Walter E. Nance - Concepedia

Author

Walter E. Nance

Virginia Commonwealth University Medical Center

Also Known As

F Or- Lebeke, W E Nance, WALTER E. NANCE, Walter E Nance, Walter E. Nance, Walter Nance

171

Publications

9.5K

Citations

H-Index

212

Concepts

All Affiliations

Virginia Commonwealth University Medical Center Virginia Commonwealth University Indiana University – Purdue University Indianapolis Gallaudet University Indiana University School of Medicine

About

Walter E. Nance is an author at Virginia Commonwealth University Medical Center specializing in medicine, genetics, and genetic epidemiology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Arts	11	11	1.4K
2	Health Sciences	5	5	247
3	Education	1	1	33
4	Engineering	1	1	64
5	Language Studies	1	1	39

Walter E. Nance

Publications

Citations

H-Index

Page 1

	Year	Citations
Genetic Factors in Determining Bone Mass David M. Smith, Walter E. Nance, Ke Won Kang, Journal of Clinical Investigation Bone DiseaseBody CompositionOrthopaedic SurgeryGeneticsGenetic Epidemiology	1973	585
Usher Syndrome 1D and Nonsyndromic Autosomal Recessive Deafness DFNB12 Are Caused by Allelic Mutations of the Novel Cadherin-Like Gene CDH23 Julie M. Bork, Linda Peters, Saima Riazuddin, The American Journal of Human Genetics Developmental BiologyAllelic MutationsMendelian DisorderGenetic DisorderGenetics	2001	551
Genetic epidemiological studies of early‐onset deafness in the U.S. school‐age population Mary L. Marazita, Lynn Ploughman, Brenda W. Rawlings, American Journal of Medical Genetics Genetic Epidemiological StudiesPediatric OtolaryngologyEarly‐onset DeafnessAudiologyPediatrics	1993	456
Prevalence and Evolutionary Origins of the del(GJB6-D13S1830) Mutation in the DFNB1 Locus in Hearing-Impaired Subjects: a Multicenter Study Ignacio del Castillo, Miguel A. Moreno‐Pelayo, Francisco Castillo, The American Journal of Human Genetics Genetic DisorderGeneticsGenetic EpidemiologyAudiologyEvolutionary Origins	2003	289
Otoancorin, an inner ear protein restricted to the interface between the apical surface of sensory epithelia and their overlying acellular gels, is defective in autosomal recessive deafness DFNB22 Ingrid Zwaenepoel, Mirna Mustapha, Michel Leibovici, Proceedings of the National Academy of Sciences OtorhinolaryngologyMolecular BiologyNeurotologyCytoskeletonOverlying Acellular Gels	2002	182
Familial branchio‐oto‐renal dysplasia: A new addition to the branchial arch syndromes Michael Melnick, David Bixler, Walter E. Nance, Clinical Genetics	1976	177
The prevalence of connexin 26 ( GJB2 ) mutations in the Chinese population Xue Liu, Xia Xia, Ke Xiao, Human Genetics Molecular Diagnostic TechniquesMendelian DisorderGenetic DisorderMedicineGenetics	2002	172
Genetic Studies of an Acardiac Monster: Evidence of Polar Body Twinning in Man Frederick R. Bieber, Walter E. Nance, Cynthia C. Morton, Science Polar Body TwinningFertilityGeneticsReproductive BiologyFertilisation	1981	172
Frequency and distribution of GJB2 (connexin 26) and GJB6 (connexin 30) mutations in a large North American repository of deaf probands Arti Pandya, Kathleen S. Arnos, Xia J. Xia, Genetics in Medicine Genetic DisorderGeneticsMolecular BiologyDeaf ProbandsMolecular Genetics	2003	160
Hypo-Functional<i>SLC26A4</i>variants associated with nonsyndromic hearing loss and enlargement of the vestibular aqueduct: Genotype-phenotype correlation or coincidental polymorphisms? Byung Yoon Choi, Andrew K. Stewart, Anne C. Madeo, Human Mutation	2009	150

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