Follow
Elizabeth Hauser
Elizabeth Hauser
Duke Molecular Physiology Institute, Duke University
Verified email at duke.edu - Homepage
Title
Cited by
Cited by
Year
Fine mapping of autistic disorder to chromosome 15q11-q13 by use of phenotypic subtypes
Y Shao, ML Cuccaro, ER Hauser, KL Raiford, MM Menold, CM Wolpert, ...
The American Journal of Human Genetics 72 (3), 539-548, 2003
4452003
Association of a peripheral blood metabolic profile with coronary artery disease and risk of subsequent cardiovascular events
SH Shah, JR Bain, MJ Muehlbauer, RD Stevens, DR Crosslin, C Haynes, ...
Circulation: Cardiovascular Genetics 3 (2), 207-214, 2010
4272010
The Finland–United States investigation of non–insulin-dependent diabetes mellitus genetics (FUSION) study. I. An autosomal genome scan for genes that predispose to type 2 diabetes
S Ghosh, RM Watanabe, TT Valle, ER Hauser, VL Magnuson, ...
The American Journal of Human Genetics 67 (5), 1174-1185, 2000
3032000
Baseline metabolomic profiles predict cardiovascular events in patients at risk for coronary artery disease
SH Shah, JL Sun, RD Stevens, JR Bain, MJ Muehlbauer, KS Pieper, ...
American heart journal 163 (5), 844-850. e1, 2012
2872012
Type 2 diabetes: evidence for linkage on chromosome 20 in 716 Finnish affected sib pairs
S Ghosh, RM Watanabe, ER Hauser, T Valle, VL Magnuson, MR Erdos, ...
Proceedings of the National Academy of Sciences 96 (5), 2198-2203, 1999
2781999
Affected‐sib‐pair interval mapping and exclusion for complex genetic traits: sampling considerations
ER Hauser, M Boehnke, SW Guo, N Risch
Genetic epidemiology 13 (2), 117-137, 1996
2471996
Ordered subset analysis in genetic linkage mapping of complex traits
ER Hauser, RM Watanabe, WL Duren, MP Bass, CD Langefeld, ...
Genetic Epidemiology: The Official Publication of the International Genetic …, 2004
1942004
A genomewide scan for early-onset coronary artery disease in 438 families: the GENECARD Study
ER Hauser, DC Crossman, CB Granger, JL Haines, CJH Jones, V Mooser, ...
The American journal of human genetics 75 (3), 436-447, 2004
1892004
Hyperammonemia in women with a mutation at the ornithine carbamoyltransferase locus: a cause of postpartum coma
PH Arn, ER Hauser, GH Thomas, G Herman, D Hess, SW Brusilow
New England Journal of Medicine 322 (23), 1652-1655, 1990
1841990
Prospective treatment of urea cycle disorders
NE Maestri, ER Hauser, D Bartholomew, SW Brusilow
The Journal of pediatrics 119 (6), 923-928, 1991
1771991
The Finland–United States investigation of non–insulin-dependent diabetes mellitus genetics (FUSION) study. II. An autosomal genome scan for diabetes-related quantitative-trait …
RM Watanabe, S Ghosh, CD Langefeld, TT Valle, ER Hauser, ...
The American Journal of Human Genetics 67 (5), 1186-1200, 2000
1612000
High heritability of metabolomic profiles in families burdened with premature cardiovascular disease
SH Shah, ER Hauser, JR Bain, MJ Muehlbauer, C Haynes, RD Stevens, ...
Molecular systems biology 5 (1), 258, 2009
1602009
Thymus transplantation in complete DiGeorge syndrome: immunologic and safety evaluations in 12 patients
ML Markert, M Sarzotti, DA Ozaki, GD Sempowski, ME Rhein, LP Hale, ...
Blood 102 (3), 1121-1130, 2003
1522003
Familiality of quantitative metabolic traits in Finnish families with non-insulin-dependent diabetes mellitus
RM Watanabe, T Valle, ER Hauser, S Ghosh, J Eriksson, K Kohtamäki, ...
Human heredity 49 (3), 159-168, 1999
1441999
Allopurinol-induced orotidinuria: a test for mutations at the ornithine carbamoyltransferase locus in women
ER Hauser, JE Finkelstein, D Valle, SW Brusilow
New England Journal of Medicine 322 (23), 1641-1645, 1990
1441990
Methods for precise sizing, automated binning of alleles, and reduction of error rates in large-scale genotyping using fluorescently labeled dinucleotide markers. FUSION …
S Ghosh, ZE Karanjawala, ER Hauser, D Ally, JI Knapp, JB Rayman, ...
Genome Research 7 (2), 165-178, 1997
1431997
Novel loci and pathways significantly associated with longevity
YI Zeng, C Nie, J Min, X Liu, M Li, H Chen, H Xu, M Wang, T Ni, Y Li, ...
Scientific reports 6 (1), 1-13, 2016
1392016
Peakwide mapping on chromosome 3q13 identifies the kalirin gene as a novel candidate gene for coronary artery disease
L Wang, ER Hauser, SH Shah, MA Pericak-Vance, C Haynes, D Crosslin, ...
The American Journal of Human Genetics 80 (4), 650-663, 2007
1342007
Genomic convergence: identifying candidate genes for Parkinson's disease by combining serial analysis of gene expression and genetic linkage
MA Hauser, YJ Li, S Takeuchi, R Walters, M Noureddine, M Maready, ...
Human molecular genetics 12 (6), 671-677, 2003
1322003
Genotype‐based association test for general pedigrees: the genotype‐PDT
ER Martin, MP Bass, JR Gilbert, MA Pericak‐Vance, ER Hauser
Genetic Epidemiology: The Official Publication of the International Genetic …, 2003
1262003
The system can't perform the operation now. Try again later.
Articles 1–20