Schmidt M - Search Results

1

Human whole-exome genotype data for Alzheimer's disease.

Leung YY, Naj AC, Chou YF, Valladares O, Schmidt M, Hamilton-Nelson K, Wheeler N, Lin H, Gangadharan P, Qu L, Clark K, Kuzma AB, Lee WP, Cantwell L, Nicaretta H; Alzheimer’s Disease Sequencing Project; Haines J, Farrer L, Seshadri S, Brkanac Z, Cruchaga C, Pericak-Vance M, Mayeux RP, Bush WS, Destefano A, Martin E, Schellenberg GD, Wang LS. Leung YY, et al. Among authors: schmidt m. Nat Commun. 2024 Jan 23;15(1):684. doi: 10.1038/s41467-024-44781-7. Nat Commun. 2024. PMID: 38263370 Free PMC article.

2

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. Among authors: schmidt s. 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.

3

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. Hum Hered. 2008;65(3):154-65. doi: 10.1159/000109732. Epub 2007 Oct 12. Hum Hered. 2008. PMID: 17934318 Free PMC article.

4

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.

5

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. Among authors: schmidt s. 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.

6

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.

7

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.

8

CAPL: a novel association test using case-control and family data and accounting for population stratification.

Chung RH, Schmidt MA, Morris RW, Martin ER. Chung RH, et al. Genet Epidemiol. 2010 Nov;34(7):747-55. doi: 10.1002/gepi.20539. Genet Epidemiol. 2010. PMID: 20878716

9

CAPL: an efficient association software package using family and case-control data and accounting for population stratification.

Chung RH, Schmidt MA, Martin ER. Chung RH, et al. BMC Bioinformatics. 2011 May 25;12:201. doi: 10.1186/1471-2105-12-201. BMC Bioinformatics. 2011. PMID: 21612626 Free PMC article.

10

Evaluation of copy number variations reveals novel candidate genes in autism spectrum disorder-associated pathways.

Griswold AJ, Ma D, Cukier HN, Nations LD, Schmidt MA, Chung RH, Jaworski JM, Salyakina D, Konidari I, Whitehead PL, Wright HH, Abramson RK, Williams SM, Menon R, Martin ER, Haines JL, Gilbert JR, Cuccaro ML, Pericak-Vance MA. Griswold AJ, et al. Among authors: schmidt ma. Hum Mol Genet. 2012 Aug 1;21(15):3513-23. doi: 10.1093/hmg/dds164. Epub 2012 Apr 27. Hum Mol Genet. 2012. PMID: 22543975 Free PMC article.

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