Xue Jun Fu - Concepedia

Author

Xue Jun Fu

Kobe University

Also Known As

X J Fu, XUE J. FU, Xue J Fu, Xue Jun Fu

Publications

971

Citations

H-Index

Concepts

All Affiliations

Kobe University Wakayama Medical University National Center For Child Health and Development University of Southampton The University of Tokyo

About

Xue Jun Fu is an author at Kobe University specializing in medicine, pathology, and genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	14	15	591
2	Molecular Genetics	5	5	191
3	Molecular Biology	2	2	37
4	Molecular Medicine	2	2	57
5	Nephrology	2	2	45

Xue Jun Fu

Publications

965

Citations

H-Index

Page 1

	Year	Citations
Genetic, Clinical, and Pathologic Backgrounds of Patients with Autosomal Dominant Alport Syndrome Naohiro Kamiyoshi, Kandai Nozu, Xue Jun Fu, Clinical Journal of the American Society of Nephrology	2016	129
Molecular analysis of digenic inheritance in Bartter syndrome with sensorineural deafness Kandai Nozu, Tetsuji Inagaki, Xue Jun Fu, Journal of Medical Genetics	2008	106
Differential diagnosis of Bartter syndrome, Gitelman syndrome, and pseudo–Bartter/Gitelman syndrome based on clinical characteristics Natsuki Matsunoshita, Kandai Nozu, Akemi Shono, Genetics in Medicine Differential DiagnosisDiagnosisPseudo–bartter/gitelman SyndromeBartter SyndromeNeuropathology	2015	89
Natural history of genetically proven autosomal recessive Alport syndrome Masafumi Oka, Kandai Nozu, Hiroshi Kaito, Pediatric Nephrology Mendelian DisorderGenetic DisorderGeneticsNatural HistoryGenetic Epidemiology	2014	88
Milder clinical aspects of X-linked Alport syndrome in men positive for the collagen IV α5 chain Yuya Hashimura, Kandai Nozu, Hiroshi Kaito, Kidney International X-linked Alport SyndromePathologyMilder Clinical AspectsSclerodermaMedicine	2013	88
Natural History and Genotype–Phenotype Correlation in Female X-Linked Alport Syndrome Tomohiko Yamamura, Kandai Nozu, Xue Jun Fu, Kidney International Reports	2017	85
Molecular Analysis of Patients With Type III Bartter Syndrome: Picking Up Large Heterozygous Deletions With Semiquantitative PCR Kandai Nozu, Xue Jun Fu, Koichi Nakanishi, Pediatric Research Mendelian DisorderGenetic DisorderGeneticsPathogenesisMolecular Analysis	2007	49
OCRL1 mutations in patients with Dent disease phenotype in Japan Takashi Sekine, Kandai Nozu, Rashmi Iyengar, Pediatric Nephrology MedicineGeneticsOral CavityPathologyDental Disease	2007	46
In vivo and in vitro splicing assay of SLC12A1 in an antenatal salt-losing tubulopathy patient with an intronic mutation Kandai Nozu, Kazumoto Iijima, Kazuo Kawai, Human Genetics Translational MedicineSodium HomeostasisGeneticsPathologyIntronic Mutation	2009	40
A Deep Intronic Mutation in the SLC12A3 Gene Leads to Gitelman Syndrome Kandai Nozu, Kazumoto Iijima, Yoshimi Nozu, Pediatric Research Developmental BiologySomatic VariantMendelian DisorderGitelman SyndromeGenetic Disorder	2009	39

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