Ben Li, MD
Associate Professor
Ob/Gyn, Reproductive Sciences
School of Medicine

Education & Training

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• Diversity, Equity, and Inclusion Champion Training University of California 2020
• Fellowship Maternal-Fetal Medicine University of California, San Francisco 2015
• Teaching Scholars Program University of California, San Francisco 2015
• Fellowship Medical Genetics University of California, San Francisco 2013
• Residency Obstetrics and Gynecology Parkland Memorial Hospital 2010
• M.D. Medicine University of California, San Francisco 2006

Publications (6)

Top publication keywords:
ClubfootEctodermal DysplasiaChromosome DuplicationMicrofilament ProteinsEhlers-Danlos SyndromeSulfotransferasesCleidocranial DysplasiaHydrops FetalisInfant MortalityConnective Tissue DiseasesMutation, MissenseContractile ProteinsOsteochondrodysplasiasDermisFilamins

• Epidemiology of Live Born Infants with Nonimmune Hydrops Fetalis-Insights from a Population-Based Dataset.
  The Journal of pediatrics 2017 Steurer MA, Peyvandi S, Baer RJ, MacKenzie T, Li BC, Norton ME, Jelliffe-Pawlowski LL, Moon-Grady AJ
• The phenotype of the musculocontractural type of Ehlers-Danlos syndrome due to CHST14 mutations.
  American journal of medical genetics. Part A 2015 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
• Nine patients with Xp22.31 microduplication, cognitive deficits, seizures, and talipes anomalies.
  American journal of medical genetics. Part A 2014 Esplin ED, Li B, Slavotinek A, Novelli A, Battaglia A, Clark R, Curry C, Hudgins L
• Clinical report: Two patients with atelosteogenesis type I caused by missense mutations affecting the same FLNB residue.
  American journal of medical genetics. Part A 2013 Li BC, Hogue J, Eilers M, Mehrotra P, Hyland J, Holm T, Prosen T, Slavotinek AM
• Intraparenchymal hemorrhage in a neonate with cleidocranial dysostosis.
  Pediatric neurology 2012 Gardner MA, Li BC, Wu YW, Slavotinek AM
• Focal facial dermal dysplasia, type IV, is caused by mutations in CYP26C1.
  Human molecular genetics 2012 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…