Research field (4):
Genomics
, Psychiatry
, Medical biochemistry
, Anesthesiology
Research keywords (11):
eQTL analysis
, MPRA
, scRNA-seq
, human behavior
, Genome-wide Association Study
, Low depth sequencing
, Whole genome sequencing
, GWAS
, 次世代シークエンサー
, Bipolar disorder
, Exome Sequencing
Research theme for competitive and other funds (1):
2012 - 2013 Identification of causative gene for Malignant Hyperthemia using exome sequencing
Papers (35):
Nana Matoba, Brandon D Le, Jordan M Valone, Justin M Wolter, Jessica Mory, Dan Liang, Nil Ayg on, K Alaine Broadaway, Marielle L Bond, Karen L Mohlke, et al. Wnt activity reveals context-specific genetic effects on gene regulation in neural progenitors. bioRxiv : the preprint server for biology. 2023
Cindy Wen, Michael Margolis, Rujia Dai, Pan Zhang, Pawel F Przytycki, Daniel D Vo, Arujun Bhattacharya, Minsoo Kim, Nana Matoba, Ellen Tsai, et al. Cross-ancestry, cell-type-informed atlas of gene, isoform, and splicing regulation in the developing human brain. medRxiv : the preprint server for health sciences. 2023
Dan Liang, Nil Aygün, Nana Matoba, Folami Y Ideraabdullah, Michael I Love, Jason L Stein. Inference of putative cell-type-specific imprinted regulatory elements and genes during human neuronal differentiation. Human molecular genetics. 2023. 32. 3. 402-416
Justin M Wolter, Brandon D Le, Nana Matoba, Michael J Lafferty, Nil Aygün, Dan Liang, Kenan Courtney, Juan Song, Joseph Piven, Mark J Zylka, et al. Cellular Genome-wide Association Study Identifies Common Genetic Variation Influencing Lithium-Induced Neural Progenitor Proliferation. Biological psychiatry. 2023. 93. 1. 8-17
Gretchen R B Saunders, Xingyan Wang, Fang Chen, Seon-Kyeong Jang, Mengzhen Liu, Chen Wang, Shuang Gao, Yu Jiang, Chachrit Khunsriraksakul, Jacqueline M Otto, et al. Genetic diversity fuels gene discovery for tobacco and alcohol use. Nature. 2022. 612. 7941. 720-724
Low coverage sequencing of 4,000 individuals in BioBank Japan Project
(The 62nd Annual Meeting of the Japanese Society of Human Genetics 2017)
Exome Sequencing Identifies De Novo Mutations in Bipolar Disorder
(the World Congress of Psychiatric Genetics XXIII 2015)
Exome Sequencing Points to Roles of De Novo and Rare Transmitted Mutations in Bipolar Disorder
(The 65th American Society of Human Genetics 2015 Annual Meeting 2015)
Professional career (1):
医科学 (東京大学大学院)
Work history (7):
2023/01 - 現在 The University of North Carolina at Chapel Hill Department of Genetics, UNC Neuroscience center research associate
2019/02 - 2023/01 University of North Carolina at Chapel Hill Department of genetics and UNC Neuroscience Center postdoctoral associate
2016/08 - 2018/12 RIKEN Center for Integrative Medical Sciences (IMS) Laboratory for Statistical Analysis Postdoctoral Researcher
2016/04 - 2016/07 RIKEN Center for Integrative Medical Sciences (IMS) Laboratory for Statistical Analysis Research associate
2014/04 - 2016/03 RIKEN Brain Science Institute Laboratory for Molecular Dynamics of Mental Disorders Junior research associate
2013/04 - 2014/03 RIKEN Brain Science Institute Laboratory for Molecular Dynamics of Mental Disorders
2011/04 - 2014/03 Saitama Medical University Researcher