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Features
Assistant
AI grounded in research
Search
Full-text citation search
Collections
Organize and monitor papers
All Features →
Integrations
MCP
Connect AI agents to Scite
API
Programmatic data access
Holdings
Full-text via your library
Zotero Plugin
Citation data in Zotero
Browser Extension
Citation badges anywhere
All Integrations →
Data
Rankings
Pricing
Log In
Start Free Trial
Akinori Miyashita
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190
Publications
7,200
Citation Statements Received
5,450
Citation Statements Given
How they've been cited
7,563
356
6,795
49
How they cite others
5,968
377
5,026
47
Affiliations
Niigata University
,
University of Toronto
Publications
Order By: Most citations
Human and mouse single-nucleus transcriptomics reveal TREM2-dependent and TREM2-independent cellular responses in Alzheimer’s disease
Zhou
1
,
Song
2
,
Andhey
3
et al.
2020
Nat Med
Abstract
Show
1,354
110
1,388
12
2
Get access via publisher
Add to collection
Cite
FUS Phase Separation Is Modulated by a Molecular Chaperone and Methylation of Arginine Cation-π Interactions
Qamar
1
,
Randle
2
,
Ruggeri
3
et al.
2018
Cell
Abstract
Show
1,035
51
1,031
2
Get access via publisher
Add to collection
Cite
ALS/FTD Mutation-Induced Phase Transition of FUS Liquid Droplets and Reversible Hydrogels into Irreversible Hydrogels Impairs RNP Granule Function
Murakami
1
,
Qamar
2
,
Lin
3
et al.
2015
Neuron
Abstract
Show
977
28
1,010
3
Get access via publisher
Add to collection
Cite
Association of HTRA1 Mutations and Familial Ischemic Cerebral Small-Vessel Disease
Hara
1
,
Shiga
2
,
Fukutake
3
et al.
2009
N Engl J Med
Abstract
Show
489
12
483
1
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Cite
SORL1 Is Genetically Associated with Late-Onset Alzheimer’s Disease in Japanese, Koreans and Caucasians
Miyashita
1
,
Koike
2
,
Jun
3
et al.
2013
PLoS ONE
Abstract
Show
222
8
177
5
1
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Add to collection
Cite
Ethnic and trans-ethnic genome-wide association studies identify new loci influencing Japanese Alzheimer’s disease risk
Shigemizu
1
,
Mitsumori
2
,
Akiyama
3
et al.
2021
Transl Psychiatry
Abstract
Show
96
7
145
1
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Cite
Neuroblastoma amplified sequence gene is associated with a novel short stature syndrome characterised by optic nerve atrophy and Pelger–Huët anomaly
Максимова
1
,
Hara
2
,
Nikolaeva
3
et al.
2010
J Med Genet
Abstract
Show
107
4
135
0
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Cite
AlzPathway: a comprehensive map of signaling pathways of Alzheimer’s disease
Mizuno
1
,
Iijima
2
,
Ogishima
3
et al.
2012
BMC Syst Biol
Abstract
Show
164
1
134
0
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Add to collection
Cite
1
2
3
4
5
6