Concepedia

Brith Otterud

BO

32

Publications

2.6K

Citations

27

H-Index

1992

Active since

Affiliations

University of Utah(Current)

Howard Hughes Medical Institute

Biomedical Informatics Research Center Antwerp

University of Washington

University of Cincinnati

Brith Otterud is an author at University of Utah specializing in medicine, genetics, and molecular genetics.

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Publications per year

1992–2018

32

Publications

32

Autosomal dominant spinocerebellar ataxia with sensory axonal neuropathy (SCA4): clinical description and genetic localization to chromosome 16q22.1.

Kevin M. Flanigan, Kathy Gardner, Kathy Alderson et al. · PubMed · 1996 · 248 citations

Bardet–Biedl syndrome is linked to DNA markers on chromosome 11 q and is genetically heterogeneous

Mark Leppert, Lisa Baird, Kent L. Anderson et al. · Nature Genetics · 1994 · 179 citations

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A locus for febrile seizures (FEB3) maps to chromosome 2q23-24

Andy Peiffer, Joel A. Thompson, Carole Charlier et al. · Annals of Neurology · 1999 · 162 citations

Genetic linkage analysis in familial benign (hypocalciuric) hypercalcemia: evidence for locus heterogeneity.

rd H Heath, Charles E. Jackson, Brith Otterud et al. · PubMed · 1993 · 156 citations

Linkage of a variant or attenuated form of adenomatous polyposis coli to the adenomatous polyposis coli (APC) locus.

Lisa Spirio, Brith Otterud, Dora Stauffer et al. · PubMed · 1992 · 148 citations

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