NAKABAYASHI Kazuhiko 中林一彦

… Alternative Names

中林一彦ナカバヤシカズヒコ

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Researcher Number	10415557
Other IDs
External Links
Affiliation (Current)	2025: 国立研究開発法人国立成育医療研究センター, 周産期病態研究部, 室長
Affiliation (based on the past Project Information) *help	2016 – 2024: 国立研究開発法人国立成育医療研究センター, 周産期病態研究部, 室長 2020: 国立研究開発法人国立国際医療研究センター, その他部局等, その他 2019: 国立研究開発法人国立国際医療研究センター, 周産期病態研究部, 室長 2015: 国立研究開発法人国立成育医療研究センター, その他部局等, その他 2015: 国立研究開発法人国立成育医療研究センター, 研究所, 室長 … More 2015: 国立成育医療研究センター, 周産期病態研究部, 室長 2013 – 2014: 独立行政法人国立成育医療研究センター, 研究所, 室長 2012: (独)国立成育医療研究センター研究所, 周産期病態研究部, 室長 2012: 独立行政法人国立成育医療研究センター, その他部局等, その他 2011: (独)国立成育医療研究センター, 研究所・周産期病態研究部, 室長 2010: 国立成育医療センター研究所, 周産期病態研究部, 室長 2010: 独立行政法人国立成育医療研究センター, 周産期病態研究部, 室長 2009: 独立行政法人国立成医療研究センター研究所, 周産期病態研究部, 室長 2006 – 2007: 国立成育医療センター(研究所), 周産期病態研究部, 室長 2006: 国立国際医療センター(研究所), 臨床病理研究部, 室長 Less
Review Section/Research Field	Principal Investigator Human genetics / Basic Section 56040:Obstetrics and gynecology-related / Biological Sciences Except Principal Investigator Basic Section 52050:Embryonic medicine and pediatrics-related / Medium-sized Section 56:Surgery related to the biological and sensory functions and related fields / Basic Section 90140:Medical technology assessment-related / Obstetrics and gynecology / Hygiene and public health / Human genetics / Sections That Are Subject to Joint Review: Basic Section90130:Medical systems-related , Basic Section90140:Medical technology assessment-related … More / Basic Section 90130:Medical systems-related / Basic Section 56040:Obstetrics and gynecology-related / Sections That Are Subject to Joint Review: Basic Section45010:Genetics-related ,Basic Section45020:Evolutionary biology-related / Basic Section 45020:Evolutionary biology-related / Basic Section 45010:Genetics-related / Medium-sized Section 63:Environmental analyses and evaluation and related fields / Pediatrics / Neurochemistry/Neuropharmacology / Genome biology / Biological Sciences / General internal medicine (including Psychosomatic medicine) Less
Keywords	Principal Investigator クロマチン高次構造 / ゲノムインプリンティング / 相関解析 / 疾患感受性遺伝子 / SNP / 関連解析 / 拒食症 / 摂食障害 / エンハンサー / スーパーエンハンサー … More / エンハンサー・プロモーター相互作用 / 子宮内膜 / 胎盤 / エピゲノム / シーケンス / アレル別エピゲノム解析 / エピゲノム診断 / インプリンティング / 遺伝学的検査 / DNAメチル化 / white adipose tissue / genomic imprinting / Klf14 / 白色脂肪組織 / KLF14 … More Except Principal Investigator DNAメチル化 / エピジェネティクス / 初期胚 / 妊娠期曝露 / 無機ヒ素 / インプリンティング / 生殖補助医療 / DOHaD / 医療技術 / 品質評価 / X染色体不活化 / X染色体 / 肝腫瘍 / 継世代影響 / 精子 / F2影響 / 初期発生 / エピゲノム / ヒストン修飾 / クロマチン / エピ変異 / 再生・移植医療 / 非侵襲的評価 / 細胞・組織構築物 / 幹細胞生物学 / 母体救命 / 母体死亡 / ゲノム解析 / 妊娠 / 羊水塞栓症 / 性分化疾患 / 胎児期低栄養環境 / オルガノイド / ガウス過程 / ヒト幹細胞 / CRISPR転写制御 / 環境因子 / female細胞 / ヒト受精胚 / 生命発動 / 器官発生 / 多能性幹細胞 / 再生・細胞医療 / バイオインフォマティクス / 凍結細胞 / 初期化 / リプログラミング / 胚 / 次世代影響 / 癌 / 女性医学 / 不育症 / 受精卵 / 生殖医学 / 胎盤発生 / 着床 / Oct4 / Xist / 標的治療 / OMICS解析 / 婦人科腫瘍学 / 分子標的治療 / バイオマーカー / 次世代シーケンサー / 遺伝子発現解析 / DNAメチル化解析 / 染色体微細構造解析 / 子宮平滑筋肉腫 / miiRNA / 発がん / 胎児期曝露 / miRNA / 早期胚 / ユビキチン化 / ヒストン / モノユビキチン化 / 運命決定 / ヒストンユビキチン化 / 未分化性維持 / モノユビキン化 / ヒストンH2B / ES細胞 / 胚盤胞 / 神経発生 / 神経幹細胞 / siRNA / 非コードRNA / 3Cアッセイ / クロマチンダイナミクス / 染色体テリトリー / 転写マシナリー / クロマチン構造 / ゲノムインプリンティング / DNA-FISH / 網羅的メチル化解析 / 網羅的 / アレイ / メチル化解析 / インプリンティング異常症 / MLID / 高齢出産 / 分子生物学的解析 / 胎盤 / 個体 / メチル化可変領域 / ヒト疾患 / iPS細胞 / 遺伝子調節 / SNP / マイクロサテライト / ゲノムワイド相関解析 / 感受性遺伝子 / 摂食障害患者 / 神経性食欲不振症 / 心療内科学 Less

Understanding the role of non-coding disease variants through dynamic-eQTL mapping
- Principal Investigator
  
  熊坂夏彦
- Project Period (FY)
  2024 – 2026
- Research Category
  
  Grant-in-Aid for Scientific Research (B)
- Review Section
  
  Basic Section 45010:Genetics-related
  Basic Section 45020:Evolutionary biology-related
  Sections That Are Subject to Joint Review: Basic Section45010:Genetics-related ,Basic Section45020:Evolutionary biology-related
- Research Institution
  The University of Tokyo
精巣体細胞栄養代謝プログラミング機構の解明
- Principal Investigator
  
  藤澤泰子
- Project Period (FY)
  2024 – 2028
- Research Category
  
  Grant-in-Aid for Scientific Research (B)
- Review Section
  
  Basic Section 52050:Embryonic medicine and pediatrics-related
- Research Institution
  Hamamatsu University School of Medicine
羊水塞栓症発症ハイリスク妊婦スクリーニング遺伝子パネル検査の開発を目指した研究
- Principal Investigator
  
  伊東宏晃
- Project Period (FY)
  2024 – 2027
- Research Category
  
  Grant-in-Aid for Scientific Research (B)
- Review Section
  
  Basic Section 56040:Obstetrics and gynecology-related
- Research Institution
  Hamamatsu University School of Medicine
ヒト幹細胞とゲノム・エピゲノム編集による初期発生原理の統合的理解
- Principal Investigator
  
  福田篤
- Project Period (FY)
  2023 – 2026
- Research Category
  
  Grant-in-Aid for Scientific Research (A)
- Review Section
  
  Medium-sized Section 56:Surgery related to the biological and sensory functions and related fields
- Research Institution
  Tokai University
Non-invasive assessment of 3D tissue constructs for regenerative medicine and cell transplantation
- Principal Investigator
  
  宮本義孝
- Project Period (FY)
  2023 – 2026
- Research Category
  
  Grant-in-Aid for Scientific Research (B)
- Review Section
  
  Basic Section 90140:Medical technology assessment-related
  Basic Section 90130:Medical systems-related
  Sections That Are Subject to Joint Review: Basic Section90130:Medical systems-related , Basic Section90140:Medical technology assessment-related
- Research Institution
  National Center for Child Health and Development
Elucidation of 3D genome architecture of human placental and endometrial cellsPrincipal Investigator
- Principal Investigator
  
  中林一彦
- Project Period (FY)
  2022 – 2024
- Research Category
  
  Grant-in-Aid for Scientific Research (B)
- Review Section
  
  Basic Section 56040:Obstetrics and gynecology-related
- Research Institution
  National Center for Child Health and Development
ヒト胎芽期・胎児期・新生児期の環境因子によるエピゲノム変異とその経時的変化の同定
- Principal Investigator
  
  秦健一郎
- Project Period (FY)
  2021 – 2023
- Research Category
  
  Grant-in-Aid for Scientific Research (B)
- Review Section
  
  Basic Section 52050:Embryonic medicine and pediatrics-related
- Research Institution
  Gunma University
Elucidating the Molecular Mechanisms in Human Fertilized Embryos Governing Developmental Initiation and Organogenesis Regulation
- Principal Investigator
  
  Akutsu Hidenori
- Project Period (FY)
  2020 – 2023
- Research Category
  
  Grant-in-Aid for Scientific Research (A)
- Review Section
  
  Medium-sized Section 56:Surgery related to the biological and sensory functions and related fields
- Research Institution
  National Center for Child Health and Development
Inheritance of environmental impacts on DNA methylation through sperm to the next generation embryos
- Principal Investigator
  
  NOHARA Keiko
- Project Period (FY)
  2018 – 2020
- Research Category
  
  Grant-in-Aid for Challenging Research (Exploratory)
- Review Section
  
  Medium-sized Section 63:Environmental analyses and evaluation and related fields
- Research Institution
  National Institute for Environmental Studies
The Fate of Frozen Cells: Development of Quality Assessment Technology for Therapeutic Cells
- Principal Investigator
  
  MIYAMOTO Yoshitaka
- Project Period (FY)
  2018 – 2020
- Research Category
  
  Grant-in-Aid for Scientific Research (B)
- Review Section
  
  Basic Section 90140:Medical technology assessment-related
- Research Institution
  National Center for Child Health and Development
Establishment and diagnostic application of epigenome sequencing methods for imprinted differentially methylated regionsPrincipal Investigator
- Principal Investigator
  
  Nakabayashi Kazuhiko
- Project Period (FY)
  2017 – 2020
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Human genetics
- Research Institution
  National Center for Child Health and Development
Omics-based analysis of specific biomarkers for leiomyosarcoma
- Principal Investigator
  
  Sonoda Kenzo
- Project Period (FY)
  2017 – 2019
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Obstetrics and gynecology
- Research Institution
  National Hospital Organization, Kyushu Cancer Center
  Kyushu University
Elucidation of oocyte molecular mechanism on imprinted X chromosome inactivation enabling a sequential development
- Principal Investigator
  
  Akutsu Hidenori
- Project Period (FY)
  2017 – 2019
- Research Category
  
  Grant-in-Aid for Scientific Research (A)
- Research Field
  
  Obstetrics and gynecology
- Research Institution
  National Center for Child Health and Development
Comprehensive analysis of somatic and germline genomic alterations for atypical leukemia in children
- Principal Investigator
  
  Kato Motohiro
- Project Period (FY)
  2017 – 2019
- Research Category
  
  Grant-in-Aid for Scientific Research (B)
- Research Field
  
  Pediatrics
- Research Institution
  National Center for Child Health and Development
Molecular mechanisms of the fate determination of neural stem cells
- Principal Investigator
  
  Hitoshi Seiji
- Project Period (FY)
  2016 – 2018
- Research Category
  
  Grant-in-Aid for Scientific Research (B)
- Research Field
  
  Neurochemistry/Neuropharmacology
- Research Institution
  Shiga University of Medical Science
Elucidation of the onset mechanism of human imprinting disorders using the method of methylation analysis with high-density DNA methylation arrays
- Principal Investigator
  
  Kagami Masayo
- Project Period (FY)
  2015 – 2017
- Research Category
  
  Grant-in-Aid for Challenging Exploratory Research
- Research Field
  
  Human genetics
- Research Institution
  National Center for Child Health and Development
Genome-wide DNA methylation analysis of sperm to explore the mechanism of hepatin tumor augmentation in the F2 by gestational arsenite exposure of F0 pregnant mice
- Principal Investigator
  
  Nohara Keiko
- Project Period (FY)
  2015 – 2016
- Research Category
  
  Grant-in-Aid for Challenging Exploratory Research
- Research Field
  
  Hygiene and public health
- Research Institution
  National Institute for Environmental Studies
Studies on epimutations that are involved in multigenerational effects of environmental chemicals in mice
- Principal Investigator
  
  Nohara Keiko
- Project Period (FY)
  2014 – 2016
- Research Category
  
  Grant-in-Aid for Scientific Research (B)
- Research Field
  
  Hygiene and public health
- Research Institution
  National Institute for Environmental Studies
KLF14 biology: its physiological roles and transcriptional regulationPrincipal Investigator
- Principal Investigator
  
  NAKABAYASHI Kazuhiko
- Project Period (FY)
  2013 – 2016
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Human genetics
- Research Institution
  National Center for Child Health and Development
Identification of chromatin factor which is associated with neuron specific chromatin dynamics.
- Principal Investigator
  
  Horike Shin-ichi
- Project Period (FY)
  2013 – 2015
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Genome biology
- Research Institution
  Kanazawa University
Clarification of (epi)genetic causes leading to the development of human imprinting disorders
- Principal Investigator
  
  OGATA Tsutomu
- Project Period (FY)
  2010 – 2012
- Research Category
  
  Grant-in-Aid for Scientific Research (A)
- Research Field
  
  Human genetics
- Research Institution
  Hamamatsu University School of Medicine
  National Research Institute for Child Health and Development
ヒト生殖系列におけるインプリンティング制御機構の解明
- Principal Investigator
  
  KAGAMI Masayo
- Project Period (FY)
  2009 – 2010
- Research Category
  
  Grant-in-Aid for Scientific Research on Priority Areas
- Review Section
  
  Biological Sciences
- Research Institution
  National Research Institute for Child Health and Development
Identification and a functional analysis of susceptibility genes of Eating Disorders by GWAS
- Principal Investigator
  
  KOMAKI Gen
- Project Period (FY)
  2008 – 2010
- Research Category
  
  Grant-in-Aid for Scientific Research (B)
- Research Field
  
  General internal medicine (including Psychosomatic medicine)
- Research Institution
  National Center of Neurology and Psychiatry
摂食障害感受性遺伝子の解明Principal Investigator
- Principal Investigator
  
  中林一彦
- Project Period (FY)
  2006 – 2007
- Research Category
  
  Grant-in-Aid for Scientific Research on Priority Areas
- Review Section
  
  Biological Sciences
- Research Institution
  National Research Institute for Child Health and Development
摂食障害感受性遺伝子の同定と機能解析Principal Investigator
- Principal Investigator
  
  中林一彦
- Project Period (FY)
  2006 – 2007
- Research Category
  
  Grant-in-Aid for Young Scientists (B)
- Research Field
  
  Human genetics
- Research Institution
  National Research Institute for Child Health and Development
  Research Institute, International Medical Center of Japan

[Book] 遺伝子医学MOOK36号　エピゲノムで新たな解明が進む「先天性疾患」2021
- Author(s)
  中林一彦
- Total Pages
  8
- Publisher
  メディカルドゥー社
- Data Source
  KAKENHI-PROJECT-17K08689
[Book] Epigenetics Methods (Volume 18 in Translational Epigenetics), 2020, Pages 117-140 (Chapter 7: The Illumina Infinium Methylation Assay for Genome-wide Methylation Analyses)2020
- Author(s)
  Kazuhiko Nakabayashi
- Total Pages
  24
- Publisher
  Springer
- Data Source
  KAKENHI-PROJECT-17K08689
[Book] Epigenetics Methods2020
- Author(s)
  Kazuhiko Nakabayashi
- Total Pages
  24
- Publisher
  Elsevier
- Data Source
  KAKENHI-PROJECT-17K08689
[Journal Article] Upregulated expression of lamin B receptor increases cell proliferation and suppresses genomic instability: implications for cellular immortalization2024
- Author(s)
  En Atsuki、Takemoto Kentaro、Yamakami Yoshimi、Nakabayashi Kazuhiko、Fujii Michihiko
- Journal Title
  
  The FEBS Journal
  
  Volume: 291 Issue: 10 Pages: 2155-2171
- DOI
  10.1111/febs.17113
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-22K11730, KAKENHI-PROJECT-23K24490
[Journal Article] Biallelic non-productive enhancer-promoter interactions precede imprinted expression of Kcnk9 during mouse neural commitment2024
- Author(s)
  Rengifo Rojas C, Cercy J, Perillous S, Gonthier-Gueret C, Montibus B, Maupetit-Mehouas S, Espinadel A, Dupre M, Hong CC, Hata K, Nakabayashi K, Plagge A, Bouschet T, Arnaud P, Vaillant I, Court F.
- Journal Title
  
  Human Genetics and Genomics Advances
  
  Volume: 5 Issue: 2 Pages: 100271-100271
- DOI
  10.1016/j.xhgg.2024.100271
- Peer Reviewed / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-23K24490
[Journal Article] Loss of NSD2 causes dysregulation of synaptic genes and altered H3K36 dimethylation in mice2024
- Author(s)
  Kinoshita Shiori、Kojima Kazuaki、Ohnishi Eriko、Takayama Yuka、Kikuchi Hiroki、Takada Shuji、Nakabayashi Kazuhiko、Kawai Tomoko、Hata Kenichiro
- Journal Title
  
  Frontiers in Genetics
  
  Volume: 15 Pages: 1308234-1308234
- DOI
  10.3389/fgene.2024.1308234
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-23K24490
[Journal Article] Gene expression signatures associated with chronic endometritis revealed by RNA sequencing2023
- Author(s)
  Oshina K, Kuroda K, Nakabayashi K, Tomikawa J, Kitade M, Sugiyama R, Hata K, Itakura A.
- Journal Title
  
  Frontiers in Medicine
  
  Volume: 10 Pages: 1185284-1185284
- DOI
  10.3389/fmed.2023.1185284
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-23K05730, KAKENHI-PROJECT-21K19584, KAKENHI-PROJECT-23K24490, KAKENHI-PROJECT-23K28470
[Journal Article] Chromosomal microdeletion leading to pituitary gigantism through hormone-gene overexpression2023
- Author(s)
  Katoh-Fukui Yuko、Hattori Atsushi、Zhang Ruogu、Terao Miho、Takada Shuji、Nakabayashi Kazuhiko、Hata Kenichiro、Yamada Yutaka、Matsuura Nobuo、Fukami Maki
- Journal Title
  
  Human Molecular Genetics
  
  Volume: 32 Issue: 14 Pages: 2318-2325
- DOI
  10.1093/hmg/ddad053
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-20H00550
[Journal Article] Reduced Representation Bisulfite Sequencing (RRBS).2023
- Author(s)
  Nakabayashi K, Yamamura M, Haseagawa K, Hata K
- Journal Title
  
  Methods Mol Biol.
  
  Volume: 2577 Pages: 39-51
- DOI
  10.1007/978-1-0716-2724-2_3
- ISBN
  9781071627235, 9781071627242
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21K19584, KAKENHI-PROJECT-23K24490
[Journal Article] Donor cord blood aging accelerates in recipients after transplantation2023
- Author(s)
  Onizuka Makoto、Imanishi Tadashi、Harada Kaito、Aoyama Yasuyuki、Amaki Jun、Toyosaki Masako、Machida Shinichiro、Kikkawa Eri、Yamada Sanetoshi、Nakabayashi Kazuhiko、Hata Kenichiro、Higashimoto Ken、Soejima Hidenobu、Ando Kiyoshi
- Journal Title
  
  Scientific Reports
  
  Volume: 13 Issue: 1 Pages: 2603-2603
- DOI
  10.1038/s41598-023-29912-2
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-20H03643, KAKENHI-PROJECT-20K08183, KAKENHI-PROJECT-21K19451, KAKENHI-PROJECT-23K24490
[Journal Article] Myelodysplasia after clonal hematopoiesis with APOBEC3-mediated CYBB inactivation in retroviral gene therapy for X-CGD2023
- Author(s)
  Uchiyama T、Kawai T、Nakabayashi K、Nakazawa Y、Goto F、Okamura K、Nishimura T、Kato K、Watanabe N、Miura A、Yasuda T、Ando Y、Minegishi T、Edasawa K、Shimura M、Akiba Y、Sato-Otsubo A、Mizukami T、Kato M、Akashi K、Nunoi H、Onodera M
- Journal Title
  
  Molecular Therapy
  
  Volume: 31 Issue: 12 Pages: 3424-3440
- DOI
  10.1016/j.ymthe.2023.09.004
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-22K07928, KAKENHI-PROJECT-22K07951, KAKENHI-PROJECT-23K24490
[Journal Article] Identification of a KDM6A somatic mutation responsible for Kabuki syndrome by excluding a conflicting KMT2D germline variant through episignature analysis.2023
- Author(s)
  Tomoko Kawai, Yuji Iwasaki, Hiroko Ogasawara, Hiromi Kamura, Kazuaki Nakamura, Kenichiro Hata, Takako Takano, Kazuhiko Nakabayashi
- Journal Title
  
  Eur J Med Genet
  
  Volume: 66(8) Issue: 8 Pages: 104806-104806
- DOI
  10.1016/j.ejmg.2023.104806
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21K02413, KAKENHI-PROJECT-20H00550, KAKENHI-PROJECT-23K24490
[Journal Article] A capture methyl-seq protocol with improved efficiency and cost-effectiveness using pre-pooling and enzymatic conversion2023
- Author(s)
  Hasegawa Keita、Nakabayashi Kazuhiko、Ishiwata Keisuke、Kasuga Yoshifumi、Hata Kenichiro、Tanaka Mamoru
- Journal Title
  
  BMC Research Notes
  
  Volume: 16 Issue: 1 Pages: 141-141
- DOI
  10.1186/s13104-023-06401-3
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-23K24490
[Journal Article] Genome-wide association study of preterm birth and gestational age in a Japanese population2023
- Author(s)
  Hasegawa Keita、Kumasaka Natsuhiko、Nakabayashi Kazuhiko、Kamura Hiromi、Maehara Kayoko、Kasuga Yoshifumi、Hata Kenichiro、Tanaka Mamoru
- Journal Title
  
  Human Genome Variation
  
  Volume: 10 Issue: 1 Pages: 1-4
- DOI
  10.1038/s41439-023-00246-9
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-23K28470
[Journal Article] Glucocorticoids increase the risk of preterm premature rupture of membranes possibly by inducing ITGA8 gene expression in the amnion2022
- Author(s)
  Okazaki Yuka、Taniguchi Kosuke、Miyamoto Yoshitaka、Kinoshita Shiori、Nakabayashi Kazuhiko、Kaneko Kayoko、Hamada Hiromi、Satoh Toyomi、Murashima Atsuko、Hata Kenichiro
- Journal Title
  
  Placenta
  
  Volume: 128 Pages: 73-82
- DOI
  10.1016/j.placenta.2022.07.012
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-22K09587, KAKENHI-PROJECT-21H02887, KAKENHI-PROJECT-20K18182, KAKENHI-PROJECT-16KK0192, KAKENHI-PROJECT-23K24490
[Journal Article] Familial Pseudohypoparathyroidism Type IB Associated with an SVA Retrotransposon Insertion in the GNAS Locus2022
- Author(s)
  Sayaka Kawashima, Akiko Yuno, Shinichiro Sano, Masayo Kagami
- Journal Title
  
  J Bone Miner Res .
  
  Volume: 10 Issue: 10 Pages: 1850-1859
- DOI
  10.1002/jbmr.4652
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-20K08178, KAKENHI-PROJECT-21K07334, KAKENHI-PROJECT-22K07858, KAKENHI-PROJECT-20H00539, KAKENHI-PROJECT-20H03641, KAKENHI-PUBLICLY-21H00342, KAKENHI-PROJECT-23K24490
[Journal Article] Development of Human Gut Organoids With Resident Tissue Macrophages as a Model of Intestinal Immune Responses2022
- Author(s)
  Tsuruta Satoru、Kawasaki Tomoyuki、Machida Masakazu、Iwatsuki Ken、Inaba Akihiko、Shibata Shinsuke、Shindo Tomoko、Nakabayashi Kazuhiko、Hakamada Kenichi、Umezawa Akihiro、Akutsu Hidenori
- Journal Title
  
  Cellular and Molecular Gastroenterology and Hepatology
  
  Volume: 14 Issue: 3 Pages: 726-729
- DOI
  10.1016/j.jcmgh.2022.06.006
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-22K08906, KAKENHI-PROJECT-22K16477, KAKENHI-PROJECT-21K07764, KAKENHI-PROJECT-23K24490
[Journal Article] Aberrant hypomethylation at imprinted differentially methylated regions is involved in biparental placental mesenchymal dysplasia2022
- Author(s)
  Aoki Saori、Higashimoto Ken、Hidaka Hidenori、Ohtsuka Yasufumi、Aoki Shigehisa、Mishima Hiroyuki、Yoshiura Koh-ichiro、Nakabayashi Kazuhiko、Hata Kenichiro、Yatsuki Hitomi、Hara Satoshi、Ohba Takashi、Katabuchi Hidetaka、Soejima Hidenobu
- Journal Title
  
  Clinical Epigenetics
  
  Volume: 14 Issue: 1 Pages: 64-64
- DOI
  10.1186/s13148-022-01280-0
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-21K07800, KAKENHI-PROJECT-20H03643, KAKENHI-PROJECT-20K08183, KAKENHI-PROJECT-21K19451, KAKENHI-PROJECT-23K24490
[Journal Article] Deleterious fibronectin type III-related gene variants may induce a spinal extradural arachnoid cyst: an exome sequencing study of identical twin cases2021
- Author(s)
  Hana Taijun、Ogiwara Hideki、Migita Ohsuke、Nakabayashi Kazuhiko、Hata Kenichiro、Morota Nobuhito
- Journal Title
  
  Child's Nervous System
  
  Volume: - Issue: 7 Pages: 2329-2334
- DOI
  10.1007/s00381-021-05137-4
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-18H03556
[Journal Article] Methylation status of genes escaping from X-chromosome inactivation in patients with X-chromosome rearrangements2021
- Author(s)
  Kawashima Sayaka、Hattori Atsushi、Suzuki Erina、Matsubara Keiko、Toki Machiko、Kosaki Rika、Hasegawa Yukihiro、Nakabayashi Kazuhiko、Fukami Maki、Kagami Masayo
- Journal Title
  
  Clinical Epigenetics
  
  Volume: 13 Issue: 1 Pages: 134-134
- DOI
  10.1186/s13148-021-01121-6
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PLANNED-17H06428, KAKENHI-PROJECT-20H00550
[Journal Article] Maintenance of mouse trophoblast stem cells in KSR-based medium allows conventional 3D culture2021
- Author(s)
  SUN Shuai、YANO Shota、NAKANISHI Momo O、HIROSE Michiko、NAKABAYASHI Kazuhiko、HATA Kenichiro、OGURA Atsuo、TANAKA Satoshi
- Journal Title
  
  J. Reprod. Dev.
  
  Volume: 67 Issue: 3 Pages: 197-205
- DOI
  10.1262/jrd.2020-119
- NAID
  130008055012
- ISSN
  0916-8818, 1348-4400
- Language
  English
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PLANNED-19H05758, KAKENHI-PROJECT-18H03556
[Journal Article] Identification of epigenetic memory candidates associated with gestational age at birth through analysis of methylome and transcriptional data2021
- Author(s)
  Kashima Kohei, Kawai Tomoko, 共同筆頭著者、他22名
- Journal Title
  
  Scientific Reports
  
  Volume: 11 Issue: 1 Pages: 3381-3381
- DOI
  10.1038/s41598-021-83016-3
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-19K11735, KAKENHI-PROJECT-17K08689, KAKENHI-PROJECT-20K16916
[Journal Article] Identification of distinct loci for de novo DNA methylation by DNMT3A and DNMT3B during mammalian development2020
- Author(s)
  Yagi Masaki、Kabata Mio、Tanaka Akito、Ukai Tomoyo、Ohta Sho、Nakabayashi Kazuhiko、Shimizu Masahito、Hata Kenichiro、Meissner Alexander、Yamamoto Takuya、Yamada Yasuhiro
- Journal Title
  
  Nature Communications
  
  Volume: 11 Issue: 1 Pages: 3199-3199
- DOI
  10.1038/s41467-020-16989-w
- NAID
  120006865709
- Peer Reviewed / Open Access / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-19K16513, KAKENHI-PUBLICLY-20H05384, KAKENHI-PROJECT-18H04026, KAKENHI-PROJECT-18H03556, KAKENHI-PROJECT-17K08689
[Journal Article] Epitranscriptomic profiling in human placenta: N6‐methyladenosine modification at the 5′‐untranslated region is related to fetal growth and preeclampsia2020
- Author(s)
  Taniguchi Kosuke、Kawai Tomoko、Kitawaki Jo、Tomikawa Junko、Nakabayashi Kazuhiko、Okamura Kohji、Sago Haruhiko、Hata Kenichiro
- Journal Title
  
  The FASEB Journal
  
  Volume: 34 Issue: 1 Pages: 494-512
- DOI
  10.1096/fj.201900619rr
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-17H01588, KAKENHI-PROJECT-17K07248, KAKENHI-PROJECT-18K15737, KAKENHI-PROJECT-18H03556
[Journal Article] Loss of imprinting of the human-specific imprinted gene ZNF597 causes prenatal growth retardation and dysmorphic features: implications for phenotypic overlap with Silver-Russell syndrome2020
- Author(s)
  Yamazawa K, Inoue T, Sakemi Y, Nakashima T, Yamashita H, Khono K, Fujita H, Enomoto K, Nakabayashi K, Hata K, Nakashima M, Matsunaga T, Nakamura A, Matsubara K, Ogata T, Kagami M.
- Journal Title
  
  Journal of Medical Genetics
  
  Volume: - Issue: 6 Pages: 107019-107019
- DOI
  10.1136/jmedgenet-2020-107019
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-17K08689, KAKENHI-PROJECT-20H00539
[Journal Article] Gestational arsenic exposure induces site-specific DNA hypomethylation in active retrotransposon subfamilies in offspring sperm in mice2020
- Author(s)
  Nohara Keiko、Nakabayashi Kazuhiko、Okamura Kazuyuki、Suzuki Takehiro、Suzuki Shigekatsu、Hata Kenichiro
- Journal Title
  
  Epigenetics & Chromatin
  
  Volume: 13 Issue: 1 Pages: 53-53
- DOI
  10.1186/s13072-020-00375-3
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-18H03556, KAKENHI-PROJECT-17K08689, KAKENHI-PROJECT-18K19860
[Journal Article] Rare variant of the epigenetic regulator SMCHD1 in a patient with pituitary hormone deficiency.2020
- Author(s)
  Kinjo K, Nagasaki K, Muroya K, Suzuki E, Ishiwata K, Nakabayashi K, Hattori A, Nagao K, Nozawa R-S, Obuse C, Miyado K, Ogata T, Fukami M and Miyado M.
- Journal Title
  
  Scientific Reports
  
  Volume: 10 Issue: 1 Pages: 10985-10985
- DOI
  10.1038/s41598-020-67715-x
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-19K09682, KAKENHI-PLANNED-17H06428, KAKENHI-PLANNED-18H05532, KAKENHI-PROJECT-19H01067, KAKENHI-PROJECT-20H00539, KAKENHI-PROJECT-19H03156, KAKENHI-PROJECT-20H03190, KAKENHI-PROJECT-17K08689
[Journal Article] ZFAT binds to centromeres to control noncoding RNA transcription through the KAT2B-H4K8ac-BRD4 axis2020
- Author(s)
  Shuhei Ishikura, Kazuhiko Nakabayashi, Masayoshi Nagai, Toshiyuki Tsunoda, Senji Shirasawa
- Journal Title
  
  Nucleic Acids Research
  
  Volume: 48(19) Issue: 19 Pages: 10848-10866
- DOI
  10.1093/nar/gkaa815
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-20K07317, KAKENHI-PROJECT-18H03556, KAKENHI-PROJECT-17K08689
[Journal Article] Contribution of gene mutations to Silver-Russell syndrome phenotype: multigene sequencing analysis in 92 etiology-unknown patients2020
- Author(s)
  Inoue Takanobu、et al
- Journal Title
  
  Clinical Epigenetics
  
  Volume: 12 Issue: 1 Pages: 86-86
- DOI
  10.1186/s13148-020-00865-x
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PLANNED-17H06428, KAKENHI-PROJECT-20H00539, KAKENHI-PROJECT-17K08689
[Journal Article] Placenta-specific epimutation at H19-DMR among common pregnancy complications: its frequency and effect on the expression patterns of H19 and IGF22019
- Author(s)
  Yamaguchi Yuko、Tayama Chiharu、Tomikawa Junko、Akaishi Rina、Kamura Hiromi、Matsuoka Kentaro、Wake Norio、Minakami Hisanori、Kato Kiyoko、Yamada Takahiro、Nakabayashi Kazuhiko、Hata Kenichiro
- Journal Title
  
  Clinical Epigenetics
  
  Volume: 11 Issue: 1 Pages: 113-113
- DOI
  10.1186/s13148-019-0712-3
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-17K08689, KAKENHI-PROJECT-17H01588, KAKENHI-PROJECT-18K19618
[Journal Article] Temple Syndrome in a Patient With Variably Methylated CpGs at the Primary MEG3/DLK1:IG-DMR and Severely Hypomethylated CpGs at the Secondary MEG3:TSS-DMR2019
- Author(s)
  Kagami M, Yanagisawa A, Ota M, Matsuoka K, Nakamura A, Matsubara K, Nakabayashi K, Takada S, Fukami M, Ogata T.
- Journal Title
  
  Clinical Epigenetics
  
  Volume: 11 Issue: 1 Pages: 41-41
- DOI
  10.1186/s13148-019-0640-2
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-18K06356, KAKENHI-PLANNED-17H06428, KAKENHI-PROJECT-17H01588, KAKENHI-PROJECT-17H04204
[Journal Article] Genome-wide single nucleotide polymorphism array analysis unveils the origin of heterozygous androgenetic complete moles2019
- Author(s)
  Usui Hirokazu、Nakabayashi Kazuhiko、Maehara Kayoko、Hata Kenichiro、Shozu Makio
- Journal Title
  
  Scientific Reports
  
  Volume: 9 Issue: 1 Pages: 12542-12542
- DOI
  10.1038/s41598-019-49047-7
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-18K09281, KAKENHI-PROJECT-17H01588, KAKENHI-PROJECT-18H03556
[Journal Article] Amplicon Sequencing-Based Noninvasive Fetal Genotyping for RHD-Positive D Antigen-Negative Alleles2019
- Author(s)
  Takahashi Ken、Migita Ohsuke、Sasaki Aiko、Nasu Michiko、Kawashima Akihiro、Sekizawa Akihiko、Sato Taisuke、Ito Yuki、Sago Haruhiko、Okamoto Aikou、Nakabayashi Kazuhiko、Hata Kenichiro
- Journal Title
  
  Clinical Chemistry
  
  Volume: 65 Issue: 10 Pages: 1307-1316
- DOI
  10.1373/clinchem.2019.307074
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-17H01588, KAKENHI-PROJECT-17K16311, KAKENHI-PROJECT-18H03556
[Journal Article] Evolution of imprinting via lineage-specific insertion of retroviral promoters2019
- Author(s)
  Bogutz Aaron B.、Brind’Amour Julie、Kobayashi Hisato、Jensen Kristoffer N.、Nakabayashi Kazuhiko、Imai Hiroo、Lorincz Matthew C.、Lefebvre Louis
- Journal Title
  
  Nature Communications
  
  Volume: 10 Issue: 1 Pages: 5674-5674
- DOI
  10.1038/s41467-019-13662-9
- Peer Reviewed / Open Access / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-17K08689, KAKENHI-PROJECT-19K21586, KAKENHI-PROJECT-17H01588, KAKENHI-PROJECT-18H04005, KAKENHI-PROJECT-18H03556
[Journal Article] Whole transcriptome sequencing reveals a KMT2A‐USP2 fusion in infant acute myeloid leukemia2019
- Author(s)
  Ikeda Junji、Shiba Norio、Tsujimoto Shin‐ichi、Yoshida Masanori、Nakabayashi Kazuhiko、Ogata‐Kawata Hiroko、Okamura Kohji、Takeuchi Masanobu、Osumi Tomoo、Tomizawa Daisuke、Hata Kenichiro、Kiyokawa Nobutaka、Ito Shuichi、Kato Motohiro
- Journal Title
  
  Genes, Chromosomes and Cancer
  
  Volume: in press Issue: 9 Pages: 1-1
- DOI
  10.1002/gcc.22751
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-16K07137, KAKENHI-PROJECT-16K20951, KAKENHI-PROJECT-19K08350, KAKENHI-PROJECT-17H04234
[Journal Article] Exploring trophoblast-specific Tead4 enhancers through chromatin conformation capture assays followed by functional screening2019
- Author(s)
  Tomikawa Junko、Takada Shuji、Okamura Kohji、Terao Miho、Ogata-Kawata Hiroko、Akutsu Hidenori、Tanaka Satoshi、Hata Kenichiro、Nakabayashi Kazuhiko
- Journal Title
  
  Nucleic Acids Research
  
  Volume: 48 Issue: 1 Pages: 278-289
- DOI
  10.1093/nar/gkz1034
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-17K08689, KAKENHI-PROJECT-19K22988, KAKENHI-PROJECT-17H01588, KAKENHI-PROJECT-17K07248, KAKENHI-PROJECT-18H03556
[Journal Article] DNA methylation changes involved in the tumor increase in F2 males born to gestationally arsenite‐exposed F1 male mice2019
- Author(s)
  Okamura Kazuyuki、Nakabayashi Kazuhiko、Kawai Tomoko、Suzuki Takehiro、Sano Tomoharu、Hata Kenichiro、Nohara Keiko
- Journal Title
  
  Cancer Science
  
  Volume: 110 Issue: 8 Pages: 2629-2642
- DOI
  10.1111/cas.14104
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-17K08689
[Journal Article] Acute promyelocytic leukemia with a cryptic insertion of RARA into TBL1XR12019
- Author(s)
  Osumi Tomoo、Watanabe Akihiro、Okamura Kohji、Nakabayashi Kazuhiko、Yoshida Masanori、Tsujimoto Shin‐ichi、Uchiyama Meri、Takahashi Hiroyuki、Tomizawa Daisuke、Hata Kenichiro、Kiyokawa Nobutaka、Kato Motohiro
- Journal Title
  
  Genes, Chromosomes and Cancer
  
  Volume: 58 Issue: 11 Pages: 820-823
- DOI
  10.1002/gcc.22791
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-19K16762, KAKENHI-PROJECT-17H01588, KAKENHI-PROJECT-17H04234
[Journal Article] A novel KMT2A-ACTN2 fusion in infant B-cell acute lymphoblastic leukemia2019
- Author(s)
  Masanori Yoshida、Kazuhiko Nakabayashi、Hiroko Ogata-Kawata、Tomoo Osumi、Shin-ichi Tsujimoto、Ryota Shirai、Kaoru Yoshida、Kohji Okamura、Kimikazu Matsumoto、Nobutaka Kiyokawa、Daisuke Tomizawa、Kenichiro Hata、Motohiro Kato
- Journal Title
  
  Pediatric Blood & Cancer
  
  Volume: in press (MPO27821) Issue: 8 Pages: 1-1
- DOI
  10.1002/pbc.27821
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-16K07137, KAKENHI-PROJECT-17H04234
[Journal Article] Characterization of parent-of-origin methylation using the Illumina Infinium MethylationEPIC array platform.2018
- Author(s)
  Mora JRH, Tayama C, Sanchez-Delgado M, Monteagudo-Sanchez A, Hata K, Ogata T, Medrano J, Eugenia Poo-Llanill M, Simón C, Moran S, Esteller M, Tenorio J, Lapunzina P, Kagami M, Monk D, Nakabayashi K
- Journal Title
  
  Epigenomics
  
  Volume: 印刷中
- Peer Reviewed / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15K15096
[Journal Article] Molecular and clinical analyses of two patients with UPD(16)mat detected by screening 94 patients with Silver-Russell syndrome phenotype of unknown aetiology2018
- Author(s)
  Inoue Takanobu、Yagasaki Hideaki、Nishioka Junko、Nakamura Akie、Matsubara Keiko、Narumi Satoshi、Nakabayashi Kazuhiko、Yamazawa Kazuki、Fuke Tomoko、Oka Akira、Ogata Tsutomu、Fukami Maki、Kagami Masayo
- Journal Title
  
  Journal of Medical Genetics
  
  Volume: 印刷中 Issue: 6 Pages: 413-418
- DOI
  10.1136/jmedgenet-2018-105463
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-17K08689, KAKENHI-PROJECT-16H05362, KAKENHI-PROJECT-17H04204
[Journal Article] Characterization of parent-of-origin methylation using the Illumina Infinium MethylationEPIC array platform2018
- Author(s)
  Hernandez Mora Jose R、Tayama Chiharu、S?nchez-Delgado Marta、Monteagudo-S?nchez Ana、Hata Kenichiro、Ogata Tsutomu、Medrano Jose、Poo-Llanillo Maria E、Sim?n Carlos、Moran Sebastian、Esteller Manel、Tenorio Jair、Lapunzina Pablo、Kagami Masayo、Monk David、Nakabayashi Kazuhiko
- Journal Title
  
  Epigenomics
  
  Volume: 10 Issue: 7 Pages: 941-954
- DOI
  10.2217/epi-2017-0172
- Peer Reviewed / Open Access / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-17K08689, KAKENHI-PROJECT-17H01588, KAKENHI-PROJECT-17H04204, KAKENHI-PROJECT-18H03556
[Journal Article] A case of paternal uniparental isodisomy for chromosome 7 associated with overgrowth2018
- Author(s)
  Nakamura Akie、Muroya Koji、Ogata-Kawata Hiroko、Nakabayashi Kazuhiko、Matsubara Keiko、Ogata Tsutomu、Kurosawa Kenji、Fukami Maki、Kagami Masayo
- Journal Title
  
  J Med Genet
  
  Volume: 55 Issue: 8 Pages: 2017-104986
- DOI
  10.1136/jmedgenet-2017-104986
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-17H04204, KAKENHI-PROJECT-15K15096, KAKENHI-PROJECT-17K08689
[Journal Article] Reciprocal changes of H3K27ac and H3K27me3 at the promoter regions of the critical genes for endometrial decidualization2018
- Author(s)
  Katoh Noriko、Kuroda Keiji、Tomikawa Junko、Ogata-Kawata Hiroko、Ozaki Rie、Ochiai Asako、Kitade Mari、Takeda Satoru、Nakabayashi Kazuhiko、Hata Kenichiro
- Journal Title
  
  Epigenomics
  
  Volume: 10 Issue: 9 Pages: 1243-1257
- DOI
  10.2217/epi-2018-0006
- Peer Reviewed / Open Access / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-17K08689, KAKENHI-PROJECT-17H01588, KAKENHI-PROJECT-18H03556
[Journal Article] Elucidation of the developmental mechanism of ovarian mature cystic teratomas using B allele-frequency plots of single nucleotide polymorphism array data2018
- Author(s)
  Usui Hirokazu、Nakabayashi Kazuhiko、Kaku Hiroshi、Maehara Kayoko、Hata Kenichiro、Shozu Makio
- Journal Title
  
  Genes, Chromosomes and Cancer
  
  Volume: 57 Issue: 8 Pages: 409-419
- DOI
  10.1002/gcc.1
- Peer Reviewed / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-17K08689, KAKENHI-PROJECT-18K09281, KAKENHI-PROJECT-17H01588, KAKENHI-PROJECT-16K11120
[Journal Article] Characterization of parent-of-origin methylation using the Illumina Infinium MethylationEPIC array platform2018
- Author(s)
  Jose Ramon Hernandez Mora, Chiharu Tayama, Marta Sanchez-Delgado, Ana Monteagudo-Sanchez, Kenichiro Hata, Tsutomu Ogata, Jose Medrano, Maria Eugenia Poo-Llanillo, Carlos Simon, Sebastian Moran, Manel Esteller, Jair Tenorio, Pablo Lapunzina, Masayo Kagami, David Monk, Kazuhiko Nakabayashi
- Journal Title
  
  Epigenomics
  
  Volume: 印刷中
- Peer Reviewed / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-17K08689
[Journal Article] Somatic MECOM mosaicism in a patient with congenital bone marrow failure without a radial abnormality2018
- Author(s)
  Osumi Tomoo、Tsujimoto Shin-ichi、Nakabayashi Kazuhiko、Taniguchi Maki、Shirai Ryota、Yoshida Masanori、Uchiyama Toru、Nagasawa Junko、Goyama Susumu、Yoshioka Takako、Tomizawa Daisuke、Kurokawa Mineo、Matsubara Yoichi、Kiyokawa Nobutaka、Matsumoto Kimikazu、Hata Kenichiro、Kato Motohiro
- Journal Title
  
  Pediatric Blood & Cancer
  
  Volume: 65 Issue: 6
- DOI
  10.1002/pbc.26959
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-17H04234, KAKENHI-PROJECT-16K15533, KAKENHI-PROJECT-15K09676
[Journal Article] Genome-wide multilocus imprinting disturbance analysis in Temple syndrome and Kagami-Ogata syndrome.2017
- Author(s)
  Kagami M, Matsubara K, Nakabayashi K, Nakamura A, Sano S, Okamura K, Hata K, Fukami M, Ogata T.
- Journal Title
  
  Genet Med.
  
  Volume: 19 Issue: 4 Pages: 476-482
- DOI
  10.1038/gim.2016.123
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-25460409, KAKENHI-PROJECT-15K09734, KAKENHI-PROJECT-16K07137, KAKENHI-PROJECT-15K15096
[Journal Article] Beckwith-Wiedemann syndrome and pseudohypoparathyroidism type Ib in a patient with multilocus methylation defects: a female-dominant phenomenon?2016
- Author(s)
  Ｓｈｉｎｉｃｈｉｒｏ　Ｓａｎｏ
- Journal Title
  
  Journal of Human Genetics
  
  Volume: 未定 Issue: 8 Pages: 765-9
- DOI
  10.1038/jhg.2016.45
- Peer Reviewed / Acknowledgement Compliant
- Data Source
  KAKENHI-PROJECT-26461537, KAKENHI-PROJECT-15K09734, KAKENHI-PROJECT-15K15096
[Journal Article] Changeability of the fully methylated status of the 15q11.2 region in induced pluripotent stem cells derived from a patient with Prader-Willi syndrome.2016
- Author(s)
  Okuno H, Nakabayashi K, Abe K, Ando T, Sanosaka T, Kohyama J, Akamatsu W, Ohyama M, Takahashi T, Kosaki K, Okano H.
- Journal Title
  
  Congenit Anom (Kyoto)
  
  Volume: Dec 21 Issue: 4 Pages: 96-103
- DOI
  10.1111/cga.12206
- NAID
  130008142312
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-25460409, KAKENHI-PROJECT-16K09677, KAKENHI-PUBLICLY-17H05706
[Journal Article] Targeted DNA demethylation in vivo using dCas9-peptide repeat and scFv-TET1 catalytic domain fusions.2016
- Author(s)
  Morita S, Noguchi H, Horii T, Nakabayashi K, Kimura M, Okamura K, Sakai A, Nakashima H, Hata K, Nakashima K, Hatada I
- Journal Title
  
  Nat Biotechnol.
  
  Volume: 34 Issue: 10 Pages: 1060-1065
- DOI
  10.1038/nbt.3658
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-25460409, KAKENHI-PROJECT-15K14452, KAKENHI-PROJECT-15K07687, KAKENHI-PROJECT-16K07137
[Journal Article] Imprinting control regions (ICRs) are marked by mono-allelic bivalent chromatin when transcriptionally inactive.2016
- Author(s)
  Maupetit-Méhouas S, Montibus B, Nury D, Tayama C, Wassef M, Kota SK, Fogli A, Cerqueira Campos F, Hata K, Feil R, Magueron R, Nakabayashi K, Court F, Arnaud P
- Journal Title
  
  Nucleic Acids Res.
  
  Volume: 44 Issue: 2 Pages: 621-635
- DOI
  10.1093/nar/gkv960
- Peer Reviewed / Open Access / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-25460409
[Journal Article] Human Oocyte-Derived Methylation Differences Persist in the Placenta Revealing Widespread Transient Imprinting.2016
- Author(s)
  Sanchez-Delgado M, Court F, Vidal E, Medrano J, Monteagudo-Sanchez A, Martin-Trujillo A, Tayama C, Iglesias-Platas I, Kondova I, Bontrop R, Poo-Llanillo ME, Marques-Bonet T, Nakabayashi K, Simon C, Monk D.
- Journal Title
  
  PLoS Genet.
  
  Volume: 12 Issue: 11 Pages: e1006427-e1006427
- DOI
  10.1371/journal.pgen.1006427
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-25460409
[Journal Article] An insulator element located at the cyclin B1 interacting protein 1 gene locus is highly conserved among mammalian species.2015
- Author(s)
  Yoshida W, Tomikawa J, Inaki M, Kimura H, Onodera M, Hata K, Nakabayashi K
- Journal Title
  
  PLoS One
  
  Volume: 10 Issue: 6 Pages: e0131204-e0131204
- DOI
  10.1371/journal.pone.0131204
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-25460409
[Journal Article] Epimutations of the IG-DMR and the MEG3-DMR at the 14q32.2 imprinted region in two patients with Silver-Russell syndrome-compatible phenotype.2015
- Author(s)
  Kagami M, Mizuno S, Matsubara K, Nakabayashi K, Sano S, Fuke T, Fukami M, Ogata T.
- Journal Title
  
  Eur J Hum Genet.
  
  Volume: 23(8) Pages: 1062-1067
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-15K15096
[Journal Article] Lists of HumanMethylation450 BeadChip probes with nucleotide-variant information obtained from the Phase 3 data of the 1000 Genomes Project.2015
- Author(s)
  Okamura K, Kawai T, Hata K, Nakabayashi K
- Journal Title
  
  Genomics Data
  
  Volume: 7 Pages: 67-9
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-25460409
[Journal Article] Exploration of hydroxymethylation in Kagami-Ogata syndrome caused by hypermethylation of imprinting control regions.2015
- Author(s)
  Matsubara K, Kagami M, Nakabayashi K, Hata K, Fukami M, Ogata T, Yamazawa K.
- Journal Title
  
  Clin Epigenetics
  
  Volume: 28;7(1) Issue: 1 Pages: 90-90
- DOI
  10.1186/s13148-015-0124-y
- Peer Reviewed / Open Access / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15K09734, KAKENHI-PROJECT-15K15096, KAKENHI-PROJECT-15K15478, KAKENHI-PROJECT-25253023, KAKENHI-PROJECT-25713040
[Journal Article] Absence of maternal methylation in biparental hydatidiform moles with NLRP7 maternal-effect mutations reveals widespread placenta-specific imprinting.2015
- Author(s)
  Sanchez-Delgado M, Martin-Trujillo A, Tayama C, Vidal E, Esteller M, Iglesias-Platas I, Deo N, Barney O, Maclean K, Hata K, Nakabayashi K, Fisher R, Monk D
- Journal Title
  
  PLoS Genet.
  
  Volume: 11
- Peer Reviewed / Open Access / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-25460409
[Journal Article] Genomic, epigenomic, and transcriptomic profiling towards identifying omics -features and specific biomarkers that distinguish uterine leiomyosarcoma and leiomyoma at molecular levels.2015
- Author(s)
  Miyata T, Sonoda K, Tomikawa J, Tayama C, Maehara K, Kobayashi H, Wake N, Kato K, Hata K, Nakabayashi K
- Journal Title
  
  Sarcoma
  
  Volume: 2015 Pages: 412068-412068
- DOI
  10.1155/2015/412068
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-25460409, KAKENHI-PROJECT-24592494
[Journal Article] DNA methylation analysis of human myoblasts during in vitro myogenic differentiation: de novo methylation of promoters of muscle-related genes and its involvement in transcriptional down-regulation2015
- Author(s)
  Miyata K, Miyata T, Nakabayashi K, Okamura K, Naito M, Kawai T, Takada S, Kato K, Miyamoto S, Hata K, Asahara H
- Journal Title
  
  Hum. Mol. Genet.
  
  Volume: 24 Issue: 2 Pages: 410-423
- DOI
  10.1093/hmg/ddu457
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-23770273, KAKENHI-PROJECT-25460409, KAKENHI-PROJECT-26560076, KAKENHI-ORGANIZER-26113001, KAKENHI-PLANNED-26113008, KAKENHI-PROJECT-15H02560
[Journal Article] Gene expression profiling of white adipose tissue reveals paternal transmission of proneness to obesity.2015
- Author(s)
  Morita S, Nakabayashi K, Kawai T, Hayashi K, Horii T, Kimura M, Kamei Y, Ogawa Y, Hata K, Hatada I
- Journal Title
  
  Sci. Rep.
  
  Volume: 6 Issue: 1 Pages: 21693-21693
- DOI
  10.1038/srep21693
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-25460409, KAKENHI-PROJECT-26560076, KAKENHI-PROJECT-15K14432, KAKENHI-PROJECT-25292076, KAKENHI-PROJECT-16H04926, KAKENHI-PROJECT-15K12669, KAKENHI-PROJECT-16K07194
[Journal Article] The role of maternal-specific H3K9me3 modification in establishing imprinted X-chromosome inactivation and embryogenesis in mice.2014
- Author(s)
  Fukuda A, Tomikawa J, Miura T, Hata K, Nakabayashi K, Eggan K, Akutsu H, Umezawa A.
- Journal Title
  
  Nat Commun.
  
  Volume: 5 Issue: 1 Pages: 5464-5464
- DOI
  10.1038/ncomms6464
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-25460409, KAKENHI-PROJECT-25670710, KAKENHI-PROJECT-25860259, KAKENHI-PROJECT-26293364, KAKENHI-PROJECT-26861350
[Journal Article] Comprehensive and quantitative multilocus methylation analysis reveals the susceptibility of specific imprinted differentially methylated regions (DMRs) to aberrant methylation in Beckwith-Wiedemann syndrome with epimutations2014
- Author(s)
  Maeda T, Higashimoto K, Jozaki K, Hitomi H, Nakabayashi K, Makita Y, Tonoki H, Okamoto N, Takada F, Ohashi H, Migita M, Kosaki R, Matsubara K, Ogata T, Matsuo M, Hamasaki Y, Ohtsuka Y, Nishioka K, Joh K, Mukai T, Hata K, Soejima H
- Journal Title
  
  Genet Med
  
  Volume: 16(12) Issue: 12 Pages: 903-912
- DOI
  10.1038/gim.2014.46
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PLANNED-22132004, KAKENHI-PROJECT-22227002, KAKENHI-PROJECT-25253023, KAKENHI-PROJECT-25460409, KAKENHI-PROJECT-25461554, KAKENHI-PROJECT-25461648, KAKENHI-PROJECT-25860898, KAKENHI-PROJECT-26670169
[Journal Article] Offspring production with sperm grown in vitro from cryopreserved testis tissues2014
- Author(s)
  Yokonishi T, Sato T, Komeya M, Katagiri K, Kubota Y, Nakabayashi K, Hata K, Inoue K, Ogonuki N, Ogura A, Ogawa T
- Journal Title
  
  Nature Communications
  
  Volume: 5 Issue: 1 Pages: 4320-4320
- DOI
  10.1038/ncomms5320
- Peer Reviewed / Acknowledgement Compliant / Open Access
- Data Source
  KAKENHI-PROJECT-24390371, KAKENHI-PLANNED-25114007, KAKENHI-PROJECT-25460409, KAKENHI-PROJECT-26713012
[Journal Article] Variable maternal methylation overlapping the nc886/vtRNA2-1 locus is locked between hypermethylated repeats and is frequently altered in cancer.2014
- Author(s)
  Romanelli V, Nakabayashi K, Vizoso M, Moran S, Iglesias-Platas I, Sugahara N, Simón C, Hata K, Esteller M, Court F, Monk D.
- Journal Title
  
  Epigenetics
  
  Volume: 9 Issue: 5 Pages: 783-790
- DOI
  10.4161/epi.28323
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-25460409
[Journal Article] Genome-wide parent-of-origin DNA methylation analysis reveals the intricacies of the human imprintome and suggests a germline methylation independent establishment of imprinting.2014
- Author(s)
  Court F, Tayama C, Romanelli V, Martin-Trujillo A, Iglesias-Platas I, Okamura K, Sugahara N, Simon C, Moore H, Harness J, Keirstead H, Vicente Sanchez-Mut J, Kaneki E, Lapunzina P, Soejima H, Wake N, Esteller M, Ogata T, Hata K, Nakabayashi K, Monk D*
- Journal Title
  
  Genome Res
  
  Volume: in press Issue: 4 Pages: 554-569
- DOI
  10.1101/gr.164913.113
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PLANNED-22132004, KAKENHI-PROJECT-22227002, KAKENHI-PROJECT-23249075, KAKENHI-PROJECT-23770273, KAKENHI-PROJECT-25253023, KAKENHI-PROJECT-25460409, KAKENHI-PROJECT-26670169
[Journal Article] Epigenetic and transcriptional features of the novel human imprinted lncRNA GPR1AS suggest it is a functional ortholog to mouse Zdbf2linc.2013
- Author(s)
  Kobayashi H, Yanagisawa E, Sakashita A, Sugawara N, Kumakura S, Ogawa H, Akutsu H, Hata K, Nakabayashi K, Kono T.
- Journal Title
  
  Epigenetics
  
  Volume: 8 (6) Issue: 6 Pages: 635-645
- DOI
  10.4161/epi.24887
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-22228004, KAKENHI-PROJECT-25450470, KAKENHI-PROJECT-25460409, KAKENHI-PROJECT-25870766
[Journal Article] Molecular and clinical studies in 138 Japanese patients with Silver-Russell syndrome2013
- Author(s)
  T. Fuke, S. Mizuno, T. Nagai, T. Hasegawa, R. Horikawa, Y. Miyoshi, K. Muroya, T. Kondoh, C. Numakura, S. Sato, K. Nakabayashi, C. Tayama, K. Hata, S. Sano, K. Matsubara, M. Kagami, K. Yamazawa, T. Ogata
- Journal Title
  
  PLoS. One
  
  Volume: 8 Issue: 3 Pages: e60105-e60105
- DOI
  10.1371/journal.pone.0060105
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-22227002, KAKENHI-PROJECT-22249010, KAKENHI-PROJECT-23390083, KAKENHI-PROJECT-24890229, KAKENHI-PROJECT-25860898
[Journal Article] Mosaic upd(7)mat in a patient with Silver-Russell syndrome: correlation between phenotype and mosaic ratio in the body and the placenta2012
- Author(s)
  Fuke-Sato T, Yamazawa K, Nakabayashi K, Matsubara K, Matsuoka K, Hasegawa T, Dobashi K, Ogata T*
- Journal Title
  
  Am J Med Genet A158A
  
  Volume: 2 Pages: 465-468
- Data Source
  KAKENHI-PROJECT-22249010
[Journal Article] Mosaic upd(7)mat in a patient with Silver-Russell syndrome: correlation between phenotype and mosaic ratio in the body and the placenta.2012
- Author(s)
  Fuke-Sato T, Yamazawa K, Nakabayashi K, Matsubara K, Matsuoka K, Hasegawa T, Dobashi K, Ogata T*
- Journal Title
  
  Am J Med Genet A
  
  Volume: 158A (2) Pages: 465-468
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-22249010
[Journal Article] Methylation screening of reciprocal genome-wide UPDs identifies novel human specific imprinted genes2011
- Author(s)
  Nakabayashi K*, Trujillo AM, Tayama C, Camprubi C, Yoshida W, Lapunzina P, Sanchez A, Soejima H, Aburatani H, Nagae G, Ogata T, Hata K, David Monk D
- Journal Title
  
  Hum Mol Genet20
  
  Volume: 16 Pages: 3188-97
- Data Source
  KAKENHI-PROJECT-22249010
[Journal Article] Androgenetic/biparental mosaicism in a girl with Beckwith-Wiedemann syndrome-like and upd(14)pat-like phenotypes2011
- Author(s)
  Yamazawa K, Nakabayashi K, Matsuoka K, Matsubara K, Hata K, Horikawa R, Ogata T*
- Journal Title
  
  J Hum Genet56
  
  Volume: 1 Pages: 91-93
- NAID
  10030657597
- Data Source
  KAKENHI-PROJECT-22249010
[Journal Article] Methylation screening of reciprocal genome-wide UPDs identifies novel human specific imprinted genes2011
- Author(s)
  Nakabayashi K, Ogata T, et al
- Journal Title
  
  Hum Mol Genet
  
  Volume: 20(16) Pages: 3188-97
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-22249010
[Journal Article] 【最近のGWAS研究の成果】神経性食欲不振症のゲノムワイド関連研究2010
- Author(s)
  中林一彦, 小牧元, 白澤専二
- Journal Title
  
  BIO Clinica
  
  Volume: 25 Pages: 494-499
- Data Source
  KAKENHI-PROJECT-20390201
[Journal Article] Androgenetic/biparental mosaicism in a girl with Beckwith-Wiedemann syndrome-like and upd (14) pat-like phenotypes2010
- Author(s)
  Yamazawa K, Nakabayashi K, Ogata T, 他
- Journal Title
  
  J Hum Genet
  
  Volume: 56(1) Pages: 91-93
- NAID
  10030657597
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-22249010
[Journal Article] A Parthenogenetic Female with a Silver-Russell Syndrome-like Phenotype and a 45, X Cell Lineage Accompanied by Biparentally Derived Autosomes.2010
- Author(s)
  Yamazawa K, Nakabayashi K, Kagami M, Satoh T, Hata K, Saitoh S, Nagai T, Horikawa R, Hizuka N, Ogata T.
- Journal Title
  
  Journal of Medical Genetics
  
  Volume: 47(11) Pages: 782-785
- Peer Reviewed
- Data Source
  KAKENHI-PUBLICLY-21028026
[Journal Article] 【最近のGWAS研究の成果】神経性食欲不振症のゲノムワイド関連研究2010
- Author(s)
  中林一彦,小牧元,白澤専二
- Journal Title
  
  BIO Clinica 25(6)
  
  Pages: 494-499
- Data Source
  KAKENHI-PROJECT-20390201
[Journal Article] Parthenogenetic chimaerism/mosaicism with a Silver-Russell Syndrome-like Phenotype2010
- Author(s)
  Yamazawa K, Nakabayashi K, Kagami M,Sato T, Saitoh S, Horikawa R, Hizuka N, Ogata T*
- Journal Title
  
  J Med Genet47
  
  Volume: 11 Pages: 782-785
- Data Source
  KAKENHI-PROJECT-22249010
[Journal Article] Parthenogenetic chimaerism/mosaicism with a Silver-Russell Syndrome-like Phenotype2010
- Author(s)
  Yamazawa K, Nakabayashi K, Kagami M, Ogata T, 他
- Journal Title
  
  J Med Genet
  
  Volume: 47(11) Pages: 782-785
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-22249010
[Journal Article] Identification of novel candidate loci for anorexia nervosa at lq41 and llq22 in Japanese by a genome-wide association analysis with micros atellite markers2009
- Author(s)
  Nakabayashi K, Komaki G, Tajima A, Ando T, Ishikawa M, Nomoto J, Hata K, Oka A, Inoko H, Sasazuki T, Japanese Genetic Research Group for Eating Disorders(JGRED), Shirasawa S.
- Journal Title
  
  J Hum Genet 54
  
  Pages: 531-537
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-20390201
[Journal Article] Japanese Genetic Research Group for Eating Disorders (JGRED), Shirasawa S.Identification of novel candidate loci for anorexia nervosa at 1q41 and 11q22 in Japanese by a genome-wide association analysis with microsatellite markers.2009
- Author(s)
  Nakabayashi K, Komaki G, Tajima A, Ando T, Ishikawa M, Nomoto J, Hata K, Oka A, Inoko H, Sasazuki T
- Journal Title
  
  J Hum Genet.(Epub) 54(9)
  
  Pages: 531-7
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-20390201
[Journal Article] ゲノムワイド解析による摂食障害遺伝子の探索と今後の課題2007
- Author(s)
  中林一彦, 白澤専二
- Journal Title
  
  心身医学 47・4
  
  Pages: 259-264
- Data Source
  KAKENHI-PROJECT-18790237
[Journal Article] ゲノムワイド解析による摂食障害遺伝子の探索と今後の課題2007
- Author(s)
  中林一彦, 白澤専二
- Journal Title
  
  心身医学 47・4
  
  Pages: 259-264
- Data Source
  KAKENHI-PROJECT-18018045
[Journal Article] Molecular and clinical studies in 138 Japanese patients with Silver-Russell syndrome
- Author(s)
  Fuke T, Mizuno S, Nagai T, Hasegawa T, Horikawa R, Miyoshi Y, Muroya K, Kondoh T, Numakura C, Sato S, Nakabayashi K, Tayama C, Hata K, Sano S, Matsubara K, Kagami M, Tamazawa K, Ogata T*
- Journal Title
  
  PLoS One (accepted)
- Data Source
  KAKENHI-PROJECT-22249010
[Journal Article] A Parthenogenetic Female with a Silver-Russell Syndrome-like Phenotype and a 45,X Cell Lineage Accompanied by Biparentally Derived Autosomes.
- Author(s)
  Yamazawa K, Nakabayashi K, Kagami M, Satoh T, Hata K, Saitoh S, Nagai T, Horikawa R, Hizuka N, Ogata T.
- Journal Title
  
  Journal of M edical Genetics (accepted)
- Peer Reviewed
- Data Source
  KAKENHI-PUBLICLY-21028026
[Patent] 慢性子宮内膜炎診断薬2022
- Inventor(s)
  大科恭子、黒田恵司、秦健一郎、中林一彦
- Industrial Property Rights Holder
  大科恭子、黒田恵司、秦健一郎、中林一彦
- Industrial Property Rights Type
  特許
- Industrial Property Number
  2022-199458
- Filing Date
  2022
- Data Source
  KAKENHI-PROJECT-23K24490
[Presentation] 上皮細胞シートの作製とナノ微粒子暴露による影響2024
- Author(s)
  宮本義孝, 岡﨑有香, 寺本直純, 河合智子, 梅澤明弘, 中林一彦
- Organizer
  第23回日本再生医療学会総会
- Data Source
  KAKENHI-PROJECT-23K28470
[Presentation] 磁性ナノ粒子暴露による細胞バリア機能の評価2024
- Author(s)
  野口彩子, 岡﨑有香, 河合智子, 中林一彦, 桝田晃司, 宮本義孝
- Organizer
  電気学会医用・生体工学研究会
- Data Source
  KAKENHI-PROJECT-23K28470
[Presentation] Application of single-cell multiomics technology to establish an effective screening method for identifying fetal nucleated red blood cells suitable for non-invasive prenatal genetic testing.2023
- Author(s)
  Ito N, Fujii T, Taniguchi1 K, Hata K, Sago H, Nakabayashi K.
- Organizer
  American Society of Human Genetics Annual Meeting 2023.11.13
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-23K24490
[Presentation] Characterization of the impact of NSD2 loss on the transcriptional and epigenetic landscape in the brain.2023
- Author(s)
  Kinoshita S, Kojima K, Ohnishi E, Takayama Y, Kikuchi H, Takada S, Nakabayashi K, Kawai T, Hata K. :
- Organizer
  American Society of Human Genetics Annual Meeting 2023.11.13
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-23K24490
[Presentation] エピシグナチャー解析による歌舞伎症候群男児症例におけるKDM6A疾患責任体細胞系列バリアントの同定2023
- Author(s)
  中林一彦,河合智子, 岩崎裕治, 緒方広子, 嘉村浩美, 中村和昭, 秦健一郎, 高野貴子
- Organizer
  第46回日本小児遺伝学会学術集会
- Data Source
  KAKENHI-PROJECT-23K24490
[Presentation] 希少遺伝性疾患ゲノム診断のためのDNAメチル化キャプチャーシーケンス法の開発2023
- Author(s)
  長谷川慶太，河合智子，春日義史，副島英伸，岡本伸彦，田中守，秦健一郎，中林一彦
- Organizer
  第31回日本医学会総会2023東京6NCリトリート 2023.4.22
- Data Source
  KAKENHI-PROJECT-23K24490
[Presentation] 健常者集団中のエピバリアントを視覚的に確認できるウェブビューワの構築2022
- Author(s)
  青砥早希、秦健一郎、中林一彦
- Organizer
  日本人類遺伝学会
- Data Source
  KAKENHI-PROJECT-23K24490
[Presentation] 希少疾患ゲノム診断率向上のためのエピゲノムアプローチ2022
- Author(s)
  中林一彦
- Organizer
  エピジェネティクス研究会
- Invited
- Data Source
  KAKENHI-PROJECT-23K24490
[Presentation] 希少遺伝性疾患ゲノム診断率向上に向けてのDNAメチル化キャプチャーシーケンス法の開発．2022
- Author(s)
  4.長谷川慶太，中林一彦，河合智子，青砥早希，春日義史，副島英伸，岡本伸彦，田中守，秦健一郎
- Organizer
  日本人類遺伝学会
- Data Source
  KAKENHI-PROJECT-21H02887
[Presentation] エピバリアントを有するプロモータ領域および検体を検出するEpimutation Finderの開発2022
- Author(s)
  青砥早希、秦健一郎、中林一彦
- Organizer
  日本分子生物学会
- Data Source
  KAKENHI-PROJECT-23K24490
[Presentation] Amplicon sequencing-based noninvasive fetal genotyping for RHDPositive D antigen-negative alleles.2022
- Author(s)
  Hori A, Sasaki A, Takahashi K, Ogata-Kawata H, Taniguchi K, Migita O, Kawashima A, Okamoto A, Sekizawa A, Sago H, Takada F, Hata K, Nakabayashi K
- Organizer
  ASHG 2022 Annual Meeting
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-23K24490
[Presentation] 先天性疾患ゲノム診断率向上のためのエピゲノムアプローチ2020
- Author(s)
  中林一彦
- Organizer
  日本人類遺伝学会
- Invited
- Data Source
  KAKENHI-PROJECT-17K08689
[Presentation] マウス妊娠期ヒ素曝露によって誘導される仔精子のLINEおよびLTRレトロトランスポゾンのDNAメチル化変化2020
- Author(s)
  野原恵子,中林一彦,岡村和幸,鈴木武博,秦健一郎
- Organizer
  第14回日本エピジェネティクス研究会年会
- Data Source
  KAKENHI-PROJECT-18K19860
[Presentation] マウス妊娠期ヒ素曝露による仔精子レトロトランスポゾン転写調節領域のメチル化低下2020
- Author(s)
  野原恵子、中林一彦、岡村和幸、鈴木武博、秦健一郎
- Organizer
  第90回日本衛生学会学術総会
- Data Source
  KAKENHI-PROJECT-18K19860
[Presentation] マウス妊娠期無機ヒ素曝露による仔精子レトロトランスポゾンのDNAメチル化低下2019
- Author(s)
  野原恵子，中林一彦，岡村和幸，鈴木武博，秦健一郎
- Organizer
  第42回日本分子生物学会年会
- Data Source
  KAKENHI-PROJECT-18K19860
[Presentation] ヒトインプリンティング制御領域の網羅的同定と疾患エピ変異診断プラットフォームへの応用2019
- Author(s)
  田山千春、鏡雅代、副島英伸、緒方勤、秦健一郎、David Monk、中林一彦
- Organizer
  エピジェネティックス研究会
- Data Source
  KAKENHI-PROJECT-17K08689
[Presentation] マウス妊娠期無機ヒ素曝露による仔精子レトロトランスポゾンのDNAメチル化低下2019
- Author(s)
  野原恵子, 中林一彦, 岡村和幸, 鈴木武博, 秦健一郎
- Organizer
  日本分子生物学会年会
- Data Source
  KAKENHI-PROJECT-18H03556
[Presentation] KLF14欠損マウスにおける腹部脂肪分布・脂質代謝の変化2019
- Author(s)
  田山千春、高梨理絵子、齋藤公亮、冨川順子、進導美幸、大喜多肇、津村秀樹、高田修治、松本健治、秦健一郎、岡村匡史、中林一彦
- Organizer
  日本分子生物学会
- Data Source
  KAKENHI-PROJECT-17K08689
[Presentation] Small RNA sequencingを用いた妊娠期無機ヒ素曝露による子世代精子で変化するtRNA fragmentsの探索2019
- Author(s)
  岡村和幸, 中林一彦, 石渡啓介, 鈴木武博, 秦健一郎, 野原恵子
- Organizer
  日本分子生物学会年会
- Data Source
  KAKENHI-PROJECT-18H03556
[Presentation] マウス妊娠期無機ヒ素曝露による仔の精子DNAメチル化変化の解析2019
- Author(s)
  野原恵子, 中林一彦, 岡村和幸, 鈴木武博, 秦健一郎
- Organizer
  第8回日本DOHaD学会学術集会
- Data Source
  KAKENHI-PROJECT-18K19860
[Presentation] pigenomics for child health and development: genomic imprinting and beyond2018
- Author(s)
  中林一彦
- Organizer
  30th Anniversary of Andrew Sass-Kortsak Award Symposium
- Invited
- Data Source
  KAKENHI-PROJECT-17K08689
[Presentation] 妊娠期無機ヒ素曝露による孫世代（F2）の肝腫瘍増加に関与する仔世代（F1）精子のエピゲノム変化2018
- Author(s)
  野原恵子、岡村和幸、鈴木武博、中林一彦、秦健一郎
- Organizer
  第41回日本分子生物学会年会
- Data Source
  KAKENHI-PROJECT-18K19860
[Presentation] 表現型可塑性におけるエピゲノムの役割2018
- Author(s)
  中林一彦
- Organizer
  第20回大会日本進化学会
- Invited
- Data Source
  KAKENHI-PROJECT-17K08689
[Presentation] F0マウス妊娠期ヒ素曝露がF1雄を介してF2世代で肝腫瘍を増加させる機序の探索：F1精子のDNAメチル化解析2018
- Author(s)
  野原恵子，岡村和幸，中林一彦，松下隼也，鈴木武博，市原学，秦健一郎
- Organizer
  第12回日本エピジェネティクス研究会年会
- Data Source
  KAKENHI-PROJECT-18K19860
[Presentation] 全エクソーム解析キット(SureSelect, TruSeq Exome)のパフォーマンス比較2018
- Author(s)
  緒方（川田）広子，渡邊豊，長井陽子，秦健一郎，中林一彦
- Organizer
  第41回日本分子生物学会年会
- Data Source
  KAKENHI-PROJECT-17K08689
[Presentation] 発生段階特異的な機能的ゲノム高次構造の探索2018
- Author(s)
  冨川順子，西園啓文，秦健一郎，中林一彦
- Organizer
  第12回日本エピジェネティクス研究会年会
- Data Source
  KAKENHI-PROJECT-17K08689
[Presentation] 霊長類エピゲノム多様性と進化（インプリンティング制御領域を中心に）2017
- Author(s)
  中林一彦
- Organizer
  日本進化学会
- Invited
- Data Source
  KAKENHI-PROJECT-17K08689
[Presentation] エピゲノム研究：最近の進歩と人類進化・多様性研究への応用2017
- Author(s)
  中林一彦
- Organizer
  日本人類学会
- Invited
- Data Source
  KAKENHI-PROJECT-17K08689
[Presentation] Novel DNA methylation changes induced by gestational arsenite exposure in hepatic tumors in F2 mice.2016
- Author(s)
  岡村和幸、中林一彦、堀部悠、河合智子、鈴木武博、秦健一郎、野原恵子
- Organizer
  第5回日本DOHaD研究会学術集会
- Place of Presentation
  国立成育医療研究センター（東京）
- Year and Date
  2016-07-23
- Data Source
  KAKENHI-PROJECT-26293154
[Presentation] 父性遺伝する食事誘導性肥満におけるインプリント遺伝子の解析と新規インプリント遺伝子の探索について．2016
- Author(s)
  森田純代，中林一彦，河合智子，林恵子，堀居拓郎，木村美香，亀井康富，小川佳宏，秦健一郎，畑田出穂
- Organizer
  第10回日本エピジェネティクス研究会年会
- Place of Presentation
  大阪
- Data Source
  KAKENHI-PROJECT-25460409
[Presentation] C3HマウスにおいてDNAメチル化変化を介して肝腫瘍形成に関与する遺伝子の探索2016
- Author(s)
  松下隼也、岡村和幸、鈴木武博、中林一彦、堀部悠、河合智子、秦健一郎、桜井敏博、市原学、野原恵子
- Organizer
  第10回日本エピジェネティクス研究会
- Place of Presentation
  千里ライフサイエンスセンター（大阪）
- Year and Date
  2016-05-19
- Data Source
  KAKENHI-PROJECT-26293154
[Presentation] KLF14 involves in controlling inflammation in the white adipose tissue.2016
- Author(s)
  Tayama C, Takanashi R, Tomikawa J, Okita H, Hata K, Okamura T, Nakabayashi K.
- Organizer
  The 13th International Congress of Human Genetics
- Place of Presentation
  Kyoto
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-25460409
[Presentation] 成育・周産期関連疾患解明のためのエピゲノム解析2016
- Author(s)
  中林一彦
- Organizer
  金沢大学学際科学実験センター・サイエンスセミナー
- Place of Presentation
  金沢
- Invited
- Data Source
  KAKENHI-PROJECT-25460409
[Presentation] 次世代シーケンサーを用いた遺伝子・ゲノム診断2015
- Author(s)
  中林一彦
- Organizer
  第25回日本サイトメトリー学会学術集会
- Place of Presentation
  東京
- Year and Date
  2015-07-12
- Invited
- Data Source
  KAKENHI-PROJECT-25460409
[Presentation] 転写因子 KLF14 の白色脂肪組織における炎症制御への関与2015
- Author(s)
  中林一彦,田山千春，高梨理絵子，冨川順子，大喜多肇，秦健一郎，岡村匡史
- Organizer
  日本人類遺伝学会第60回大会
- Place of Presentation
  東京
- Year and Date
  2015-10-15
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-25460409
[Presentation] 14番染色体インプリンティング異常症エピ変異例に対する網羅的DMRメチル化解析および臨床像についての検討2015
- Author(s)
  鏡雅代、松原圭子、中林一彦、嘉村浩美、中村明枝、深見真紀、緒方勤
- Organizer
  第49回日本小児内分泌学会学術集会
- Place of Presentation
  東京
- Year and Date
  2015-10-08
- Data Source
  KAKENHI-PROJECT-15K15096
[Presentation] KLF14 involves in controlling inflammation in the white adipose tissue.2015
- Author(s)
  Tayama C, Takanashi E, Tomikawa J, Okita H, Hata K, Okamura T, Nakabayashi K
- Organizer
  The 65th Annual Meeting of the American Society of Human Genetics
- Place of Presentation
  Baltimore
- Year and Date
  2015-10-07
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-25460409
[Presentation] 転写因子KLF14の白色脂肪組織における炎症制御への関与2014
- Author(s)
  田山千春，高梨(矢延) 理絵子，富川順子，大喜多肇，秦健一郎，岡村匡史，中林一彦
- Organizer
  第37回日本分子生物学会年会
- Place of Presentation
  横浜
- Year and Date
  2014-11-25
- Data Source
  KAKENHI-PROJECT-25460409
[Presentation] ヒトインプリントーム解析から見えてきたヒト（霊長類）特異的エピゲノム進化2014
- Author(s)
  中林一彦
- Organizer
  京都大学霊長類研究所・研究会「霊長類への展開に向けた幹細胞・生殖細胞・エピゲノム研究」
- Place of Presentation
  京都大学・霊長類研究所
- Year and Date
  2014-08-27
- Invited
- Data Source
  KAKENHI-PROJECT-25460409
[Presentation] Japanese Genetic Research Group For Eating Disorders (JGRED) : Genetic study for Japanese anorexia nervosa patients bygenome-wide association analysis with microsatellite markers.2010
- Author(s)
  Komaki G, Nakabayashi K, Ando T, Inoko H, Shirasawa S
- Organizer
  The 14th Congress of the Asian College of Psychosomatic Medicine
- Place of Presentation
  Beijing,
- Data Source
  KAKENHI-PROJECT-20390201
[Presentation] SNP相関解析による摂食障害感受性遺伝子の探索2007
- Author(s)
  中林一彦
- Organizer
  日本人類遺伝学会
- Place of Presentation
  東京
- Year and Date
  2007-09-14
- Data Source
  KAKENHI-PROJECT-18790237
[Presentation] SNP相関解析による摂食障害感受性遺伝子の探索2007
- Author(s)
  中林一彦
- Organizer
  日本人類遺伝学会
- Place of Presentation
  東京
- Year and Date
  2007-09-14
- Data Source
  KAKENHI-PROJECT-18018045

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NAKABAYASHI Kazuhiko 中林 一彦

中林 一彦 ナカバヤシ カズヒコ

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Elucidation of 3D genome architecture of human placental and endometrial cellsPrincipal Investigator

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Establishment and diagnostic application of epigenome sequencing methods for imprinted differentially methylated regionsPrincipal Investigator

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NAKABAYASHI Kazuhiko 中林一彦

中林一彦ナカバヤシカズヒコ