Author

Orin Mishkit

NYU Langone HealthORCID 0000-0002-0858-5053Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

Click to filter author papers

Signature Assays, Organisms & Methods

Click to filter · or open tag

Approach:experimental assay· 1 Organism:mouse· 1 Research Focus:variant calling· 1 Assay:whole-genome sequencing· 1

Frequent Co-Authors

Aleksandra M. WudzinskaiD· 1 shared Christine A. VaineiD· 1 shared D. Cristopher BraggiD· 1 shared Gwen EllisiD· 1 shared H. T. Marc TimmersiD· 1 shared Heather L. Appleby· 1 shared Jef D. BoekeiD· 1 shared Kelly Barriball· 1 shared

Activity by Year

2025-2025 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

Click any collaborator node to inspect or filter shared papers

Focal author (center)Selected co-authorORCID co-authorUnlinked name

Curved chords = mutual co-authorship

1 shared paperGenetics

Aleksandra M. WudzinskaORCID

Mutual co-authors in cluster

Author profile →

1 paper

Recent·Most cited

Genome writing to dissect consequences of SVA retrotransposon disease X-Linked Dystonia Parkinsonism

Weimin Zhang, Yu Zhao, Priya Prakash, Heather L. Appleby, Kelly Barriball, Simona Capponi, Qingwen Jiang, Aleksandra M. Wudzinska, Christine A. Vaine, Gwen Ellis, Neha Rahman, Stefan Markovic, Orin Mishkit, Kerry C. Limberg, Matthew T. Maurano, , Jef D. Boeke

The paper genomically rewrote a mouse Taf1 allele with a human XDP patient-derived TAF1 allele, revealing that intronic SVA retrotransposons reduce TAF1 levels and cause neurodegeneration.

bioRxiv · Oct 7, 2025 · PreprintGenetics