Linda Akloul

Mutational Spectrum in Holoprosencephaly Shows That FGF is a New Major Signaling Pathway

Christèle Dubourg, Wilfrid Carré, Houda Hamdi‐Rozé et al. · Human Mutation · 2016 · 74 citations

Life Sciences, Genetics, Molecular Genetics +17

New insights into the genetic basis of premature ovarian insufficiency: Novel causative variants and candidate genes revealed by genomic sequencing

Sylvie Jaillard, Katrina M. Bell, Linda Akloul et al. · Maturitas · 2020 · 64 citations · Full text

Medicine, Genetics, Molecular Genetics +13

STAG3 homozygous missense variant causes primary ovarian insufficiency and male non-obstructive azoospermia

Sylvie Jaillard, Kenneth McElreavy, Gorjana Robevska et al. · Molecular Human Reproduction · 2020 · 61 citations · Full text

Medicine, Genetics, Molecular Genetics +15

Integrated clinical and omics approach to rare diseases: novel genes and oligogenic inheritance in holoprosencephaly

Artem Kim, Clara Savary, Christèle Dubourg et al. · Brain · 2018 · 59 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

Common Variants at the 19p13.1 and <i>ZNF365</i> Loci Are Associated with ER Subtypes of Breast Cancer and Ovarian Cancer Risk in <i>BRCA1</i> and <i>BRCA2</i> Mutation Carriers

Fergus J. Couch, Mia M. Gaudet, Antonis C. Antoniou et al. · Cancer Epidemiology Biomarkers & Prevention · 2012 · 57 citations · Full text

Medicine, Genetics, Oncology +17