Author

Mark A. Reimers

Michigan State UniversityORCID 0000-0001-9023-2785Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetic & Genomic Medicine· 1 Genetics· 1 Neuroscience· 1

Signature Assays, Organisms & Methods

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Approach:statistical model· 3 Organism:human· 2 Research Focus:cell type annotation· 1 Research Focus:differential expression· 1 Research Focus:gene regulatory network inference· 1 Assay:GWAS summary statistics· 1 Organism:rat· 1 Assay:spatial transcriptomics· 1

Frequent Co-Authors

Aarno V. PalotieiD· 1 shared Aaron R. WoleniD· 1 shared Abraham ReichenbergiD· 1 shared Alexander L. RichardsiD· 1 shared Andrew J. ChessiD· 1 shared Andrew J. PocklingtoniD· 1 shared Aniket ShettyiD· 1 shared Anirban ChakrabortyiD· 1 shared

Activity by Year

2023-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 36 mutual co-author links

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1 shared paperGenetic & Genomic Medicine

Aarno V. PalotieORCID

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3 papers

Recent·Most cited

NeurosciencebioRxivPreprintMar 16, 2026

A systematic analysis of brain tissue response to microelectrode material and size with single-cell spatial transcriptomics

Cort H. Thompson, Anirban Chakraborty, Lauren C. Wade-Kleyn…·Erin K. Purcell

This study uses single-cell spatial transcriptomics to analyze the brain's response to different microelectrode materials and sizes in rats, finding that electrode dimensions have a greater impact on tissue response than material type.

2 citations

ratspatial transcriptomics

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GeneticsPLoS ONEPeer-reviewedMay 16, 2024

Functional classes of SNPs related to psychiatric disorders and behavioral traits contrast with those related to neurological disorders

Mark A. Reimers, Kenneth S. Kendler

The paper identifies distinct functional SNP classes associated with psychiatric disorders, behavioral traits, and neurological disorders, highlighting differences in genomic regions involved.

3 citations

humanGWAS summary statistics

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Genetic & Genomic MedicineCell GenomicsPeer-reviewedJul 6, 2023

Schizophrenia-associated somatic copy number variants from 12,834 cases reveal contribution to risk and recurrent, isoform-specific NRXN1 disruptions

Eduardo A. Maury, Maxwell A. Sherman, Giulio Genovese…·Brandon K. Wormley

This study identifies somatic copy number variants (sCNVs) in schizophrenia cases, revealing their contribution to risk and specific NRXN1 disruptions.

47 citationstop 2%

humanwhole-genome sequencing

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