Author

Ryan R. White

Regeneron (United States)ORCID 0000-0001-8344-2549Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetic & Genomic Medicine· 1 Genetics· 1

Signature Assays, Organisms & Methods

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Approach:experimental assay· 1 Organism:human· 1 Organism:mouse· 1 Approach:statistical model· 1 Research Focus:variant effect prediction· 1 Assay:whole-exome sequencing· 1

Frequent Co-Authors

Adam E. LockeiD· 1 shared Agata SmogorzewskaiD· 1 shared Alan R. ShuldineriD· 1 shared Amy DamaskiD· 1 shared Aris BarasiD· 1 shared Audrey M. GoldfarbiD· 1 shared Charles PauldingiD· 1 shared Christopher E. GilliesiD· 1 shared

Activity by Year

2021-2025 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 24 mutual co-author links

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1 shared paperGenetic & Genomic Medicine

Adam E. LockeORCID

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2 papers

Recent·Most cited

GeneticsThe Journal of Cell BiologyPeer-reviewedMay 3, 2025

ALDH9A1 Deficiency as a Source of Endogenous DNA Damage that Requires Repair by the Fanconi Anemia Pathway

Moonjung Jung, Jung-Woo Kim, Yeji Park…·Agata Smogorzewska

The paper identifies ALDH9A1 deficiency as a source of endogenous DNA damage that requires FA pathway repair, leading to genomic instability and tumorigenesis in FA-deficient cells.

13 citations

mouseexperimental assay

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Genetic & Genomic MedicinemedRxivPreprintDec 29, 2021

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

Michael D. Kessler, Amy Damask, Sean O’Keeffe…·Eric Jorgenson

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

21 citations

humanwhole-exome sequencing

𝕏 PostBluesky