Elizabeth Hauser
Elizabeth Hauser
Duke Molecular Physiology Institute, Duke University
Потвърден имейл адрес: duke.edu - Начална страница
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
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
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
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
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
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
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
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
Prospective treatment of urea cycle disorders
NE Maestri, ER Hauser, D Bartholomew, SW Brusilow
The Journal of pediatrics 119 (6), 923-928, 1991
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
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), 21243, 2016
Harmonizing genetic ancestry and self-identified race/ethnicity in genome-wide association studies
H Fang, Q Hui, J Lynch, J Honerlaw, TL Assimes, J Huang, M Vujkovic, ...
The American Journal of Human Genetics 105 (4), 763-772, 2019
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
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
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
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
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
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
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
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
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