Tsutomu Ogata

21.3k total citations · 1 hit paper
490 papers, 11.7k citations indexed

About

Tsutomu Ogata is a scholar working on Molecular Biology, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Tsutomu Ogata has authored 490 papers receiving a total of 11.7k indexed citations (citations by other indexed papers that have themselves been cited), including 286 papers in Molecular Biology, 272 papers in Genetics and 69 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Tsutomu Ogata's 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). Tsutomu Ogata is often cited by papers focused on 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). Tsutomu Ogata collaborates with scholars based in Japan, United States and Germany. Tsutomu Ogata's 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 and has published in prestigious journals such as Journal of Biological Chemistry, Nature Genetics and SHILAP Revista de lepidopterología.

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

Tsutomu Ogata

GENET

PPCH

EDM

Berenice B. Mendonça Brazil

Egbert Bakker Netherlands

Outi Hovatta Sweden

Subburaman Mohan United States

Hannu Sariola Finland

David J. Baylink United States

Paul A. Overbeek United States

Thomas L. Saunders United States

Wesley G. Beamer United States

Thomas Doetschman United States

Berenice B. Mendonça Brazil

Tsutomu Ogata

8.3k ×1.2

5.6k ×0.8

GENET

767 ×0.4

PPCH

6.8k ×4.8

EDM

3.5k ×2.8

Citations per year, relative to Tsutomu Ogata Tsutomu Ogata (= 1×) peers Berenice B. Mendonça

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

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

Soejima, Hidenobu, Akie Nakamura, Sayaka Kawashima, et al.. (2024). Comprehensive molecular and clinical findings in 29 patients with multi-locus imprinting disturbance. Clinical Epigenetics. 16(1). 138–138. 4 indexed citations

Nagasaki, Keisuke, Tomohiro Saito, Shun Soneda, et al.. (2024). Comprehensive Study on Central Precocious Puberty: Molecular and Clinical Analyses in 90 Patients. The Journal of Clinical Endocrinology & Metabolism. 110(4). 1023–1036. 1 indexed citations

Unuma, Kana, Taka‐aki Matsuyama, Yohsuke Makino, et al.. (2023). Case Report: Molecular autopsy underlie COVID-19-associated sudden, unexplained child mortality. Frontiers in Immunology. 14. 1121059–1121059. 4 indexed citations

Matsubara, Keiko, Akie Nakamura, Shinichiro Sano, et al.. (2023). Risk assessment of assisted reproductive technology and parental age at childbirth for the development of uniparental disomy-mediated imprinting disorders caused by aneuploid gametes. Clinical Epigenetics. 15(1). 78–78. 3 indexed citations

Sano, Shinichiro, Sayaka Kawashima, Akie Nakamura, et al.. (2023). (Epi)genetic and clinical characteristics in 84 patients with pseudohypoparathyroidism type 1B. European Journal of Endocrinology. 189(6). 590–600. 1 indexed citations

Hiraide, Takuya, Kazuki Watanabe, Kimiyoshi Sakaguchi, et al.. (2023). RNA sequencing and target long-read sequencing reveal an intronic transposon insertion causing aberrant splicing. Journal of Human Genetics. 69(2). 91–99. 7 indexed citations

Fuke, Tomoko, Akie Nakamura, Takanobu Inoue, et al.. (2022). 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). 607–611. 2 indexed citations

Hiraide, Takuya, Yohei Masunaga, Hidetaka Yamada, et al.. (2021). Genetic and phenotypic analysis of 101 patients with developmental delay or intellectual disability using whole‐exome sequencing. Clinical Genetics. 100(1). 40–50. 27 indexed citations

Binder, Gerhard, Akie Nakamura, Roland Schweizer, et al.. (2021). Long-term Effect of Aromatase Inhibition in Aromatase Excess Syndrome. The Journal of Clinical Endocrinology & Metabolism. 106(5). 1491–1500. 3 indexed citations

10.

Matsubara, Keiko, Tomoko Fuke, Kazuki Yamazawa, et al.. (2020). Genome-wide methylation analysis in Silver–Russell syndrome, Temple syndrome, and Prader–Willi syndrome. Clinical Epigenetics. 12(1). 11 indexed citations

11.

Fuke, Tomoko, Akie Nakamura, Takanobu Inoue, et al.. (2020). Role of Imprinting Disorders in Short Children Born SGA and Silver-Russell Syndrome Spectrum. The Journal of Clinical Endocrinology & Metabolism. 106(3). 802–813. 16 indexed citations

12.

Yamazawa, Kazuki, Takanobu Inoue, Hiroharu Yamashita, et al.. (2020). 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). 427–432. 7 indexed citations

13.

Inoue, Takanobu, Akie Nakamura, Keiko Matsubara, et al.. (2020). Contribution of gene mutations to Silver-Russell syndrome phenotype: multigene sequencing analysis in 92 etiology-unknown patients. Clinical Epigenetics. 12(1). 86–86. 33 indexed citations

14.

Kagami, Masayo, Miyuki Ota, Kentaro Matsuoka, et al.. (2019). 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. Clinical Epigenetics. 11(1). 42–42. 18 indexed citations

15.

Houge, Gunnar, et al.. (2017). Mosaic upd(14)pat in a patient with mild features of Kagami–Ogata syndrome. Clinical Case Reports. 6(1). 91–95. 9 indexed citations

16.

Isojima, Tsuyoshi, Ryuzo Takaya, Eiichiro Satake, et al.. (2015). 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. BMC Public Health. 15(1). 1121–1121. 11 indexed citations

17.

Yamazawa, Kazuki, Kazuhiko Nakabayashi, Kentaro Matsuoka, et al.. (2010). Androgenetic/biparental mosaicism in a girl with Beckwith–Wiedemann syndrome-like and upd(14)pat-like phenotypes. Journal of Human Genetics. 56(1). 91–93. 24 indexed citations

18.

Wada, Yuka, et al.. (2008). Premature ovarian failure and androgen receptor gene CAG repeat lengths weighted by X chromosome inactivation patterns. Fertility and Sterility. 91(2). 649–652. 18 indexed citations

19.

Wada, Yuka, Michiyo Okada, Maki Fukami, Isoji Sasagawa, & Tsutomu Ogata. (2006). Association of cryptorchidism with Gly146Ala polymorphism in the gene for steroidogenic factor-1. Fertility and Sterility. 85(3). 787–790. 34 indexed citations

20.

Ogata, Tsutomu, et al.. (1994). Deterioration estimating system for 200-Ah sealed lead-acid batteries. International Telecommunications Energy Conference. 256–262. 8 indexed citations

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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