David Chin, MD

CA3 Resident
What I do: 

Medical School:
Rutgers NJMS

Livingston, NJ

Hobbies and Interests: 
Spending time w/ my pup, squash, basketball, eating

Favorite part about UCSF:
Amazing co-residents both in and out of the anesthesia department!


Priya Ramaswamy, MD, MEng; David T. Chin, MD; David Robinowitz, MD, MHS, MS. Open Anesthesia Records: Guidance for Anesthesia Providers on Implementing the Cures Act. ASA Monitor. 2021; 85(2):e3-4.
Amin MD, Chin D, Amin S, Patel A. Anesthetic Challenges in a Child with Pulmonary Agenesis: A Case Report and Review of Literature. Journal of Anesthesia and Clinical Research. 2018; 6(9).
Diep J, Chin DT, Gupta S, Syed F, Xiong M, Cheng J. Kratom, an Emerging Drug of Abuse: A Case Report of Overdose and Management of Withdrawal. A A Pract. 2018 Apr 15; 10(8):192-194.
Amin M, Diep J, Chin D, Kahn JA, Monteiro I, Jackson D, Shulman SM . The Use of Smartphone Video Feature for Diagnosis and Counseling of a Propofol-Induced Acute Dystonic Reaction in a Pediatric Patient. Journal of Clinical Anesthesia and Management. 2017; 2(2).
Zhou Q, Wang H, Schwartz DM, Stoffels M, Park YH, Zhang Y, Yang D, Demirkaya E, Takeuchi M, Tsai WL, Lyons JJ, Yu X, Ouyang C, Chen C, Chin DT, Zaal K, Chandrasekharappa SC, Hanson EP, Yu Z, Mullikin JC, Hasni SA, Wertz IE, Ombrello AK, Stone DL, Hoffmann P, Jones A, Barham BK, Leavis HL, van Royen-Kerkof A, Sibley C, Batu ED, Gül A, Siegel RM, Boehm M, Milner JD, Ozen S, Gadina M, Chae J, Laxer RM, Kastner DL, Aksentijevich I. Loss-of-function mutations in TNFAIP3 leading to A20 haploinsufficiency cause an early-onset autoinflammatory disease. Nat Genet. 2016 01; 48(1):67-73.
Zhou Q, Yang D, Ombrello AK, Zavialov AV, Toro C, Zavialov AV, Stone DL, Chae JJ, Rosenzweig SD, Bishop K, Barron KS, Kuehn HS, Hoffmann P, Negro A, Tsai WL, Cowen EW, Pei W, Milner JD, Silvin C, Heller T, Chin DT, Patronas NJ, Barber JS, Lee CC, Wood GM, Ling A, Kelly SJ, Kleiner DE, Mullikin JC, Ganson NJ, Kong HH, Hambleton S, Candotti F, Quezado MM, Calvo KR, Alao H, Barham BK, Jones A, Meschia JF, Worrall BB, Kasner SE, Rich SS, Goldbach-Mansky R, Abinun M, Chalom E, Gotte AC, Punaro M, Pascual V, Verbsky JW, Torgerson TR, Singer NG, Gershon TR, Ozen S, Karadag O, Fleisher TA, Remmers EF, Burgess SM, Moir SL, Gadina M, Sood R, Hershfield MS, Boehm M, Kastner DL, Aksentijevich I. Early-onset stroke and vasculopathy associated with mutations in ADA2. N Engl J Med. 2014 Mar 06; 370(10):911-20.
Zhou Q, Laxer R, Pelletier M, Ramaswamy M, Wang H-Y, Chin D, Gül A, Sibley C, Barat-Houari M, Siegel R, Kastner DL, Aksentijevich I. Exome Sequencing in Monogenic Behçet-like Disease. Pediatric Rheumatology Online Journal. 2013; (11).
Zhou Q, Zavialov A, Chae J, Hershfield M, Sood R, Burgess S, Zavialov A, Chin D, Gadina M, Goldbach-Mansky R, Ombrello A, Stone D, Aksentijevich I, Kastner D. Loss-of-function mutations in CECR1, encoding adenosine deaminase 2 (ADA2), cause recurrent fevers and early onset strokes. 2013.
Zhou Q, Ombrello AK, Chin D, Kastner DL, Aksentijevich I. Pediatric Rheumatology Online Journal. NLRP3 mosaicism as a cause of late-onset CAPS. 2013; (11).
Honors and Awards: 
Alpha Omega Alpha, 2017