Tsutomu Ogata

21.3k citations

490 papers · 11.7k indexed · 1 hit paper · h-index 52

Molecular Biology top 0.5%
Genetics top 0.05%
Pediatrics, Perinatology and Child Health top 0.5%
Endocrinology, Diabetes and Metabolism top 0.5%
Reproductive Medicine top 0.5%

Co-authors: Maki Fukami Masayo Kagami Nobutake Matsuo Koji Muroya Tomonobu Hasegawa Anne C. Ferguson‐Smith Toshiro Nagai Reiko Horikawa
Topics: Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (125 papers)Sexual Differentiation and Disorders (107 papers)Genetic Syndromes and Imprinting (90 papers)
Cited by: Genetics Reproductive Medicine Urology
Journals: Journal of Biological Chemistry Nature GeneticsSHILAP Revista de lepidopterología
Partner nations: Japan United States Germany

In The Last Decade

Tsutomu Ogata

473 papers receiving 11.3k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Pseudoautosomal deletions encompassing a novel homeobox gene cause growth failure in idiopathic short stature and Turner syndrome

1997 701 citations Maki Fukami, Gerhard Binder et al. profile →

Peers

Countries citing papers authored by Tsutomu Ogata

Since Specialization

Citations

This map shows the geographic impact of Tsutomu Ogata's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Tsutomu Ogata with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Tsutomu Ogata more than expected).

Fields of papers citing papers by Tsutomu Ogata

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Tsutomu Ogata. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Tsutomu Ogata. The network helps show where Tsutomu Ogata may publish in the future.

Co-authorship network of co-authors of Tsutomu Ogata

This figure shows the co-authorship network connecting the top 25 collaborators of Tsutomu Ogata. A scholar is included among the top collaborators of Tsutomu Ogata based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Tsutomu Ogata. Tsutomu Ogata is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

#	Work	Indexed citations
1	Comprehensive molecular and clinical findings in 29 patients with multi-locus imprinting disturbance 2024 ·Clinical Epigenetics ·(unknown),Hidenobu Soejima,(unknown),(unknown),Akie Nakamura,Sayaka Kawashima,(unknown),Rika Kosaki,Yutaka Nishimura,Kazuki Yamazawa,Tetsuo Hattori,(unknown),Takanobu Inoue,Keiko Matsubara,Maki Fukami,Shinji Saitoh,Tsutomu Ogata,Masayo Kagami	4
2	Comprehensive Study on Central Precocious Puberty: Molecular and Clinical Analyses in 90 Patients 2024 ·The Journal of Clinical Endocrinology & Metabolism ·(unknown),(unknown),(unknown),Keisuke Nagasaki,(unknown),Tomohiro Saito,Shun Soneda,Saori Kinjo,Shin‐ichiro Sano,Mitsukazu Mamada,(unknown),Sumito Dateki,Satoshi Narumi,Yasuhiro Naiki,Reiko Horikawa,Tsutomu Ogata,Maki Fukami,Masayo Kagami	1
3	Case Report: Molecular autopsy underlie COVID-19-associated sudden, unexplained child mortality 2023 ·Frontiers in Immunology ·Kana Unuma,(unknown),(unknown),(unknown),Taka‐aki Matsuyama,Yohsuke Makino,Atsushi Hijikata,(unknown),Tsutomu Ogata,Nobuhiko Okamoto,Satoshi Okada,Kenichi Ohashi,Koichi Uemura,Hirokazu Kanegane	4
4	Risk assessment of assisted reproductive technology and parental age at childbirth for the development of uniparental disomy-mediated imprinting disorders caused by aneuploid gametes 2023 ·Clinical Epigenetics ·(unknown),Keiko Matsubara,Akie Nakamura,Shinichiro Sano,Takanobu Inoue,Sayaka Kawashima,Tomoko Fuke,Kazuki Yamazawa,Maki Fukami,Tsutomu Ogata,Masayo Kagami	3
5	(Epi)genetic and clinical characteristics in 84 patients with pseudohypoparathyroidism type 1B 2023 ·European Journal of Endocrinology ·(unknown),Shinichiro Sano,Sayaka Kawashima,Akie Nakamura,Hirohito Shima,(unknown),Yuki Yamada,(unknown),(unknown),Yoshiaki Ohtsu,Keiko Matsubara,Sumito Dateki,Yoshihiro Maruo,Maki Fukami,Tsutomu Ogata,Masayo Kagami	1
6	RNA sequencing and target long-read sequencing reveal an intronic transposon insertion causing aberrant splicing 2023 ·Journal of Human Genetics ·(unknown),Takuya Hiraide,Kazuki Watanabe,(unknown),(unknown),(unknown),(unknown),Kimiyoshi Sakaguchi,Masato Maekawa,(unknown),Tokiko Fukuda,Isao Miyairi,Tsutomu Ogata,Hirotomo Saitsu	7
7	Frequency and clinical characteristics of distinct etiologies in patients with Silver-Russell syndrome diagnosed based on the Netchine-Harbison clinical scoring system 2022 ·Journal of Human Genetics ·Tomoko Fuke,Akie Nakamura,Takanobu Inoue,Sayaka Kawashima,(unknown),Keiko Matsubara,Shinichiro Sano,Kazuki Yamazawa,Maki Fukami,Tsutomu Ogata,Masayo Kagami	2
8	Genetic and phenotypic analysis of 101 patients with developmental delay or intellectual disability using whole‐exome sequencing 2021 ·Clinical Genetics ·Takuya Hiraide,(unknown),Yohei Masunaga,(unknown),(unknown),(unknown),(unknown),(unknown),Hidetaka Yamada,Kumiko Yanagi,Mitsuko Nakashima,(unknown),Haruhiko Sugimura,Tokiko Fukuda,Tsutomu Ogata,Hirotomo Saitsu	27
9	Long-term Effect of Aromatase Inhibition in Aromatase Excess Syndrome 2021 ·The Journal of Clinical Endocrinology & Metabolism ·Gerhard Binder,Akie Nakamura,Roland Schweizer,Tsutomu Ogata,Maki Fukami,Keisuke Nagasaki	3
10	Genome-wide methylation analysis in Silver–Russell syndrome, Temple syndrome, and Prader–Willi syndrome 2020 ·Clinical Epigenetics ·(unknown),Keiko Matsubara,Tomoko Fuke,Kazuki Yamazawa,Kazuhito Satou,Nobuyuki Murakami,Shinji Saitoh,Kazuhiko Nakabayashi,Kenichiro Hata,Tsutomu Ogata,Maki Fukami,Masayo Kagami	11
11	Role of Imprinting Disorders in Short Children Born SGA and Silver-Russell Syndrome Spectrum 2020 ·The Journal of Clinical Endocrinology & Metabolism ·Tomoko Fuke,Akie Nakamura,Takanobu Inoue,Sayaka Kawashima,Kaori Hara,Keiko Matsubara,Shinichiro Sano,Kazuki Yamazawa,Maki Fukami,Tsutomu Ogata,Masayo Kagami	16
12	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 2020 ·Journal of Medical Genetics ·Kazuki Yamazawa,Takanobu Inoue,(unknown),(unknown),Hiroharu Yamashita,(unknown),Hideki Fujita,Keisuke Enomoto,Kazuhiko Nakabayashi,Kenichiro Hata,(unknown),Tatsuo Matsunaga,Akie Nakamura,Keiko Matsubara,Tsutomu Ogata,Masayo Kagami	7
13	Contribution of gene mutations to Silver-Russell syndrome phenotype: multigene sequencing analysis in 92 etiology-unknown patients 2020 ·Clinical Epigenetics ·Takanobu Inoue,Akie Nakamura,(unknown),(unknown),Keiko Matsubara,Junko Nishioka,Yoshihiro Maruo,Yukihiro Hasegawa,Hiroshi Suzumura,Seiji Sato,Yoshiyuki Kobayashi,Nobuyuki Murakami,Kazuhiko Nakabayashi,Kazuki Yamazawa,Tomoko Fuke,Satoshi Narumi,Akira Oka,Tsutomu Ogata,Maki Fukami,Masayo Kagami	33
14	Temple syndrome in a patient with variably methylated CpGs at the primary MEG3/DLK1:IG-DMR and severely hypomethylated CpGs at the secondary MEG3:TSS-DMR 2019 ·Clinical Epigenetics ·Masayo Kagami,(unknown),Miyuki Ota,Kentaro Matsuoka,Akie Nakamura,Keiko Matsubara,Kazuhiko Nakabayashi,Shuji Takada,Maki Fukami,Tsutomu Ogata	18
15	Mosaic upd(14)pat in a patient with mild features of Kagami–Ogata syndrome 2017 ·Clinical Case Reports ·(unknown),(unknown),Gunnar Houge,Masayo Kagami,Tsutomu Ogata	9
16	Development of waist circumference percentiles for Japanese children and an examination of their screening utility for childhood metabolic syndrome: a population-based cross-sectional study 2015 ·BMC Public Health ·(unknown),Tsuyoshi Isojima,Ryuzo Takaya,Eiichiro Satake,Rie Shigetomi Yamaguchi,(unknown),(unknown),Shin‐ichiro Sano,(unknown),Yuichi Nakagawa,Takehiko Ohzeki,Tsutomu Ogata,Yasuko Fujisawa	11
17	Androgenetic/biparental mosaicism in a girl with Beckwith–Wiedemann syndrome-like and upd(14)pat-like phenotypes 2010 ·Journal of Human Genetics ·Kazuki Yamazawa,Kazuhiko Nakabayashi,Kentaro Matsuoka,(unknown),Kenichiro Hata,Reiko Horikawa,Tsutomu Ogata	24
18	Premature ovarian failure and androgen receptor gene CAG repeat lengths weighted by X chromosome inactivation patterns 2008 ·Fertility and Sterility ·(unknown),Yuka Wada,Tetsuo Maruyama,Hiroshi Uchida,Bunpei Ishizuka,Tsutomu Ogata	18
19	Association of cryptorchidism with Gly146Ala polymorphism in the gene for steroidogenic factor-1 2006 ·Fertility and Sterility ·Yuka Wada,Michiyo Okada,Maki Fukami,Isoji Sasagawa,Tsutomu Ogata	34
20	Deterioration estimating system for 200-Ah sealed lead-acid batteries 1994 ·International Telecommunications Energy Conference ·(unknown),(unknown),(unknown),(unknown),(unknown),Tsutomu Ogata	8

About Tsutomu Ogata

Tsutomu Ogata is a scholar working on Genetics, Reproductive Medicine and Urology, having authored 490 papers that have together received 11.7k indexed citations. Recurring topics across this work include Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (125 papers), Sexual Differentiation and Disorders (107 papers) and Genetic Syndromes and Imprinting (90 papers). The work is most often cited by research in Genetics (6.8k citations), Reproductive Medicine (1.3k citations) and Urology (696 citations). Tsutomu Ogata has collaborated with scholars based in Japan, United States and Germany. Frequent co-authors include Maki Fukami, Masayo Kagami, Nobutake Matsuo, Koji Muroya, Tomonobu Hasegawa, Anne C. Ferguson‐Smith, Toshiro Nagai, Reiko Horikawa, Gudrun Rappold and Naoki Matsuo. Their work appears in journals such as Journal of Biological Chemistry, Nature Genetics and SHILAP Revista de lepidopterología.

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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