Author

Madison Hincher

Harvard University

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

Biology Disciplines

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Genetic & Genomic Medicine· 1 Genetics· 1

Signature Assays, Organisms & Methods

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Organism:human· 2 Assay:bulk RNA-seq· 1 Approach:deep learning· 1 Research Focus:differential expression· 1 Research Focus:gene regulatory network inference· 1 Assay:imaging· 1 Approach:statistical model· 1

Frequent Co-Authors

Aloysius DomingoiD· 2 shared Laurie J. OzeliusiD· 2 shared Michael E. TalkowskiiD· 2 shared Nutan SharmaiD· 2 shared Rachita YadaviD· 2 shared Alan Mejia MazaiD· 1 shared Ayumi NishiyamaiD· 1 shared Bailey Reese· 1 shared

Activity by Year

2025-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 41 mutual co-author links

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2 shared papersGenetic & Genomic Medicine

Aloysius DomingoORCID

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2 papers

Recent·Most cited

Genetic & Genomic MedicinemedRxivPreprintOct 21, 2026

Perisynaptic matrix gene variants underlie DystoniaGeneNet endophenotypes in isolated focal dystonia

Aloysius Domingo, Dongren Yao, Nyah Kshatriya…·Laurie J. Ozelius

This paper uses a deep learning model to identify genetic variants associated with isolated focal dystonia by leveraging neuroimaging endophenotypes.

DOI 10.64898/2026.10.19.26365640

GeneticsbioRxivPreprintMay 14, 2025

MSH3 is a genetic modifier of somatic repeat instability in X-linked dystonia parkinsonism

Alan Mejia Maza, Madison Hincher, Kevin Correia…·Vanessa Chantal Wheeler

This study identifies MSH3 as a genetic modifier of CCCTCT repeat instability in XDP, showing its impact on both expansion and contraction in blood and brain tissues.

1 citation

humanbulk RNA-seq