Schmidt MA - Search Results

1

Exome sequencing of extended families with autism reveals genes shared across neurodevelopmental and neuropsychiatric disorders.

Cukier HN, Dueker ND, Slifer SH, Lee JM, Whitehead PL, Lalanne E, Leyva N, Konidari I, Gentry RC, Hulme WF, Booven DV, Mayo V, Hofmann NK, Schmidt MA, Martin ER, Haines JL, Cuccaro ML, Gilbert JR, Pericak-Vance MA. Cukier HN, et al. Among authors: schmidt ma. Mol Autism. 2014 Jan 10;5(1):1. doi: 10.1186/2040-2392-5-1. Mol Autism. 2014. PMID: 24410847 Free PMC article.

2

Linkage disequilibrium inflates type I error rates in multipoint linkage analysis when parental genotypes are missing.

Boyles AL, Scott WK, Martin ER, Schmidt S, Li YJ, Ashley-Koch A, Bass MP, Schmidt M, Pericak-Vance MA, Speer MC, Hauser ER. Boyles AL, et al. Among authors: schmidt m, schmidt s. Hum Hered. 2005;59(4):220-7. doi: 10.1159/000087122. Epub 2005 Jul 26. Hum Hered. 2005. PMID: 16093727 Free PMC article.

3

Extension of the SIMLA package for generating pedigrees with complex inheritance patterns: environmental covariates, gene-gene and gene-environment interaction.

Schmidt M, Hauser ER, Martin ER, Schmidt S. Schmidt M, et al. Stat Appl Genet Mol Biol. 2005;4:Article15. doi: 10.2202/1544-6115.1133. Epub 2005 Jun 6. Stat Appl Genet Mol Biol. 2005. PMID: 16646832 Free PMC article.

4

Linkage analysis with gene-environment interaction: model illustration and performance of ordered subset analysis.

Schmidt S, Schmidt MA, Qin X, Martin ER, Hauser ER. Schmidt S, et al. Among authors: schmidt ma. Genet Epidemiol. 2006 Jul;30(5):409-22. doi: 10.1002/gepi.20152. Genet Epidemiol. 2006. PMID: 16671105

5

Interpreting analyses of continuous covariates in affected sibling pair linkage studies.

Schmidt S, Qin X, Schmidt MA, Martin ER, Hauser ER. Schmidt S, et al. Among authors: schmidt ma. Genet Epidemiol. 2007 Sep;31(6):541-52. doi: 10.1002/gepi.20227. Genet Epidemiol. 2007. PMID: 17410529

6

Increased efficiency of case-control association analysis by using allele-sharing and covariate information.

Schmidt S, Schmidt MA, Qin X, Martin ER, Hauser ER. Schmidt S, et al. Among authors: schmidt ma. Hum Hered. 2008;65(3):154-65. doi: 10.1159/000109732. Epub 2007 Oct 12. Hum Hered. 2008. PMID: 17934318 Free PMC article.

7

The future is now - will the real disease gene please stand up?

Martin ER, Schmidt MA. Martin ER, et al. Among authors: schmidt ma. Hum Hered. 2008;66(2):127-35. doi: 10.1159/000119112. Epub 2008 Mar 31. Hum Hered. 2008. PMID: 18382092 Free PMC article.

8

Two-stage study designs for analyzing disease-associated covariates: linkage thresholds and case-selection strategies.

Schmidt M, Qin X, Martin ER, Hauser ER, Schmidt S. Schmidt M, et al. BMC Proc. 2007;1 Suppl 1(Suppl 1):S138. doi: 10.1186/1753-6561-1-s1-s138. Epub 2007 Dec 18. BMC Proc. 2007. PMID: 18466481 Free PMC article.

9

Exome sequencing of a multigenerational human pedigree.

Hedges DJ, Burges D, Powell E, Almonte C, Huang J, Young S, Boese B, Schmidt M, Pericak-Vance MA, Martin E, Zhang X, Harkins TT, Züchner S. Hedges DJ, et al. Among authors: schmidt m. PLoS One. 2009 Dec 14;4(12):e8232. doi: 10.1371/journal.pone.0008232. PLoS One. 2009. PMID: 20011588 Free PMC article.

10

SeqEM: an adaptive genotype-calling approach for next-generation sequencing studies.

Martin ER, Kinnamon DD, Schmidt MA, Powell EH, Zuchner S, Morris RW. Martin ER, et al. Among authors: schmidt ma. Bioinformatics. 2010 Nov 15;26(22):2803-10. doi: 10.1093/bioinformatics/btq526. Epub 2010 Sep 21. Bioinformatics. 2010. PMID: 20861027 Free PMC article.

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