Hiroto Fujigasaki - Concepedia

Author

Hiroto Fujigasaki

Tokyo Medical and Dental University

Also Known As

Benjamin Frishberg, H Fujigasaki, H. Fujigasaki, HIROTO FUJIGASAKI, Hiroto Fujigasaki, Hiroto Fuｊigasaki, S Tsuji

Publications

4.3K

Citations

H-Index

Concepts

All Affiliations

Tokyo Medical and Dental University Jikei University School of Medicine Inserm Tokyo Metropolitan Institute of Medical Science Tokyo Metropolitan Neurological Hospital

About

Hiroto Fujigasaki is an author at Tokyo Medical and Dental University specializing in medicine, neurology, and neurodegenerative diseases.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	15	18	1.2K
2	Social Sciences	4	4	200
3	Natural Sciences	2	2	172
4	Public Health	1	1	18
5	Allergy	1	1	34

Hiroto Fujigasaki

Publications

Citations

H-Index

Page 1

	Year	Citations
Rivaroxaban or aspirin for patent foramen ovale and embolic stroke of undetermined source: a prespecified subgroup analysis from the NAVIGATE ESUS trial Scott E. Kasner, Balakumar Swaminathan, Pablo M. Lavados, The Lancet Neurology	2018	177
CAG repeat expansion in the TATA box-binding protein gene causes autosomal dominant cerebellar ataxia Hiroto Fujigasaki Brain Neurodegenerative DiseasesMendelian DisorderExpanded RepeatExpanded PolyglutamineNeurological Disorder	2001	164
Neuronal intranuclear inclusions in spinocerebellar ataxia type 2: triple-labeling immunofluorescent study Shigeru Koyano, Toshiki Uchihara, Hiroto Fujigasaki, Neuroscience Letters Triple-labeling Immunofluorescent StudyNeuronal Intranuclear InclusionsNeuroanatomyMedicineExperimental Neuropathology	1999	128
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
Spinocerebellar Ataxia Type 6 Mutation Alters P-type Calcium Channel Function Shuta Toru, Takayuki Murakoshi, Kinya Ishikawa, Journal of Biological Chemistry	2000	119
SCA12 is a rare locus for autosomal dominant cerebellar ataxia: A study of an Indian family Hiroto Fujigasaki, Ishwar C. Verma, A. Camuzat, Annals of Neurology	2001	103
Ataxin-3 Is Translocated into the Nucleus for the Formation of Intranuclear Inclusions in Normal and Machado–Joseph Disease Brains Hiroto Fujigasaki, Toshiki Uchihara, Shigeru Koyano, Experimental Neurology Neurodegenerative DiseasesMachado–joseph Disease BrainsNeurobiology Of DiseaseCellular NeurobiologyNeuroanatomy	2000	98
A clinical and genetic study in a large cohort of patients with spinocerebellar ataxia type 6 Hiroki Takahashi, Kinya Ishikawa, Takeshi Tsutsumi, Journal of Human Genetics Mendelian DisorderNeurological DisorderGenetic DisorderSpinocerebellar AtaxiaGenetic Epidemiology	2004	95
SUMOylation attenuates the aggregation propensity and cellular toxicity of the polyglutamine expanded ataxin-7 Alexandre Janer, Andreas Werner, Junko Takahashi‐Fujigasaki, Human Molecular Genetics Molecular BiologyCytoskeletonAggregation PropensityToxicological MechanismCellular Toxicity	2009	92
Non-expanded polyglutamine proteins in intranuclear inclusions of hereditary ataxias – triple-labeling immunofluorescence study Toshiki Uchihara, Hiroto Fujigasaki, Shigeru Koyano, Acta Neuropathologica Neurodegenerative DiseasesAutoimmune DiseaseMolecular BiologyDegenerative DiseaseAutoimmunity	2001	89

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