Karen Grønskov

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

Population-based risk estimates of Wilms tumor in sporadic aniridia

Karen Grønskov, Jørgen H. Olsen, Annie Sand et al. · Human Genetics · 2001 · 137 citations

Wilms Tumor, Medicine, Histopathology +4

Mutations in C10orf11, a Melanocyte-Differentiation Gene, Cause Autosomal-Recessive Albinism

Karen Grønskov, Christopher M. Dooley, Elsebet Østergaard et al. · The American Journal of Human Genetics · 2013 · 125 citations · Full text

Developmental Biology, Mendelian Disorder, Genetic Disorder +4

Molecular genetic analysis using targeted NGS analysis of 677 individuals with retinal dystrophy

Cathrine Jespersgaard, Mingyan Fang, Mette Bertelsen et al. · Scientific Reports · 2019 · 120 citations · Full text

Angelman syndrome in Denmark. Birth incidence, genetic findings, and age at diagnosis

Line Granild Bie Mertz, Rikke Christensen, Ida Vogel et al. · American Journal of Medical Genetics Part A · 2013 · 107 citations