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Assisted reproduction treatment and epigenetic inheritance

Human reproduction update, 2012-03, Vol.18 (2), p.171-197

2012

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Exome sequencing reveals novel causes as well as new candidate genes for human globozoospermia

Human reproduction (Oxford), 2020-01, Vol.35 (1), p.240-252

2020

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Recent developments in genetics and medically assisted reproduction: from research to clinical applications

European journal of human genetics : EJHG, 2018-01, Vol.26 (1), p.12-33

2018

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Assisted oocyte activation overcomes fertilization failure in globozoospermic patients regardless of the DPY19L2 status

Human reproduction (Oxford), 2013-04, Vol.28 (4), p.1054-1061

2013

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Pathogenic missense variation in PABPC1L/EPAB causes female infertility due to oocyte maturation arrest at the germinal vesicle stage

Journal of assisted reproduction and genetics, 2024-02, Vol.41 (2), p.311-322

2024

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C10 hESc and IPSc as models for genetic defects

Reproductive biomedicine online, 2010, Vol.20, p.S3-S3

Viville, S

2010

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ESHRE PGD consortium data collection VII: cycles from January to December 2004 with pregnancy follow-up to October 2005

Human reproduction (Oxford), 2008-04, Vol.23 (4), p.741-755

2008

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ESHRE PGD Consortium data collection VI: cycles from January to December 2003 with pregnancy follow-up to October 2004

Human reproduction (Oxford), 2007-02, Vol.22 (2), p.323-336

2007

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What next for preimplantation genetic screening? More randomized controlled trials needed?

Human reproduction (Oxford), 2008-12, Vol.23 (12), p.2626-2628

2008

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ESHRE PGD Consortium data collection IV: May–December 2001

Human reproduction (Oxford), 2005-01, Vol.20 (1), p.19-34

2005

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Increased pregnancy rate using standardized coculture on autologous endometrial cells and single blastocyst transfer : a multicentre randomized controlled trial

Cellular and molecular biology (Noisy-le-Grand, France), 2015-01, Vol.61 (8), p.79

2015

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Genetic aspects of male infertility: From bench to clinic

Gynécologie, obstétrique, fertilité & sénologie, 2019-01, Vol.47 (1), p.54-62

2019

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Chromosome abnormalities in sperm from infertile men with normal somatic karyotypes: teratozoospermia

Cytogenetic and genome research, 2005-01, Vol.111 (3-4), p.352-357

2005

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P-714 Clinical utility of FMR1 screening: risk factor or monogenic cause for POI

Human reproduction (Oxford), 2023-06, Vol.38 (Supplement_1)

2023

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Creation of a registry for human embryonic stem cells carrying an inherited defect: joint collaboration between ESHRE and hESCreg

Human reproduction (Oxford), 2009-07, Vol.24 (7), p.1556-1560

2009

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P-522 Custom design gene panel as a diagnostic for human non-syndromic infertility

Human reproduction (Oxford), 2022-06, Vol.37 (Supplement_1)

2022

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Strategies and outcomes of PGD of familial adenomatous polyposis

Molecular human reproduction, 2007-02, Vol.13 (2), p.95-101

2007

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Recent developments in genetics and medically-assisted reproduction: from research to clinical applications

Human reproduction open, 2017-01, Vol.2017 (3), p.hox015

2017

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TRIM28 repression of retrotransposon-based enhancers is necessary to preserve transcriptional dynamics in embryonic stem cells

Genome research, 2013-03, Vol.23 (3), p.452-461

2013

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Red blood cell generation from human induced pluripotent stem cells: perspectives for transfusion medicine

Haematologica (Roma), 2010-10, Vol.95 (10), p.1651-1659

2010

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P108 - Étude descriptive rétrospective sur une série de 20 hommes diabétiques pris en charge en CECOS pour infertilité

Diabetes & metabolism, 2011, Vol.37 (1), p.A60-A60

2011

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Genomic Structure and Parent-of-Origin-Specific Methylation of Peg1

Human molecular genetics, 1997-10, Vol.6 (11), p.1907-1915

1997

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Homozygous Mutation in SPATA16 Is Associated with Male Infertility in Human Globozoospermia

American journal of human genetics, 2007-10, Vol.81 (4), p.813-820

2007

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A Silencer Element Identified in Drosophila Is Required for Imprinting of H19 Reporter Transgenes in Mice

Proceedings of the National Academy of Sciences - PNAS, 1999-08, Vol.96 (16), p.9242-9247

1999

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Human embryo research in France

Human reproduction (Oxford), 2002-02, Vol.17 (2), p.261-263

2002

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Assisted reproduction treatment and epigenetic inheritance

Exome sequencing reveals novel causes as well as new candidate genes for human globozoospermia

Recent developments in genetics and medically assisted reproduction: from research to clinical applications

Assisted oocyte activation overcomes fertilization failure in globozoospermic patients regardless of the DPY19L2 status

Pathogenic missense variation in PABPC1L/EPAB causes female infertility due to oocyte maturation arrest at the germinal vesicle stage

C10 hESc and IPSc as models for genetic defects

ESHRE PGD consortium data collection VII: cycles from January to December 2004 with pregnancy follow-up to October 2005

ESHRE PGD Consortium data collection VI: cycles from January to December 2003 with pregnancy follow-up to October 2004

What next for preimplantation genetic screening? More randomized controlled trials needed?

ESHRE PGD Consortium data collection IV: May–December 2001

Increased pregnancy rate using standardized coculture on autologous endometrial cells and single blastocyst transfer : a multicentre randomized controlled trial

Genetic aspects of male infertility: From bench to clinic

Chromosome abnormalities in sperm from infertile men with normal somatic karyotypes: teratozoospermia

P-714 Clinical utility of FMR1 screening: risk factor or monogenic cause for POI

Creation of a registry for human embryonic stem cells carrying an inherited defect: joint collaboration between ESHRE and hESCreg

P-522 Custom design gene panel as a diagnostic for human non-syndromic infertility

Strategies and outcomes of PGD of familial adenomatous polyposis

Recent developments in genetics and medically-assisted reproduction: from research to clinical applications

TRIM28 repression of retrotransposon-based enhancers is necessary to preserve transcriptional dynamics in embryonic stem cells

Red blood cell generation from human induced pluripotent stem cells: perspectives for transfusion medicine

P108 - Étude descriptive rétrospective sur une série de 20 hommes diabétiques pris en charge en CECOS pour infertilité

Genomic Structure and Parent-of-Origin-Specific Methylation of Peg1

Homozygous Mutation in SPATA16 Is Associated with Male Infertility in Human Globozoospermia

A Silencer Element Identified in Drosophila Is Required for Imprinting of H19 Reporter Transgenes in Mice

Human embryo research in France

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