Works by Otterud, Brith

Results: 9

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

Published in:

1999

By:

Peiffer, Andy;
Thompson, Joel;
Charlier, Carole;
Otterud, Brith;
Varvil, Tena;
Pappas, Chris;
Barnitz, Craig;
Gruenthal, Kristen;
Kuhn, Renée;
Leppert, Mark;
Peiffer, A;
Thompson, J;
Charlier, C;
Otterud, B;
Varvil, T;
Pappas, C;
Barnitz, C;
Gruenthal, K;
Kuhn, R;
Leppert, M

Publication type:

journal article

Genetic linkage of the human gene for phenylethanol-amine N-methyltransferase (PNMT), the adrenaline-synthesizing enzyme, to DNA markers on chromosome 17q21–q22.

Published in:

Human Molecular Genetics, 1992, v. 1, n. 3, p. 175

By:

Hoehe, Margret R.;
Plaetke, Rosemarie;
Otterud, Brith;
Stauffer, Dora;
Holik, John;
Byerley, William F.;
Baetge, E. Edward;
Gershon, Elliot S.;
Lalouel, Jean-Marc;
Leppert, Mark

Publication type:

Article

Identification of rare DNA sequence variants in high-risk autism families and their prevalence in a large case/control population.

Published in:

Molecular Autism, 2014, v. 5, n. 1, p. 3, doi. 10.1186/2040-2392-5-5

By:

Matsunami, Nori;
Hensel, Charles H.;
Baird, Lisa;
Stevens, Jeff;
Otterud, Brith;
Leppert, Tami;
Varvil, Tena;
Hadley, Dexter;
Glessner, Joseph T.;
Pellegrino, Renata;
Kim, Cecilia;
Thomas, Kelly;
Wang, Fengxiang;
Otieno, Frederick G.;
Ho, Karen;
Christensen, Gerald B.;
Dongying Li;
Prekeris, Rytis;
Lambert, Christophe G.;
Hakonarson, Hakon

Publication type:

Article

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.

Published in:

Human Genetics, 2003, v. 112, n. 5/6, p. 567, doi. 10.1007/s00439-003-0911-y

By:

Drayna, Dennis;
Coon, Hilary;
Un-Kyung Kim;
Elsner, Tami;
Cromer, Kevin;
Otterud, Brith;
Baird, Lisa;
Peiffer, Andy P.;
Leppert, Mark

Publication type:

Article

Identification of Rare Recurrent Copy Number Variants in High-Risk Autism Families and Their Prevalence in a Large ASD Population.

Published in:

PLoS ONE, 2013, v. 8, n. 1, p. 1, doi. 10.1371/journal.pone.0052239

By:

Matsunami, Nori;
Hadley, Dexter;
Hensel, Charles H.;
Christensen, G. Bryce;
Kim, Cecilia;
Frackelton, Edward;
Thomas, Kelly;
Silva, Renata Pellegrino da;
Stevens, Jeff;
Baird, Lisa;
Otterud, Brith;
Ho, Karen;
Varvil, Tena;
Leppert, Tami;
Lambert, Christophe G.;
Leppert, Mark;
Hakonarson, Hakon

Publication type:

Article

Identification of a Herpes Simplex Labialis Susceptibility Region on Human Chromosome 21.

Published in:

Journal of Infectious Diseases, 2008, v. 197, n. 3, p. 340, doi. 10.1086/525540

By:

Hobbs, Maurine R.;
Jones, Brandt B.;
Otterud, Brith E.;
Leppert, Mark;
Kriesel, John D.

Publication type:

Article

The identical 5′ splice-site acceptor mutation in five attenuated APC families from Newfoundland demonstrates a founder effect.

Published in:

2000

By:

Spirio, Lisa;
Green, Jane;
Robertson, Jennifer;
Robertson, Margaret;
Otterud, Brith;
Sheldon, John;
Howse, Erica;
Green, Roger;
Groden, Joanna;
White, Ray;
Leppert, Mark

Publication type:

Erratum

A hyperactivating proinflammatory RIPK2 allele associated with early-onset osteoarthritis.

Published in:

Human Molecular Genetics, 2018, v. 27, n. 13, p. 2383, doi. 10.1093/hmg/ddy132

By:

Jurynec, Michael J.;
Sawitzke, Allen D.;
Beals, Timothy C.;
Redd, Michael J.;
Stevens, Jeff;
Otterud, Brith;
Leppert, Mark F.;
Grunwald, David Jonah

Publication type:

Article

Description of a second microsatellite marker and linkage analysis of the muscle glycogen synthase locus in familial NIDDM.

Published in:

1994

By:

Elbein, Steven C.;
Hoffman, Michael;
Ridinger, David;
Otterud, Brith;
Leppert, Mark;
Elbein, S C;
Hoffman, M;
Ridinger, D;
Otterud, B;
Leppert, M

Publication type:

journal article