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Mechanisms of Mendelian dominance

Clinical genetics, 2018-03, Vol.93 (3), p.419-428

2018

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The genetic make‐up of ovarian development and function: the focus on the transcription factor FOXL2

Clinical genetics, 2017-02, Vol.91 (2), p.173-182

2017

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P-015: Association of FOXD1 variants with pregnancy failures in mice and humans

Thrombosis research, 2017-03, Vol.151, p.S114-S114

2017

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Structure, evolution and expression of the FOXL2 transcription unit

Cytogenetic and genome research, 2003-01, Vol.101 (3-4), p.206-211

2003

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A non-sense MCM9 mutation in a familial case of primary ovarian insufficiency

Clinical genetics, 2016-05, Vol.89 (5), p.603-607

2016

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Clinical Genetics in the age of Genomics and Genome editing

Clinical genetics, 2016-01, Vol.89 (1), p.3-4

Veitia, R. A.

2016

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Evolution and expression of FOXL2

Journal of medical genetics, 2002-12, Vol.39 (12), p.916-921

2002

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Adult ovarian granulosa cell tumor transcriptomics: prevalence of FOXL2 target genes misregulation gives insights into the pathogenic mechanism of the p.Cys134Trp somatic mutation

Oncogene, 2013-05, Vol.32 (22), p.2739-2746

2013

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Three‐dimensional genome architecture in health and disease

Clinical genetics, 2019-02, Vol.95 (2), p.189-198

2019

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A role for SOX9 in post-transcriptional processes: insights from the amphibian oocyte

Scientific reports, 2018-05, Vol.8 (1), p.7191-14, Article 7191

2018

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Paralogs in polyploids: one for all and all for one?

The Plant cell, 2005, Vol.17 (1), p.4-11

Veitia, R.A

2005

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Deletions Involving Long-Range Conserved Nongenic Sequences Upstream and Downstream of FOXL2 as a Novel Disease-Causing Mechanism in Blepharophimosis Syndrome

American journal of human genetics, 2005-08, Vol.77 (2), p.205-218

2005

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The mutations and potential targets of the forkhead transcription factor FOXL2

Molecular and cellular endocrinology, 2008-01, Vol.282 (1), p.2-11

2008

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Genes encoding subunits of stable complexes are clustered on the yeast chromosomes: an interpretation from a dosage balance perspective

Genetics (Austin), 2004-08, Vol.167 (4), p.2121-2125

2004

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FOXL2 copy number changes in the molecular pathogenesis of BPES: unique cohort of 17 deletions

Human mutation, 2010-05, Vol.31 (5), p.E1332-E1347

2010

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Coding repeats and evolutionary "agility"

BioEssays, 2005-06, Vol.27 (6), p.581-587

2005

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Sense and antisense Foxl2 transcripts in mouse

Genomics (San Diego, Calif.), 2005-05, Vol.85 (5), p.531-541

2005

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Gene expression regulation in the context of mouse interspecific mosaic genomes

Genome Biology, 2008-01, Vol.9 (8), p.R133-R133

2008

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A Genomic Basis for the Evolution of Vertebrate Transcription Factors Containing Amino Acid Runs

Genetics (Austin), 2004-08, Vol.167 (4), p.1813-1820

2004

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Genetic basis of human sex determination: An overview

Theriogenology, 1997, Vol.47 (1), p.83-91

1997

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Testis determination in mammals: more questions than answers

Molecular and cellular endocrinology, 2001-06, Vol.179 (1), p.3-16

2001

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The identification and characterization of a FOXL2 response element provides insights into the pathogenesis of mutant alleles

Human molecular genetics, 2008, Vol.17, p.3118-3127

2008

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Swyer Syndrome and 46,XY Partial Gonadal Dysgenesis Associated with 9p Deletions in the Absence of Monosomy-9p Syndrome

American journal of human genetics, 1998-09, Vol.63 (3), p.901-905

1998

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Amino Acid Repeats and the Structure and Evolution of Proteins

Gene and Protein Evolution, 2007, Vol.3, p.119-130

2007

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A novel human gene, encoding a potential membrane protein conserved from yeast to man, is strongly expressed in testis and cancer cell lines

Cytogenetics and cell genetics, 1999-01, Vol.85 (3-4), p.217

1999

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Mechanisms of Mendelian dominance

The genetic make‐up of ovarian development and function: the focus on the transcription factor FOXL2

P-015: Association of FOXD1 variants with pregnancy failures in mice and humans

Structure, evolution and expression of the FOXL2 transcription unit

A non-sense MCM9 mutation in a familial case of primary ovarian insufficiency

Clinical Genetics in the age of Genomics and Genome editing

Evolution and expression of FOXL2

Adult ovarian granulosa cell tumor transcriptomics: prevalence of FOXL2 target genes misregulation gives insights into the pathogenic mechanism of the p.Cys134Trp somatic mutation

Three‐dimensional genome architecture in health and disease

A role for SOX9 in post-transcriptional processes: insights from the amphibian oocyte

Paralogs in polyploids: one for all and all for one?

Deletions Involving Long-Range Conserved Nongenic Sequences Upstream and Downstream of FOXL2 as a Novel Disease-Causing Mechanism in Blepharophimosis Syndrome

The mutations and potential targets of the forkhead transcription factor FOXL2

Genes encoding subunits of stable complexes are clustered on the yeast chromosomes: an interpretation from a dosage balance perspective

FOXL2 copy number changes in the molecular pathogenesis of BPES: unique cohort of 17 deletions

Coding repeats and evolutionary "agility"

Sense and antisense Foxl2 transcripts in mouse

Gene expression regulation in the context of mouse interspecific mosaic genomes

A Genomic Basis for the Evolution of Vertebrate Transcription Factors Containing Amino Acid Runs

Genetic basis of human sex determination: An overview

Testis determination in mammals: more questions than answers

The identification and characterization of a FOXL2 response element provides insights into the pathogenesis of mutant alleles

Swyer Syndrome and 46,XY Partial Gonadal Dysgenesis Associated with 9p Deletions in the Absence of Monosomy-9p Syndrome

Amino Acid Repeats and the Structure and Evolution of Proteins

A novel human gene, encoding a potential membrane protein conserved from yeast to man, is strongly expressed in testis and cancer cell lines

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