Author

Michael Van Meter

Regeneron (United States)

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 Molecular Biology· 1

Signature Assays, Organisms & Methods

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Organism:human· 2 Approach:statistical model· 2 Research Focus:variant effect prediction· 2 Research Focus:cell-cell communication· 1 Assay:DNA methylation· 1 Approach:experimental assay· 1 Research Focus:gene regulatory network inference· 1 Assay:proteomics· 1

Frequent Co-Authors

Aaron J. WolfeiD· 1 shared Adam D. HudginsiD· 1 shared Adam E. LockeiD· 1 shared Advait AthreyaiD· 1 shared Alan R. ShuldineriD· 1 shared Alexis Pope· 1 shared Amy DamaskiD· 1 shared Andrei SeluanoviD· 1 shared

Activity by Year

2021-2022 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 21 mutual co-author links

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1 shared paperMolecular Biology

Aaron J. WolfeORCID

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Author profile →

2 papers

Recent·Most cited

A rare human centenarian variant of SIRT6 enhances genome stability and interaction with Lamin A

Matthew A. Simon, Jiping Yang, Jonathan Gigas, Eric J. Earley, Eric C. Hillpot, Lei Justan Zhang, Maria Zagorulya, Greg Tombline, Michael B. Gilbert, Samantha L. Yuen, Alexis Pope, Michael Van Meter, Stephan Emmrich, Denis Firsanov, Advait Athreya, , Vera A. Gorbunova

The paper identifies a SIRT6 variant enriched in centenarians that improves genome stability through enhanced mADPr activity and interaction with Lamin A.

The EMBO Journal · Oct 10, 2022Peer-reviewedMolecular Biology

Exome sequencing of 628,388 individuals identifies common and rare variant associations with clonal hematopoiesis phenotypes

Michael D. Kessler, Amy Damask, Sean O’Keeffe, Michael Van Meter, Nilanjana Banerjee, Stefan Semrau, Dadong Li, Kyoko Watanabe, Julie E. Horowitz, Yariv J. Houvras, Christopher E. Gillies, Joelle S. Mbatchou, Ryan R. White, Jack A. Kosmicki, Michelle G. LeBlanc, , Eric Jorgenson

This study uses exome sequencing of 628,388 individuals to identify genetic variants associated with clonal hematopoiesis and its health outcomes.

medRxiv · Dec 29, 2021 · PreprintGenetic & Genomic Medicine