Ben Li, MD

Title(s)Associate Professor, Ob/Gyn, Reproductive Sciences
SchoolSchool of Medicine
Address490 Illinois Street, #10249
San Francisco CA 94158
Phone415-343-2566
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    University of California, San FranciscoM.D.2006 Medicine
    Parkland Memorial HospitalResidency2010Obstetrics and Gynecology
    University of California, San FranciscoFellowship2013Medical Genetics
    University of California, San FranciscoFellowship2015Maternal-Fetal Medicine
    University of California, San Francisco2015Teaching Scholars Program
    University of California, San Francisco, CA2020Diversity, Equity, and Inclusion Champion Training

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    Publications listed below are automatically derived from MEDLINE/PubMed and other sources, which might result in incorrect or missing publications. Researchers can login to make corrections and additions, or contact us for help. to make corrections and additions.
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    Altmetrics Details 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. Some publications (especially newer ones and publications not in PubMed) might not yet be assigned Field or Translation tags.) Click a Field or Translation tag to filter the publications.
    1. Epidemiology of Live Born Infants with Nonimmune Hydrops Fetalis-Insights from a Population-Based Dataset. J Pediatr. 2017 08; 187:182-188.e3. Steurer MA, Peyvandi S, Baer RJ, MacKenzie T, Li BC, Norton ME, Jelliffe-Pawlowski LL, Moon-Grady AJ. PMID: 28533037.
      View in: PubMed   Mentions: 14     Fields:    Translation:Humans
    2. The phenotype of the musculocontractural type of Ehlers-Danlos syndrome due to CHST14 mutations. Am J Med Genet A. 2016 Jan; 170A(1):103-15. Janecke AR, Li B, Boehm M, Krabichler B, Rohrbach M, Müller T, Fuchs I, Golas G, Katagiri Y, Ziegler SG, Gahl WA, Wilnai Y, Zoppi N, Geller HM, Giunta C, Slavotinek A, Steinmann B. PMID: 26373698; PMCID: PMC5115638.
      View in: PubMed   Mentions: 32     Fields:    Translation:HumansCells
    3. Nine patients with Xp22.31 microduplication, cognitive deficits, seizures, and talipes anomalies. Am J Med Genet A. 2014 Aug; 164A(8):2097-103. Esplin ED, Li B, Slavotinek A, Novelli A, Battaglia A, Clark R, Curry C, Hudgins L. PMID: 24800990.
      View in: PubMed   Mentions: 19     Fields:    Translation:HumansCells
    4. Clinical report: Two patients with atelosteogenesis type I caused by missense mutations affecting the same FLNB residue. Am J Med Genet A. 2013 Mar; 161A(3):619-25. Li BC, Hogue J, Eilers M, Mehrotra P, Hyland J, Holm T, Prosen T, Slavotinek AM. PMID: 23401428.
      View in: PubMed   Mentions: 3     Fields:    Translation:HumansCells
    5. Intraparenchymal hemorrhage in a neonate with cleidocranial dysostosis. Pediatr Neurol. 2012 Dec; 47(6):455-7. Gardner MA, Li BC, Wu YW, Slavotinek AM. PMID: 23127269.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
    6. Focal facial dermal dysplasia, type IV, is caused by mutations in CYP26C1. Hum Mol Genet. 2013 Feb 15; 22(4):696-703. Slavotinek AM, Mehrotra P, Nazarenko I, Tang PL, Lao R, Cameron D, Li B, Chu C, Chou C, Marqueling AL, Yahyavi M, Cordoro K, Frieden I, Glaser T, Prescott T, Morren MA, Devriendt K, Kwok PY, Petkovich M, Desnick RJ. PMID: 23161670; PMCID: PMC3554199.
      View in: PubMed   Mentions: 20     Fields:    Translation:HumansAnimalsCells
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