Mike Schmidt

Research assistant professor

  • 565 Citations
20052019
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Research Output 2005 2019

  • 565 Citations
  • 20 Article
  • 1 Conference contribution
  • 1 Comment/debate
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Article
2019
3 Citations (Scopus)

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

Alzheimer's Disease Sequencing Project, Mar 1 2019, In : Alzheimer's and Dementia. 15, 3, p. 441-452 12 p.

Research output: Contribution to journalArticle

Open Access
Alzheimer Disease
Hispanic Americans
Genome-Wide Association Study
Case-Control Studies
Alzheimer disease type 2
2018
1 Citation (Scopus)

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), Jan 1 2018, (Accepted/In press) In : Genomics.

Research output: Contribution to journalArticle

Quality Control
Alzheimer Disease
Genotype
Genome
Atlases
17 Citations (Scopus)

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, Jan 1 2018, (Accepted/In press) In : Molecular Psychiatry.

Research output: Contribution to journalArticle

Exome
Alzheimer Disease
Hispanic Americans
Genes
Long Noncoding RNA
2016
21 Citations (Scopus)

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

Genome-Wide Association Study
Multiple Sclerosis
T-Lymphocytes
Genes
Noise
2015
20 Citations (Scopus)

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

High-Throughput Nucleotide Sequencing
Genes
Genome-Wide Association Study
Autism Spectrum Disorder
Mutation
2014
93 Citations (Scopus)

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., Martin, E. R., Haines, J. L., Cuccaro, M., Gilbert, J. & Pericak-Vance, M. A., Jan 10 2014, In : Molecular Autism. 5, 1, 1.

Research output: Contribution to journalArticle

Exome
Autistic Disorder
Genes
Neurodevelopmental Disorders
Autism Spectrum Disorder
2013
18 Citations (Scopus)

Evaluating Mitochondrial DNA Variation in Autism Spectrum Disorders

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

Research output: Contribution to journalArticle

Mitochondrial DNA
Autistic Disorder
Autism Spectrum Disorder
Genome-Wide Association Study
Fathers
7 Citations (Scopus)

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

Pedigree
Nuclear Family
Pathway
Genes
Genome-Wide Association Study
2012
95 Citations (Scopus)

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

Griswold, A., Ma, D., Cukier, H. N., Nations, L. D., Schmidt, M., 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., Cuccaro, M. & Pericak-Vance, M. A., Aug 1 2012, In : Human Molecular Genetics. 21, 15, p. 3513-3523 11 p., dds164.

Research output: Contribution to journalArticle

GABA Receptors
Genes
GABA Plasma Membrane Transport Proteins
Neural Pathways
Genetic Loci
2011
1 Citation (Scopus)
Case-control Data
Stratification
Software Package
Software packages
Genome
2010
15 Citations (Scopus)

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

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

Research output: Contribution to journalArticle

Population
Sample Size
Siblings
Genotype
Genome-Wide Association Study
50 Citations (Scopus)

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

Martin, E. R., Kinnamon, D. D., Schmidt, M., Powell, E. H., Zuchner, S. L. & Morris, R. W., Nov 1 2010, In : Bioinformatics. 26, 22, p. 2803-2810 8 p., btq526.

Research output: Contribution to journalArticle

Genotype
Sequencing
Nucleotides
Classifiers
Error Rate
2009
63 Citations (Scopus)

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. R., Zhang, X., Harkins, T. T. & Zuchner, S. L., Dec 1 2009, In : PLoS One. 4, 12, e8232.

Research output: Contribution to journalArticle

Exome
Pedigree
pedigree
Genotype
genotype
2008

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

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

Research output: Contribution to journalArticle

Genes
Pedigree
Alleles
Genome
Viverridae
2007
4 Citations (Scopus)

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

Schmidt, S., Schmidt, M., 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

Information Dissemination
Quantitative Trait Loci
Alleles
Gene-Environment Interaction
Case-Control Studies
6 Citations (Scopus)

Interpreting analyses of continuous covariates in affected sibling pair linkage studies

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

Research output: Contribution to journalArticle

Quantitative Trait Loci
Disease Susceptibility
Lod Score
Macular Degeneration
Genes
2006
5 Citations (Scopus)

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

Schmidt, S., Schmidt, M., 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

Gene-Environment Interaction
Genotype
Lod Score
Genetic Heterogeneity
Genetic Models
2005
37 Citations (Scopus)
Gene-environment Interaction
Inheritance Patterns
Gene-Environment Interaction
Pedigree
Linkage
66 Citations (Scopus)

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

Linkage Disequilibrium
Genotype
Economic Inflation
Gene Frequency
Haplotypes
5 Citations (Scopus)

Searching for epistatic interactions in nuclear families using conditional linkage analysis

Shah, S. H., Schmidt, M., 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

Nuclear Family
Chromosomes
Single Nucleotide Polymorphism
Siblings
Education