Page Sorensen

Title(s)Research Development Specialis, Vice Chanc Research
vCardDownload vCard

    Collapse Biography 
    Collapse Education and Training
    University of California, DavisBachelor's of ScienceHuman Development
    University of California, Los AngelesMaster's DegreeMedical Anthropology

    Collapse Overview 
    Collapse Overview
    I am a long-time UC-System community member, having worked and studied at 3 campuses. I received my undergraduate degree in Child Development from UC-Davis where I also spent several years managing clinical research studies focused on patients with fragile X mutations. I completed a Master’s Degree in Medical Anthropology at UCLA where my work focused on patient interactions with healthcare systems, specifically around issues of genetic testing.

    I currently work on large grants and manage the Team Science Program within the UCSF Research Development Office (RDO). The RDO serves at the nexus of research and research administration to promote, support, strengthen, and grow the research enterprise at UCSF. Working with faculty, administration staff, and leadership partners, the RDO seeks to attract extramural research funding, increase institutional competitiveness, create research relationships, and foster innovation.

    Collapse ORNG Applications 
    Collapse Websites

    Collapse Bibliographic 
    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.
    List All   |   Timeline
    1. Sorensen PL, Gane LW, Yarborough M, Hagerman RJ, Tassone F. Newborn screening and cascade testing for FMR1 mutations. Am J Med Genet A. 2013 Jan; 161A(1):59-69. PMID: 23239591; PMCID: PMC3980469.
    2. Sorensen PL, Basuta K, Mendoza-Morales G, Gane LW, Schneider A, Hagerman R, Tassone F. A fragile X sibship from a consanguineous family with a compound heterozygous female and partially methylated full mutation male. Am J Med Genet A. 2012 May; 158A(5):1221-4. PMID: 22488807; PMCID: PMC3331966.
    3. Chonchaiya W, Nguyen DV, Au J, Campos L, Berry-Kravis EM, Lohse K, Mu Y, Utari A, Hervey C, Wang L, Sorensen P, Cook K, Gane L, Tassone F, Hagerman RJ. Clinical involvement in daughters of men with fragile X-associated tremor ataxia syndrome. Clin Genet. 2010 Jul; 78(1):38-46. PMID: 20497189; PMCID: PMC4031089.