Phenotypic variability of patients homozygous for the GJB2 mutation 35delG cannot be explained by the influence of one major modifier gene

Novel Crohn Disease Locus Identified by Genome-Wide Association Maps to a Gene Desert on 5p13.1 and Modulates Expression of PTGER4

Cécile Libioulle, Édouard Louis, Sarah Hansoul et al. · PLoS Genetics · 2007 · 563 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

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 · 559 citations · Full text

Medicine, Genetics, Otolaryngology +12

High carrier frequency of the 35delG deafness mutation in European populations

Paolo Gasparini, Raquel Rabionet, Guido Barbujani et al. · European Journal of Human Genetics · 2000 · 390 citations · Full text

Life Sciences, Genetics, Molecular Genetics +13

GRR: graphical representation of relationship errors

Gonçalo R. Abecasis, Stacey S. Cherny, William Cookson et al. · Bioinformatics · 2001 · 390 citations · Full text

Life Sciences, Bioinformatics, Genetics +13

Transplacental Uptake of Glucose Is Decreased in Embryonic Lethal Connexin26-deficient Mice

Heinz‐Dieter Gabriel, Dirk Jung, C Bützler et al. · The Journal of Cell Biology · 1998 · 293 citations · Full text

Life Sciences, Biochemistry, Developmental Biology +17