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153 results

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Page 1
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: speer mc. Genet Epidemiol. 2001;21 Suppl 1:S546-51. doi: 10.1002/gepi.2001.21.s1.s546. Genet Epidemiol. 2001. PMID: 11793734
False positive rates in a genomic screen for complex quantitative traits.
Scott WK, Speer MC, Leal SM, Brzustowicz LM, Haynes CS, Pericak-Vance MA. Scott WK, et al. Among authors: speer mc. Genet Epidemiol. 1997;14(6):891-6. doi: 10.1002/(SICI)1098-2272(1997)14:6<891::AID-GEPI55>3.0.CO;2-H. Genet Epidemiol. 1997. PMID: 9433596 Free PMC article. Clinical Trial.
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: speer mc. Genet Epidemiol. 1999;17 Suppl 1:S473-8. doi: 10.1002/gepi.1370170776. Genet Epidemiol. 1999. PMID: 10597478
Mapping strategies for multiple linked markers.
Speer MC, Sherman SL, Haynes CS, Pericak-Vance MA. Speer MC, et al. Prog Clin Biol Res. 1989;329:75-80. Prog Clin Biol Res. 1989. PMID: 2622966 No abstract available.
High-density single nucleotide polymorphism screen in a large multiplex neural tube defect family refines linkage to loci at 7p21.1-pter and 2q33.1-q35.
Stamm DS, Rampersaud E, Slifer SH, Mehltretter L, Siegel DG, Xie J, Hu-Lince D, Craig DW, Stephan DA, George TM, Gilbert JR, Speer MC; NTD Collaborative Group. Stamm DS, et al. Among authors: speer mc. Birth Defects Res A Clin Mol Teratol. 2006 Jun;76(6):499-505. doi: 10.1002/bdra.20272. Birth Defects Res A Clin Mol Teratol. 2006. PMID: 16933213 Free PMC article.
Phenotypic definition of Chiari type I malformation coupled with high-density SNP genome screen shows significant evidence for linkage to regions on chromosomes 9 and 15.
Boyles AL, Enterline DS, Hammock PH, Siegel DG, Slifer SH, Mehltretter L, Gilbert JR, Hu-Lince D, Stephan D, Batzdorf U, Benzel E, Ellenbogen R, Green BA, Kula R, Menezes A, Mueller D, Oro' JJ, Iskandar BJ, George TM, Milhorat TH, Speer MC. Boyles AL, et al. Among authors: speer mc. Am J Med Genet A. 2006 Dec 15;140(24):2776-85. doi: 10.1002/ajmg.a.31546. Am J Med Genet A. 2006. PMID: 17103432
Linkage analysis in familial amyotrophic lateral sclerosis.
Siddique T, Pericak-Vance MA, Brooks BR, Roos RP, Hung WY, Antel JP, Munsat TL, Phillips K, Warner K, Speer M, et al. Siddique T, et al. Neurology. 1989 Jul;39(7):919-25. doi: 10.1212/wnl.39.7.919. Neurology. 1989. PMID: 2739919
153 results