Kouji Narahara - Concepedia

Author

Kouji Narahara

Okayama University

Also Known As

K Narahara, K. A. Narahara, K. NARAHARA, K. Narahara, KOUJI NARAHARA, Kouji Narahara, Kumiko Narahara

Publications

1.2K

Citations

H-Index

Concepts

All Affiliations

Okayama University Matsuyama Red Cross Hospital Boston Children's Hospital Nagasaki University Saitama Children's Medical Center

About

Kouji Narahara is an author at Okayama University specializing in medicine, genetics, and cytogenetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	13	16	461
2	Natural Sciences	4	4	141
3	Biochemistry	3	3	119
4	Social Sciences	1	1	12
5	Biology	1	1	38

Kouji Narahara

Publications

797

Citations

H-Index

Page 1

	Year	Citations
Regional mapping of catalase and Wilms tumor?aniridia, genitourinary abnormalities, and mental retardation triad loci to the chromosome segment 11p1305?p1306 Kouji Narahara, Kiyoshi Kikkawa, S. Kimira, Human Genetics Developmental AnomalyUrologyChromosome Segment 11P1305Somatic VariantCytogenetics	1984	83
Probable assignment of soluble isocitrate dehydrogenase (IDH1) to 2q33.3 Kouji Narahara, Shunsuke Kimura, Kiyoshi Kikkawa, Human Genetics Aldehyde DehydrogenaseBiochemistryNatural SciencesMolecular BiologyStructural Biology	1985	63
Assignment of human porphobilinogen deaminase to 11q24.1→q24.2 by in situ hybridization and gene dosage studies Hiroshi Namba, Kouji Narahara, Kazushiro Tsuji, Cytogenetic and Genome Research	1991	63
Isolation of a Testis-Specific cDNA on Chromosome 17q from a Region Adjacent to the Breakpoint of t(12, 17) Observed in a Patient with Acampomelic Campomelic Dysplasia and Sex Reversal Shinsuke Ninomiya, Minoru Isomura, Kouji Narahara, Human Molecular Genetics	1996	50
Localisation of a 10q breakpoint within the PAX2 gene in a patient with a de novo t(10;13) translocation and optic nerve coloboma-renal disease. Kouji Narahara, E Baker, Sakiko Ito, Journal of Medical Genetics	1997	48
Autosomal dominant congenital cataract and microphthalmia associated with a familial t(2;16) translocation Yuji Yokoyama, Kouji Narahara, Kazushiro Tsuji, Human Genetics Ocular DiseaseFamilial TOphthalmologyPediatric OphthalmologyGlaucoma	1992	45
Growth hormone deficiency and empty sella syndrome in a boy with dup(x)(q13.3→q21.2) Yuji Yokoyama, Kouji Narahara, Kazushiro Tsuji, American Journal of Medical Genetics	1992	44
Renal and skin involvement in a patient with complete Kearns‐Sayre syndrome Kazuhiro Mori, Kouji Narahara, Shinsuke Ninomiya, American Journal of Medical Genetics	1991	40
Vastus lateralis cytochrome oxidase activity and its relationship to maximal oxygen consumption in man Frank W. Booth, Kouji Narahara Pflügers Archiv - European Journal of Physiology BiologyBiochemistryCytochrome Oxidase ActivityNatural SciencesHeme Homeostasis	1974	38
Interstitial deletion of the long arm of chromosome 2: A case report and review of the literature Yukio Takahashi, Kouji Narahara, Kiyoshi Kikkawa, The Japanese Journal of Human Genetics ChromatinChromosome DynamicsCytogeneticsGenetic DisorderGenetics	1985	33

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