Brith Otterud
University of Utah(US)
Publications by Year
Research Areas
Neurogenetic and Muscular Disorders Research, Hereditary Neurological Disorders, Neurological diseases and metabolism, T-cell and B-cell Immunology, Immunotherapy and Immune Responses
Most-Cited Works
- Autosomal dominant spinocerebellar ataxia with sensory axonal neuropathy (SCA4): clinical description and genetic localization to chromosome 16q22.1.(1996)
- → Bardet–Biedl syndrome is linked to DNA markers on chromosome 11 q and is genetically heterogeneous(1994)179 cited
- → Genetic Mapping of Ossification of the Posterior Longitudinal Ligament of the Spine(1998)170 cited
- → A locus for febrile seizures (FEB3) maps to chromosome 2q23-24(1999)162 cited
- Genetic linkage analysis in familial benign (hypocalciuric) hypercalcemia: evidence for locus heterogeneity.(1993)
- → Genetic analysis of a complex trait in the Utah Genetic Reference Project: a major locus for PTC taste ability on chromosome 7q and a secondary locus on chromosome 16p(2003)148 cited
- Linkage of a variant or attenuated form of adenomatous polyposis coli to the adenomatous polyposis coli (APC) locus.(1992)
- Autosomal dominant familial spastic paraplegia: tight linkage to chromosome 15q.(1995)
- → Molecular cloning and physical and genetic mapping of a novel human Na+/H+ exchanger (NHE5/SLC9A5) to chromosome 16q22.1(1995)134 cited
- Paroxysmal dystonic choreoathetosis: tight linkage to chromosome 2q.(1996)