Sumito Dateki

995 total citations
40 papers, 592 citations indexed

About

Sumito Dateki is a scholar working on Molecular Biology, Genetics and Endocrinology, Diabetes and Metabolism. According to data from OpenAlex, Sumito Dateki has authored 40 papers receiving a total of 592 indexed citations (citations by other indexed papers that have themselves been cited), including 25 papers in Molecular Biology, 22 papers in Genetics and 9 papers in Endocrinology, Diabetes and Metabolism. Recurrent topics in Sumito Dateki's work include Growth Hormone and Insulin-like Growth Factors (7 papers), Congenital heart defects research (6 papers) and Genetic Syndromes and Imprinting (5 papers). Sumito Dateki is often cited by papers focused on Growth Hormone and Insulin-like Growth Factors (7 papers), Congenital heart defects research (6 papers) and Genetic Syndromes and Imprinting (5 papers). Sumito Dateki collaborates with scholars based in Japan, United States and Malaysia. Sumito Dateki's co-authors include Tsutomu Ogata, Maki Fukami, Hiroyuki Moriuchi, Naoko Sato, Satoshi Watanabe, Koji Muroya, Masanori Adachi, Eiichi Kinoshita, Koh-ichiro Yoshiura and Katsuaki Motomura and has published in prestigious journals such as PLoS ONE, The Journal of Clinical Endocrinology & Metabolism and Molecular Endocrinology.

In The Last Decade

Sumito Dateki

39 papers receiving 587 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Sumito Dateki Japan 14 293 286 177 134 75 40 592
Dolores Segura Spain 15 67 0.2× 249 0.9× 141 0.8× 152 1.1× 36 0.5× 25 630
Francesca Romana Lepri Italy 18 429 1.5× 608 2.1× 33 0.2× 74 0.6× 46 0.6× 62 972
Chalurmpon Srichomthong Thailand 16 356 1.2× 342 1.2× 51 0.3× 74 0.6× 59 0.8× 49 676
Caroline Buckway United States 12 304 1.0× 323 1.1× 627 3.5× 62 0.5× 22 0.3× 16 891
E. Futo Switzerland 10 139 0.5× 400 1.4× 605 3.4× 70 0.5× 11 0.1× 11 807
Patricia Krief France 14 253 0.9× 118 0.4× 144 0.8× 166 1.2× 26 0.3× 31 575
Mariana F.A. Funari Brazil 17 400 1.4× 368 1.3× 232 1.3× 44 0.3× 17 0.2× 35 736
Florence Dastot France 16 487 1.7× 385 1.3× 764 4.3× 129 1.0× 33 0.4× 19 1.0k
Masaki Takagi Japan 14 290 1.0× 236 0.8× 141 0.8× 65 0.5× 22 0.3× 54 514
S. Mohan United States 13 118 0.4× 324 1.1× 428 2.4× 55 0.4× 14 0.2× 18 701

Countries citing papers authored by Sumito Dateki

Since Specialization
Citations

This map shows the geographic impact of Sumito Dateki'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 Sumito Dateki with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Sumito Dateki more than expected).

Fields of papers citing papers by Sumito Dateki

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Sumito Dateki. 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 Sumito Dateki. The network helps show where Sumito Dateki may publish in the future.

Co-authorship network of co-authors of Sumito Dateki

This figure shows the co-authorship network connecting the top 25 collaborators of Sumito Dateki. A scholar is included among the top collaborators of Sumito Dateki 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 Sumito Dateki. Sumito Dateki is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
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
2.
Kitaoka, Taichi, Takuo Kubota, Junko Kanno, et al.. (2024). Clinical outcomes and medical management of achondroplasia in Japanese children: A retrospective medical record review of clinical data. American Journal of Medical Genetics Part A. 194(8). e63612–e63612. 3 indexed citations
3.
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
4.
Kawano, Hiroaki, Takeharu Kato, Sumito Dateki, et al.. (2023). An Iron-chelating Agent Improved the Cardiac Function in a Patient with Severe Heart Failure Due to Hereditary Hemochromatosis. Internal Medicine. 63(2). 253–258.
5.
Hashimoto, Nobuhiro, Sumito Dateki, Takatoshi Tsuchihashi, et al.. (2020). Compound heterozygous variants in the ABCG8 gene in a Japanese girl with sitosterolemia. Human Genome Variation. 7(1). 25–25. 2 indexed citations
6.
Watanabe, Satoshi, et al.. (2019). KAT6B-related disorder in a patient with a novel frameshift variant (c.3925dup). Human Genome Variation. 6(1). 54–54. 1 indexed citations
7.
Watanabe, Satoshi, Akira Kinoshita, Hiroyuki Mishima, et al.. (2019). Identification of a homozygous frameshift variant in RFLNA in a patient with a typical phenotype of spondylocarpotarsal synostosis syndrome. Journal of Human Genetics. 64(5). 467–471. 3 indexed citations
8.
Dateki, Sumito, Satoshi Watanabe, Hiroyuki Mishima, et al.. (2019). A homozygous splice site ROBO1 mutation in a patient with a novel syndrome with combined pituitary hormone deficiency. Journal of Human Genetics. 64(4). 341–346. 13 indexed citations
9.
Nakashima, Yumiko, Satoshi Watanabe, Mariko Kinoshita, et al.. (2018). A novel heterozygous GLI2 mutation in a patient with congenital urethral stricture and renal hypoplasia/dysplasia leading to end-stage renal failure. CEN Case Reports. 7(1). 94–97. 7 indexed citations
10.
Watanabe, Satoshi, Akiko Nakatomi, Tatsuro Kondoh, et al.. (2018). A hot-spot mutation in CDC42 (p.Tyr64Cys) and novel phenotypes in the third patient with Takenouchi-Kosaki syndrome. Journal of Human Genetics. 63(3). 387–390. 32 indexed citations
11.
Dateki, Sumito, Akiko Nakatomi, Satoshi Watanabe, et al.. (2017). Identification of a novel heterozygous mutation of the Aggrecan gene in a family with idiopathic short stature and multiple intervertebral disc herniation. Journal of Human Genetics. 62(7). 717–721. 29 indexed citations
12.
Dateki, Sumito, Masayo Kagami, Keiko Matsubara, et al.. (2017). Maternally derived 15q11.2-q13.1 duplication and H19-DMR hypomethylation in a patient with Silver–Russell syndrome. Journal of Human Genetics. 62(10). 919–922. 1 indexed citations
13.
Hashimoto, Yukiko, Sumito Dateki, Masakazu Hirose, et al.. (2016). Molecular and clinical features of KATP-channel neonatal diabetes mellitus in Japan. Pediatric Diabetes. 18(7). 532–539. 25 indexed citations
14.
Suzuki, Junichi, Noriyuki Azuma, Sumito Dateki, et al.. (2014). Mutation spectrum and phenotypic variation in nine patients with SOX2 abnormalities. Journal of Human Genetics. 59(6). 353–356. 12 indexed citations
15.
Song, Yuan‐Zong, Zhan‐Hui Zhang, Mei Deng, et al.. (2013). SLC25A13 Gene Analysis in Citrin Deficiency: Sixteen Novel Mutations in East Asian Patients, and the Mutation Distribution in a Large Pediatric Cohort in China. PLoS ONE. 8(9). e74544–e74544. 50 indexed citations
16.
Fukami, Maki, Tetsuo Maruyama, Sumito Dateki, et al.. (2010). Hypothalamic Dysfunction in a Female with Isolated Hypogonadotropic Hypogonadism and Compound Heterozygous TACR3 Mutations and Clinical Manifestation in Her Heterozygous Mother. Hormone Research in Paediatrics. 73(6). 477–481. 16 indexed citations
17.
Ashkenazi‐Hoffnung, Liat, Yael Lebenthal, Alexander W. Wyatt, et al.. (2010). A novel loss-of-function mutation in OTX2 in a patient with anophthalmia and isolated growth hormone deficiency. Human Genetics. 127(6). 721–729. 35 indexed citations
18.
Dateki, Sumito, Kosei Hasegawa, Hiroyuki Tanaka, et al.. (2010). Heterozygous Orthodenticle Homeobox 2 Mutations Are Associated with Variable Pituitary Phenotype. Molecular Endocrinology. 24(1). 275–275. 5 indexed citations
19.
Fukami, Maki, Sumito Dateki, Fumiko Kato, et al.. (2008). Identification and characterization of cryptic SHOX intragenic deletions in three Japanese patients with Léri–Weill dyschondrosteosis. Journal of Human Genetics. 53(5). 454–459. 15 indexed citations
20.
Dateki, Sumito, Tatsuro Kondoh, Gen Nishimura, et al.. (2007). A Japanese patient with a mild Lenz–Majewski syndrome. Journal of Human Genetics. 52(8). 686–689. 6 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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