Concepedia
Statistics
Publications
8
Citations
390
H-Index
Active since
1999
Affiliations
University of Antwerp(Current)
Radboud University Nijmegen
Radboud University Medical Center
University of Iowa
Kris Flothmann is an author at University of Antwerp specializing in genetics, life sciences, and human genetics.
Publications per year
1999–2004
Determination of the carrier frequency of the common GJB2 (connexin-26) 35delG mutation in the Belgian population using an easy and reliable screening method
Katrien Storm, Sandra Willocx, Kris Flothmann et al. · Human Mutation · 1999 · 98 citations
Life Sciences, Genetics, Molecular Genetics +14
Mutations in the WFS1 gene that cause low-frequency sensorineural hearing loss are small non-inactivating mutations
Kim Cryns, Markus Pfister, Ronald J. E. Pennings et al. · Human Genetics · 2002 · 90 citations · Full text
Life Sciences, Genetics, Molecular Genetics +11
The ABCA4 2588G>C Stargardt mutation: single origin and increasing frequency from South-West to North-East Europe
Alessandra Maugeri, Kris Flothmann, Nadine Hemmrich et al. · European Journal of Human Genetics · 2002 · 48 citations · Full text
Life Sciences, Genetics, Molecular Genetics +5
A gene for autosomal dominant hearing impairment (DFNA14) maps to a region on chromosome 4p16.3 that does not overlap the DFNA6 locus
Guy Van Camp, Henricus P. M. Kunst, Kris Flothmann et al. · Journal of Medical Genetics · 1999 · 46 citations · Full text
Life Sciences, Audiology, Genetics +11
Progression of Low-Frequency Sensorineural Hearing Loss (DFNA6/14-WFS1)
Ronald J. E. Pennings, Steven J. H. Bom, Kim Cryns et al. · Archives of Otolaryngology - Head and Neck Surgery · 2003 · 42 citations
Health Professions, Audiology, Genetics +15
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