Kei Ohashi

628 total citations
22 papers, 266 citations indexed

About

Kei Ohashi is a scholar working on Molecular Biology, Genetics and Cognitive Neuroscience. According to data from OpenAlex, Kei Ohashi has authored 22 papers receiving a total of 266 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Molecular Biology, 8 papers in Genetics and 5 papers in Cognitive Neuroscience. Recurrent topics in Kei Ohashi's work include Genetics and Neurodevelopmental Disorders (5 papers), Autism Spectrum Disorder Research (4 papers) and Genomics and Rare Diseases (2 papers). Kei Ohashi is often cited by papers focused on Genetics and Neurodevelopmental Disorders (5 papers), Autism Spectrum Disorder Research (4 papers) and Genomics and Rare Diseases (2 papers). Kei Ohashi collaborates with scholars based in Japan, Qatar and United States. Kei Ohashi's co-authors include Shinji Saitoh, Yutaka Negishi, Ikumi Hori, Takao Togawa, Koichi Ito, Shigeo Kure, Takeshi Endo, Ayako Hattori, Toyoichiro Kudo and Tokio Sugiura and has published in prestigious journals such as Carbon, The Journal of Pediatrics and Journal of Autism and Developmental Disorders.

In The Last Decade

Kei Ohashi

20 papers receiving 262 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Kei Ohashi Japan 9 93 83 80 47 30 22 266
C. Nowak Germany 13 88 0.9× 144 1.7× 49 0.6× 50 1.1× 28 0.9× 41 369
Kotaro Yuge Japan 10 40 0.4× 109 1.3× 31 0.4× 72 1.5× 32 1.1× 35 295
Tara Wenger United States 11 196 2.1× 144 1.7× 73 0.9× 26 0.6× 50 1.7× 42 377
Andrew Evans Australia 11 42 0.5× 160 1.9× 50 0.6× 41 0.9× 55 1.8× 18 410
Jamie K. Capal United States 12 156 1.7× 115 1.4× 19 0.2× 146 3.1× 35 1.2× 29 523
Jochem K. H. Spoor Netherlands 9 22 0.2× 55 0.7× 53 0.7× 21 0.4× 48 1.6× 40 265
Anne P. Bouvy Netherlands 8 47 0.5× 41 0.5× 55 0.7× 36 0.8× 7 0.2× 13 464
Michael Pope United Kingdom 6 271 2.9× 95 1.1× 51 0.6× 33 0.7× 14 0.5× 11 431
Anton Mlikotic United States 11 80 0.9× 66 0.8× 58 0.7× 28 0.6× 12 0.4× 19 371
Michael Davenport United States 9 28 0.3× 44 0.5× 64 0.8× 20 0.4× 10 0.3× 21 284

Countries citing papers authored by Kei Ohashi

Since Specialization
Citations

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

Fields of papers citing papers by Kei Ohashi

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Kei Ohashi

This figure shows the co-authorship network connecting the top 25 collaborators of Kei Ohashi. A scholar is included among the top collaborators of Kei Ohashi 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 Kei Ohashi. Kei Ohashi 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.
Goto, Takuma, et al.. (2023). Safe and damage-less dry-purification of carbon nanotubes using FeCl3 vapor. Carbon. 212. 118171–118171. 5 indexed citations
2.
Tsuchida, Naomi, Shuichi Shimakawa, Kei Ohashi, et al.. (2022). Three KINSSHIP syndrome patients with mosaic and germline AFF3 variants. Clinical Genetics. 103(5). 590–595. 1 indexed citations
3.
Ohashi, Kei, et al.. (2022). Two case reports of extended‐release guanfacine overdose in children. Pediatrics International. 65(1). e15424–e15424.
4.
Ohashi, Kei, Taishi Miyachi, Tomoko Asai, et al.. (2021). Comprehensive Genetic Analysis of Non-syndromic Autism Spectrum Disorder in Clinical Settings. Journal of Autism and Developmental Disorders. 51(12). 4655–4662. 7 indexed citations
5.
Ohashi, Kei, et al.. (2021). Impact of School Closures due to COVID-19 on Children with Neurodevelopmental Disorders in Japan. Journal of Autism and Developmental Disorders. 52(5). 2149–2155. 24 indexed citations
6.
Hori, Ikumi, Daisuke Ieda, Y. Nakamura, et al.. (2021). Peripheral nerves are involved in hypomyelinating leukodystrophy-3 caused by a homozygous AIMP1 variant. Brain and Development. 43(4). 590–595. 1 indexed citations
7.
Kato, Aki, et al.. (2021). A case series from a single family of familial retinal arteriolar tortuosity with common history of sudden visual loss. American Journal of Ophthalmology Case Reports. 24. 101230–101230. 1 indexed citations
8.
Uematsu, Mitsugu, Tomoko Kobayashi, Noriko Togashi, et al.. (2020). Behavioral problems and family distress in tuberous sclerosis complex. Epilepsy & Behavior. 111. 107321–107321. 4 indexed citations
9.
Nakamura, Y., Yusuke Okuno, Hideki Muramatsu, et al.. (2019). A novel CUL4B splice site variant in a young male exhibiting less pronounced features. Human Genome Variation. 6(1). 43–43. 4 indexed citations
10.
Ieda, Daisuke, Ikumi Hori, Y. Nakamura, et al.. (2019). A novel splicing mutation in SLC9A6 in a boy with Christianson syndrome. Human Genome Variation. 6(1). 15–15. 7 indexed citations
11.
Ohashi, Kei, et al.. (2019). Direct formation of continuous multilayer graphene films with controllable thickness on dielectric substrates. Thin Solid Films. 675. 136–142. 3 indexed citations
12.
Kato, Kohji, Seiji Mizuno, Shinobu Fukumura, et al.. (2018). Distinctive facies, macrocephaly, and developmental delay are signs of a PTEN mutation in childhood. Brain and Development. 40(8). 678–684. 16 indexed citations
13.
Hayano, Junichiro, Kei Ohashi, Yutaka Yoshida, et al.. (2018). Increase in random component of heart rate variability coinciding with developmental and degenerative stages of life. Physiological Measurement. 39(5). 54004–54004. 14 indexed citations
14.
Kato, Koji, Fuyuki Miya, Ikumi Hori, et al.. (2017). A novel missense mutation in the HECT domain of NEDD4L identified in a girl with periventricular nodular heterotopia, polymicrogyria and cleft palate. Journal of Human Genetics. 62(9). 861–863. 18 indexed citations
15.
Mizuno, Haruo, Takao Togawa, Yutaka Negishi, et al.. (2017). Molecular genetic and clinical delineation of 22 patients with congenital hypogonadotropic hypogonadism. Journal of Pediatric Endocrinology and Metabolism. 30(10). 1111–1118. 19 indexed citations
16.
Ohashi, Kei, Takao Togawa, Tokio Sugiura, et al.. (2017). Combined genetic analyses can achieve efficient diagnostic yields for subjects with Alagille syndrome and incomplete Alagille syndrome. Acta Paediatrica. 106(11). 1817–1824. 9 indexed citations
17.
Togawa, Takao, Tokio Sugiura, Koichi Ito, et al.. (2016). Molecular Genetic Dissection and Neonatal/Infantile Intrahepatic Cholestasis Using Targeted Next-Generation Sequencing. The Journal of Pediatrics. 171. 171–177.e4. 80 indexed citations
18.
Hori, Ikumi, Fuyuki Miya, Kei Ohashi, et al.. (2016). Novel splicing mutation in the ASXL3 gene causing Bainbridge–Ropers syndrome. American Journal of Medical Genetics Part A. 170(7). 1863–1867. 24 indexed citations
19.
Ohashi, Kei, et al.. (2015). Concordance of DSM‐5 and DSM‐IV‐TR classifications for autism spectrum disorder. Pediatrics International. 57(6). 1097–1100. 8 indexed citations
20.
Ohashi, Kei, et al.. (2008). Improvement Method of the Detection Accuracy of the Information Leakage in Diffusion Tracing Function of Classified Information. IPSJ SIG Notes. 2008(21). 97–102. 2 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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