 David Chin, MD
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| Title(s) | Resident, Anesthesia |
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| School | School of Medicine |
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| Address | 513 Parnassus Ave, MSB
San Francisco CA 94117
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| Phone | -- |
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| vCard | Download vCard |
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 Biography | Rutgers New Jersey Medical School, Newark, NJ | MD | 05/2018 | Medicine | | Georgetown University, Washington, DC | BS | 05/2012 | Biology |
Bibliographic
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PMC Citations indicate the number of times the publication was cited by articles in PubMed Central, and the Altmetric score represents citations in news articles and social media.
(Note that publications are often cited in additional ways that are not shown here.)
Fields are based on how the National Library of Medicine (NLM) classifies the publication's journal and might not represent the specific topic of the publication.
Translation tags are based on the publication type and the MeSH terms NLM assigns to the publication.
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Open Anesthesia Records: Guidance for Anesthesia Providers on Implementing the Cures Act. ASA Monitor. 2021; 85(2):e3-4.
Priya Ramaswamy, MD, MEng; David T. Chin, MD; David Robinowitz, MD, MHS, MS. View Publication.
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Anesthetic Challenges in a Child with Pulmonary Agenesis: A Case Report and Review of Literature. Journal of Anesthesia and Clinical Research. 2018; 6(9).
Amin MD, Chin D, Amin S, Patel A. View Publication.
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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.
Diep J, Chin DT, Gupta S, Syed F, Xiong M, Cheng J. PMID: 29652682.
View in: PubMed Mentions: 2 Fields:
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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).
Amin M, Diep J, Chin D, Kahn JA, Monteiro I, Jackson D, Shulman SM . View Publication.
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Loss-of-function mutations in TNFAIP3 leading to A20 haploinsufficiency cause an early-onset autoinflammatory disease. Nat Genet. 2016 01; 48(1):67-73.
PMID: 26642243.
View in: PubMed Mentions: 117 Fields: Translation: Humans
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Early-onset stroke and vasculopathy associated with mutations in ADA2. N Engl J Med. 2014 Mar 06; 370(10):911-20.
PMID: 24552284.
View in: PubMed Mentions: 125 Fields: Translation: HumansAnimals
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Exome Sequencing in Monogenic Behçet-like Disease. Pediatric Rheumatology Online Journal. 2013; (11).
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. View Publication.
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Pediatric Rheumatology Online Journal. NLRP3 mosaicism as a cause of late-onset CAPS. 2013; (11).
Zhou Q, Ombrello AK, Chin D, Kastner DL, Aksentijevich I. View Publication.
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Loss-of-function mutations in CECR1, encoding adenosine deaminase 2 (ADA2), cause recurrent fevers and early onset strokes. 2013.
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. View Publication.
This graph shows the total number of publications by year. To see the data as text, click here.
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| Year | Publications |
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| 2013 | 3 | | 2014 | 1 | | 2015 | 1 | | 2017 | 1 | | 2018 | 2 | | 2021 | 1 |
This graph shows the number and percent of publications by field.
Fields are based on how the National Library of Medicine (NLM) classifies the publications' journals and might not represent the specific topics of the publications.
Note that an individual publication can be assigned to more than one field. As a result, the publication counts in this graph might add up to more than the number of publications the person has written.
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This graph shows the number and percent of publications by field.
Fields are based on how the National Library of Medicine (NLM) classifies the publications' journals and might not represent the specific topics of the publications.
Note that an individual publication can be assigned to more than one field. As a result, the publication counts in this graph might add up to more than the number of publications the person has written.
To see the data as text, click here.
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