2022

Ghevaria, H., Sengupta, S., Naja, R., Odia, R., Exeter, H., Serhal, P., ...Delhanty, J. (2022). Next Generation Sequencing Detects Premeiotic Errors in Human Oocytes. International Journal of Molecular Sciences, 23 (2), doi:10.3390/ijms23020665
Ghevaria, H., SenGupta, S., Naja, R., Odia, R., Serhal, P., Gonzalez, X.V., ...Delhanty, J. (2022). Simple and complex aneuploidy in premeiotic oocytes detected by aCGH & NGS: evidence for genetic influence and effect on fertility.

2020

Ghevaria, H., SenGupta, S., Naja, R., Odia, R., Serhal, P., Gonzalez, X.V., ...Delhanty, J. (2020). Next generation sequencing detects premeiotic errors in human oocytes and provides evidence of genetic influence.
Theobald, R., SenGupta, S., Harper, J. (2020). The status of preimplantation genetic testing in the UK and USA. Human Reproduction, 35 (4), 986-998. doi:10.1093/humrep/deaa034
Mantzouratou, A., Xanthopoulou, L., Mania, A., Serhal, P., Delhanty, J., SenGupta, S. (2020). Whole genome insights into male infertility.

2019

Delhanty, J.D.A., SenGupta, S.B., Ghevaria, H. (2019). Correction to: How common is germinal mosaicism that leads to premeiotic aneuploidy in the female?. Journal of Assisted Reproduction and Genetics, doi:10.1007/s10815-019-01644-1
Delhanty, J.D.A., SenGupta, S.B., Ghevaria, H. (2019). How common is germinal mosaicism that leads to premeiotic aneuploidy in the female?. Journal of Assisted Reproduction and Genetics, doi:10.1007/s10815-019-01596-6
Ben-Nagi, J., Jones, B., Naja, R., Amer, A., Sunkara, S., SenGupta, S., Serhal, P. (2019). Live birth rate is associated with oocyte yield and number of biopsied and suitable blastocysts to transfer in preimplantation genetic testing (PGT) cycles for monogenic disorders and chromosomal structural rearrangements. European Journal of Obstetrics and Gynecology and Reproductive Biology: X, doi:10.1016/j.eurox.2019.100055
Ghevaria, H., Sengupta, S., Naja, R., Odia, R., Serhal, P., Gonzalez, X.V., Delhanty, J. (2019). Next generation sequencing detects premeiotic errors in human oocytes and provides evidence of genetic influence.
Ben-Nagi, J., Odia, R., Gonzalez, X.V., Heath, C., Babariya, D., SenGupta, S., ...Wells, D. (2019). The first ongoing pregnancy following comprehensive aneuploidy assessment using a combined blastocenetesis, cell free DNA and trophectoderm biopsy strategy. Journal of Reproduction and Infertility, 20 (1), 57-62.
Sun, X., Odia, R., Williams, C., Campbell-Forde, M., Orach, I., Sugumar, G., ...Sen Gupta, S. (2019). The influence of ploidy status on the expression of DNA repair and cell cycle checkpoint genes in human preimplantation embryos.

2017

Jawdat, R., Sengupta, S., Lane, N. (2017). Investigation of possible incompatibilities between the mitochondrial and nuclear genomes that affect preimplantation embryo development.
Ghevaria, H., Naja, R., SenGupta, S., Serhal, P., Delhanty, J. (2017). Meiotic outcome in two carriers of Y autosome reciprocal translocations: selective elimination of certain segregants. Molecular Cytogenetics, 10 (1), 1-8. doi:10.1186/s13039-017-0303-y

2016

Tulay, P., Doshi, A., Serhal, P., SenGupta, S.B. (2016). Differential expression of parental alleles of BRCA1 in human preimplantation embryos.. European journal of human genetics : EJHG, doi:10.1038/ejhg.2016.121
TULAY, P., JAROUDI, S., DOSHI, A., SEN GUPTA, S.B. (2016). Functional assessment for elimination of mismatches in nuclear and whole cell extracts obtained from mouse and human blastocysts. Systems Biology in Reproductive Medicine, doi:10.1080/19396368.2016.1232447
Tulay, P., Sengupta, S.B. (2016). MicroRNA expression and its association with DNA repair in preimplantation embryos. JOURNAL OF REPRODUCTION AND DEVELOPMENT, 62 (3), 225-234.
Ben-Nagi, J., Serhal, P., SenGupta, S., Doye, K., Wells, D. (2016). Preimplantation genetic diagnosis: an overview and recent advances. The Obstetrician & Gynaecologist, 18 (2), 99-106. doi:10.1111/tog.12264
SenGupta, S.B., Dhanjal, S., Harper, J.C. (2016). Quality control standards in PGD and PGS. Reproductive BioMedicine Online, 32 (3), 263-270. doi:10.1016/j.rbmo.2015.11.020
Naja, R.P., Dhanjal, S., Doshi, A., Serhal, P., Delhanty, J., SenGupta, S.B. (2016). The impact of mosaicism in preimplantation genetic diagnosis (PGD): approaches to PGD for dominant disorders in couples without family history. PRENATAL DIAGNOSIS, 36 (9), 864-870. doi:10.1002/pd.4874
Ghevaria, H., SenGupta, S., Shmitova, N., Serhal, P., Delhanty, J. (2016). The origin and significance of additional aneuploidy events in couples undergoing preimplantation genetic diagnosis for translocations by array comparative genomic hybridization. Reproductive BioMedicine Online, 32 (2), 178-189. doi:10.1016/j.rbmo.2015.11.017

2015

Coonen, E., De Rycke, M., Kokkali, G., Moutou, C., SenGupta, S., Synodinos, T.-.J., Goossens, V. (2015). Data from the ESHRE PGD consortium.
De Rycke, M., Belva, F., Goossens, V., Moutou, C., SenGupta, S.B., Traeger-Synodinos, J., Coonen, E. (2015). ESHRE PGD Consortium data collection XIII: cycles from January to December 2010 with pregnancy follow-up to October 2011. HUMAN REPRODUCTION, 30 (8), 1763-1789. doi:10.1093/humrep/dev122
Tulay, P., Naja, R.P., Cascales-Roman, O., Doshi, A., Serhal, P., SenGupta, S.B. (2015). Investigation of microRNA expression and DNA repair gene transcripts in human oocytes and blastocysts. Journal of Assisted Reproduction and Genetics, 32 (12), 1757-1764. doi:10.1007/s10815-015-0585-0
Girardet, A., Viart, V., Plaza, S., Daina, G., De Rycke, M., Des Georges, M., ...Navarro, J. (2015). The improvement of the best practice guidelines for preimplantation genetic diagnosis of cystic fibrosis: Toward an international consensus. European Journal of Human Genetics, 24 (4), 469-478. doi:10.1038/ejhg.2015.99
Ghevaria, H., SenGupta, S., Serhal, P., Delhanty, J. (2015). The origin and significance of additional aneuploidy events in couples undergoing preimplantation genetic diagnosis for translocations by array comparative genomic hybridisation.

2014

Ghevaria, H., Naja, R.P., Dhanjal, S., Herman, B., Silcock, L., SenGupta, S., Delhanty, J.D. (2014). Analysis of untransferred embryos after PGD for reciprocal translocations by array-Comparative Hybridization (aCGH)-incidence meiotic and mitotic errors.
Traeger-Synodinos, J., Coonen, E.C., De Rycke, M., Moutou, C., SenGupta, S., Goossens, V. (2014). Data from the ESHRE PGD Consortium.
Moutou, C., Goossens, V., Coonen, E., De Rycke, M., Kokkali, G., Renwick, P., ...Traeger-Synodinos, J. (2014). ESHRE PGD Consortium data collection XII: cycles from January to December 2009 with pregnancy follow-up to October 2010. HUMAN REPRODUCTION, 29 (5), 880-903. doi:10.1093/humrep/deu012
Dreesen, J., Destouni, A., Kourlaba, G., Degn, B., Mette, W.C., Carvalho, F., ...Renwick, P. (2014). Evaluation of PCR-based preimplantation genetic diagnosis applied to monogenic diseases: A collaborative ESHRE PGD consortium study. European Journal of Human Genetics, 22 (8), 1012-1018. doi:10.1038/ejhg.2013.277
Mania, A., Mantzouratou, A., Delhanty, J.D.A., Baio, G., Serhal, P., Sengupta, S.B. (2014). Telomere length in human blastocysts.. REPRODUCTIVE BIOMEDICINE ONLINE, 28 (5), 624-637. doi:10.1016/j.rbmo.2013.12.010
Ghevaria, H., SenGupta, S., Sarna, U., Sargeant, S., Serhal, P., Delhanty, J. (2014). The Contribution of Germinal Mosaicism to Human Aneuploidy. CYTOGENETIC AND GENOME RESEARCH, 144 (4), 264-274. doi:10.1159/000381073

2013

Kakourou, G., Jaroudi, S., Tulay, P., Heath, C., Serhal, P., Harper, J.C., Sengupta, S.B. (2013). Investigation of gene expression profiles before and after embryonic genome activation and assessment of functional pathways at the human metaphase II oocyte and blastocyst stage.. FERTILITY AND STERILITY, 99 (3), 803-+. doi:10.1016/j.fertnstert.2012.10.036
Harper, J., SenGupta, S. (2013). Quality assessment and control in PGD.
Deans, Z., Fiorentino, F., Biricik, A., Traeger-Synodinos, J., Moutou, C., De Rycke, M., ...Harton, G. (2013). The experience of 3 years of external quality assessment of preimplantation genetic diagnosis for cystic fibrosis. European Journal of Human Genetics, 21 (8), 800-806. doi:10.1038/ejhg.2012.244

2012

Harton, G., Dreesen, J., Destouni, A., Degn, B., Christensen, M.W., Moutou, C., ...Davies, S. (2012). Analysis of PCR-based monogenic preimplantation genetic diagnosis by follow up of untransferred embryos, a multi-center study.
Mamas, T., Gordon, A., Brown, A., Harper, J., Sengupta, S. (2012). Detection of aneuploidy by array comparative genomic hybridization using cell lines to mimic a mosaic trophectoderm biopsy.. FERTILITY AND STERILITY, 97 (4), 943-947. doi:10.1016/j.fertnstert.2011.12.048
Mamas, T., Xanthopoulou, L., Heath, C., Doshi, A., Serhal, P., SenGupta, S.B. (2012). Incidence of aneuploidy in embryos from fertile couples.
Tulay, P., Naja, R.P., Cascales-Roman, O., Cawood, S., Doshi, A., Serhal, P., SenGupta, S.B. (2012). Investigation of microRNA expression with DNA repair in human oocytes and preimplantation embryos.
SenGupta, S.B., Vadaparampil, S.T., Menon, U. (2012). Preimplantation genetic diagnosis for hereditary cancers.. REPRODUCTIVE HEALTH AND CANCER IN ADOLESCENTS AND YOUNG ADULTS, 732 103-113. doi:10.1007/978-94-007-2492-1_8
SenGupta, S.B., Delhanty, J.D.A. (2012). Preimplantation genetic diagnosis: recent triumphs and remaining challenges.. EXPERT REVIEW OF MOLECULAR DIAGNOSTICS, 12 (6), 585-592. doi:10.1586/ERM.12.61
Harper, J.C., Sengupta, S.B. (2012). Preimplantation genetic diagnosis: state of the art 2011.. HUMAN GENETICS, 131 (2), 175-186. doi:10.1007/s00439-011-1056-z
Harper, J.C., Wilton, L., Traeger-Synodinos, J., Goossens, V., Moutou, C., SenGupta, S.B., ...Geraedts, J.P.M. (2012). The ESHRE PGD Consortium: 10 years of data collection.. HUMAN REPRODUCTION UPDATE, 18 (3), 234-247. doi:10.1093/humupd/dmr052

2011

Harton, G.L., De Rycke, M., Fiorentino, F., Moutou, C., SenGupta, S., Traeger-Synodinos, J., Harper, J.C. (2011). ESHRE PGD consortium best practice guidelines for amplification-based PGD. Hum.Reprod., 26 (1), 33-40. doi:10.1093/humrep/deq231
Tulay, P., Jaroudi, S., Harper, J., SenGupta, S. (2011). Functional assessment of mismatch repair.
Xanthopoulou, L., Delhanty, J.D.A., Mania, A., Mamas, T., Serhal, P., Sengupta, S.B., Mantzouratou, A. (2011). The nature and origin of binucleate cells in human preimplantation embryos: relevance to placental mesenchymal dysplasia.. REPRODUCTIVE BIOMEDICINE ONLINE, 22 (4), 362-370. doi:10.1016/j.rbmo.2011.01.001

2010

Harper, J.C., Sengupta, S., Vesela, K., Thornhill, A., Dequeker, E., Coonen, E., Morris, M.A. (2010). Accreditation of the PGD laboratory.. Hum.Reprod., 25 (4), 1051-1065. doi:10.1093/humrep/dep450
Kakourou, G., Dhanjal, S., Mamas, T., Serhal, P., Delhanty, J.D., SenGupta, S.B. (2010). Modification of the triplet repeat primed polymerase chain reaction method for detection of the CTG repeat expansion in myotonic dystrophy type 1: application in preimplantation genetic diagnosis.. FERTILITY AND STERILITY, 94 (5), 1674-1679. doi:10.1016/j.fertnstert.2009.10.050
Harper, J., Coonen, E., De Rycke, M., Fiorentino, F., Geraedts, J., Goossens, V., ...Renwick, P. (2010). What next for preimplantation genetic screening (PGS)? A position statement from the ESHRE PGD Consortium Steering Committee.. Hum.Reprod., 25 (4), 821-823. doi:10.1093/humrep/dep476

2009

Mamas, T., SenGupta, S., Sultan, H., Dafou, D., Gordon, T., Harper, J.C. (2009). Detection of chromosomal abnormalities in single cells from epithelial cell lines by array comparative genomic hybridisation.
Jaroudi, S., Kakourou, G., Cawood, S., Doshi, A., Ranieri, D.M., Serhal, P., ...SenGupta, S.B. (2009). Expression profiling of DNA repair genes in human oocytes and blastocysts using microarrays. Hum.Reprod., 24 (10), 2649-2655. doi:10.1093/humrep/dep224
Kakourou, G., Jaroudi, S., Gotts, S., Doshi, A., Serhal, P., Harper, J.C., ...SenGupta, S.B. (2009). Gene expression profiling of human oocytes and embryo blastocysts.
Glentis, S., SenGupta, S., Thornhill, A., Wang, R., Craft, I., Harper, J.C. (2009). Molecular comparison of single cell MDA products derived from different cell types.. Reprod.Biomed.Online., 19 (1), 89-98.

2008

Mamas, T., Kakourou, G., Dhanjal, S., Doshi, A., Gotts, S., Serhal, P., ...SenGupta, S. (2008). Detection of aneuploidy in embryos from PGD cases for single gene disorders.
Harper, J.C., de Die-Smulders, C., Goossens, V., Harten, G., Moutou, C., Repping, S., ...Van Rij, M.C. (2008). ESHRE PGD consortium data collection VII: cycles from January to December 2004 with pregnancy follow-up to October 2005. Human Reproduction, 23 (4), 741-755. doi:10.1093/humrep/dem354
Jaroudi, S., Harper, J.C., SenGupta, S.B. (2008). Functional assessment of mismatch repair in human nuclear extracts.
Kakourou, G., Dhanjal, S., Mamas, T., Doshi, A., Gotts, S., Cawood, S., ...Harper, J.C. (2008). Inheritance of the DMPK CTG repeat in couples undergoing PGD for DM1.
Kakourou, G., Dhanjal, S., Mamas, T., Gotts, S., Doshi, A., Fordham, K., ...Harper, J.C. (2008). Preimplantation genetic diagnosis for myotonic dystrophy type 1 in the UK.. NEUROMUSCULAR DISORDERS, 18 (2), 131-136. doi:10.1016/j.nmd.2007.10.002
Dhanjal, S., Kakourou, G., Mamas, T., Doshi, A., Gotts, S., Serhal, P., ...SenGupta, S.B. (2008). The pursuit of a diagnosis for every embryo in PGD.
Harper, J.C., Sermon, K., Geraedts, J., Vesela, K., Harton, G., Thornhill, A., ...de Die-Smulders, C. (2008). What next for Preimplantation Genetic Screening (PGS)?. Human Reproduction, 23 (3), 487-480. doi:10.1093/humrep/dem424

2007

Jaroudi, S., SenGupta, S. (2007). DNA repair in mammalian embryos. Mutat.Res., 635 (1), 53-77. doi:10.1016/j.mrrev.2006.09.002
Sermon, K.D., Michiels, A., Harton, G., Moutou, C., Repping, S., Scriven, P.N., ...Viville, S. (2007). ESHRE PGD Consortium data collection VI: cycles from January to December 2003 with pregnancy follow-up to October 2004. HUMAN REPRODUCTION, 22 (2), 323-336. doi:10.1093/humrep/del402
Mamas, T., Dhanjal, S., Jaroudi, S., Kakourou, G., SenGupta, S. (2007). Preimplantation genetic diagnosis for inherited cancer predisposition - Different strategies.
Kakourou, G., Dhanjal, S., Daphnis, D., Doshi, A., Nuttall, S., Gotts, S., ...Sen Gupta, S. (2007). Preimplantation genetic diagnosis for myotonic dystrophy type 1: detection of crossover between the gene and the linked marker APOC2. Prenatal Diagnosis, 27 (2), 111-116. doi:10.1002/pd.1611
Dhanjal, S., Kakourou, G., Mamas, T., Saleh, N., Doshi, A., Gotts, S., ...Delhanty, J. (2007). Preimplantation genetic diagnosis for retinoblastoma predisposition. British Journal of Ophthalmology, 91 (8), 1090-1091. doi:10.1136/bjo.2006.108597
Dhanjal, S., Kakourou, G., Mamas, T., Saleh, N., Doshi, A., Gotts, S., ...Delhanty, J. (2007). Preimplantation genetic diagnosis for retinoblastoma predisposition.. Br J Ophthalmol, 91 (8), 1090-1091. doi:10.1136/bjo.2006.108597

2006

Harper, J.C., Boelaert, K., Geraedts, J., Harton, G., Kearns, W.G., Moutou, C., ...Scriven, P.N. (2006). ESHRE PGD Consortium data collection V: Cycles from January to December 2002 with pregnancy follow-up to October 2003. Human Reproduction, 21 (1), 3-21. doi:10.1093/humrep/dei292
Lawes, D.A., Pearson, T., Sen Gupta, S., Boulos, P.B. (2006). Is MSI-H of value in predicting the development of metachronous colorectal cancer?. European Journal of Cancer, 42 (4), 473-476. doi:10.1016/j.ejca.2005.11.019
Glentis, S., SenGupta, S., Thornhill, A., Craft, I., Carter, N., Rickman, L., Harper, C.J. (2006). Multiple displacement amplification as a method of whole genome amplification for preimplantation genetic diagnosis.
Kakourou, G., Dhanjal, S., Sud, R., Mamas, T., Doshi, A., Nuttall, S., ...Harper, J.C. (2006). Preimplantation genetic diagnosis for non-syndrornic deafness.
Dhanjal, S., Kakourou, G., Saleh, N., Mamas, T., Doshi, A., Gotts, S., ...Delhanty, J. (2006). Preimplantation genetic diagnosis for retinoblastoma predisposition.

2005

Lawes, D.A., Pearson, T., Sen Gupta, S., Boulos, P.B. (2005). The role of MLH1, MSH2 and MSH6 in the development of multiple colorectal cancers. British Journal of Cancer, 93 (4), 472-477. doi:10.1038/sj.bjc.6602708

2004

Lawes, D.A., SenGupta, S., Boulos, P.B. (2004). The incidence of HNPCC in patients with metachronous colorectal cancer.
Lawes, D.A., SenGupta, S., Boulos, P.B. (2004). The incidence of HNPCC in patients with metachronous colorectal cancer.

2003

Lawes, D.A., SenGupta, S.B., Boulos, P.B. (2003). The clinical importance and prognostic implications of microsatellite instability in sporadic cancer. European Journal of Surgical Oncology, 29 (3), 201-212.

2002

Lawes, D.A., SenGupta, S.B., Boulos, P.B. (2002). Pathogenesis and clinical management of hereditary non-polyposis colorectal cancer. British Journal Of Surgery, 89 (11), 1357-1369.
Lawes, D., Pearson, T., Sen Gupta, S., Taylor, I., Boulos, P.B. (2002). Patients with left-sided colorectal cancer demonstrating microsatellite instability are at risk of developing a second cancer.

2000

(2000). Evaluation of colonoscopic sized biopsies for microsatellite instability and adenomatous polyposis coli (APC) variants. Colorectal Disease, 2 (5), 304-308.

1998

Fajobi, O., Yiu, C.Y., Sen-Gupta, S.B., Boulos, P.B. (1998). Metachronous colorectal cancers.. Br.J.Surg., 85 (7), 897-901. doi:10.1046/j.1365-2168.1998.00800.x

1997

Sengupta, S.B., Yiu, C.Y., Boulos, P.B. (1997). Are colonic biopsies of value in genetic analysis?.
Sengupta, S.B., Yiu, C.Y., Boulos, P.B., De Silva, M., Sams, V.R., Delhanty, J.D.A. (1997). Genetic instability in patients with metachronous colorectal cancers. BR J SURG, 84 996-1000.

1994

Gayther, S.A., Wells, D., SenGupta, S.B., Chapman, N., K, T., K, D., J, D. (1994). Regionally clustered APC mutations are associated with a severe phenotype and occur at a high frequency in new mutation cases of adenomatous polyposis coli. Human Molecular Genetics, 3 (1), 53-56.

1993

Sen-Gupta, S., Van der Luijt, R.B., Bowles, L.V., Meera, K.P., Delhanty, J.D. (1993). Somatic mutation of APC gene in desmoid tumour in familial adenomatous polyposis. Lancet, 342 (8870), 552-553.