Hans‐Henrik M. Dahl

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

Genetic Disorder, Genetics, Audiology +9

A reduction of mitochondrial DNA molecules during embryogenesis explains the rapid segregation of genotypes

Lynsey Cree, David C. Samuels, Susana M. Chuva de Sousa Lopes et al. · Nature Genetics · 2008 · 505 citations

Developmental Biology, Rapid Segregation, Cell Division +10

Strikingly Different Clinicopathological Phenotypes Determined by Progranulin-Mutation Dosage

Katherine R. Smith, John A. Damiano, Silvana Franceschetti et al. · The American Journal of Human Genetics · 2012 · 479 citations · Full text

Neurodegenerative Diseases, Mendelian Disorder, Genetic Disorder +15

Prevalence and Evolutionary Origins of the del(GJB6-D13S1830) Mutation in the DFNB1 Locus in Hearing-Impaired Subjects: a Multicenter Study

Ignacio del Castillo, Miguel A. Moreno‐Pelayo, Francisco Castillo et al. · The American Journal of Human Genetics · 2003 · 289 citations · Full text

Genetic Disorder, Genetics, Genetic Epidemiology +9

High frequency hearing loss correlated with mutations in the GJB2 gene

Stephen Wilcox, Kerryn Saunders, Amelia H. Osborn et al. · Human Genetics · 2000 · 209 citations

Genetic Disorder, Genetics, Audiology +12