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Reiner A. Veitia

Reiner A. Veitia

D-Index & Metrics

Genetics

D-Index
74
Citations
15437
World Ranking
1986
National Ranking
89

Research.com Recognitions

  • 2015 - Member of Academia Europaea

Overview

Reiner A. Veitia is affiliated with Université Paris Cité in France and has contributed extensively to the field of Biochemistry, Genetics, and Molecular Biology. Their research covers a broad spectrum of topics, focusing primarily on molecular and genetic mechanisms with applications in reproductive biology, chromatin dynamics, and genetic engineering.

The scientist's work prominently involves the study of FOXO transcription factor regulation, DNA repair mechanisms, and genetic and clinical aspects of sex determination and chromosomal abnormalities. Other primary research topics include chromosomal and genetic variations, reproductive biology and fertility, CRISPR and genetic engineering, and genomics and chromatin dynamics.

Frequent co-authors in their body of work include:

  • Anne-Laure Todeschini
  • Luís Aragón
  • Mohan Babu
  • Ronald Berezney
  • Hannah Correia

They have published many articles in a range of scientific journals, with frequent appearances in the following venues:

  • BioEssays
  • Clinical Genetics
  • Trends in Genetics
  • Human Genetics
  • Journal of Clinical Research in Pediatric Endocrinology

Among the recent publications featuring their research contributions are:

  • "Forkhead Transcription Factors in Health and Disease," 2020, Trends in Genetics
  • "One Hundred Years of Gene Balance: How Stoichiometric Issues Affect Gene Expression, Genome Evolution, and Quantitative Traits," 2021, Cytogenetic and Genome Research
  • "Primary ovarian insufficiency, meiosis and DNA repair," 2020, Biomedical Journal
  • "A missense in HSF2BP causing primary ovarian insufficiency affects meiotic recombination by its novel interactor C19ORF57/BRME1," 2020, eLife
  • "The Oncogenic FOXL2 C134W Mutation Is a Key Driver of Granulosa Cell Tumors," 2022, Cancer Research

Veitia's research incorporates elements of molecular biology, genetics, plant science, public health, environmental and occupational health, and reproductive medicine. Their multidisciplinary approach reflects a comprehensive engagement with both fundamental biological processes and clinical applications.

The scientist was recognized with membership in the Academia Europaea in 2015, indicating involvement and acknowledgment within a European scholarly community.

Best Publications

  • Gene balance hypothesis: connecting issues of dosage sensitivity across biological disciplines

    James A. Birchler;Reiner A. Veitia

  • The gene balance hypothesis: from classical genetics to modern genomics.

    James A. Birchler;Reiner A. Veitia

  • Dosage balance in gene regulation: biological implications.

    James A. Birchler;Nicole C. Riddle;Donald L. Auger;Reiner A. Veitia

  • The Gene Balance Hypothesis: implications for gene regulation, quantitative traits and evolution

    James A. Birchler;Reiner A. Veitia;Reiner A. Veitia

  • Exploring the etiology of haploinsufficiency.

    Reiner A. Veitia

  • Mutations and sequence variants in GDF9 and BMP15 in patients with premature ovarian failure

    Paul Laissue;Sophie Christin-Maitre;Philippe Touraine;Frederique Kuttenn

  • Evolution and expression of FOXL2

    J Cocquet;E Pailhoux;F Jaubert;N Servel

  • Spectrum of FOXL2 gene mutations in blepharophimosis-ptosis-epicanthus inversus (BPES) families demonstrates a genotype–phenotype correlation

    Elfride De Baere;Michael J. Dixon;Kent W. Small;Ethylin W. Jabs

  • Cellular reactions to gene dosage imbalance: genomic, transcriptomic and proteomic effects

    Reiner A. Veitia;Samuel Bottani;Samuel Bottani;Samuel Bottani;James A. Birchler

  • Mutant Cohesin in Premature Ovarian Failure

    Sandrine Caburet;Valerie A. Arboleda;Elena Llano;Paul A. Overbeek

  • FOXL2 and BPES: Mutational hotspots, phenotypic variability, and revision of the genotype-phenotype correlation

    Elfride De Baere;Diane Beysen;Christine Oley;Birgit Lorenz

  • FOXL2 activates P450 aromatase gene transcription: towards a better characterization of the early steps of mammalian ovarian development.

    Maëlle Pannetier;Stéphane Fabre;Frank Batista;Ayhan Kocer

  • The transience of transient overexpression

    Toby J Gibson;Markus Seiler;Reiner A Veitia

  • An evolutionary and functional analysis of FoxL2 in rainbow trout gonad differentiation.

    Daniel Baron;Julie Cocquet;Xuhua Xia;Marc Fellous

  • Transcription factors: specific DNA binding and specific gene regulation

    Anne-Laure Todeschini;Adrien Georges;Reiner A. Veitia

  • Structure, evolution and expression of the FOXL2 transcription unit

    J. Cocquet;E. De Baere;M. Gareil;M. Pannetier

  • FOXL2: a central transcription factor of the ovary.

    Adrien Georges;Aurelie Auguste;Laurianne Bessière;Anne Vanet

  • Recent male-mediated gene flow over a linguistic barrier in Iberia, suggested by analysis of a Y-chromosomal DNA polymorphism.

    Matthew E. Hurles;Reiner Veitia;Eduardo Arroyo;Manuel Armenteros

  • Gene dosage effects: nonlinearities, genetic interactions, and dosage compensation

    Reiner A. Veitia;Reiner A. Veitia;Samuel Bottani;James A. Birchler

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

    D. Beysen;J. Raes;B.P. Leroy;B.P. Leroy;A. Lucassen

Frequent Co-Authors

Marc Fellous
Marc Fellous Bayer Pharmaceuticals
Daniel Vaiman
Daniel Vaiman Université Paris Cité
Elfride De Baere
Elfride De Baere Ghent University
James A. Birchler
James A. Birchler University of Missouri
Ken McElreavey
Ken McElreavey Institut Pasteur
Elizabeth M. Simpson
Elizabeth M. Simpson University of British Columbia
Ludwine Messiaen
Ludwine Messiaen University of Alabama at Birmingham
Wyeth W. Wasserman
Wyeth W. Wasserman University of British Columbia
Peggy J. Farnham
Peggy J. Farnham University of Southern California
Bruce E. Torbett
Bruce E. Torbett Seattle Children's Hospital

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