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Catharine Freyer, MBA

Title(s)Division Administrator, Neurology
SchoolSchool of Medicine
Address1001 Potrero Ave
San Francisco CA 94110
Phone628-206-6182
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    Other Positions
    Title(s)UCSF Weill Institute for Neurosciences


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    University of California, San Francisco, CA2019Diversity, 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. Return of individual results in epilepsy genomic research: A view from the field. Epilepsia. 2018 09; 59(9):1635-1642. Ottman R, Freyer C, Mefford HC, Poduri A, Lowenstein DH. PMID: 30098010.
      View in: PubMed   Mentions: 1     Fields:    Translation:Humans
    2. Phenotypic analysis of 303 multiplex families with common epilepsies. Brain. 2017 Aug 01; 140(8):2144-2156. PMID: 28899008.
      View in: PubMed   Mentions: 4     Fields:    Translation:Humans
    3. Heterozygous HNRNPU variants cause early onset epilepsy and severe intellectual disability. Hum Genet. 2017 07; 136(7):821-834. Bramswig NC, Lüdecke HJ, Hamdan FF, Altmüller J, Beleggia F, Elcioglu NH, Freyer C, Gerkes EH, Demirkol YK, Knupp KG, Kuechler A, Li Y, Lowenstein DH, Michaud JL, Park K, Stegmann APA, Veenstra-Knol HE, Wieland T, Wollnik B, Engels H, Strom TM, Kleefstra T, Wieczorek D. PMID: 28393272.
      View in: PubMed   Mentions: 8     Fields:    Translation:HumansCells
    4. Ultra-rare genetic variation in common epilepsies: a case-control sequencing study. Lancet Neurol. 2017 Feb; 16(2):135-143. PMID: 28102150.
      View in: PubMed   Mentions: 41     Fields:    Translation:Humans
    5. Surpassing the Target: How a Recruitment Campaign Transformed the Participant Accrual Trajectory in the Epilepsy Phenome/Genome Project. Clin Transl Sci. 2015 Oct; 8(5):518-25. McGovern K, Karn CF, Fox K. PMID: 26176343.
      View in: PubMed   Mentions: 1     Fields:    Translation:Humans
    6. The epilepsy phenome/genome project. Clin Trials. 2013 Aug; 10(4):568-86. Abou-Khalil B, Alldredge B, Bautista J, Berkovic S, Bluvstein J, Boro A, Cascino G, Consalvo D, Cristofaro S, Crumrine P, Devinsky O, Dlugos D, Epstein M, Fahlstrom R, Fiol M, Fountain N, Fox K, French J, Freyer Karn C, Friedman D, Geller E, Glauser T, Glynn S, Haas K, Haut S, Hayward J, Helmers S, Joshi S, Kanner A, Kirsch H, Knowlton R, Kossoff E, Kuperman R, Kuzniecky R, Lowenstein D, McGuire S, Motika P, Nesbitt G, Novotny E, Ottman R, Paolicchi J, Parent J, Park K, Poduri A, Risch N, Sadleir L, Scheffer I, Shellhaas R, Sherr E, Shih JJ, Shinnar S, Singh R, Sirven J, Smith M, Sullivan J, Thio LL, Venkat A, Vining E, von Allmen G, Weisenberg J, Widdess-Walsh P, Winawer M. PMID: 23818435.
      View in: PubMed   Mentions: 19     Fields:    Translation:Humans
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