Chen Yin, PhD

Title(s)Postdoctoral Scholar, Neurology
SchoolSchool of Medicine
Address1550 Fourth St
San Francisco CA 94158
Phone--
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    Other Positions
    Title(s)UCSF Weill Institute for Neurosciences


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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. Mutations in Metabotropic Glutamate Receptor 1 Contribute to Natural Short Sleep Trait. Curr Biol. 2021 01 11; 31(1):13-24.e4. Shi G, Yin C, Fan Z, Xing L, Mostovoy Y, Kwok PY, Ashbrook LH, Krystal AD, Ptácek LJ, Fu YH. PMID: 33065013.
      View in: PubMed   Mentions: 2     Fields:    Translation:HumansAnimals
    2. Potential digenic inheritance of familial hypertrophic cardiomyopathy identified by whole-exome sequencing. Mol Genet Genomic Med. 2020 03; 8(3):e1150. Ren MB, Chai XR, Li L, Wang X, Yin C. PMID: 31960626.
      View in: PubMed   Mentions: 2     Fields:    Translation:HumansCells
    3. TDRD6 is associated with oligoasthenoteratozoospermia by sequencing the patient from a consanguineous family. Gene. 2018 Jun 15; 659:84-88. Sha YW, Wang X, Su ZY, Wang C, Ji ZY, Mei LB, Zhang L, Deng BB, Huang XJ, Yan W, Chen J, Li P, Cui YQ, Qu QL, Yin C, He XM. PMID: 29551503.
      View in: PubMed   Mentions: 2     Fields:    Translation:HumansCells
    4. A novel mutation in HAUS7 results in severe oligozoospermia in two brothers. Gene. 2018 Jan 10; 639:106-110. Li L, Sha YW, Su ZY, Mei LB, Ji ZY, Zhang Q, Lin SB, Wang X, Qiu PP, Li P, Yin C. PMID: 29017965.
      View in: PubMed   Mentions: 6     Fields:    Translation:Humans