Kinya Ishikawa - Concepedia

Author

Kinya Ishikawa

Tokyo Medical and Dental University ORCID

Also Known As

Elisabetta Indelicato, Ishikawa Kinya, Ishikawa, K., K Ishikawa, K. Ishikawa, KINYA ISHIKAWA, KYOZO ISHIKAWA, Kenji Nakashima, Kinya ISHIKAWA, Kinya Ishikawa

235

Publications

5.2K

Citations

H-Index

149

Concepts

All Affiliations

Tokyo Medical and Dental University National Center of Neurology and Psychiatry The University of Tokyo Niigata University University of Tsukuba

About

Kinya Ishikawa is an author at Tokyo Medical and Dental University specializing in medicine, neurology, and neuroscience.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	27	45	2.5K
2	Natural Sciences	10	10	609
3	Health Sciences	7	7	342
4	Engineering	5	5	85
5	Public Health	2	2	45

Kinya Ishikawa

Publications

4.9K

Citations

H-Index

Page 1

	Year	Citations
Spinocerebellar Ataxia Type 31 Is Associated with “Inserted” Penta-Nucleotide Repeats Containing (TGGAA)n Nozomu Sato, Takeshi Amino, Kazuhiro Kobayashi, The American Journal of Human Genetics Neurodegenerative DiseasesMolecular NeuroscienceNeurological DisorderNeuroanatomyGenetics	2009	291
Inhibition of microbial growth by ajoene, a sulfur-containing compound derived from garlic Rie Naganawa, Nami Iwata, Kinya Ishikawa, Applied and Environmental Microbiology Microbial GrowthSulfur-containing CompoundDisulfide BondAntibioticsBiochemistry	1996	191
Efficacy and safety of leuprorelin in patients with spinal and bulbar muscular atrophy (JASMITT study): a multicentre, randomised, double-blind, placebo-controlled trial Masahisa Katsuno, Haruhiko Banno, Keisuke Suzuki, The Lancet Neurology Jasmitt StudyClinical InjuryNeurological DisorderClinical TrialsPlacebo-controlled Trial	2010	187
Spinocerebellar ataxia type 6 knockin mice develop a progressive neuronal dysfunction with age-dependent accumulation of mutant Ca <sub>V</sub> 2.1 channels Kei Watase, Curtis F. Barrett, Taisuke Miyazaki, Proceedings of the National Academy of Sciences	2008	166
Japanese Families with Autosomal Dominant Pure Cerebellar Ataxia Map to Chromosome 19p13.1-p13.2 and Are Strongly Associated with Mild CAG Expansions in the Spinocerebellar Ataxia Type 6 Gene in Chromosome 19p13.1 Kinya Ishikawa, Hajime Tanaka, Masaaki Saito, The American Journal of Human Genetics Mendelian DisorderGenetic DisorderGeneticsJapanese FamiliesMild Cag Expansions	1997	150
Quantitation of amyloid beta-protein (A beta) in the cortex during aging and in Alzheimer's disease. Hiromasa Funato, Masahiro Yoshimura, Kaoru Kusui, PubMed	1998	146
Regulatory Role of RNA Chaperone TDP-43 for RNA Misfolding and Repeat-Associated Translation in SCA31 Taro Ishiguro, Nozomu Sato, Morio Ueyama, Neuron Rna Chaperone Tdp-43Regulatory RoleNatural SciencesRna BiologyMolecular Biology	2017	133
An Autosomal Dominant Cerebellar Ataxia Linked to Chromosome 16q22.1 Is Associated with a Single-Nucleotide Substitution in the 5′ Untranslated Region of the Gene Encoding a Protein with Spectrin Repeat and Rho Guanine-Nucleotide Exchange-Factor Domains Kinya Ishikawa, Shuta Toru, Taiji Tsunemi, The American Journal of Human Genetics Neurodegenerative DiseasesNeurobiology Of DiseaseMendelian DisorderGenetic DisorderSpectrin Repeat	2005	128
Bi-allelic CSF1R Mutations Cause Skeletal Dysplasia of Dysosteosclerosis-Pyle Disease Spectrum and Degenerative Encephalopathy with Brain Malformation Long Guo, Débora Romeo Bertola, Asako Takanohashi, The American Journal of Human Genetics Neurodegenerative DiseasesMendelian DisorderDysosteosclerosis-pyle Disease SpectrumBrain MalformationGenetics	2019	125
Spinocerebellar Ataxia Type 6 Mutation Alters P-type Calcium Channel Function Shuta Toru, Takayuki Murakoshi, Kinya Ishikawa, Journal of Biological Chemistry	2000	119

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