Yoshimi Nozu

1.1k citations

21 papers · 600 indexed · h-index 14

Co-authors: Kandai Nozu Kazumoto Iijima Koichi Nakanishi Hiroshi Kaito Xue Jun Fu Tomohiko Yamamura Norishige Yoshikawa Shogo Minamikawa
Topics: Renal and related cancers (7 papers)Ion Transport and Channel Regulation (7 papers)Cell Adhesion Molecules Research (7 papers)
Cited by: Immunology and Allergy Nephrology Hematology
Journals: PEDIATRICS Kidney International Clinical Journal of the American Society of Nephrology
Partner nations: Japan United Kingdom

In The Last Decade

Yoshimi Nozu

21 papers receiving 593 citations

Peers

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

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

20 of 20 papers shown

#	Work	Indexed citations
1	Genotype-phenotype correlations influence the response to angiotensin-targeting drugs in Japanese patients with male X-linked Alport syndrome 2020 ·Kidney International ·Tomohiko Yamamura,Tomoko Horinouchi,China Nagano,Takashi Omori,Nana Sakakibara,Yuya Aoto,Shinya Ishiko,Koichi Nakanishi,Yuko Shima,Hiroaki Nagase,Hiroki Takeda,Rini Rossanti,Ming Juan Ye,Yoshimi Nozu,Shingo Ishimori,Takeshi Ninchoji,Hiroshi Kaito,Naoya Morisada,Kazumoto Iijima,Kandai Nozu	63
2	Clinical spectrum of male patients with OFD1 mutations 2018 ·Journal of Human Genetics ·Nana Sakakibara,Naoya Morisada,Kandai Nozu,(unknown),Toshiyuki Ohta,Junya Shimizu,(unknown),Yuko Shima,Tomohiko Yamamura,Shogo Minamikawa,Junya Fujimura,Tomoko Horinouchi,China Nagano,Akemi Shono,Ming Juan Ye,Yoshimi Nozu,Koichi Nakanishi,Kazumoto Iijima	9
3	Clinical and Genetic Characteristics in Patients With Gitelman Syndrome 2018 ·Kidney International Reports ·Junya Fujimura,Kandai Nozu,Tomohiko Yamamura,Shogo Minamikawa,Keita Nakanishi,Tomoko Horinouchi,China Nagano,Nana Sakakibara,Koichi Nakanishi,Yuko Shima,Kenichi Miyako,Yoshimi Nozu,Naoya Morisada,Hiroaki Nagase,Takeshi Ninchoji,Hiroshi Kaito,Kazumoto Iijima	37
4	Detection of copy number variations by pair analysis using next-generation sequencing data in inherited kidney diseases 2018 ·Clinical and Experimental Nephrology ·China Nagano,Kandai Nozu,Naoya Morisada,Masahiko Yazawa,Daisuke Ichikawa,(unknown),(unknown),(unknown),(unknown),Ryojiro Tanaka,Tomohiko Yamamura,Shogo Minamikawa,Tomoko Horinouchi,Keita Nakanishi,Junya Fujimura,Nana Sakakibara,Yoshimi Nozu,Ming Juan Ye,Hiroshi Kaito,Kazumoto Iijima	21
5	Development of ultra-deep targeted RNA sequencing for analyzing X-chromosome inactivation in female Dent disease 2018 ·Journal of Human Genetics ·Shogo Minamikawa,Kandai Nozu,Yoshimi Nozu,Tomohiko Yamamura,Mariko Taniguchi‐Ikeda,Keita Nakanishi,Junya Fujimura,Tomoko Horinouchi,Yuko Shima,Koichi Nakanishi,(unknown),Kyoko Kanda,Ryojiro Tanaka,Naoya Morisada,China Nagano,Nana Sakakibara,Hiroaki Nagase,Ichiro Morioka,Hiroshi Kaito,Kazumoto Iijima	10
6	Detection of a Splice Site Variant in a Patient with Glomerulopathy and Fibronectin Deposits 2017 ·The Nephron journals/Nephron journals ·(unknown),Kandai Nozu,Tadashi Sofue,Shigeo Hara,Keita Nakanishi,Tomohiko Yamamura,Shogo Minamikawa,Yoshimi Nozu,Hiroshi Kaito,Junya Fujimura,Tomoko Horinouchi,Naoya Morisada,Ichiro Morioka,Mariko Taniguchi‐Ikeda,Masafumi Matsuo,Kazumoto Iijima	6
7	Natural History and Genotype–Phenotype Correlation in Female X-Linked Alport Syndrome 2017 ·Kidney International Reports ·Tomohiko Yamamura,Kandai Nozu,Xue Jun Fu,Yoshimi Nozu,Ming Juan Ye,Akemi Shono,(unknown),Shogo Minamikawa,Naoya Morisada,Koichi Nakanishi,Yuko Shima,Norishige Yoshikawa,Takeshi Ninchoji,Ichiro Morioka,Hiroshi Kaito,Kazumoto Iijima	59
8	A birth of bipartite exon by intragenic deletion 2017 ·Molecular Genetics & Genomic Medicine ·Kandai Nozu,Kazumoto Iijima,Toru Igarashi,Shiro YAMADA,Jana Královičová,Yoshimi Nozu,Tomohiko Yamamura,Shogo Minamikawa,Ichiro Morioka,Takeshi Ninchoji,Hiroshi Kaito,Koichi Nakanishi,Igor Vořechovský	4
9	Cryptic exon activation in SLC12A3 in Gitelman syndrome 2016 ·Journal of Human Genetics ·Kandai Nozu,Yoshimi Nozu,Keita Nakanishi,(unknown),Tomoko Horinouchi,Akemi Shono,Naoya Morisada,Shogo Minamikawa,Tomohiko Yamamura,Junya Fujimura,Koichi Nakanishi,Takeshi Ninchoji,Hiroshi Kaito,Ichiro Morioka,Mariko Taniguchi‐Ikeda,Igor Vořechovský,Kazumoto Iijima	11
10	Female X-linked Alport syndrome with somatic mosaicism 2016 ·Clinical and Experimental Nephrology ·(unknown),Kandai Nozu,Shogo Minamikawa,Tomohiko Yamamura,Keita Nakanishi,Hisashi Kaneda,Riku Hamada,Yoshimi Nozu,Akemi Shono,Takeshi Ninchoji,Naoya Morisada,Shingo Ishimori,Junya Fujimura,Tomoko Horinouchi,Hiroshi Kaito,Koichi Nakanishi,Ichiro Morioka,Mariko Taniguchi‐Ikeda,Kazumoto Iijima	16
11	Genetic, Clinical, and Pathologic Backgrounds of Patients with Autosomal Dominant Alport Syndrome 2016 ·Clinical Journal of the American Society of Nephrology ·Naohiro Kamiyoshi,Kandai Nozu,Xue Jun Fu,Naoya Morisada,Yoshimi Nozu,Ming Juan Ye,Aya Imafuku,Kenichiro Miura,Tomohiko Yamamura,Shogo Minamikawa,Akemi Shono,Takeshi Ninchoji,Ichiro Morioka,Koichi Nakanishi,Norishige Yoshikawa,Hiroshi Kaito,Kazumoto Iijima	84
12	Differential diagnosis of Bartter syndrome, Gitelman syndrome, and pseudo–Bartter/Gitelman syndrome based on clinical characteristics 2015 ·Genetics in Medicine ·(unknown),Kandai Nozu,Akemi Shono,Yoshimi Nozu,Xue Jun Fu,Naoya Morisada,Naohiro Kamiyoshi,(unknown),Takeshi Ninchoji,Shogo Minamikawa,Tomohiko Yamamura,Koichi Nakanishi,Norishige Yoshikawa,Yuko Shima,Hiroshi Kaito,Kazumoto Iijima	56
13	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 2015 ·Clinical and Experimental Nephrology ·Xue Jun Fu,Kandai Nozu,(unknown),Yoshimi Nozu,Naoya Morisada,Akemi Shono,Mariko Taniguchi‐Ikeda,Yuko Shima,Koichi Nakanishi,Igor Vořechovský,Kazumoto Iijima	14
14	Different phenotypes of HNF1? deletion mutants in familial multicystic dysplastic kidneys 2012 ·Clinical Nephrology ·Masafumi Hasui,Kazunari Kaneko,Shoji Tsuji,Yuka Isozaki,Takahisa Kimata,Yoshimi Nozu,Kandai Nozu,Kazumoto Iijima	8
15	Recurrent EIARF and PRES With Severe Renal Hypouricemia by Compound Heterozygous SLC2A9 Mutation 2011 ·PEDIATRICS ·Yuko Shima,Kandai Nozu,Yoshimi Nozu,Hiroko Togawa,Hiroshi Kaito,Masafumi Matsuo,Kazumoto Iijima,Koichi Nakanishi,Norishige Yoshikawa	28
16	A Deep Intronic Mutation in the SLC12A3 Gene Leads to Gitelman Syndrome 2009 ·Pediatric Research ·Kandai Nozu,Kazumoto Iijima,Yoshimi Nozu,(unknown),(unknown),Xue Jun Fu,Hiroshi Kaito,Koichi Nakanishi,Norishige Yoshikawa,Masafumi Matsuo	25
17	In vivo and in vitro splicing assay of SLC12A1 in an antenatal salt-losing tubulopathy patient with an intronic mutation 2009 ·Human Genetics ·Kandai Nozu,Kazumoto Iijima,(unknown),Yoshimi Nozu,Atsushi Nishida,Yasuhiro Takeshima,Xue Jun Fu,Yuya Hashimura,Hiroshi Kaito,Koichi Nakanishi,Norishige Yoshikawa,Masafumi Matsuo	32
18	Atypical phenotype of type I Bartter syndrome accompanied by focal segmental glomerulosclerosis 2008 ·Pediatric Nephrology ·Hajime Yamazaki,Kandai Nozu,Ichiei Narita,Michio Nagata,Yoshimi Nozu,Xue Jun Fu,Masafumi Matsuo,Kazumoto Iijima,Fumitake Gejyo	22
19	Molecular analysis of digenic inheritance in Bartter syndrome with sensorineural deafness 2008 ·Journal of Medical Genetics ·Kandai Nozu,(unknown),Xue Jun Fu,Yoshimi Nozu,Hiroshi Kaito,Kyoko Kanda,Takashi Sekine,T. Igarashi,Koichi Nakanishi,N. Yoshikawa,Kazumoto Iijima,Masafumi Matsuo	71
20	Detection of large deletion mutations in the COL4A5 gene of female Alport syndrome patients 2008 ·Pediatric Nephrology ·Kandai Nozu,(unknown),Yasufumi Ohtsuka,Koichi Nakanishi,Norishige Yoshikawa,Yoshimi Nozu,Hiroshi Kaito,Kyoko Kanda,Yuya Hashimura,Yuhei Hamasaki,Kazumoto Iijima,Masafumi Matsuo	3

About Yoshimi Nozu

Yoshimi Nozu is a scholar working on Immunology and Allergy, Nephrology and Hematology, having authored 21 papers that have together received 600 indexed citations. Recurring topics across this work include Renal and related cancers (7 papers), Ion Transport and Channel Regulation (7 papers) and Cell Adhesion Molecules Research (7 papers). The work is most often cited by research in Immunology and Allergy (227 citations), Nephrology (156 citations) and Hematology (84 citations). Yoshimi Nozu has collaborated with scholars based in Japan and United Kingdom. Frequent 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. Their work appears in journals such as PEDIATRICS, Kidney International and Clinical Journal of the American Society of Nephrology.

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