Shrawan Kumar

SIX1 mutations cause branchio-oto-renal syndrome by disruption of EYA1–SIX1–DNA complexes

Rainer Ruf, Pin‐Xian Xu, Derek Silvius et al. · Proceedings of the National Academy of Sciences · 2004 · 417 citations · Full text

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

Genomewide Search and Genetic Localization of a Second Gene Associated with Autosomal Dominant Branchio-Oto-Renal Syndrome: Clinical and Genetic Implications

Shrawan Kumar, Karen Deffenbacher, Henri A. M. Marres et al. · The American Journal of Human Genetics · 2000 · 93 citations · Full text

Second Gene Associated, Developmental Biology, Mendelian Disorder +9

Localization of the gene for branchiootorenal syndrome to chromosome 8q

Richard J. Smith, Kevin B. Coppage, Jennifer K.B. Ankerstjerne et al. · Genomics · 1992 · 69 citations

Developmental Biology, Cytogenetics, Genetic Disorder +7

Autosomal dominant branchio-oto-renal syndrome—localization of a disease gene to chromosome 8q by linkage in a Dutch family

Shrawan Kumar, William J. Kimberling, Judy B. Kenyon et al. · Human Molecular Genetics · 1992 · 65 citations

Genetics, Disease Gene, Genetic Epidemiology +23