Tomomi Aoi

622 total citations
10 papers, 228 citations indexed

About

Tomomi Aoi is a scholar working on Molecular Biology, Genetics and Pathology and Forensic Medicine. According to data from OpenAlex, Tomomi Aoi has authored 10 papers receiving a total of 228 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 Pathology and Forensic Medicine. Recurrent topics in Tomomi Aoi's work include Genetic factors in colorectal cancer (2 papers), Genomics and Rare Diseases (1 paper) and Retinal Development and Disorders (1 paper). Tomomi Aoi is often cited by papers focused on Genetic factors in colorectal cancer (2 papers), Genomics and Rare Diseases (1 paper) and Retinal Development and Disorders (1 paper). Tomomi Aoi collaborates with scholars based in Japan, Italy and United States. Tomomi Aoi's co-authors include Michiaki Kubo, Kyota Ashikawa, Naoyuki Kamatani, Atsushi Takahashi, Kazuaki Kadonosono, Naoya Hosono, Shigeru Honda, Yuji Oshima, Miho Yasuda and Satoshi Arakawa and has published in prestigious journals such as Nature Genetics, Gastroenterology and Human Molecular Genetics.

In The Last Decade

Tomomi Aoi

8 papers receiving 224 citations

Peers

Tomomi Aoi

OPHTH

MB

GENET

RNMI

IMMUN

Beate J. Wegscheider Austria

Maria Chiara Gelmi Netherlands

Debasis Chakrabarti United States

Elena Zinovieva France

Mitsuko Takamoto Japan

BE DAMATO United Kingdom

Emanuel Bs United States

Lidia Ostanek Poland

E S Concepcion United States

H. Tönnies Germany

Beate J. Wegscheider Austria

Tomomi Aoi

212 ×2.6

OPHTH

78 ×1.1

MB

9 ×0.1

GENET

73 ×1.2

RNMI

58 ×1.1

IMMUN

Citations per year, relative to Tomomi Aoi Tomomi Aoi (= 1×) peers Beate J. Wegscheider

Countries citing papers authored by Tomomi Aoi

Since Specialization

Citations

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

Fields of papers citing papers by Tomomi Aoi

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Tomomi Aoi

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

All Works

Sort: Min cites: Since: Top N: Style:

10 of 10 papers shown

1.

Uno, Yasuhiro, Koya Fukunaga, Norie Murayama, et al.. (2025). Genetic variants in dog cytochrome P450 2B6 and their relevance to interindividual variability of oxidations of probe drug propofol. Drug Metabolism and Disposition. 53(12). 100189–100189.

2.

Matsumura, Naoki, Keijiro Mizukami, Yuko Goto‐Koshino, et al.. (2024). Investigation of the mutations in the genes involved in Janus kinase/signal transducer and activator of transcription pathway in canine large cell gastrointestinal lymphoma. Journal of Veterinary Medical Science. 86(10). 1052–1055.

3.

Koyanagi, Yoshito, Yusuke Murakami, Kohta Fujiwara, et al.. (2022). Likely pathogenic structural variants in genetically unsolved patients with retinitis pigmentosa revealed by long-read sequencing. Journal of Medical Genetics. 59(11). 1133–1138. 13 indexed citations

4.

Suzuki, Toshimitsu, Yoshinao Koike, Kyota Ashikawa, et al.. (2021). Genome‐wide association study of epilepsy in a Japanese population identified an associated region at chromosome 12q24. Epilepsia. 62(6). 1391–1400. 7 indexed citations

5.

Iwasaki, Yusuke, Tomomi Aoi, Mikiko Endo, et al.. (2021). OUP accepted manuscript. Human Molecular Genetics. 31(12). 1962–1969. 6 indexed citations

6.

Fujita, Masashi, Xiaoxi Liu, Yusuke Iwasaki, et al.. (2020). Population-based Screening for Hereditary Colorectal Cancer Variants in Japan. Clinical Gastroenterology and Hepatology. 20(9). 2132–2141.e9. 20 indexed citations

7.

Liu, Xiaoxi, Sadaaki Takata, Kyota Ashikawa, et al.. (2020). Prevalence and Spectrum of Pathogenic Germline Variants in Japanese Patients With Early-Onset Colorectal, Breast, and Prostate Cancer. JCO Precision Oncology. 4(4). 183–191. 5 indexed citations

8.

Okada, Yukinori, Keiko Yamazaki, Junji Umeno, et al.. (2011). HLA-Cw*1202-B*5201-DRB1*1502 Haplotype Increases Risk for Ulcerative Colitis but Reduces Risk for Crohn's Disease. Gastroenterology. 141(3). 864–871.e5. 58 indexed citations

9.

Arakawa, Satoshi, Atsushi Takahashi, Kyota Ashikawa, et al.. (2011). Genome-wide association study identifies two susceptibility loci for exudative age-related macular degeneration in the Japanese population. Nature Genetics. 43(10). 1001–1004. 101 indexed citations

10.

Chisuwa, Hisanao, Shin Kawasaki, Junya Ozawa, et al.. (1997). Systemic reactive amyloidosis associated with Castleman's disease: serial changes of the concentrations of acute phase serum amyloid A and interleukin 6 in serum.. Journal of Clinical Pathology. 50(11). 965–967. 18 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.

Explore authors with similar magnitude of impact