Shun Soneda

683 total citations
18 papers, 401 citations indexed

About

Shun Soneda is a scholar working on Genetics, Molecular Biology and Surgery. According to data from OpenAlex, Shun Soneda has authored 18 papers receiving a total of 401 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Genetics, 7 papers in Molecular Biology and 5 papers in Surgery. Recurrent topics in Shun Soneda's work include Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (6 papers), Genetic Syndromes and Imprinting (3 papers) and Sexual Differentiation and Disorders (3 papers). Shun Soneda is often cited by papers focused on Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (6 papers), Genetic Syndromes and Imprinting (3 papers) and Sexual Differentiation and Disorders (3 papers). Shun Soneda collaborates with scholars based in Japan, United States and South Korea. Shun Soneda's co-authors include Tsutomu Ogata, Maki Fukami, Tomonobu Hasegawa, Reiko Horikawa, Yasuhiro Naiki, Gen Nishimura, Nobutake Matsuo, Naoko Sato, Seiji Sato and Keiko Homma and has published in prestigious journals such as PLoS ONE, The Journal of Clinical Endocrinology & Metabolism and Cytogenetic and Genome Research.

In The Last Decade

Shun Soneda

17 papers receiving 397 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Shun Soneda Japan 10 184 153 109 102 79 18 401
Han Wook Yoo South Korea 10 116 0.6× 87 0.6× 77 0.7× 73 0.7× 67 0.8× 50 416
Andrew Y. Shuen Canada 11 190 1.0× 138 0.9× 12 0.1× 75 0.7× 34 0.4× 16 412
Takashi Hamajima Japan 12 137 0.7× 80 0.5× 118 1.1× 25 0.2× 41 0.5× 33 317
Haïfa Sanhaji Tunisia 12 69 0.4× 51 0.3× 37 0.3× 57 0.6× 46 0.6× 36 319
Katalin Sümegi Hungary 11 202 1.1× 70 0.5× 32 0.3× 16 0.2× 37 0.5× 24 402
Stella Feld United States 8 167 0.9× 66 0.4× 170 1.6× 30 0.3× 45 0.6× 9 416
C. A. Haiman United States 3 197 1.1× 162 1.1× 76 0.7× 7 0.1× 20 0.3× 3 388
Lucy Y.-H. Tseng United States 12 320 1.7× 142 0.9× 471 4.3× 25 0.2× 86 1.1× 15 618
Mary Anne Preece United Kingdom 11 162 0.9× 46 0.3× 41 0.4× 166 1.6× 56 0.7× 20 377
Bert Bachrach United States 9 67 0.4× 141 0.9× 106 1.0× 20 0.2× 39 0.5× 13 293

Countries citing papers authored by Shun Soneda

Since Specialization
Citations

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

Fields of papers citing papers by Shun Soneda

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Shun Soneda

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

All Works

18 of 18 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.
3.
Mochizuki, M., Yoshiya Ito, Hiroshi Yokomichi, et al.. (2020). Increasing secular trends in height and obesity in children with type 1 diabetes: JSGIT cohort. PLoS ONE. 15(11). e0242259–e0242259. 3 indexed citations
4.
Satoh, Mari, Noriyuki Takubo, Chikahiko Numakura, et al.. (2020). Retrospective study of the renal function using estimated glomerular filtration rate and congenital anomalies of the kidney‐urinary tract in pediatric Turner syndrome. Congenital Anomalies. 60(6). 175–179. 5 indexed citations
5.
Hattori, Atsushi, Erina Suzuki, Hirohito Shima, et al.. (2019). DNA Methylation Status of SHOX-Flanking CpG Islands in Healthy Individuals and Short Stature Patients with Pseudoautosomal Copy Number Variations. Cytogenetic and Genome Research. 158(2). 56–62. 5 indexed citations
6.
Suzuki, Erina, Hirohito Shima, Masayo Kagami, et al.. (2019). (Epi)genetic defects of MKRN3 are rare in Asian patients with central precocious puberty. Human Genome Variation. 6(1). 7–7. 9 indexed citations
7.
Yorifuji, Tohru, Reiko Horikawa, Tomonobu Hasegawa, et al.. (2017). Clinical practice guidelines for congenital hyperinsulinism. Clinical Pediatric Endocrinology. 26(3). 127–152. 56 indexed citations
8.
Fukami, Maki, Yasuhiro Naiki, Koji Muroya, et al.. (2015). Rare pseudoautosomal copy-number variations involving SHOX and/or its flanking regions in individuals with and without short stature. Journal of Human Genetics. 60(9). 553–556. 28 indexed citations
9.
Kim, Ok‐Hwa, Christine M Hall, Amaka C Offiah, et al.. (2014). Acroscyphodysplasia as a phenotypic variation of pseudohypoparathyroidism and acrodysostosis type 2. American Journal of Medical Genetics Part A. 164(10). 2529–2534. 12 indexed citations
10.
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
11.
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
12.
Urakami, Tatsuhiko, Reiko Horikawa, Tomoyuki Kawamura, et al.. (2012). Usefulness of insulin detemir in Japanese children with type 1 diabetes. Pediatrics International. 54(6). 773–779. 4 indexed citations
13.
Fukami, Maki, Makio Shozu, Shun Soneda, et al.. (2011). Aromatase Excess Syndrome: Identification of Cryptic Duplications and Deletions Leading to Gain of Function ofCYP19A1and Assessment of Phenotypic Determinants. The Journal of Clinical Endocrinology & Metabolism. 96(6). E1035–E1043. 22 indexed citations
14.
Soneda, Shun, Takashi Yazawa, Maki Fukami, et al.. (2011). Proximal Promoter of the Cytochrome P450 Oxidoreductase Gene: Identification of Microdeletions Involving the Untranslated Exon 1 and Critical Function of the SP1 Binding Sites. The Journal of Clinical Endocrinology & Metabolism. 96(11). E1881–E1887. 14 indexed citations
15.
Shigeta, Takanobu, Mureo Kasahara, Takuya Kimura, et al.. (2009). Liver transplantation for an infant with neonatal intrahepatic cholestasis caused by citrin deficiency using heterozygote living donor. Pediatric Transplantation. 14(7). E86–8. 34 indexed citations
16.
Nakazawa, Ryuto, Shun Soneda, Akitoshi Kinoshita, et al.. (2009). A case report: Primary extragonadal yolk sac tumor of penile shaft in a 2‐year‐old child. International Journal of Urology. 16(4). 413–415. 3 indexed citations
17.
Soneda, Shun, Maki Fukami, Masatoshi Fujimoto, et al.. (2005). Association of Micropenis with Pro185Ala Polymorphism of the Gene for Aryl Hydrocarbon Receptor Repressor Involved in Dioxin Signaling. Endocrine Journal. 52(1). 83–88. 21 indexed citations
18.
Fukami, Maki, Reiko Horikawa, Toshiro Nagai, et al.. (2005). Cytochrome P450 Oxidoreductase Gene Mutations and Antley-Bixler Syndrome with Abnormal Genitalia and/or Impaired Steroidogenesis: Molecular and Clinical Studies in 10 Patients. The Journal of Clinical Endocrinology & Metabolism. 90(1). 414–426. 122 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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