David B. Beck | |
|---|---|
 | |
| Born | David Benjamin Beck New Haven, Connecticut, USA |
| Nationality | American |
| Alma mater | |
| Known for | VEXAS Syndrome, Autoinflammatory Disease, Rare Genetic Disease |
| Scientific career | |
| Fields | Clinical Genetics |
| Institutions | |
| Doctoral advisor | Danny Reinberg |
| Website | https://davidbecklab.org/ |
David B. Beck is an American physician-scientist, clinical geneticist, and researcher who co-discovered VEXAS Syndrome.[1][2][3] He holds dual appointments as an assistant professor in the Department of Medicine and the Department of Biochemistry and Molecular Pharmacology, and is a member of the Center for Human Genetics and Genomics and the Division of Rheumatology at New York University Grossman School of Medicine and NYU Langone Health.[4][5]
- ^ Beck, David B.; Ferrada, Marcela A.; Sikora, Keith A.; Ombrello, Amanda K.; Collins, Jason C.; Pei, Wuhong; Balanda, Nicholas; Ross, Daron L.; Ospina Cardona, Daniela; Wu, Zhijie; Patel, Bhavisha (31 December 2020). "Somatic Mutations in UBA1 and Severe Adult-Onset Autoinflammatory Disease". New England Journal of Medicine. 383 (27): 2628–2638. doi:10.1056/NEJMoa2026834. ISSN 0028-4793. PMC 7847551. PMID 33108101.
- ^ Marcela Ferrada, M. D. (2022-01-18). "VEXAS Syndrome". National Institute of Arthritis and Musculoskeletal and Skin Diseases. Retrieved 2023-01-20.
- ^ Azvolinsky, Anna (24 January 2021). "The Vexing VEXAS Syndrome". American Society of Hematology Clinical News.
- ^ "Renowned Clinician-Scientist Joins Division of Rheumatology at NYU Langone Health". finance.yahoo.com. 18 October 2021. Retrieved 18 July 2022.
- ^ Bammert, David (21 June 2022). "The Relapsing Polychondritis Foundation Invests in Potentially Groundbreaking Collaborative Research". polychondritis.org. Relapsing Polychondritis Foundation. Retrieved 19 July 2022.