SUZUKI Hisato

Affiliation

Institute of Medicine

Official title

Associate Professor

ORCID

0000-0002-8122-7180

Research fields

Human genetics
Pediatrics

Research keywords

rare disease
exome analysis, exome sequencing
metagenome
genetic analysis

Research projects

新規ウイルス探索を含めた川崎病患者に対するショットガンメタゲノム解析	2022-04 -- (current)	Hisato Suzuki	Kakenhi//科学研究費助成事業（学術研究助成基金助成金）基盤研究(c)(一般）
超長寿者を比較対象とした肺高血圧患者の遺伝子構造異常解析とリスク評価	2020-04 -- 2022-03	Hisato Suzuki	Kakenhi/若手研究
食物アレルギーの発症における腸内細菌叢の役割の解明	2017-04 -- 2021-03	Hisato Suzuki	Kakenhi/Grants-in-Aid for Scientific Research(若手研究(B))

Academic background

2014-04 -- 2017-03	Universit of Tsukuba Graduate School of Comprehensive Human Sciences Doctoral program in Clinical Sciences
2003-04 -- 2009-03	University of Tsukuba 医学専門学群 医学類

Degree

2009-03	M.D.	University of Tsukuba
2017-03	Ph.D.	University of Tsukuba

Licenses and qualifications

2019-11	臨床遺伝専門医
2019-04	日本アレルギー学会専門医
2014-10	日本小児科学会専門医
2009-04	Medical license

Academic societies

2017 -- (current)	日本小児遺伝学会
2017 -- (current)	JAPANESE TERATOLOGY SOCIETY
2012 -- (current)	JAPANESE SOCIETY OF ALLERGOLOGY
2015 -- (current)	THE JAPAN SOCIETY OF HUMAN GENETICS
2011 -- (current)	JAPAN PEDIATRIC SOCIETY

Articles

• Forebrain commissure formation in zebrafish embryo requires the binding of KLC1 to CRMP2
  Li Simo; Guo Youjia; Takahashi Miyuki; Suzuki Hisato; ...
  Developmental neurobiology/84(3)/pp.203-216, 2024-07-01
  
  PubMed
• Janus kinase inhibitors ameliorate clinical symptoms in patients with STAT3 gain-of-function
  Kaneko Shuya; Sakura Fumiaki; Tanita Kay; Shimbo Asam...
  Immunotherapy advances/3(1)/p.ltad027, 2023-04-01
  
  PubMed
• Biallelic loss-of-function variants in the centriolar protein CCP110 leads to a ciliopathy-like phenotype(s)
  Suzuki Hisato; Muramatsu Yukako; Miya Fuyuki; Asada H...
  European journal of medical genetics, 2024-06-08
  
  PubMed
• Gut microbiota of one-and-a-half-year-old food-allergic and healthy children
  Hara Monami; Suzuki Hisato; Hayashi Daisuke; Morii Wa...
  Allergology international : official journal of the Japanese Society of Allergology, 2024-04-09
  
  PubMed
• Gene-specific somatic epigenetic mosaicism of FDFT1 underlies a non-hereditary localized form of porokeratosis
  Saito Sonoko; Saito Yuki; Sato Showbu; Aoki Satomi; F...
  The American Journal of Human Genetics, 2024-04
• Truncating variants of the sterol recognition region of SHH cause hypertelorism phenotype rather than hypotelorism-holoprosencephaly
  Yamada Mamiko; Mizuno Seiji; Inaba Mie; Uehara Tomoko...
  American journal of medical genetics. Part A, 2024-04-02
  
  PubMed
• A novel missense variant of FGD1 disrupts critical cysteine residues of the FYVE domain in Japanese siblings with Aarskog-Scott syndrome
  Takahashi Ikuko; Noguchi Atsuko; Kondo Daiki; Sato Yo...
  Clinical pediatric endocrinology : case reports and clinical investigations : official journal of the Japanese Society for Pediatric Endocrinology/33(1)/pp.39-42, 2024-04-01
  
  PubMed
• Successful skipping of abnormal pseudoexon by antisense oligonucleotides in vitro for a patient with beta-propeller protein-associated neurodegeneration
  Yamada Mamiko; Maeta Kazuhiro; Suzuki Hisato; Kurosawa...
  Scientific reports/14(1)/p.6506, 2024-03-18
  
  PubMed
• Identification of a novel splice-site WWOX variant with paternal uniparental isodisomy in a patient with infantile epileptic encephalopathy
  Nishino Megumi; Tanaka Mai; Imagawa Kazuo; Yaita Kats...
  AMERICAN JOURNAL OF MEDICAL GENETICS PART A/194(7), 2024-02-26
  
  PubMed
• SALL4 deletion and kidney and cardiac defects associated with VACTERL association
  Watanabe Daisuke; Nakato Daisuke; Yamada Mamiko; Suzuk...
  Pediatric nephrology (Berlin, Germany), 2024-02-08
  
  PubMed
• X -linked inheritance of primary ciliary dyskinesia and retinitis pigmentosa due to RPGR variant: A case report and literature review
  Kuroda Aoi; Namkoong Ho; Iwami Eri; Tsutsumi Akihiro; ...
  Respirology case reports/11(12), 2023-12-01
  
  PubMed
• BMP2 is a potential causative gene for isolated dextrocardia situs solitus
  Yogi Analia; Iemura Ryosei; Nakatani Hisae; Takasawa ...
  European journal of medical genetics/66(9), 2023-09-01
  
  PubMed
• Heterozygous loss-of-function DHX9 variants are associated with neurodevelopmental disorders: Human genetic and experimental evidences
  Yamada Mamiko; Nitta Yohei; Uehara Tomoko; Suzuki His...
  European journal of medical genetics/66(8), 2023-08-01
  
  PubMed
• Café-au-lait Spots and Cleft Palate: Not a Chance Association
  Yamada Mamiko; Tanito Katsumi; Suzuki Hisato; Nakato ...
  The Cleft palate-craniofacial journal : official publication of the American Cleft Palate-Craniofacial Association, 2023-07-14
  
  PubMed
• Oculofaciocardiodental syndrome caused by a novel BCOR variant
  Yamashita Tomoyo; Hotta Junko; Jogu Yukiko; Sakai Eri...
  Human genome variation/10(1)/p.18, 2023-06-12
  
  PubMed
• Parkinsonism in spinocerebellar ataxia with axonal neuropathy caused by adult-onset COA7 variants: a case report
  Ouchi Shogo; Ishii Kazuhiro; Kosaki Kenjiro; Suzuki H...
  BMC NEUROLOGY/23(1)/p.211, 2023-06-01
  
  PubMed
• Ketogenic diet in action: Metabolic profiling of pyruvate dehydrogenase deficiency
  Ogawa Eri; Hishiki Takako; Hayakawa Noriyo; Suzuki Hi...
  Molecular genetics and metabolism reports/35, 2023-06-01
  
  PubMed
• Involvement of mTOR pathway in neurodegeneration in NSF-related developmental and epileptic encephalopathy
  Hayashi Takahiro; Yano Naoko; Kora Kengo; Yokoyama At...
  Human molecular genetics/32(10)/pp.1683-1697, 2023-05-05
  
  PubMed
• Marked hypertriglyceridemia with a novel splicing mutation in GPIHBP1
  Kawahara Sakura; Imagawa Kazuo; Suzuki Hisato; Ohto T...
  PEDIATRICS INTERNATIONAL/65(1), 2023-04-01
  
  PubMed
• Oral Baclofen Therapy for Multifocal Spinal Myoclonus with TBC1D24 Variant
  Murofushi Yuka; Hayakawa Itaru; Kawai Michiko; Abe Yu...
  Movement disorders clinical practice/10(4)/pp.719-721, 2023-04-01
  
  PubMed
• Precise definition of the breakpoints of an apparently balanced translocation between chromosome 3q26 and chromosome 7q36: Role of KMT2C disruption
  Yamada Mamiko; Suzuki Hisato; Miya Fuyuki; Kosugiyama ...
  Congenital anomalies, 2023-03-22
  
  PubMed
• Familial café-au-lait macules associated with in-frame deletion of NF1 p.Met992del mimicking Legius syndrome
  Nakato Daisuke; Yamada Mamiko; Suzuki Hisato; Takenouc...
  Congenital anomalies/63(2)/pp.54-55, 2023-03-01
  
  PubMed
• A novel variant of ARPC4-related neurodevelopmental disorder
  Kuroda Yukiko; Kumaki Tatsuro; Saito Yoko; Enomoto Yu...
  American journal of medical genetics. Part A/191(3)/pp.893-895, 2023-03-01
  
  PubMed
• Diagnosis of Prader-Willi syndrome and Angelman syndrome by targeted nanopore long-read sequencing
  Yamada Mamiko; Okuno Hironobu; Okamoto Nobuhiko; Suzuk...
  European journal of medical genetics/66(2), 2023-02-01
  
  PubMed
• De novo non-synonymous DPYSL2 (CRMP2) variants in two patients with intellectual disabilities and documentation of functional relevance through zebrafish rescue and cellular transfection experiments
  Suzuki Hisato; Li Simo; Tokutomi Tomoharu; Takeuchi C...
  Human molecular genetics/31(24)/pp.4173-4182, 2022-12-16
  
  PubMed
• more...

Conference, etc.

• 小児遺伝性疾患患者を対象としたPubcaseFinderを用いた疾患候補遺伝子パネルの検討
  鈴木 寿人
  第46回日本小児遺伝学会学術集会/2023-12-08--2023-12-09
• Genetic analysis in preventive medicine and following medical management
  SUZUKI Hisato
  Human Genetics Asia 2023/2023-10-11--2023-10-14
• 小児遺伝性疾患の診断技術と創薬における将来展望
  鈴木 寿人
  BioJapan2023/2023-10-11--2023-10-13
• IRUDに関わって
  鈴木 寿人
  2023年IRUDワークショップ/2023-07-14--2023-07-14
• 重症新生児・乳幼児に対する迅速なゲノム診断の全国ネットワーク構築
  鈴木 寿人
  第126回日本小児科学会学術集会/2023-04-14--2023-04-16
• 脳梗塞を契機に診断に至ったアデノシンデアミナーゼ2欠損症の21歳女性例
  奥根祥; 早川幹人; 穂坂 翔; 鈴木寿人; 高田英俊; 斉木臣二; 松丸祐司
  第247回日本神経学会関東・甲信越地方会/2023-12-2

Teaching

2023-04 -- (current)	小児の成長・発達と疾患系	筑波大学　医学専門学群医学類

Talks

• 単因子遺伝・ゲノム解析の基礎
  鈴木 寿人
  第10回総合アレルギー講習会/2024-03-16--2024-03-17

Professional activities

2023-11 -- 2025-03	JAPANESE TERATOLOGY SOCIETY	評議員

(Last updated: 2024-07-23)