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2023 |
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2023 |
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2023 |
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2023 |
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2023 |
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2023 |
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2023 |
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2023 |
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2023 |
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The first mitotic division: a perilous bridge connecting the zygote and the early embryo
Giovanni Coticchio, Danilo Cimadomo, Greta Chiara Cermisoni, Laura Rienzi, Enrico Papaleo, Filippo Maria Ubaldi, Andrea Borini, Lucia De Santis
Human Reproduction, Volume 38, Issue 6, June 2023, Pages 1019–1027, https://doi.org/10.1093/humrep/dead067. 2023 doi:
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2022 |
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2022 |
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2022 |
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2022 |
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2022 |
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2022 |
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2022 |
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2022 |
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2021 |
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The cyto-protective effects of LH on ovarian reserve and female fertility during exposure to gonadotoxic alkylating agents in an adult mouse model.
Del Castillo LM, Buigues A, Rossi V, Soriano MJ, Martinez J, De Felici M, Lamsira HK, Di Rella F, Klinger FG, Pellicer A, Herraiz S
Hum Reprod. 2021 doi:
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2021 |
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2021 |
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2021 |
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2021 |
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2021 |
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2021 |
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2021 |
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2021 |
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2021 |
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2021 |
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2021 |
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2019 |
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2018 |
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2017 |
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Analysis of implantation and ongoing pregnancy rates following the transfer of mosaic diploid-aneuploid blastocysts.
Fragouli, E, Alfarawati, S, Spath, K, Babariya, D, Tarozzi, N, Borini, A, Wells, D,
Hum Genet. 2017 doi:
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2017 |
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2017 |
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Survey of Fertility Preservation Options Available to Patients With Cancer Around the Globe. J Glob Oncol. 4, pp. 1 - 16. 28/06/2017.
Rashedi, AS, de, Roo, SF, Ataman, LM, Edmonds, ME, Silva, AA, Scarella, A, Horbaczewska, A, Anazodo, A, Arvas, A, Ramalho, de, Carvalho, B, Sartorio, C, Beerendonk, CCM, Diaz-Garcia, C, Anazodo, A,
2017 doi:
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2017 |
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2016 |
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2016 |
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2016 |
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2016 |
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2016 |
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A randomized and blinded comparison of qpcr and NGS based detection of aneuploidy in a cell line mixture model of blastocyst biopsy mosaicism.
Goodrich, D, Tao, X, Bohrer, C, Lonczak, A, Xing, T, Zimmerman, R, Zhan, Y, Scott, R T, Treff, NR, Scott, R T,
Hum Reprod. 2016 doi:
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2016 |
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2016 |
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Causes and estimated incidences of sex-chromosome misdiagnosis in preimplantation genetic diagnosis of aneuploidy.
Ravichandran, K, Guzman, L, Escudero, T, Zheng, X, Colls, P, Jordan, A, Cohen, J, Wells, D, Munne, S, Wells, D,
RBM Online. 2016 doi:
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2016 |
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2016 |
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2016 |
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Development and validation of concurrent preimplantation genetic diagnosis for single gene disorders and comprehensive chromosomal aneuploidy screening without whole-genome amplification.
Zimmerman, RS, Jalas, C, Tao, X, Fedick, AM, Kim, J, Pepe, RJ, Northrop, LE, Scott, R T, Treff, NR, , Scott, R T,
Fertil Steril. 2016 doi:
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2016 |
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Embryonic aneuploidy does not differ among genetic ancestry according to continental origin as determined by ancestry informative markers.
Franasiak, J M, Olcha, M, Shastri, S, Molinaro, T A, Congdon, H, Treff, NR, Scott, R T,
Hum Reprod. 2016 doi:
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2016 |
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2016 |
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2016 |
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Next Generation Sequencing Based Comprehensive Chromosome Screening in Mouse Polar Bodies, Oocytes, and Embryos.
Treff, NR, Krisher, R, Tao, X, Garnsey, H, Bohrer, C, Silva, E, Landis, J, Taylor, D, Scott, R T, Woodruff, TK, Duncan, FE, Taylor, D,
Biol Reprod. 2016 doi:
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2016 |
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2016 |
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2016 |
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2016 |
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2016 |
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Why do euploid embryos miscarry? A case-control study comparing the rate of aneuploidy within presumed euploid embryos that resulted in miscarriage or live birth using next-generation sequencing.
Maxwell, SM, Colls, P, Hodes-Wertz, B, McCulloh, DH, McCaffrey, C, Wells, D, Munne, S, Grifo, J,
Fertil Steril. 2016 doi:
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2016 |
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2015 |
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2015 |
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2015 |
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2015 |
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2015 |
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2015 |
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2015 |
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2015 |
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2015 |
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Karyomapping allows preimplantation genetic diagnosis of a de-novo deletion undetectable using conventional PGD technology.
Gimenez, C, Sarasa, J, Arjona, C, Vilamajo, E, Martinez-Pasarell, O, Wheeler, K, Valls, G, Garcia-Guixe, E, Wells, D, Garcia-Guixe, E,
RBM Online. 2015 doi:
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2015 |
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Live births following Karyomapping of human blastocysts: experience from clinical application of the method.
Konstantinidis, M, Prates, R, Goodall, N, Fischer, J, Tecson, V, Lemma, T, Chua, B, Jordan, A, Armenti, E, Wells, D, Munne, S, Jordan, A,
RBM Online. 2015 doi:
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2015 |
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Routine use of next-generation sequencing for preimplantation genetic diagnosis of blastomeres obtained from embryos on day 3 in fresh in~vitro fertilization cycles.
Ukaszuk K, Pukszta, S, Wells, D, Cybulska, C, Liss, J, P?ociennik, ?, Kuczy?ski, W, Zabielska, J,
Fertil Steril. 2015 doi:
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2015 |
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2015 |
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2014 |
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2014 |
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2014 |
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Clinical utilization of a rapid low-pass whole genome sequencing technique for the diagnosis of aneuploidy in human embryos prior to implantation.
Wells, D, Kaur, K, Grifo, J, Glassner, M, Taylor, JC, Fragouli, E, Munne, S,
J Med Genet. 2014 doi:
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2014 |
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2014 |
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2014 |
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2014 |
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2014 |
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2014 |
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2014 |
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Increasing the probability of selecting chromosomally normal embryos by time-lapse morphokinetic analysis.
Basile, N, Bronet, F, Nogales, MC, Martinez, E, Ariza, M, Agudo, D, Florensa, M, Riqueros, M, Meseguer, M, Riqueros, M,
Fertil Steril. 2014 doi:
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2014 |
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Live birth after PGD with confirmation by a comprehensive approach (karyomapping) for simultaneous detection of monogenic and chromosomal disorders.
Natesan, SA, Handyside, AH, Thornhill, AR, Ottolini, CS, Sage, K, Summers, MC, Konstantinidis, M, Wells, D, Griffin, DK,
RBM Online. 2014 doi:
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2014 |
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2014 |
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2014 |
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2014 |
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2014 |
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Simultaneous assessment of aneuploidy, polymorphisms, and mitochondrial DNA content in human polar bodies and embryos with the use of a novel microarray platform.
Konstantinidis, M, Alfarawati, S, Hurd, D, Paolucci, M, Shovelton, J, Fragouli, E, Wells, D,
Fertil Steril. 2014 doi:
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2014 |
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2014 |
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2014 |
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The nature of aneuploidy with increasing age of the female partner: a review of 15,169 consecutive trophectoderm biopsies evaluated with comprehensive chromosomal screening.
Franasiak, J M, Forman, EJ, Hong, KH, Werner, M D, Upham, KM, Treff, NR,
Fertil Steril. 2014 doi:
|
2014 |
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Uniparental disomy in the human blastocyst is exceedingly rare.
Gueye, N, Devkota, B, Taylor, D, Pfundt, R, Scott, R T, Tref, N,
Fertil Steril. 2014 doi:
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2014 |
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2013 |
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2013 |
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Additive effect of factors related to assisted conception on the reduction of maternal serum pregnancy-associated plasma protein A concentrations and the increased false-positive rates in first-trimester Down syndrome screening.
Bellver, J, Casanova, C, Garrido, N, Lara, C, Remohi, J, Pellicer, A, Serra, V,
Fertil Steril. 2013 doi:
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2013 |
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2013 |
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2013 |
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Embryos whose polar bodies contain isolated reciprocal chromosome aneuploidy are almost always euploid.
Forman, EJ, Treff, NR, Stevens, JM, Garnsey, HM, Katz-Jaffe, MG, Scott, R T, Schoolcraft, WB,
Hum Reprod. 2013 doi:
|
2013 |
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Evaluation of targeted next-generation sequencing based preimplantation genetic diagnosis of monogenic disease.
Treff, NR, Fedick, A, Tao, X, Devkota, B, Taylor, D, Scott, R T,
Fertil Steril. 2013 doi:
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2013 |
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2013 |
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2013 |
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2013 |
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2013 |
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2013 |
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2013 |
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2013 |
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2013 |
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2013 |
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2013 |
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The origin and impact of embryonic aneuploidy.
Fragouli, E, Alfarawati, S, Spath, K, Jaroudi, S, Sarasa, J, Enciso, M, Wells, D,
Hum Genet. 2013 doi:
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2013 |
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2013 |
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2012 |
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2012 |
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2012 |
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Alteration of gene expression in human cumulus cells as a potential indicator of oocyte aneuploidy.
Fragouli, E, Wells, D, Iager, AE, Kayisli, UA, Patrizio, P,
Hum Reprod. 2012 doi:
|
2012 |
|
2012 |
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Blastocyst preimplantation genetic diagnosis of a mitochondrial DNA disorder.
Treff, NR, Tao, X, Campos, J, Su, J, Ferry, KM, Levy, B, Scott, R T,
Fertil Steril. 2012 doi:
|
2012 |
|
2012 |
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Characterization of two heterozygous mutations of the oocyte activation factor phospholipase C zeta (PLC?) from an infertile man by use of minisequencing of individual sperm and expression in somatic cells.
Kashir, J, Konstantinidis, M, Jones, C, Heindryckx, B, Sutter, P, De, Parrington, J, Wells, D, Coward, K,
Fertil Steril. 2012 doi:
|
2012 |
|
2012 |
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Comprehensive chromosome screening is highly predictive of the reproductive potential of human embryos: a prospective, blinded, nonselection study.
Scott, R T, Ferry, KM, Su, J, Tao, X, Scott, KL, Treff, NR,
Fertil Steril. 2012 doi:
|
2012 |
|
2012 |
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Development and validation of an accurate quantitative real-time polymerase chain reaction – based assay for human blastocyst comprehensive chromosomal aneuploidy screening. Seminal Contribution.
Treff, NR, Tao, X, Ferry, KM, Su, J, Taylor, D, Scott, R T,
Fertil Steril. 2012 doi:
|
2012 |
|
2012 |
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Intra-age, intercenter, and intercycle differences in chromosome abnormalities in oocytes.
Munne, S, Held, KR, Magli, CM, Ata, B, Wells, D, Fragouli, E, Baukloh, V, Fischer, R, Gianaroli, L, Fischer, R,
Fertil Steril. 2012 doi:
|
2012 |
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2012 |
|
2012 |
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Single embryo transfer with comprehensive chromosome screening results in improved ongoing pregnancy rates and decreased miscarriage rates.
Forman, EJ, Tao, X, Ferry, KM, Taylor, D, Treff, NR, Scott, R T,
Hum Reprod. 2012 doi:
|
2012 |
-
Successful Live Birth following Preimplantation Genetic Diagnosis for Phenylketonuria in Day 3 Embryos by Specific Mutation Analysis and Elective Single Embryo Transfer.
Lavery, S, Abdo, D, JIMD, Reports, Kotrotsou, M, Trew, G, Konstantinidis, M, Wells, D,
JIMD Reports. 2012 doi:
|
2012 |
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2012 |
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2011 |
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A maternally inherited autosomal point mutation in human phospholipase C zeta (PLC?) leads to male infertility.
Kashir, J, Konstantinidis, M, Jones, C, Lemmon, B, Lee, HC, Hamer, R, Heindryckx, B, Deane, CM, De, Sutter, P, Fissore, RA, Parrington, J, Wells, D, Coward, K, Deane, CM,
Hum Reprod. 2011 doi:
|
2011 |
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2011 |
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2011 |
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Effect of sperm DNA fragmentation on pregnancy outcome depends on oocyte quality
Meseguer, M, Santiso, R, Garrido, N, Garcia-Herrero, S, Remohi, J, Fernandez, JL,
Fertil Steril. 2011 doi:
|
2011 |
|
2011 |
|
2011 |
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SNP Microarray Based Concurrent Screening of 24 Chromosome Aneuploidy and Unbalanced Translocations in Preimplantation Human Embryos.
Treff, NR, Northrop, L, Kasabwala, K, Su, J, Levy, B, Scott, R T,
Fertil Steril. 2011 doi:
|
2011 |
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2011 |
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2011 |
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2011 |
-
Validation of microarray comparative genomic hybridization for comprehensive chromosome analysis of embryos.
Gutierrez-Mateo, C, Colls, P, Sanchez-Garcia, J, Escudero, T, Prates, R, Ketterson, K, Wells, D, Munne, S,
Fertil Steril. 2011 doi:
|
2011 |
-
Accurate single cell 24 chromosome aneuploidy screening using whole genome amplification and single nucleotide polymorphism microarrays.
Treff, NR, Su, J, Tao, X, Levy, B, Scott, R T,
Fertil Steril. 2010 doi:
|
2010 |
-
Aneploidies in embryos and spermatozoa from patients with Y chromosome microdelections.
Mateu, E, Rodrigo, L, Martinez, MC, Peinedo, V, Delagado, A, MIr, P, Simon, C, Remohi, J,
RBM Online. 2010 doi:
|
2010 |
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2010 |
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Cytogenetic analysis of human blastocysts with the use of FISH, CGH and aCGH: scientific data and technical evaluation.
Fragouli, E, Alfarawati, S, Daphnis, D, Goodall, N, Mania, A, Griffiths, T, Gordon, T, Wells, D,
Hum Reprod. 2010 doi:
|
2010 |
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2010 |
-
GnRH agonist administration at the time of implantation does not improve pregnancy outcome in intrauterine insemination cycles: a randomized controlled tria
Bellver, J, E, Labarta, Bosch, E, Melo, MAB, Vidal, C, Remohi, J, Pellicer, A,
Fertil Steril. 2010 doi:
|
2010 |
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2010 |
-
Improved detection of aneuploid blastocysts using a new 12-chromosome FISH test.
Munne, S, Fragouli, E, Colls, P, Katz-Jaffe, MG, Schoolcraft, WB, Wells, D,
RBM Online. 2010 doi:
|
2010 |
-
Improving FISH diagnosis for preimplantation genetic aneploidy screening
Mir, P, Rodrigo, L, Mateu, E, Milan, M, Mercader, A, Buendia, P, Delgado, A, Pellicer, A, Remohi, J, Rubio, C,
Hum Reprod. 2010 doi:
|
2010 |
|
2010 |
-
Robust embryo identification using polar body single nucleotide polymorphism microarray based DNA fingerprinting.
Treff, NR, Su, J, Kasabwala, N, Tao, X, Miller, KA, Scott, R T,
Fertil Steril. 2010 doi:
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2010 |
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2010 |
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2010 |
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2010 |
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2010 |
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2010 |
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2010 |
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2010 |
-
Transmission of Mitochondrial DNA Diseases and Ways to Prevent Them.
Poulton, J, Chiaratti, MR, Meirelles, FV, Kennedy, S, Wells, D, Holt, IJ,
PLoS Genet. 2010 doi:
|
2010 |
-
Y chromosome microdeletions, sperm DNA fragmentation and sperm oxidative stress as causes of recurrent spontaneous abortion of unknown etiology.
Bellver, J, Meseguer, M, Muriel, L, Garcia-Herrero, S, Barreto, MAM, Garda, AL, Remohi, J, Pellicer, A, Garrido, N, Pellicer, A,
Hum Reprod. 2010 doi:
|
2010 |
-
Comparative genomic hybridization of oocytes and first polar bodies from young donors.
Fragouli, E, Escalona, A, Gutierrez-Mateo, C, Tormasi, S, Alfarawati, S, Sepulveda, S, Wells, D, Munne, S,
RBM Online. 2009 doi:
|
2009 |
|
2008 |
-
Birth of a healthy boy after a double factor PGD in a couple carrying a genetic disease and at risk for aneuploidy.
Obradors, A, Fernandez, E, Oliver-Bonet, M, Rius, M, de, la, Fuente, A, Wells, D, Benet, J, Navarro, J,
Hum Reprod. 2008 doi:
|
2008 |
|
2008 |
-
Técnica de B-Lynch en el control de la hemorragia posparto Progresos de Obstetricia
Blanco, M, Gomez, E, Manosalvas, P, Izquierdo, A, Puente, J M, Hernandez, Garcia, JM,
Ginecología. 2008 doi:
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2008 |
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2007 |
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2007 |
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2007 |
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2006 |
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2006 |
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2006 |
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Heteroparental blastocyst production from microsurgically corrected tripronucleated human embryos.
Escriba, M J, Martin, J, Rubio, C, Valbuena, D, Remohi, J, Pellicer, A, Simon, C,
Fertil Steril. 2006 doi:
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2006 |
-
J.Ultrastructure of preimplantation genetic diagnosis-derived human blastocysts grown in a coculture system after vitrification.
Escriba, M J, Escobedo-Lucea, C, Mercader, A, De, Los, Santos, MJ, Pellicer, A, Remohi, J,
Fertil Steril. 2006 doi:
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2006 |
|
2006 |
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2006 |
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2005 |
-
Association of abnormal morphology and altered gene expression in human preimplantation embryos.
Wells, D, Bermúdez, MG, Steuerwald, N, Malter, HE, Thornhill, AR, Cohen, J,
Fertil Steril. 2005 doi:
|
2005 |
|
2005 |
-
Expression of genes regulating chromosome segregation, the cell cycle and apoptosis during human preimplantation development.
Wells, D, Bermudez, MG, Steuerwald, N, Thornhill, AR, Walker, DL, Malter, H, Delhanty, JDA, Cohen, J,
Hum Reprod. 2005 doi:
|
2005 |
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2005 |
|
2005 |
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2004 |
-
Reliability of comparative genomic hybridization to detect chromosome abnormalities in first polar bodies and metaphase II oocytes.
Gutierrez-Mateo, C, Wells, D, Benet, J, Sanchez-Garcia, JF, Bermúdez, MG, Belil, I, Egozcue, J, Munne, S, Navarro, J, Munne, S,
Hum Reprod. 2004 doi:
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2004 |
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2003 |
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2003 |
-
Single-cell sequencing and mini-sequencing for preimplantation genetic diagnosis.
Bermudez, MG, Piyamongkol, W, Tomaz, S, Dudman, E, Sherlock, JK, Wells, D,
Prenat Diagn. 2003 doi:
|
2003 |
|
2002 |
-
First clinical application of comparative genomic hybridization and polar body testing for preimplantation genetic diagnosis of aneuploidy.
Wells, D, Escudero, T, Levy, B, Hirschhorn, K, Delhanty, JDA, Munne, S,
Fertil Steril. 2002 doi:
|
2002 |
|
2002 |
-
Preimplantation genetic diagnosis for single gene disorders: experience with five single gene disorders.
Harper, JC, Wells, D, Piyamongkol, W, Abou-Sleiman, P, Apessos, A, Ioulianos, A, Davis, M, Doshi, A, Serhal, P, Ranieri, M, Rodeck, C, Delhanty, JDA,
Prenat Diagn. 2002 doi:
|
2002 |
|
2002 |
-
The "vanishing embryo" phenomenon in an oocyte donation programme.
Rodriguez-Gonzalez, M, Serra, V, Garcia-Velasco, J A, Pellicer, A, Remohi, J,
Fertil Steril. 2002 doi:
|
2002 |
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2002 |
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2002 |
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2002 |
-
A successful strategy for preimplantation genetic diagnosis of myotonic dystrophy using multiplex fluorescent PCR.
Piyamongkol, W, Harper, JC, Sherlock, JK, Doshi, A, Serhal, PF, Delhanty, JDA, Wells, D,
Prenat Diagn. 2001 doi:
|
2001 |
-
Acrocentric chromosome disomy is increased in spermatozoa from fathers of Turner syndrome patients
Soares, S R, Vidal, F, Bosch, M, Martinez-Pasarell, O, Nogues, C, Egozcue, J, Templado, C,
Hum Genet. 2001 doi:
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2001 |
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2001 |
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2001 |
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2001 |
-
Numerical chromosome abnormalities in the spermatozoa of the fathers of children with trisomy 21 of paternal origin: generalised tendency to meiotic non-disjunction.
Soares, S R, Templado, C, Blanco, J, Egozcue, J, Vidal, F,
Hum Genet. 2001 doi:
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2001 |
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2001 |
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2001 |
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2001 |
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2000 |
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2000 |
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2000 |
-
Deletion and duplication of the adenomatous polyposis coli gene resulting from an interchromosomal insertion involving 5 (q22q23.3) in the father.
Hastings, RJ, Svennevik, EC, Setterfield, B, Wells, D, Delhanty, JDA, Mackinnon, H,
J Med Genet. 2000 doi:
|
2000 |
|
2000 |
-
Positive outcome after preimplantation diagnosis of aneuploidy in human embryos.
Munne, S, Magli, C, Cohen, J, Morton, P, Sadowy, S, Gianaroli, L, Tucker, M, Marquez, C, Sable, D, Ferraretti, AP, Massey, JB, Scott, R T,
Hum Reprod. 1999 doi:
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1999 |
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1998 |
|
1998 |
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1997 |
|
1997 |
-
APC gene mutation and DNA microsatellite instability in pancreatic cancers of UK origin.
See, CG, Sud, R, Wells, D, Bowles, L, Ding, S, Habib, N, Delhanty, JDA,
GI Cancer 2. 1996 doi:
|
1996 |
|
1996 |
|
1995 |
-
Rapid detection of rare variants and common polymorphisms in the APC gene by PCR-SSCP for presymptomatic diagnosis and showing allele loss.
Gayther, SA, Sud, R, Wells, D, Tsioupra, K, Delhanty, JD,
J Med Genet. 1995 doi:
|
1995 |