Concepedia
Statistics
Publications
3
Citations
301
H-Index
Active since
2013
Affiliations
Inserm(Current)
Hôpital Armand-Trousseau
Sorbonne Université
Hôpital Albert-Chenevier
Maladies génétiques d’expression pédiatrique
Benoit Vallette is an author at Inserm specializing in ciliary motility defects, medicine, and genetic disorders.
Publications per year
2013–2017
Loss-of-Function Mutations in RSPH1 Cause Primary Ciliary Dyskinesia with Central-Complex and Radial-Spoke Defects
Esther Kott, Marie Legendre, Bruno Copin et al. · The American Journal of Human Genetics · 2013 · 183 citations · Full text
Medicine, Molecular Genetics, Neuroscience +6
Mutations in DNAJB13 , Encoding an HSP40 Family Member, Cause Primary Ciliary Dyskinesia and Male Infertility
Elma El Khouri, Lucie Thomas, Ludovic Jeanson et al. · The American Journal of Human Genetics · 2016 · 104 citations · Full text
Medicine, Genetics, Molecular Genetics +9
A Novel System for the Quantification of the ADCC Activity of Therapeutic Antibodies
Christophe Lallemand, Feifei Liang, Flore Staub et al. · Journal of Immunology Research · 2017 · 14 citations · Full text
Life Sciences, Immunology, Oncology +17
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