Yoshimi Nozu

1.1k total citations
21 papers, 600 citations indexed

About

Yoshimi Nozu is a scholar working on Molecular Biology, Immunology and Allergy and Hematology. According to data from OpenAlex, Yoshimi Nozu has authored 21 papers receiving a total of 600 indexed citations (citations by other indexed papers that have themselves been cited), including 17 papers in Molecular Biology, 7 papers in Immunology and Allergy and 5 papers in Hematology. Recurrent topics in Yoshimi Nozu's work include Renal and related cancers (7 papers), Ion Transport and Channel Regulation (7 papers) and Cell Adhesion Molecules Research (7 papers). Yoshimi Nozu is often cited by papers focused on Renal and related cancers (7 papers), Ion Transport and Channel Regulation (7 papers) and Cell Adhesion Molecules Research (7 papers). Yoshimi Nozu collaborates with scholars based in Japan and United Kingdom. Yoshimi Nozu's co-authors include Kandai Nozu, Kazumoto Iijima, Koichi Nakanishi, Hiroshi Kaito, Xue Jun Fu, Tomohiko Yamamura, Norishige Yoshikawa, Shogo Minamikawa, Takeshi Ninchoji and Yuko Shima and has published in prestigious journals such as PEDIATRICS, Kidney International and Clinical Journal of the American Society of Nephrology.

In The Last Decade

Yoshimi Nozu

21 papers receiving 593 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Yoshimi Nozu Japan 14 412 227 156 146 84 21 600
Naoya Morisada Japan 15 367 0.9× 159 0.7× 89 0.6× 205 1.4× 58 0.7× 46 585
Alison Homstad United States 6 187 0.5× 76 0.3× 287 1.8× 64 0.4× 35 0.4× 8 406
Nanami Gotoh Japan 10 191 0.5× 17 0.1× 136 0.9× 62 0.4× 84 1.0× 26 483
Harald O. Schöcklmann Germany 12 151 0.4× 74 0.3× 138 0.9× 29 0.2× 26 0.3× 17 401
Britta George Germany 11 277 0.7× 25 0.1× 408 2.6× 148 1.0× 19 0.2× 20 603
Rita Foti Australia 9 135 0.3× 34 0.1× 163 1.0× 21 0.1× 27 0.3× 12 451
Jiamin Teng United States 11 358 0.9× 23 0.1× 133 0.9× 46 0.3× 45 0.5× 21 441
Purba Biswas United States 7 141 0.3× 94 0.4× 38 0.2× 19 0.1× 54 0.6× 9 336
Shoichiro Kanda Japan 13 267 0.6× 13 0.1× 165 1.1× 56 0.4× 11 0.1× 36 442
Mohamed H. Al‐Hamed Saudi Arabia 13 227 0.6× 10 0.0× 65 0.4× 128 0.9× 22 0.3× 44 456

Countries citing papers authored by Yoshimi Nozu

Since Specialization
Citations

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

Fields of papers citing papers by Yoshimi Nozu

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Yoshimi Nozu

This figure shows the co-authorship network connecting the top 25 collaborators of Yoshimi Nozu. A scholar is included among the top collaborators of Yoshimi Nozu 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 Yoshimi Nozu. Yoshimi Nozu 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.
Yamamura, Tomohiko, Tomoko Horinouchi, China Nagano, et al.. (2020). Genotype-phenotype correlations influence the response to angiotensin-targeting drugs in Japanese patients with male X-linked Alport syndrome. Kidney International. 98(6). 1605–1614. 63 indexed citations
2.
Sakakibara, Nana, Naoya Morisada, Kandai Nozu, et al.. (2018). Clinical spectrum of male patients with OFD1 mutations. Journal of Human Genetics. 64(1). 3–9. 9 indexed citations
3.
Fujimura, Junya, Kandai Nozu, Tomohiko Yamamura, et al.. (2018). Clinical and Genetic Characteristics in Patients With Gitelman Syndrome. Kidney International Reports. 4(1). 119–125. 37 indexed citations
4.
Nagano, China, Kandai Nozu, Naoya Morisada, et al.. (2018). Detection of copy number variations by pair analysis using next-generation sequencing data in inherited kidney diseases. Clinical and Experimental Nephrology. 22(4). 881–888. 21 indexed citations
5.
Minamikawa, Shogo, Kandai Nozu, Yoshimi Nozu, et al.. (2018). Development of ultra-deep targeted RNA sequencing for analyzing X-chromosome inactivation in female Dent disease. Journal of Human Genetics. 63(5). 589–595. 10 indexed citations
6.
Nozu, Kandai, Tadashi Sofue, Shigeo Hara, et al.. (2017). Detection of a Splice Site Variant in a Patient with Glomerulopathy and Fibronectin Deposits. ˜The œNephron journals/Nephron journals. 138(2). 166–171. 6 indexed citations
7.
Yamamura, Tomohiko, Kandai Nozu, Xue Jun Fu, et al.. (2017). Natural History and Genotype–Phenotype Correlation in Female X-Linked Alport Syndrome. Kidney International Reports. 2(5). 850–855. 59 indexed citations
8.
Nozu, Kandai, Kazumoto Iijima, Toru Igarashi, et al.. (2017). A birth of bipartite exon by intragenic deletion. Molecular Genetics & Genomic Medicine. 5(3). 287–294. 4 indexed citations
9.
Nozu, Kandai, Yoshimi Nozu, Keita Nakanishi, et al.. (2016). Cryptic exon activation in SLC12A3 in Gitelman syndrome. Journal of Human Genetics. 62(2). 335–337. 11 indexed citations
10.
Nozu, Kandai, Shogo Minamikawa, Tomohiko Yamamura, et al.. (2016). Female X-linked Alport syndrome with somatic mosaicism. Clinical and Experimental Nephrology. 21(5). 877–883. 16 indexed citations
11.
Kamiyoshi, Naohiro, Kandai Nozu, Xue Jun Fu, et al.. (2016). Genetic, Clinical, and Pathologic Backgrounds of Patients with Autosomal Dominant Alport Syndrome. Clinical Journal of the American Society of Nephrology. 11(8). 1441–1449. 84 indexed citations
12.
Nozu, Kandai, Akemi Shono, Yoshimi Nozu, et al.. (2015). Differential diagnosis of Bartter syndrome, Gitelman syndrome, and pseudo–Bartter/Gitelman syndrome based on clinical characteristics. Genetics in Medicine. 18(2). 180–188. 56 indexed citations
13.
Fu, Xue Jun, Kandai Nozu, Yoshimi Nozu, et al.. (2015). X-linked Alport syndrome associated with a synonymous p.Gly292Gly mutation alters the splicing donor site of the type IV collagen alpha chain 5 gene. Clinical and Experimental Nephrology. 20(5). 699–702. 14 indexed citations
14.
Hasui, Masafumi, Kazunari Kaneko, Shoji Tsuji, et al.. (2012). Different phenotypes of HNF1? deletion mutants in familial multicystic dysplastic kidneys. Clinical Nephrology. 79(6). 484–487. 8 indexed citations
15.
Shima, Yuko, Kandai Nozu, Yoshimi Nozu, et al.. (2011). Recurrent EIARF and PRES With Severe Renal Hypouricemia by Compound Heterozygous SLC2A9 Mutation. PEDIATRICS. 127(6). e1621–e1625. 28 indexed citations
16.
Nozu, Kandai, Kazumoto Iijima, Yoshimi Nozu, et al.. (2009). A Deep Intronic Mutation in the SLC12A3 Gene Leads to Gitelman Syndrome. Pediatric Research. 66(5). 590–593. 25 indexed citations
17.
Nozu, Kandai, Kazumoto Iijima, Yoshimi Nozu, et al.. (2009). In vivo and in vitro splicing assay of SLC12A1 in an antenatal salt-losing tubulopathy patient with an intronic mutation. Human Genetics. 126(4). 533–538. 32 indexed citations
18.
Yamazaki, Hajime, Kandai Nozu, Ichiei Narita, et al.. (2008). Atypical phenotype of type I Bartter syndrome accompanied by focal segmental glomerulosclerosis. Pediatric Nephrology. 24(2). 415–418. 22 indexed citations
19.
Nozu, Kandai, Xue Jun Fu, Yoshimi Nozu, et al.. (2008). Molecular analysis of digenic inheritance in Bartter syndrome with sensorineural deafness. Journal of Medical Genetics. 45(3). 182–186. 71 indexed citations
20.
Nozu, Kandai, Yasufumi Ohtsuka, Koichi Nakanishi, et al.. (2008). Detection of large deletion mutations in the COL4A5 gene of female Alport syndrome patients. Pediatric Nephrology. 23(11). 2085–2090. 3 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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