Reiner A Veitia (R A Veitia)

Publication Activity (10 Years)

Years Active: 2016-2024
Publications (10 Years): 24

Top Topics

Dna Methylation

Age Related Macular Degeneration

Top Venues

Clinical genetics

BioEssays : news and reviews in molecular, cellular and developmental biology

This page only lists publications with an associated author ORCID identifier.

Publications

Elfride De Baere, Eric Legius, Reiner A Veitia, Kathleen Claes
In memory of Ludwine Messiaen, Ph.D. (1956-2024). Clinical genetics (2024)
Caroline Zutterling, Anne-Laure Todeschini, Deborah Fourmy, Didier Busso, Xavier Veaute, Frédéric Ducongé, Reiner A Veitia
The forkhead DNA-binding domain binds specific G2-rich RNA sequences. Nucleic acids research (2023)
Reiner A Veitia
Dominant negative variants and cotranslational assembly of macromolecular complexes. BioEssays : news and reviews in molecular, cellular and developmental biology (2023)
Monica M Franca, Yazmine B Condezo, Maëva Elzaiat, Natalia Felipe-Medina, Fernando Sánchez-Sáez, Sergio Muñoz, Raquel Sainz-Urruela, M Rosario Martín-Hervás, Rodrigo García-Valiente, Manuel A Sanchez-Martin, Aurora Astudillo, Juan Méndez, Elena Llano, Reiner A Veitia, Berenice Bilharinho de Mendonca, Alberto M Pendas
A truncating variant of RAD51B associated with primary ovarian insufficiency provides insights into its meiotic and somatic functions. Cell death and differentiation (2022)
Olivier Ariste, Pierre de la Grange, Reiner A Veitia
Recurrent missense variants in clonal hematopoiesis-related genes present in the general population. Clinical genetics (2022)
Elena Llano, Anne Laure Todeschini, Natalia Felipe-Medina, María Daniela Corte-Torres, Yazmine B Condezo, Manuel A Sanchez-Martin, Sara López-Tamargo, María Aurora Astudillo, Xose S Puente, Alberto M Pendas, Reiner A Veitia
The oncogenic FOXL2 C134W mutation is a key driver of granulosa cell tumors. Cancer research (2022)
Hideki Innan, Daniel Vaiman, Reiner A Veitia
Predictable increase in female reproductive window: A simple model connecting age of reproduction, menopause, and longevity. BioEssays : news and reviews in molecular, cellular and developmental biology 43 (5) (2021)
Reiner A Veitia, Jessica Pilsworth, Anne-Laure Todeschini, David Huntsman
Reply to "An alternative miRISC targets a cancer-associated coding sequence mutation in FOXL2". The EMBO journal 40 (16) (2021)
Laetitia Herman, Bérangère Legois, Anne Laure Todeschini, Reiner A Veitia
Genomic exploration of the targets of FOXL2 and ESR2 unveils their implication in cell migration, invasion, and adhesion. FASEB journal : official publication of the Federation of American Societies for Experimental Biology 35 (4) (2021)
Luis Bermúdez-Guzmán, Reiner A Veitia
Insights into the pathogenicity of missense variants in the forkhead domain of FOX proteins underlying Mendelian disorders. Human genetics 140 (7) (2021)
Reiner A Veitia
A reply to: Longitudinal changes in the frequency of mosaic chromosome Y loss in peripheral blood cells of aging men varies profoundly between individuals. European journal of human genetics : EJHG 29 (9) (2021)
Natalia Felipe-Medina, Sandrine Caburet, Fernando Sánchez-Sáez, Yazmine B Condezo, Dirk G de Rooij, Laura Gómez-H, Rodrigo García-Valiente, Anne Laure Todeschini, Paloma Duque, Manuel Adolfo Sánchez-Martin, Stavit A Shalev, Elena Llano, Reiner A Veitia, Alberto M Pendas
A missense in HSF2BP causing primary ovarian insufficiency affects meiotic recombination by its novel interactor C19ORF57/BRME1. eLife 9 (2020)
Reiner A Veitia
Clinical Genetics paving the way to the future. Clinical genetics 99 (2) (2020)
Maëva Elzaiat, Delphine Flatters, Diana Carolina Sierra-Díaz, Berangère Legois, Paul Laissue, Reiner A Veitia
DHH pathogenic variants involved in 46,XY disorders of sex development differentially impact protein self-cleavage and structural conformation. Human genetics 139 (11) (2020)
Maria Isabel Alvarez-Mora, Anne-Laure Todeschini, Sandrine Caburet, Lilach Peled Perets, Montserrat Mila, Johnny S Younis, Stavit Shalev, Reiner A Veitia
An exome-wide exploration of cases of primary ovarian insufficiency uncovers novel sequence variants and candidate genes. Clinical genetics 98 (3) (2020)
Adam F Johnson, Ha Thi Nguyen, Reiner A Veitia
Causes and effects of haploinsufficiency. Biological reviews of the Cambridge Philosophical Society 94 (5) (2019)
Reiner A Veitia
Further quantitative insights into the decrease of heteroplasmy of m.3243A>G with age in leukocytes. Clinical genetics 95 (4) (2019)
Felix Grassmann, null null, Bernhard H F Weber, Reiner A Veitia
Insights into the loss of the Y chromosome with age in control individuals and in patients with age-related macular degeneration using genotyping microarray data. Human genetics 139 (3) (2019)
J-F Ouimette, C Rougeulle, Reiner A Veitia
Three-dimensional genome architecture in health and disease. Clinical genetics 95 (2) (2018)
Reiner A Veitia
On the loss of human sex chromosomes in lymphocytes with age: a quantitative treatment. European journal of human genetics : EJHG 26 (12) (2018)
Reiner A Veitia, S Caburet, J A Birchler
Mechanisms of Mendelian dominance. Clinical genetics 93 (3) (2017)
Baptiste Fouquet, Patrycja Pawlikowska, Sandrine Caburet, Celine Guigon, Marika Mäkinen, Laura Tanner, Marja Hietala, Kaja Urbanska, Laura Bellutti, Bérangère Legois, Bettina Bessieres, Alain Gougeon, Alexandra Benachi, Gabriel Livera, Filippo Rosselli, Reiner A Veitia, Abdelkader Heddar
A homozygous FANCM mutation underlies a familial case of non-syndromic primary ovarian insufficiency. eLife 6 (2017)
Francoise Paris, Delphine Flatters, Sandrine Caburet, Bérangère Legois, Nadège Servant, Hervé Lefebvre, Charles Sultan, Reiner A Veitia
A novel variant of DHH in a familial case of 46,XY disorder of sex development: Insights from molecular dynamics simulations. Clinical endocrinology 87 (5) (2017)
Dorien Baetens, Hans Stoop, Frank Peelman, Anne-Laure Todeschini, Toon Rosseel, Frauke Coppieters, Reiner A Veitia, Leendert H J Looijenga, Elfride De Baere, Martine Cools
NR5A1 is a novel disease gene for 46,XX testicular and ovotesticular disorders of sex development. Genetics in medicine : official journal of the American College of Medical Genetics 19 (4) (2016)