskoot, L.C., Russell, L.L., Peakman, G., Convery, R.S., Greaves, C.V., Bocchetta, M., ...van Swieten, J.C. (2023). The Benson Complex Figure Test detects deficits in visuoconstruction and visual memory in symptomatic familial frontotemporal dementia: A GENFI study. Journal of the Neurological Sciences, 446 doi:10.1016/j.jns.2023.120590
Scotton, W.J., Shand, C., Todd, E., Bocchetta, M., Cash, D.M., VandeVrede, L., ...Oxtoby, N. (2023). Uncovering spatiotemporal patterns of atrophy in progressive supranuclear palsy using unsupervised machine learning. Brain Communications, 5 (2), doi:10.1093/braincomms/fcad048

2022

Scotton, W.J., Bocchetta, M., Todd, E., Cash, D.M., Oxtoby, N., Vande Vrede, L., ...Morris, H.R. (2022). A data-driven model of brain volume changes in progressive supranuclear palsy. Brain Communications, doi:10.1093/braincomms/fcac098
Tregidgo, H., Soskic, S., Althonayan, J., Maffei, C., Van Leemput, K., Golland, P., ...Rohrer, J. (2022). Accurate Bayesian segmentation of thalamic nuclei using diffusion MRI and an improved histological atlas. .
Boeve, B.F., Boxer, A.L., Kumfor, F., Pijnenburg, Y., Rohrer, J.D. (2022). Advances and controversies in frontotemporal dementia: diagnosis, biomarkers, and therapeutic considerations. The Lancet Neurology, 21 (3), 258-272. doi:10.1016/S1474-4422(21)00341-0
Premi, E., Costa, T., Gazzina, S., Benussi, A., Cauda, F., Gasparotti, R., ...Sanchez-Valle, R. (2022). An Automated Toolbox to Predict Single Subject Atrophy in Presymptomatic Granulin Mutation Carriers.. Journal of Alzheimer's Disease, doi:10.3233/JAD-215447
Bouzigues, A., Russell, L.L., Peakman, G., Bocchetta, M., Greaves, C.V., Convery, R.S., ...Galimberti, D. (2022). Anomia is present pre-symptomatically in frontotemporal dementia due to MAPT mutations. Journal of Neurology, doi:10.1007/s00415-022-11068-0
Poos, J.M., Moore, K.M., Nicholas, J., Russell, L.L., Peakman, G., Convery, R.S., ...Papma, J.M. (2022). Cognitive composites for genetic frontotemporal dementia: GENFI-Cog. Alzheimer's Research & Therapy, 14 (1), doi:10.1186/s13195-022-00958-0
Keshavan, A., O'Shea, F., Chapman, M.D., Hart, M.S., Lunn, M.P., Paterson, R.W., ...Zetterberg, H. (2022). CSF biomarkers for dementia.. Practical Neurology, doi:10.1136/practneurol-2021-003310
Woollacott, I.O.C., Swift, I.J., Sogorb-Esteve, A., Heller, C., Knowles, K., Bouzigues, A., ...Convery, R. (2022). CSF glial markers are elevated in a subset of patients with genetic frontotemporal dementia. Annals of Clinical and Translational Neurology, doi:10.1002/acn3.51672
McCarthy, J., Borroni, B., Sanchez-Valle, R., Moreno, F., Laforce, R., Graff, C., ...Masellis, M. (2022). Data-driven staging of genetic frontotemporal dementia using multi-modal MRI. HUMAN BRAIN MAPPING, 43 (6), 1821-1835. doi:10.1002/hbm.25727
Wilson, K.M., Katona, E., Glaria, I., Carcolé, M., Swift, I.J., Sogorb-Esteve, A., ...Keshavan, A. (2022). Development of a sensitive trial-ready poly(GP) CSF biomarker assay for C9orf72-associated frontotemporal dementia and amyotrophic lateral sclerosis. Journal of Neurology, Neurosurgery & Psychiatry, doi:10.1136/jnnp-2021-328710
Sogorb-Esteve, A., Nilsson, J., Swift, I., Heller, C., Russell, L., Peakman, G., ...Borroni, B. (2022). Differential Impairment Of Cerebrospinal Fluid Synaptic Biomarkers In The Genetic Forms Of Frontotemporal Dementia.
Sogorb-Esteve, A., Nilsson, J., Swift, I.J., Heller, C., Bocchetta, M., Russell, L.L., ...Seelaar, H. (2022). Differential impairment of cerebrospinal fluid synaptic biomarkers in the genetic forms of frontotemporal dementia. Alzheimer's Research & Therapy, 14 doi:10.1186/s13195-022-01042-3
van der Ende, E.L., Heller, C., Sogorb-Esteve, A., Swift, I.J., McFall, D., Peakman, G., ...Panman, J.L. (2022). Elevated CSF and plasma complement proteins in genetic frontotemporal dementia: results from the GENFI study. Journal of Neuroinflammation, 19 (1), 217. doi:10.1186/s12974-022-02573-0
Foster, P.H., Russell, L.L., Peakman, G., Convery, R.S., Bouzigues, A., Greaves, C.V., ...Jiskoot, L.C. (2022). Examining empathy deficits across familial forms of frontotemporal dementia within the GENFI cohort. Cortex, doi:10.1016/j.cortex.2022.01.012
Tookey, S., Greaves, C.V., Rohrer, J.D., Desai, R., Stott, J. (2022). Exploring experiences and needs of spousal carers of people with behavioural variant frontotemporal dementia (bvFTD) including those with familial FTD (fFTD): a qualitative study. BMC Geriatrics, 22 (1), doi:10.1186/s12877-022-02867-1
Schönecker, S., Martinez-Murcia, F.J., Rauchmann, B.-.S., Franzmeier, N., Prix, C., Wlasich, E., ...Laforce, R. (2022). Frequency and Longitudinal Course of Motor Signs In Genetic Frontotemporal Dementia.. Neurology, 10.1212/WNL.0000000000200. doi:10.1212/WNL.0000000000200828
Bruffaerts, R., Gors, D., Bárcenas Gallardo, A., Vandenbulcke, M., Van Damme, P., Suetens, P., ...Moreno, F. (2022). Hierarchical spectral clustering reveals brain size and shape changes in asymptomatic carriers of C9orf72. Brain Communications, 4 (4), doi:10.1093/braincomms/fcac182
Shapiro, N.L., Todd, E.G., Billot, B., Cash, D.M., Iglesias, J.E., Warren, J.D., ...Bocchetta, M. (2022). In vivo hypothalamic regional volumetry across the frontotemporal dementia spectrum. NeuroImage: Clinical, 35 doi:10.1016/j.nicl.2022.103084
Samra, K., MacDougall, A.M., Bouzigues, A., Bocchetta, M., Cash, D.M., Greaves, C.V., ...Jiskoot, L. (2022). Language impairment in the genetic forms of behavioural variant frontotemporal dementia. Journal of Neurology, doi:10.1007/s00415-022-11512-1
Samra, K., MacDougall, A., Bouzigues, A., Bocchetta, M., Cash, D., Greaves, C., ...Moreno, F. (2022). Language Impairment in the Genetic Forms of Behavioural Variant Frontotemporal Dementia. .
Poos, J.M., MacDougall, A., van den Berg, E., Jiskoot, L.C., Papma, J.M., van der Ende, E.L., ...Convery, R. (2022). Longitudinal Cognitive Changes in Genetic Frontotemporal Dementia Within the GENFI Cohort. Neurology, doi:10.1212/WNL.0000000000200384
Pérez-Millan, A., Borrego-Écija, S., van Swieten, J.C., Jiskoot, L., Moreno, F., Laforce, R., ...Rowe, J.B. (2022). Loss of brainstem white matter predicts onset and motor neuron symptoms in C9orf72 expansion carriers: a GENFI study. Journal of Neurology, doi:10.1007/s00415-022-11435-x
Samra, K., MacDougall, A.M., Peakman, G., Bouzigues, A., Bocchetta, M., Cash, D.M., ...Jiskoot, L. (2022). Motor symptoms in genetic frontotemporal dementia: developing a new module for clinical rating scales. Journal of Neurology, doi:10.1007/s00415-022-11442-y
Shafiei, G., Bazinet, V., Dadar, M., Manera, A.L., Collins, D.L., Dagher, A., ...Laforce, R. (2022). Network structure and transcriptomic vulnerability shape atrophy in frontotemporal dementia. Brain, doi:10.1093/brain/awac069
Finger, E., Malik, R., Bocchetta, M., Coleman, K., Graff, C., Borroni, B., ...Russell, L.L. (2022). Neurodevelopmental effects of genetic frontotemporal dementia in young adult mutation carriers.. Brain, doi:10.1093/brain/awac446
Chelban, V., Nikram, E., Perez-Soriano, A., Wilke, C., Foubert-Samier, A., Vijiaratnam, N., ...Gonzalez, M. (2022). Neurofilament light levels predict clinical progression and death in multiple system atrophy.. Brain, doi:10.1093/brain/awac253
Shribman, S., Burrows, M., Convery, R., Bocchetta, M., Sudre, C.H., Acosta‐Cabronero, J., ...Bandmann, O. (2022). Neuroimaging Correlates of Cognitive Deficits in Wilson's Disease. Movement Disorders, doi:10.1002/mds.29123
Requena-Komuro, M.-.C., Jiang, J., Dobson, L., Benhamou, E., Russell, L., Bond, R., ...Rohrer, J. (2022). Neuropsychological assessments for dementia research in the COVID-19 era: comparing remote and face-to-face testing.
Harper, L., Lindberg, O., Bocchetta, M., Todd, E.G., Strandberg, O., van Westen, D., ...Hansson, O. (2022). Prenatal Gyrification Pattern Affects Age at Onset in Frontotemporal Dementia.. Cereb Cortex, doi:10.1093/cercor/bhab457
Chokesuwattanaskul, A., Marshall, C.R., Van Harskamp, N., Houlden, H., Rohrer, J., Hardy, C.J.D., Warren, J.D. (2022). Primary progressive aphasia: ReADing the clinical GRANularity. Practical Neurology, doi:10.1136/practneurol-2022-003460
Drazich-Taylor, E.H.S., Todd, E., Convery, R., Bocchetta, M., Clarke, M., Warren, J.D., ...Rohrer, J.D. (2022). Q351R MAPT mutation is associated with a mixed 3R/4R tauopathy and a slowly progressive cognitive, behavioural and parkinsonian syndrome.. Journal of Neurology, Neurosurgery and Psychiatry, doi:10.1136/jnnp-2022-329330
Requena-Komuro, M.-.C., Jiang, J., Dobson, L., Benhamou, E., Russell, L., Bond, R.L., ...Rohrer, J.D. (2022). Remote versus face-to-face neuropsychological testing for dementia research: a comparative study in people with Alzheimer's disease, frontotemporal dementia and healthy older individuals. BMJ Open, 12 (11), doi:10.1136/bmjopen-2022-064576
Gazzina, S., Grassi, M., Premi, E., Alberici, A., Benussi, A., Archetti, S., ...Todd, E.G. (2022). Structural brain splitting is a hallmark of Granulin-related Frontotemporal Dementia. Neurobiology of Aging, doi:10.1016/j.neurobiolaging.2022.02.009
Moore, K., Convery, R.S., Rohrer, J.D. (2022). Study protocol: computerised cognitive testing in a cohort of people with frontotemporal dementia. BMJ Open, 12 (8), doi:10.1136/bmjopen-2021-055211
Whiteside, D.J., Malpetti, M., Jones, P.S., Ghosh, B.C.P., Coyle-Gilchrist, I., van Swieten, J.C., ...Sanchez-Valle, R. (2022). Temporal dynamics predict symptom onset and cognitive decline in familial frontotemporal dementia. Alzheimer's & Dementia, doi:10.1002/alz.12824
Staffaroni, A.M., Quintana, M., Wendelberger, B., Heuer, H.W., Russell, L.L., Cobigo, Y., ...Gendron, T.F. (2022). Temporal order of clinical and biomarker changes in familial frontotemporal dementia.. Nat Med, doi:10.1038/s41591-022-01942-9
Bocchetta, M., Todd, E.G., Tse, N.Y., Devenney, E.M., Tu, S., Caga, J., ...Piguet, O. (2022). Thalamic and Cerebellar Regional Involvement across the ALS–FTD Spectrum and the Effect of C9orf72. Brain Sciences, 12 (3), doi:10.3390/brainsci12030336
Nelson, A., Russell, L.L., Peakman, G., Convery, R.S., Bouzigues, A., Greaves, C., ...Jiskoot, L. (2022). The CBI-R detects early behavioural impairment in genetic frontotemporal dementia. Annals of Clinical and Translational Neurology, doi:10.1002/acn3.51544
Belder, C.R.S., Chokesuwattanaskul, A., Marshall, C.R., Hardy, C.J.D., Rohrer, J.D., Warren, J.D. (2022). The problematic syndrome of right temporal lobe atrophy: Unweaving the phenotypic rainbow. Frontiers in Neurology, 13 doi:10.3389/fneur.2022.1082828
Zetterberg, H., Teunissen, C., van Swieten, J., Kuhle, J., Boxer, A., Rohrer, J.D., ...McCaughey, S.M. (2022). The role of neurofilament light in genetic frontotemporal lobar degeneration. Brain Communications, doi:10.1093/braincomms/fcac310
Mok, T.H., Nihat, A., Majbour, N., Sequeira, D., Holm-Mercer, L., Coysh, T., ...Orrù, C. (2022). Trajectories of neurodegeneration and seed amplification biomarkers prior to disease onset in individuals at risk of prion disease.

2021

Gordon, E., Bocchetta, M., Nicholas, J., Cash, D.M., Rohrer, J.D. (2021). A comparison of automated atrophy measures across the frontotemporal dementia spectrum: Implications for trials. NeuroImage: Clinical, 32 doi:10.1016/j.nicl.2021.102842
van der Ende, E.L., Bron, E.E., Poos, J.M., Jiskoot, L.C., Panman, J.L., Papma, J.M., ...Synofzik, M. (2021). A data-driven disease progression model of fluid biomarkers in genetic frontotemporal dementia.. Brain, doi:10.1093/brain/awab382
Bergstrom, S., Oijerstedt, L., Remnestal, J., Olofsson, J., Ullgren, A., Seelaar, H., ...Moreno, F. (2021). A panel of CSF proteins separates genetic frontotemporal dementia from presymptomatic mutation carriers: a GENFI study. Molecular Neurodegeneration, 16 (1), doi:10.1186/s13024-021-00499-4
Lux, D., Wu, L., Ling, H., Warner, T., Lees, A., Revesz, T., ...Morris, H. (2021). An evaluation of the application of clinical research criteria for corticobasal degeneration in a large clinico-pathological series.
Bussy, A., Levy, J., Best, T., Patel, R., Cupo, L., Van Langenhove, T., ...Remes, A. (2021). Cerebellar and subcortical atrophy contribute to psychiatric symptoms in frontotemporal dementia. .
Young, A.L., Bocchetta, M., Russell, L.L., Convery, R.S., Peakman, G., Todd, E., ...Jiskoot, L. (2021). Characterizing the Clinical Features and Atrophy Patterns of MAPT-Related Frontotemporal Dementia With Disease Progression Modeling. Neurology, doi:10.1212/WNL.0000000000012410
Poos, J., Moore, K., Nicholas, J., Russell, L., Peakman, G., Convery, R., ...Papma, J. (2021). Cognitive Composites for Genetic Frontotemporal Dementia: GENFI-Cog.
Peakman, G., Russell, L.L., Convery, R.S., Nicholas, J.M., van Swieten, J.C., Jiskoot, L.C., ...Graff, C. (2021). Comparison of clinical rating scales in genetic frontotemporal dementia within the GENFI cohort. Journal of Neurology, Neurosurgery and Psychiatry, doi:10.1136/jnnp-2021-326868
Benussi, A., Alberici, A., Samra, K., Russell, L.L., Greaves, C.V., Bocchetta, M., ...Galimberti, D. (2021). Conceptual framework for the definition of preclinical and prodromal frontotemporal dementia. Alzheimer's & Dementia, doi:10.1002/alz.12485
Benhamou, E., Zhao, S., Sivasathiaseelan, H., Johnson, J.C.S., Requena-Komuro, M.-.C., Bond, R.L., ...Nelson, A. (2021). Decoding expectation and surprise in dementia: the paradigm of music. Brain Communications, 3 (3), doi:10.1093/braincomms/fcab173
Wilson, K., Katona, E., Glaria, I., Swift, I., Sogorb-Esteve, A., Heller, C., ...Mohapatra, S. (2021). Development of a sensitive trial-ready poly(GP) CSF biomarker assay for C9orf72-associated frontotemporal dementia and amyotrophic lateral sclerosis.
Sogorb-Esteve, A., Swift, I.J., Woollacott, I.O.C., Warren, J.D., Zetterberg, H., Rohrer, J.D. (2021). Differential chemokine alteration in the variants of primary progressive aphasia-a role for neuroinflammation. Journal of Neuroinflammation, 18 (1), doi:10.1186/s12974-021-02247-3
Bocchetta, M., Todd, E.G., Peakman, G., Cash, D.M., Convery, R.S., Russell, L.L., ...Jiskoot, L.C. (2021). Differential early subcortical involvement in genetic FTD within the GENFI cohort. NeuroImage: Clinical, 102646. doi:10.1016/j.nicl.2021.102646
Sogorb-Esteve, A., Colas, R.A., Dalli, J., Rohrer, J.D. (2021). Differential Lipid Mediator Involvement in the Different Forms of Genetic Frontotemporal Dementia: Novel Insights into Neuroinflammation.. J Alzheimers Dis, doi:10.3233/JAD-210559
Borrego-Écija, S., Sala-Llonch, R., van Swieten, J., Borroni, B., Moreno, F., Masellis, M., ...Laforce, R. (2021). Disease-related cortical thinning in presymptomatic granulin mutation carriers.. Neuroimage Clin, 29 102540. doi:10.1016/j.nicl.2020.102540
Premi, E., Giunta, M., Iraji, A., Rachakonda, S., Calhoun, V.D., Gazzina, S., ...Bocchetta, M. (2021). Dissemination in time and space in presymptomatic granulin mutation carriers: a GENFI spatial chronnectome study. Neurobiology of Aging, 108 155-167. doi:10.1016/j.neurobiolaging.2021.09.001
Clarke, M.T.M., St-Onge, F., Beauregard, J.M., Bocchetta, M., Todd, E., Cash, D.M., ...Laforce, R. (2021). Early anterior cingulate involvement is seen in presymptomatic MAPT P301L mutation carriers. Alzheimer's Research and Therapy, 13 (1), doi:10.1186/s13195-021-00777-9
Seto-Salvia, N., Esteras, N., de Silva, R., de Pablo-Fernandez, E., Arber, C., Toomey, C.E., ...Abramov, A.Y. (2021). Elevated 4R-tau in astrocytes from asymptomatic carriers of the MAPT 10+16 intronic mutation. Journal of Cellular and Molecular Medicine, doi:10.1111/jcmm.17136
Thompson, A.G.B., Anastasiadis, P., Druyeh, R., Whitworth, I., Nayak, A., Nihat, A., ...Rohrer, J. (2021). Evaluation of plasma tau and neurofilament light chain biomarkers in a 12-year clinical cohort of human prion diseases. Molecular Psychiatry, doi:10.1038/s41380-021-01045-w
Tookey, S., Greaves, C., Rohrer, J., Desai, R., Stott, J. (2021). Exploring Experiences and Needs of Spousal Carers of People with Behavioural variant Frontotemporal Dementia (bvFTD) including those with familial FTD (fFTD): A Qualitative Study.
Russell, L.L., Greaves, C.V., Convery, R.S., Bocchetta, M., Warren, J.D., Kaski, D., Rohrer, J.D. (2021). Eye movements in frontotemporal dementia: Abnormalities of fixation, saccades and anti-saccades. Alzheimer's & Dementia: Translational Research & Clinical Interventions, 7 (1), doi:10.1002/trc2.12218
Koriath, C.A.M., Kenny, J., Ryan, N.S., Rohrer, J.D., Schott, J.M., Houlden, H., ...Mead, S. (2021). Genetic testing in dementia — utility and clinical strategies. Nature Reviews Neurology, doi:10.1038/s41582-020-00416-1
Shafiei, G., Bazinet, V., Dadar, M., Manera, A., Collins, L., Dagher, A., ...Laforce, R. (2021). Global network structure and local transcriptomic vulnerability shape atrophy in sporadic and genetic behavioral variant frontotemporal dementia.
Poos, J.M., Russell, L.L., Peakman, G., Bocchetta, M., Greaves, C.V., Jiskoot, L.C., ...van den Berg, E. (2021). Impairment of episodic memory in genetic frontotemporal dementia: A GENFI study.. Alzheimer's and Dementia: Diagnosis, Assessment and Disease Monitoring, 13 (1), e12185. doi:10.1002/dad2.12185
Sivasathiaseelan, H., Marshall, C.R., Benhamou, E., van Leeuwen, J.E.P., Bond, R.L., Russell, L.L., ...Frost, C. (2021). Laughter as a paradigm of socio-emotional signal processing in dementia. Cortex, doi:10.1016/j.cortex.2021.05.020
Bocchetta, M., Malpetti, M., Todd, E.G., Rowe, J.B., Rohrer, J.D. (2021). Looking beneath the surface: the importance of subcortical structures in frontotemporal dementia. Brain Communications, doi:10.1093/braincomms/fcab158
Panman, J.L., Venkatraghavan, V., van der Ende, E.L., Steketee, R.M.E., Jiskoot, L.C., Poos, J.M., ...Rombouts, S.A.R.B. (2021). Modelling the cascade of biomarker changes in GRN-related frontotemporal dementia.. J Neurol Neurosurg Psychiatry, doi:10.1136/jnnp-2020-323541
Manera, A.L., Dadar, M., Van Swieten, J.C., Borroni, B., Sanchez-Valle, R., Moreno, F., ...Galimberti, D. (2021). MRI data-driven algorithm for the diagnosis of behavioural variant frontotemporal dementia.. J Neurol Neurosurg Psychiatry, doi:10.1136/jnnp-2020-324106
Shribman, S., Bocchetta, M., Sudre, C.H., Acosta-Cabronero, J., Burrows, M., Cook, P., ...Bandmann, O. (2021). Neuroimaging correlates of brain injury in Wilson's disease: a multimodal, whole-brain MRI study.. Brain, doi:10.1093/brain/awab274
Russell, L.L., Greaves, C.V., Convery, R.S., Nicholas, J., Warren, J.D., Kaski, D., Rohrer, J.D. (2021). Novel instructionless eye tracking tasks identify emotion recognition deficits in frontotemporal dementia.. Alzheimers Res Ther, 13 (1), 39. doi:10.1186/s13195-021-00775-x
Dewan, R., Chia, R., Ding, J., Hickman, R.A., Stein, T.D., Abramzon, Y., ...Tucci, A. (2021). Pathogenic Huntingtin Repeat Expansions in Patients with Frontotemporal Dementia and Amyotrophic Lateral Sclerosis.. Neuron, doi:10.1016/j.neuron.2020.11.005
Mahoney, C.J., Ahmed, R.M., Huynh, W., Tu, S., Rohrer, J.D., Bedlack, R.S., ...Kiernan, M.C. (2021). Pathophysiology and Treatment of Non-motor Dysfunction in Amyotrophic Lateral Sclerosis. CNS DRUGS, 35 (5), 483-505. doi:10.1007/s40263-021-00820-1
Rojas, J.C., Wang, P., Staffaroni, A.M., Heller, C., Cobigo, Y., Wolf, A., ...Fong, J.C. (2021). Plasma Neurofilament Light for Prediction of Disease Progression in Familial Frontotemporal Lobar Degeneration. Neurology, doi:10.1212/WNL.0000000000011848
Öijerstedt, L., Andersson, C., Jelic, V., van Swieten, J.C., Jiskoot, L.C., Seelaar, H., ...Laforce, R. (2021). Practice effects in genetic frontotemporal dementia and at-risk individuals: a GENFI study. Journal of neurology, neurosurgery, and psychiatry, doi:10.1136/jnnp-2021-327005
El-Wahsh, S., Finger, E.C., Piguet, O., Mok, V., Rohrer, J.D., Kiernan, M.C., Ahmed, R.M. (2021). Predictors of survival in frontotemporal lobar degeneration syndromes. Journal of Neurology, Neurosurgery and Psychiatry, doi:10.1136/jnnp-2020-324349
Benussi, A., Premi, E., Gazzina, S., Brattini, C., Bonomi, E., Alberici, A., ...Moreno, F. (2021). Progression of Behavioral Disturbances and Neuropsychiatric Symptoms in Patients With Genetic Frontotemporal Dementia.. JAMA Netw Open, 4 (1), e2030194. doi:10.1001/jamanetworkopen.2020.30194
Barbier, M., Camuzat, A., Hachimi, K.E., Guegan, J., Rinaldi, D., Lattante, S., ...Antonell, A. (2021). SLITRK2, an X-linked modifier of the age at onset in C9orf72 frontotemporal lobar degeneration. Brain, 144 (9), 2798-2811. doi:10.1093/brain/awab171
Tookey, S.A., Greaves, C.V., Rohrer, J.D., Stott, J. (2021). Specific support needs and experiences of carers of people with frontotemporal dementia: A systematic review.. Dementia, 14713012211022982. doi:10.1177/14713012211022982
Wilke, C., Reich, S., van Swieten, J.C., Borroni, B., Sanchez-Valle, R., Moreno, F., ...Rowe, J.B. (2021). Stratifying the presymptomatic phase of genetic frontotemporal dementia by serum NfL and pNfH: a longitudinal multicentre study. Annals of Neurology, doi:10.1002/ana.26265
Johnson, J.C.S., McWhirter, L., Hardy, C.J.D., Crutch, S.J., Marshall, C.R., Mummery, C.J., ...Weil, R.S. (2021). Suspecting dementia: canaries, chameleons and zebras.. Practical Neurology, doi:10.1136/practneurol-2021-003019
Ahmed, R.M., Bocchetta, M., Todd, E.G., Tse, N.Y., Devenney, E.M., Tu, S., ...Irish, M. (2021). Tackling clinical heterogeneity across the Amyotrophic Lateral Sclerosis-Frontotemporal Dementia spectrum using a transdiagnostic approach. Brain Communications, doi:10.1093/braincomms/fcab257
Rohrer, J.D., Boxer, A.L. (2021). The Frontotemporal Dementia Prevention Initiative: Linking Together Genetic Frontotemporal Dementia Cohort Studies.. In (pp. 113-121). .
Franklin, H.D., Russell, L.L., Peakman, G., Greaves, C.V., Bocchetta, M., Nicholas, J., ...van Swieten, J. (2021). The Revised Self-Monitoring Scale detects early impairment of social cognition in genetic frontotemporal dementia within the GENFI cohort. Alzheimer's Research & Therapy, 13 (1), doi:10.1186/s13195-021-00865-w

2020

Adams-Carr, K.L., Bocchetta, M., Neason, M., Holton, J.L., Lashley, T., Warren, J.D., Rohrer, J.D. (2020). A case of TDP-43 type C pathology presenting as nonfluent variant primary progressive aphasia.. Neurocase, 1-6. doi:10.1080/13554794.2019.1690665
de Pablo-Fernández, E., González-Herrero, B., Cerdán Santacruz, D., Rossor, M.N., Schott, J.M., Lashley, T., ...Warren, J.D. (2020). A Clinicopathologic Study of Movement Disorders in Frontotemporal Lobar Degeneration.. Mov Disord, doi:10.1002/mds.28356
Moore, K., Convery, R., Bocchetta, M., Neason, M., Cash, D.M., Greaves, C., ...van Swieten, J. (2020). A modified Camel and Cactus Test detects presymptomatic semantic impairment in genetic frontotemporal dementia within the GENFI cohort.. Applied Neuropsychology: Adult, 1-8. doi:10.1080/23279095.2020.1716357
Convery, R.S., Bocchetta, M., Greaves, C.V., Moore, K.M., Cash, D.M., Van Swieten, J., ...Laforce, R. (2020). Abnormal pain perception is associated with thalamo-cortico-striatal atrophy in C9orf72 expansion carriers in the GENFI cohort.. J Neurol Neurosurg Psychiatry, doi:10.1136/jnnp-2020-323279
Jimenez, D.A., Bond, R.L., Requena-Komuro, M.-.C., Sivasathiaseelan, H., Marshall, C.R., Russell, L.L., ...Shafei, R. (2020). Altered phobic reactions in frontotemporal dementia: a behavioural and neuroanatomical analysis. Cortex, doi:10.1016/j.cortex.2020.05.016
Requena-Komuro, M.-.C., Marshall, C.R., Bond, R.L., Russell, L.L., Greaves, C., Moore, K.M., ...Hardy, C.J.D. (2020). Altered Time Awareness in Dementia. Frontiers in Neurology, 11 291. doi:10.3389/fneur.2020.00291
Altmann, A., Cash, D.M., Bocchetta, M., Heller, C., Reynolds, R., Moore, K., ...Moreno, F. (2020). Analysis of brain atrophy and local gene expression in genetic frontotemporal dementia. Brain Communications, doi:10.1093/braincomms/fcaa122
Malpetti, M., Jones, P.S., Tsvetanov, K.A., Rittman, T., van Swieten, J.C., Borroni, B., ...Graff, C. (2020). Apathy in presymptomatic genetic frontotemporal dementia predicts cognitive decline and is driven by structural brain changes. Alzheimer's and Dementia, doi:10.1002/alz.12252
Zimmerer, V., Hardy, C., Eastman, J., Dutta, S., Varnet, L., Bond, R., ...Varley, R. (2020). Automated profiling of spontaneous speech in primary progressive aphasia and behavioral-variant frontotemporal dementia: An approach based on usage-frequency. Cortex,
Billot, B., Bocchetta, M., Todd, E., Dalca, A.V., Rohrer, J.D., Iglesias, J.E. (2020). Automated segmentation of the Hypothalamus and associated subunits in brain MRI.. Neuroimage, 117287. doi:10.1016/j.neuroimage.2020.117287
Convery, R.S., Neason, M., Cash, D.M., Cardoso, M.J., Modat, M., Ourselin, S., ...Bocchetta, M. (2020). Basal forebrain atrophy in frontotemporal dementia. NeuroImage: Clinical, 102210. doi:10.1016/j.nicl.2020.102210
Tsvetanov, K.A., Gazzina, S., Jones, P.S., van Swieten, J., Borroni, B., Sanchez-Valle, R., ...Synofzik, M. (2020). Brain functional network integrity sustains cognitive function despite atrophy in presymptomatic genetic frontotemporal dementia.. Alzheimers Dement, doi:10.1002/alz.12209
Woollacott, I.O.C., Nicholas, J.M., Heller, C., Foiani, M.S., Moore, K.M., Russell, L.L., ...Warren, J.D. (2020). Cerebrospinal Fluid YKL-40 and Chitotriosidase Levels in Frontotemporal Dementia Vary by Clinical, Genetic and Pathological Subtype.. Dement Geriatr Cogn Disord, 1-21. doi:10.1159/000506282
Mansur, A., Rabiner, E.A., Comley, R.A., Lewis, Y., Middleton, L.T., Huiban, M., ...Martarello, L. (2020). Characterization of 3 PET Tracers for Quantification of Mitochondrial and Synaptic Function in Healthy Human Brain: F-18-BCPP-EF, C-11-SA-4503, and C-11-UCB-J. JOURNAL OF NUCLEAR MEDICINE, 61 (1), 96-103. doi:10.2967/jnumed.119.228080
Miki, Y., Ling, H., Crampsie, S., Mummery, C.J., Rohrer, J.D., Jaunmuktane, Z., ...Holton, J.L. (2020). Corticospinal tract degeneration and temporal lobe atrophy in frontotemporal lobar degeneration TDP-43 type C pathology.. Neuropathology and Applied Neurobiology, doi:10.1111/nan.12582
Tavares, T.P., Mitchell, D.G.V., Coleman, K.K., Coleman, B.L., Shoesmith, C.L., Butler, C.R., ...de Mendonca, A. (2020). Early symptoms in symptomatic and preclinical genetic frontotemporal lobar degeneration.. J Neurol Neurosurg Psychiatry, doi:10.1136/jnnp-2020-322987
Thompson, P.M., Jahanshad, N., Ching, C.R.K., Salminen, L.E., Thomopoulos, S.I., Bright, J., ...Bruin, W.B. (2020). ENIGMA and global neuroscience: A decade of large-scale studies of the brain in health and disease across more than 40 countries.. Transl Psychiatry, 10 (1), 100. doi:10.1038/s41398-020-0705-1
Le Blanc, G., Jetté Pomerleau, V., McCarthy, J., Borroni, B., van Swieten, J., Galimberti, D., ...Synofzik, M. (2020). Faster Cortical Thinning and Surface Area Loss in Presymptomatic and Symptomatic C9orf72 Repeat Expansion Adult Carriers.. Ann Neurol, doi:10.1002/ana.25748
Swift, I.J., Sogorb-Esteve, A., Heller, C., Synofzik, M., Otto, M., Graff, C., ...Van Der Ende, E.L. (2020). Fluid biomarkers in frontotemporal dementia: Past, present and future. Journal of Neurology, Neurosurgery and Psychiatry, doi:10.1136/jnnp-2020-323520
Bocchetta, M., Rohrer, J. (2020). Frontotemporal dementia. In Dening, T., Thomas, A., Stewart, R., Taylor, J.-.P. (Eds.), Oxford Textbook of Old Age Psychiatry. Oxford University Press.
Johnson, J.C.S., Jiang, J., Bond, R.L., Benhamou, E., Requena‐Komuro, M., Russell, L.L., ...Marshall, C.R. (2020). Impaired phonemic discrimination in logopenic variant primary progressive aphasia. Annals of Clinical and Translational Neurology, doi:10.1002/acn3.51101
Bocchetta, M., Iglesias Espinosa, M.D.M., Lashley, T., Warren, J.D., Rohrer, J.D. (2020). In vivo staging of frontotemporal lobar degeneration TDP-43 type C pathology. Alzheimer's Research & Therapy, 12 (1), doi:10.1186/s13195-020-00600-x
Rajewsky, N., Almouzni, G., Gorski, S.A., Aerts, S., Amit, I., Bertero, M.G., ...Chiocca, S. (2020). LifeTime and improving European healthcare through cell-based interceptive medicine. Nature, doi:10.1038/s41586-020-2715-9
Woollacott, I.O.C., Toomey, C.E., Strand, C., Courtney, R., Benson, B.C., Rohrer, J.D., Lashley, T. (2020). Microglial burden, activation and dystrophy patterns in frontotemporal lobar degeneration.. J Neuroinflammation, 17 (1), 234. doi:10.1186/s12974-020-01907-0
Magen, I., Yacovzada, N.-.S., Warren, J., Heller, C., Swift, I., Bobeva, Y., ...Fratta, P. (2020). microRNA-based predictor for diagnosis of frontotemporal dementia. .
van der Ende, E.L., Xiao, M., Xu, D., Poos, J.M., Panman, J.L., Jiskoot, L.C., ...Heller, C. (2020). Neuronal pentraxin 2: a synapse-derived CSF biomarker in genetic frontotemporal dementia.. J Neurol Neurosurg Psychiatry, doi:10.1136/jnnp-2019-322493
Boxer, A.L., Gold, M., Feldman, H., Boeve, B.F., Dickinson, S.L.-.J., Fillit, H., ...Sutherland, M. (2020). New directions in clinical trials for frontotemporal lobar degeneration: Methods and outcome measures.. Alzheimer's and Dementia, doi:10.1016/j.jalz.2019.06.4956
Heller, C., Chan, E., Foiani, M.S., Todd, E., Russell, L.L., Greaves, C.V., ...Bocchetta, M. (2020). Plasma glial fibrillary acidic protein and neurofilament light chain are measures of disease severity in semantic variant primary progressive aphasia. Journal of Neurology, Neurosurgery & Psychiatry, doi:10.1136/jnnp-2020-325085
Heller, C., Foiani, M.S., Moore, K., Convery, R., Bocchetta, M., Neason, M., ...Woollacott, I.O.C. (2020). Plasma glial fibrillary acidic protein is raised in progranulin-associated frontotemporal dementia. Journal of Neurology, Neurosurgery & Psychiatry, doi:10.1136/jnnp-2019-321954
Shribman, S., Heller, C., Burrows, M., Heslegrave, A., Swift, I., Foiani, M.S., ...Gerhard, A. (2020). Plasma Neurofilament Light as a Biomarker of Neurological Involvement in Wilson's Disease. Movement Disorders, doi:10.1002/mds.28333
Russell, L.L., Greaves, C.V., Bocchetta, M., Nicholas, J., Convery, R.S., Moore, K., ...Moreno, F. (2020). Social cognition impairment in genetic frontotemporal dementia within the GENFI cohort. Cortex, doi:10.1016/j.cortex.2020.08.023
Bauermeister, S., Orton, C., Thompson, S., Barker, R.A., Bauermeister, J.R., Ben-Shlomo, Y., ...Calvin, C. (2020). The Dementias Platform UK (DPUK) Data Portal. European Journal of Epidemiology, doi:10.1007/s10654-020-00633-4
Benhamou, E., Marshall, C.R., Russell, L.L., Hardy, C.J.D., Bond, R.L., Sivasathiaseelan, H., ...Warren, J.D. (2020). The neurophysiological architecture of semantic dementia: spectral dynamic causal modelling of a neurodegenerative proteinopathy.. Sci Rep, 10 (1), 16321. doi:10.1038/s41598-020-72847-1
Swift, I., Bocchetta, M., Benotmane, H., Woollacott, I.O.C., Shafei, R., Rohrer, J.D. (2020). Variable clinical phenotype in TBK1 mutations: case report of a novel mutation causing primary progressive aphasia and review of the literature. Neurobiology of Aging, doi:10.1016/j.neurobiolaging.2020.08.014

2019

Clarke, M.T., Woollacott, I., Shafei, R., Moore, K., Greaves, C., Russell, L., ...Rohrer, J. (2019). [11C]PBR28 inflammatory PET imaging in frontotemporal dementia.
Lamb, R., Rohrer, J.D., Real, R., Lubbe, S.J., Waite, A.J., Blake, D.J., ...Holton, J.L. (2019). A novel TBK1 mutation in a family with diverse frontotemporal dementia spectrum disorders.. Cold Spring Harb Mol Case Stud, 5 (3), doi:10.1101/mcs.a003913
Moore, K.M., Nicholas, J., Grossman, M., McMillan, C.T., Irwin, D.J., Massimo, L., ...Rossor, M.N. (2019). Age at symptom onset and death and disease duration in genetic frontotemporal dementia: an international retrospective cohort study. The Lancet Neurology, doi:10.1016/s1474-4422(19)30394-1
Jimenez, D., Bond, R.L., Sivasathiaseelan, H., Russell, L.L., Greaves, C., Moore, K., ...Rohrer, J.D. (2019). ALTERED PHOBIC RESPONSES IN FRONTOTEMPORAL DEMENTIA.
Bocchetta, M., Iglesias, J.E., Cash, D.M., Warren, J.D., Rohrer, J.D. (2019). Amygdala subnuclei are differentially affected in the different genetic and pathological forms of frontotemporal dementia. Alzheimer's and Dementia: Diagnosis, Assessment and Disease Monitoring, 11 136-141. doi:10.1016/j.dadm.2018.12.006
Greaves, C.V., Rohrer, J.D. (2019). An update on genetic frontotemporal dementia.. J Neurol, doi:10.1007/s00415-019-09363-4
Koriath, C., Lashley, T., Taylor, W., Druyeh, R., Dimitriadis, A., Denning, N., ...Schott, J.M. (2019). ApoE4 lowers age at onset in patients with frontotemporal dementia and tauopathy independent of amyloid-β copathology. Alzheimer's & Dementia: Diagnosis, Assessment & Disease Monitoring, 11 277-280. doi:10.1016/j.dadm.2019.01.010
Bocchetta, M., Iglesias, J.E., Chelban, V., Jabbari, E., Lamb, R., Russell, L.L., ...Thomas, D.L. (2019). Automated Brainstem Segmentation Detects Differential Involvement in Atypical Parkinsonian Syndromes. Journal of Movement Disorders, doi:10.14802/jmd.19030
Jabbari, E., Woodside, J., Chelban, V., Costantini, A., Holland, N., Leigh, N., ...Kobylecki, C. (2019). Baseline analysis of PROSPECT-M-UK: a longitudinal study of PSP, CBS and MSA.
Mutsaerts, H.J.M.M., Mirza, S.S., Petr, J., Thomas, D.L., Cash, D.M., Bocchetta, M., ...Robertson, A.D. (2019). Cerebral perfusion changes in presymptomatic genetic frontotemporal dementia: a GENFI study. Brain. A Journal of Neurology, doi:10.1093/brain/awz039
Mutsaerts, H.J.M.M., Mirza, S.S., Petr, J., Thomas, D.L., Cash, D.M., Bocchetta, M., ...Robertson, A.D. (2019). Cerebral perfusion changes in presymptomaticgenetic frontotemporal dementia: a GENFIstudy (vol 142, pg 1108, 2019). BRAIN, 142 doi:10.1093/brain/awz103
Meeter, L.H.H., Steketee, R.M.E., Salkovic, D., Vos, M.E., Grossman, M., McMillan, C.T., ...Olney, N.T. (2019). Clinical value of cerebrospinal fluid neurofilament light chain in semantic dementia.. J Neurol Neurosurg Psychiatry, doi:10.1136/jnnp-2018-319784
Holland, N., Jones, S., Woodside, J., Jabbari, E., Chelban, V., Costantini, A., ...Gerhard, A. (2019). Cortical and subcortical atrophy in typical and variant Parkinson-plus syndromes: PROSPECT-M-UK study.
Clarke, M.T.M., Brinkmalm, A., Foiani, M.S., Woollacott, I.O.C., Heller, C., Heslegrave, A., ...Warren, J.D. (2019). CSF synaptic protein concentrations are raised in those with atypical Alzheimer's disease but not frontotemporal dementia.. Alzheimers Res Ther, 11 (1), 105. doi:10.1186/s13195-019-0564-2
Chelban, V., Woodside, J., Jabbari, E., Lamb, R., Bocchetta, M., Rohrer, J., ...Houlden, H. (2019). DEFINING CLINICAL AND GENETIC BIOMARKERS IN MSA.
Jabbari, E., Holland, N., Chelban, V., Jones, P.S., Lamb, R., Rawlinson, C., ...Heslegrave, A.J. (2019). Diagnosis Across the Spectrum of Progressive Supranuclear Palsy and Corticobasal Syndrome.. JAMA Neurol, doi:10.1001/jamaneurol.2019.4347
Gazzina, S., Grassi, M., Premi, E., Cosseddu, M., Alberici, A., Archetti, S., ...Sanchez-Valle, R. (2019). Education modulates brain maintenance in presymptomatic frontotemporal dementia.. J Neurol Neurosurg Psychiatry, doi:10.1136/jnnp-2019-320439
Hardy, C.J.D., Frost, C., Sivasathiaseelan, H., Johnson, J.C.S., Agustus, J.L., Bond, R.L., ...Rohrer, J.D. (2019). Findings of Impaired Hearing in Patients With Nonfluent/Agrammatic Variant Primary Progressive Aphasia. JAMA Neurology, doi:10.1001/jamaneurol.2018.4799
Zetterberg, H., van Swieten, J.C., Boxer, A.L., Rohrer, J.D. (2019). Fluid biomarkers for frontotemporal dementias.. Neuropathol Appl Neurobiol, doi:10.1111/nan.12530
Sivasathiaseelan, H., Marshall, C.R., Agustus, J.L., Benhamou, E., Bond, R.L., Van Leeuwen, J.E.P., ...Warren, J.D. (2019). Frontotemporal Dementia: A Clinical Review. Seminars in Neurology, 39 (2), 251-263. doi:10.1055/s-0039-1683379
Rittman, T., Borchert, R., Jones, S., van Swieten, J., Borroni, B., Galimberti, D., ...Tagliavini, F. (2019). Functional network resilience to pathology in presymptomatic genetic frontotemporal dementia.. Neurobiol Aging, 77 169-177. doi:10.1016/j.neurobiolaging.2018.12.009
Pottier, C., Ren, Y., Perkerson, R.B., Baker, M., Jenkins, G.D., van Blitterswijk, M., ...Christopher, E. (2019). Genome-wide analyses as part of the international FTLD-TDP whole-genome sequencing consortium reveals novel disease risk factors and increases support for immune dysfunction in FTLD. Acta Neuropathologica, doi:10.1007/s00401-019-01962-9
Swarup, V., Hinz, F.I., Rexach, J.E., Noguchi, K.I., Toyoshiba, H., Oda, A., ...Cheng, C. (2019). Identification of evolutionarily conserved gene networks mediating neurodegenerative dementia. Nature Medicine, doi:10.1038/s41591-018-0223-3
Convery, R.S., Jiao, J., Clarke, M.T.M., Moore, K.M., Koriath, C.A.M., Woollacott, I.O.C., ...Cash, D.M. (2019). Longitudinal (¹⁸F)AV-1451 PET imaging in a patient with frontotemporal dementia due to a Q351R MAPT mutation. Journal of Neurology, Neurosurgery & Psychiatry, doi:10.1136/jnnp-2019-320904
Harrison, I.F., Whitaker, R., Bertelli, P.M., O'Callaghan, J.M., Csincsik, L., Bocchetta, M., ...Murray, T.K. (2019). Optic nerve thinning and neurosensory retinal degeneration in the rTg4510 mouse model of frontotemporal dementia.. Acta Neuropathol Commun, 7 (1), 4. doi:10.1186/s40478-018-0654-6
Foiani, M.S., Jackson-Morgan, T., Cicognola, C., Ermann, N., Ye, K., Kornhuber, J., ...Blennow, K. (2019). Profiling of tauopathies in frontotemporal dementia.
Shafei, R., Toomey, C., Foiani, M., Mills, K., Lashley, T., Rohrer, J. (2019). PROTEOMIC ANALYSIS OF TDP-43 PATHOLOGY IN FRONTOTEMPORAL DEMENTIA.
Foiani, M.S., Cicognola, C., Ermann, N., Woollacott, I.O.C., Heller, C., Heslegrave, A.J., ...Kornhuber, J. (2019). Searching for novel cerebrospinal fluid biomarkers of tau pathology in frontotemporal dementia: an elusive quest.. J Neurol Neurosurg Psychiatry, doi:10.1136/jnnp-2018-319266
Bocchetta, M., Iglesias, J.E., Russell, L., Greaves, C.V., Marshall, C., Scelsi, M.A., ...Rohrer, J. (2019). Segmentation of medial temporal subregions reveals early right-sided involvement in semantic variant PPA. Alzheimer's Research and Therapy, doi:10.1186/s13195-019-0489-9
van der Ende, E.L., Meeter, L.H., Poos, J.M., Panman, J.L., Jiskoot, L.C., Dopper, E.G.P., ...Teunissen, C. (2019). Serum neurofilament light chain in genetic frontotemporal dementia: a longitudinal, multicentre cohort study. The Lancet Neurology, 18 (12), 1103-1111. doi:10.1016/s1474-4422(19)30354-0
Paterson, R.W., Gabelle, A., Lucey, B.P., Barthélemy, N.R., Leckey, C.A., Hirtz, C., ...West, T. (2019). SILK studies - capturing the turnover of proteins linked to neurodegenerative diseases.. Nat Rev Neurol, doi:10.1038/s41582-019-0222-0
Sani, T.P., Bond, R.L., Marshall, C.R., Hardy, C.J.D., Russell, L.L., Moore, K.M., ...Wendi, I.P. (2019). Sleep symptoms in syndromes of frontotemporal dementia and Alzheimer's disease: A proof-of-principle behavioural study. eNeurologicalSci, 17 doi:10.1016/j.ensci.2019.100212
Cury, C., Durrleman, S., Cash, D.M., Lorenzi, M., Nicholas, J.M., Bocchetta, M., ...Masellis, M. (2019). Spatiotemporal analysis for detection of pre-symptomatic shape changes in neurodegenerative diseases: Initial application to the GENFI cohort.. Neuroimage, 188 doi:10.1016/j.neuroimage.2018.11.063
Volkmer, A., Rogalski, E., Henry, M., Taylor-Rubin, C., Ruggero, L., Khayum, R., ...Rohrer, J.D. (2019). Speech and language therapy approaches to managing primary progressive aphasia. Practical Neurology, doi:10.1136/practneurol-2018-001921
Mauricio, R., Benn, C., Davis, J., Dawson, G., Dawson, L.A., Evans, A., ...Isaac, J. (2019). Tackling gaps in developing life-changing treatments for dementia. Alzheimer's & Dementia: Translational Research & Clinical Interventions, 5 241-253. doi:10.1016/j.trci.2019.05.001
Bocchetta, M., Iglesias, J.E., Neason, M., Cash, D.M., Warren, J.D., Rohrer, J.D. (2019). Thalamic nuclei in frontotemporal dementia: Mediodorsal nucleus involvement is universal but pulvinar atrophy is unique to C9orf72. Human Brain Mapping, doi:10.1002/hbm.24856
Marshall, C.R., Hardy, C.J.D., Russell, L.L., Bond, R.L., Sivasathiaseelan, H., Greaves, C., ...Wastling, S.J. (2019). The functional neuroanatomy of emotion processing in frontotemporal dementias.. Brain, doi:10.1093/brain/awz204
Premi, E., Calhoun, V.D., Diano, M., Gazzina, S., Cosseddu, M., Alberici, A., ...van Swieten, J. (2019). The inner fluctuations of the brain in presymptomatic Frontotemporal Dementia: The chronnectome fingerprint. NeuroImage, 189 645-654. doi:10.1016/j.neuroimage.2019.01.080
Desmarais, P., Rohrer, J.D., Nguyen, Q.D., Herrmann, N., Stuss, D.T., Lang, A.E., ...Van Swieten, J.C. (2019). Therapeutic trial design for frontotemporal dementia and related disorders. Journal of Neurology, Neurosurgery and Psychiatry, doi:10.1136/jnnp-2018-318603
Shafei, R., Woollacott, I.O.C., Mummery, C.J., Bocchetta, M., Guerreiro, R., Bras, J., ...Rohrer, J.D. (2019). Two pathologically confirmed cases of novel mutations in the MAPT gene causing frontotemporal dementia. Neurobiology of Aging, doi:10.1016/j.neurobiolaging.2019.11.009
Tavares, T.P., Mitchell, D.G.V., Coleman, K., Shoesmith, C., Bartha, R., Cash, D.M., ...Galimberti, D. (2019). Ventricular volume expansion in presymptomatic genetic frontotemporal dementia.. Neurology, doi:10.1212/WNL.0000000000008386
Sudre, C.H., Bocchetta, M., Heller, C., Convery, R., Neason, M., Moore, K.M., ...Foiani, M. (2019). White matter hyperintensities in progranulin-associated frontotemporal dementia – a longitudinal GENFI study. NeuroImage: Clinical, 102077. doi:10.1016/j.nicl.2019.102077

2018

Zhang, M., Ferrari, R., Tartaglia, M.C., Keith, J., Surace, E.I., Wolf, U., ...Xi, Z. (2018). A C6orf10/LOC101929163 locus is associated with age of onset in C9orf72 carriers.. Brain, doi:10.1093/brain/awy238
Chelban, V., Bocchetta, M., Hassanein, S., Haridy, N.A., Houlden, H., Rohrer, J.D. (2018). An update on advances in magnetic resonance imaging of multiple system atrophy. Journal of Neurology, doi:10.1007/s00415-018-9121-3
Marshall, C.R., Hardy, C.J.D., Allen, M., Russell, L.L., Clark, C.N., Bond, R.L., ...Kilner, J.M. (2018). Cardiac responses to viewing facial emotion differentiate frontotemporal dementias. Annals of Clinical and Translational Neurology, doi:10.1002/acn3.563
Paterson, R.W., Slattery, C.F., Poole, T., Nicholas, J.M., Magdalinou, N.K., Toombs, J., ...Foiani, M.S. (2018). Cerebrospinal fluid in the differential diagnosis of Alzheimer's disease: clinical utility of an extended panel of biomarkers in a specialist cognitive clinic.. Alzheimer's research & therapy, 10 (1), 32. doi:10.1186/s13195-018-0361-3
Meeter, L.H., Steketee, R., Salkovic, D., Vos, M., Grossman, M., McMillan, C., ...Sanchez-Valle, R. (2018). Cerebrospinal fluid neurofilament light chain illustrates that semantic dementia is a distinctive neurodegenerative disease.
Woollacott, I.O.C., Nicholas, J.M., Heslegrave, A., Heller, C., Foiani, M.S., Dick, K.M., ...Fox, N.C. (2018). Cerebrospinal fluid soluble TREM2 levels in frontotemporal dementia differ by genetic and pathological subgroup. Alzheimer's Research and Therapy, 10 (1), doi:10.1186/s13195-018-0405-8
Convery, R., Mead, S., Rohrer, J.D. (2018). Clinical, genetic and neuroimaging features of frontotemporal dementia.. Neuropathol Appl Neurobiol, doi:10.1111/nan.12535
Heywood, W.E., Hallqvist, J., Heslegrave, A.J., Zetterberg, H., Fenoglio, C., Scarpini, E., ...Mills, K. (2018). CSF pro-orexin and amyloid-β38 expression in Alzheimer's disease and frontotemporal dementia.. Neurobiol Aging, 72 171-176. doi:10.1016/j.neurobiolaging.2018.08.019
Bonham, L.W., Karch, C.M., Fan, C.C., Tan, C., Geier, E.G., Wang, Y., ...Barkovich, M.J. (2018). CXCR4 involvement in neurodegenerative diseases.. Translational psychiatry, 8 (1), 73. doi:10.1038/s41398-017-0049-7
Owen, D., Melbourne, A., Eaton-Rosen, Z., Thomas, D.L., Marlow, N., Rohrer, J.D., Ourselin, S. (2018). Deep Convolutional Filtering for Spatio-Temporal Denoising and Artifact Removal in Arterial Spin Labelling MRI..
Sellami, L., Bocchetta, M., Masellis, M., Cash, D.M., Dick, K.M., van Swieten, J., ...Rowe, J.B. (2018). Distinct Neuroanatomical Correlates of Neuropsychiatric Symptoms in the Three Main Forms of Genetic Frontotemporal Dementia in the GENFI Cohort. Journal of Alzheimer's Disease, 1-16. doi:10.3233/JAD-180053
Fumagalli, G.G., Basilico, P., Arighi, A., Bocchetta, M., Dick, K.M., Cash, D.M., ...Pietroboni, A.M. (2018). Distinct patterns of brain atrophy in Genetic Frontotemporal Dementia Initiative (GENFI) cohort revealed by visual rating scales. Alzheimer's Research and Therapy, 10 (1), doi:10.1186/s13195-018-0376-9
Schneider, R., McKeever, P., Kim, T., Graff, C., van Swieten, J.C., Karydas, A., ...Laforce, R. (2018). Downregulation of exosomal miR-204-5p and miR-632 as a biomarker for FTD: a GENFI study.. Journal of Neurology, Neurosurgery and Psychiatry, doi:10.1136/jnnp-2017-317492
Bocchetta, M., Iglesias, J.E., Scelsi, M., Cash, D., Cardoso, M.J., Modat, M., ...Rohrer, J.D. (2018). Hippocampal subfield volumetry: differential pattern of atrophy in different forms of genetic frontotemporal dementia. Journal of Alzheimer's Disease, doi:10.3233/JAD-180195
Broce, I., Karch, C.M., Wen, N., Fan, C.C., Wang, Y., Tan, C.H., ...Muller, U. (2018). Immune-related genetic enrichment in frontotemporal dementia: An analysis of genome-wide association studies. PLOS MEDICINE, 15 (1), doi:10.1371/journal.pmed.1002487
Mahoney, C.J., Simpson, I.J.A., Nicholas, J.M., Rohrer, J.D., Warren, J.D. (2018). LONGITUDINAL DIFFUSION TENSOR IMAGING IN THE PRIMARY PROGRESSIVE APHASIAS.
Lashley, T., Schott, J.M., Weston, P., Murray, C.E., Wellington, H., Keshavan, A., ...Rohrer, J.D. (2018). Molecular biomarkers of Alzheimer's disease: progress and prospects.. Disease models & mechanisms, 11 (5), doi:10.1242/dmm.031781
Marshall, C.R., Hardy, C.J.D., Russell, L.L., Clark, C.N., Bond, R.L., Dick, K.M., ...Rohrer, J.D. (2018). Motor signatures of emotional reactivity in frontotemporal dementia. SCIENTIFIC REPORTS, 8 doi:10.1038/s41598-018-19528-2
Clark, C.N., Golden, H.L., McCallion, O., Nicholas, J.M., Cohen, M.H., Slattery, C.F., ...Rohrer, J.D. (2018). Music models aberrant rule decoding and reward valuation in dementia.. Soc Cogn Affect Neurosci, doi:10.1093/scan/nsx140
Woollacott, I.O.C., Bocchetta, M., Sudre, C.H., Ridha, B.H., Strand, C., Courtney, R., ...Rossor, M.N. (2018). Pathological correlates of white matter hyperintensities in a case of progranulin mutation associated frontotemporal dementia.. Neurocase, 1-9. doi:10.1080/13554794.2018.1506039
Foiani, M.S., Woollacott, I.O., Heller, C., Bocchetta, M., Heslegrave, A., Dick, K.M., ...Schott, J.M. (2018). Plasma tau is increased in frontotemporal dementia.. Journal of Neurology, Neurosurgery and Psychiatry, doi:10.1136/jnnp-2017-317260
Meeter, L.H.H., Gendron, T.F., Sias, A.C., Jiskoot, L.C., Russo, S.P., Donker Kaat, L., ...Dopper, E.G. (2018). Poly(GP), neurofilament and grey matter deficits in C9orf72 expansion carriers.. Annals of Clinical and Translational Neurology, 5 (5), 583-597. doi:10.1002/acn3.559
Pottier, C., Zhou, X., Perkerson, R.B., Baker, M., Jenkins, G.D., Serie, D.J., ...López de Munain, A. (2018). Potential genetic modifiers of disease risk and age at onset in patients with frontotemporal lobar degeneration and GRN mutations: a genome-wide association study.. The Lancet Neurology, doi:10.1016/s1474-4422(18)30126-1
Koriath, C., Kenny, J., ADAMSON, G., Druyeh, R., Taylor, W., Quinn, L., ...Mead, S. (2018). Predictors for a dementia gene mutation based on gene-panel next-generation sequencing of a large dementia referral series. Molecular Psychiatry, doi:10.1038/s41380-018-0224-0
Jiskoot, L.C., Bocchetta, M., Nicholas, J.M., Cash, D.M., Thomas, D., Modat, M., ...Meeter, L.H. (2018). Presymptomatic white matter integrity loss in familial frontotemporal dementia in the GENFI cohort: A cross-sectional diffusion tensor imaging study. Annals of Clinical and Translational Neurology, doi:10.1002/acn3.601
Bergeron, D., Gorno-Tempini, M.L., Rabinovici, G.D., Santos-Santos, M.A., Seeley, W., Miller, B.L., ...van Berckel, B.N.M. (2018). Prevalence of amyloid-β pathology in distinct variants of primary progressive aphasia.. Annals of Neurology, doi:10.1002/ana.25333
Marshall, C.R., Hardy, C.J.D., Volkmer, A., Russell, L.L., Bond, R.L., Fletcher, P.D., ...Rossor, M.N. (2018). Primary progressive aphasia: a clinical approach.. Journal of neurology, doi:10.1007/s00415-018-8762-6
Hardy, C.J.D., Marshall, C.R., Bond, R.L., Russell, L.L., Dick, K., Ariti, C., ...Crutch, S.J. (2018). Retained capacity for perceptual learning of degraded speech in primary progressive aphasia and Alzheimer's disease. Alzheimer's research & therapy, 10 (1), 70. doi:10.1186/s13195-018-0399-2
Hardy, C.J.D., Bond, R.L., Jaisin, K., Marshall, C.R., Russell, L.L., Dick, K., ...Warren, J.D. (2018). Sensitivity of Speech Output to Delayed Auditory Feedback in Primary Progressive Aphasias. Frontiers in Neurology, 9 doi:10.3389/fneur.2018.00894
Bocchetta, M., Gordon, E., Cardoso, M.J., Modat, M., Ourselin, S., Warren, J., Rohrer, J. (2018). Thalamic atrophy in frontotemporal dementia - not just a C9orf72 problem. NeuroImage: Clinical, doi:10.1016/j.nicl.2018.02.019
Semedo, C., Cardoso, M.J., Vos, S.B., Sudre, C.H., Bocchetta, M., Ribbens, A., ...Ourselin, S. (2018). Thalamic nuclei segmentation using tractography, population-specific priors and local fibre orientation.
Young, A., Marinescu, R., Oxtoby, N., Bocchetta, M., Yong, K., Firth, N., ...Cardoso, J. (2018). Uncovering the heterogeneity and temporal complexity of neurodegenerative diseases with Subtype and Stage Inference. Nature Commun, 9 4273. doi:10.1038/s41467-018-05892-0

2017

Kenny, J., Woollacott, I., Koriath, C., Hosszu, L., Adamson, G., Rudge, P., ...Mead, S. (2017). A novel prion protein variant in a patient with semantic dementia.. Journal of neurology, neurosurgery, and psychiatry, doi:10.1136/jnnp-2017-315577
Owen, D., Melbourne, A., Thomas, D.L., Beckmann, J., Rohrer, J., Marlow, N., Ourselin, S. (2017). ADRIMO: Anatomy-DRIven MOdelling of spatial correlation to improve analysis of arterial spin labelling data.
Owen, D., Melbourne, A., Eaton-Rosen, Z., Thomas, D.L., Marlow, N., Rohrer, J., Ourselin, S. (2017). Anatomy-driven modelling of spatial correlation for regularisation of arterial spin labelling images.
Clark, C.N., Nicholas, J.M., Agustus, J.L., Hardy, C.J.D., Russell, L.L., Brotherhood, E.V., ...Rohrer, J.D. (2017). Auditory conflict and congruence in frontotemporal dementia.. Neuropsychologia, doi:10.1016/j.neuropsychologia.2017.08.009
Owen, D., Melbourne, A., Sokolska, M., Thomas, D.L., Rohrer, J., Ourselin, S. (2017). Bayesian experimental design for multi-parametric T1/T2 relaxometry and diffusion.
Hardy, C.J.D., Agustus, J.L., Marshall, C.R., Clark, C.N., Russell, L.L., Bond, R.L., ...Rohrer, J.D. (2017). Behavioural and neuroanatomical correlates of auditory speech analysis in primary progressive aphasias.. Alzheimers Res Ther, 9 (1), 53. doi:10.1186/s13195-017-0278-2
Zetterberg, H., Rohrer, J.D., Schott, J.M. (2017). Cerebrospinal fluid in the dementias.. Handbook of Clinical Neurology, 146 85-97. doi:10.1016/b978-0-12-804279-3.00006-x
Premi, E., Grassi, M., van Swieten, J., Galimberti, D., Graff, C., Masellis, M., ...Laforce, R. (2017). Cognitive reserve and TMEM106B genotype modulate brain damage in presymptomatic frontotemporal dementia: a GENFI study.. Brain : a journal of neurology, doi:10.1093/brain/awx103
Mutsaerts, H.J.M.M., Petr, J., Thomas, D.L., Vita, E.D., Cash, D.M., Osch, M.J.P.V., ...Swieten, J.V. (2017). Comparison of arterial spin labeling registration strategies in the multi-center GENetic frontotemporal dementia initiative (GENFI).. Journal of magnetic resonance imaging : JMRI, doi:10.1002/jmri.25751
Lamb, R., Darvell, M., Woodside, J., Weil, R., Rohrer, J., Lees, A., Morris, H. (2017). EUROPEAN REGISTRY OF CORTICOBASAL DEGENERATION A PROSPECT SISTER STUDY: RECRUITMENT OF PATIENTS WITH CORTICOBASAL SYNDROME VIA THE BNSU.
Primativo, S., Clark, C., Yong, K.X.X., Firth, N.C., Nicholas, J., Alexander, D., ...Crutch, S.J. (2017). Eyetracking metrics reveal impaired spatial anticipation in behavioural variant frontotemporal dementia. Neuropsychologia, 106 328-340. doi:10.1016/j.neuropsychologia.2017.10.014
Hardy, C.J.D., Agustus, J.L., Marshall, C.R., Clark, C.N., Russell, L.L., Brotherhood, E.V., ...Thomas, D.L. (2017). Functional neuroanatomy of speech signal decoding in primary progressive aphasias. Neurobiology of Ageing, doi:10.1016/j.neurobiolaging.2017.04.026
Ferrari, R., Wang, Y., Vandrovcova, J., G.u.e.l.f.i., Witeolar, A., Karch, C.M., ......I.F.G.C. (2017). Genetic architecture of sporadic frontotemporal dementia and overlap with Alzheimer’s and Parkinson’s diseases. Journal of Neurology, Neurosurgery, and Psychiatry, doi:10.1136/jnnp-2016-314411
Turner, M.R., Al-Chalabi, A., Chio, A., Hardiman, O., Kiernan, M.C., Rohrer, J.D., ...Talbot, K. (2017). Genetic screening in sporadic ALS and FTD.. Journal of Neurology, Neurosurgery, and Psychiatry, doi:10.1136/jnnp-2017-315995
Meeter, L.H., Kaat, L.D., Rohrer, J.D., van Swieten, J.C. (2017). Imaging and fluid biomarkers in frontotemporal dementia. NATURE REVIEWS NEUROLOGY, 13 (7), 406-419. doi:10.1038/nrneurol.2017.75
Moody, C.J., Mitchell, D., Kiser, G., Aarsland, D., Berg, D., Brayne, C., ...Rohrer, J.D. (2017). Maximizing the Potential of Longitudinal Cohorts for Research in Neurodegenerative Diseases: A Community Perspective. FRONTIERS IN NEUROSCIENCE, 11 doi:10.3389/fnins.2017.00467
Esteras, N., Rohrer, J.D., Hardy, J., Wray, S., Abramov, A.Y. (2017). Mitochondrial hyperpolarization in iPSC-derived neurons from patients of FTDP-17 with 10+16 MAPT mutation leads to oxidative stress and neurodegeneration. Redox Biology, 12 410-422. doi:10.1016/j.redox.2017.03.008
Cash, D.M., Bocchetta, M., Thomas, D., Dick, K.M., van Swieten, J.C., Borroni, B., ...Rowe, J.B. (2017). Patterns of grey matter atrophy in genetic frontotemporal dementia: results from the GENFI study. Neurobiology of Aging, doi:10.1016/j.neurobiolaging.2017.10.008
Galimberti, D., Fumagalli, G.G., Fenoglio, C., Cioffi, S.M.G., Arighi, A., Serpente, M., ...Masellis, M. (2017). Progranulin plasma levels predict the presence of GRN mutations in asymptomatic subjects and do not correlate with brain atrophy: Results from the GENFI study. Neurobiology of Aging, doi:10.1016/j.neurobiolaging.2017.10.016
Lakshmanan, R., Adams, M.E., Lynch, D.S., Kinsella, J.A., Phadke, R., Schott, J.M., ...Houlden, H. (2017). Redefining the phenotype of ALSP and AARS2 mutation-related leukodystrophy.. Neurology. Genetics, 3 (2), e135. doi:10.1212/nxg.0000000000000135
Bond, R., Russell, L., Marshall, C., Hardy, C., Dick, K., Woollacott, I.O.C., ...Warren, J. (2017). Self-schema alterations in dementia.
Harding, S.R., Bocchetta, M., Gordon, E., Cash, D.M., Cardoso, M.J., Druyeh, R., ...Rohrer, J.D. (2017). The TMEM106B risk allele is associated with lower cortical volumes in a clinically diagnosed frontotemporal dementia cohort.. Journal of neurology, neurosurgery, and psychiatry, doi:10.1136/jnnp-2017-315641
Sudre, C.H., Bocchetta, M., Cash, D., Thomas, D.L., Woollacott, I., Dick, K.M., ...Masellis, M. (2017). White matter hyperintensities are seen only in GRN mutation carriers in the GENFI cohort. NeuroImage: Clinical, 15 171-180. doi:10.1016/j.nicl.2017.04.015

2016

Fletcher, P.D., Nicholas, J.M., Downey, L.E., Golden, H.L., Clark, C.N., Pires, C., ...Rohrer, J.D. (2016). A physiological signature of sound meaning in dementia. CORTEX, 77 13-23. doi:10.1016/j.cortex.2016.01.007
Primativo, S., Clark, C., Yong, K., Warren, J., Rohrer, J., Crutch, S. (2016). A spatial anticipation deficit is revealed by eyetracking metrics in behavioural variant frontotemporal dementia..
Gordon, E., Rohrer, J.D., Fox, N.C. (2016). Advances in neuroimaging in frontotemporal dementia. Journal of Neurochemistry, 193-210. doi:10.1111/jnc.13656
Clark, C.N., Nicholas, J.M., Gordon, E., Golden, H.L., Cohen, M.H., Woodward, F.J., ...Schott, J.M. (2016). Altered sense of humor in dementia. Journal of Alzheimer's Disease, 49 (1), 111-119. doi:10.3233/JAD-150413
Warren, J.D., Hardy, C.J., Fletcher, P.D., Marshall, C.R., Clark, C.N., Rohrer, J.D., Rossor, M.N. (2016). Binary reversals in primary progressive aphasia. Cortex, 82 287-289. doi:10.1016/j.cortex.2016.05.017
Marshall, C.R., Bocchetta, M., Rohrer, J.D., Warren, J.D. (2016). C9orf72 mutations and the puzzle of cerebro-cerebellar network degeneration.. Brain : a journal of neurology, 139 (8), 103. doi:10.1093/brain/aww103
Sander, K., Lashley, T., Gami, P., Gendron, T., Lythgoe, M.F., Rohrer, J., ...Arstad, E. (2016). Characterisation of tau PET tracer [18F]AV-1451 binding to post-mortem tissue in Alzheimer's disease, primary tauopathies and other dementias. Alzheimer's & Dementia, doi:10.1016/j.jalz.2016.01.003
Abdelkarim, S., Morgan, S., Plagnol, V., Lu, C.-.H., Adamson, G., Howard, R., ...Sidle, K. (2016). CHCHD10 Pro34Ser is not a highly penetrant pathogenic variant for amyotrophic lateral sclerosis and frontotemporal dementia. BRAIN, 139 E9-U13. doi:10.1093/brain/awv223
Gordon, E., Bocchetta, M., Cardoso, M.J., Ourselin, S., Warren, J.D., Rohrer, J.D. (2016). Clinical, genetic and pathological stratification in frontotemporal dementia: implications for clinical trial design.
Lamb, R., Darvell, M., Woodside, J., Rohrer, J., Lees, A., Morris, H. (2016). CORTICOBASAL SYNDROME AND CORTICOBASAL DEGENERATION.
Lamb, R.C., Darvell, M.C., Woodside, J.D.S., Rohrer, J.D., Lees, A.J., Morris, H.R. (2016). Defining the pathology underlying cortico-basal syndrome: A European study.
Rossor, M., Collinge, J., Fox, N., Mead, S., Mummery, C., Rohrer, J., ...Warren, J. (2016). Dementia and Cognitive Impairment. In Neurology: A Queen Square Textbook: Second Edition. (pp. 289-336). .
Fumagalli, G.G., Basilico, P., Harding, S., Arighi, A., Bocchetta, M., Mercurio, M., ...Graff, C. (2016). Distinct patterns of brain atrophy in genetic frontotemporal dementia: visual rating scales in the GENFI cohort.
Marshall, C., Hardy, C., Russell, L., Clark, C., Dick, K., Brotherhood, E., ...Warren, J. (2016). Embodied cognition of dynamic emotion in frontotemporal lobar degeneration.
Clark, C., Golden, H., McCallion, O., Nicholas, J., Cohen, M., Slattery, C., ...Schott, J. (2016). Expectation and reward in frontotemporal dementia: the case of music.
Hardy, C., Marshall, C., Clark, C., Russell, L., Brotherhood, E., Thomas, D., ...Warren, J. (2016). Functional neuroanatomy of speech signal decoding in primary progressive aphasias.
Panman, J.L., Meeter, L.H.H., Dopper, E.G.P., Jiskoot, L.C., Bouts, M.J.M., Moller, C., ...Graff, C. (2016). Increased neurofilament light chain correlates with decreased white matter integrity in presymptomatic and symptomatic granulin carriers.
Russell, L., Bocchetta, M., Harding, S., Crutch, S., Warren, J., Rohrer, J. (2016). Investigating the role of face processing in behavioural variant frontotemporal dementia.
Harper, L., Fumagalli, G.G., Barkhof, F., Scheltens, P., O'Brien, J.T., Bouwman, F., ...Ridgway, G.R. (2016). MRI visual rating scales in the diagnosis of dementia: evaluation in 184 post-mortem confirmed cases. BRAIN, 139 1211-1225. doi:10.1093/brain/aww005
Bocchetta, M., Toussaint, N., Hutel, M., Modat, M., Cardoso, M.J., Gordon, E., ...Borroni, B. (2016). Multimodal imaging analysis of C9orf72-associated FTD in the Genetic Frontotemporal dementia Initiative (GENFI) study.
Agustus, J.L., Clark, C.N., Golden, H.L., Slattery, C.F., Fletcher, P.D., Rohrer, J.D., Warren, J.D. (2016). Music defines fMRI signatures of molecular nexopathies.
Meeter, L., Dopper, E., Jiskoot, L., Sanchez-Valle, R., Graff, C., Benussi, L., ...Galimberti, D. (2016). Neurofilament light chain: a biomarker for disease onset and survival in genetic frontotemporal dementia.
Meeter, L.H., Dopper, E.G., Jiskoot, L.C., Sanchez-Valle, R., Graff, C., Benussi, L., ...Galimberti, D. (2016). Neurofilament light chain: a biomarker for genetic frontotemporal dementia.. Annals of Clinical and Translational Neurology, 3 (8), 623-636. doi:10.1002/acn3.325
Ahmed, R.M., Devenney, E.M., Irish, M., Ittner, A., Naismith, S., Ittner, L.M., ...Hodges, J.R. (2016). Neuronal network disintegration: Common pathways linking neurodegenerative diseases. Journal of Neurology, Neurosurgery and Psychiatry, doi:10.1136/jnnp-2014-308350
Sellami, L., Bocchetta, M., van Swieten, J., Borroni, B., Galimberti, D., Masellis, M., ...Frisoni, G. (2016). Neuropsychiatric symptoms in the genetic frontotemporal dementia initiative (GENFI) cohort.
Owen, D., Melbourne, A., Thomas, D., de Vita, E., Rohrer, J., Ourselin, S. (2016). Optimisation of arterial spin labelling using Bayesian experimental design.
Rohrer, J., Bocchetta, M., Gordon, E., Cash, D., Dick, K., Thomas, D., ...van Swieten, J. (2016). Patterns of longitudinal neuroanatomical change in genetic FTD: results from the Genetic FTD Initiative (GENFI).
Bocchetta, M., Cardoso, M.J., Cash, D.M., Ourselin, S., Warren, J.D., Rohrer, J.D. (2016). Patterns of regional cerebellar atrophy in genetic frontotemporal dementia. NeuroImage: Clinical, 11 287-290. doi:10.1016/j.nicl.2016.02.008
Gordon, E., Warren, J.D., Rohrer, J.D. (2016). Phenomenology and anatomy of abnormal behaviours in frontotemporal dementia as measured by the Cambridge Behavioural Inventory.
Mutsaerts, H., Mirza, S.S., Rohrer, J., Thomas, D., Cash, D., De Vita, E., ...Galimberti, D. (2016). Presymptomatic cerebral perfusion biomarker changes in genetic frontotemporal dementia: results from the GENetic Frontotemporal dementia Initiative (GENFI).
Koriath, C., Adamson, G., Druyeh, R., Kenny, J., Rossor, M., Schott, J., ...Collinge, J. (2016). Probing FTD genetics with a next-generation sequencing gene panel.
Koriath, C., Adamson, G., Druyeh, R., Kenny, J., Rossor, M., Schott, J., ...Mead, S. (2016). PROBING FTD GENETICS WITH NEXT-GENERATION SEQUENCING.
Cohen, M.H., Carton, A.M., Hardy, C.J., Golden, H.L., Clark, C.N., Fletcher, P.D., ...Rohrer, J.D. (2016). Processing emotion from abstract art in frontotemporal lobar degeneration. Neuropsychologia, 81 245-254. doi:10.1016/j.neuropsychologia.2015.12.031
Clark, C., Agustus, J., Nicholas, J., Hardy, C., Mummery, C., Schott, J., ...Warren, J. (2016). Processing of auditory conflict in frontotemporal dementia.
Hardy, C., Marshall, C., Clark, C., Russell, L., Brotherhood, E., Thomas, D., ...Warren, J. (2016). Progressive aphasias as disorders of auditory information processing: behavioural signatures and structural neuroanatomy.
Lamb, R., Rohrer, J.D., Lees, A.J., Morris, H.R. (2016). Progressive Supranuclear Palsy and Corticobasal Degeneration: Pathophysiology and Treatment Options. CURRENT TREATMENT OPTIONS IN NEUROLOGY, 18 (9), doi:10.1007/s11940-016-0422-5
Woollacott, I., Dick, K., Gordon, E., Bocchetta, M., Harding, S., Sidle, K., ...Rohrer, J. (2016). Right temporal variant frontotemporal dementia with motor neuron disease: a novel association with the C9orf72 expansion.
Woollacott, I., Rohrer, J., Dick, K., Brotherhood, E., Gordon, E., Fellows, A., ...Ourselin, S. (2016). Serum neurofilament light chain protein is a measure of disease intensity in frontotemporal dementia.
Rohrer, J.D., Woollacott, I.O.C., Dick, K.M., Brotherhood, E., Gordon, E., Fellows, A., ...Ourselin, S. (2016). Serum neurofilament light chain protein is a measure of disease intensity in frontotemporal dementia. NEUROLOGY, 87 (13), 1329-1336. doi:10.1212/WNL.0000000000003154
Cury, C., Lorenzi, M., Cash, D., Nicholas, J.M., Routier, A., Rohrer, J., ...Modat, M. (2016). Spatio-temporal shape analysis of cross-sectional data for detection of early changes in neurodegenerative disease.
Woollacott, I.O.C., Rohrer, J.D. (2016). The clinical spectrum of sporadic and familial forms of frontotemporal dementia. Journal of Neurochemistry, 6-31. doi:10.1111/jnc.13654
Koriath, C.A.M., Bocchetta, M., Brotherhood, E., Woollacott, I., Norsworthy, P., Simon-Sanchez, J., ...Harding, S. (2016). The clinical, neuroanatomical, and neuropathologic phenotype of TBK1-associated frontotemporal dementia: A longitudinal case report. Alzheimer's and Dementia, doi:10.1016/j.dadm.2016.10.003
Hardy, C.J.D., Buckley, A.H., Downey, L.E., Lehmann, M., Zimmerer, V.C., Varley, R.A., ...Warren, J.D. (2016). The Language Profile of Behavioral Variant Frontotemporal Dementia. JOURNAL OF ALZHEIMERS DISEASE, 50 (2), 359-371. doi:10.3233/JAD-150806
Harding, S.R., Bocchetta, M., Gordon, E., Cash, D.M., Cardoso, M.J., Adamson, G., ...Rohrer, J.D. (2016). TMEM106B polymorphism is associated with lower cortical volumes in a clinically diagnosed FTD cohort.
Thompson, A.E., Clark, C.N., Hardy, C.J., Fletcher, P.D., Greene, J., Rohrer, J.D., Warren, J.D. (2016). Two cases of food aversion with semantic dementia. NEUROCASE, 22 (3), 312-316. doi:10.1080/13554794.2016.1149592
Brotherhood, E., Drummond, J., Swapp, D., Russell, L., Primativo, S., Hardy, C., ...Warren, J. (2016). Virtual reality as an assessment of cognition in behavioural variant Frontotemporal Dementia: A Feasibility Study.
Brotherhood, E.V., Drummond, J., Russell, L., Primativo, S., Steed, A., Slater, M., ...Crutch, S. (2016). Virtual reality as an assessment of social cognition in behavioural variant Frontotemporal Dementia: A Pilot Study..

2015

Marshall, C.R., Guerreiro, R., Thust, S., Fletcher, P., Rohrer, J.D., Fox, N.C. (2015). A Novel MAPT Mutation Causing Corticobasal Syndrome Led by Progressive Apraxia of Speech. JOURNAL OF ALZHEIMERS DISEASE, 48 (4), 923-926. doi:10.3233/JAD-150477
Rollinson, S., Bennion Callister, J., Young, K., Ryan, S.J., Druyeh, R., Rohrer, J.D., ...Harris, J. (2015). A small deletion in C9orf72 hides a proportion of expansion carriers in FTLD. Neurobiology of Aging, 36 (3), 1601.e1-1601.e5. doi:10.1016/j.neurobiolaging.2014.12.009
Fletcher, P., Rohrer, J., Schott, J., Rossor, M., Warren, J. (2015). ABNORMAL PAIN AND TEMPERATURE PROCESSING IN DEMENTIA.
Fletcher, P.D., Downey, L.E., Golden, H.L., Clark, C.N., Slattery, C.F., Paterson, R.W., ...Warren, J.D. (2015). Auditory hedonic phenotypes in dementia: A behavioural and neuroanatomical analysis. Cortex, 67 95-105. doi:10.1016/j.cortex.2015.03.021
Rohrer, J.D., Isaacs, A.M., Mizlienska, S., Mead, S., Lashley, T., Wray, S., ...Hardy, J. (2015). C9orf72 expansions in frontotemporal dementia and amyotrophic lateral sclerosis. LANCET NEUROLOGY, 14 (3), 291-301. doi:10.1016/S1474-4422(14)70233-9
Woollacott, I.O.C., Fletcher, P.D., Massey, L.A., Pasupathy, A., Rossor, M.N., Caine, D., ...Warren, J.D. (2015). Compulsive versifying after treatment of transient epileptic amnesia.. Neurocase, 21 (5), 548-553. doi:10.1080/13554794.2014.953178
Bocchetta, M., Gordon, E., Manning, E., Barnes, J., Cash, D.M., Espak, M., ...Warren, J.D. (2015). Detailed volumetric analysis of the hypothalamus in behavioral variant frontotemporal dementia. Journal of Neurology, 262 (12), 2635-2642. doi:10.1007/s00415-015-7885-2
Clark, C.N., Nicholas, J.M., Henley, S.M., Downey, L.E., Woollacott, I.O., Golden, H.L., ...Rohrer, J.D. (2015). Humour processing in frontotemporal lobar degeneration: A behavioural and neuroanatomical analysis. Cortex, 69 47-59. doi:10.1016/j.cortex.2015.03.024
Fletcher, P.D., Downey, L.E., Golden, H.L., Clark, C.N., Slattery, C.F., Paterson, R.W., ...Warren, J.D. (2015). Pain and temperature processing in dementia: a clinical and neuroanatomical analysis. Brain: a journal of neurology, 138 (11), 3360-3372. doi:10.1093/brain/awv276
Rohrer, J.D., Nicholas, J.M., Cash, D.M., van Swieten, J., Dopper, E., Jiskoot, L., ...Clegg, S. (2015). Presymptomatic cognitive and neuroanatomical changes in genetic frontotemporal dementia in the Genetic Frontotemporal dementia Initiative (GENFI) study: a cross-sectional analysis.. Lancet Neurol, 14 (3), 253-262. doi:10.1016/S1474-4422(14)70324-2
Lashley, T., Rohrer, J.D., Mead, S., Revesz, T. (2015). Review: An update on clinical, genetic and pathological aspects of frontotemporal lobar degenerations. Neuropathology and Applied Neurobiology, 41 (7), 858-881. doi:10.1111/nan.12250
Lashley, T., Rohrer, J.D., Mead, S., Revesz, T. (2015). Review: An update on clinical, genetic and pathological aspects of frontotemporal lobar degenerations. NEUROPATHOLOGY AND APPLIED NEUROBIOLOGY, 41 (7), 858-881. doi:10.1111/nan.12250
Clark, C.N., Lashley, T., Mahoney, C.J., Warren, J.D., Revesz, T., Rohrer, J.D. (2015). Temporal Variant Frontotemporal Dementia Is Associated with Globular Glial Tauopathy. COGNITIVE AND BEHAVIORAL NEUROLOGY, 28 (2), 92-97. doi:10.1097/WNN.0000000000000060
Bocchetta, M., Gordon, E., Marshall, C.R., Slattery, C.F., Cardoso, M.J., Cash, D.M., ...Frisoni, G.B. (2015). The habenula: an under-recognised area of importance in frontotemporal dementia?. Journal of Neurology, Neurosurgery and Psychiatry, doi:10.1136/jnnp-2015-312067
Walton, J., Ryan, N., Crutch, S., Rohrer, J.D., Fox, N. (2015). The importance of dementia support groups.. BMJ (Clinical research ed.), 351 h3875-. doi:10.1136/bmj.h3875

2014

Lashley, T., Rohrer, J.D., Mahoney, C., Gordon, E., Beck, J., Mead, S., ...Revesz, T. (2014). A pathogenic progranulin mutation and C9orf72 repeat expansion in a family with frontotemporal dementia.
Ahmed, R.M., Murphy, E., Davagnanam, I., Parton, M., Schott, J.M., Mummery, C.J., ...Fox, N.C. (2014). A practical approach to diagnosing adult onset leukodystrophies. JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY, 85 (7), 770-781. doi:10.1136/jnnp-2013-305888
Downey, L.E., Fletcher, P.D., Golden, H.L., Mahoney, C.J., Agustus, J.L., Schott, J.M., ...Rossor, M.N. (2014). Altered body schema processing in frontotemporal dementia with C9ORF72 mutations.. JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY, 85 (9), 1016-1023. doi:10.1136/jnnp-2013-306995
Rohrer, J.D., Zetterberg, H. (2014). Biomarkers in frontotemporal dementia.. BIOMARKERS IN MEDICINE, 8 (4), 519-521. doi:10.2217/bmm.14.30
Woollacott, I.O.C., Fletcher, P.D., Massey, L.A., Pasupathy, A., Rossor, M.N., Rohrer, J.D., Warren, J.D. (2014). COMPULSIVE VERSIFYING IN TRANSIENT EPILEPTIC AMNESIA.
Maruta, C., Makhmood, S., Downey, L.E., Golden, H.L., Fletcher, P.D., Witoonpanich, P., ...Warren, J.D. (2014). Delayed auditory feedback simulates features of nonfluent primary progressive aphasia. Journal of the Neurological Sciences, 347 (1-2), 345-348. doi:10.1016/j.jns.2014.09.039
Maruta, C., Makhmood, S., Downey, L.E., Golden, H.L., Fletcher, P.D., Witoonpanich, P., ...Warren, J.D. (2014). Delayed auditory feedback simulates features of nonfluent primary progressive aphasia.. J Neurol Sci, 347 (1-2), 345-348. doi:10.1016/j.jns.2014.09.039
Rohrer, J.D., Devine, H., Foulkes, A., Johnston, A., Mallam, B., Marshall, C., ...Blackburn, D. (2014). DEVELOPING A NEUROLOGY MENTORING PROGRAMME FOR TRAINEES.
Ferrari, R., Hernandez, D.G., Nalls, M.A., Rohrer, J.D., Ramasamy, A., Kwok, J.B.J., ...Halliday, G.M. (2014). Frontotemporal dementia and its subtypes: a genome-wide association study.. LANCET NEUROLOGY, 13 (7), 686-699. doi:10.1016/S1474-4422(14)70065-1
Cash, D.M., Rohrer, J.D., Ryan, N.S., Ourselin, S., Fox, N.C. (2014). Imaging endpoints for clinical trials in Alzheimer's disease. Alzheimer's Research & Therapy, 6 doi:10.1186/s13195-014-0087-9
Mahoney, C.J., Simpson, I.J.A., NIcholas, J.M., Fletcher, P.D., Downey, L.E., Golden, H.L., ...Schott, J.M. (2014). Longitudinal diffusion tensor imaging in frontotemporal dementia. Annals of Neurology, doi:10.1002/ana.24296
Mahoney, C.J., Ridgway, G.R., Malone, I.B., Downey, L.E., Beck, J., Kinnunen, K.M., ...Schott, J.M. (2014). Profiles of white matter tract pathology in frontotemporal dementia.. Human Brain Mapping, 35 (8), 4163-4179. doi:10.1002/hbm.22468
Slattery, C.F., Beck, J.A., Harper, L., Adamson, G., Abdi, Z., Uphill, J., ...Rohrer, J.D. (2014). R47H TREM2 variant increases risk of typical early-onset Alzheimer's disease but not of prion or frontotemporal dementia.. ALZHEIMERS & DEMENTIA, 10 (6), 602-608. doi:10.1016/j.jalz.2014.05.1751
Rohrer, J.D. (2014). The genetics of primary progressive aphasia. Aphasiology, 28 (8-9), 941-947. doi:10.1080/02687038.2014.911242
Rohrer, J.D. (2014). The genetics of primary progressive aphasia. APHASIOLOGY, 28 (8-9), 941-947. doi:10.1080/02687038.2014.911242
Gallagher, M.D., Suh, E., Grossman, M., Elman, L., McCluskey, L., Van Swieten, J.C., ...Ghetti, B. (2014). TMEM106B is a genetic modifier of frontotemporal lobar degeneration with C9orf72 hexanucleotide repeat expansions. Acta Neuropathologica, 127 (3), 407-418. doi:10.1007/s00401-013-1239-x
Slattery, C.F., Beck, J., Harper, L., Adamson, G., Abdi, Z., Uphill, J., ...Rohrer, J.D. (2014). TREM2 VARIANTS INCREASE RISK OF TYPICAL EARLY-ONSET ALZHEIMER'S DISEASE BUT NOT OF PRION OR FRONTOTEMPORAL DEMENTIA. JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY, 85 (8), doi:10.1136/jnnp-2014-308883.7
Beck, J., Pittman, A., Adamson, G., Campbell, T., Kenny, J., Houlden, H., ...Uphill, J. (2014). Validation of next-generation sequencing technologies in genetic diagnosis of dementia. Neurobiology of Aging, 35 (1), 261-265. doi:10.1016/j.neurobiolaging.2013.07.017

2013

Liang, Y., Gordon, E., Rohrer, J., Downey, L., de Silva, R., Jäger, H.R., ...Mahoney, C. (2013). A cognitive chameleon: Lessons from a novel MAPT mutation case. Neurocase, doi:10.1080/13554794.2013.826697
Ahmed, R., Guerreiro, R., Rohrer, J.D., Guven, G., Rossor, M.N., Hardy, J., Fox, N.C. (2013). A novel A781V mutation in the CSF1R gene causes hereditary diffuse leucoencephalopathy with axonal spheroids. Journal of the Neurological Sciences, 332 (1-2), 141-144. doi:10.1016/j.jns.2013.06.007
Guerreiro, R., Brás, J., Bilgic, B., Lohmann, E., Hanagasi, H., Gurvit, H., ...Rohrer, J. (2013). A novel compound heterozygous mutation in TREM2 found in a Turkish frontotemporal dementia-like family. Neurobiology of Aging, 34 (12), 2890.e1-2890.e5. doi:10.1016/j.neurobiolaging.2013.06.005
Lashley, T., Rohrer, J.D., Mahoney, C., Gordon, E., Beck, J., Mead, S., ...Revesz, T. (2013). A pathogenic progranulin mutation and C9orf72 repeat expansion in a family with frontotemporal dementia.. Neuropathology and Applied Neurobiology, 40 (4), 502-513. doi:10.1111/nan.12100
Rascovsky, K., Hodges, J., Knopman, D., Mendez, M., Kramer, J., Neuhaus, J., ...Onyike, C. (2013). Can Clinical Features Predict Tau Pathology in Patients with Behavioral Variant Frontotemporal Dementia (bvFTD)?.
Lashley, T., Rohrer, J.D., Mahoney, C.J., Polke, J.M., Ryan, N.S., Isaacs, A., ...Revesz, T. (2013). Clinical and pathological features of frontotemporal dementia linked to C9ORF72 homozygosity.
Warren, J.D., Rohrer, J.D., Rossor, M.N. (2013). Clinical review. Frontotemporal dementia.. BMJ, 347 doi:10.1136/bmj.f4827
Rohrer, J.D., Beck, J., Plagnol, V., Gordon, E., Lashley, T., Revesz, T., ...Rossor, M.N. (2013). Exome sequencing reveals a novel partial deletion in the progranulin gene causing primary progressive aphasia. Journal of Neurology, Neurosurgery and Psychiatry, 84 (12), 1411-1412. doi:10.1136/jnnp-2013-306116
Fratta, P., Poulter, M., Lashley, T., Rohrer, J.D., Polke, J.M., Beck, J., ...Waite, A.J. (2013). Homozygosity for the C9orf72 GGGGCC repeat expansion in frontotemporal dementia.. Acta Neuropathologica, 126 (3), 401-409. doi:10.1007/s00401-013-1147-0
Beck, J., Poulter, M., Hensman, D., Rohrer, J.D., Mahoney, C.J., Adamson, G., ...Fratta, P. (2013). Large C9orf72 hexanucleotide repeat expansions are seen in multiple neurodegenerative syndromes and are more frequent than expected in the UK population.. AMERICAN JOURNAL OF HUMAN GENETICS, 92 (3), 345-353. doi:10.1016/j.ajhg.2013.01.011
Warren, J.D., Rohrer, J.D., Schott, J.M., Fox, N.C., Hardy, J., Rossor, M.N. (2013). Molecular nexopathies: A new paradigm of neurodegenerative disease. Trends Neurosci, 36 (10), 561-569. doi:10.1016/j.tins.2013.06.007
Rohrer, J.D., Rosen, H.J. (2013). Neuroimaging in frontotemporal dementia.. INTERNATIONAL REVIEW OF PSYCHIATRY, 25 (2), 221-229. doi:10.3109/09540261.2013.778822
Rohrer, J.D., Caso, F., Mahoney, C., Henry, M., Rosen, H.J., Rabinovici, G., ...Fox, N.C. (2013). Patterns of longitudinal brain atrophy in the logopenic variant of primary progressive aphasia.. Brain and Language, 127 (2), 121-126. doi:10.1016/j.bandl.2012.12.008
Rohrer, J.D., Warren, J.D., Fox, N.C., Rossor, M.N. (2013). Presymptomatic studies in genetic frontotemporal dementia.. REVUE NEUROLOGIQUE, 169 (10), 820-824. doi:10.1016/j.neurol.2013.07.010
Doherty, K.M., Rohrer, J.D., Lees, A.J., Holton, J.L., Warren, J. (2013). Primary progressive aphasia with parkinsonism.. MOVEMENT DISORDERS, 28 (6), 741-746. doi:10.1002/mds.25341
Rohrer, J.D. (2013). Recent advances in Alzheimer's disease and other dementias. JOURNAL OF NEUROLOGY, 260 S9.
Mahoney, C., Yeatman, T., Rohrer, J., Manning, E., Leung, K., Rossor, M., ...Fox, N. (2013). THE EVOLUTION OF FRONTOTEMPORAL DEMENTIA DUE TO THE MAPT MUTATION: A SEVENTEEN YEAR NATURAL HISTORY STUDY.. JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY, 84 (11), doi:10.1136/jnnp-2013-306573.86
Crutch, S.J., Lehmann, M., Warren, J.D., Rohrer, J.D. (2013). The language profile of posterior cortical atrophy.. Journal of Neurology, Neurosurgery and Psychiatry, 84 (4), 460-466. doi:10.1136/jnnp-2012-303309
Stutzbach, L.D., Xie, S.X., Naj, A.C., Albin, R., Gilman, S., Lee, V.M.Y., ...Schellenberg, G.D. (2013). The unfolded protein response is activated in disease-affected brain regions in progressive supranuclear palsy and Alzheimer's disease. ACTA NEUROPATHOLOGICA COMMUNICATIONS, 1 doi:10.1186/2051-5960-1-31
Guerreiro, R.J., Lohmann, E., Brás, J.M., Gibbs, J.R., Rohrer, J.D., Gurunlian, N., ...Gurvit, H. (2013). Using exome sequencing to reveal mutations in TREM2 presenting as a frontotemporal dementia-like syndrome without bone involvement.. JAMA NEUROLOGY, 70 (1), 78-84. doi:10.1001/jamaneurol.2013.579

2012

Rohrer, J.D., Rossor, M.N., Warren, J.D. (2012). Alzheimer's pathology in primary progressive aphasia.. NEUROBIOLOGY OF AGING, 33 (4), 744-752. doi:10.1016/j.neurobiolaging.2010.05.020
Ryan, N.S., Bastos-Leite, A.J., Rohrer, J.D., Werring, D.J., Fox, N.C., Rossor, M.N., Schott, J.M. (2012). Cerebral microbleeds in familial Alzheimer's disease. BRAIN, 135 doi:10.1093/brain/awr126
Rascovsky, K., Hodges, J.R., Knopman, D., Mendez, M.F., Kramer, J.H., Xie, S., ...Onyike, C.U. (2012). Determinants of Survival in Autopsy-Confirmed Patients with Behavioral Variant Frontotemporal Dementia (bvFTD).
Rascovsky, K., Hodges, J.R., Knopman, D., Mendez, M.F., Kramer, J.H., Xie, S., ...Onyike, C.U. (2012). Determinants of Survival in Autopsy-Confirmed Patients with Behavioral Variant Frontotemporal Dementia (bvFTD).
Warren, J.D., Rohrer, J.D., Hardy, J. (2012). Disintegrating brain networks: from syndromes to molecular nexopathies.. NEURON, 73 (6), 1060-1062. doi:10.1016/j.neuron.2012.03.006
Ridgway, G.R., Lehmann, M., Barnes, J., Rohrer, J.D., Warren, J.D., Crutch, S.J., Fox, N.C. (2012). Early-onset Alzheimer disease clinical variants: multivariate analyses of cortical thickness.. NEUROLOGY, 79 (1), 80-84. doi:10.1212/WNL.0b013e31825dce28
Englund, E., Gustafson, L., Passant, U., Majounie, E., Renton, A.E., Traynor, B.J., ...Hardy, J. (2012). Familial Lund frontotemporal dementia caused by C9ORF72 hexanucleotide expansion. Neurobiol Aging, 33 (8), doi:10.1016/j.neurobiolaging.2012.02.019
Majounie, E., Renton, A.E., Mok, K., Dopper, E.G.P., Waite, A., Rollinson, S., ...Simon-Sanchez, J. (2012). Frequency of the C9orf72 hexanucleotide repeat expansion in patients with amyotrophic lateral sclerosis and frontotemporal dementia: A cross-sectional study. Lancet Neurology, 11 (4), 323-330. doi:10.1016/S1474-4422(12)70043-1
Mahoney, C.J., Beck, J., Rohrer, J.D., Lashley, T., Mok, K., Shakespeare, T., ...Fox, N.C. (2012). Frontotemporal dementia with the C9ORF72 hexanucleotide repeat expansion: Clinical, neuroanatomical and neuropathological features. Brain, 135 (3), 736-750. doi:10.1093/brain/awr361
Mahoney, C., Beck, J., Rohrer, J., Lashley, T., Mok, K., Yeatman, T., ...Fox, N. (2012). Frontotemporal dementia with the C9ORF72 hexanucleotide repeat expansion: clinical, neuroanatomical and neuropathological features.
Guerreiro, R., Kara, E., Le Ber, I., Bras, J., Rohrer, J., Taipa, R., ...Mochel, F. (2012). Genetic analysis of inherited leukodystrophies: genotype phenotype correlations in the CSF1R gene.
Guerreiro, R., Kara, E., Le Ber, I., Bras, J., Rohrer, J., Taipa, R., ...Mochel, F. (2012). Genetic analysis of inherited leukodystrophies: genotype phenotype correlations in the CSF1R gene.
Guerreiro, R., Kara, E., Le Ber, I., Bras, J., Rohrer, J.D., Taipa, R., ...Mochel, F. (2012). Genetic analysis of inherited leukodystrophies: genotype-phenotype correlations in the CSF1R gene..
Rohrer, J., Frisoni, G.B., Galimberti, D., Masellis, M., Rowe, J.B., Borroni, B., ...Graff, C. (2012). GENFI - The GENetic Frontotemporal dementia Initiative.
Mead, S., Beck, J., Poulter, M., Rohrer, J., Adamson, G., Hensman, D., ...Borg, A. (2012). Large C9ORF72 hexanucleotide expansions arise spontaneously in the healthy population but can be distinguished from pathogenic mutations by Sothern Blotting.
Mahoney, C.J., Downey, L.E., Ridgway, G.R., Beck, J., Clegg, S., Blair, M., ...Golden, H. (2012). Longitudinal neuroimaging and neuropsychological profiles of frontotemporal dementia with C9ORF72 expansions.. Alzheimer's Research & Therapy, 4 (5), 41-. doi:10.1186/alzrt144
Crutch, S., Lehmann, M., Warrington, E.K., Warren, J.D., Rohrer, J.D. (2012). PARIETAL CONTRIBUTIONS TO LANGUAGE PROCESSING: PROGRESSIVE APHASIA IN POSTERIOR CORTICAL ATROPHY.
Rohrer, J.D., Caso, F., Mahoney, C., Henry, M., Rosen, H., Rossor, M.N., ...Gorno-Tempini, M.L. (2012). Patterns of Longitudinal Brain Atrophy in the Logopenic Variant of Primary Progressive Aphasia.
Rohrer, J.D., Clarkson, M.J., Kittus, R., Rossor, M.N., Ourselin, S., Warren, J.D., Fox, N.C. (2012). Rates of hemispheric and lobar atrophy in the language variants of frontotemporal lobar degeneration.. JOURNAL OF ALZHEIMERS DISEASE, 30 (2), 407-411. doi:10.3233/JAD-2012-111556
Rohrer, J.D., Sauter, D., Scott, S., Rossor, M.N., Warren, J.D. (2012). Receptive prosody in nonfluent primary progressive aphasias.. CORTEX, 48 (3), 308-316. doi:10.1016/j.cortex.2010.09.004
Rohrer, J.D. (2012). Structural brain imaging in frontotemporal dementia.. BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE, 1822 (3), 325-332. doi:10.1016/j.bbadis.2011.07.014
Mahoney, C., Yeatman, T., Rohrer, J., Manning, E., Leung, K., Downey, L., ...Fox, N. (2012). The evolution of Frontotemporal Dementia due to the MAPT mutation: a seventeen year natural history study.
Warren, J., Rohrer, J.D., Lashley, T., Schott, J.M., Beck, J., Mead, S., ...Rossor, M.N. (2012). The frontotemporal lobar degenerations as 'molecular nexopathies'.
Warren, J., Rohrer, J.D., Lashley, T., Schott, J.M., Beck, J., Mead, S., ...Rossor, M.N. (2012). The frontotemporal lobar degenerations as 'molecular nexopathies'.
Kara, E., Ling, H., Pittman, A.M., Shaw, K., de Silva, R., Simone, R., ...Xiromerisiou, G. (2012). The MAPT p.A152T variant is a risk factor associated with tauopathies with atypical clinical and neuropathological features. Neurobioly of Aging, 33 (9), 2231.e7-2231.e14. doi:10.1016/j.neurobiolaging.2012.04.006
Guerreiro, R.J., Lohmann, E., Brás, J.M., Gibbs, J.R., Rohrer, J.D., Gurunlian, N., ...Gurvit, H. (2012). Using Exome Sequencing to Reveal Mutations in TREM2 Presenting as a Frontotemporal Dementia-like Syndrome Without Bone Involvement.. Arch Neurol, 1-7. doi:10.1001/archneurol.2013.579

2011

Lashley, T., Rohrer, J.D., Bandopadhyay, R., Fry, C., Ahmed, Z., Isaacs, A.M., ...Troakes, C. (2011). A comparative clinical, pathological, biochemical and genetic study of fused in sarcoma proteinopathies.. BRAIN, 134 2548-2564. doi:10.1093/brain/awr160
Clarkson, M.J., Cardoso, M.J., Modat, M., Ridgway, G.R., Leung, K.K., Rohrer, J.D., ...Fox, N. (2011). A Comparative Study of Voxel and Surface Based Cortical Thickness Methods in Frontotemporal Dementia.
Clarkson, M.J., Cardoso, M.J., Ridgway, G.R., Modat, M., Leung, K.K., Rohrer, J.D., ...Ourselin, S. (2011). A comparison of voxel and surface based cortical thickness estimation methods. NeuroImage, 57 (3), 856-865. doi:10.1016/j.neuroimage.2011.05.053
Rohrer, J.D., Warren, J.D., Reiman, D., Uphill, J., Beck, J., Collinge, J., ...Mead, S. (2011). A novel exon 2 I27V VCP variant is associated with dissimilar clinical syndromes.. JOURNAL OF NEUROLOGY, 258 (8), 1494-1496. doi:10.1007/s00415-011-5966-4
Ridgway, G.R., Lehmann, M., Rohrer, J., Clarkson, M., Warren, J., Ourselin, S., Fox, N. (2011). Balanced sensitivity and specificity on unbalanced data using support vector machine re-thresholding.
Rohrer, J.D. (2011). Behavioural variant frontotemporal dementia--defining genetic and pathological subtypes.. JOURNAL OF MOLECULAR NEUROSCIENCE, 45 (3), 583-588. doi:10.1007/s12031-011-9542-2
Gorno-Tempini, M.L., Hillis, A.E., Weintraub, S., Kertesz, A., Mendez, M., Cappa, S.F., ...Boeve, B.F. (2011). Classification of primary progressive aphasia and its variants. NEUROLOGY, 76 (11), 1006-1014. doi:10.1212/WNL.0b013e31821103e6
Rohrer, J.D., Lashley, T., Schott, J.M., Warren, J.E., Mead, S., Isaacs, A.M., ...Warrington, E. (2011). Clinical and neuroanatomical signatures of tissue pathology in frontotemporal lobar degeneration. Brain, 134 (9), 2565-2581.
Seelaar, H., Rohrer, J.D., Pijnenburg, Y.A.L., Fox, N.C., van Swieten, J.C. (2011). Clinical, genetic and pathological heterogeneity of frontotemporal dementia: a review. JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY, 82 (5), 476-486. doi:10.1136/jnnp.2010.212225
Clarkson, M.J., Cardoso, M., Modat, M., Ridgway, G.R., Leung, K.K., Rohrer, J., ...Ourselin, S. (2011). Cross-sectional analysis using voxel or surface based cortical thickness methods: a comparison study.
Alner, K., Hyare, H., Mead, S., Rudge, P., Wroe, S., Rohrer, J.D., ...Hunt, H. (2011). Distinct neuropsychological profiles correspond to distribution of cortical thinning in inherited prion disease caused by insertional mutation.. Journal of Neurology, Neurosurgery & Psychiatry, doi:10.1136/jnnp-2011-300167
Rollinson, S., Mead, S., Snowden, J., Richardson, A., Rohrer, J., Halliwell, N., ...Hardy, J. (2011). Frontotemporal lobar degeneration genome wide association study replication confirms a risk locus shared with amyotrophic lateral sclerosis. NEUROBIOLOGY OF AGING, 32 (4), doi:10.1016/j.neurobiolaging.2010.12.005
Chen-Plotkin, A.S., Martinez-Lage, M., Sleiman, P.M.A., Hu, W., Greene, R., Wood, E.M., ...Hatanpaa, K.J. (2011). Genetic and Clinical Features of Progranulin-Associated Frontotemporal Lobar Degeneration. ARCHIVES OF NEUROLOGY, 68 (4), 488-497. doi:10.1001/archneurol.2011.53
Höglinger,, G.U., Melhem, N.M., Dickson, D.W., Sleiman, P.M., Wang, L.S., Klei, L., ...Riley, D.E. (2011). Identification of common variants influencing risk of the tauopathy progressive supranuclear palsy. Nature Genetics, 43 (7), 699-705. doi:10.1038/ng.859
Höglinger, G.U., Melhem, N.M., Dickson, D.W., Sleiman, P.M.A., Wang, L.-.S., Klei, L., ...Riley, D.E. (2011). Identification of common variants influencing risk of the tauopathy progressive supranuclear palsy.. Nat Genet, 43 (7), 699-705. doi:10.1038/ng.859
Mahoney, C.J., Rohrer, J.D., Omar, R., Rossor, M.N., Warren, J.D. (2011). Neuroanatomical profiles of personality change in frontotemporal lobar degeneration.. BRITISH JOURNAL OF PSYCHIATRY, 198 (5), 365-372. doi:10.1192/bjp.bp.110.082677
Rollinson, S., Rohrer, J.D., van der Zee, J., Sleegers, K., Mead, S., Engelborghs, S., ...Van Broeckhoven, C. (2011). No association of PGRN 3'UTR rs5848 in frontotemporal lobar degeneration.. NEUROBIOLOGY OF AGING, 32 (4), 754-755. doi:10.1016/j.neurobiolaging.2009.04.009
Rohrer, J.D., Paviour, D., Vandrovcova, J., Hodges, J., de Silva, R., Rossor, M. (2011). Novel L284R MAPT mutation in a family with an autosomal dominant progressive supranuclear palsy syndrome. Neurodegenerative Diseases, doi:10.1159/000319454
Lehmann, M., Rohrer, J.D., Clarkson, M.J., Ridgway, G.R., Scahill, R.I., Modat, M., ...Rossor, M.N. (2011). Patterns of cortical thickness in pathologically-confirmed typical and atypical Alzheimer's disease. In Handbook of Imaging the Alzheimer Brain. (pp. 57-67). IOS Press.
Rohrer, J.D., Warren, J.D. (2011). Phenotypic signatures of genetic frontotemporal dementia.. CURRENT OPINION IN NEUROLOGY, 24 (6), 542-549. doi:10.1097/WCO.0b013e32834cd442
Rohrer, J.D., Schott, J.M. (2011). Primary progressive aphasia: defining genetic and pathological subtypes.. Curr Alzheimer Res, 8 (3), 266-272.
Rascovsky, K., Hodges, J.R., Knopman, D., Mendez, M.F., Kramer, J.H., Van Swieten, J.C., ...Hillis, A. (2011). Sensitivity of Diagnostic Criteria in Autopsy-Confirmed Patients with Behavioral Variant Frontotemporal Dementia (bvFTD): First Report of the International bvFTD Criteria Consortium (FTDC).
Rascovsky, K., Hodges, J.R., Knopman, D., Mendez, M.F., Kramer, J.H., Neuhaus, J., ...Onyike, C.U. (2011). Sensitivity of revised diagnostic criteria for the behavioural variant of frontotemporal dementia.. BRAIN, 134 2456-2477. doi:10.1093/brain/awr179
Omar, R., Rohrer, J.D., Hailstone, J.C., Warren, J.D. (2011). Structural neuroanatomy of face processing in frontotemporal lobar degeneration.. Journal of Neurology, Neurosurgery and Psychiatry, 82 (12), 1341-1343. doi:10.1136/jnnp.2010.227983
Mahoney, C.J., Rohrer, J.D., Goll, J.C., Fox, N.C., Rossor, M.N., Warren, J.D. (2011). Structural neuroanatomy of tinnitus and hyperacusis in semantic dementia.. JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY, 82 (11), 1274-1278. doi:10.1136/jnnp.2010.235473
Rohrer, J.D., Lashley, T., Holton, J., Revesz, T., Urwin, H., Isaacs, A.M., ...Warren, J. (2011). The clinical and neuroanatomical phenotype of FUS associated frontotemporal lobar degeneration.. JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY, 82 (12), 1405-1407. doi:10.1136/jnnp.2010.214437

2010

Rohrer, J.D., Lashley, T., Mead, S., Fox, N., Holton, J., Revesz, T., ...Warren, J. (2010). An Anatomopathological Classification of Frontotemporal Lobar Degeneration.
Rohrer, J.D., Rossor, M.N., Warren, J.D. (2010). Apraxia in progressive nonfluent aphasia.. Journal of Neurology, 257 (4), 569-574. doi:10.1007/s00415-009-5371-4
Van Deerlin, V.M., Sleiman, P.M.A., Martinez-Lage, M., Chen-Plotkin, A., Wang, L.-.S., Graff-Radford, N.R., ...Grossman, M. (2010). Common variants at 7p21 are associated with frontotemporal lobar degeneration with TDP43 inclusions. NATURE GENETICS, 42 (3), 234-U34. doi:10.1038/ng.536
Rudge, P., Fox, N.C., Cipolotti, L., Mead, S., Hyare, H., Rohrer, J., Collinge, J. (2010). DISTINCT NEUROPSYCHOLOGICAL PROFILES CORRESPOND TO DISTRIBUTION OF CORTICAL THINNING IN INHERITED PRION DISEASE CAUSED BY INSERTIONAL MUTATION. JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY, 81 (11), E42-E43. doi:10.1136/jnnp.2010.226340.103
Rohrer, J.D., Ridgway, G.R., Modat, M., Ourselin, S., Mead, S., Fox, N.C., ...Warren, J.D. (2010). Distinct profiles of brain atrophy in frontotemporal lobar degeneration caused by progranulin and tau mutations.. Neuroimage, doi:10.1016/j.neuroimage.2009.12.088
Lashley, T., Rohrer, J., Bandopadhyay, R., Ahmed, Z., Borroni, B., Warren, J., ...Bojsen-Moller, M. (2010). Frontotemporal lobar degeneration with FUS-positive inclusions.
Urwin, H., Josephs, K.A., Rohrer, J.D., Mackenzie, I.R., Neumann, M., Authier, A., ...Johannsen, P. (2010). FUS pathology defines the majority of tau- and TDP-43-negative frontotemporal lobar degeneration.. ACTA NEUROPATHOLOGICA, 120 (1), 33-41. doi:10.1007/s00401-010-0698-6
Gordon, E., Rohrer, J.D., Kim, L.G., Omar, R., Rossor, M.N., Fox, N.C., Warren, J.D. (2010). Measuring disease progression in frontotemporal lobar degeneration: a clinical and MRI study.. NEUROLOGY, 74 (8), 666-673. doi:10.1212/WNL.0b013e3181d1a879
Goll, J.C., Crutch, S.J., Loo, J.H.Y., Rohrer, J.D., Frost, C., Bamiou, D.E., Warren, J.D. (2010). Non-verbal sound processing in the primary progressive aphasias.. Brain, 133 (1), 272-285. doi:10.1093/brain/awp235
Newsway, V., Fish, M., Rohrer, J.D., Majounie, E., Williams, N., Hack, M., ...Morris, H.R. (2010). Perry Syndrome Due to the DCTN1 G71R Mutation: A Distinctive Levodopa Responsive Disorder with Behavioral Syndrome, Vertical Gaze Palsy, and Respiratory Failure. MOVEMENT DISORDERS, 25 (6), 767-770. doi:10.1002/mds.22950
Newsway, V., Fish, M., Rohrer, J.D., Majounie, E., Williams, N., Hack, M., ...Morris, H.R. (2010). Perry syndrome due to the DCTN1 G71R mutation: a distinctive levodopa responsive disorder with behavioral syndrome, vertical gaze palsy, and respiratory failure.. Movement disorders : official journal of the Movement Disorder Society, 25 (6), 759-762.
Rohrer, J.D., Warren, J.D. (2010). Phenomenology and anatomy of abnormal behaviours in primary progressive aphasia.. JOURNAL OF THE NEUROLOGICAL SCIENCES, 293 (1-2), 35-38. doi:10.1016/j.jns.2010.03.012
Rohrer, J.D., Crutch, S.J., Warrington, E.K., Warren, J.D. (2010). Progranulin-associated primary progressive aphasia: a distinct phenotype?. NEUROPSYCHOLOGIA, 48 (1), 288-297. doi:10.1016/j.neuropsychologia.2009.09.017
Rohrer, J.D., Ridgway, G.R., Crutch, S.J., Hailstone, J., Goll, J.C., Clarkson, M.J., ...Ourselin, S. (2010). Progressive logopenic/phonological aphasia: erosion of the language network.. NEUROIMAGE, 49 (1), 984-993. doi:10.1016/j.neuroimage.2009.08.002
Rohrer, J.D., Paviour, D., Bronstein, A.M., O'Sullivan, S.S., Lees, A., Warren, J.D. (2010). Progressive supranuclear palsy syndrome presenting as progressive nonfluent aphasia: a neuropsychological and neuroimaging analysis.. MOVEMENT DISORDERS, 25 (2), 179-188. doi:10.1002/mds.22946
Lehmann, M., Rohrer, J.D., Clarkson, M.J., Ridgway, G.R., Scahill, R.I., Modat, M., ...Rossor, M.N. (2010). Reduced cortical thickness in the posterior cingulate gyrus is characteristic of both typical and atypical Alzheimer's disease.. J Alzheimer Dis, 20 (2), 587-598. doi:10.3233/JAD-2010-1401
Rohrer, J.D., Rossor, M.N., Warren, J.D. (2010). Syndromes of nonfluent primary progressive aphasia: a clinical and neurolinguistic analysis.. NEUROLOGY, 75 (7), 603-610. doi:10.1212/WNL.0b013e3181ed9c6b
Rohrer, J.D., Geser, F., Zhou, J., Gennatas, E.D., Sidhu, M., Trojanowski, J.Q., ...Seeley, W.W. (2010). TDP-43 subtypes are associated with distinct atrophy patterns in frontotemporal dementia.. NEUROLOGY, 75 (24), 2204-2211.
Revesz, T., Lashley, T., Ahmed, Z., Rohrer, J., Warren, J., Al-Saraj, S., ...Lees, A. (2010). The Spectrum of FUS-Positive Pathology in Frontotemporal Lobar Degenerations.

2009

Kloeppel, S., Stonnington, C.M., Chu, C., Draganski, B., Scahill, R.I., Rohrer, J.D., ...Frackowiak, R.S.J. (2009). A plea for confidence intervals and consideration of generalizability in diagnostic studies. Brain, 132 (4), e102-. doi:10.1093/brain/awn091
Rohrer, J.D., Warren, J.D., Rossor, M.N. (2009). Abnormal laughter-like vocalisations replacing speech in primary progressive aphasia.. JOURNAL OF THE NEUROLOGICAL SCIENCES, 284 (1-2), 120-123. doi:10.1016/j.jns.2009.04.021
Rohrer, J.D., Beck, J., Warren, J.D., King, A., Al Sarraj, S., Holton, J., ...Mead, S. (2009). Corticobasal syndrome associated with a novel 1048_1049insG progranulin mutation.. JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY, 80 (11), 1297-1298. doi:10.1136/jnnp.2008.169383
Rohrer, J.D., Rossor, M.N., Warren, J.D. (2009). Neologistic jargon aphasia and agraphia in primary progressive aphasia. Journal of the Neurological Sciences, 277 (1-2), 155-159. doi:10.1016/j.jns.2008.10.014
Rohrer, J.D., Warren, J.D., Modat, M., Ridgway, G.R., Douiri, A., Rossor, M.N., ...Fox, N.C. (2009). Patterns of cortical thinning in the language variants of frontotemporal lobar degeneration. Neurology, 72 (18), 1562-1569. doi:10.1212/WNL.0b013e3181a4124e
Rohrer, J.D., Ahsan, R.L., Isaacs, A.M., Nielsen, J.E., Ostergaard, L., Scahill, R., ...Johannsen, P. (2009). Presymptomatic generalized brain atrophy in frontotemporal dementia caused by CHMP2B mutation. Dementia and Geriatric Cognitive Disorders, 27 (2), 182-186. doi:10.1159/000200466
Warren, J.D., Rohrer, J.D. (2009). Ravel's last illness: a unifying hypothesis. Brain, 132 (6), e114-. doi:10.1093/brain/awn245
Ryan, N., Rohrer, J., Warrington, E., Galton, M., Fox, N., Rossor, M., Warren, J. (2009). Selective preservation of visual motion perception in posterior cortical degeneration.
Rohrer, J.D., Guerreiro, R., Vandrovcova, J., Uphill, J., Reiman, D., Beck, J., ...Fox, N.C. (2009). The heritability and genetics of frontotemporal lobar degeneration. Neurology, 73 (18), 1451-1456. doi:10.1212/WNL.0b013e3181bf997a
Rollinson, S., Rizzu, P., Sikkink, S., Baker, M., Halliwell, N., Snowden, J., ...Rohrer, J.D. (2009). Ubiquitin associated protein 1 is a risk factor for frontotemporal lobar degeneration. Neurobiology of Aging, 30 (4), 656-665. doi:10.1016/j.neurobiolaging.2009.01.009

2008

Beck, J., Rohrer, J.D., Campbell, T., Isaacs, A., Morrison, K.E., Goodall, E.F., ...Holton, J. (2008). A distinct clinical, neuropsychological and radiological phenotype is associated with progranulin gene mutations in a large UK series. Brain, 131 (3), 706-720. doi:10.1093/brain/awm320
Kloppel, S., Stonnington, C.M., Chu, C., Draganski, B., Scahill, R.I., Rohrer, J.D., ...Frackowiak, R.S. (2008). Automatic classification of MR scans in Alzheimer's disease. Brain, 131 (3), 681-689. doi:10.1093/brain/awm319
Rohrer, J.D., Warren, J.D., Barnes, J., Mead, S., Beck, J., Pepple, T., ...Stevens, J.M. (2008). Mapping the progression of progranulin-associated frontotemporal lobar degeneration. Nature Clinical Practice Neurology, 4 (8), 455-460. doi:10.1038/ncpneuro0869
Rohrer, J.D., Warren, J.D., Omar, R., Mead, S., Beck, J., Revesz, T., ...Pickering-Brown, S.M. (2008). Parietal lobe deficits in frontotemporal lobar degeneration caused by a mutation in the progranulin gene. Archives of Neurology, 65 (4), 506-513. doi:10.1001/archneur.65.4.506
Ridgway, G.R., Henley, S.M.D., Rohrer, J.D., Scahill, R.I., Warren, J.D., Fox, N.C. (2008). Ten simple rules for reporting voxel-based morphometry studies. NeuroImage, 40 (4), 1429-1435. doi:10.1016/j.neuroimage.2008.01.003
Rohrer, J.D., McNaught, E., Foster, J., Clegg, S.L., Barnes, J., Omar, R., ...Warren, J.D. (2008). Tracking progression in frontotemporal lobar degeneration: serial MRI in semantic dementia.. Neurology, 71 (18), 1445-1451. doi:10.1212/01.wnl.0000327889.13734.cd
Rohrer, J.D., Schapira, A.H. (2008). Transient Horner's syndrome during lumbar epidural anaesthesia. European Journal of Neurology, 15 (5), 530-531. doi:10.1111/j.1468-1331.2008.02120.x
Rohrer, J.D., Knight, W.D., Warren, J.E., Fox, N.C., Rossor, M.N., Warren, J.D. (2008). Word-finding difficulty: a clinical analysis of the progressive aphasias. Brain, 131 (1), 8-38. doi:10.1093/brain/awm251

2007

Rohrer, J.D., Fox, N.C., Rossor, M.N., Warrington, E.K., Warren, J.D. (2007). Jargon language in frontotemporal lobar degeneration.
Rohrer, J.D., Warren, J.D., Omar, R., Barnes, J., Mead, S., Beck, J., ...Rossor, M.N. (2007). Longitudinal clinical, radiological and neuropsychological profile of an at-risk family member from a kindred with progranulin-associated frontotemporal lobar degeneration.
Rohrer, J.D., Kennedy, J., Knight, W.D. (2007). Myths of MTAS and MMC. Journal of the Royal Society of Medicine, 100 (6), 252-254. doi:10.1258/jrsm.100.6.252
Rohrer, J.D., Warren, J.D., Omar, R., Mead, S., Beck, J., Stevens, J.M., ...Hardy, J. (2007). Parietal lobe deficits are a feature of frontotemporal lobar degeneration caused by a mutation in the progranulin gene.

2006

Rohrer, J.D., Smith, S.J., Warren, J.D. (2006). Craving for music after treatment for partial epilepsy.. Epilepsia, 47 (5), 939-940.
Rohrer, J.D., Mead, S., Omar, R., Poulter, M., Warren, J.D., Collinge, J., Rossor, M.N. (2006). Prion protein (PRNP) genotypes in frontotemporal lobar degeneration syndromes.. Annals of Neurology, 60 (5), 616.

2005

Tahir, H., Rohrer, J., Bhatia, A., Wegener, W.A., Isenberg, D.A. (2005). Humanized anti-CD20 monoclonal antibody in the treatment of severe resistant systemic lupus erythematosus in a patient with antibodies against rituximab.. RHEUMATOLOGY, 44 (4), 561-562. doi:10.1093/rheumatology/keh533

1900

Pavisic, I., Primativo, S., Yong, K., Russell, L., Hardy, C., Bond, R., ...Crutch, S. (1900). Can Eyetracking Metrics Provide Insight into the Diagnosis of Different Dementia Types? A Spatial Anticipation Task. Presented at: Alzheimer's Association International Conference 2018 Chicago, USA.
Sogorb-Esteve, A., Nilsson, J., Swift, I.J., Heller, C., Russell, L.L., Peakman, G., ...Borroni, B. (1900). Differential Impairment of Cerebrospinal Fluid Synaptic Biomarkers in the Genetic Forms of Frontotemporal Dementia. .
Mahoney, C.J., Downey, L.E., Ridgway, G.R., Beck, J., Clegg, S., Blair, M., ...Golden, H. (1900). Longitudinal neuroimaging and neuropsychological profiles of frontotemporal dementia with C9ORF72 expansions.. Alzheimers Res Ther, doi:10.1186/alzrt144
Woollacott, I., Toomey, C., Benson, B., Lim, Y., Strand, C., Courtney, R., ...Lashley, T. (1900). MICROGLIAL PHENOTYPES DIFFER ACCORDING TO GENE MUTATION IN FAMILIAL FRONTOTEMPORAL DEMENTIA. Presented at: 11th International Conference on Frontotemporal Dementias .
Foiani, M., Cicognola, C., Jackson-Morgan, T., Ermann, N., Woollacott, I., Heller, C., ...Ye, K. (1900). Searching for novel CSF biomarkers of primary tauopathies. Presented at: 11th International Conference on Frontotemporal Dementias .
Walton, J., Ryan, N.S., Crutch, S., Rohrer, J.D., Fox, N.C. (1900). The importance of dementia support groups. BMJ, 351 1. doi:10.1136/bmj.h3875