Tsutomu Ogata

ORCID

Publication Activity (10 Years)

Years Active: 2015-2024
Publications (10 Years): 44

Top Venues

Journal of human genetics

Clinical epigenetics

American journal of medical genetics. Part A

Human genome variation

Hamamatsu University School of Medicine

This page only lists publications with an associated author ORCID identifier.

Affiliation History

Hamamatsu University School of Medicine May 16 2011

Japan

Professor :: Pediatrics

Publications

Kaori Yamoto, Hirotomo Saitsu, Yumiko Ohkubo, Masayo Kagami, Tsutomu Ogata
Pathogenic sequence variant and microdeletion affecting HMGA2 in Silver-Russell syndrome: case reports and literature review. Clinical epigenetics 16 (1) (2024)
Kaori Yamoto, Hirotomo Saitsu, Yumiko Ohkubo, Masayo Kagami, Tsutomu Ogata
Pathogenic sequence variant and microdeletion affecting HMGA2 in Silver-Russell syndrome: case reports and literature review. Clinical epigenetics 16 (1) (2024)
Kaori Yamoto, Hirotomo Saitsu, Yumiko Ohkubo, Masayo Kagami, Tsutomu Ogata
Pathogenic sequence variant and microdeletion affecting HMGA2 in Silver-Russell syndrome: case reports and literature review. Clinical epigenetics 16 (1) (2024)
Tsutomu Ogata, Atsushi Hattori, Maki Fukami
SHOX and sex difference in height: a hypothesis. Endocrine journal (2024)
Kaori Yamoto, Hirotomo Saitsu, Yumiko Ohkubo, Masayo Kagami, Tsutomu Ogata
Pathogenic sequence variant and microdeletion affecting HMGA2 in Silver-Russell syndrome: case reports and literature review. Clinical epigenetics 16 (1) (2024)
Ryota Kawakami, Takuya Hiraide, Kazuki Watanabe, Sachiko Miyamoto, Kota Hira, Kazuyuki Komatsu, Hidetoshi Ishigaki, Kimiyoshi Sakaguchi, Masato Maekawa, Keita Yamashita, Tokiko Fukuda, Isao Miyairi, Tsutomu Ogata, Hirotomo Saitsu
RNA sequencing and target long-read sequencing reveal an intronic transposon insertion causing aberrant splicing. Journal of human genetics (2023)
Ryota Kawakami, Takuya Hiraide, Kazuki Watanabe, Sachiko Miyamoto, Kota Hira, Kazuyuki Komatsu, Hidetoshi Ishigaki, Kimiyoshi Sakaguchi, Masato Maekawa, Keita Yamashita, Tokiko Fukuda, Isao Miyairi, Tsutomu Ogata, Hirotomo Saitsu
RNA sequencing and target long-read sequencing reveal an intronic transposon insertion causing aberrant splicing. Journal of human genetics 69 (2) (2023)
Tatsuki Urakawa, Shinichiro Sano, Sayaka Kawashima, Akie Nakamura, Hirohito Shima, Motoki Ohta, Yuki Yamada, Ai Nishida, Hiromune Narusawa, Yoshiaki Ohtsu, Keiko Matsubara, Sumito Dateki, Yoshihiro Maruo, Maki Fukami, Tsutomu Ogata, Masayo Kagami
(Epi)genetic and clinical characteristics in 84 patients with pseudohypoparathyroidism type 1B. European journal of endocrinology (2023)
Takuya Hiraide, Kenji Shimizu, Yoshinori Okumura, Sachiko Miyamoto, Mitsuko Nakashima, Tsutomu Ogata, Hirotomo Saitsu
A deep intronic TCTN2 variant activating a cryptic exon predicted by SpliceRover in a patient with Joubert syndrome. Journal of human genetics (2023)
Yohei Masunaga, Yasuko Fujisawa, Francesco Massart, Claudio Spinelli, Yoshiyuki Kojima, Kentaro Mizuno, Yutaro Hayashi, Isoji Sasagawa, Rie Yoshida, Fumiko Kato, Maki Fukami, Naoyuki Kamatani, Hirotomo Saitsu, Tsutomu Ogata
Microdeletion at ESR1 Intron 6 (DEL_6_75504) Is a Susceptibility Factor for Cryptorchidism and Hypospadias. The Journal of clinical endocrinology and metabolism (2023)
Ryota Kawakami, Takuya Hiraide, Kazuki Watanabe, Sachiko Miyamoto, Kota Hira, Kazuyuki Komatsu, Hidetoshi Ishigaki, Kimiyoshi Sakaguchi, Masato Maekawa, Keita Yamashita, Tokiko Fukuda, Isao Miyairi, Tsutomu Ogata, Hirotomo Saitsu
RNA sequencing and target long-read sequencing reveal an intronic transposon insertion causing aberrant splicing. Journal of human genetics 69 (2) (2023)
Tomoko Fuke, Akie Nakamura, Takanobu Inoue, Sayaka Kawashima, Kaori Hara-Isono, Keiko Matsubara, Shinichiro Sano, Kazuki Yamazawa, Maki Fukami, Tsutomu Ogata, Masayo Kagami
Frequency and clinical characteristics of distinct etiologies in patients with Silver-Russell syndrome diagnosed based on the Netchine-Harbison clinical scoring system. Journal of human genetics 67 (10) (2022)
Tsuyoshi Isojima, Satoru Sakazume, Tomonobu Hasegawa, Tsutomu Ogata, Toshio Nakanishi, Toshiro Nagai, Susumu Yokoya
Correction to: Growth references for Japanese individuals with Noonan syndrome. Pediatric research (2022)
Yohei Masunaga, Yumiko Ohkubo, Gen Nishimura, Taizo Ueno, Yasuko Fujisawa, Maki Fukami, Hirotomo Saitsu, Tsutomu Ogata
ACAN biallelic variants in a girl with severe idiopathic short stature. Journal of human genetics 67 (8) (2022)
Takuya Hiraide, Kenji Shimizu, Sachiko Miyamoto, Kazushi Aoto, Mitsuko Nakashima, Tomomi Yamaguchi, Tomoki Kosho, Tsutomu Ogata, Hirotomo Saitsu
Genome sequencing and RNA sequencing of urinary cells reveal an intronic FBN1 variant causing aberrant splicing. Journal of human genetics 67 (7) (2022)
Kaori Hara-Isono, Akie Nakamura, Tomoko Fuke, Takanobu Inoue, Sayaka Kawashima, Keiko Matsubara, Shinichiro Sano, Kazuki Yamazawa, Maki Fukami, Tsutomu Ogata, Masayo Kagami
Pathogenic Copy Number and Sequence Variants in Children Born SGA With Short Stature Without Imprinting Disorders. The Journal of clinical endocrinology and metabolism 107 (8) (2022)
Kaori Yamoto, Satoshi Okada, Fumiko Kato, Yasuko Fujisawa, Maki Fukami, Hirotomo Saitsu, Tsutomu Ogata
A novel intronic PORCN variant creating an alternative splice acceptor site in a mother and her daughter with focal dermal hypoplasia. American journal of medical genetics. Part A 188 (5) (2022)
Maki Fukami, Junya Shindo, Tsutomu Ogata, Ikuko Kageyama, Tsutomu Kamimaki
SHOX far-downstream deletion in a patient with nonsyndromic short stature. American journal of medical genetics. Part A 188 (7) (2022)
Yasuko Fujisawa, Hiroyuki Ono, Alu Konno, Ikuko Yao, Hiroaki Itoh, Takashi Baba, Kenichirou Morohashi, Yuko Katoh-Fukui, Mami Miyado, Maki Fukami, Tsutomu Ogata
Intrauterine Hyponutrition Reduces Fetal Testosterone Production and Postnatal Sperm Count in the Mouse. Journal of the Endocrine Society 6 (4) (2022)
Kyoko Fukahori, Kaori Yamoto, Hirotomo Saitsu, Tsutomu Ogata, Keisuke Nagasaki
PORCN-related microphthalmia with limb anomalies: Case report and literature review. American journal of medical genetics. Part A (2022)
Takuya Hiraide, Yohei Masunaga, Akira Honda, Fumiko Kato, Tokiko Fukuda, Maki Fukami, Mitsuko Nakashima, Hirotomo Saitsu, Tsutomu Ogata
Retrotransposition disrupting EBP in a girl and her mother with X-linked dominant chondrodysplasia punctata. Journal of human genetics 67 (5) (2022)
Takuya Hiraide, Taihei Tanaka, Yohei Masunaga, Yumiko Ohkubo, Mitsuko Nakashima, Tokiko Fukuda, Tsutomu Ogata, Hirotomo Saitsu
Global developmental delay, systemic dysmorphism and epilepsy in a patient with a de novo U2AF2 variant. Journal of human genetics 66 (12) (2021)
Yohei Masunaga, Masayo Kagami, Fumiko Kato, Takeshi Usui, Takako Yonemoto, Kazuo Mishima, Maki Fukami, Kazushi Aoto, Hirotomo Saitsu, Tsutomu Ogata
Parthenogenetic mosaicism: generation via second polar body retention and unmasking of a likely causative PER2 variant for hypersomnia. Clinical epigenetics 13 (1) (2021)
Kaori Hara-Isono, Keiko Matsubara, Riku Hamada, Shun Shimada, Tomomi Yamaguchi, Keiko Wakui, Osamu Miyazaki, Koji Muroya, Kenji Kurosawa, Maki Fukami, Tsutomu Ogata, Tomoki Kosho, Masayo Kagami
A patient with Silver-Russell syndrome with multilocus imprinting disturbance, and Schimke immuno-osseous dysplasia unmasked by uniparental isodisomy of chromosome 2. Journal of human genetics 66 (11) (2021)
Sachiko Nishina, Katsuhiro Hosono, Shizuka Ishitani, Kenjiro Kosaki, Tadashi Yokoi, Tomoyo Yoshida, Kaoru Tomita, Maki Fukami, Hirotomo Saitsu, Tsutomu Ogata, Tohru Ishitani, Yoshihiro Hotta, Noriyuki Azuma
Biallelic CDK9 variants as a cause of a new multiple-malformation syndrome with retinal dystrophy mimicking the CHARGE syndrome. Journal of human genetics 66 (10) (2021)
Satoshi Tamaoka, Erina Suzuki, Atsushi Hattori, Tsutomu Ogata, Maki Fukami, Yuko Katoh-Fukui
NDNF variants are rare in patients with congenital hypogonadotropic hypogonadism. Human genome variation 8 (1) (2021)
Takaaki Hayashi, Katsuhiro Hosono, Akiko Kubo, Kentaro Kurata, Satoshi Katagiri, Kei Mizobuchi, Minehiro Kurai, Norihito Mamiya, Mineo Kondo, Toshiaki Tachibana, Hirotomo Saitsu, Tsutomu Ogata, Tadashi Nakano, Yoshihiro Hotta
Long-term observation of a Japanese mucolipidosis IV patient with a novel homozygous p.F313del variant of MCOLN1. American journal of medical genetics. Part A 182 (6) (2020)
Kazuki Yamazawa, Takanobu Inoue, Yoshihiro Sakemi, Toshinori Nakashima, Hironori Yamashita, Kaduki Khono, Hideki Fujita, Keisuke Enomoto, Kazuhiko Nakabayashi, Kenichiro Hata, Moeko Nakashima, Tatsuo Matsunaga, Akie Nakamura, Keiko Matsubara, Tsutomu Ogata, Masayo Kagami
Loss of imprinting of the human-specific imprinted gene ZNF597 causes prenatal growth retardation and dysmorphic features: implications for phenotypic overlap with Silver-Russell syndrome. Journal of medical genetics 58 (6) (2020)
Jessica Omark, Yohei Masunaga, Mark Hannibal, Brandon Shaw, Maki Fukami, Fumiko Kato, Hirotomo Saitsu, Masayo Kagami, Tsutomu Ogata
Kagami-Ogata syndrome in a patient with 46,XX,t(2;14)(q11.2;q32.2)mat disrupting MEG3. Journal of human genetics 66 (4) (2020)
Kaori Yamoto, Hirotomo Saitsu, Yasuko Fujisawa, Fumiko Kato, Keiko Matsubara, Maki Fukami, Masayo Kagami, Tsutomu Ogata
Coffin-Lowry syndrome in a girl with 46,XX,t(X;11)(p22;p15)dn: Identification of RPS6KA3 disruption by whole genome sequencing. Clinical case reports 8 (6) (2020)
Takuya Hiraide, Seiji Watanabe, Tomoko Matsubayashi, Kumiko Yanagi, Mitsuko Nakashima, Tsutomu Ogata, Hirotomo Saitsu
A de novo TOP2B variant associated with global developmental delay and autism spectrum disorder. Molecular genetics & genomic medicine 8 (3) (2020)
Daisuke Shimizu, Rieko Sakamoto, Kaori Yamoto, Hirotomo Saitsu, Maki Fukami, Gen Nishimura, Tsutomu Ogata
De novo AFF3 variant in a patient with mesomelic dysplasia with foot malformation. Journal of human genetics 64 (10) (2019)
Erina Suzuki, Hirohito Shima, Masayo Kagami, Shun Soneda, Toshiaki Tanaka, Shuichi Yatsuga, Junko Nishioka, Yuji Oto, Toshiya Kamiya, Yasuhiro Naiki, Tsutomu Ogata, Yasuko Fujisawa, Akie Nakamura, Sayaka Kawashima, Shuntaro Morikawa, Reiko Horikawa, Shinichiro Sano, Maki Fukami
(Epi)genetic defects of MKRN3 are rare in Asian patients with central precocious puberty. Human genome variation 6 (2019)
Kaori Yamoto, Hirotomo Saitsu, Gen Nishimura, Rika Kosaki, Shinichiro Takayama, Nobuhiko Haga, Hidefumi Tonoki, Akihisa Okumura, Emiko Horii, Nobuhiko Okamoto, Hiroshi Suzumura, Shiro Ikegawa, Fumiko Kato, Yasuko Fujisawa, Eiko Nagata, Shuji Takada, Maki Fukami, Tsutomu Ogata
Comprehensive clinical and molecular studies in split-hand/foot malformation: identification of two plausible candidate genes (LRP6 and UBA2). European journal of human genetics : EJHG 27 (12) (2019)
Akira Ohishi, Yohei Masunaga, Shigeo Iijima, Kaori Yamoto, Fumiko Kato, Maki Fukami, Hirotomo Saitsu, Tsutomu Ogata
De novo ZBTB7A variant in a patient with macrocephaly, intellectual disability, and sleep apnea: implications for the phenotypic development in 19p13.3 microdeletions. Journal of human genetics 65 (2) (2019)
Mami Miyado, Maki Fukami, Shuji Takada, Miho Terao, Kazuhiko Nakabayashi, Kenichiro Hata, Yoichi Matsubara, Yoko Tanaka, Goro Sasaki, Keisuke Nagasaki, Masaaki Shiina, Kazuhiro Ogata, Youhei Masunaga, Hirotomo Saitsu, Tsutomu Ogata
Germline-Derived Gain-of-Function Variants of Gsα-Coding GNAS Gene Identified in Nephrogenic Syndrome of Inappropriate Antidiuresis. Journal of the American Society of Nephrology : JASN 30 (5) (2019)
Hiroyuki Ono, Hirotomo Saitsu, Reiko Horikawa, Shinichi Nakashima, Yumiko Ohkubo, Kumiko Yanagi, Kazuhiko Nakabayashi, Maki Fukami, Yasuko Fujisawa, Tsutomu Ogata
Partial androgen insensitivity syndrome caused by a deep intronic mutation creating an alternative splice acceptor site of the AR gene. Scientific reports 8 (1) (2018)
Shigeru Nakamura, Yoshitomo Kobori, Yoshihiko Ueda, Yoko Tanaka, Hiromichi Ishikawa, Atsumi Yoshida, Momori Katsumi, Kazuki Saito, Akie Nakamura, Tsutomu Ogata, Hiroshi Okada, Hideo Nakai, Mami Miyado, Maki Fukami
STX2 is a causative gene for nonobstructive azoospermia. Human mutation 39 (6) (2018)
Daisuke Shimizu, Satoru Iwashima, Keisuke Sato, Satoshi Hayano, Maki Fukami, Hirotomo Saitsu, Tsutomu Ogata
GATA4 variant identified by whole-exome sequencing in a Japanese family with atrial septal defect: Implications for male sex development. Clinical case reports 6 (11) (2018)
Kaori Yamoto, Shingo Okamoto, Yasuko Fujisawa, Maki Fukami, Hirotomo Saitsu, Tsutomu Ogata
FGFR1 disruption identified by whole genome sequencing in a male with a complex chromosomal rearrangement and hypogonadotropic hypogonadism. American journal of medical genetics. Part A 176 (1) (2017)
Marte G Haug, Atle Brendehaug, Gunnar Houge, Masayo Kagami, Tsutomu Ogata
Mosaic upd(14)pat in a patient with mild features of Kagami-Ogata syndrome. Clinical case reports 6 (1) (2017)
Kaori Yamoto, Hirotomo Saitsu, Norio Nakagawa, Hisakazu Nakajima, Tatsuji Hasegawa, Yasuko Fujisawa, Masayo Kagami, Maki Fukami, Tsutomu Ogata
De novo IGF2 mutation on the paternal allele in a patient with Silver-Russell syndrome and ectrodactyly. Human mutation 38 (8) (2017)
Tadashi Yokoi, Sachiko Nishina, Maki Fukami, Tsutomu Ogata, Katsuhiro Hosono, Yoshihiro Hotta, Noriyuki Azuma
Genotype-phenotype correlation of PAX6 gene mutations in aniridia. Human genome variation 3 (2016)
Masayo Kagami, Keiko Matsubara, Kazuhiko Nakabayashi, Akie Nakamura, Shinichiro Sano, Kohji Okamura, Kenichiro Hata, Maki Fukami, Tsutomu Ogata
Genome-wide multilocus imprinting disturbance analysis in Temple syndrome and Kagami-Ogata syndrome. Genetics in medicine : official journal of the American College of Medical Genetics 19 (4) (2016)
Tsuyoshi Isojima, Satoru Sakazume, Tomonobu Hasegawa, Tsutomu Ogata, Toshio Nakanishi, Toshiro Nagai, Susumu Yokoya
Growth references for Japanese individuals with Noonan syndrome. Pediatric research 79 (4) (2015)
Misako Okuno, Tsutomu Ogata, Kazuhiko Nakabayashi, Tatsuhiko Urakami, Maki Fukami, Keisuke Nagasaki
Endocrinopathies in a boy with cryptic copy-number variations on 4q, 7q and Xp. Human genome variation 2 (2015)

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Publication Activity (10 Years)

Top Topics

Top Venues

Tsutomu Ogata