IGARASHI Maki 五十嵐麻希

Researcher Number	10623035
Other IDs
Affiliation (Current)	2025: 国立研究開発法人国立成育医療研究センター, 分子内分泌研究部, (非)研究員 2025: 国立研究開発法人国立がん研究センター, がん対策研究所, 特任研究員
Affiliation (based on the past Project Information) *help	2024 – 2025: 国立研究開発法人国立がん研究センター, がん対策研究所, 特任研究員 2021: 東京大学, 大学院農学生命科学研究科(農学部), 特任助教 2020: 東京大学, 大学院農学生命科学研究科(農学部), 特任研究員 2017 – 2020: 国立研究開発法人国立成育医療研究センター, 分子内分泌研究部, (非)研究員 2016 – 2018: 国立研究開発法人国立成育医療研究センター, 分子内分泌研究部, 共同研究員 … More 2016: 国立成育医療研究センター, 分子内分泌研究部, 研究員 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, 研究員 2014: 独立行政法人国立成育医療研究センター, 分子内分泌研究部, 研究員 2013 – 2014: 独立行政法人国立成育医療研究センター, その他部局等, 研究員 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 Less
Review Section/Research Field	Principal Investigator Pediatrics / Basic Section 58020:Hygiene and public health-related: including laboratory approach / Basic Section 59040:Nutrition science and health science-related Except Principal Investigator Basic Section 38050:Food sciences-related / Urology / Endocrinology / Human genetics
Keywords	Principal Investigator 性分化疾患（DSD） / アレイCGH / 次世代シークエンス / 性分化疾患 / プレシジョン栄養 / ゲノム編集 / NR5A1 / 次世代シークエンス（NGS） / 腸内細菌 / 大腸腫瘍 … More / 短鎖脂肪酸 / ALDH2*2 / 栄養疫学 / ノックインマウス / ゲノム編集技術 / 12q24領域 / 多因子疾患予防 / 食嗜好 / オンライン料理画像調査 / フェノムワイド関連解析 / ゲノムワイド関連解析 / ゲノム編集マウス / BMI / 食事画像調査 / アルコール脱水素酵素 / 食事調査法 / うまみ嗜好性 / 食行動 / rs671 / ALDH2 / 一塩基多型 / テーラーメイド栄養 / 次世代シークエンサ－ / ゲノム解析 / スプライス異常 / 機能亢進変異 / エクソーム解析 / PROKR2 / GATA4 / 遺伝子変異 / ナンセンス随伴性スプライス変更 / AR / MAP3K1 / 遺伝子解析 / NR0B1 / SOX9 / ｱﾚｲCGH / ベトナム / 国際情報交換 … More Except Principal Investigator ゲノム / 遺伝子 / 疾患 / メチル化 / エピゲノム / 個別化栄養 / プレシジョン栄養学 / 分析科学 / 人類学 / 遺伝学 / 停留精巣 / 先天性尿道形成異常 / 無精子症 / 尿道下裂 / 先天性尿道形成異常症 / 生殖内分泌 / 内分泌学 / 生殖 / 性分化 / 内分泌 / 染色体 / 染色体微細構造異常 / 細胞遺伝学 Less

Association between dietary fiber intake and colorectal tumors depending on the abundance of short-chain fatty acid-producing microbiotaPrincipal Investigator
- Principal Investigator
  
  五十嵐麻希
- Project Period (FY)
  2025 – 2027
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Review Section
  
  Basic Section 58020:Hygiene and public health-related: including laboratory approach
- Research Institution
  National Cancer Center Japan
Establishment of precision nutrition platform based on interaction of genome and epigenome
- Principal Investigator
  
  加藤久典
- Project Period (FY)
  2024 – 2026
- Research Category
  
  Grant-in-Aid for Scientific Research (B)
- Review Section
  
  Basic Section 38050:Food sciences-related
- Research Institution
  Kagawa Nutrition University
Molecular basis research for personalized nutritionPrincipal Investigator
- Principal Investigator
  
  Igarashi Maki
- Project Period (FY)
  2019 – 2021
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Review Section
  
  Basic Section 59040:Nutrition science and health science-related
- Research Institution
  The University of Tokyo
  National Center for Child Health and Development
Elucidation of the pathogenic mechanism of congenital urethral anomaly by comprehensive genetic and endocrine analysis
- Principal Investigator
  
  Nakamura Shigeru
- Project Period (FY)
  2017 – 2020
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Urology
- Research Institution
  Jichi Medical University
  National Center for Child Health and Development
Elucidation of pathogenic mechanisms of disorders of sex development using systematic molecular analysisPrincipal Investigator
- Principal Investigator
  
  Igarashi Maki
- Project Period (FY)
  2016 – 2018
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Pediatrics
- Research Institution
  National Center for Child Health and Development
Identification and functional elucidation of genetic abnormalities in patients with disorders of sex development using next-generation approachesPrincipal Investigator
- Principal Investigator
  
  IGARASHI MAKI
- Project Period (FY)
  2014 – 2015
- Research Category
  
  Grant-in-Aid for Young Scientists (B)
- Research Field
  
  Pediatrics
- Research Institution
  National Center for Child Health and Development
Clarification of molecular basis of pubertal disorders and disorders of sex development
- Principal Investigator
  
  Fukami Maki
- Project Period (FY)
  2014 – 2016
- Research Category
  
  Grant-in-Aid for Scientific Research (B)
- Research Field
  
  Endocrinology
- Research Institution
  National Center for Child Health and Development
Genetic and environmental factors involved in human genomic instability
- Principal Investigator
  
  FUKAMI maki
- Project Period (FY)
  2013 – 2014
- Research Category
  
  Grant-in-Aid for Challenging Exploratory Research
- Research Field
  
  Human genetics
- Research Institution
  National Research Institute for Child Health and Development
Identification and functional elucidation of novel causative genes in patients with disorders of sex developmentPrincipal Investigator
- Principal Investigator
  
  IGARASHI Maki
- Project Period (FY)
  2012 – 2013
- Research Category
  
  Grant-in-Aid for Young Scientists (B)
- Research Field
  
  Pediatrics
- Research Institution
  National Research Institute for Child Health and Development

All 2022 2021 2020 2019 2018 2017 2016 2015 2014 2013 2012 Other

All Journal Article Presentation Book

[Book] 日常診療における性分化の診かた。性分化疾患と遺伝子異常。2014
- Author(s)
  五十嵐　麻希、深見　真紀
- Total Pages
  5
- Publisher
  小児内科
- Data Source
  KAKENHI-PROJECT-26860837
[Journal Article] Collection of 2429 constrained headshots of 277 volunteers for deep learning2022
- Author(s)
  Aoto Saki、Hangai Mayumi、Ueno-Yokohata Hitomi、Ueda Aki、Igarashi Maki、Ito Yoshikazu、Tsukamoto Motoko、Jinno Tomoko、Sakamoto Mika、Okazaki Yuka、Hasegawa Fuyuki、Ogata-Kawata Hiroko、Namura Saki、Kojima Kazuaki、Kikuya Masao、Matsubara Keiko、Taniguchi Kosuke、Okamura Kohji
- Journal Title
  
  Scientific reports
  
  Volume: 12 Issue: 1 Pages: 3730-3730
- DOI
  10.1038/s41598-022-07560-2
- Peer Reviewed / Open Access / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-19K11709, KAKENHI-PROJECT-19J21185, KAKENHI-PROJECT-21K06143
[Journal Article] Dietary supplement use in elementary school children: a Japanese web-based survey2021
- Author(s)
  Ishitsuka Kazue、Sasaki Satoshi、Mezawa Hidetoshi、Konishi Mizuho、Igarashi Maki、Yamamoto-Hanada Kiwako、Nakayama Shoji F.、Ohya Yukihiro
- Journal Title
  
  Environmental Health and Preventive Medicine
  
  Volume: 26 Issue: 1 Pages: 63-63
- DOI
  10.1186/s12199-021-00985-7
- NAID
  210000159107
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-19K11709
[Journal Article] Female-dominant estrogen production in healthy young children before adrenarche.2021
- Author(s)
  Maki Igarashi, Tadayuki Ayabe, Kiwako Yamamoto-Hanada, Keiko Matsubara, Hatoko Sasaki, Mayako Saito-Abe, Miori Sato, Nathan Mise, Akihiko Ikegami, Masayuki Shimono, Reiko Suga, Shouichi Ohga, Masafumi Sanefuji, Masako Oda, Hiroshi Mitsubuchi, Takehiro Michikawa, Shin Yamazaki, Shoji Nakayama, Yukihiro Ohya, Maki Fukami
- Journal Title
  
  Endocrine connections
  
  Volume: 10 Issue: 10 Pages: 1221-1226
- DOI
  10.1530/ec-21-0134
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-19K11709, KAKENHI-PLANNED-17H06428, KAKENHI-PROJECT-20H00550
[Journal Article] A Genome-wide association study identifies the association between the 12q24 locus and black tea consumption in Japanese populations.2020
- Author(s)
  Furukawa, K., Igarashi, M., Jia, H., Nogawa, S., Kawafune, K., Hachiya, T., Takahashi, S., Saito, K. and Kato, H.
- Journal Title
  
  Nutrients
  
  Volume: 12 Issue: 10 Pages: 3182-3182
- DOI
  10.3390/nu12103182
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-19K11709, KAKENHI-PROJECT-19J01450, KAKENHI-PROJECT-16H06277
[Journal Article] Dihydrotestosterone induces minor transcriptional alterations in genital skin fibroblasts of children with and without androgen insensitivity2019
- Author(s)
  Tanase-Nakao Kanako、Mizuno Kentaro、Hayashi Yutaro、Kojima Yoshiyuki、Hara Mariko、Matsumoto Kenji、Matsubara Yoichi、Igarashi Maki、Miyado Mami、Fukami Maki
- Journal Title
  
  Endocr J
  
  Volume: 66 Issue: 4 Pages: 387-393
- DOI
  10.1507/endocrj.EJ18-0494
- NAID
  130007636463
- ISSN
  0918-8959, 1348-4540
- Language
  English
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PLANNED-17H06428, KAKENHI-PROJECT-17J40246, KAKENHI-PROJECT-18J21048, KAKENHI-PROJECT-16K08603, KAKENHI-PROJECT-16K09979, KAKENHI-PROJECT-17K11204
[Journal Article] A Follow-Up from Infancy to Puberty in a Japanese Male with SRY-Negative 46,XX Testicular Disorder of Sex Development Carrying a p.Arg92Trp Mutation in NR5A12019
- Author(s)
 Saito-Hakoda Akiko、Kanno Junko、Suzuki Dai、Kawashima Sayaka、Kamimura Miki、Hirano Koji、Sakai Kiyohide、Igarashi Maki、Fukami Maki、Fujiwara Ikuma
- Journal Title
 
 Sexual Development
 
 Volume: 印刷中 Issue: 2 Pages: 60-66
- DOI
 10.1159/000496777
- Peer Reviewed
- Data Source
 KAKENHI-PLANNED-17H06428, KAKENHI-PROJECT-17J40246, KAKENHI-PROJECT-16K09979
[Journal Article] Identification of the 12q24 locus associated with fish intake frequency by genome-wide meta-analysis in Japanese populations.2019
- Author(s)
  Igarashi M, Nogawa S, Kawafune K, Hachiya T, Takahashi S, Jia H, Saito K, Kato H.
- Journal Title
  
  Gene and Nutrition.
  
  Volume: 5 Issue: 1 Pages: 21-21
- DOI
  10.1186/s12263-019-0646-6
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-19K11709, KAKENHI-PROJECT-17J40246
[Journal Article] GWAS of habitual coffee consumption reveals a sex difference in the genetic effect of the 12q24 locus in the Japanese population.2019
- Author(s)
  Jia H, Nogawa S, Kawafune K, Hachiya T, Takahashi S, Igarashi M, Saito K, Kato H.
- Journal Title
  
  BMC Genet.
  
  Volume: 20 Issue: 1 Pages: 20-20
- DOI
  10.1186/s12863-019-0763-7
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-19K11709, KAKENHI-PROJECT-17J40246
[Journal Article] Phenotypic Variation in 46,XX Disorders of Sex Development due to the NR5A1 p.R92W Variant: A Sibling Case Report and Literature Review.2018
- Author(s)
  Takasawa K, Igarashi M, Ono M, Takemoto A, Takada S, Yamataka A, Ogata T, Morio T, Fukami M, Kashimada K.
- Journal Title
  
  Sexual Development
  
  Volume: 24 Issue: 5-6 Pages: 5-6
- DOI
  10.1159/000485868
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-16K09979, KAKENHI-PLANNED-17H06428, KAKENHI-PROJECT-17J40246
[Journal Article] Gain-of-function mutations in G-protein coupled receptor genes associated with human endocrine disorders.2018
- Author(s)
  Fukami M, Suzuki E, Igarashi M, Miyado M and Ogata T.
- Journal Title
  
  Clin Endocrinol (Oxf).
  
  Volume: 88 Issue: 3 Pages: 351-359
- DOI
  10.1111/cen.13496
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-16K08603, KAKENHI-PROJECT-16K09979, KAKENHI-PLANNED-17H06428, KAKENHI-PROJECT-17J40246, KAKENHI-PROJECT-17H04204
[Journal Article] GATA4 mutations are uncommon in patients with 46,XY disorders of sex development without heart anomaly.2018
- Author(s)
  Igarashi M, Mizuno K, Kon M, Narumi S, Kojima Y, Hayashi Y, Ogata T, Fukami M
- Journal Title
  
  Asian journal of andrology
  
  Volume: 印刷中 Issue: 6 Pages: 0-0
- DOI
  10.4103/aja.aja_20_18
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-16K09979, KAKENHI-PLANNED-17H06428, KAKENHI-PROJECT-17K11194, KAKENHI-PROJECT-17H06490, KAKENHI-PROJECT-17J40246
[Journal Article] MIRAGE syndrome is a rare cause of 46,XY DSD born SGA without adrenal insufficiency.2018
- Author(s)
  Shima H, Hayashi M, Tachibana T, Oshiro M, Amano N, Ishii T, Haruna H, Igarashi M, Kon M, Fukuzawa R, Tanaka Y, Fukami M, Hasegawa T, Narumi S.
- Journal Title
  
  PLoS One.
  
  Volume: 13 Issue: 11 Pages: e0206184-e0206184
- DOI
  10.1371/journal.pone.0206184
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-17K11194, KAKENHI-PROJECT-18K08527, KAKENHI-PLANNED-17H06428, KAKENHI-PROJECT-17J40246, KAKENHI-PROJECT-16K09979
[Journal Article] A novel C-terminal truncating NR5A1 mutation in dizygotic twins.2017
- Author(s)
  Hattori A, Zukeran H, Igarashi M, Toguchi S, Toubaru Y, Inoue T, Katoh-Fukui Y, Fukami M.
- Journal Title
  
  Hum Genome Var.
  
  Volume: 印刷中 Issue: 1 Pages: 17008-17008
- DOI
  10.1038/hgv.2017.8
- Peer Reviewed / Acknowledgement Compliant / Open Access / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-26293224, KAKENHI-PROJECT-15K06917, KAKENHI-PROJECT-16K09979
[Journal Article] Paradoxical gain-of-function mutant of the G-protein-coupled receptor PROKR2 promotes early puberty.2017
- Author(s)
  Fukami M, Suzuki E, Izumi Y, Torii T, Narumi S, Igarashi M, Miyado M, Katsumi M, Fujisawa Y, Nakabayashi K, Hata K, Umezawa A, Matsubara Y, Yamauchi J, Ogata T.
- Journal Title
  
  Journal of Cellular and Molecular Medicine
  
  Volume: - Issue: 10 Pages: 2623-2626
- DOI
  10.1111/jcmm.13146
- Peer Reviewed / Acknowledgement Compliant / Open Access
- Data Source
  KAKENHI-PROJECT-15K19538, KAKENHI-PROJECT-16K08603, KAKENHI-PROJECT-16K09979, KAKENHI-PROJECT-17K10074, KAKENHI-PROJECT-17J40246
[Journal Article] Identical NR5A1 Missense Mutations in Two Unrelated 46,XX Individuals with Testicular Tissues.2017
- Author(s)
  Igarashi M, Fukami M et al.
- Journal Title
  
  Hum Mutat.
  
  Volume: 38 Issue: 1 Pages: 39-42
- DOI
  10.1002/humu.23116
- Peer Reviewed / Open Access / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-26293224, KAKENHI-PROJECT-16K08593, KAKENHI-PROJECT-16K08603, KAKENHI-PROJECT-16K09979
[Journal Article] Copy Number Variations of the Azoospermia Factor Region and SRY Are Not Associated with the Risk of Hypospadias.2016
- Author(s)
  Kon M, Saito K, Mitsui T, Miyado M, Igarashi M, Moriya K, Nonomura K, Shinohara N, Ogata T, Fukami M.
- Journal Title
  
  Sexual Development
  
  Volume: 10 Issue: 1 Pages: 1-4
- DOI
  10.1159/000444938
- Peer Reviewed / Acknowledgement Compliant
- Data Source
  KAKENHI-PROJECT-26860837, KAKENHI-PROJECT-26870887, KAKENHI-PROJECT-16K09979
[Journal Article] The p.R92W variant of NR5A1/Nr5a1 induces testicular development of 46,XX gonads in humans, but not in mice: phenotypic comparison of human patients and mutation-induced mice2016
- Author(s)
  Miyado M, Inui M, Igarashi M, Katoh-Fukui Y, Takasawa K, Hakoda A, Kanno J, Kashimada K, Miyado K, Tamano M, Ogata T, Takada S, Fukami M
- Journal Title
  
  Biol Sex Differ
  
  Volume: 7 Issue: 1 Pages: 56-56
- DOI
  10.1186/s13293-016-0114-6
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-26293363, KAKENHI-PROJECT-26670733, KAKENHI-PROJECT-15K06917, KAKENHI-PROJECT-16K08603, KAKENHI-PROJECT-16K09979
[Journal Article] Copy-Number Variations of the Azoospermia Factor Region or SRY Are Not Associated with the Risk of Hypospadias2016
- Author(s)
  Kon M, Saito K, Mitsui T, Miyado M, Igarashi M, Moriya K, Nonomura K, Shinohara N, Ogata T, Fukami M
- Journal Title
  
  Sex Dev
  
  Volume: 未定
- Peer Reviewed / Acknowledgement Compliant / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-26293224
[Journal Article] Novel splice site mutation in MAMLD1 in a patient with hypospadias.2015
- Author(s)
  10.1038/ejhg.2015.13
- Journal Title
  
  Sex Dev
  
  Volume: 3 Issue: 3 Pages: 1-1
- DOI
  10.1159/000380842
- Peer Reviewed / Acknowledgement Compliant
- Data Source
  KAKENHI-PLANNED-22132004, KAKENHI-PROJECT-22227002, KAKENHI-PROJECT-26860837, KAKENHI-PROJECT-26462421, KAKENHI-PROJECT-25253023, KAKENHI-PROJECT-25462541, KAKENHI-PROJECT-25670686, KAKENHI-PROJECT-24390372
[Journal Article] Novel Splice Site Mutation in MAMLD1 in a Patient with Hypospadias2015
- Author(s)
  Igarashi M, Wada Y, Kojima Y, Miyado M, Nakamura M, Muroya K, Mizuno K, Hayashi Y, Nonomura K, Kohri K, Ogata T, Fukami M
- Journal Title
  
  Sex Dev
  
  Volume: 未定
- Peer Reviewed / Acknowledgement Compliant
- Data Source
  KAKENHI-PROJECT-26293224
[Journal Article] Molecular basis of non-syndromic hypospadias: Systematic mutation screening and genome-wide copy-number analysis of 62 patients.2015
- Author(s)
  Kon M, Suzu ki E, Dung VC, Hasegawa Y, Mitsui T, Muroya K, Ueoka K, Igarashi N, Nagasaki K, Oto Y, Hamajima T, Yoshino K, Igarashi M, Kato-Fukui Y, Nakabayashi K, Hayashi K, Hata K, Matsubara Y, Moriya K, Ogata T, Nonomura K, Fukami M
- Journal Title
  
  Hum Reprod
  
  Volume: 30(3) Issue: 3 Pages: 499-506
- DOI
  10.1093/humrep/deu364
- Peer Reviewed / Acknowledgement Compliant / Open Access
- Data Source
  KAKENHI-PLANNED-22132004, KAKENHI-PROJECT-25253023, KAKENHI-PROJECT-26293224, KAKENHI-PROJECT-26860837, KAKENHI-PROJECT-15K06917
[Journal Article] SOX3 overdosage permits normal sex development in females with random X inactivation2015
- Author(s)
  Igarashi M, Mikami H, Katsumi M, Miyado M, Izumi Y, Ogata T, Fukami M
- Journal Title
  
  Sex Dev
  
  Volume: 3 Issue: 3 Pages: 1-1
- DOI
  10.1159/000377653
- Peer Reviewed / Acknowledgement Compliant
- Data Source
  KAKENHI-PLANNED-22132004, KAKENHI-PROJECT-22227002, KAKENHI-PROJECT-25253023, KAKENHI-PROJECT-26860837
[Journal Article] SOX3 Overdosage Permits Normal Sex Development in Females with Random X Inactivation2015
- Author(s)
  Igarashi M, Mikami H, Katsumi M, Miyado M, Izumi Y, Ogata T, Fukami M
- Journal Title
  
  Sex Dev
  
  Volume: 未定
- Peer Reviewed / Acknowledgement Compliant
- Data Source
  KAKENHI-PROJECT-25670173
[Journal Article] Fertility preservation in a family with a novel NR5A1 mutation2015
- Author(s)
 Yagi H, Takagi M, Kon M, Igarashi M, Fukami M, Hasegawa Y.
- Journal Title
 
 Endocr J
 
 Volume: 62 Issue: 3 Pages: 289-295
- DOI
 10.1507/endocrj.EJ14-0340
- NAID
 130005060861
- ISSN
 0918-8959, 1348-4540
- Language
 English
- Peer Reviewed / Acknowledgement Compliant
- Data Source
 KAKENHI-PROJECT-26860837
[Journal Article] SOX3 Overdosage Permits Normal Sex Development in Females with Random X Inactivation2015
- Author(s)
  Igarashi M, Mikami H, Katsumi M, Miyado M, Izumi Y, Ogata T, Fukami M.
- Journal Title
  
  Sex Dev
  
  Volume: 未定
- Peer Reviewed / Acknowledgement Compliant
- Data Source
  KAKENHI-PROJECT-26293224
[Journal Article] Lack of Skeletal Dysplasia in Patients with Missense Mutations and Upstream Deletion of SOX9.2015
- Author(s)
  Katoh-Fukui Y, Igarashi M, Nagasaki K, Horikawa R, Nagai T, Tsuchiya T, Suzuki E, Miyado M, Hata K, Nakabayashi K, Hayashi K, Matsubara Y, Baba T, Morohashi K, Igarashi A, Ogata T, Takada S, and Fukami M
- Journal Title
  
  Molecular Genetics & Genomic Medicine
  
  Volume: 3 Issue: 6 Pages: 550-557
- DOI
  10.1002/mgg3.165
- Peer Reviewed / Open Access / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15K06917, KAKENHI-PROJECT-15K19439, KAKENHI-PROJECT-15K19538, KAKENHI-PLANNED-22132002, KAKENHI-PROJECT-25253023, KAKENHI-PROJECT-26860837, KAKENHI-PROJECT-26870887, KAKENHI-PROJECT-26293224
[Journal Article] Genome-wide copy number analysis and systematic mutation screening in 58 patients with hypogonadotropic hypogonadism2014
- Author(s)
  Izumi Y, Suzuki E, Kanzaki S, Yatsuga S, Kinjo S, Igarashi M, Maruyama T, Sano S, Horikawa R, Sato N, Nakabayashi K, Hata K, Umezawa A, Ogata T, Yoshimura Y, Fukami M
- Journal Title
  
  Fertil Steril
  
  Volume: 102(4) Issue: 4 Pages: 1130-1136
- DOI
  10.1016/j.fertnstert.2014.06.017
- Peer Reviewed / Acknowledgement Compliant
- Data Source
  KAKENHI-PLANNED-22132004, KAKENHI-PROJECT-22227002, KAKENHI-PROJECT-24390381, KAKENHI-PROJECT-24591512, KAKENHI-PROJECT-25670706, KAKENHI-PROJECT-25860891, KAKENHI-PROJECT-26293224, KAKENHI-PROJECT-26860837
[Journal Article] Rapid generation of mouse models with defined point mutations by the CRISPR/Cas9 system2014
- Author(s)
  Inui M, Miyado M, Igarashi M, Tamano M, Kubo A, Yamashita S, Asahara H, Fukami M, Takada S.
- Journal Title
  
  Scientific Reports
  
  Volume: 4 Issue: 1 Pages: 5396-5396
- DOI
  10.1038/srep05396
- Peer Reviewed / Acknowledgement Compliant / Open Access
- Data Source
  KAKENHI-PUBLICLY-25132713, KAKENHI-PROJECT-25871177, KAKENHI-PROJECT-26860837, KAKENHI-PROJECT-26870887, KAKENHI-PROJECT-26870891
[Journal Article] De Novo Frameshift Mutation in Fibroblast Growth Factor 8 in a Male Patient with Gonadotropin Deficiency.2014
- Author(s)
  Suzuki E, Yatsuga S, Igarashi M, Miyado M, Nakabayashi K, Hayashi K, Hata K, Umezawa A, Yamada G, Ogata T, Fukami M.
- Journal Title
  
  Hormone Research in Paediatrics
  
  Volume: 81 Pages: 139-144
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-24791103
[Journal Article] Tamoxifen Treatment for Pubertal Gynecomastia in Two Siblings with Partial Androgen Insensitivity Syndrome.2014
- Author(s)
  Saito R, Yamamoto Y, Goto M, Araki S, Kubo K, Kawagoe R, Kawada Y, Kusuhara K, Igarashi M, Fukami M.
- Journal Title
  
  Hormone Research in Paediatrics
  
  Volume: 81 Pages: 211-216
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-24791103
[Journal Article] Tamoxifen treatment for pubertal gynecomastia in two siblings with partial androgen insensitivity syndrome2014
- Author(s)
  Saito R, Tamamoto Y, Goto M, Araki S, Kubo K, Kawada Y, Kusuhara K, Igarashi M, Fukami M
- Journal Title
  
  Hormone Research in Paediatrics
  
  Volume: 81 Pages: 211-6
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-24791103
[Journal Article] Clinical and molecular studies in four patients with SRY-positive 46,XX testicular disorders of sex development: implications for variable sex development and genomic rearrangements.2014
- Author(s)
  Nakashima S, Oishi A, Takada F, Kawamura H, Igarashi M, Fukami M, Ogata T
- Journal Title
  
  J Hum Genet
  
  Volume: 59(10) Issue: 10 Pages: 549-553
- DOI
  10.1038/jhg.2014.70
- Peer Reviewed / Acknowledgement Compliant / Open Access
- Data Source
  KAKENHI-PLANNED-22132004, KAKENHI-PROJECT-22227002, KAKENHI-PROJECT-25253023, KAKENHI-PROJECT-26860837, KAKENHI-PROJECT-25860905
[Journal Article] Submicroacopic deletion incolving the fibroblast growth factor receptor 1 gene in a patient with combinedpituitary hormone deficiency2013
- Author(s)
  Fukami M, Iso M, Sato N, Igarashi M, Seo M, Kazukawa I, Kinoshita E, Dateki S, Ogata T
- Journal Title
  
  Endcr. J
- URL
  https://www.jstage.jst.go.jp/article/endocrj/60/8/60_EJ13-0023/_article
- Data Source
  KAKENHI-PROJECT-24791103
[Journal Article] Submicroscopic deletion involving the fibroblast growth factor receptor 1 gene in a patient with combined pituitary hormone deficiency.2013
- Author(s)
  Fukami M, Iso M, Sato N, Igarashi M, Seo M, Kazukawa I, Kinoshita E, Dateki S, Ogata T.
- Journal Title
  
  Endocrine Journal
  
  Volume: 60 Pages: 1013-1020
- NAID
  10031195771
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-24791103
[Journal Article] Cyptic genomic rearrangements in three patients with 46, XY disorders of sex development2013
- Author(s)
  Igarashi M, Dung VC, Suzuki E, Ida S, Nakacho M, Nakabayashi K, Mizuno K, Hayashi Y, Kohri K, Kojima Y, Ogata T, Fukami M
- Journal Title
  
  PLOS One
  
  Volume: Vol. 8
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-24791103
[Journal Article] Cryptic genomic rearrangements in three patients with 46,XY disorders of sex development2013
- Author(s)
  M. Igarashi, V. C. Dung, E. Suzuki, S. Ida, M. Nakacho, K. Nakabayashi, K. Mizuno, Y. Hayashi, K. Kohri, Y. Kojima, T. Ogata, M. Fukami
- Journal Title
  
  PLoS. One
  
  Volume: 8 Issue: 7 Pages: e68194-e68194
- DOI
  10.1371/journal.pone.0068194
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-22227002, KAKENHI-PROJECT-23390249, KAKENHI-PROJECT-24390372, KAKENHI-PROJECT-25462541, KAKENHI-PROJECT-25670173, KAKENHI-PROJECT-25670686
[Journal Article] De novo frameshift mutation in fibroblast growth factor 8 in a male patient with gonadotropin deficiency2013
- Author(s)
  Suzuki E, Yatsuga S, Igarashi M, Miyado M, Nakabayashi K, Hayashi K, Hata K, Umezawa A, Yamada G, Ogata T, Fukami M*
- Journal Title
  
  Horm Res Paediatr ,
  
  Volume: 81 Issue: 2 Pages: 139-144
- DOI
  10.1159/000355380
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PLANNED-22132004, KAKENHI-PROJECT-22227002, KAKENHI-PROJECT-24790303, KAKENHI-PROJECT-24791103, KAKENHI-PROJECT-25253023, KAKENHI-PROJECT-25860891
[Journal Article] Cryptic genomic rearrangements in three patients with 46,XY disorders of sex development.2013
- Author(s)
  Igarashi M, Dung VC, Suzuki E, Ida S, Nakacho M, Nakabayashi K, Mizuno K, Hayashi Y, Kohri K, Kojima Y, Ogata T, Fukami M.
- Journal Title
  
  PLoS One
  
  Volume: 8
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-24791103
[Journal Article] 性分化疾患の新知見－新規男性ホルモン産生経路.2012
- Author(s)
  五十嵐麻希、深見真紀．
- Journal Title
  
  医学のあゆみ
  
  Volume: 241 Pages: 788-789
- Data Source
  KAKENHI-PROJECT-24791103
[Presentation] Development of precision nutrition AI for weight control2022
- Author(s)
  Miyuki Chijiiwa, Maki Igarashi, Shun Nogawa, Tsuyoshi Hachiya, Kyohei Furukawa, Shoko Takahashi, Huijuan Jia, Kenji Saito, Hisanori Kato
- Organizer
  International Congress of Nutrition
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-19K11709
[Presentation] Validity of Calculation Value of Nutrient Intake by Photographic Dietary Assessment2022
- Author(s)
  Tomomi Nagahata, Maki Igarashi, Yuko Mekata, Yuki Kokubo, Naoki Takayanagi, Noriko Suzuki- Kemuriyama, Sosuke Amano, Kiyoharu Aizawa, and Hisanori Kato.
- Organizer
  International Congress of Nutrition
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-19K11709
[Presentation] Association between dietary behaviors and BMI modified by the ALDH2 rs671 polymorphism2022
- Author(s)
  Maki Igarashi, Shun Nogawa, Tsuyoshi Hachiya, Kyohei Furukawa, Shoko Takahashi, Huijuan Jia, Kenji Saito, Hisanori Kato
- Organizer
  International Congress of Nutrition
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-19K11709
[Presentation] Asian-specific SNP influences dietary behaviors in Japanese youth2022
- Author(s)
  Maki Igarashi, Tomomi Nagahata, Yuko Mekata, Yuki Kokubo, Naoki Takayanagi, Noriko Suzuki-Kemuriyama, Hisanori Kato
- Organizer
  The 8th Asian Congress of Dietetics
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-19K11709
[Presentation] アルコール感受性一塩基多型はヒトおよびマウスのうま味嗜好性に影響する2022
- Author(s)
  五十嵐　麻希、野川　駿、中出恵梨香、近都航太、古川　恭平、煙山紀子、福井由宇子、高田修治、八谷　剛史、高橋　祥子、斉藤　憲司、賈　慧娟、加藤　久典
- Organizer
  第76回　日本栄養食糧学会
- Data Source
  KAKENHI-PROJECT-19K11709
[Presentation] 個別化栄養を目指した飲酒関連一塩基多型の遺伝型別・食行動と BMI の特徴解析2021
- Author(s)
  五十嵐　麻希、野川　駿、古川　恭平、八谷　剛史、高橋　祥子、斉藤　憲司、賈　慧娟、加藤　久典
- Organizer
  第75回　日本栄養食糧学会
- Data Source
  KAKENHI-PROJECT-19K11709
[Presentation] 肥満に対するアルコールの摂取量と代謝酵素遺伝子多型の関連、季節の関連2021
- Author(s)
  古郡かすみ、可児美月、五十嵐麻希、後藤千穂、栗木清典
- Organizer
  第80回　日本公衆衛生学会総会
- Data Source
  KAKENHI-PROJECT-19K11709
[Presentation] 日本人集団における一塩基多型と緑茶摂取量の関連解析2021
- Author(s)
  染谷　駿一、野川　駿、五十嵐　麻希、古川　恭平、八谷　剛史、賈　慧娟、加藤　久典
- Organizer
  第75回　日本栄養食糧学会
- Data Source
  KAKENHI-PROJECT-19K11709
[Presentation] アルコール代謝遺伝子上のSNPは多彩な食行動および味覚嗜好と関連する－個別化栄養を目指したニュートリジェネティクス研究－2020
- Author(s)
  五十嵐麻希、野川駿、川舩かおる、八谷剛史、高橋祥子、齋藤藤憲司、賈慧娟、加藤久典
- Organizer
  第74回日本栄養・食糧学会大会
- Data Source
  KAKENHI-PROJECT-19K11709
[Presentation] 肥満に対するアルコール摂取量と遺伝要因の関連：四季食事調査の横断的検討2020
- Author(s)
  古郡かすみ、根津のあ、袴田菜月、可児美月、五十嵐麻希、後藤千穂、栗木清典
- Organizer
  第79回日本公衆衛生学会総会
- Data Source
  KAKENHI-PROJECT-19K11709
[Presentation] AIによる食品画像の識別に向けた寿司ネタの判別の試み2020
- Author(s)
  五十嵐麻希、齋藤憲司、　野川駿、　高橋祥子、　賈慧娟、　加藤久典
- Organizer
  第67回　日本栄養改善学会
- Data Source
  KAKENHI-PROJECT-19K11709
[Presentation] 12q24 locus affects BMI through alcohol drinking and dietary behaviors2020
- Author(s)
  Maki Igarashi, Shun Nogawa, Kaoru Kawafune, Tsuyoshi Hachiya, Huijuan Jia, Kyohei Furukawa, Shoko Takahashi, Kenji Saito and Hisanori Kato
- Organizer
  European Society of Human Genetics
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-19K11709
[Presentation] 日本人集団を用いたphenome-wide関連解析により明らかとなった12ｑ24領域と食行動の相関2020
- Author(s)
  五十嵐　麻希
- Organizer
  コホート・生体試料支援プラットフォーム・若手支援研究成果発表会
- Data Source
  KAKENHI-PROJECT-19K11709
[Presentation] アルコール代謝遺伝子上のSNPは多彩な食嗜好および食行動と関連する－個別化栄養を目指したニュートリジェネティクス研究－2020
- Author(s)
  五十嵐麻希, 野川駿, 川舩かおる, 八谷剛史, 高橋祥子, 斉藤憲司, 賈慧娟 , 加藤久典
- Organizer
  第74回日本栄養・食糧学会大会
- Data Source
  KAKENHI-PROJECT-19K11709
[Presentation] 日本人GWASから見えてきた12ｑ24領域と食の関連2019
- Author(s)
  五十嵐麻希、賈慧娟、野川駿、川舩かおる、八谷剛史、高橋祥子、斉藤憲司、加藤久典
- Organizer
  第4回食欲・食嗜好研究会
- Data Source
  KAKENHI-PROJECT-19K11709
[Presentation] 食にまつわるGWAS研究2019
- Author(s)
  五十嵐麻希、賈慧娟、野川駿、川舩かおる、八谷剛史、高橋祥子、斉藤憲司、加藤久典
- Organizer
  第4回　ゲノムコホート研究における遺伝統計学
- Data Source
  KAKENHI-PROJECT-19K11709
[Presentation] 東アジア系集団に特有の12ｑ24領域は多彩な摂取行動に関連する2019
- Author(s)
  五十嵐麻希、賈慧娟、野川駿、川舩かおる、八谷剛史、高橋祥子、斉藤憲司、加藤久典
- Organizer
  弟42回日本分子生物学会年会
- Data Source
  KAKENHI-PROJECT-19K11709
[Presentation] 食にまつわるGWAS研究2019
- Author(s)
  五十嵐麻希
- Organizer
  イルミナセミナー「消費者向け遺伝子解析サービスを活用した研究最前線」多検体解析によるビッグデータ活用から見えてくる複雑な疾患克服への展望
- Invited
- Data Source
  KAKENHI-PROJECT-19K11709
[Presentation] GWASによって見出された12q24遺伝子座と紅茶消費量との関連2019
- Author(s)
  五十嵐麻希、賈慧娟、野川駿、川舩かおる、八谷剛史、高橋祥子、斉藤憲司、加藤久典
- Organizer
  第73回日本栄養・食糧学会大会
- Data Source
  KAKENHI-PROJECT-19K11709
[Presentation] GWAS reveals the association between black tea consumption and 12q24 locus in Japanese population2019
- Author(s)
  Maki Igarashi, Huijuan Jia, Shun Nogawa, Kaoru Kawafune, Tsuyoshi Hachiya, Shoko Takahashi, Kenji Saito, Hisanori Kato
- Organizer
  Asian congress of Nutrition 2019
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-19K11709
[Presentation] ナンセンス随伴スプライス変更による 46,XY 性分化疾患の発症2018
- Author(s)
  五十嵐麻希
- Organizer
  性スペクトラム-連続する表現型としての雌雄　第一回班会議
- Data Source
  KAKENHI-PROJECT-16K09979
[Presentation] MAP3K1遺伝子のナンセンス随伴スプライス変更による46,XY性分化疾患の発症2018
- Author(s)
  五十嵐麻希、金城健一、中尾美奈子、宮戸真美、堀川玲子、　緒方勤、　深見真紀
- Organizer
  性スペクトラムー連続する表現型としての雌雄　第2 回領域会議
- Data Source
  KAKENHI-PROJECT-16K09979
[Presentation] NR5A1ミスセンス変異p.R92Wは、ヒトとマウスに共通する46,XY精巣形成不全とヒト特異的46,XX精巣形成を招く2017
- Author(s)
  宮戸真美, 乾雅史, 五十嵐麻希, 福井由宇子, 玉野萌恵, 宮戸健二, 緒方勤, 高田修治, 深見真紀
- Organizer
  第21回日本生殖内分泌学会
- Place of Presentation
  大阪
- Data Source
  KAKENHI-PROJECT-16K09979
[Presentation] Nonsense-associated altered splicing leading to a human disorder: Identification of MAP3K1 mutations in two brothers with 46,XY disorders of sex development2017
- Author(s)
  五十嵐麻希、金城健一、堀川玲子、緒方勤、深見真紀
- Organizer
  第40回日本分子生物学会年会
- Data Source
  KAKENHI-PROJECT-16K09979
[Presentation] 46,XY性分化疾患兄弟例におけるMAP3K1変異の同定2017
- Author(s)
  五十嵐麻希、金城健一、堀川玲子、緒方勤、深見真紀
- Organizer
  日本人類遺伝学会
- Data Source
  KAKENHI-PROJECT-16K09979
[Presentation] 内分泌疾患の原因となる新たなGタンパク共役型受容体機能亢進メカニズムの解明.2016
- Author(s)
  鈴木江莉奈, 泉陽子, 鳥居知宏, 五十嵐麻希, 宮戸真美, 勝見桃理, 鳴海覚志, 山内淳司, 藤澤泰子, 緒方勤, 深見真紀
- Organizer
  第50回日本小児内分泌学会学術集会
- Place of Presentation
  東京
- Data Source
  KAKENHI-PROJECT-16K09979
[Presentation] NR5A1は、46,XX精巣性性分化疾患の新規発症責任遺伝子である.2016
- Author(s)
  五十嵐麻希, 高澤啓, 箱田明子, 菅野潤子, 高田修治, 乾雅史, 宮戸真美, 福井由宇子, 鳴海覚志, 田島敏広, 秦健一郎, 中林一彦, 松原洋一, 緒方勤, 鹿島田健一,深見真紀
- Organizer
  第39回日本分子生物学会年会
- Place of Presentation
  神奈川
- Data Source
  KAKENHI-PROJECT-16K09979
[Presentation] Sequence Variations in Genes of the GH-IGF-1 Axis in Children with Idiopathic Short Stature.2016
- Author(s)
  Hattori A, Katoh-Fukui Y, Matsubara K, Igarashi M, Suzuki E, Nakamura A, Tanaka H, Nagasaki K, Muroya K, Horikawa R, Ida S, Tanaka T, Kamimaki T, Mitani M, Ogata T, Fukami M
- Organizer
  The 9th Biennial Scientific Meeting of the Asia Pacific Paediatric Endocrine Society
- Place of Presentation
  東京
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-16K09979
[Presentation] Identical NR5A1 Missense Mutations in Two Unrelated 46,XX Individuals with Testicular Tissues.2016
- Author(s)
  Igarashi M, Takasawa K, Hakoda A, Kanno J, Takada S, Miyado M, Tajima T, Sekido R, Ogata T, Kashimada K, Fukami M
- Organizer
  第50回日本小児内分泌学会学術集会
- Place of Presentation
  東京
- Data Source
  KAKENHI-PROJECT-16K09979
[Presentation] Identical NR5A1 Missense Mutations in Two Unrelated 46,XX Individuals with Testicular Tissues.2016
- Author(s)
  Igarashi M, Takasawa K, Hakoda A, Kanno J, Takada S, Miyado M, Tajima T, Sekido R, Ogata T, Kashimada K, Fukami M.
- Organizer
  The 9th Biennial Scientific Meeting of the Asia Pacific Paediatric Endocrine Society,
- Place of Presentation
  東京
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-16K09979
[Presentation] NR5A1は、46,XX精巣性性分化疾患の新規発症責任遺伝子である2016
- Author(s)
  五十嵐麻希, 高澤啓, 箱田明子, 菅野潤子, 高田修治, 乾雅史, 宮戸真美, 福井由宇子, 田島敏広, 秦健一郎, 中林一彦, 松原洋一, 緒方勤, 鹿島田健一,深見真紀
- Organizer
  第39回日本小児遺伝学会学術集会
- Place of Presentation
  東京
- Data Source
  KAKENHI-PROJECT-16K09979
[Presentation] Identical NR5A1 Missense Mutations in Two Unrelated 46,XX Individuals with Testicular Tissues.2016
- Author(s)
  Igarashi M, Takasawa K, Hakoda A, Kanno J, Takada S, Miyado M, Tajima T, Sekido R, Ogata T, Kashimada K, Fukami M.
- Organizer
  The 9th Biennial Scientific Meeting of the Asia Pacific Paediatric Endocrine Society
- Place of Presentation
  東京
- Year and Date
  2016-11-18
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-26293224
[Presentation] SRY陰性46,XX精巣性性分化疾患患者2例に共通するNR5A1ミスセンス変異の同定2015
- Author(s)
  五十嵐　麻希、鹿島田　健一、箱田　明子、高澤　啓、菅野　潤子、宮戸　真美、加藤　朋子、乾　雅史、関戸　良平、高田　修治、緒方　勤、深見　真紀
- 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-26860837
[Presentation] 低ゴナドトロピン性性腺機能低下症58例の網羅的遺伝子解析2015
- Author(s)
  鈴木江莉奈, 泉陽子, 神崎晋, 八ツ賀秀一, 金城さおり, 五十嵐麻希, 中林一彦, 梅沢明弘, 秦健一郎, 緒方勤, 深見真紀
- Organizer
  第19回日本生殖内分泌学会学術集会
- Place of Presentation
  大阪
- Year and Date
  2015-01-10
- Data Source
  KAKENHI-PROJECT-26860837
[Presentation] SOX9伸長変異（p.Q496fsX578）はタンパク不安定性を介してacampomelic campomelic dysplasiaを招く2015
- Author(s)
  山口理惠, 楢村哲生, 加藤芙弥子, 門奈央子, 五十嵐麻希, 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-26860837
[Presentation] ヒト性分化疾患の網羅的遺伝子変異解析.2015
- Author(s)
  五十嵐麻希、今雅史、泉陽子、福井由宇子、鈴木　江莉奈、和田友香、宮戸真美、緒方勤、深見真紀
- Organizer
  日本内分泌学会学術総会
- Place of Presentation
  東京
- Year and Date
  2015-04-23
- Data Source
  KAKENHI-PROJECT-26860837
[Presentation] Systematic mutation analysis of　patients with disorders of sex development.2015
- Author(s)
  Maki Igarashi, Yoko Izumi, Masafumi Kon, Yuko Kato-Fukui, Erina Suzuki, Yuka Wada, Mami Miyado, Tsutomu Ogata, Maki Fukami
- Organizer
  Seventh international symposium in the biology of vertebrate sex determination
- Place of Presentation
  ハワイ島
- Year and Date
  2015-04-13
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-26860837
[Presentation] SRY陰性46,XX精巣性性分化疾患患者2例に共通するNR5A1ミスセンス変異の同定2015
- Author(s)
  五十嵐　麻希、鹿島田　健一、箱田　明子、高澤　啓、菅野　潤子、宮戸　真美、加藤　朋子、乾　雅史、関戸　良平、高田　修治、緒方　勤、深見　真紀
- Organizer
  日本人類遺伝学会第60回大会
- Place of Presentation
  東京
- Year and Date
  2015-10-14
- Data Source
  KAKENHI-PROJECT-26860837
[Presentation] SOX9伸長変異（p.Q496fsX578）はタンパク不安定性を介してacampomelic campomelic dysplasiaを招く2015
- Author(s)
  山口理惠, 楢村哲生, 加藤芙弥子, 門奈央子, 五十嵐麻希, 深見真紀, 緒方勤
- Organizer
  日本人類遺伝学会第60回大会
- Place of Presentation
  東京
- Year and Date
  2015-10-14
- Data Source
  KAKENHI-PROJECT-26860837
[Presentation] Vanishing Testis SyndromeにおけるDSD関連遺伝子の網羅的変異解析2015
- Author(s)
  福井由宇子, 五十嵐麻希, 長崎啓祐, 位田忍, 堀川玲子, 鈴木江莉奈, 宮戸真美, 中村明枝, 緒方勤, 深見真紀
- 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-26860837
[Presentation] ヒト性分化疾患の網羅的遺伝子変異解析2015
- Author(s)
  五十嵐麻希、今雅史、泉陽子、福井由宇子、鈴木江莉奈、和田友香、宮戸真美、緒方勤、深見真紀
- Organizer
  第88回日本内分泌学会学術総会
- Place of Presentation
  東京
- Year and Date
  2015-04-25
- Data Source
  KAKENHI-PROJECT-26293224
[Presentation] Systematic mutation analysis of　patients with disorders of sex development2015
- Author(s)
  Igarashi M, Izumi Y, Kon M, Kato-Fukui Y, Suzuki E, Wada Y, Miyado M, Ogata T, Fukami M
- Organizer
  Seventh international symposium in the biology of vertebrate sex determination
- Place of Presentation
  Hawai
- Year and Date
  2015-04-15
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-26293224
[Presentation] 新規MAMLD1 イントロン変異による尿道下裂発症機序の解明2013
- Author(s)
  五十嵐麻希, 宮戸真美, 和田友香, 中村美智子, 小島祥敬, 水野健太郎, 林祐太郎, 郡健二郎, 緒方勤, 深見真紀
- Organizer
  日本人類遺伝学会第58回大会
- Place of Presentation
  仙台
- Year and Date
  2013-11-21
- Data Source
  KAKENHI-PROJECT-24791103
[Presentation] Kallmann 症候群患者におけるFGF8 フレームシフト変異の同定2013
- Author(s)
  鈴木江莉奈, 八ツ賀秀一, 五十嵐麻希, 宮戸真美, 中林一彦, 秦健一郎, 緒方勤, 深見真紀
- Organizer
  第47回日本小児内分泌学会学術集会
- Place of Presentation
  東京
- Year and Date
  2013-10-10
- Data Source
  KAKENHI-PROJECT-24791103
[Presentation] Kallmann症候群患者におけるFGF8フレームシフト変異の同定2013
- Author(s)
  鈴木江莉奈, 八ツ賀秀一, 五十嵐麻希, 宮戸真美, 中林一彦, 秦健一郎, 緒方勤, 深見真紀
- Organizer
  第18回日本生殖内分泌学会学術集会
- Place of Presentation
  東京
- Data Source
  KAKENHI-PROJECT-24791103
[Presentation] 新規MAMLD1イントロン変異による尿道下裂発症機序の解明2013
- Author(s)
  五十嵐麻希, 宮戸真美, 和田友香, 中村美智子, 小島祥敬, 水野健太郎, 林祐太郎, 郡健二郎, 緒方勤, 深見真紀
- Organizer
  日本人類遺伝学会第58回大会
- Place of Presentation
  仙台
- Data Source
  KAKENHI-PROJECT-24791103
[Presentation] 特発性低ゴナドトロピン性性腺機能低下症患者25 例のゲノムコピー数解析2013
- Author(s)
  泉陽子, 金城さおり, 鈴木江莉奈, 五十嵐麻希, 中林一彦, 緒方勤, 吉村泰典, 深見真紀
- Organizer
  第47回日本小児内分泌学会学術集会
- Place of Presentation
  東京
- Year and Date
  2013-10-12
- Data Source
  KAKENHI-PROJECT-24791103
[Presentation] MAMLD1変異による尿道下裂発症機序の探索2013
- Author(s)
  五十嵐麻希, 宮戸真美, 和田友香, 中村美智子, 小島祥敬, 水野健太郎, 林祐太郎, 郡健二郎, 緒方勤, 深見真紀
- Organizer
  第18回日本生殖内分泌学会学術集会
- Place of Presentation
  東京
- Data Source
  KAKENHI-PROJECT-24791103
[Presentation] 特発性低ゴナドトロピン性性腺機能低下症患者25例のゲノムコピー数解析2013
- Author(s)
  泉陽子, 金城さおり, 鈴木江莉奈, 五十嵐麻希, 中林一彦, 緒方勤, 吉村泰典, 深見真紀
- Organizer
  第18回日本生殖内分泌学会学術集会
- Place of Presentation
  東京
- Data Source
  KAKENHI-PROJECT-24791103
[Presentation] 女性化乳房14例における遺伝子解析2013
- Author(s)
  志原大蔵, 長崎啓祐, 五十嵐麻希, 緒方勤, 宮戸真美, 深見真紀
- Organizer
  第36回日本分子生物学会年会
- Place of Presentation
  兵庫
- Data Source
  KAKENHI-PROJECT-24791103
[Presentation] Molecular analyses using next-generation technologies for 141 patients with disorders of sex development.2013
- Author(s)
  2. Igarashi M, Vu Chi Dung, Suzuki E, Ida S, Mizuno K, Kojima Y, Muroya K, Takakuwa S, Oto Y, Takazawa K, Stuji Y, Hasegawa Y, Horikawa R, Ogata T, Fukami M
- Organizer
  9th Joint Meeting of Paediatric Endocrinology
- Place of Presentation
  Milan, Italy
- Data Source
  KAKENHI-PROJECT-24791103
[Presentation] 新規MAMLD1イントロン変異による尿道下裂発症機序の解明2013
- Author(s)
  五十嵐麻希, 宮戸真美, 和田友香, 中村美智子, 小島祥敬, 水野健太郎, 林祐太郎, 郡健二郎, 緒方勤, 深見真紀
- Organizer
  第47回日本小児内分泌学会学術集会
- Place of Presentation
  東京
- Data Source
  KAKENHI-PROJECT-24791103
[Presentation] Molecular analyses using next-generation technologies for 141 patients with disorders of sex development2013
- Author(s)
  Igarashi M, Vu Chi Dung, Suzuki E, Ida S, Mizuno K, Kojima Y, Muroya K, Takakuwa S, Oto Y, Takazawa K, Stuji Y, Hasegawa Y, Horikawa R, Ogata T, Fukami M
- Organizer
  9th Joint Meeting of Paediatric Endocrinology
- Place of Presentation
  Milan, Italy
- Year and Date
  2013-09-20
- Data Source
  KAKENHI-PROJECT-24791103
[Presentation] 高度尿道下裂の原因にアンドロゲン受容体遺伝子の関与が考えられるクラインフェルター症候群(KS)の一例2013
- Author(s)
  上田理誉, 宮下健悟, 高橋千恵, 内木康博, 泉陽子, 五十嵐麻希, 深見真紀, 堀川玲子
- Organizer
  第47回日本小児内分泌学会学術集会
- Place of Presentation
  東京
- Data Source
  KAKENHI-PROJECT-24791103
[Presentation] MAMLD1 変異による尿道下裂発症機序の探索2013
- Author(s)
  五十嵐麻希, 宮戸真美, 和田友香, 中村美智子, 小島祥敬, 水野健太郎, 林祐太郎, 郡健二郎, 緒方勤, 深見真紀
- Organizer
  第18回日本生殖内分泌学会学術集会
- Place of Presentation
  東京
- Year and Date
  2013-12-07
- Data Source
  KAKENHI-PROJECT-24791103
[Presentation] Kallmann症候群患者におけるFGF8 フレームシフト変異の同定2013
- Author(s)
  鈴木江莉奈, 八ツ賀秀一, 五十嵐麻希, 宮戸真美, 中林一彦, 秦健一郎, 緒方勤, 深見真紀
- Organizer
  第47回日本小児内分泌学会学術集会
- Place of Presentation
  東京
- Data Source
  KAKENHI-PROJECT-24791103
[Presentation] 尿道下裂患者における既知発症責任遺伝子および感受性遺伝子変異解析2013
- Author(s)
  今雅史, 鈴木江莉奈, 長谷川行洋, 五十嵐麻希, 福井由宇子, 水野健太郎, 小島祥敬, 林祐太郎, 群健二郎, Dung Vu Chi , 緒方勤, 野々村克也, 深見真紀
- Organizer
  第47回日本小児内分泌学会学術集会
- Place of Presentation
  東京
- Year and Date
  2013-10-12
- Data Source
  KAKENHI-PROJECT-24791103
[Presentation] 新規MAMLD1 イントロン変異による尿道下裂発症機序の解明2013
- Author(s)
  五十嵐麻希, 宮戸真美, 和田友香, 中村美智子, 小島祥敬, 水野健太郎, 林祐太郎, 郡健二郎, 緒方勤, 深見真紀
- Organizer
  第47回日本小児内分泌学会学術集会
- Place of Presentation
  東京
- Year and Date
  2013-10-10
- Data Source
  KAKENHI-PROJECT-24791103
[Presentation] 特発性低ゴナドトロピン性性腺機能低下症患者25例のゲノムコピー数解析2013
- Author(s)
  泉陽子, 金城さおり, 鈴木江莉奈, 五十嵐麻希, 中林一彦, 緒方勤, 吉村泰典, 深見真紀
- Organizer
  第47回日本小児内分泌学会学術集会
- Place of Presentation
  東京
- Data Source
  KAKENHI-PROJECT-24791103
[Presentation] 尿道下裂患者における既知発症責任遺伝子および感受性遺伝子変異解析2013
- Author(s)
  今雅史, 鈴木江莉奈, 長谷川行洋, 五十嵐麻希, 福井由宇子, 秦健一郎, 水野健太郎, 小島祥敬, 林祐太郎, 群健二郎, Dung Vu Chi , 緒方勤, 野々村克也, 深見真紀
- Organizer
  第18回日本生殖内分泌学会学術集会
- Place of Presentation
  東京
- Data Source
  KAKENHI-PROJECT-24791103
[Presentation] A rare case of siblings with partial androgen insensitivity syndrome diagnosed following gynaecomastia and the successful management of gynaecomastia using tamoxifen.2013
- Author(s)
  Saito R, Yamamoto Y, Gotoh M, Araki S, Kubo K, Kawagoe R, Kawada Y, Kusuhara K, Igarashi M, Kato F, Fukami M
- Organizer
  9th Joint Meeting of Paediatric Endocrinology
- Place of Presentation
  Milan, Italy
- Data Source
  KAKENHI-PROJECT-24791103
[Presentation] SRY陽性46,XXDSD(disorders of sex development)4症例の遺伝学的解析2013
- Author(s)
  中島信一, 大石彰, 高田史男, 永田絵子, 加藤芙弥子, 山口理惠, 五十嵐麻希, 深見真紀, 緒方勤
- Organizer
  日本人類遺伝学会第58回大会
- Place of Presentation
  仙台
- Data Source
  KAKENHI-PROJECT-24791103
[Presentation] A rare case of siblings with partial androgen insensitivity syndrome diagnosed following gynaecomastia and the successful management of gynaecomastia using tamoxifen2013
- Author(s)
  Saito R, Yamamoto Y, Gotoh M, Araki S, Kubo K, Kawagoe R, Kawada Y, Kusuhara K, Igarashi M, Kato F, Fukami M
- Organizer
  9th Joint Meeting of Paediatric Endocrinology
- Place of Presentation
  Milan, Italy
- Year and Date
  2013-09-21
- Data Source
  KAKENHI-PROJECT-24791103
[Presentation] 次世代遺伝子解析技術を用いた性分化疾患141例の病因解析2012
- Author(s)
  五十嵐麻希、Dung Chi Vu、小島祥敬、堀川玲子、緒方勤、深見真紀．
- Organizer
  第46回日本小児内分泌学会学術集会.
- Place of Presentation
  大阪
- Data Source
  KAKENHI-PROJECT-24791103
[Presentation] Silent mutations of androgen receptor gene in two patients with partial androgen insensitivity syndrome2012
- Author(s)
  Igarashi M, Kato F, Tsuji Y, Hasegawa Y, Ogata T, Fukami M
- Organizer
  6th International Symposium on the Biology of Vertebrate Sex Determination
- Place of Presentation
  Kona, Hawaii, USA
- Data Source
  KAKENHI-PROJECT-24791103
[Presentation] 次世代遺伝子解析技術を用いた性分化疾患141例の病因解析2012
- Author(s)
  五十嵐麻希, ブゥジュンイチ, 小島祥敬, 堀川玲子, 緒方勤, 深見真紀
- Organizer
  第35回日本分子生物学会
- Place of Presentation
  福岡
- Data Source
  KAKENHI-PROJECT-24791103
[Presentation] 次世代遺伝子解析技術を用いた性分化疾患141例の病因解析2012
- Author(s)
  五十嵐麻希、ブゥジュンイチ、小島祥敬、堀川玲子、緒方勤、深見真紀．
- Organizer
  第35回日本分子生物学会．
- Place of Presentation
  福岡
- Data Source
  KAKENHI-PROJECT-24791103
[Presentation] Silent mutations of androgen receptor gene in two patients with partial androgen insensitivity syndrome.2012
- Author(s)
  Igarashi M, Kato F, Tsuji Y, Hasegawa Y, Ogata T, Fukami M.
- Organizer
  6th International Symposium on the Biology of Vertebrate Sex Determination
- Place of Presentation
  Kona, Hawaii, USA
- Data Source
  KAKENHI-PROJECT-24791103
[Presentation] 男性における乳房腫大(女性化乳房)2012
- Author(s)
  深見真紀, 五十嵐麻希, 阿部修司, 山本幸代, 金城さおり, 緒方勤
- Organizer
  第46回小児内分泌学会とっておきの症例
- Place of Presentation
  大阪
- Data Source
  KAKENHI-PROJECT-24791103
[Presentation] 次世代遺伝子解析技術を用いた性分化疾患141例の病因解析2012
- Author(s)
  五十嵐麻希, Dung Chi Vu, 小島祥敬, 堀川玲子, 緒方勤, 深見真紀
- Organizer
  第17回日本生殖内分泌学会
- Place of Presentation
  東京
- Year and Date
  2012-12-08
- Data Source
  KAKENHI-PROJECT-24791103
[Presentation] 次世代遺伝子解析技術を用いた性分化疾患142例の病因解析2012
- Author(s)
  五十嵐麻希、Dung Chi Vu、小島祥敬、堀川玲子、緒方勤、深見真紀．
- Organizer
  新学術領域研究「性差構築の分子基盤」若手研究会．
- Place of Presentation
  和歌山
- Data Source
  KAKENHI-PROJECT-24791103
[Presentation] 次世代遺伝子解析技術を用いた性分化疾患141例の病因解析2012
- Author(s)
  五十嵐麻希, Dung Chi Vu, 小島祥敬, 堀川玲子, 緒方勤, 深見真紀
- Organizer
  日本人類遺伝学会第57回大会
- Place of Presentation
  東京
- Data Source
  KAKENHI-PROJECT-24791103
[Presentation] 次世代遺伝子解析技術を用いた性分化疾患141例の病因解析2012
- Author(s)
  五十嵐麻希、Dung Chi Vu、小島祥敬、堀川玲子、緒方勤、深見真紀．
- Organizer
  日本人類遺伝学会第57回大会．
- Place of Presentation
  東京
- Data Source
  KAKENHI-PROJECT-24791103
[Presentation] 次世代遺伝子解析技術を用いた性分化疾患141例の病因解析2012
- Author(s)
  五十嵐麻希, Dung Chi Vu, 小島祥敬, 堀川玲子, 緒方勤, 深見真紀
- Organizer
  第46回日本小児内分泌学会学術集会
- Place of Presentation
  大阪
- Data Source
  KAKENHI-PROJECT-24791103
[Presentation] Identification of a missense MAP3K1 mutation in a patient with hypospadias.
- Author(s)
  Igarashi M, Horikawa R, Nakabayashi K, Hata K, Ogata T, Fukami M.
- Organizer
  53th annual ESPE meeting
- Place of Presentation
  Dublin
- Year and Date
  2014-09-18 – 2014-09-20
- Data Source
  KAKENHI-PROJECT-26860837
[Presentation] 妊孕性が確認できた新規SF1遺伝子異常症の父子例
- Author(s)
  八木弘子, 高木優樹, 長谷川行洋, 五十嵐麻希, 今雅史, 深見真紀
- Organizer
  第87回日本内分泌学会学術総会
- Place of Presentation
  福岡
- Year and Date
  2014-04-24 – 2014-04-26
- Data Source
  KAKENHI-PROJECT-26860837
[Presentation] 46,XX精巣性性分化疾患を伴わない母娘例におけるSOX3重複の同定
- Author(s)
  五十嵐麻希, 三上仁, 勝見桃理, 泉陽子, 緒方勤, 深見真紀
- Organizer
  第48回日本小児内分泌学会学術集会
- Place of Presentation
  静岡
- Year and Date
  2014-09-25 – 2014-09-27
- Data Source
  KAKENHI-PROJECT-26860837
[Presentation] SOX9 frameshift mutation in a patient with acampomelic campomelic dysplasia:the second case
- Author(s)
  37.山口理惠, 楢村哲生, 加藤芙弥子, 永田絵子, 中島信一, 馬場崇, 諸橋憲一郎, 五十嵐麻希, 深見真紀, 緒方勤
- Organizer
  第48回日本小児内分泌学会学術集会
- Place of Presentation
  静岡
- Year and Date
  2014-09-25 – 2014-09-27
- Data Source
  KAKENHI-PROJECT-26860837
[Presentation] 非症候性尿道下裂発症における単一遺伝子変異の寄与の解明
- Author(s)
  今雅史, 室谷浩二, 長谷川行洋, 長崎啓祐, Dung Vu Chi, 上岡克彦, 大戸佑二, 五十嵐登, 三井貴彦, 鈴木江莉奈, 五十嵐麻希, 福井由宇子, 守屋仁彦, 野々村克也, 緒方勤, 深見真紀
- Organizer
  第48回日本小児内分泌学会学術集会
- Place of Presentation
  静岡
- Year and Date
  2014-09-25 – 2014-09-27
- Data Source
  KAKENHI-PROJECT-26860837
[Presentation] Mutation analysis of KDM3A (lysine-specific demethylase 3A) in patients with hypospadias.
- Author(s)
  Kon M, Igarashi M, Izumi Y, Kato-Fukui Y, Mizuno K, Hayashi Y, Kohri K, Kojima Y, Nonomura K, Ogata T, Fukami M.
- Organizer
  53rd Annual ESPE Meeting
- Place of Presentation
  Dublin
- Year and Date
  2014-09-18 – 2014-09-20
- Data Source
  KAKENHI-PROJECT-26860837
[Presentation] ヒト性分化疾患の網羅的遺伝子変異解析
- Author(s)
  五十嵐麻希、今雅史、泉陽子、福井由宇子、鈴木　江莉奈、和田友香、宮戸真美、緒方勤、深見真紀
- Organizer
  第88回　日本内分泌学会各術総会
- Place of Presentation
  東京
- Year and Date
  2015-04-23 – 2015-04-25
- Data Source
  KAKENHI-PROJECT-26860837
[Presentation] SRY陽性46,XX DSD(disorders of sex development)4症例の遺伝学的解析
- Author(s)
  中島信一, 大石彰, 高田史男, 永田絵子, 加藤芙弥子, 山口理惠, 五十嵐麻希, 深見真紀, 中西俊樹, 緒方勤
- Organizer
  第87回日本内分泌学会学術総会
- Place of Presentation
  福岡
- Year and Date
  2014-04-24 – 2014-04-26
- Data Source
  KAKENHI-PROJECT-26860837
[Presentation] ヒト性分化異常症の網羅的遺伝子変異解析
- Author(s)
  五十嵐麻希、今雅史、泉陽子、福井由宇子、鈴木　江莉奈、和田友香、宮戸真美、緒方勤、深見真紀
- Organizer
  第37回日本分子生物学会年会
- Place of Presentation
  神奈川
- Year and Date
  2014-11-25 – 2014-11-27
- Data Source
  KAKENHI-PROJECT-26860837
[Presentation] Systematic mutation analysis of　patients with disorders of sex development.
- Author(s)
  Igarashi M, Izumi Y, Kon M, Kato-Fukui Y, Suzuki E, Wada Y, Miyado M, Ogata T, Fukami M
- Organizer
  Seventh international symposium in the biology of vertebrate sex determination
- Place of Presentation
  ﾊﾜｲ
- Year and Date
  2015-04-13 – 2015-04-17
- Data Source
  KAKENHI-PROJECT-26860837
[Presentation] SRY(+)46,XX精巣性性分化疾患4症例における性分化決定因子と転座発症機序の解析
- Author(s)
  中島信一, 大石彰, 高田史男, 河村秀樹, 小野裕之, 五十嵐麻希, 深見真紀, 緒方勤
- Organizer
  第48回日本小児内分泌学会学術集会
- Place of Presentation
  静岡
- Year and Date
  2014-09-25 – 2014-09-27
- Data Source
  KAKENHI-PROJECT-26860837

1. FUKAMI maki (40265872)

# of Collaborated Projects: 3 results

# of Collaborated Products: 27 results
2. 高田修治 (20382856)

# of Collaborated Projects: 2 results

# of Collaborated Products: 9 results
3. 加藤久典 (40211164)

# of Collaborated Projects: 2 results

# of Collaborated Products: 19 results
4. AYABE Tadayuki (80566555)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
5. Nakamura Shigeru (50420477)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
6. 小島祥敬 (60305539)

# of Collaborated Projects: 1 results

# of Collaborated Products: 1 results
7. 宮戸真美 (00386252)

# of Collaborated Projects: 1 results

# of Collaborated Products: 1 results
8. 中井秀郎 (50167540)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
9. 栗木清典 (20543705)

# of Collaborated Projects: 1 results

# of Collaborated Products: 2 results
10. 福井由宇子 (50342639)

# of Collaborated Projects: 1 results

# of Collaborated Products: 4 results
11. 賈慧娟 (60456324)

# of Collaborated Projects: 1 results

# of Collaborated Products: 17 results
12. 目加田優子 (60617281)

# of Collaborated Projects: 1 results

# of Collaborated Products: 2 results
13. 長幡友実 (40512512)

# of Collaborated Projects: 1 results

# of Collaborated Products: 2 results
14. 小久保友貴 (10610066)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
15. OGATA Tsutomu

# of Collaborated Projects: 0 results

# of Collaborated Products: 6 results
16. 鈴木友貴

# of Collaborated Projects: 0 results

# of Collaborated Products: 2 results
17. 鈴木江莉奈

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
18. 宮戸健二

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results

IGARASHI Maki 五十嵐 麻希

Research Projects

Research Products

Co-Researchers

Association between dietary fiber intake and colorectal tumors depending on the abundance of short-chain fatty acid-producing microbiotaPrincipal Investigator

Principal Investigator

Project Period (FY)

Research Category

Review Section

Research Institution

Establishment of precision nutrition platform based on interaction of genome and epigenome

Principal Investigator

Project Period (FY)

Research Category

Review Section

Research Institution

Molecular basis research for personalized nutritionPrincipal Investigator

Principal Investigator

Project Period (FY)

Research Category

Review Section

Research Institution

Elucidation of the pathogenic mechanism of congenital urethral anomaly by comprehensive genetic and endocrine analysis

Principal Investigator

Project Period (FY)

Research Category

Research Field

Research Institution

Elucidation of pathogenic mechanisms of disorders of sex development using systematic molecular analysisPrincipal Investigator

Principal Investigator

Project Period (FY)

Research Category

Research Field

Research Institution

Identification and functional elucidation of genetic abnormalities in patients with disorders of sex development using next-generation approachesPrincipal Investigator

Principal Investigator

Project Period (FY)

Research Category

Research Field

Research Institution

Clarification of molecular basis of pubertal disorders and disorders of sex development

Principal Investigator

Project Period (FY)

Research Category

Research Field

Research Institution

Genetic and environmental factors involved in human genomic instability

Principal Investigator

Project Period (FY)

Research Category

Research Field

Research Institution

Identification and functional elucidation of novel causative genes in patients with disorders of sex developmentPrincipal Investigator

Principal Investigator

Project Period (FY)

Research Category

Research Field

Research Institution

[Book] 日常診療における性分化の診かた。性分化疾患と遺伝子異常。2014

Author(s)

Total Pages

Publisher

Data Source

[Journal Article] Collection of 2429 constrained headshots of 277 volunteers for deep learning2022

Author(s)

Journal Title

DOI

Data Source

[Journal Article] Dietary supplement use in elementary school children: a Japanese web-based survey2021

Author(s)

Journal Title

DOI

NAID

Data Source

[Journal Article] Female-dominant estrogen production in healthy young children before adrenarche.2021

Author(s)

Journal Title

DOI

Data Source

[Journal Article] A Genome-wide association study identifies the association between the 12q24 locus and black tea consumption in Japanese populations.2020

IGARASHI Maki 五十嵐麻希