Concepedia
Statistics
Publications
19
Citations
2K
H-Index
18
Active since
2000
Affiliations
Inserm(Current)
Hôpital Necker-Enfants Malades
Université Paris Cité
Assistance Publique – Hôpitaux de Paris
Institut Necker Enfants Malades
Nathalie Dagoneau is an author at Inserm specializing in genetics, life sciences, and molecular genetics.
Publications per year
2000–2017
ADAMTS10 Mutations in Autosomal Recessive Weill-Marchesani Syndrome
Nathalie Dagoneau, Catherine Benoist-Lasselin, Céline Huber et al. · The American Journal of Human Genetics · 2004 · 281 citations · Full text
Life Sciences, Genetics, Molecular Genetics +8
In frame fibrillin-1 gene deletion in autosomal dominant Weill-Marchesani syndrome: Figure 1
Laurence Faivre, Robert J. Gorlin, Mary K. Wirtz et al. · Journal of Medical Genetics · 2003 · 281 citations · Full text
Life Sciences, Genetics, Molecular Genetics +17
DYNC2H1 Mutations Cause Asphyxiating Thoracic Dystrophy and Short Rib-Polydactyly Syndrome, Type III
Nathalie Dagoneau, Marie Goulet, David Geneviève et al. · The American Journal of Human Genetics · 2009 · 258 citations · Full text
Life Sciences, Genetics, Molecular Genetics +4
ADAMTSL2 mutations in geleophysic dysplasia demonstrate a role for ADAMTS-like proteins in TGF-β bioavailability regulation
Carine Le Goff, Fanny Morice‐Picard, Nathalie Dagoneau et al. · Nature Genetics · 2008 · 245 citations · Full text
Life Sciences, Genetics, Molecular Biology +9
Null Leukemia Inhibitory Factor Receptor (LIFR) Mutations in Stüve-Wiedemann/Schwartz-Jampel Type 2 Syndrome
Nathalie Dagoneau, Déborah Scheffer, Céline Huber et al. · The American Journal of Human Genetics · 2004 · 187 citations · Full text
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