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 | 504 | 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 | 463 | 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 | 347 | 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 | 309 | 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 | 287 | 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 | 251 | 1996 |
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 | 201 | 1990 |
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 | 199 | 2004 |
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 | 197 | 2019 |
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 | 196 | 2004 |
Prospective treatment of urea cycle disorders NE Maestri, ER Hauser, D Bartholomew, SW Brusilow The Journal of pediatrics 119 (6), 923-928, 1991 | 191 | 1991 |
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 | 187 | 2016 |
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 | 169 | 2009 |
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 | 169 | 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 | 169 | 2000 |
Dissecting the shared genetic architecture of suicide attempt, psychiatric disorders, and known risk factors N Mullins, JE Kang, AI Campos, JRI Coleman, AC Edwards, H Galfalvy, ... Biological psychiatry 91 (3), 313-327, 2022 | 158 | 2022 |
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 | 157 | 1990 |
Large-scale genome-wide association study of coronary artery disease in genetically diverse populations C Tcheandjieu, X Zhu, AT Hilliard, SL Clarke, V Napolioni, S Ma, KM Lee, ... Nature medicine 28 (8), 1679-1692, 2022 | 151 | 2022 |
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 | 151 | 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 | 149 | 1999 |