Author

Stephen Wincovitch

National Institutes of HealthORCID 0000-0002-5820-0174Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetics· 2 Developmental Biology· 1 Neuroscience· 1

Signature Assays, Organisms & Methods

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Research Focus:cell type annotation· 3 Organism:zebrafish· 3 Assay:bulk RNA-seq· 2 Research Focus:differential expression· 2 Approach:experimental assay· 2 Approach:statistical model· 2 Research Focus:drug response / drug discovery· 1 Organism:human· 1

Frequent Co-Authors

Blake CarringtoniD· 2 shared Claire C. SleviniD· 2 shared Kevin S. BishopiD· 2 shared Martha KirbyiD· 2 shared Raman B. SoodiD· 2 shared Shawn Michael BurgessiD· 2 shared Alberto RissoneiD· 1 shared Alice YoungiD· 1 shared

Activity by Year

2019-2025 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 27 mutual co-author links

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2 shared papersGenetics

Blake CarringtonORCID

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Author profile →

4 papers

Recent·Most cited

Comparative study of enriched dopaminergic neurons from siblings with Gaucher disease discordant for parkinsonism

Ellen Hertz, Gani Perez, Ying Hao, Krystyna Rytel, Charis Ma, Martha Kirby, Stacie M. Anderson, Stephen Wincovitch, Katherine M. Andersh, Tim Ahfeldt, Joel Blanchard, Yue Andy Qi, López. Grisel, Nahid Tayebi, Ellen Sidransky, Yu Chen

The paper compares dopaminergic neurons from siblings with Gaucher disease to investigate genetic factors contributing to Parkinsonism.

Movement Disorders · Jun 26, 2025Peer-reviewedNeuroscience

Redundant mechanisms driven independently by RUNX1 and GATA2 for hematopoietic development

Erica Bresciani, Blake Carrington, Kai Yu, Erika M. Kim, Tao Zhen, Victoria Sanchez Guzman, Elizabeth Broadbridge, Kevin S. Bishop, Martha Kirby, Ursula L. Harper, Stephen Wincovitch, Stefania Dell’Orso, Vittorio Sartorelli, Raman B. Sood, Paul Liu

The paper identifies RUNX1-independent mechanisms for hematopoietic stem cell generation and shows that GATA2 and RUNX1 functionally complement each other in hematopoiesis.

Blood Advances · Sep 7, 2021Peer-reviewedGenetics

A subset of SMN complex members have a specific role in tissue regeneration via ERBB pathway-mediated proliferation

Wuhong Pei, Lisha Xu, Zelin Chen, Claire C. Slevin, Kade P. Pettie, Stephen Wincovitch, NISC Comparative Sequencing Program, Beatrice B. Barnabas, Sean Black, Gerard G. Bouffard, Shelise Y. Brooks, Holly Coleman, Lyudmila Dekhtyar, Xiaobin Guan, Joel Han, , Shawn Michael Burgess

The paper identifies gemin3 as a regeneration-essential gene in zebrafish and shows smn1, gemin3, and gemin5 inhibit the ErbB pathway to promote cell proliferation during tissue regeneration.

npj Regenerative Medicine · Mar 25, 2020Peer-reviewedGenetics

A model for reticular dysgenesis shows impaired sensory organ development and hair cell regeneration linked to cellular stress

Alberto Rissone, Erin Jimenez, Kevin S. Bishop, Blake Carrington, Claire C. Slevin, Stephen Wincovitch, Raman B. Sood, Fabio Candotti, Shawn Michael Burgess

This study uses zebrafish models to show that AK2 deficiency impairs sensory hair cell development and regeneration, induces oxidative stress, and can be partially rescued by glutathione treatment.

Disease Models & Mechanisms · Jan 1, 2019Peer-reviewedDevelopmental Biology