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238 results

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Page 1
A genomewide scan for early-onset coronary artery disease in 438 families: the GENECARD Study.
Hauser ER, Crossman DC, Granger CB, Haines JL, Jones CJ, Mooser V, McAdam B, Winkelmann BR, Wiseman AH, Muhlestein JB, Bartel AG, Dennis CA, Dowdy E, Estabrooks S, Eggleston K, Francis S, Roche K, Clevenger PW, Huang L, Pedersen B, Shah S, Schmidt S, Haynes C, West S, Asper D, Booze M, Sharma S, Sundseth S, Middleton L, Roses AD, Hauser MA, Vance JM, Pericak-Vance MA, Kraus WE. Hauser ER, et al. Among authors: hauser ma. Am J Hum Genet. 2004 Sep;75(3):436-47. doi: 10.1086/423900. Epub 2004 Jul 22. Am J Hum Genet. 2004. PMID: 15272420 Free PMC article.
BRCA1 maps proximal to D17S579 on chromosome 17q21 by genetic analysis.
Chamberlain JS, Boehnke M, Frank TS, Kiousis S, Xu J, Guo SW, Hauser ER, Norum RA, Helmbold EA, Markel DS, et al. Chamberlain JS, et al. Among authors: hauser er. Am J Hum Genet. 1993 Apr;52(4):792-8. Am J Hum Genet. 1993. PMID: 8460646 Free PMC article.
Complete genomic screen for disease susceptibility loci in nuclear families.
Anderson JL, Hauser ER, Martin ER, Scott WK, Ashley-Koch A, Kim KJ, Monks SA, Haynes CS, Speer MC, Pericak-Vance MA. Anderson JL, et al. Among authors: hauser er. Genet Epidemiol. 1999;17 Suppl 1:S473-8. doi: 10.1002/gepi.1370170776. Genet Epidemiol. 1999. PMID: 10597478
Genetic studies in autistic disorder and chromosome 15.
Bass MP, Menold MM, Wolpert CM, Donnelly SL, Ravan SA, Hauser ER, Maddox LO, Vance JM, Abramson RK, Wright HH, Gilbert JR, Cuccaro ML, DeLong GR, Pericak-Vance MA. Bass MP, et al. Among authors: hauser er. Neurogenetics. 2000 Mar;2(4):219-26. doi: 10.1007/s100489900081. Neurogenetics. 2000. PMID: 10983717
Genetic analysis for common complex disease.
Hauser ER, Pericak-Vance MA. Hauser ER, et al. Am Heart J. 2000 Oct;140(4):S36-44. doi: 10.1067/mhj.2000.108946. Am Heart J. 2000. PMID: 11011322 Review. No abstract available.
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.
Ghosh S, Watanabe RM, Valle TT, Hauser ER, Magnuson VL, Langefeld CD, Ally DS, Mohlke KL, Silander K, Kohtamäki K, Chines P, Balow J Jr, Birznieks G, Chang J, Eldridge W, Erdos MR, Karanjawala ZE, Knapp JI, Kudelko K, Martin C, Morales-Mena A, Musick A, Musick T, Pfahl C, Porter R, Rayman JB. Ghosh S, et al. Among authors: hauser er. Am J Hum Genet. 2000 Nov;67(5):1174-85. Epub 2000 Oct 13. Am J Hum Genet. 2000. PMID: 11032783 Free PMC article.
The Finland-United States investigation of non-insulin-dependent diabetes mellitus genetics (FUSION) study. II. An autosomal genome scan for diabetes-related quantitative-trait loci.
Watanabe RM, Ghosh S, Langefeld CD, Valle TT, Hauser ER, Magnuson VL, Mohlke KL, Silander K, Ally DS, Chines P, Blaschak-Harvan J, Douglas JA, Duren WL, Epstein MP, Fingerlin TE, Kaleta HS, Lange EM, Li C, McEachin RC, Stringham HM, Trager E, White PP, Balow J Jr, Birznieks G, Chang J, Eldridge W. Watanabe RM, et al. Among authors: hauser er. Am J Hum Genet. 2000 Nov;67(5):1186-200. Epub 2000 Oct 13. Am J Hum Genet. 2000. PMID: 11032784 Free PMC article.
Life after the screen: making sense of many P-values.
Schmidt S, Shao Y, Hauser ER, Slifer SH, Martin ER, Scott WK, Speer MC, Pericak-Vance MA. Schmidt S, et al. Among authors: hauser er. Genet Epidemiol. 2001;21 Suppl 1:S546-51. doi: 10.1002/gepi.2001.21.s1.s546. Genet Epidemiol. 2001. PMID: 11793734
Fine mapping of autistic disorder to chromosome 15q11-q13 by use of phenotypic subtypes.
Shao Y, Cuccaro ML, Hauser ER, Raiford KL, Menold MM, Wolpert CM, Ravan SA, Elston L, Decena K, Donnelly SL, Abramson RK, Wright HH, DeLong GR, Gilbert JR, Pericak-Vance MA. Shao Y, et al. Among authors: hauser er. Am J Hum Genet. 2003 Mar;72(3):539-48. doi: 10.1086/367846. Epub 2003 Feb 3. Am J Hum Genet. 2003. PMID: 12567325 Free PMC article.
238 results