Mike Schmidt

Research assistant professor

  • 721 Citations
20052020

Research output per year

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Research Output

  • 721 Citations
  • 20 Article
  • 1 Conference contribution
  • 1 Comment/debate
2020
1 Scopus citations

Whole exome sequencing study identifies novel rare and common Alzheimer’s-Associated variants involved in immune response and transcriptional regulation

Alzheimer’s Disease Sequencing Project, Aug 1 2020, In : Molecular psychiatry. 25, 8, p. 1859-1875 17 p.

Research output: Contribution to journalArticle

38 Scopus citations
2019

A rare missense variant of CASP7 is associated with familial late-onset Alzheimer's disease

Alzheimer's Disease Sequencing Project, Mar 2019, In : Alzheimer's and Dementia. 15, 3, p. 441-452 12 p.

Research output: Contribution to journalArticle

Open Access
5 Scopus citations

Quality control and integration of genotypes from two calling pipelines for whole genome sequence data in the Alzheimer's disease sequencing project

Alzheimer's Disease Sequencing Project (ADSP), Jul 2019, In : Genomics. 111, 4, p. 808-818 11 p.

Research output: Contribution to journalArticle

4 Scopus citations
2016

GWAS analysis implicates NF-κB-mediated induction of inflammatory T cells in multiple sclerosis

Hussman, J. P., Beecham, A. H., Schmidt, M., Martin, E. R., McCauley, J. L., Vance, J. M., Haines, J. L. & Pericak-Vance, M. A., Jun 9 2016, (Accepted/In press) In : Genes and Immunity.

Research output: Contribution to journalArticle

28 Scopus citations
2015

Targeted massively parallel sequencing of autism spectrum disorder-associated genes in a case control cohort reveals rare loss-of-function risk variants

Griswold, A., Dueker, N. D., Van Booven, D., Rantus, J. A., Jaworski, J. M., Slifer, S. H., Schmidt, M., Hulme, W., Konidari, I., Whitehead, P. L., Cuccaro, M., Martin, E. R., Haines, J. L., Gilbert, J., Hussman, J. P. & Pericak-Vance, M. A., Jul 7 2015, In : Molecular Autism. 6, 1, 43.

Research output: Contribution to journalArticle

26 Scopus citations
2014

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

Cukier, H. N., Dueker, N. D., Slifer, S. H., Lee, J. M., Whitehead, P. L., Lalanne, E., Leyva, N., Konidari, I., Gentry, R. C., Hulme, W. F., Booven, D. V., Mayo, V., Hofmann, N. K., Schmidt, M. A., Martin, E. R., Haines, J. L., Cuccaro, M. L., Gilbert, J. R. & Pericak-Vance, M. A., Jan 10 2014, In : Molecular Autism. 5, 1, 1.

Research output: Contribution to journalArticle

103 Scopus citations
2013

Evaluating Mitochondrial DNA Variation in Autism Spectrum Disorders

Hadjixenofontos, A., Schmidt, M. A., Whitehead, P. L., Konidari, I., Hedges, D. J., Wright, H. H., Abramson, R. K., Menon, R., Williams, S. M., Cuccaro, M. L., Haines, J. L., Gilbert, J. R., Pericak-Vance, M. A., Martin, E. R. & McCauley, J. L., Jan 2013, In : Annals of Human Genetics. 77, 1, p. 9-21 13 p.

Research output: Contribution to journalArticle

20 Scopus citations

Pathway-PDT: A flexible pathway analysis tool for nuclear families

Park, Y. S., Schmidt, M., Martin, E. R., Pericak-Vance, M. A. & Chung, R. H., Sep 4 2013, In : BMC Bioinformatics. 14, 1, 267.

Research output: Contribution to journalArticle

8 Scopus citations
2012

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

Griswold, A. J., Ma, D., Cukier, H. N., Nations, L. D., Schmidt, M. A., Chung, R. H., Jaworski, J. M., Salyakina, D., Konidari, I., Whitehead, P. L., Wright, H. H., Abramson, R. K., Williams, S. M., Menon, R., Martin, E. R., Haines, J. L., Gilbert, J. R., Cuccaro, M. L. & Pericak-Vance, M. A., Aug 2012, In : Human molecular genetics. 21, 15, p. 3513-3523 11 p., dds164.

Research output: Contribution to journalArticle

111 Scopus citations
2011
2 Scopus citations
2010

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

Chung, R. H., Schmidt, M. A., Morris, R. W. & Martin, E. R., Nov 1 2010, In : Genetic Epidemiology. 34, 7, p. 747-755 9 p.

Research output: Contribution to journalArticle

15 Scopus citations

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

Martin, E. R., Kinnamon, D. D., Schmidt, M. A., Powell, E. H., Zuchner, S. & Morris, R. W., Nov 2010, In : Bioinformatics. 26, 22, p. 2803-2810 8 p., btq526.

Research output: Contribution to journalArticle

50 Scopus citations
2009

Exome sequencing of a multigenerational human pedigree

Hedges, D., Burges, D., Powell, E., Almonte, C., Huang, J., Young, S., Boese, B., Schmidt, M., Pericak-Vance, M. A., Martin, E., Zhang, X., Harkins, T. T. & Züchner, S., 2009, In : PloS one. 4, 12, e8232.

Research output: Contribution to journalArticle

64 Scopus citations
2008

Generating linkage disequilibrium patterns in data simulations using genomeSIMLA

Edwards, T. L., Bush, W. S., Turner, S. D., Dudek, S. M., Torstenson, E. S., Schmidt, M., Martin, E. & Ritchie, M. D., Jul 21 2008, Evolutionary Computation, Machine Learning and Data Mining in Bioinformatics - 6th European Conference, EvoBIO 2008, Proceedings. p. 24-35 12 p. (Lecture Notes in Computer Science (including subseries Lecture Notes in Artificial Intelligence and Lecture Notes in Bioinformatics); vol. 4973 LNCS).

Research output: Chapter in Book/Report/Conference proceedingConference contribution

39 Scopus citations

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

Martin, E. R. & Schmidt, M. A., Mar 1 2008, In : Human Heredity. 66, 2, p. 127-135 9 p.

Research output: Contribution to journalArticle

2007

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

Schmidt, S., Schmidt, M. A., Qin, X., Martin, E. R. & Hauser, E. R., Dec 1 2007, In : Human Heredity. 65, 3, p. 154-165 12 p.

Research output: Contribution to journalArticle

4 Scopus citations

Interpreting analyses of continuous covariates in affected sibling pair linkage studies

Schmidt, S., Qin, X., Schmidt, M. A., Martin, E. R. & Hauser, E. R., Sep 1 2007, In : Genetic Epidemiology. 31, 6, p. 541-552 12 p.

Research output: Contribution to journalArticle

6 Scopus citations
2006

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

Schmidt, S., Schmidt, M. A., Qin, X., Martin, E. R. & Hauser, E. R., Jul 1 2006, In : Genetic Epidemiology. 30, 5, p. 409-422 14 p.

Research output: Contribution to journalArticle

5 Scopus citations
2005
37 Scopus citations

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

Boyles, A. L., Scott, W. K., Martin, E. R., Schmidt, S., Li, Y. J., Ashley-Koch, A., Bass, M. P., Schmidt, M., Pericak-Vance, M. A., Speer, M. C. & Hauser, E. R., Aug 1 2005, In : Human Heredity. 59, 4, p. 220-227 8 p.

Research output: Contribution to journalArticle

67 Scopus citations

Searching for epistatic interactions in nuclear families using conditional linkage analysis

Shah, S. H., Schmidt, M. A., Mei, H., Scott, W. K., Hauser, E. R. & Schmidt, S., Dec 30 2005, In : BMC genetics. 6, SUPPL.1, S148.

Research output: Contribution to journalArticle

5 Scopus citations