Your account is not claimed yet. You can sign up with ORCID to claim your account.

Laura Mary

ORCID

Publication Activity (10 Years)

Years Active: 2019-2023
Publications (10 Years): 7

Top Venues

Genes

American journal of medical genetics. Part A

Human mutation

Human genetics

Université de Strasbourg (PHD)

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

Education History

Université de Strasbourg - Sep 4o 2018

France

PHD :: Faculté de médecine

Publications

Laura Mary, Delphine Leclerc, Audrey Labalme, Pascale Bellaud, Severine Mazaud-Guittot, Stéphane Dréano, Bertrand Evrard, Antoine Bigand, Aurélie Cauchoix, Philippe Loget, Anna Lokchine, Laurence Cluzeau, David Gilot, Marc-Antoine Belaud-Rotureau, Sylvie Jaillard
Functional Assessment of a New PBX1 Variant in a 46,XY Fetus with Severe Syndromic Difference of Sexual Development through CRISPR-Cas9 Gene Editing. Genes 14 (2) (2023)
Laura Mary, Delphine Leclerc, Audrey Labalme, Pascale Bellaud, Severine Mazaud-Guittot, Stéphane Dréano, Bertrand Evrard, Antoine Bigand, Aurélie Cauchoix, Philippe Loget, Anna Lokchine, Laurence Cluzeau, David Gilot, Marc-Antoine Belaud-Rotureau, Sylvie Jaillard
Functional Assessment of a New PBX1 Variant in a 46,XY Fetus with Severe Syndromic Difference of Sexual Development through CRISPR-Cas9 Gene Editing. Genes 14 (2) (2023)
Laura Mary, Delphine Leclerc, Audrey Labalme, Pascale Bellaud, Severine Mazaud-Guittot, Stéphane Dréano, Bertrand Evrard, Antoine Bigand, Aurélie Cauchoix, Philippe Loget, Anna Lokchine, Laurence Cluzeau, David Gilot, Marc-Antoine Belaud-Rotureau, Sylvie Jaillard
Functional Assessment of a New PBX1 Variant in a 46,XY Fetus with Severe Syndromic Difference of Sexual Development through CRISPR-Cas9 Gene Editing. Genes 14 (2) (2023)
Laura Mary, Delphine Leclerc, Audrey Labalme, Pascale Bellaud, Severine Mazaud-Guittot, Stéphane Dréano, Bertrand Evrard, Antoine Bigand, Aurélie Cauchoix, Philippe Loget, Anna Lokchine, Laurence Cluzeau, David Gilot, Marc-Antoine Belaud-Rotureau, Sylvie Jaillard
Functional Assessment of a New PBX1 Variant in a 46,XY Fetus with Severe Syndromic Difference of Sexual Development through CRISPR-Cas9 Gene Editing. Genes 14 (2) (2023)
Laura Mary, Delphine Leclerc, David Gilot, Marc-Antoine Belaud-Rotureau, Sylvie Jaillard
The TALE never ends: A comprehensive overview of the role of PBX1, a TALE transcription factor, in human developmental defects. Human mutation 43 (9) (2022)
Laura Mary, Elsa Nourisson, Claire Feger, Vincent Laugel, Denys Chaigne, Boris Keren, Alexandra Afenjar, Thierry Billette, Detlef Trost, Cécile Cieuta-Walti, Bénédicte Gerard, Amélie Piton, Elise Schaefer
Pathogenic variants in KCNQ2 cause intellectual deficiency without epilepsy: Broadening the phenotypic spectrum of a potassium channelopathy. American journal of medical genetics. Part A 185 (6) (2021)
Laura Mary, Vincent Zvénigorosky, Alexey Kovalev, Angéla Gonzalez, Jean-Luc Fausser, Florence Jagorel, Marina Kilunovskaya, Vladimir Semenov, Eric Crubézy, Bertrand Ludes, Christine Keyser
Genetic kinship and admixture in Iron Age Scytho-Siberians. Human genetics 138 (4) (2019)

Laura Mary.css-eqlu8i{font-size:small;padding-left:4px;}

Publication Activity (10 Years)

Top Topics

Top Venues

Laura Mary