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Ben Li, MD

TitleAssistant Professor
SchoolUCSF School of Medicine
DepartmentOb/Gyn, Reproductive Sciences
Address550 16th. Street
San Francisco CA 94158
Phone415-343-2566
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    Collapse Biography 
    Collapse Education and Training
    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

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    Collapse Publications
    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.
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    1. Steurer MA, Peyvandi S, Baer RJ, MacKenzie T, Li B, Norton ME, Jelliffe-Pawlowski LL, Moon-Grady AJ. Epidemiology of Live Born Infants with Nonimmune Hydrops Fetalis-Insights from a Population-Based Dataset. J Pediatr. 2017 Aug; 187:182-188.e3. PMID: 28533037.
      View in: PubMed
    2. 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. 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. PMID: 26373698.
      View in: PubMed
    3. Esplin ED, Li B, Slavotinek A, Novelli A, Battaglia A, Clark R, Curry C, Hudgins L. Nine patients with Xp22.31 microduplication, cognitive deficits, seizures, and talipes anomalies. Am J Med Genet A. 2014 Aug; 164A(8):2097-103. PMID: 24800990.
      View in: PubMed
    4. Li B, Hogue J, Eilers M, Mehrotra P, Hyland J, Holm T, Prosen T, Slavotinek AM. 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. PMID: 23401428.
      View in: PubMed
    5. Gardner MA, Li B, Wu YW, Slavotinek AM. Intraparenchymal hemorrhage in a neonate with cleidocranial dysostosis. Pediatr Neurol. 2012 Dec; 47(6):455-7. PMID: 23127269.
      View in: PubMed
    6. 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. Focal facial dermal dysplasia, type IV, is caused by mutations in CYP26C1. Hum Mol Genet. 2013 Feb 15; 22(4):696-703. PMID: 23161670; PMCID: PMC3554199.
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