KATO Takema 加藤武馬

Researcher Number	20387690
Affiliation (based on the past Project Information) *help	2022 – 2023: 藤田医科大学, 医科学研究センター, 助教 2018 – 2021: 藤田医科大学, 総合医科学研究所, 助教 2013 – 2017: 藤田保健衛生大学, 総合医科学研究所, 助教
Review Section/Research Field	Principal Investigator Human genetics / Basic Section 45010:Genetics-related / Obstetrics and gynecology Except Principal Investigator Basic Section 52050:Embryonic medicine and pediatrics-related / Basic Section 56040:Obstetrics and gynecology-related
Keywords	Principal Investigator 初期胚 / 受精卵 / パリンドローム / 染色体転座 / PATRR / 染色体不安定性 / 染色体 / niPGT / 機械学習 / Single cell RNA sequence … More / TE / ICM / PGS / PGD / Chromosome / Trophectoderm / Inner Cell Mass / Blastocyst / 胚盤胞 / NGS / PGT-SR / PGT-A / 着床前診断 / モザイク / 染色体異常 / PGT / 回分配列 / ゲノム再構成 / 染色体脆弱部位 / FRA3B / t(3;8)(p14;q24) … More Except Principal Investigator ゲノム編集 / アンチセンス療法 / SVA型レトロトランスポゾン / 尿中細胞 / レトロトランスポゾン / ロングリードシークエンサー / SVA / 福山型筋ジストロフィー / 着床前遺伝学的検査 / 初期胚 / モザイク / 着床前染色体検査 / 染色体異常 Less

初期胚における染色体不安定性を起こす要因の探索Principal Investigator
- Principal Investigator
  
  加藤武馬
- Project Period (FY)
  2021
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Review Section
  
  Basic Section 45010:Genetics-related
- Research Institution
  Fujita Health University
Establishing Diagnostic Methods and Elucidating the Pathogenesis of Fukuyama Congenital Muscular Dystrophy Using Long-Read Sequencers
- Principal Investigator
  
  Nagasaka Miwako
- Project Period (FY)
  2021 – 2023
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Review Section
  
  Basic Section 52050:Embryonic medicine and pediatrics-related
- Research Institution
  Aijinkai Healthcare Corporation Takatsuki General Hospital Clinical Research Center
Risk factors related to chromosomal aneuploidy in human blastocysts
- Principal Investigator
  
  Miyai Shunsuke
- Project Period (FY)
  2019 – 2021
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Review Section
  
  Basic Section 56040:Obstetrics and gynecology-related
- Research Institution
  Fujita Health University
Molecular origin of chromosomal abnormalities in early embryonic cellsPrincipal Investigator
- Principal Investigator
  
  Kato Takema
- Project Period (FY)
  2017 – 2019
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Obstetrics and gynecology
- Research Institution
  Fujita Health University
Spatial proximity of PATRRs and their translocation frequenciesPrincipal Investigator
- Principal Investigator
  
  KATO TAKEMA
- Project Period (FY)
  2015 – 2016
- Research Category
  
  Grant-in-Aid for Young Scientists (B)
- Research Field
  
  Human genetics
- Research Institution
  Fujita Health University
FRA3B and the Palindromic AT-rich repeatPrincipal Investigator
- Principal Investigator
  
  KATO Takema
- Project Period (FY)
  2013 – 2014
- Research Category
  
  Grant-in-Aid for Young Scientists (B)
- Research Field
  
  Human genetics
- Research Institution
  Fujita Health University

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

All Journal Article Presentation Patent

[Journal Article] Target enrichment long-read sequencing with adaptive sampling can determine the structure of the small supernumerary marker chromosomes2022
- Author(s)
  Mariya T, Kato T, Sugimoto T, Miyai S, Inagaki H, Ohye T, Sugihara E, Muramatsu Y, Mizuno S, Kurahashi H.
- Journal Title
  
  Journal of human genetics
  
  Volume: Jan 14 Issue: 6 Pages: 363-368
- DOI
  10.1038/s10038-021-01004-x
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-19K09790, KAKENHI-PROJECT-21K06283, KAKENHI-PROJECT-19K07902
[Journal Article] Usefulness of combined NGS and QF-PCR analysis for product of conception karyotyping2022
- Author(s)
  Kato T, Miyai S, Suzuki H, Murase Y, Ota S, Yamauchi H, Ammae M, Nakano T, Nakaoka Y, Inoue T, Morimoto Y, Fukuda A, Utsunomiya T, Nishizawa H, Kurahashi H.
- Journal Title
  
  Reproductive medicine and biology
  
  Volume: Feb 27;21(1) Issue: 1
- DOI
  10.1002/rmb2.12449
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-19K09790, KAKENHI-PROJECT-21K06283
[Journal Article] Identification of a Novel Mutation in Carboxyl Ester Lipase Gene in a Patient with MODY-like Diabetes2022
- Author(s)
  Kondoh Tomomi、Nakajima Yoko、Yokoi Katsuyuki、Matsumoto Yuji、Inagaki Hidehito、Kato Takema、Nakajima Yoichi、Ito Tetsuya、Yoshikawa Tetsushi、Kurahashi Hiroki
- Journal Title
  
  Tohoku J. Exp. Med.
  
  Volume: 256 Issue: 1 Pages: 37-41
- DOI
  10.1620/tjem.256.37
- NAID
  130008144085
- ISSN
  0040-8727, 1349-3329
- Language
  English
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21K06283
[Journal Article] Genotype-phenotype correlation of renal lesions in the tuberous sclerosis complex2022
- Author(s)
  Muto Y, Sasaki H, Sumitomo M, Inagaki H, Kato M, Kato T, Miyai S, Kurahashi H, Shiroki R.
- Journal Title
  
  Human Genome Variation
  
  Volume: Feb 10;9(1) Issue: 1 Pages: 5-5
- DOI
  10.1038/s41439-022-00181-1
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-19K09790, KAKENHI-PROJECT-21K06283
[Journal Article] Coexistence of RASA1 and COL4A2 variants caused pial arteriovenous fistula (AVF) in a patient with capillary malformation-arteriovenous malformation2021
- Author(s)
  Kumai Tadashi、Sadato Akiyo、Kurahashi Hiroki、Kato Takema、Adachi Kazuhide、Hirose Yuichi
- Journal Title
  
  Clinical Neurology and Neurosurgery
  
  Volume: 204 Pages: 106612-106612
- DOI
  10.1016/j.clineuro.2021.106612
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21K06283
[Journal Article] Myoinositol to Total Choline Ratio in Glioblastomas as a Potential Prognostic Factor in Preoperative Magnetic Resonance Spectroscopy2021
- Author(s)
  KUMON Masanobu、NAKAE Shunsuke、MURAYAMA Kazuhiro、KATO Takema、OHBA Shigeo、INAMASU Joji、YAMADA Seiji、ABE Masato、SASAKI Hikaru、OHNO Yoshiharu、HASEGAWA Mitsuhiro、KURAHASHI Hiroki、HIROSE Yuichi
- Journal Title
  
  Neurol. Med. Chir.(Tokyo)
  
  Volume: 61 Issue: 8 Pages: 453-460
- DOI
  10.2176/nmc.oa.2020-0312
- NAID
  130008074598
- ISSN
  0470-8105, 1349-8029
- Language
  English
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-19K09464, KAKENHI-PROJECT-19K09468, KAKENHI-PROJECT-19K09490, KAKENHI-PROJECT-21K06283, KAKENHI-PROJECT-21K09161
[Journal Article] Analysis of the Origin of Double Mosaic Aneuploidy in Two Cases.2020
- Author(s)
  Kato T, Kawai M, Miyai S, Suzuki F, Tsutsumi M, Mizuno S, Ikeda T, Kurahashi H.
- Journal Title
  
  Cytogenet Genome Res.
  
  Volume: - Issue: 3 Pages: 118-123
- DOI
  10.1159/000507177
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-19K09790, KAKENHI-PROJECT-17K11259
[Journal Article] A case of a parthenogenetic 46,XX/46,XY chimera presenting ambiguous genitalia.2020
- Author(s)
  Kawamura R, Kato T, Miyai S, Suzuki F, Naru Y, Kato M, Tanaka K, Nagasaka M, Tsutsumi M, Inagaki H, Ioroi T, Yoshida M, Nao T, Conlin LK, Iijima K, Kurahashi H, Taniguchi-Ikeda M.
- Journal Title
  
  J Hum Genet.
  
  Volume: - Issue: 8 Pages: 705-709
- DOI
  10.1038/s10038-020-0748-4
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-19K09790, KAKENHI-PROJECT-17K00481, KAKENHI-PROJECT-17K11259
[Journal Article] The involvement of U-type dicentric chromosomes in the formation of terminal deletions with or without adjacent inverted duplications.2020
- Author(s)
  Kato T, Inagaki H, Miyai S, Suzuki F, Naru Y, Shinkai Y, Kato A, Kanyama K, Mizuno S, Muramatsu Y, Yamamoto T, Shinya M, Tazaki Y, Hiwatashi S, Ikeda T, Ozaki M, Kurahashi H.
- Journal Title
  
  Hum Genet.
  
  Volume: 139(11) Issue: 11 Pages: 1417-1427
- DOI
  10.1007/s00439-020-02186-8
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-19K09790, KAKENHI-PROJECT-18K07803
[Journal Article] Novel mutation in the KITLG gene in familial progressive hyperpigmentation with or without hypopigmentation2020
- Author(s)
  Kato Maki、Yagami Akiko、Tsukamoto Tetsuya、Shinkai Yasuko、Kato Takema、Kurahashi Hiroki
- Journal Title
  
  The Journal of Dermatology
  
  Volume: - Issue: 6 Pages: 669-672
- DOI
  10.1111/1346-8138.15313
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-17K11259
[Journal Article] DNA methylation accumulation in gastric mucosa adjacent to cancer after Helicobacter pylori eradication.2019
- Author(s)
  Tahara S, Tahara T, Horiguchi N, Kato T, Shinkai Y, Yamashita H, Yamada H, Kawamura T, Terada T, Okubo M, Nagasaka M, Nakagawa Y, Shibata T, Yamada S, Urano M, Tsukamoto T, Kurahashi H, Kuroda M, Ohmiya N.
- Journal Title
  
  Int J Cancer.
  
  Volume: 144 Issue: 1 Pages: 80-88
- DOI
  10.1002/ijc.31667
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-17K11259
[Journal Article] Preimplantation genetic testing for aneuploidy: a comparison of live birth rates in patients with recurrent pregnancy loss due to embryonic aneuploidy or recurrent implantation failure.2019
- Author(s)
  Sato T, Sugiura-Ogasawara M, Ozawa F, Yamamoto T, Kato T, Kurahashi H, Kuroda T, Aoyama N, Kato K, Kobayashi R, Fukuda A, Utsunomiya T, Kuwahara A, Saito H, Takeshita T, Irahara M.
- Journal Title
  
  Hum Reprod.
  
  Volume: 34 Issue: 12 Pages: 2340-2348
- DOI
  10.1093/humrep/dez229
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-18K07803, KAKENHI-PROJECT-18K09267, KAKENHI-PROJECT-17K11259
[Journal Article] Exome-First Approach in Fetal Akinesia Reveals Chromosome 1p36 Deletion Syndrome.2019
- Author(s)
  Toshimitsu M, Nagaoka S, Kobori S, Ogawa M, Suzuki F, Kato T, Miyai S, Kawamura R, Inagaki H, Kurahashi H, Murotsuki J.
- Journal Title
  
  Case Rep Obstet Gynecol.
  
  Volume: - Pages: 1-5
- DOI
  10.1155/2019/6753184
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-19K09790, KAKENHI-PROJECT-17K11259
[Journal Article] Prostate stem cell antigen gene polymorphism is associated with H. pylori-related promoter DNA methylation in non-neoplastic gastric epithelium2019
- Author(s)
  Tahara Tomomitsu、Tahara Sayumi、Horiguchi Noriyuki、Kato Takema、Shinkai Yasuko、Okubo Masaaki、Terada Tsuyoshi、Yoshida Dai、Funasaka Kohei、Nagasaka Mitsuo、Nakagawa Yoshihito、Kurahashi Hiroki、Shibata Tomoyuki、Tsukamoto Tetsuya、Ohmiya Naoki
- Journal Title
  
  Cancer Prevention Research
  
  Volume: - Issue: 9 Pages: 579-584
- DOI
  10.1158/1940-6207.capr-19-0035
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-17K11259
[Journal Article] A female patient with retinoblastoma and severe intellectual disability carrying an X;13 balanced translocation without rearrangement in the RB1 gene: a case report2019
- Author(s)
  Tsutsumi Makiko、Hattori Hiroyoshi、Akita Nobuhiro、Maeda Naoko、Kubota Toshinobu、Horibe Keizo、Fujita Naoko、Kawai Miki、Shinkai Yasuko、Kato Maki、Kato Takema、Kawamura Rie、Suzuki Fumihiko、Kurahashi Hiroki
- Journal Title
  
  BMC Medical Genomics
  
  Volume: 12 Issue: 1 Pages: 1-8
- DOI
  10.1186/s12920-019-0640-2
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-17K11259, KAKENHI-PROJECT-18K15291
[Journal Article] Obstetric complication-associated ANXA5 promoter polymorphisms may affect gene expression via DNA secondary structures.2019
- Author(s)
  Inagaki H, Ota S, Nishizawa H, Miyamura H, Nakahira K, Suzuki M, Nishiyama S, Kato T, Yanagihara I, Kurahashi H.
- Journal Title
  
  J Hum Genet.
  
  Volume: 64 Issue: 5 Pages: 459-466
- DOI
  10.1038/s10038-019-0578-4
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-17K11259, KAKENHI-PROJECT-17H04237
[Journal Article] A case of dihydropyrimidinase deficiency incidentally detected by urine metabolome analysis.2019
- Author(s)
  Tsuchiya H, Akiyama T, Kuhara T, Nakajima Y, Ohse M, Kurahashi H, Kato T, Maeda Y, Yoshinaga H, Kobayashi K.
- Journal Title
  
  Brain Dev.
  
  Volume: 41 Issue: 3 Pages: 280-284
- DOI
  10.1016/j.braindev.2018.10.005
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-17K11259
[Journal Article] Prenatal diagnosis of premature chromatid separation/mosaic variegated aneuploidy (PCS/MVA) syndrome.2018
- Author(s)
  Yamaguchi T, Yamaguchi M, Akeno K, Fujisaki M, Sumiyoshi K, Ohashi M, Sameshima H, Ozaki M, Kato M, Kato T, Hosoba E, Kurahashi H.
- Journal Title
  
  J Obstet Gynaecol Res.
  
  Volume: 44 Issue: 7 Pages: 1313-1317
- DOI
  10.1111/jog.13647
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-17K11259, KAKENHI-PROJECT-18K15291
[Journal Article] Potential role for nectin-4 in the pathogenesis of pre-eclampsia: a molecular genetic study.2018
- Author(s)
  Ito M, Nishizawa H, Tsutsumi M, Kato A, Sakabe Y, Noda Y, Ohwaki A, Miyazaki J, Kato T, Shiogama K, Sekiya T, Kurahashi H, Fujii T.
- Journal Title
  
  BMC Med Genet.
  
  Volume: 19 Issue: 1 Pages: 166-166
- DOI
  10.1186/s12881-018-0681-y
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-17K11259, KAKENHI-PROJECT-16H05174
[Journal Article] Twin pregnancy with chromosomal abnormalities mimicking a gestational trophoblastic disorder and coexistent foetus on ultrasound2018
- Author(s)
  Ohwaki Akiko、Nishizawa Haruki、Aida Noriko、Kato Takema、Kambayashi Asuka、Miyazaki Jun、Ito Mayuko、Urano Makoto、Kiriyama Yuka、Kuroda Makoto、Nakayama Masahiro、Sonta Shin-Ichi、Suzumori Kaoru、Sekiya Takao、Kurahashi Hiroki、Fujii Takuma
- Journal Title
  
  Journal of Obstetrics and Gynaecology
  
  Volume: - Issue: 7 Pages: 1-3
- DOI
  10.1080/01443615.2017.1401598
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-17K11259, KAKENHI-PROJECT-17K11300
[Journal Article] FOXA2 gene mutation in a patient with congenital complex pituitary hormone deficiency.2018
- Author(s)
  Boda H, Miyata M, Inagaki H, Shinkai Y, Kato T, Yoshikawa T, Kurahashi H.
- Journal Title
  
  Eur J Med Genet.
  
  Volume: S1769-7212 Issue: 11 Pages: 30408-7
- DOI
  10.1016/j.ejmg.2018.11.004
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-17K11259
[Journal Article] Multiplex PCR in noninvasive prenatal diagnosis for FGFR3-related disorders2018
- Author(s)
  Terasawa Sumire、Kato Asuka、Nishizawa Haruki、Kato Takema、Yoshizawa Hikari、Noda Yoshiteru、Miyazaki Jun、Ito Mayuko、Sekiya Takao、Fujii Takuma、Kurahashi Hiroki
- Journal Title
  
  Congenital Anomalies
  
  Volume: - Issue: 1 Pages: 1-7
- DOI
  10.1111/cga.12278
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-17K11259, KAKENHI-PROJECT-17K11300, KAKENHI-PROJECT-15H04710
[Journal Article] Lethal persistent pulmonary hypertension of the newborn in Bohring-Opitz syndrome.2018
- Author(s)
  Kibe M, Ibara S, Inagaki H, Kato T, Kurahashi H, Ikeda T.
- Journal Title
  
  Am J Med Genet A.
  
  Volume: 176 Issue: 5 Pages: 1245-1248
- DOI
  10.1002/ajmg.a.38681
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-17K11259
[Journal Article] PCS/MVA syndrome caused by an Alu insertion in the BUB1B gene2017
- Author(s)
  Kato Maki、Kato Takema、Hosoba Eriko、Ohashi Masanao、Fujisaki Midori、Ozaki Mamoru、Yamaguchi Masatoshi、Sameshima Hiroshi、Kurahashi Hiroki
- Journal Title
  
  Human Genome Variation
  
  Volume: 4 Issue: 1 Pages: 17021-17021
- DOI
  10.1038/hgv.2017.21
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-17K11259, KAKENHI-PROJECT-15H04710
[Journal Article] Remote intracranial recurrence of <i>IDH</i> mutant gliomas is associated with <i>TP53</i> mutations and an 8q gain2017
- Author(s)
  Nakae Shunsuke、Kato Takema、Murayama Kazuhiro、Sasaki Hikaru、Abe Masato、Kumon Masanobu、Kumai Tadashi、Yamashiro Kei、Inamasu Joji、Hasegawa Mitsuhiro、Kurahashi Hiroki、Hirose Yuichi
- Journal Title
  
  Oncotarget
  
  Volume: 8 Issue: 49 Pages: 84729-84742
- DOI
  10.18632/oncotarget.20951
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-17K11259, KAKENHI-PROJECT-15H04710, KAKENHI-PROJECT-15K10343, KAKENHI-PROJECT-16K20029
[Journal Article] A Japanese case of β-ureidopropionase deficiency with dysmorphic features2017
- Author(s)
  Akiyama, T., Shibata, T., Yoshinaga, H., Kuhara, T., Nakajima, Y., Kato, T., Maeda, Y., Ohse, M., Oka, M., Kageyama, M., Kobayashi, K.
- Journal Title
  
  Brain and Development
  
  Volume: 39 Issue: 1 Pages: 58-61
- DOI
  10.1016/j.braindev.2016.08.001
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-ORGANIZER-15H05871, KAKENHI-PLANNED-15H05874, KAKENHI-PROJECT-15K19042, KAKENHI-PROJECT-16K18961, KAKENHI-INTERNATIONAL-15K21731, KAKENHI-PROJECT-17K11259
[Journal Article] Genomic Characterization of Chromosomal Insertions: Insights into the Mechanisms Underlying Chromothripsis2017
- Author(s)
  Kato Takema、Ouchi Yuya、Inagaki Hidehito、Makita Yoshio、Mizuno Seiji、Kajita Mitsuharu、Ikeda Toshiro、Takeuchi Kazuhiro、Kurahashi Hiroki
- Journal Title
  
  Cytogenetic and Genome Research
  
  Volume: 153 Issue: 1 Pages: 1-9
- DOI
  10.1159/000481586
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-17K11259, KAKENHI-PROJECT-16K12941, KAKENHI-PROJECT-15H04710, KAKENHI-PROJECT-15K08287
[Journal Article] Palindrome-mediated translocations in humans: a new mechanistic model for gross chromosomal rearrangements.2016
- Author(s)
  Inagaki H, Kato T, Tsutsumi M, Ouchi Y, Ohye T, *Kurahashi H.
- Journal Title
  
  Front Genet
  
  Volume: 7 Pages: 125-125
- DOI
  10.3389/fgene.2016.00125
- Peer Reviewed / Acknowledgement Compliant / Open Access
- Data Source
  KAKENHI-PROJECT-15H04710, KAKENHI-PROJECT-15K19042, KAKENHI-PROJECT-15K08287, KAKENHI-PROJECT-16K08981
[Journal Article] Increased levels of soluble corin in pre-eclampsia and fetal growth restriction.2016
- Author(s)
  Miyazaki J, *Nishizawa H, Kambayashi A, Ito M, Noda Y, Terasawa S, Kato T, Miyamura H, Shiogama K, Sekiya T, Kurahashi H, Fujii T.
- Journal Title
  
  Placenta
  
  Volume: 48 Pages: 20-25
- DOI
  10.1016/j.placenta.2016.10.002
- Peer Reviewed / Acknowledgement Compliant
- Data Source
  KAKENHI-PROJECT-15H04710, KAKENHI-PROJECT-15K19042
[Journal Article] Emergence and Characterization of Unusual DS-1-Like G1P[8] Rotavirus Strains in Children with Diarrhea in Thailand2015
- Author(s)
  Komoto S, Tacharoenmuang R, Guntapong R, Ide T, Haga K, Katayama K, Kato T, Ouchi Y, Kurahashi H, Tsuji T, Sangkitporn S, Taniguchi K.
- Journal Title
  
  PLoS One
  
  Volume: 10(11) Issue: 11 Pages: 1-22
- DOI
  10.1371/journal.pone.0141739
- Peer Reviewed / Acknowledgement Compliant / Open Access / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15K08505, KAKENHI-PROJECT-15K19042, KAKENHI-PROJECT-26670171
[Journal Article] Preimplantation genetic diagnosis/screening by comprehensive molecular testing2015
- Author(s)
  Kurahashi H, Kato T, Miyazaki J, Nishizawa H, Nishio E, Furukawa H, Miyamura H, Ito M, Endo T, Ouchi Y, Inagaki H, Fujii T
- Journal Title
  
  Reprod Med Biol
  
  Volume: 15 Issue: 1 Pages: 13-19
- DOI
  10.1007/s12522-015-0216-6
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-15K19042, KAKENHI-PROJECT-26670171
[Journal Article] Intragenic duplication in the PKHD1 gene in autosomal recessive polycystic kidney disease.2015
- Author(s)
  Miyazaki J, et al.
- Journal Title
  
  BMC Med Genet
  
  Volume: 16 Issue: 1 Pages: 98-98
- DOI
  10.1186/s12881-015-0245-3
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-15K08287, KAKENHI-PROJECT-15K19042, KAKENHI-PROJECT-26670171
[Journal Article] Whole Genomic Analysis of an Unusual Human G6P[14] Rotavirus Strain Isolated from a Child with Diarrhea in Thailand: Evidence for Bovine-To-Human Interspecies Transmission and Reassortment Events2015
- Author(s)
  Tacharoenmuang R, Komoto S, Guntapong R, Ide T, Haga K, Katayama K, Kato T, Ouchi Y, Kurahashi H, Tsuji T, Sangkitporn S, Taniguchi K.
- Journal Title
  
  PLoS One
  
  Volume: 10(9) Issue: 9 Pages: 1-23
- DOI
  10.1371/journal.pone.0139381
- Peer Reviewed / Acknowledgement Compliant / Open Access / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15K08505, KAKENHI-PROJECT-15K19042, KAKENHI-PROJECT-26670171
[Journal Article] Breakpoint analysis of the recurrent constitutional t(8;22)(q24.13;q11.21) translocation2014
- Author(s)
  Mishra D, Kato T, Inagaki H, Kosho T, Wakui K, Kido Y, Sakazume S, Taniguchi-Ikeda M, Morisada N, Iijima K, Fukushima Y, Emanuel BS, Kurahashi H
- Journal Title
  
  Mol Cytogenet
  
  Volume: 7 Issue: 1 Pages: 55-55
- DOI
  10.1186/s13039-014-0055-x
- Peer Reviewed / Acknowledgement Compliant / Open Access
- Data Source
  KAKENHI-PROJECT-24390085, KAKENHI-PROJECT-24501307, KAKENHI-PROJECT-25860256, KAKENHI-PROJECT-26670171, KAKENHI-PROJECT-221S0002
[Journal Article] Analysis of the t(3;8) of hereditary renal cell carcinoma: A palindrome mediated translocation2014
- Author(s)
  Kato T, Franconi CP, Sheridan MB, Hacker AM, Inagakai H, Glover TW, Arlt MF, Drabkin HA, Gemmill RM, Kurahashi H, Emanuel BS
- Journal Title
  
  Cancer Genet
  
  Volume: 207 Issue: 4 Pages: 133-140
- DOI
  10.1016/j.cancergen.2014.03.004
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-24390085, KAKENHI-PROJECT-25860256, KAKENHI-PROJECT-26670171
[Journal Article] Prevalence of Emanuel syndrome: theoretical frequency and surveillance result2014
- Author(s)
  Ohye T, Inagaki H, Kato T, Tsutsumi M, Kurahashi H
- Journal Title
  
  Pediatr Int
  
  Volume: 56 Issue: 4 Pages: 462-466
- DOI
  10.1111/ped.12437
- Peer Reviewed / Acknowledgement Compliant / Open Access
- Data Source
  KAKENHI-PROJECT-24390085, KAKENHI-PROJECT-25860256, KAKENHI-PROJECT-26670171
[Journal Article] Age-related decrease of meiotic cohesins in human oocyte2014
- Author(s)
  Tsutsumi M, Fujiwara R, Nishizawa H, Ito M, Kogo H, Inagaki H, Ohye T, Kato T, Fujii T, Kurahashi H
- Journal Title
  
  PLoS One
  
  Volume: 9, Issue: 5 Pages: 1-8
- DOI
  10.1371/journal.pone.0096710
- Peer Reviewed / Acknowledgement Compliant / Open Access
- Data Source
  KAKENHI-PROJECT-24390085, KAKENHI-PROJECT-24590263, KAKENHI-PROJECT-25860255, KAKENHI-PROJECT-25860256, KAKENHI-PROJECT-26462540, KAKENHI-PROJECT-26670171
[Journal Article] Two sequential cleavage reactions on cruciform DNA structures cause palindrome-mediated chromosomal translocations2013
- Author(s)
  Inagaki H, Ohye T, Kogo H, Tsutsumi M, Kato T, Tong M, Emanuel BS, Kurahashi H
- Journal Title
  
  Nat Commun
  
  Volume: 4 Issue: 1 Pages: 1592-1592
- DOI
  10.1038/ncomms2595
- Peer Reviewed
- Data Source
  KAKENHI-PUBLICLY-23013019, KAKENHI-PROJECT-23659182, KAKENHI-PROJECT-24390085, KAKENHI-PROJECT-24501307, KAKENHI-PROJECT-24590263, KAKENHI-PROJECT-25860256
[Patent] 胎児成分の検出方法2017
- Inventor(s)
  加藤武馬
- Industrial Property Rights Holder
  藤田保健衛生大学
- Industrial Property Rights Type
  特許
- Filing Date
  2017-04-19
- Data Source
  KAKENHI-PROJECT-15K19042
[Presentation] 初期分割不良は胚盤胞到達後の正倍数率に影響しない2020
- Author(s)
  渡辺真一、吉貝香里、冨田麻莉、鈴木篤智、野呂麻理子、松田有希野、宮井俊輔、加藤武馬、中野英子、倉橋浩樹、澤田富夫
- Organizer
  第61回　日本卵子学会
- Data Source
  KAKENHI-PROJECT-19K09790
[Presentation] タイムラプスモニタリングで胚発生能と正倍数性はどこまで評価できるか2020
- Author(s)
  渡辺真一、吉貝香里、冨田麻莉、鈴木篤智、松田有希野、宮井俊輔、加藤武馬、中野英子、倉橋浩樹、澤田富夫
- Organizer
  第38回　日本受精着床学会（ワークショップ）
- Data Source
  KAKENHI-PROJECT-19K09790
[Presentation] NGS解析データより胚移植順位の基準を再構築する2019
- Author(s)
  吉貝香里，松田有希野，加藤武馬，宮井俊輔，新井千登勢，鈴木篤智，冨田麻莉，中野英子，倉橋浩樹，澤田富夫
- Organizer
  第64回日本生殖医学会学術講演会
- Data Source
  KAKENHI-PROJECT-19K09790
[Presentation] 精子因子が異数性に与える影響2019
- Author(s)
  鈴木篤智、吉貝香里、加藤武馬、宮井俊輔、松田有希野、新井千登勢、冨田麻莉、中野英子、倉橋浩樹、澤田富夫
- Organizer
  第64回日本生殖医学会学術講演会
- Data Source
  KAKENHI-PROJECT-19K09790
[Presentation] NGS分析を用いた胚発育の後方視的解析2019
- Author(s)
  松田有希野、吉貝香里、加藤武馬、宮井俊輔、新井千登勢、鈴木篤智、冨田麻莉、中野英子、倉橋浩樹、澤田富夫
- Organizer
  第64回日本生殖医学会学術講演会
- Data Source
  KAKENHI-PROJECT-19K09790
[Presentation] How does DNA break for formation of three-way translocations?2019
- Author(s)
  Takema Kato
- Organizer
  日本人類遺伝学会第64回大会
- Data Source
  KAKENHI-PROJECT-17K11259
[Presentation] Genetic counseling for preimplantation genetic diagnosis2019
- Author(s)
  河村理恵，森山育実，加藤麻希，河合美紀，宮井俊輔，倉橋浩樹
- Organizer
  第43回日本遺伝カウンセリング学会学術集会
- Data Source
  KAKENHI-PROJECT-19K09790
[Presentation] 染色体構造異常の解析2019
- Author(s)
  加藤武馬、倉橋浩樹
- Organizer
  小児遺伝学会
- Invited
- Data Source
  KAKENHI-PROJECT-17K11259
[Presentation] PGT解析手法の現状2019
- Author(s)
  加藤武馬
- Organizer
  第21回東北ART研究会
- Invited
- Data Source
  KAKENHI-PROJECT-17K11259
[Presentation] 凍結融解胚移植において異数胚を避けるための条件2019
- Author(s)
  松田有希野、吉貝香里、加藤武馬、宮井俊輔、新井千登勢、鈴木篤智、冨田麻莉、中野英子、倉橋浩樹、澤田富夫
- Organizer
  第64回日本生殖医学会学術講演会
- Data Source
  KAKENHI-PROJECT-19K09790
[Presentation] PGT解析技術の現状と問題点2019
- Author(s)
  加藤武馬
- Organizer
  第26回セント・ルカセミナー
- Invited
- Data Source
  KAKENHI-PROJECT-17K11259
[Presentation] 着床前・出生前のゲノム解析2019
- Author(s)
  加藤武馬
- Organizer
  第5回日本産科婦人科遺伝診療学会
- Invited
- Data Source
  KAKENHI-PROJECT-17K11259
[Presentation] Optimization of PGD for recurrent t(11;22) carrier2018
- Author(s)
  Takema Kato, Maki Kato, Yasuko Shinkai, Haruki Nishizawa, Toshiaki Endo, Chikako Kani, Masanori Ochi, Shin Hayashi, Johji Inazawa, Hiroki Kurahashi
- Organizer
  PGDIS
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-17K11259
[Presentation] How does DNA break for formation of three-way translocations?2018
- Author(s)
  Takema Kato, Hidehito Inagaki, Yasuko Shinkai, Asuka Kato, Rie Kawamura, Makiko Tsutsumi, Mariko Taniguchi-Ikeda, Seiji Mizuno, Yoshio Makita, Nakamichi Saito, Nobuhiko Ochi, Hiroki Kurahashi
- Organizer
  The American Society of Human Genetics
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-17K11259
[Presentation] Mosaicism for two abnormal cell lines, one with trisomy 5 and one with trisomy 82018
- Author(s)
  加藤武馬
- Organizer
  Chubu Cytoegenetics Conference
- Invited
- Data Source
  KAKENHI-PROJECT-17K11259
[Presentation] 次世代シーケンサーを用いた着床前診断染色体解析の解析精度と限界2018
- Author(s)
  加藤武馬、加藤麻希、宮井俊輔、遠藤俊明、中岡義晴、福田愛作、澤井英明、田中温、宇津宮隆史、竹内一浩、倉橋浩樹
- Organizer
  受精着床学会
- Data Source
  KAKENHI-PROJECT-17K11259
[Presentation] 均衡型染色体構造異常保因者にInter-chromosomal effectは見られるか2018
- Author(s)
  加藤武馬、遠藤俊明、中岡義晴、福田愛作、澤井英明、田中温、宇津宮隆史、竹内一浩、倉橋浩樹
- Organizer
  生殖医学会
- Data Source
  KAKENHI-PROJECT-17K11259
[Presentation] 染色体構造異常の発生機構2018
- Author(s)
  加藤武馬、稲垣秀人、新海保子、堤真紀子、山本俊至、水野誠司、倉橋浩樹
- Organizer
  先天異常学会
- Invited
- Data Source
  KAKENHI-PROJECT-17K11259
[Presentation] 網羅的手法によるPGDの現状と問題点2018
- Author(s)
  加藤武馬
- Organizer
  JISART
- Invited
- Data Source
  KAKENHI-PROJECT-17K11259
[Presentation] 染色体挿入の発生機序2018
- Author(s)
  加藤武馬、稲垣秀人、藤田尚子、新海保子、蒔田芳男、水野誠司、梶田光晴、池田敏郎、竹内一浩、柘植郁哉、倉橋浩樹
- Organizer
  小児遺伝学会
- Data Source
  KAKENHI-PROJECT-17K11259
[Presentation] Fetoplacental chromosomal structural abnormalities are originated from repeated breakage-fusion-bridge cycles.2018
- Author(s)
  Takema Kato, Syunsuke Miyai, Fumihiko Suzuki, Yuki Naru, Maki Kato, Hidehito Inagaki, Mitsuhisa Shinya, Toshiro Ikeda, Hiroki Kurahashi
- Organizer
  人類遺伝学会
- Data Source
  KAKENHI-PROJECT-17K11259
[Presentation] Comprehensive chromosomal analysis of blastomeres with developmental arrest2017
- Author(s)
  Takema Kato, Sachie Nishiyama, Yukio Nishyama, Kaori Yoshikai, Yukino Matsuda, Tomio Sawada, Hikari Yoshizawa, Hiroshi Furukawa, Haruki Nishizawa, Maki Kato, Asuka Kanbayashi, Hiroki Kurahashi
- Organizer
  International Conference on Prenatal Diagnosis and Therapy
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-17K11259
[Presentation] Mate Pair Sequencing for Chromosomal Rearrangements2017
- Author(s)
  Takema Kato, Hidehito Inagaki, Yasuko Shinkai, Makiko Tsutsumi, Naoko Fujita, Toshiyuki Yamamoto, Hiroki Kurahashi
- Organizer
  分子生物学会
- Data Source
  KAKENHI-PROJECT-17K11259
[Presentation] 全ゲノムシーケンスとゲノム再構成について2017
- Author(s)
  加藤武馬
- Organizer
  染色体研究会
- Invited
- Data Source
  KAKENHI-PROJECT-17K11259
[Presentation] Chromosomal abnormalities in ICM and TE of human blastocysts2017
- Author(s)
  Takema kato, Maki Kato, Kaori Yoshikai, Yukino Matsuda, Chitose Arai, Naomi Asai, Eiko nakano, Tomio Sawada, Hiroki Kurahashi
- Organizer
  日本人類遺伝学会
- Data Source
  KAKENHI-PROJECT-17K11259
[Presentation] Mechanisms of Interchromosomal Insertional Translocation2016
- Author(s)
  Takema Kato, Yuya Ouchi, Hidehito Inagaki, Yoshio Makita, Seiji Mizuno, Hiroki Kurahashi
- Organizer
  ICHG2016（the 13th International Congress of Human Genetics in 2016）
- Place of Presentation
  京都国際会館
- Year and Date
  2016-04-03
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15K19042
[Presentation] Mechanistic analysis and prediction of interchromosomal insertional translocation2016
- Author(s)
  Takema Kato, Yuya Ouchi, Hidehito Inagaki, Yoshio Makita, Seiji Mizuno, Hiroki Kurahashi
- Organizer
  The American Society of Human Genetics Annual Meeting
- Place of Presentation
  Vancouver
- Year and Date
  2016-10-19
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15K19042
[Presentation] Breakpoint analysis of the recurrent constitutional t(8;22)(q24;q11) translocation2015
- Author(s)
  Takema Kato, Hidehito Inagaki, Divya Mishra, Yuya Ouchi, Makiko Tsutsumi, Tamae Ohye, Hiroki Kurahashi
- Organizer
  第11回国際ゲノム会議
- Place of Presentation
  学術総合センター　一橋講堂
- Year and Date
  2015-05-20
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15K19042
[Presentation] t(8;22)(q24.1;q11.2)の2家系2015
- Author(s)
  加藤武馬、Divya Mishra、稲垣秀人、池田真理子、森貞直哉、飯島一誠、城戸康宏、坂爪悟、古庄知己、涌井敬子、福嶋義光、倉橋浩樹
- Organizer
  第55回日本先天異常学会学術集会／第38回小児遺伝学会学術大会
- Place of Presentation
  パシフィコ横浜会議センター
- Year and Date
  2015-07-25
- Data Source
  KAKENHI-PROJECT-15K19042
[Presentation] 染色体挿入の発生機序2015
- Author(s)
  加藤武馬、大内雄矢、稲垣秀人、蒔田芳男、水野誠司、倉橋浩樹
- Organizer
  日本人類遺伝学会第60回大会
- Place of Presentation
  京王プラザホテル
- Year and Date
  2015-10-14
- Data Source
  KAKENHI-PROJECT-15K19042
[Presentation] 染色体挿入の発生機序2015
- Author(s)
  加藤武馬、大内雄矢、稲垣秀人、蒔田芳男、水野誠司、倉橋浩樹
- Organizer
  BMB2015（第38回日本分子生物学会年会　第88回日本生化学大会　合同大会)
- Place of Presentation
  神戸ポートアイランド
- Year and Date
  2015-12-01
- Data Source
  KAKENHI-PROJECT-15K19042
[Presentation] 染色体挿入の発生機序2015
- Author(s)
  加藤武馬、大内雄矢、稲垣秀人、倉橋浩樹
- Organizer
  新学術ゲノム支援拡大班会議
- Place of Presentation
  京都国際会館
- Year and Date
  2015-08-27
- Data Source
  KAKENHI-PROJECT-15K19042
[Presentation] t(8;22)(q24.1;q11.2)の2家系2014
- Author(s)
  加藤武馬、Divya Mishra、稲垣秀人、大江瑞恵、堤真紀子、池田真理子、森貞直哉、飯島一誠、城戸康宏、坂爪悟、古庄知己、涌井敬子、福嶋義光、倉橋浩樹
- Organizer
  第5回東海小児遺伝カンファレンス
- Place of Presentation
  名古屋市立大学
- Data Source
  KAKENHI-PROJECT-25860256
[Presentation] パリンドロームを介した染色体転座の発生メカニズムの解明2013
- Author(s)
  加藤武馬、稲垣秀人、倉橋浩樹
- Organizer
  新学術「ゲノム支援」拡大班会議
- Place of Presentation
  神戸ポートピアホテル
- Data Source
  KAKENHI-PROJECT-25860256
[Presentation] FRA3B and the Palindromic AT-rich repeat2013
- Author(s)
  Takema Kato, Molly B. Sheridan, April M. Hacker, Hidehito Inagakai, Thomas Glover, Sharon Plon, Harry Drabkin, Robert Gemmill, Beverly S. Emanuel, Hiroki Kurahashi
- Organizer
  日本人類遺伝学会第58回大会
- Place of Presentation
  仙台江陽グランドホテル
- Data Source
  KAKENHI-PROJECT-25860256
[Presentation] 染色体転座頻度と染色体間距離の因果関係2013
- Author(s)
  加藤武馬、稲垣秀人、大江瑞恵、堤真紀子、倉橋浩樹
- Organizer
  第36日本分子生物学会
- Place of Presentation
  神戸ポートピアホテル
- Data Source
  KAKENHI-PROJECT-25860256
[Presentation] 染色体脆弱部位FRA3Bとパリンドローム配列2013
- Author(s)
  加藤武馬
- Organizer
  第45回藤田学園医学会
- Place of Presentation
  藤田保健衛生大学
- Data Source
  KAKENHI-PROJECT-25860256
[Presentation] Breakpoint analysis of the recurrent constitutional t(8;22)(q24.13;q11.21) translocation
- Author(s)
  加藤武馬、Divya Mishra、稲垣秀人、池田真理子、森貞直哉、飯島一誠、城戸康宏、坂爪悟、古庄知己、涌井敬子、福嶋義光、倉橋浩樹
- Organizer
  第37回日本分子生物学会
- Place of Presentation
  パシフィコ横浜
- Year and Date
  2014-11-25 – 2014-11-27
- Data Source
  KAKENHI-PROJECT-25860256
[Presentation] ヒトゲノムに散在するパリンドローム配列の同定
- Author(s)
  加藤武馬、稲垣秀人、大内雄矢、倉橋浩樹
- Organizer
  新学術「ゲノム支援」拡大班会議
- Place of Presentation
  神戸ポートピアホテル
- Year and Date
  2014-08-20 – 2014-08-21
- Data Source
  KAKENHI-PROJECT-25860256
[Presentation] Breakpoint analysis of the recurrent constitutional t(8;22)(q24.13;q11.21) translocation
- Author(s)
  加藤武馬、Divya Mishra、稲垣秀人、池田真理子、森貞直哉、飯島一誠、城戸康宏、坂爪悟、古庄知己、涌井敬子、福嶋義光、倉橋浩樹
- Organizer
  第59回日本人類遺伝学会第21回日本遺伝子診療学会合同大会
- Place of Presentation
  タワーホール船堀
- Year and Date
  2014-11-19 – 2014-11-22
- Data Source
  KAKENHI-PROJECT-25860256

1. Miyai Shunsuke (50563350)

# of Collaborated Projects: 1 results

# of Collaborated Products: 14 results
2. Nagasaka Miwako (70723998)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
3. 河村理恵 (20735534)

# of Collaborated Projects: 1 results

# of Collaborated Products: 3 results
4. 池田真理子 (00410738)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
5. 粟野宏之 (30437470)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
6. 倉橋浩樹

# of Collaborated Projects: 0 results

# of Collaborated Products: 7 results
7. 山本俊至

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
8. 河本聡志

# of Collaborated Projects: 0 results

# of Collaborated Products: 2 results

KATO Takema 加藤 武馬

Research Projects

Research Products

Co-Researchers

初期胚における染色体不安定性を起こす要因の探索Principal Investigator

Principal Investigator

Project Period (FY)

Research Category

Review Section

Research Institution

Establishing Diagnostic Methods and Elucidating the Pathogenesis of Fukuyama Congenital Muscular Dystrophy Using Long-Read Sequencers

Principal Investigator

Project Period (FY)

Research Category

Review Section

Research Institution

Risk factors related to chromosomal aneuploidy in human blastocysts

Principal Investigator

Project Period (FY)

Research Category

Review Section

Research Institution

Molecular origin of chromosomal abnormalities in early embryonic cellsPrincipal Investigator

Principal Investigator

Project Period (FY)

Research Category

Research Field

Research Institution

Spatial proximity of PATRRs and their translocation frequenciesPrincipal Investigator

Principal Investigator

Project Period (FY)

Research Category

Research Field

Research Institution

FRA3B and the Palindromic AT-rich repeatPrincipal Investigator

Principal Investigator

Project Period (FY)

Research Category

Research Field

Research Institution

[Journal Article] Target enrichment long-read sequencing with adaptive sampling can determine the structure of the small supernumerary marker chromosomes2022

Author(s)

Journal Title

DOI

Data Source

[Journal Article] Usefulness of combined NGS and QF-PCR analysis for product of conception karyotyping2022

Author(s)

Journal Title

DOI

Data Source

[Journal Article] Identification of a Novel Mutation in Carboxyl Ester Lipase Gene in a Patient with MODY-like Diabetes2022

Author(s)

Journal Title

DOI

NAID

ISSN

Language

Data Source

[Journal Article] Genotype-phenotype correlation of renal lesions in the tuberous sclerosis complex2022

Author(s)

Journal Title

DOI

Data Source

[Journal Article] Coexistence of RASA1 and COL4A2 variants caused pial arteriovenous fistula (AVF) in a patient with capillary malformation-arteriovenous malformation2021

Author(s)

Journal Title

DOI

Data Source

[Journal Article] Myoinositol to Total Choline Ratio in Glioblastomas as a Potential Prognostic Factor in Preoperative Magnetic Resonance Spectroscopy2021

Author(s)

Journal Title

DOI

NAID

ISSN

Language

Data Source

[Journal Article] Analysis of the Origin of Double Mosaic Aneuploidy in Two Cases.2020

Author(s)

Journal Title

DOI

KATO Takema 加藤武馬