Concepedia

Scott C. Wildenberg

SC

8

Publications

1.2K

Citations

8

H-Index

1995

Active since

Affiliations

University of Minnesota(Current)

National Institutes of Health

National Human Genome Research Institute

Institute of Human Genetics

Scott C. Wildenberg is an author at University of Minnesota specializing in genetics, medicine, and cytogenetics.

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Publications per year

1995–2003

8

Publications

8

Evidence That a Locus for Familial High Myopia Maps to Chromosome 18p

Terri L. Young, Shawn M. Ronan, Leslie A. Drahozal et al. · The American Journal of Human Genetics · 1998 · 279 citations · Full text

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A Second Locus for Familial High Myopia Maps to Chromosome 12q

Terri L. Young, Shawn M. Ronan, Alison B. Alvear et al. · The American Journal of Human Genetics · 1998 · 266 citations · Full text

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Mutation in and lack of expression of tyrosinase-related protein-1 (TRP-1) in melanocytes from an individual with brown oculocutaneous albinism: a new subtype of albinism classified as "OCA3".

Raymond E. Boissy, Hongyi Zhao, William S. Oetting et al. · PubMed · 1996 · 195 citations · Full text

New Locus for Autosomal Dominant High Myopia Maps to the Long Arm of Chromosome 17

Prasuna Paluru, Shawn M. Ronan, Elise Héon et al. · Investigative Ophthalmology & Visual Science · 2003 · 180 citations · Full text

The mouse pale ear ( <i>ep</i> ) mutation is the homologue of human Hermansky–Pudlak syndrome

John M. Gardner, Scott C. Wildenberg, Natalie M. Keiper et al. · Proceedings of the National Academy of Sciences · 1997 · 133 citations · Full text

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