Judith B. Kenyon

Autosomal dominant polycystic kidney disease: Localization of the second gene to chromosome 4q13–q23

William J. Kimberling, Shrawan Kumar, Patricia A. Gabow et al. · Genomics · 1993 · 293 citations

Mendelian Disorder, Genetic Disorder, Medicine +12

Linkage Heterogeneity of Autosomal Dominant Polycystic Kidney Disease

William J. Kimberling, Pamela R. Fain, Judith B. Kenyon et al. · New England Journal of Medicine · 1988 · 219 citations

Family Members, Genetics, Genetic Epidemiology +21

Linkage of usher syndrome type I gene (USH1B) to the long arm of chromosome 11

William J. Kimberling, Claes Möller, Sandra L. H. Davenport et al. · Genomics · 1992 · 182 citations

Usher Syndrome Type, Developmental Biology, Genetic Disorder +8

Tietz syndrome (hypopigmentation/deafness) caused by mutation of<i>MITF</i>: Figure 1

Shelley D. Smith, Philip M. Kelley, Judith B. Kenyon et al. · Journal of Medical Genetics · 2000 · 151 citations · Full text

Consanguineous nuclear families used to identify a new locus for recessive non-syndromic hearing loss on 14q

Kunihiro Fukushima, Arabandi Ramesh, C. R. Srikumari Srisailapathy et al. · Human Molecular Genetics · 1995 · 55 citations

Genetics, Genetic Epidemiology, Pathology +18