Author details

Full Name

Brith Otterud

Affiliation

ORCID

Career Start Year

1990

Papers

H Index

Expertise

CM4AI Collaborator

PMID	Paper Title	Journal Title	Published Year
29659823	A hyperactivating proinflammatory RIPK2 allele associated with early-onset osteoarthritis.	Hum Mol Genet	2018
29860498	A hyperactivating proinflammatory RIPK2 allele associated with early-onset osteoarthritis.	Hum Mol Genet	2018
24467814	Identification of rare DNA sequence variants in high-risk autism families and their prevalence in a large case/control population.	Mol Autism	2014
23341896	Identification of rare recurrent copy number variants in high-risk autism families and their prevalence in a large ASD population.	PLoS One	2013
22337856	Exome analysis of a family with pleiotropic congenital heart disease.	Circ Cardiovasc Genet	2012
20203263	Leukemia-associated minor histocompatibility antigen discovery using T-cell clones isolated by in vitro stimulation of naive CD8+ T cells.	Blood	2010
20522424	Colorectal adenomas and cancer link to chromosome 13q22.1-13q31.3 in a large family with excess colorectal cancer.	J Med Genet	2010
19318250	A novel form of juvenile recessive ALS maps to loci on 6p25 and 21q22.	Neuromuscul Disord	2009
18199027	Identification of a herpes simplex labialis susceptibility region on human chromosome 21.	J Infect Dis	2008
19001137	Toward targeting B cell cancers with CD4+ CTLs: identification of a CD19-encoded minor histocompatibility antigen using a novel genome-wide analysis.	J Exp Med	2008
16322791	A frameshift polymorphism in P2X5 elicits an allogeneic cytotoxic T lymphocyte response associated with remission of chronic myeloid leukemia.	J Clin Invest	2005
15585611	Allogeneic hematopoietic cell transplantation for metastatic renal cell carcinoma after nonmyeloablative conditioning: toxicity, clinical response, and immunological response to minor histocompatibility antigens.	Clin Cancer Res	2004
12624758	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.	Hum Genet	2003
12135428	Feasibility of using genetic linkage analysis to identify the genes encoding T cell-defined minor histocompatibility antigens.	Tissue Antigens	2002
10598803	The identical 5' splice-site acceptor mutation in five attenuated APC families from Newfoundland demonstrates a founder effect.	Hum Genet	1999
9973294	Novel locus for autosomal dominant hereditary spastic paraplegia, on chromosome 8q.	Am J Hum Genet	1999
10514109	A locus for febrile seizures (FEB3) maps to chromosome 2q23-24.	Ann Neurol	1999
10371253	Genetic linkage of the dentinogenesis imperfecta type III locus to chromosome 4q.	J Dent Res	1999
9818901	Analysis of microtubule-associated protein 1a gene in hereditary spastic paraplegia.	Neurology	1998
9463332	Mutations in CYP1B1, the gene for cytochrome P4501B1, are the predominant cause of primary congenital glaucoma in Saudi Arabia.	Am J Hum Genet	1998
9728933	Localization to chromosome 11 of a gene encoding a human minor histocompatibility antigen.	Exp Hematol	1998
9585596	Genetic mapping of ossification of the posterior longitudinal ligament of the spine.	Am J Hum Genet	1998
9345096	Genetic linkage of Paget disease of the bone to chromosome 18q.	Am J Hum Genet	1997
8618696	Hereditary spastic paraplegia linked to chromosome 15q: Analysis of candidate genes.	Neurology	1996
8955193	Localization to chromosome 22 of a gene encoding a human minor histocompatibility antigen.	J Immunol	1996
8946299	A gene for primary congenital glaucoma is not linked to the locus on chromosome 1q for autosomal dominant juvenile-onset open angle glaucoma.	J Glaucoma	1996
8755926	Autosomal dominant spinocerebellar ataxia with sensory axonal neuropathy (SCA4): clinical description and genetic localization to chromosome 16q22.1.	Am J Hum Genet	1996
8659518	Paroxysmal dystonic choreoathetosis: tight linkage to chromosome 2q.	Am J Hum Genet	1996
8652836	Linkage of a familial platelet disorder with a propensity to develop myeloid malignancies to human chromosome 21q22.1-22.2.	Blood	1996
7847375	A gene for familial total anomalous pulmonary venous return maps to chromosome 4p13-q12.	Am J Hum Genet	1995
7759094	Molecular cloning and physical and genetic mapping of a novel human Na+/H+ exchanger (NHE5/SLC9A5) to chromosome 16q22.1.	Genomics	1995
7825577	Autosomal dominant familial spastic paraplegia: tight linkage to chromosome 15q.	Am J Hum Genet	1995
7583452	Genetic mapping of adrenergic receptor genes in humans.	J Mol Med (Berl)	1995
8533764	A YAC contig encompassing the recessive Stargardt disease gene (STGD) on chromosome 1p.	Am J Hum Genet	1995
7854534	Autosomal dominant, familial spastic paraplegia, type I: clinical and genetic analysis of a large North American family.	Neurology	1995
8001971	Molecular cloning and physical and genetic mapping of the human anion exchanger isoform 3 (SLC2C) gene to chromosome 2q36.	Genomics	1994
8075632	Bardet-Biedl syndrome is linked to DNA markers on chromosome 11q and is genetically heterogeneous.	Nat Genet	1994
7913686	Description of a second microsatellite marker and linkage analysis of the muscle glycogen synthase locus in familial NIDDM.	Diabetes	1994
7977374	A gene for distal arthrogryposis type I maps to the pericentromeric region of chromosome 9.	Am J Hum Genet	1994
7874147	Dinucleotide repeat polymorphism from a cosmid containing the human anion exchanger isoform 3 (SLC2C) gene.	Hum Mol Genet	1994
8252630	Alleles of the APC gene: an attenuated form of familial polyposis.	Cell	1993
8428511	The human endothelin-1 gene (EDN1) encoding a peptide with potent vasoactive properties maps distal to HLA on chromosome arm 6p in close linkage to D6S89.	Cytogenet Cell Genet	1993
8317484	Genetic linkage analysis in familial benign (hypocalciuric) hypercalcemia: evidence for locus heterogeneity.	Am J Hum Genet	1993
7683738	Genetic susceptibility in familial multiple sclerosis not linked to the myelin basic protein gene.	Lancet	1993
1303174	Genetic linkage of the human gene for phenylethanolamine N-methyltransferase (PNMT), the adrenaline-synthesizing enzyme, to DNA markers on chromosome 17q21-q22.	Hum Mol Genet	1992
1319115	Linkage of a variant or attenuated form of adenomatous polyposis coli to the adenomatous polyposis coli (APC) locus.	American Journal of Human Genetics	1992
1672750	D7S448 detects a HindIII polymorphism located in the centromere region of chromosome 7.	Nucleic Acids Res	1991
1971808	Mapping recessive ophthalmic diseases: linkage of the locus for Usher syndrome type II to a DNA marker on chromosome 1q.	Genomics	1990
1979868	D7S449 detects a HindIII polymorphism tightly linked to the MET gene on chromosome 7.	Nucleic Acids Res	1990