Frank Declau

A New Autosomal Recessive Form of Stickler Syndrome Is Caused by a Mutation in the COL9A1 Gene

Guy Van Camp, Rikkert L. Snoeckx, Nele Hilgert et al. · The American Journal of Human Genetics · 2006 · 181 citations · Full text

Stickler Syndrome Is, Autoimmune Disease, Mendelian Disorder +10

Recommendations for the Description of Genetic and Audiological Data for Families with Nonsyndromic Hereditary Hearing Impairment

Manuela Mazzoli, Guy Van Camp, Valerie Newton et al. · Audiological Medicine · 2003 · 173 citations

Audiological Medicine, Genetics, Genetic Epidemiology +11

Nonmuscle Myosin Heavy-Chain Gene MYH14 Is Expressed in Cochlea and Mutated in Patients Affected by Autosomal Dominant Hearing Impairment (DFNA4)

Francesca Donaudy, Rik L. Snoeckx, Markus Pfister et al. · The American Journal of Human Genetics · 2004 · 167 citations · Full text

Patients Affected, Genetic Disorder, Genetics +8

High Prevalence of Symptoms of Meniere's Disease in three Families With a Mutation in the COCH Gene

Erik Fransén, Margriet Verstreken, W. I. M. Verhagen et al. · Human Molecular Genetics · 1999 · 145 citations · Full text

Prevalence of Otosclerosis in an Unselected Series of Temporal Bones

Frank Declau, M. van Spaendonck, Jean‐Pierre Timmermans et al. · Otology & Neurotology · 2001 · 140 citations