Judith B. Kenyon - Concepedia

Concepedia

Author

Judith B. Kenyon

Boys Town National Research Hospital

Also Known As

J. B. KENYON, J.B. Kenyon, Judith B Kenyon, Judith B. Kenyon, Judith B.Kenyon, Judith Kenyon

13

Publications

1.1K

Citations

9

H-Index

26

Concepts

All Affiliations

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

JB

About

Judith B. Kenyon is an author at Boys Town National Research Hospital specializing in genetics, medicine, and genetic epidemiology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	5	5	798
2	Molecular Genetics	3	3	286
3	Arts	2	2	104
4	Public Health	2	2	512
5	Nephrology	2	2	512

Judith B. Kenyon

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9

Publications

1.1K

Citations

9

H-Index

	Year	Citations
Autosomal dominant polycystic kidney disease: Localization of the second gene to chromosome 4q13–q23 William J. Kimberling, Shrawan Kumar, Patricia A. Gabow, Genomics Mendelian DisorderGenetic DisorderMedicineGeneticsRenal Pathology	1993	293
Linkage Heterogeneity of Autosomal Dominant Polycystic Kidney Disease William J. Kimberling, Pamela R. Fain, Judith B. Kenyon, New England Journal of Medicine Family MembersGeneticsGenetic EpidemiologyHuman PolymorphismPathology	1988	219
Linkage of usher syndrome type I gene (USH1B) to the long arm of chromosome 11 William J. Kimberling, Claes Möller, Sandra L. H. Davenport, Genomics Usher Syndrome TypeDevelopmental BiologyGenetic DisorderGeneticsLong Arm	1992	182
Tietz syndrome (hypopigmentation/deafness) caused by mutation of<i>MITF</i>: Figure 1 Shelley D. Smith, Philip M. Kelley, Judith B. Kenyon, Journal of Medical Genetics	2000	151
Consanguineous nuclear families used to identify a new locus for recessive non-syndromic hearing loss on 14q Kunihiro Fukushima, Arabandi Ramesh, C. R. Srikumari Srisailapathy, Human Molecular Genetics GeneticsGenetic EpidemiologyPathologyMolecular GeneticsDisease Gene Identification	1995	55
Splice-altering variant in COL11A1 as a cause of nonsyndromic hearing loss DFNA37 Kevin T. Booth, James W. Askew, Zohreh Talebizadeh, Genetics in Medicine	2018	53
A Novel Locus for Autosomal Dominant Nonsyndromic Hearing Loss, DFNA13, Maps to Chromosome 6p Matthew Brown, Michael S. Tomek, L. Van Laer, The American Journal of Human Genetics Developmental BiologyGenetic DisorderGeneticsAudiologyAuditory Physiology	1997	49
Autosomal-dominant, prelingual, nonprogressive sensorineural hearing loss: localization of the gene (DFNA8) to chromosome 11q by linkage in an Austrian family Karin Kirschhofer, Judith B. Kenyon, D.M. Hoover, Cytogenetic and Genome Research	1998	43
Genetic Studies of Usher Syndrome William J. Kimberling, Michael D. Weston, S. Pieke Dahl, Annals of the New York Academy of Sciences Mendelian DisorderGenetic DisorderGeneticsGenetic EpidemiologyUsher Syndrome	1991	13

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