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Genki Hayashi, PhD

Title(s)Postdoctoral Scholar, Ophthalmology
SchoolSchool of Medicine
Address10 Koret Way
San Francisco CA 94117
Phone--
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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. COL4A1 Mutations Cause Neuromuscular Disease with Tissue-Specific Mechanistic Heterogeneity. Am J Hum Genet. 2019 05 02; 104(5):847-860. Labelle-Dumais C, Schuitema V, Hayashi G, Hoff K, Gong W, Dao DQ, Ullian EM, Oishi P, Margeta M, Gould DB. PMID: 31051113.
      View in: PubMed   Mentions: 4     Fields:    Translation:HumansAnimals
    2. Use of sodium 4-phenylbutyrate to define therapeutic parameters for reducing intracerebral hemorrhage and myopathy in Col4a1 mutant mice. Dis Model Mech. 2018 07 04; 11(7). Hayashi G, Labelle-Dumais C, Gould DB. PMID: 29895609.
      View in: PubMed   Mentions: 2     Fields:    Translation:Animals
    3. Dimethyl fumarate mediates Nrf2-dependent mitochondrial biogenesis in mice and humans. Hum Mol Genet. 2017 08 01; 26(15):2864-2873. Hayashi G, Jasoliya M, Sahdeo S, Saccà F, Pane C, Filla A, Marsili A, Puorro G, Lanzillo R, Brescia Morra V, Cortopassi G. PMID: 28460056.
      View in: PubMed   Mentions: 20     Fields:    Translation:HumansAnimalsCells
    4. Lymphoblast Oxidative Stress Genes as Potential Biomarkers of Disease Severity and Drug Effect in Friedreich's Ataxia. PLoS One. 2016; 11(4):e0153574. Hayashi G, Cortopassi G. PMID: 27078885.
      View in: PubMed   Mentions: 4     Fields:    Translation:HumansCells
    5. Oxidative stress in inherited mitochondrial diseases. Free Radic Biol Med. 2015 Nov; 88(Pt A):10-7. Hayashi G, Cortopassi G. PMID: 26073122.
      View in: PubMed   Mentions: 37     Fields:    Translation:Humans
    6. Frataxin deficiency increases cyclooxygenase 2 and prostaglandins in cell and animal models of Friedreich's ataxia. Hum Mol Genet. 2014 Dec 20; 23(25):6838-47. Hayashi G, Shen Y, Pedersen TL, Newman JW, Pook M, Cortopassi G. PMID: 25104852.
      View in: PubMed   Mentions: 11     Fields:    Translation:HumansAnimalsCells
    7. Frataxin deficiency leads to defects in expression of antioxidants and Nrf2 expression in dorsal root ganglia of the Friedreich's ataxia YG8R mouse model. Antioxid Redox Signal. 2013 Nov 01; 19(13):1481-93. Shan Y, Schoenfeld RA, Hayashi G, Napoli E, Akiyama T, Iodi Carstens M, Carstens EE, Pook MA, Cortopassi GA. PMID: 23350650.
      View in: PubMed   Mentions: 53     Fields:    Translation:HumansAnimalsCells
    8. Rare and common variants in CARD14, encoding an epidermal regulator of NF-kappaB, in psoriasis. Am J Hum Genet. 2012 May 04; 90(5):796-808. Jordan CT, Cao L, Roberson ED, Duan S, Helms CA, Nair RP, Duffin KC, Stuart PE, Goldgar D, Hayashi G, Olfson EH, Feng BJ, Pullinger CR, Kane JP, Wise CA, Goldbach-Mansky R, Lowes MA, Peddle L, Chandran V, Liao W, Rahman P, Krueger GG, Gladman D, Elder JT, Menter A, Bowcock AM. PMID: 22521419.
      View in: PubMed   Mentions: 90     Fields:    Translation:HumansCells
    9. Protective effect of human endogenous retrovirus K dUTPase variants on psoriasis susceptibility. J Invest Dermatol. 2012 Jul; 132(7):1833-40. Lai OY, Chen H, Michaud HA, Hayashi G, Kuebler PJ, Hultman GK, Ariza ME, Williams MV, Batista MD, Nixon DF, Foerster J, Bowcock AM, Liao W. PMID: 22437317.
      View in: PubMed   Mentions: 11     Fields:    Translation:HumansCells
    10. Psoriasis patients are enriched for genetic variants that protect against HIV-1 disease. PLoS Genet. 2012 Feb; 8(2):e1002514. Chen H, Hayashi G, Lai OY, Dilthey A, Kuebler PJ, Wong TV, Martin MP, Fernandez Vina MA, McVean G, Wabl M, Leslie KS, Maurer T, Martin JN, Deeks SG, Carrington M, Bowcock AM, Nixon DF, Liao W. PMID: 22577363.
      View in: PubMed   Mentions: 29     Fields:    Translation:HumansCells
    11. Association analysis identifies ZNF750 regulatory variants in psoriasis. BMC Med Genet. 2011 Dec 20; 12:167. Birnbaum RY, Hayashi G, Cohen I, Poon A, Chen H, Lam ET, Kwok PY, Birk OS, Liao W. PMID: 22185198.
      View in: PubMed   Mentions: 7     Fields:    Translation:HumansCells
    12. Mechanism behind Pruritus in Psoriasis. Journal of Psoriasis and Psoriatic Arthritis. 2009 Jun 1; 15a(1):15-18. Genki Hayashi, Mei-Lin Pang. .
      View in: Publisher Site   Mentions:
    13. TNF-a Blocker-Induced Psoriasiform Dermatitis. Journal of Psoriasis and Psoriatic Arthritis. 2008 Dec 1; 14a(2):8-18. Genki Hayashi, Emily Becker, Tim Berger, John Koo. .
      View in: Publisher Site   Mentions:
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