Futoshi Sekiguchi

504 total citations
12 papers, 94 citations indexed

About

Futoshi Sekiguchi is a scholar working on Molecular Biology, Genetics and Cellular and Molecular Neuroscience. According to data from OpenAlex, Futoshi Sekiguchi has authored 12 papers receiving a total of 94 indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Molecular Biology, 3 papers in Genetics and 2 papers in Cellular and Molecular Neuroscience. Recurrent topics in Futoshi Sekiguchi's work include RNA modifications and cancer (3 papers), Genomics and Rare Diseases (3 papers) and Genetics and Neurodevelopmental Disorders (2 papers). Futoshi Sekiguchi is often cited by papers focused on RNA modifications and cancer (3 papers), Genomics and Rare Diseases (3 papers) and Genetics and Neurodevelopmental Disorders (2 papers). Futoshi Sekiguchi collaborates with scholars based in Japan, Iran and Malaysia. Futoshi Sekiguchi's co-authors include Naomichi Matsumoto, Takeshi Mizuguchi, Satoko Miyatake, Noriko Miyake, Atsushi Takata, Eriko Koshimizu, Kazuhiro Ogata, Mahdiyeh Behnam, Kohei Hamanaka and Mitsuko Nakashima and has published in prestigious journals such as American Journal of Obstetrics and Gynecology, Clinical Genetics and Brain and Development.

In The Last Decade

Futoshi Sekiguchi

12 papers receiving 93 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Futoshi Sekiguchi Japan 7 59 27 16 14 9 12 94
Edward J. Romasko United States 4 52 0.9× 58 2.1× 5 0.3× 8 0.6× 7 0.8× 6 118
Caroline Scholz Germany 6 86 1.5× 62 2.3× 7 0.4× 6 0.4× 14 1.6× 8 127
Julie Steffann France 8 100 1.7× 26 1.0× 26 1.6× 6 0.4× 51 5.7× 22 142
Jennifer L. Kemppainen United States 8 56 0.9× 50 1.9× 11 0.7× 5 0.4× 6 0.7× 15 116
Birgitta Bernhard United Kingdom 7 58 1.0× 57 2.1× 15 0.9× 10 0.7× 2 0.2× 10 114
Damara Ortiz United States 6 40 0.7× 19 0.7× 8 0.5× 7 0.5× 5 0.6× 14 127
Ghunwa Nakouzi United States 8 103 1.7× 56 2.1× 17 1.1× 6 0.4× 63 7.0× 15 180
Daphne M. van Beek Netherlands 3 81 1.4× 19 0.7× 38 2.4× 3 0.2× 4 0.4× 4 116
Paul R. Mark United States 7 70 1.2× 58 2.1× 14 0.9× 5 0.4× 14 1.6× 11 123
Angela Hübner Germany 8 134 2.3× 42 1.6× 8 0.5× 4 0.3× 20 2.2× 13 165

Countries citing papers authored by Futoshi Sekiguchi

Since Specialization
Citations

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

Fields of papers citing papers by Futoshi Sekiguchi

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Futoshi Sekiguchi

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

All Works

12 of 12 papers shown
1.
Nagai, Koichi, et al.. (2022). MED12 mutations in uterine leiomyomas: prediction of volume reduction by gonadotropin-releasing hormone agonists. American Journal of Obstetrics and Gynecology. 228(2). 207.e1–207.e9. 6 indexed citations
2.
Saida, Ken, Masayuki Sasaki, Eriko Koshimizu, et al.. (2021). Pathogenic variants in the survival of motor neurons complex gene GEMIN5 cause cerebellar atrophy. Clinical Genetics. 100(6). 722–730. 18 indexed citations
3.
Nishi, Eriko, Yuko Mishima, Futoshi Sekiguchi, et al.. (2021). Novel variants in aromatic L-amino acid decarboxylase deficiency: Case report of sisters with mild phenotype. Brain and Development. 43(10). 1023–1028. 4 indexed citations
4.
Iwama, Kazuhiro, Futoshi Sekiguchi, Satoko Kumada, et al.. (2020). Novel EXOSC9 variants cause pontocerebellar hypoplasia type 1D with spinal motor neuronopathy and cerebellar atrophy. Journal of Human Genetics. 66(4). 401–407. 13 indexed citations
5.
Haginoya, Kazuhiro, Futoshi Sekiguchi, Mitsutoshi Munakata, et al.. (2020). A patient with a 6q22.1 deletion and a phenotype of non-progressive early-onset generalized epilepsy with tremor. Epilepsy & Behavior Reports. 15. 100405–100405. 5 indexed citations
6.
Sekiguchi, Futoshi, et al.. (2020). A Novel SETBP1 Gene Disruption by a De Novo Balanced Translocation in a Patient with Speech Impairment, Intellectual, and Behavioral Disorder. Journal of Pediatric Genetics. 11(2). 135–138. 2 indexed citations
7.
Hamanaka, Kohei, Futoshi Sekiguchi, Masataka Taguri, et al.. (2019). Comparison of mitochondrial DNA variants detection using short- and long-read sequencing. Journal of Human Genetics. 64(11). 1107–1116. 11 indexed citations
8.
Sekiguchi, Futoshi, Maryam Sedghi, Mansoor Salehi, et al.. (2018). A novel homozygous DPH1 mutation causes intellectual disability and unique craniofacial features. Journal of Human Genetics. 63(4). 487–491. 10 indexed citations
9.
Suzuki, Toshifumi, Mahdiyeh Behnam, Mansoor Salehi, et al.. (2018). A homozygous NOP14 variant is likely to cause recurrent pregnancy loss. Journal of Human Genetics. 63(4). 425–430. 13 indexed citations
10.
Ishikawa, Hiroshi, et al.. (2018). Predicting the intrauterine fetal death of fetuses with cystic hygroma in early pregnancy. Congenital Anomalies. 58(5). 167–170. 6 indexed citations
11.
Ishibashi, Kohei, Kajuro Komeda, Futoshi Sekiguchi, & Yasuhiko Kanazawa. (1989). Creeping: a new mutant rat with neurological disease.. PubMed. 39(2). 132–6. 5 indexed citations
12.
Ishikawa, Yoshihiro, et al.. (1986). [Childhood liposarcoma of the eyelid--a case report].. PubMed. 32(5). 506–12. 1 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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