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Mike Schmidt

Research Profile

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Publications

TOP 3
Anthony J Griswold; Jonathan L Haines; James M Jaworski; Ioanna Konidari; Deqiong Ma; Eden R Martin; Ramkumar Menon; Laura D Nations; Ruth K Abramson; Ren-Hua Chung; Michael Cuccaro; Holly N Cukier; John Gilbert; Daria Salyakina; Mike Schmidt; Patrice L Whitehead; Scott M Williams; Harry H Wright; Margaret Pericak-Vance
Evaluation of copy number variations reveals novel candidate genes in autism spectrum disorder-associated pathways.
Ren-Hua Chung; Mike Schmidt; Eden R Martin
CAPL: an efficient association software package using family and case-control data and accounting for population stratification.
Eden R Martin; D D Kinnamon; Mike Schmidt; Eric Halsey Powell; Stephan Zuchner; R W Morris
SeqEM: an adaptive genotype-calling approach for next-generation sequencing studies.

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All Publications

2012: Anthony J Griswold; Jonathan L Haines; James M Jaworski; Ioanna Konidari; Deqiong Ma; Eden R Martin; Ramkumar Menon; Laura D Nations; Ruth K Abramson; Ren-Hua Chung; Michael Cuccaro; Holly N Cukier; John Gilbert; Daria Salyakina; Mike Schmidt; Patrice L Whitehead; Scott M Williams; Harry H Wright; Margaret Pericak-Vance
Evaluation of copy number variations reveals novel candidate genes in autism spectrum disorder-associated pathways.
Human molecular genetics 2012;21(15):3513-23.
2011: Ren-Hua Chung; Mike Schmidt; Eden R Martin
CAPL: an efficient association software package using family and case-control data and accounting for population stratification.
BMC bioinformatics 2011;12():201.
2010: Eden R Martin; D D Kinnamon; Mike Schmidt; Eric Halsey Powell; Stephan Zuchner; R W Morris
SeqEM: an adaptive genotype-calling approach for next-generation sequencing studies.
Bioinformatics (Oxford, England) 2010;26(22):2803-10.
2010: Ren-Hua Chung; Mike Schmidt; Richard W Morris; Eden R Martin
CAPL: a novel association test using case-control and family data and accounting for population stratification.
Genetic epidemiology 2010;34(7):747-55.
2009: Dale J Hedges; Dale Hedges; Dan Burges; Eric Powell; Cherylyn Almonte; Jia Huang; Stuart Young; Benjamin Boese; Mike Schmidt; Margaret Pericak-Vance; Eden R Martin; Xinmin Zhang; Timothy T Harkins; Stephan Zuchner
Exome sequencing of a multigenerational human pedigree.
PloS one 2009;4(12):e8232.
2009: Ellen L Goode; Csilla Szabo; Ludmila Prokunina-Olsson; Robert A Vierkant; Zachary S Fredericksen; Francis S Collins; Kristin L White; Mike Schmidt; Brooke L Fridley; Fergus J Couch
No association between a candidate TCF7L2 variant and risk of breast or ovarian cancer.
BMC cancer 2009;9():312.
2008: Eden R Martin; Mike Schmidt
The future is now - will the real disease gene please stand up?
Human heredity 2008;66(2):127-35.
2008: Silke Schmidt; Mike Schmidt; Xuejun Qin; Eden R Martin; Elizabeth R Hauser
Increased efficiency of case-control association analysis by using allele-sharing and covariate information.
Human heredity 2008;65(3):154-65.
2007: Silke Schmidt; Xuejun Qin; Mike Schmidt; Eden R Martin; Elizabeth R Hauser
Interpreting analyses of continuous covariates in affected sibling pair linkage studies.
Genetic epidemiology 2007;31(6):541-52.
2007: Mike Schmidt; Xuejun Qin; Eden R Martin; Elizabeth R Hauser; Silke Schmidt
Two-stage study designs for analyzing disease-associated covariates: linkage thresholds and case-selection strategies.
BMC proceedings 2007;1 Suppl 1():S138.
2006: Silke Schmidt; Mike Schmidt; Xuejun Qin; Eden R Martin; Elizabeth R Hauser
Linkage analysis with gene-environment interaction: model illustration and performance of ordered subset analysis.
Genetic epidemiology 2006;30(5):409-22.
2005: Mike Schmidt; Elizabeth R Hauser; Eden R Martin; Silke Schmidt
Extension of the SIMLA package for generating pedigrees with complex inheritance patterns: environmental covariates, gene-gene and gene-environment interaction.
Statistical applications in genetics and molecular biology 2005;4():Article15.
2005: Svati H Shah; Mike Schmidt; Hao Mei; William Scott; Elizabeth R Hauser; Silke Schmidt
Searching for epistatic interactions in nuclear families using conditional linkage analysis.
BMC genetics 2005;6 Suppl 1():S148.
2005: Abee L Boyles; William Scott; Eden R Martin; Silke Schmidt; Yi-Ju Li; Allison Ashley-Koch; Meredyth P Bass; Mike Schmidt; Margaret Pericak-Vance; Marcy C Speer; Elizabeth R Hauser
Linkage disequilibrium inflates type I error rates in multipoint linkage analysis when parental genotypes are missing.
Human heredity 2005;59(4):220-7.