Tetsuro Noguchi

1.7k total citations
31 papers, 1.0k citations indexed

About

Tetsuro Noguchi is a scholar working on Molecular Biology, Genetics and Cancer Research. According to data from OpenAlex, Tetsuro Noguchi has authored 31 papers receiving a total of 1.0k indexed citations (citations by other indexed papers that have themselves been cited), including 20 papers in Molecular Biology, 9 papers in Genetics and 6 papers in Cancer Research. Recurrent topics in Tetsuro Noguchi's work include BRCA gene mutations in cancer (7 papers), DNA Repair Mechanisms (6 papers) and Cancer Genomics and Diagnostics (5 papers). Tetsuro Noguchi is often cited by papers focused on BRCA gene mutations in cancer (7 papers), DNA Repair Mechanisms (6 papers) and Cancer Genomics and Diagnostics (5 papers). Tetsuro Noguchi collaborates with scholars based in France, Japan and United States. Tetsuro Noguchi's co-authors include Akira Fujishima, Kazuhito Hashimoto, Phillip Sawunyama, Hagay Sobol, Rodrigo Bravo, Lihong Chen, Marie‐Geneviève Mattéi, Daniel E. Carrasco, R Metz and Daniel Birnbaum and has published in prestigious journals such as Nucleic Acids Research, Environmental Science & Technology and PLoS ONE.

In The Last Decade

Tetsuro Noguchi

30 papers receiving 981 citations

Peers

Tetsuro Noguchi
Yanzhu Yang United States
Shuai Gao China
Jinyu Li China
Yaqing Li China
Fei Zhu China
Zhan Wang China
Tetsuro Noguchi
Citations per year, relative to Tetsuro Noguchi Tetsuro Noguchi (= 1×) peers Jingjia Li

Countries citing papers authored by Tetsuro Noguchi

Since Specialization
Citations

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

Fields of papers citing papers by Tetsuro Noguchi

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Tetsuro Noguchi

This figure shows the co-authorship network connecting the top 25 collaborators of Tetsuro Noguchi. A scholar is included among the top collaborators of Tetsuro Noguchi 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 Tetsuro Noguchi. Tetsuro Noguchi 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.
Hamadou, Walid Sabri, Nouha Bouali, Violaine Bourdon, et al.. (2021). Mutational analysis of apoptotic genes in familial aggregation of hematological malignancies. Bulletin du Cancer. 108(9). 798–805.
2.
Ishida, Kyoko, Masamitsu Shimazawa, Tetsuro Noguchi, et al.. (2017). Movement of retinal vessels toward the optic nerve head after increasing intraocular pressure in monkey eyes with experimental glaucoma. Experimental Eye Research. 162. 110–115. 7 indexed citations
3.
Kadota, Kazunori, et al.. (2017). DEM Modelling of Granule Rearrangement and Fracture Behaviours During a Closed-Die Compaction. AAPS PharmSciTech. 18(6). 2368–2377. 15 indexed citations
4.
Noguchi, Tetsuro, Violaine Bourdon, & Hagay Sobol. (2014). About Sequence Quality: Impact on Clinical Applications. Genetic Testing and Molecular Biomarkers. 18(5). 299–305. 1 indexed citations
5.
Gilabert, Marine, Christophe Ginestier, François Bertucci, et al.. (2014). Poly(ADP-Ribose) Polymerase 1 (PARP1) Overexpression in Human Breast Cancer Stem Cells and Resistance to Olaparib. PLoS ONE. 9(8). e104302–e104302. 55 indexed citations
6.
Hassanein, Mohamed, Laëtitia Huiart, Violaine Bourdon, et al.. (2013). Prediction of BRCA1 Germ-Line Mutation Status in Patients with Breast Cancer Using Histoprognosis Grade, MS110, Lys27H3, Vimentin, and KI67. Pathobiology. 80(5). 219–227. 10 indexed citations
7.
Soeda, Fumio, et al.. (2013). Effect of tipepidine with novel antidepressant-like action on c-fos-like protein expression in rat brain. Brain Research. 1513. 135–142. 11 indexed citations
8.
Gensollen, Thomas, Christophe Bourges, Pascal Rihet, et al.. (2013). Functional Polymorphisms in the Regulatory Regions of the VNN1 Gene Are Associated with Susceptibility to Inflammatory Bowel Diseases. Inflammatory Bowel Diseases. 19(11). 2315–2325. 41 indexed citations
9.
Rousseau, Guillaume, Tetsuro Noguchi, Violaine Bourdon, Hagay Sobol, & Sylviane Olschwang. (2011). SMARCB1/INI1 germline mutations contribute to 10% of sporadic schwannomatosis. BMC Neurology. 11(1). 9–9. 52 indexed citations
11.
Lassailly, François, Julien Mozziconacci, Tetsuro Noguchi, et al.. (2007). Comparison of a Selection of Rapid Automated DNA and RNA Extraction Technologies for Detection of Somatic or Constitutional Gene Abnormalities in Cancer Diagnosis. 5(1). 2–15. 3 indexed citations
12.
Sobol, Hagay, Norbert Vey, R Sauvan, et al.. (2002). Re: Familial multiple myeloma: A family study and review of the literature (multiple letters). JNCI Journal of the National Cancer Institute. 94(6). 461–463. 8 indexed citations
13.
Sauvan, R, Tetsuro Noguchi, Daniel Serin, et al.. (2001). Three novel BRCA1 germline mutations (1104delAA, 1276delTT, 3747delGA) detected in breast/ovarian cancer families identified in the south of France. Human Mutation. 17(2). 154–154. 2 indexed citations
14.
Sobol, Hagay, F Kerangueven, Yin Luo, et al.. (2001). Genome‐wide search for loss of heterozygosity in Burkitt lymphoma cell lines. Genes Chromosomes and Cancer. 33(2). 217–224. 12 indexed citations
15.
Eisinger, François, Jean‐Philippe Peyrat, Tetsuro Noguchi, et al.. (1999). Novel indications forBRCA1 screening using individual clinical and morphological features. International Journal of Cancer. 84(3). 263–267. 39 indexed citations
16.
Allione, Florence, François Eisinger, Patricia Parc, et al.. (1998). Loss of heterozygosity at loci from chromosome arm 22Q in human sporadic breast carcinomas. International Journal of Cancer. 75(2). 181–186. 39 indexed citations
17.
Kerangueven, F, François Eisinger, Tetsuro Noguchi, et al.. (1997). Loss of heterozygosity in human breast carcinomas in the ataxia telangiectasia, Cowden disease and BRCA1 gene regions. Oncogene. 14(3). 339–347. 54 indexed citations
18.
Chaffanet, Max, Laurent Essioux, Tetsuro Noguchi, et al.. (1996). Integrated Map of the Chromosome 8p12–p21 Region, a Region Involved in Human Cancers and Werner Syndrome. Genomics. 32(1). 29–38. 31 indexed citations
19.
Lazo, Pedro S., et al.. (1992). Structure and mapping of thefosB gene. FosB downregulates the activity of thefosB promotero. Nucleic Acids Research. 20(2). 343–350. 62 indexed citations
20.

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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