Michael A. Schmidt - Concepedia

Author

Michael A. Schmidt

Also Known As

Helena Schmidt, Kara Hamilton-Nelson, M Schmidt, M. A. Schmidt, M. Schmidt, Michael A Schmidt, Michael A. Schmidt, Michael Schmidt, Schmidt, M., Schmidt, Michael A.

Publications

2.3K

Citations

H-Index

Concepts

All Affiliations

University of Miami Dr. John T. Macdonald Foundation Case Western Reserve University Center for Human Genetics Vanderbilt University

About

Michael A. Schmidt is an author at University of Miami specializing in medicine, public health, and genetic epidemiology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	8	8	460
2	Public Health	5	5	276
3	Health Sciences	1	1	22
4	Allergy	1	1	74
5	Biology	1	1	44

Michael A. Schmidt

Publications

1.6K

Citations

H-Index

Page 1

	Year	Citations
Exome sequencing of extended families with autism reveals genes shared across neurodevelopmental and neuropsychiatric disorders Holly N. Cukier, Nicole Dueker, Susan H. Slifer, Molecular Autism	2014	328
Whole exome sequencing study identifies novel rare and common Alzheimer’s-Associated variants involved in immune response and transcriptional regulation Joshua C. Bis, Xueqiu Jian, Brian W. Kunkle, Molecular Psychiatry	2018	257
Physical Mapping of a Translocation Breakpoint in Neurofibromatosis Jane W. Fountain, Margaret R. Wallace, M BRUCE, Science	1989	141
Fragile X Syndrome: Diagnosis, Treatment, and Research Michael A. Schmidt JAMA GeneticsGenetic EpidemiologyWright BrothersGenetic MedicineClinical Genetics	1997	96
Cases of neurofibromatosis with rearrangements of chromosome 17 involving band 17q11.2 Michael A. Schmidt, Virginia V. Michels, Gordon W. Dewald, American Journal of Medical Genetics Recklinghausen NeurofibromatosisMendelian DisorderCytogeneticsNeurofibromatosis GeneGenetics	1987	88
Intellectual Disability Is Associated with Increased Runs of Homozygosity in Simplex Autism Ece D. Gamsiz Uzun, Emma Viscidi, A. Matsen Frederick, The American Journal of Human Genetics	2013	88
Linkage Disequilibrium Inflates Type I Error Rates in Multipoint Linkage Analysis when Parental Genotypes Are Missing Abee L. Boyles, William K. Scott, Eden R. Martin, Human Heredity	2005	82
SeqEM: an adaptive genotype-calling approach for next-generation sequencing studies Eden R. Martin, Daniel D. Kinnamon, Michael A. Schmidt, Bioinformatics	2010	76
GWAS analysis implicates NF-κB-mediated induction of inflammatory T cells in multiple sclerosis John P. Hussman, Ashley Beecham, Michael A. Schmidt, Genes and Immunity ImmunologyImmune RegulationGenetic EpidemiologyPathologyMultiomics	2016	74
Targeted massively parallel sequencing of autism spectrum disorder-associated genes in a case control cohort reveals rare loss-of-function risk variants Anthony J. Griswold, Nicole Dueker, Derek Van Booven, Molecular Autism	2015	68

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