Concepedia

Delphine Feldmann

DF

32

Publications

3.6K

Citations

27

H-Index

1984

Active since

Affiliations

Hôpital Armand-Trousseau(Current)

Sorbonne Université

Inserm

Assistance Publique – Hôpitaux de Paris

Hôpital Necker-Enfants Malades

Delphine Feldmann is an author at Hôpital Armand-Trousseau specializing in medicine, genetics, and molecular genetics.

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Publications per year

1984–2013

32

Publications

32

GJB2 Mutations and Degree of Hearing Loss: A Multicenter Study

Rikkert L. Snoeckx, P.L.M. Huygen, Delphine Feldmann et al. · The American Journal of Human Genetics · 2005 · 551 citations · Full text

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Mutation of BSND causes Bartter syndrome with sensorineural deafness and kidney failure

Ralf Birkenhäger, Edgar A. Otto, Maria J. Schürmann et al. · Nature Genetics · 2001 · 529 citations

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Mutations in the Chloride Channel Gene CLCNKB as a Cause of Classic Bartter Syndrome

Martin Konrad, Martin Vollmer, Henny H. Lemmink et al. · Journal of the American Society of Nephrology · 2000 · 288 citations

Spectrum of CFTR mutations in cystic fibrosis and in congenital absence of the vas deferens in France

Mireille Claustres, Caroline Guittard, Dominique Bozon et al. · Human Mutation · 2000 · 250 citations

SLC26A4 gene is frequently involved in nonsyndromic hearing impairment with enlarged vestibular aqueduct in Caucasian populations

Sébastien Albert, Hélène Blons, Laurence Jonard et al. · European Journal of Human Genetics · 2006 · 240 citations · Full text

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