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Microarray analysis reveals abnormal chromosomal complements in over 70% of 14 normally developing human embryos

Human reproduction (Oxford), 2013-01, Vol.28 (1), p.256-264

2013

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Genetic and epigenetic instability in human pluripotent stem cells

Human reproduction update, 2013-03, Vol.19 (2), p.187-205

2013

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Gain of 20q11.21 in human embryonic stem cells improves cell survival by increased expression of Bcl-xL

Molecular human reproduction, 2014-02, Vol.20 (2), p.168-177

2014

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Sustained intrinsic WNT and BMP4 activation impairs hESC differentiation to definitive endoderm and drives the cells towards extra-embryonic mesoderm

Scientific reports, 2021-04, Vol.11 (1), p.8242-8242, Article 8242

2021

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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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The effect of polymorphisms in FSHR gene on late follicular phase progesterone and estradiol serum levels in predicted normoresponders

Human reproduction (Oxford), 2022-10, Vol.37 (11), p.2646-2654

2022

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The effect of polymorphisms in FSHR and FSHB genes on ovarian response: a prospective multicenter multinational study in Europe and Asia

Human reproduction (Oxford), 2021-05, Vol.36 (6), p.1711-1721

2021

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Mitotic spindle disruption in human preimplantation embryos activates the spindle assembly checkpoint but not apoptosis until Day 5 of development

Molecular human reproduction, 2017-05, Vol.23 (5), p.321-329

2017

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Chromosome constitution of human embryos generated after in vitro maturation including 3-isobutyl-1-methylxanthine in the oocyte collection medium

Human reproduction (Oxford), 2015-03, Vol.30 (3), p.653-663

2015

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Gain of 20q11.21 in Human Pluripotent Stem Cells Impairs TGF-β-Dependent Neuroectodermal Commitment

Stem cell reports, 2019-07, Vol.13 (1), p.163-176

2019

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Evolution of aneuploidy up to Day 4 of human preimplantation development

Human reproduction (Oxford), 2013-06, Vol.28 (6), p.1716-1724

2013

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Female human pluripotent stem cells rapidly lose X chromosome inactivation marks and progress to a skewed methylation pattern during culture

Molecular human reproduction, 2016-04, Vol.22 (4), p.285-298

2016

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The role of methylation, DNA polymorphisms and microRNAs on HLA-G expression in human embryonic stem cells

Stem cell research, 2017-03, Vol.19, p.118-127

2017

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Optimization and evaluation of single-cell whole-genome multiple displacement amplification

Human mutation, 2006-05, Vol.27 (5), p.496-503

2006

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Stem cell therapy: facts and fiction

Facts, views & vision in ObGyn, 2012-01, Vol.4 (3), p.195-197

Spits, C

2012

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Characterization of CD30 expression in human embryonic stem cell lines cultured in serum-free media and passaged mechanically

Human reproduction (Oxford), 2009-10, Vol.24 (10), p.2477-2489

2009

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Methylation of the CpG sites in the myotonic dystrophy locus does not correlate with CTG expansion size or with the congenital form of the disease

Journal of medical genetics, 2010-10, Vol.47 (10), p.700-703

2010

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Preimplantation genetic diagnosis for cancer predisposition syndromes

Prenatal diagnosis, 2007-05, Vol.27 (5), p.447-456

2007

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Real and expected delivery rates of patients with myotonic dystrophy undergoing intracytoplasmic sperm injection and preimplantation genetic diagnosis

Human reproduction (Oxford), 2008-07, Vol.23 (7), p.1654-1660

2008

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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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P-660 Polymorphisms in FSHR gene do not affect late follicular phase steroidogenic response in predicted normoresponders. Secondary analysis of a prospective multicenter cohort study

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

2022

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P-662 Association between polymorphisms in FSHR and reproductive outcomes following IVF. Secondary analysis of a prospective cohort study in Europe and Asia

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

2022

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O-205 Aneuploidy induces proteotoxic stress and autophagy-mediated apoptosis in human preimplantation embryos

Human reproduction (Oxford), 2021-08, Vol.36 (Supplement_1)

2021

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Preimplantation genetic diagnosis for neurofibromatosis type 1

Molecular human reproduction, 2005-05, Vol.11 (5), p.381-387

2005

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Screening ethnically diverse human embryonic stem cells identifies a chromosome 20 minimal amplicon conferring growth advantage

Nature biotechnology, 2011-12, Vol.29 (12), p.1132-1144

2011

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Microarray analysis reveals abnormal chromosomal complements in over 70% of 14 normally developing human embryos

Genetic and epigenetic instability in human pluripotent stem cells

Gain of 20q11.21 in human embryonic stem cells improves cell survival by increased expression of Bcl-xL

Sustained intrinsic WNT and BMP4 activation impairs hESC differentiation to definitive endoderm and drives the cells towards extra-embryonic mesoderm

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

The effect of polymorphisms in FSHR gene on late follicular phase progesterone and estradiol serum levels in predicted normoresponders

The effect of polymorphisms in FSHR and FSHB genes on ovarian response: a prospective multicenter multinational study in Europe and Asia

Mitotic spindle disruption in human preimplantation embryos activates the spindle assembly checkpoint but not apoptosis until Day 5 of development

Chromosome constitution of human embryos generated after in vitro maturation including 3-isobutyl-1-methylxanthine in the oocyte collection medium

Gain of 20q11.21 in Human Pluripotent Stem Cells Impairs TGF-β-Dependent Neuroectodermal Commitment

Evolution of aneuploidy up to Day 4 of human preimplantation development

Female human pluripotent stem cells rapidly lose X chromosome inactivation marks and progress to a skewed methylation pattern during culture

The role of methylation, DNA polymorphisms and microRNAs on HLA-G expression in human embryonic stem cells

Optimization and evaluation of single-cell whole-genome multiple displacement amplification

Stem cell therapy: facts and fiction

Characterization of CD30 expression in human embryonic stem cell lines cultured in serum-free media and passaged mechanically

Methylation of the CpG sites in the myotonic dystrophy locus does not correlate with CTG expansion size or with the congenital form of the disease

Preimplantation genetic diagnosis for cancer predisposition syndromes

Real and expected delivery rates of patients with myotonic dystrophy undergoing intracytoplasmic sperm injection and preimplantation genetic diagnosis

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

P-660 Polymorphisms in FSHR gene do not affect late follicular phase steroidogenic response in predicted normoresponders. Secondary analysis of a prospective multicenter cohort study

P-662 Association between polymorphisms in FSHR and reproductive outcomes following IVF. Secondary analysis of a prospective cohort study in Europe and Asia

O-205 Aneuploidy induces proteotoxic stress and autophagy-mediated apoptosis in human preimplantation embryos

Preimplantation genetic diagnosis for neurofibromatosis type 1

Screening ethnically diverse human embryonic stem cells identifies a chromosome 20 minimal amplicon conferring growth advantage

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