Session Details
[O14]Complex Disorders
Fri. Nov 20, 2026 10:40 AM - 11:40 AM JST
Fri. Nov 20, 2026 1:40 AM - 2:40 AM UTC
Fri. Nov 20, 2026 1:40 AM - 2:40 AM UTC
Room 5 (Meeting Room 2, Exhibition Building, Sendai International Center)
Chair: Kinya Ishikawa (Institute of Science Tokyo), Mayumi Tamari (The Jikei University School of Medicine, Division of Molecular Genetics)
[O14-01]Proteomic patterns associated with serum urate level and dysfunctional ABCG2 urate transporter variants
Masahiro Nakatochi1, Yuki Ohashi1, Sahoko Ichihara2, Ken Yamamoto3, Yuki Kitamura2, Tatsuaki Matsubara4, Ruriha Beppo1, Fumie Kinoshita5, Tomoko S Kato6, Yu Toyoda7, Yusuke Kawamura7, Hirotaka Matsuo7, Kimiyoshi Ichida8, Mitsuhiro Yokota9 (1. Public Health Informatics Unit, Department of Integrated Health Sciences, Nagoya University Graduate School of Medicine, Nagoya, Japan, 2. Department of Environmental and Preventive Medicine, Jichi Medical University School of Medicine, Shimotsuke, Japan, 3. Department of Medical Biochemistry, Kurume University School of Medicine, Kurume, Japan, 4. Faculty of Human Sciences, Aichi Mizuho College, Nagoya, Japan, 5. Department of Advanced Medicine, Data Science Division, Data Coordinating Center, Nagoya University Hospital, Nagoya, Japan, 6. Division of Cardio-Vascular Medicine, Department of Internal Medicine, Kurume University School of Medicine, Kurume, Japan, 7. Department of Integrative Physiology and Bio-Nano Medicine, National Defense Medical College, Tokorozawa, Japan, 8. School of Pharmacy, Tokyo University of Pharmacy and Life Sciences, Tokyo, Japan, 9. Kurume University School of Medicine, Kurume, Japan)
[O14-02]Functional analyses of SHARPIN variants associated with the risk of late-onset Alzheimer's disease using genome editing
Yuya Asanomi1, Tetsuaki Kimura1, Nobuyoshi Shimoda1, Satoshi Kamijo2,3, Hideki Miwa2, Daichi Shigemizu1,4, Shumpei Niida5, Kouichi Ozaki1,4,6,7 (1. Medical Genome Center, Research Institute, National Center for Geriatrics and Gerontology, Obu, Japan, 2. Department of Neuropsychopharmacology, National Institute of Mental Health, National Center of Neurology and Psychiatry, Kodaira, Japan, 3. Department of Physiology, National Defense Medical College, Tokorozawa, Japan, 4. Department of Cardiovascular Medicine, Hiroshima University Graduate School of Biomedical and Health Sciences, Hiroshima, Japan, 5. Research Institute, National Center for Geriatrics and Gerontology, Obu, Japan, 6. RIKEN Center for Integrative Medical Sciences, Yokohama, Japan, 7. Department of Aging Research, Nagoya University Graduate School of Medicine, Nagoya, Japan)
[O14-03]Polygenic risk analyses reveal shared genetic architecture between narcolepsy type 1 and type 2 beyond HLA-DQB1*06:02
Taku Miyagawa1, Mihoko Shimada1,2, Tohru Kodama2,3, Katsushi Tokunaga2, Makoto Honda2,3 (1. Sleep Disorders Project, Tokyo Metropolitan Institute of Medical Science, Tokyo, Japan, 2. Genome Medical Science Project, National Institute of Global Health and Medicine, Japan Institute for Health Security, 3. Japan Somnology Center and Seiwa Hospital, Tokyo, Japan)
[O14-04]Longitudinal Analysis of HBV Mutations in Serum Samples Using Survival Analysis
Nao Nishida1, Masaya Sugiyama2, Jun Ohashi3, Takayo Tsuchiura1, Katsushi Tokunaga1 (1. Japan Institute for Health Security, Toyama, 2. Japan Institute for Health Security, Kohnodai, 3. University of Tokyo)
[O14-05]Association analysis between tryptase genotypes and food allergy in Japanese population
Yamato Sasaki1,2, Shunsuke Kuriyama1, Kazuhiro Hosoya1, Takako Nakamura1, Teruaki Matsui3, Shiro Sugiura3, Kiwako Yamamoto4, Tatsuki Hukuie4, Yukihiro Ohya5, Emiko Noguti1 (1. Department of Medical Genetics, Institute of Medicine, University of Tsukuba, Ibaraki, Japan, 2. Graduate School of Comprehensive Human Sciences, Master's Program in Medical Sciences, 3. Division of Allergy, Allergy Center, Aichi Children Health and Medical Center, Aichi, Japan, 4. Division of General Allergy, Allergy Center, National Center for Child Health and Development, Tokyo, Japan, 5. Department of Occupational and Environmental Health, Graduate School of Medical Sciences, Nagoya City University)
[O14-06]Multi-ancestry genome-wide association studies elucidate spatio-cellular features of multiple sclerosis genetics
Rintaro Fujimoto1,2, Kotaro Ogawa3, Shinichi Namba1,2, Yosuke Ogawa1, Ryuya Edahiro2,4, Kyuto Sonehara1,2,5, Shiori Tagawa1, Mitsuru Watanabe6, Tomohiro Yata3, Yuya Shirai4, Yuji Yamamoto4, Go Sato1,2, Chifune Kai7, Tasuhiko Naito1, Koichi Matsuda8, Makoto Kinoshita3, Jun-ichi Kira6, Tatsusada Okuno3, Noriko Isobe6, Yukinori Okada1,2 (1. Department of Genome Informatics, Graduate School of Medicine, the University of Tokyo, 2. Laboratory for Systems Genetics, RIKEN Center for Integrative Medical Sciences, Yokohama, Japan, 3. Department of Neurology, Graduate School of Medicine, The University of Osaka, Suita, Japan, 4. Department of Respiratory Medicine and Clinical Immunology, Graduate School of Medicine, The University of Osaka, Suita, Japan, 5. Wellcome Sanger Institute, Wellcome Genome Campus, Cambridge, UK, 6. Department of Neurology, Neurological Institute, Graduate School of Medical Sciences, Kyushu University, Fukuoka, Japan, 7. Department of Ophthalmology, Graduate School of Medicine, The University of Osaka, Suita, Japan, 8. Laboratory of Clinical Genome Sequencing, Graduate School of Frontier Sciences, The University of Tokyo, Tokyo, Japan)
