Concepedia

Jacqueline Levilliers

JL

Statistics

Publications

41

Citations

6.7K

H-Index

29

Active since

1974

Affiliations

Institut Pasteur(Current)

Centre National de la Recherche Scientifique

Inserm

Sorbonne Université

Centre de Référence Déficits Immunitaires Héréditaires

Jacqueline Levilliers is an author at Institut Pasteur specializing in genetics, life sciences, and human genetics.

Publications per year

1974–2014

41

Publications

41

Defective myosin VIIA gene responsible for Usher syndrome type IB

Dominique Well, Stéphane Blanchard, Josseline Kaplan et al. · Nature · 1995 · 1.1K citations

, , +7

Loss-of-function mutations in FGFR1 cause autosomal dominant Kallmann syndrome

Catherine Dodé, Jacqueline Levilliers, Jean‐Michel Dupont et al. · Nature Genetics · 2003 · 830 citations

, , +9

The candidate gene for the X-linked Kallmann syndrome encodes a protein related to adhesion molecules

Renaud Legouis, Jean‐Pierre Hardelin, Jacqueline Levilliers et al. · Cell · 1991 · 684 citations

, , +8

Prelingual Deafness: High Prevalence of a 30delG Mutation in the Connexin 26 Gene

Françoise Denoyelle, Dominique Weil, Marion A. Maw et al. · Human Molecular Genetics · 1997 · 636 citations · Full text

, , +11

Kallmann Syndrome: Mutations in the Genes Encoding Prokineticin-2 and Prokineticin Receptor-2

Catherine Dodé, Luís Teixeira, Jacqueline Levilliers et al. · PLoS Genetics · 2006 · 452 citations · Full text

, , +16

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