Stuart A. Holmes - Concepedia

Author

Stuart A. Holmes

University of Wisconsin–Madison

Also Known As

S A Holmes, Stuart A. Holmes, Stuart Holmes

Publications

Citations

H-Index

Concepts

All Affiliations

University of Wisconsin–Madison Children's Hospital of Philadelphia Oregon Health & Science University Hospital for Sick Children NYU Langone Health

About

Stuart A. Holmes is an author at University of Wisconsin–Madison specializing in medicine, genetics, and molecular genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	9	9	555
2	Biochemistry	2	2	260
3	Engineering	1	1	29
4	Health Sciences	1	1	20
5	Natural Sciences	1	1	238

Stuart A. Holmes

Publications

Citations

H-Index

Page 1

	Year	Citations
<i>SSC1</i>, an Essential Member of the Yeast HSP70 Multigene Family, Encodes a Mitochondrial Protein Elizabeth A. Craig, Julie Kramer, Jeffery Shilling, Molecular and Cellular Biology Protein FunctionMitochondrial BiogenesisMitochondrial FunctionBiochemistryHsp70 Yeast Protein	1989	238
Dominant negative and loss of function mutations of the c-kit (mast/stem cell growth factor receptor) proto-oncogene in human piebaldism. Richard A. Spritz, Lutz B. Giebel, Stuart A. Holmes PubMed	1992	159
Novel mutations and deletions of the KIT (steel factor receptor) gene in human piebaldism. Kazuhiko Ezoe, Stuart A. Holmes, L. Ho, PubMed	1995	111
Mutations of the KIT (mast/stem cell growth factor receptor) proto-oncogene account for a continuous range of phenotypes in human piebaldism. Richard A. Spritz, Stuart A. Holmes, Raj Ramesar, PubMed	1992	94
Autosomal recessive ocular albinism associated with a functionally significant tyrosinase gene polymorphism Kazuyoshi Fukai, Stuart A. Holmes, Neil J. Lucchese, Nature Genetics Ocular DiseaseMendelian DisorderOphthalmologyGenetic DisorderGenetics	1995	78
Novel mutations of the tyrosinase (TYR) gene in type I oculocutaneous albinism (OCA1) Richard A. Spritz, Jangsuk Oh, Kazuyoshi Fukai, Human Mutation Oculocutaneous AlbinismGenetic DisorderGeneticsNovel MutationsMolecular Biology	1997	71
Frequent intragenic deletion of the P gene in Tanzanian patients with type II oculocutaneous albinism (OCA2). Richard A. Spritz, Kazuyoshi Fukai, Stuart A. Holmes, PubMed	1995	62
Novel Mutations of the KIT (Mast/Stem Cell Growth Factor Receptor) Proto-Oncogene in Human Piebaldism Richard A. Spritz, Stuart A. Holmes, Peter Itin, Journal of Investigative Dermatology Cell LineageDevelopmental GeneticsGeneticsNovel MutationsStem Cell Research	1993	50
Mutations of the tyrosinase gene in Indo-Pakistani patients with type I (tyrosinase-deficient) oculocutaneous albinism (OCA). R. K. Tripathi, Sarah Bundey, M A Musarella, PubMed	1993	37
A Non-radioactive Method for Simultaneous Detection of Single-strand Conformation Polymorphisms (SSCPs) and Heteroduplexes Seung‐Taek Lee, Sang Kyu Park, Kyoung Hwa Lee, Molecules and Cells Simultaneous DetectionEngineeringSingle-strand Conformation PolymorphismsGeneticsDna Analysis	1995	29

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