Shinsuke Ninomiya

671 total citations
31 papers, 444 citations indexed

About

Shinsuke Ninomiya is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Shinsuke Ninomiya has authored 31 papers receiving a total of 444 indexed citations (citations by other indexed papers that have themselves been cited), including 18 papers in Genetics, 17 papers in Molecular Biology and 7 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Shinsuke Ninomiya's work include Genomic variations and chromosomal abnormalities (12 papers), Prenatal Screening and Diagnostics (6 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (5 papers). Shinsuke Ninomiya is often cited by papers focused on Genomic variations and chromosomal abnormalities (12 papers), Prenatal Screening and Diagnostics (6 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (5 papers). Shinsuke Ninomiya collaborates with scholars based in Japan, Finland and United States. Shinsuke Ninomiya's co-authors include Kouji Narahara, Yuji Yokoyama, Yoshiki Seino, Kazushiro Tsuji, Sakari Knuutila, Minoru Isomura, Chiaki Inoue, Ikuya Nonaka, Yu‐ichi Goto and Erkki Elonen and has published in prestigious journals such as Human Molecular Genetics, Journal of Medical Genetics and Human Genetics.

In The Last Decade

Shinsuke Ninomiya

31 papers receiving 436 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Shinsuke Ninomiya Japan 14 268 210 57 48 43 31 444
Amy Knight Johnson United States 12 196 0.7× 164 0.8× 32 0.6× 67 1.4× 28 0.7× 16 396
Eden Haverfield United States 13 241 0.9× 277 1.3× 95 1.7× 44 0.9× 18 0.4× 23 536
Ilenia Simeoni United Kingdom 12 391 1.5× 125 0.6× 16 0.3× 36 0.8× 40 0.9× 16 608
Lilia Romdhane Tunisia 12 150 0.6× 189 0.9× 18 0.3× 40 0.8× 15 0.3× 29 394
Salwati Shuib Malaysia 7 193 0.7× 104 0.5× 27 0.5× 77 1.6× 53 1.2× 17 321
Johji Inazawa Japan 10 308 1.1× 54 0.3× 69 1.2× 47 1.0× 12 0.3× 16 452
Adriano Torres Antonucci Italy 13 242 0.9× 78 0.4× 21 0.4× 54 1.1× 17 0.4× 41 452
Sonia Avila Spain 5 460 1.7× 103 0.5× 23 0.4× 62 1.3× 28 0.7× 9 579
S. Todd United States 9 252 0.9× 160 0.8× 12 0.2× 55 1.1× 43 1.0× 17 353
Howard Mulhern United States 8 198 0.7× 139 0.7× 45 0.8× 11 0.2× 63 1.5× 9 497

Countries citing papers authored by Shinsuke Ninomiya

Since Specialization
Citations

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

Fields of papers citing papers by Shinsuke Ninomiya

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Shinsuke Ninomiya

This figure shows the co-authorship network connecting the top 25 collaborators of Shinsuke Ninomiya. A scholar is included among the top collaborators of Shinsuke Ninomiya 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 Shinsuke Ninomiya. Shinsuke Ninomiya 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.
Suzuki, Yoshiro, Hirotake Sawada, Shigeru Suzuki, et al.. (2020). Novel TRPV6 mutations in the spectrum of transient neonatal hyperparathyroidism. The Journal of Physiological Sciences. 70(1). 33–33. 21 indexed citations
2.
Takeuchi, Akihito, Nobuhiko Okamoto, Junya Shimizu, et al.. (2015). Progressive brain atrophy in Schinzel–Giedion syndrome with a SETBP1 mutation. European Journal of Medical Genetics. 58(8). 369–371. 17 indexed citations
3.
Yamamoto, Toshiyuki, Shino Shimada, Keiko Shimojima, et al.. (2015). Leukoencephalopathy associated with 11q24 deletion involving the gene encoding hepatic and glial cell adhesion molecule in two patients. European Journal of Medical Genetics. 58(9). 492–496. 8 indexed citations
4.
Shimbo, Hiroko, Shinsuke Ninomiya, Kenji Kurosawa, & Takahito Wada. (2014). A case report of two brothers with ATR-X syndrome due to low maternal frequency of somatic mosaicism for an intragenic deletion in the ATRX. Journal of Human Genetics. 59(7). 408–410. 1 indexed citations
5.
Ninomiya, Shinsuke, Ioana Borze, Riikka Räty, et al.. (2012). Integrated Analysis of Gene Copy Number, Copy Neutral LOH, and microRNA Profiles in Adult Acute Lymphoblastic Leukemia. Cytogenetic and Genome Research. 136(4). 246–255. 16 indexed citations
6.
Masuno, Mitsuo, Atsushi Watanabe, Takashi Shimada, et al.. (2011). Ehlers‐Danlos syndrome, vascular type: A novel missense mutation in the COL3A1 gene. Congenital Anomalies. 52(4). 207–210. 3 indexed citations
7.
Borze, Ioana, Eeva Juvonen, Shinsuke Ninomiya, et al.. (2010). High-resolution oligonucleotide array comparative genomic hybridization study and methylation status of the RPS14 gene in de novo myelodysplastic syndromes. Cancer Genetics and Cytogenetics. 197(2). 166–173. 5 indexed citations
8.
Ninomiya, Shinsuke, Riikka Räty, Jaakko Hollmén, et al.. (2009). Focal 9p instability in hematologic neoplasias revealed by comparative genomic hybridization and single‐nucleotide polymorphism microarray analyses. Genes Chromosomes and Cancer. 49(4). 309–318. 24 indexed citations
9.
Lehtonen, Heli, Kowan Ja Jee, Shinsuke Ninomiya, et al.. (2009). Array comparative genomic hybridization identifies a distinct DNA copy number profile in renal cell cancer associated with hereditary leiomyomatosis and renal cell cancer. Genes Chromosomes and Cancer. 48(7). 544–551. 20 indexed citations
10.
Yokoyama, Yuji, et al.. (2001). Maternal origin of a unique extra chromosome, der(9)(pter?q13::q13?q12:) in a girl with typical trisomy 9p syndrome. American Journal of Medical Genetics. 102(1). 25–28. 5 indexed citations
11.
Ninomiya, Shinsuke, Yuji Yokoyama, Rintaro Mori, et al.. (2000). A novel mutation (296 del G) of the SOX9 gene in a patient with campomelic syndrome and sex reversal. Clinical Genetics. 58(3). 224–227. 10 indexed citations
12.
Yokoyama, Yuji, et al.. (2000). Rapid screening method to detect mutations inCYP21, the gene for 21-hydroxylase. American Journal of Medical Genetics. 94(1). 28–31. 3 indexed citations
13.
Yokoyama, Yuji, et al.. (1999). Two novel mutations of SURF1 in Leigh syndrome with cytochrome c oxidase deficiency. Human Genetics. 105(6). 560–563. 29 indexed citations
14.
15.
Ninomiya, Shinsuke, et al.. (1995). Acampomelic campomelic syndrome and sex reversal associated with de novo t(12;17) translocation. American Journal of Medical Genetics. 56(1). 31–34. 18 indexed citations
16.
Tsuji, Kazushiro, Kouji Narahara, Kiyoshi Kikkawa, et al.. (1994). Craniosynostosis and hemizygosity for D7S135 caused by a de novo and apparently balanced t(6;7) translocation. American Journal of Medical Genetics. 49(1). 98–102. 15 indexed citations
17.
Tsuji, Kazushiro, Kouji Narahara, Yuji Yokoyama, et al.. (1993). Reproductive risk in mating between two translocation carriers: Case report and review of the literature. American Journal of Medical Genetics. 46(5). 524–528. 13 indexed citations
18.
Narahara, Kouji, Susumu Miyake, Kazushiro Tsuji, et al.. (1992). Unique karyotypes in two patients with Prader‐Willi syndrome. American Journal of Medical Genetics. 42(5). 671–677. 6 indexed citations
19.
Narahara, Kouji, Kazushiro Tsuji, Yuji Yokoyama, et al.. (1992). De novo complex chromosome rearrangement in identical twins with multiple congenital anomalies. Human Genetics. 88(5). 596–598. 11 indexed citations
20.
Narahara, Kouji, Masahiro Kamada, Yukio Takahashi, et al.. (1992). Case of ovarian dysgenesis and dilated cardiomyopathy supports existence of malouf syndrome. American Journal of Medical Genetics. 44(3). 369–373. 10 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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