William J. Kimberling

Quantitative Trait Locus for Reading Disability on Chromosome 6

Lon R. Cardon, Shelley D. Smith, David W. Fulker et al. · Science · 1994 · 540 citations

Haplotype Determination, Quantitative Genetics, Genotype-phenotype Association +14

Mutations in the human α-tectorin gene cause autosomal dominant non-syndromic hearing impairment

Kristien Verhoeven, Lut Van Laer, Karin Kirschhofer et al. · Nature Genetics · 1998 · 335 citations

Developmental Biology, Genetic Disorder, Genetics +10

Localization of two genes for usher syndrome type I to chromosome 11

Richard J. Smith, E.C. Lee, William J. Kimberling et al. · Genomics · 1992 · 221 citations

Usher Syndrome Type, Genetic Disorder, Genetics +6

Localization of Usher syndrome type II to chromosome 1q

William J. Kimberling, Michael D. Weston, Claes Möller et al. · Genomics · 1990 · 217 citations

Medicine, Molecular Genetics, Genetics +1

Myosin VIIA mutation screening in 189 Usher syndrome type 1 patients.

Michael D. Weston, P M Kelley, L D Overbeck et al. · PubMed · 1996 · 109 citations