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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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2019 |
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2018 |
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2017 |
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2017 |
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2017 |
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2017 |
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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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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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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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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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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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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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2012 |
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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:
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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:
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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:
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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:
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Interleukin-10 haplotypes in Celiac Disease in the Spanish population.
Nuñez C, Alecsandru D, Varade J, Polanco I, Maluenda C, Fernandez-Arquero M, G de la Concha E, Urcelay E, Martinez A, Urcelay E,
BMC Med Genet. 2006 doi:
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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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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:
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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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