William J. Kimberling

Author

Also Known As

Sczaniecka, Anna, W J Kimberling, W Kimberling, W. J. KIMBERLING, W. J. Kimberling, W. Kimberling, W.J. Kimberling, WILLIAM J KIMBERLING PhD, WILLIAM J. KIMBERLING, WILLIAM KIMBERLING

240

Publications

15.8K

Citations

H-Index

206

Concepts

All Affiliations

Boys Town National Research Hospital Boys Town University of Iowa Radboud University Nijmegen Creighton University

About

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

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	43	74	8.5K
2	Arts	13	14	1.3K
3	Health Sciences	6	6	444
4	Education	2	2	434
5	Language Studies	1	1	101

William J. Kimberling

138

Publications

14.7K

Citations

H-Index

Page 1

	Year	Citations
<b> <i>PKD2</i> </b> , a Gene for Polycystic Kidney Disease That Encodes an Integral Membrane Protein Toshio Mochizuki, Guanqing Wu, Tomohito Hayashi, Science	1996	1.4K
Defective myosin VIIA gene responsible for Usher syndrome type IB Dominique Well, Stéphane Blanchard, Josseline Kaplan, Nature Mendelian DisorderGenetic DisorderGeneticsPathologyMedicine	1995	1.1K
Factors affecting the progression of renal disease in autosomal-dominant polycystic kidney disease Patricia A. Gabow, Margaret Johnson, William D. Kaehny, Kidney International GlomerulonephritisUrologyRenal DiseaseRenal FunctionMedicine	1992	507
Novel Mutations in the Connexin 26 Gene (GJB2) That Cause Autosomal Recessive (DFNB1) Hearing Loss Philip M. Kelley, David J. Harris, B.C. Comer, The American Journal of Human Genetics Developmental BiologyMendelian DisorderGenetic DisorderGeneticsAudiology	1998	505
Hereditary nonpolyposis colorectal cancer (lynch syndromes I and II). I. Clinical description of resource Henry T. Lynch, William J. Kimberling, William A. Albano, Cancer	1985	398
Mutation of a Gene Encoding a Protein with Extracellular Matrix Motifs in Usher Syndrome Type IIa James D. Eudy, Michael D. Weston, Su-Fang Yao, Science Molecular PhysiologyDevelopmental BiologyMarkers Afm268zd1Genetic DisorderExtracellular Matrix Motifs	1998	391
Clinical diagnosis of the Usher syndromes Richard J. Smith, Charles I. Berlín, J. Fielding Hejtmancik, American Journal of Medical Genetics	1994	341
Mutations in the VLGR1 Gene Implicate G-Protein Signaling in the Pathogenesis of Usher Syndrome Type II Michael D. Weston, Mirjam W.J. Luijendijk, Kurt Humphrey, The American Journal of Human Genetics Signal TransductionMolecular PhysiologySignaling PathwayG Protein-coupled ReceptorGenetic Disorder	2004	338
Specific Reading Disability: Identification of an Inherited Form Through Linkage Analysis Shelley D. Smith, William J. Kimberling, Bruce F. Pennington, Science Family MedicineDevelopmental DisabilityChromosome 15Genetic DisorderMedicine	1983	333
Linkage of a Gene Causing High Bone Mass to Human Chromosome 11 (11q12-13) Mark L. Johnson, Guodong Gong, William J. Kimberling, The American Journal of Human Genetics Bone DiseaseChromatinDevelopmental BiologyGeneticsGenetic Epidemiology	1997	319

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