Joon Yong An, PhD

TitlePostdoctoral Scholar
SchoolUCSF School of Medicine
Address1550 Fourth St
San Francisco CA 94158
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    Collapse Biography 
    Collapse Education and Training
    University of Queensland (Australia)PhD2016Neuroscience
    University of Queensland (Australia)MSc2011Molecular Biology
    Konkuk University (South Korea)BSc2010Molecular Biology
    Collapse Awards and Honors
    Apex Foundation Charitable Trust2014Research Grant for Australian Autism Study
    University of Queensland2012International Student Research Fellowship
    University of Queensland2011Dean’s Commendation for High Achievement

    Collapse Overview 

    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.
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    1. Sanders SJ, Neale BM, Huang H, Werling DM, An JY, Dong S, Abecasis G, Arguello PA, Blangero J, Boehnke M, Daly MJ, Eggan K, Geschwind DH, Glahn DC, Goldstein DB, Gur RE, Handsaker RE, McCarroll SA, Ophoff RA, Palotie A, Pato CN, Sabatti C, State MW, Willsey AJ, Hyman SE, Addington AM, Lehner T, Freimer NB. Whole genome sequencing in psychiatric disorders: the WGSPD consortium. Nat Neurosci. 2017 Dec; 20(12):1661-1668. PMID: 29184211.
      View in: PubMed
    2. An JY. National human genome projects: an update and an agenda. Epidemiol Health. 2017; 39:e2017045. PMID: 29056031.
      View in: PubMed
    3. An J, Sanders SJ. Appreciating the Population-wide Impact of Copy Number Variants on Cognition. Biol Psychiatry. 2017 Jul 15; 82(2):78-80. PMID: 28645357.
      View in: PubMed
    4. Collins RL, Brand H, Redin CE, Hanscom C, Antolik C, Stone MR, Glessner JT, Mason T, Pregno G, Dorrani N, Mandrile G, Giachino D, Perrin D, Walsh C, Cipicchio M, Costello M, Stortchevoi A, An JY, Currall BB, Seabra CM, Ragavendran A, Margolin L, Martinez-Agosto JA, Lucente D, Levy B, Sanders SJ, Wapner RJ, Quintero-Rivera F, Kloosterman W, Talkowski ME. Defining the diverse spectrum of inversions, complex structural variation, and chromothripsis in the morbid human genome. Genome Biol. 2017 Mar 06; 18(1):36. PMID: 28260531.
      View in: PubMed
    5. Ben-Shalom R, Keeshen CM, Berrios KN, An JY, Sanders SJ, Bender KJ. Opposing Effects on NaV1.2 Function Underlie Differences Between SCN2A Variants Observed in Individuals With Autism Spectrum Disorder or Infantile Seizures. Biol Psychiatry. 2017 Aug 01; 82(3):224-232. PMID: 28256214.
      View in: PubMed
    6. An J, Claudianos C, et al. Genetic heterogeneity in autism: From single gene to a pathway perspective. Neurosci Biobehav Rev. 2016 Sep; 68:442-453. PMID: 27317861.
      View in: PubMed
    7. An JY, Cristino AS, Zhao Q, Edson J, Williams SM, Ravine D, Wray J, Marshall VM, Hunt A, Whitehouse AJ, Claudianos C. Towards a molecular characterization of autism spectrum disorders: an exome sequencing and systems approach. Transl Psychiatry. 2014 Jun 03; 4:e394. PMID: 24893065; PMCID: PMC4080319.
    8. Cristino AS, Williams SM, Hawi Z, An JY, Bellgrove MA, Schwartz CE, Costa Lda F, Claudianos C. Neurodevelopmental and neuropsychiatric disorders represent an interconnected molecular system. Mol Psychiatry. 2014 Mar; 19(3):294-301. PMID: 23439483.
      View in: PubMed
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