Abdelkader Heddar (Micheline Misrahi, M Misrahi)

ORCID

Publication Activity (10 Years)

Years Active: 2017-2021
Publications (10 Years): 9

Top Venues

Clinical genetics

Human mutation

EMBO molecular medicine

Journal of medical genetics

Université Paris-Sud Faculté de Médecine

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

Affiliation History

Université Paris-Sud Faculté de Médecine Jun 30 2016

France

Prof.

Publications

Abdelkader Heddar, Abdelkader Heddar
Should FANCL heterozygous pathogenic variants be considered as potentially causative of primary ovarian insufficiency? Human mutation 41 (9) (2021)
Abdelkader Heddar, Nathalie Guichoux, Nathalie Auger, Abdelkader Heddar
A SPIDR homozygous nonsense pathogenic variant in isolated primary ovarian insufficiency with chromosomal instability. Clinical genetics (2021)
Olayiwola O Oduwole, Ilpo T Huhtaniemi, Abdelkader Heddar
The Roles of Luteinizing Hormone, Follicle-Stimulating Hormone and Testosterone in Spermatogenesis and Folliculogenesis Revisited. International journal of molecular sciences 22 (23) (2021)
Abdelkader Heddar, Abdelkader Heddar
Concerns regarding the potentially causal role of FANCA heterozygous variants in human primary ovarian insufficiency. Human genetics 140 (4) (2020)
Sandrine Caburet, Abdelkader Heddar, Elodie Dardillac, Héléne Creux, Marie Lambert, Sébastien Messiaen, Sophie Tourpin, Gabriel Livera, Bernard S Lopez, Abdelkader Heddar
Homozygous hypomorphic BRCA2 variant in primary ovarian insufficiency without cancer or Fanconi anaemia trait. Journal of medical genetics (2020)
Abdelkader Heddar, Philippe Dessen, Delphine Flatters, Abdelkader Heddar
Novel STAG3 mutations in a Caucasian family with primary ovarian insufficiency. Molecular genetics and genomics : MGG 294 (6) (2019)
Abdelkader Heddar
β-Klotho sustains postnatal GnRH biology and spins the thread of puberty. EMBO molecular medicine 9 (10) (2018)
A Mayer, B Fouquet, M Pugeat, Abdelkader Heddar
BMP15 "knockout-like" effect in familial premature ovarian insufficiency with persistent ovarian reserve. Clinical genetics 92 (2) (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)

Abdelkader Heddar.css-eqlu8i{font-size:small;padding-left:4px;} (Micheline Misrahi, M Misrahi)

Publication Activity (10 Years)

Top Topics

Top Venues

Abdelkader Heddar (Micheline Misrahi, M Misrahi)