Michael A. Schmidt

2.4k total citations
37 papers, 1.2k citations indexed

About

Michael A. Schmidt is a scholar working on Molecular Biology, Genetics and Clinical Psychology. According to data from OpenAlex, Michael A. Schmidt has authored 37 papers receiving a total of 1.2k indexed citations (citations by other indexed papers that have themselves been cited), including 21 papers in Molecular Biology, 17 papers in Genetics and 5 papers in Clinical Psychology. Recurrent topics in Michael A. Schmidt's work include Epigenetics and DNA Methylation (13 papers), Genetic Associations and Epidemiology (9 papers) and Genetics and Neurodevelopmental Disorders (6 papers). Michael A. Schmidt is often cited by papers focused on Epigenetics and DNA Methylation (13 papers), Genetic Associations and Epidemiology (9 papers) and Genetics and Neurodevelopmental Disorders (6 papers). Michael A. Schmidt collaborates with scholars based in United States and Germany. Michael A. Schmidt's co-authors include Eden R. Martin, Virginia V. Michels, Gordon W. Dewald, Lissette Gomez, Juan I. Young, John M. Opitz, James F. Reynolds, John R. Gilbert, Michael L. Cuccaro and Ioanna Konidari and has published in prestigious journals such as Science, JAMA and Nature Communications.

In The Last Decade

Michael A. Schmidt

36 papers receiving 1.1k citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Michael A. Schmidt United States 18 519 487 266 149 84 37 1.2k
Jeff M. Milunsky United States 22 822 1.6× 704 1.4× 252 0.9× 85 0.6× 79 0.9× 70 1.7k
Deborah K. Sokol United States 19 431 0.8× 303 0.6× 374 1.4× 125 0.8× 174 2.1× 56 1.1k
Erwin Petek Austria 21 469 0.9× 669 1.4× 229 0.9× 77 0.5× 35 0.4× 60 1.5k
Josette Mancini France 19 454 0.9× 484 1.0× 305 1.1× 79 0.5× 224 2.7× 29 1.2k
Beth Wilmot United States 22 319 0.6× 711 1.5× 227 0.9× 153 1.0× 277 3.3× 70 2.0k
Kiran K. Mantripragada United Kingdom 22 853 1.6× 773 1.6× 274 1.0× 304 2.0× 241 2.9× 41 1.8k
Julie S. Cohen United States 22 578 1.1× 617 1.3× 76 0.3× 121 0.8× 176 2.1× 44 1.4k
Juliette Nectoux France 23 775 1.5× 602 1.2× 207 0.8× 60 0.4× 78 0.9× 58 1.3k
Xingchao Wang China 20 281 0.5× 623 1.3× 355 1.3× 168 1.1× 141 1.7× 55 1.8k
Elisabetta Bolognesi Italy 21 207 0.4× 257 0.5× 202 0.8× 88 0.6× 96 1.1× 50 973

Countries citing papers authored by Michael A. Schmidt

Since Specialization
Citations

This map shows the geographic impact of Michael A. Schmidt's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Michael A. Schmidt with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Michael A. Schmidt more than expected).

Fields of papers citing papers by Michael A. Schmidt

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Michael A. Schmidt. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Michael A. Schmidt. The network helps show where Michael A. Schmidt may publish in the future.

Co-authorship network of co-authors of Michael A. Schmidt

This figure shows the co-authorship network connecting the top 25 collaborators of Michael A. Schmidt. A scholar is included among the top collaborators of Michael A. Schmidt based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Michael A. Schmidt. Michael A. Schmidt is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Zhang, Wei, Juan I. Young, Lissette Gomez, et al.. (2025). Blood DNA methylation signature for incident dementia: Evidence from longitudinal cohorts. Alzheimer s & Dementia. 21(3). e14496–e14496. 3 indexed citations
2.
Zhang, Wei, David Lukacsovich, Juan I. Young, et al.. (2025). DNA methylation signature of a lifestyle-based resilience index for cognitive health. Alzheimer s Research & Therapy. 17(1). 88–88. 2 indexed citations
3.
Wang, Lily, Juan I. Young, Lissette Gomez, et al.. (2023). Distinct CSF biomarker‐associated DNA methylation in Alzheimer’s disease and cognitively normal subjects. Alzheimer s & Dementia. 19(S15). 2 indexed citations
4.
Silva, Tiago C., Juan I. Young, Lissette Gomez, et al.. (2022). Cross-tissue analysis of blood and brain epigenome-wide association studies in Alzheimer’s disease. Nature Communications. 13(1). 4852–4852. 23 indexed citations
5.
Silva, Tiago C., Juan I. Young, Lissette Gomez, et al.. (2022). Distinct sex-specific DNA methylation differences in Alzheimer’s disease. Alzheimer s Research & Therapy. 14(1). 133–133. 17 indexed citations
6.
Zhang, Lanyu, Juan I. Young, Lissette Gomez, et al.. (2021). Sex-specific DNA methylation differences in Alzheimer’s disease pathology. Acta Neuropathologica Communications. 9(1). 77–77. 35 indexed citations
7.
Kunkle, Brian W., Kara L. Hamilton‐Nelson, Michael A. Schmidt, et al.. (2021). APOE‐stratified genome‐wide association analysis identifies novel Alzheimer disease candidate risk loci for African Americans. Alzheimer s & Dementia. 17(S3). 3 indexed citations
8.
Zhang, Lanyu, Tiago C. Silva, Juan I. Young, et al.. (2020). Epigenome-wide meta-analysis of DNA methylation differences in prefrontal cortex implicates the immune processes in Alzheimer’s disease. Nature Communications. 11(1). 6114–6114. 87 indexed citations
9.
Hussman, John P., Ashley Beecham, Michael A. Schmidt, et al.. (2016). GWAS analysis implicates NF-κB-mediated induction of inflammatory T cells in multiple sclerosis. Genes and Immunity. 17(5). 305–312. 55 indexed citations
10.
Griswold, Anthony J., Nicole Dueker, Derek Van Booven, et al.. (2015). Targeted massively parallel sequencing of autism spectrum disorder-associated genes in a case control cohort reveals rare loss-of-function risk variants. Molecular Autism. 6(1). 43–43. 46 indexed citations
11.
Uzun, Ece D. Gamsiz, Emma Viscidi, A. Matsen Frederick, et al.. (2013). Intellectual Disability Is Associated with Increased Runs of Homozygosity in Simplex Autism. The American Journal of Human Genetics. 93(1). 103–109. 52 indexed citations
12.
Chung, Ren-Hua, Michael A. Schmidt, & Eden R. Martin. (2011). CAPL: an efficient association software package using family and case-control data and accounting for population stratification. BMC Bioinformatics. 12(1). 201–201. 4 indexed citations
13.
Martin, Eden R., Daniel D. Kinnamon, Michael A. Schmidt, et al.. (2010). SeqEM: an adaptive genotype-calling approach for next-generation sequencing studies. Bioinformatics. 26(22). 2803–2810. 49 indexed citations
14.
Chung, Ren‐Hua, Michael A. Schmidt, Richard Morris, & Eden R. Martin. (2010). CAPL: a novel association test using case‐control and family data and accounting for population stratification. Genetic Epidemiology. 34(7). 747–755. 13 indexed citations
15.
Schmidt, Silke, Michael A. Schmidt, Xuejun Qin, Eden R. Martin, & Elizabeth R. Hauser. (2007). Increased Efficiency of Case-Control Association Analysis by Using Allele-Sharing and Covariate Information. Human Heredity. 65(3). 154–165. 6 indexed citations
16.
Schmidt, Silke, Michael A. Schmidt, Xuejun Qin, Eden R. Martin, & Elizabeth R. Hauser. (2006). Linkage analysis with gene‐environment interaction: model illustration and performance of ordered subset analysis. Genetic Epidemiology. 30(5). 409–422. 7 indexed citations
17.
Shah, Svati H., Michael A. Schmidt, Hao Mei, et al.. (2005). Searching for epistatic interactions in nuclear families using conditional linkage analysis. BMC Genetics. 6(S1). S148–S148. 6 indexed citations
18.
Schmidt, Michael A., Anjan Chakrabarti, Claire S. Duvernoy, et al.. (2003). Interactive effects of the ACE DD polymorphism with the NOS III homozygous G849T (Glu298-Asp) variant in determining endothelial function in coronary artery disease. Journal of the American College of Cardiology. 41(6). 309–309. 1 indexed citations
19.
Schmidt, Michael A., et al.. (1989). Autosomal dominant supravalvular aortic stenosis: Large three‐generation family. American Journal of Medical Genetics. 32(3). 384–389. 20 indexed citations
20.
Schmidt, Michael A. & Warren G. Sanger. (1981). Sister chromatid exchange in aged human lymphocytes. A brief note. Mechanisms of Ageing and Development. 16(1). 67–70. 21 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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