| 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 | 445 | 2003 |
| 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 | 427 | 2010 |
| 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 | 303 | 2000 |
| 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 | 287 | 2012 |
| 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 | 278 | 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 | 247 | 1996 |
| 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 | 194 | 2004 |
| 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 | 189 | 2004 |
| 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 | 184 | 1990 |
| Prospective treatment of urea cycle disorders NE Maestri, ER Hauser, D Bartholomew, SW Brusilow The Journal of pediatrics 119 (6), 923-928, 1991 | 177 | 1991 |
| 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 | 161 | 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 | 160 | 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 | 152 | 2003 |
| 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 | 144 | 1999 |
| 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 | 144 | 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 | 143 | 1997 |
| 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 | 139 | 2016 |
| 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 | 134 | 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 | 132 | 2003 |
| 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 | 126 | 2003 |
