William J. Kimberling

Author

Also Known As

W J Kimberling, William J. Kimberling

Publications

1.6K

Citations

H-Index

Concepts

All Affiliations

William J. Kimberling is an author at Boys Town National Research Hospital specializing in genetics, medicine, and genetic epidemiology.

#	Concept	H-Index	Publications	Citations
1	Medicine	5	5	1.4K
2	Molecular Genetics	2	2	438
3	Arts	1	1	335
4	Public Health	1	1	540
5	Biostatistics	1	1	540

William J. Kimberling

Publications

1.6K

Citations

H-Index

Page 1

	Year	Citations
Quantitative Trait Locus for Reading Disability on Chromosome 6 Lon R. Cardon, Shelley D. Smith, David W. Fulker, Science Haplotype DeterminationQuantitative GeneticsGenotype-phenotype AssociationGenetic DisorderMedicine	1994	540
Mutations in the human α-tectorin gene cause autosomal dominant non-syndromic hearing impairment Kristien Verhoeven, Lut Van Laer, Karin Kirschhofer, Nature Genetics Developmental BiologyGenetic DisorderGeneticsAudiologyAuditory Physiology	1998	335
Localization of two genes for usher syndrome type I to chromosome 11 Richard J. Smith, E.C. Lee, William J. Kimberling, Genomics Usher Syndrome TypeGenetic DisorderGeneticsLinkage AnalysisPathology	1992	221
Localization of Usher syndrome type II to chromosome 1q William J. Kimberling, Michael D. Weston, Claes Möller, Genomics MedicineMolecular GeneticsGeneticsGenetic Disorder	1990	217
Myosin VIIA mutation screening in 189 Usher syndrome type 1 patients. Michael D. Weston, P M Kelley, L D Overbeck, PubMed	1996	109
Connexin 26 gene (GJB2) mutation modulates the severity of hearing loss associated with the 1555A?G mitochondrial mutation Satoko Abe, Philip M. Kelley, William J. Kimberling, American Journal of Medical Genetics	2001	81
Genetic Heterogeneity of Usher Syndrome: Analysis of 151 Families with Usher Type I Lisa M. Astuto, Michael D. Weston, Carol A. Carney, The American Journal of Human Genetics Mendelian DisorderGenetic DisorderGeneticsGenetic EpidemiologyGenetic Heterogeneity	2000	71

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