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The clinical value of optical genome mapping in the rapid characterization of RB1 duplication and 15q23q24.2 triplication, for more appropriate prenatal genetic counselling

Molecular genetics & genomic medicine, 2024-04, Vol.12 (4), p.e2437-n/a

2024

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Chromosome methylation patterns during mammalian preimplantation development

Genes & development, 1998-07, Vol.12 (14), p.2108-2113

1998

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Are de novo rea(21;21) chromosomes really de novo?

Clinical case reports, 2015-10, Vol.3 (10), p.786-789

2015

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Genetic polymorphisms influence the ovarian response to rFSH stimulation in patients undergoing in vitro fertilization programs with ICSI

PloS one, 2012-06, Vol.7 (6), p.e38700-e38700

2012

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Associations between Individual and Combined Polymorphisms of the TNF and VEGF Genes and the Embryo Implantation Rate in Patients Undergoing In Vitro Fertilization (IVF) Programs

PloS one, 2014-09, Vol.9 (9), p.e108287-e108287

2014

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Sperm FISH analysis of a 46,XY,t(3;6)(p24;p21.2),inv (8)(p11;2q21.2) double chromosomal rearrangement

Reproductive biomedicine online, 2012-02, Vol.24 (2), p.219-223

2012

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The chromosomal risk in sperm from heterozygous Robertsonian translocation carriers is related to the sperm count and the translocation type

Fertility and sterility, 2011-12, Vol.96 (6), p.1337-1343

2011

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The High Frequency of Sperm Aneuploidy in Klinefelter Patients and in Nonobstructive Azoospermia Is Due to Meiotic Errors in Euploid Spermatocytes

Journal of andrology, 2012-11, Vol.33 (6), p.1352-1359

2012

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Sperm chromosome analysis of an infertile patient with a 95% mosaic r(21) karyotype and normal phenotype

Fertility and sterility, 2009-03, Vol.91 (3), p.930.e13-930.e15

2009

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Is classic pericentric inversion of chromosome 2 inv(2)(p11q13) associated with an increased risk of unbalanced chromosomes?

Fertility and sterility, 2009-10, Vol.92 (4), p.1497.e1-1497.e4

2009

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Prenatal diagnosis of 2q13 duplications: The crucial role of the family survey in genetic counseling on novel copy number variations

European journal of medical genetics, 2020-08, Vol.63 (8), p.103956, Article 103956

2020

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Next Generation Sequencing Should Be Proposed to Every Woman With “Idiopathic” Primary Ovarian Insufficiency

Journal of the Endocrine Society, 2021-07, Vol.5 (7), p.bvab032-bvab032

2021

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Associations between Individual and Combined Polymorphisms of the TNF and VEGF Genes and the Embryo Implantation Rate in Patients Undergoing In Vitro Fertilization

PloS one, 2014-09, Vol.9 (9)

2014

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RHOXF2 gene, a new candidate gene for spermatogenesis failure

Basic and Clinical Andrology, 2014-01, Vol.24 (1), p.3-3, Article 3

2014

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Contribution of first polar body analysis to understanding of human aneuploidy mechanism

Bulletin de l'Académie nationale de médecine, 2005-11, Vol.189 (8), p.1761-72; discussion 1772

2005

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Associations between Individual and Combined Polymorphisms of the TNF and VEGF Genes and the Embryo Implantation Rate in Patients Undergoing In Vitro Fertilization (IVF) Programs: e108287

PloS one, 2014-09, Vol.9 (9)

2014

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Meiotic segregation of X-autosome translocation in two carriers and implications for assisted reproduction

Reproductive biomedicine online, 2009, Vol.18 (6), p.850-855

2009

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cDNA cloning, tissue distribution and chromosomal localization of the human ID4 gene

DNA research, 1998, Vol.5 (5), p.309-313

1998

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Structure and Physical Mapping of DR1, a TATA-Binding Protein-Associated Phosphoprotein Gene, to Chromosome 1p22.1 and Its Exclusion in Stargardt Disease (STGD)

Genomics (San Diego, Calif.), 1996-09, Vol.36 (3), p.554-556

1996

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Contribution de l'analyse du premier globule polaire à la compréhension du mécanisme des aneuploïdies humaines

Bulletin de l'Académie nationale de médecine, 2005-11, Vol.189 (8), p.1761-1772

2005

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Influence de la congélation sur le taux de fragmentation de l'ADN des spermes normaux à sévèrement altérés

Andrologie (Lille, France), 2007-03, Vol.17 (1), p.55-70

2007

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Génétique et place d’une présence affectivo-confirmante dans l’annonce d’une pathologie

Présence haptonomique, 2012-01, Vol.N° 10 (1), p.303-315

Molina Gomes-Mortelier, Denise

2012

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Le risque chromosomique pour un patient porteur d'une translocation t(X;2) concerne non seulement la translocation mais aussi la ségrégation XY

Andrologie (Lille, France), 2005-09, Vol.15 (3), p.328-333

2005

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Are de novo rea(21;21) chromosomes really de novo?

Clinical case reports, 2015, Vol.3 (10), p.786-789

2015

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The clinical value of optical genome mapping in the rapid characterization of RB1 duplication and 15q23q24.2 triplication, for more appropriate prenatal genetic counselling

Chromosome methylation patterns during mammalian preimplantation development

Are de novo rea(21;21) chromosomes really de novo?

Genetic polymorphisms influence the ovarian response to rFSH stimulation in patients undergoing in vitro fertilization programs with ICSI

Associations between Individual and Combined Polymorphisms of the TNF and VEGF Genes and the Embryo Implantation Rate in Patients Undergoing In Vitro Fertilization (IVF) Programs

Sperm FISH analysis of a 46,XY,t(3;6)(p24;p21.2),inv (8)(p11;2q21.2) double chromosomal rearrangement

The chromosomal risk in sperm from heterozygous Robertsonian translocation carriers is related to the sperm count and the translocation type

The High Frequency of Sperm Aneuploidy in Klinefelter Patients and in Nonobstructive Azoospermia Is Due to Meiotic Errors in Euploid Spermatocytes

Sperm chromosome analysis of an infertile patient with a 95% mosaic r(21) karyotype and normal phenotype

Is classic pericentric inversion of chromosome 2 inv(2)(p11q13) associated with an increased risk of unbalanced chromosomes?

Prenatal diagnosis of 2q13 duplications: The crucial role of the family survey in genetic counseling on novel copy number variations

Next Generation Sequencing Should Be Proposed to Every Woman With “Idiopathic” Primary Ovarian Insufficiency

Associations between Individual and Combined Polymorphisms of the TNF and VEGF Genes and the Embryo Implantation Rate in Patients Undergoing In Vitro Fertilization

RHOXF2 gene, a new candidate gene for spermatogenesis failure

Contribution of first polar body analysis to understanding of human aneuploidy mechanism

Associations between Individual and Combined Polymorphisms of the TNF and VEGF Genes and the Embryo Implantation Rate in Patients Undergoing In Vitro Fertilization (IVF) Programs: e108287

Meiotic segregation of X-autosome translocation in two carriers and implications for assisted reproduction

cDNA cloning, tissue distribution and chromosomal localization of the human ID4 gene

Structure and Physical Mapping of DR1, a TATA-Binding Protein-Associated Phosphoprotein Gene, to Chromosome 1p22.1 and Its Exclusion in Stargardt Disease (STGD)

Contribution de l'analyse du premier globule polaire à la compréhension du mécanisme des aneuploïdies humaines

Influence de la congélation sur le taux de fragmentation de l'ADN des spermes normaux à sévèrement altérés

Génétique et place d’une présence affectivo-confirmante dans l’annonce d’une pathologie

Le risque chromosomique pour un patient porteur d'une translocation t(X;2) concerne non seulement la translocation mais aussi la ségrégation XY

Are de novo rea(21;21) chromosomes really de novo?

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