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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
Hoon‐Chul Kang
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569
Publications
9,013
Citation Statements Received
14,354
Citation Statements Given
How they've been cited
10,119
421
8,531
61
How they cite others
15,722
935
13,242
177
Affiliations
Yonsei University
,
Severance Hospital
Publications
Order By: Most citations
Optimal clinical management of children receiving dietary therapies for epilepsy: Updated recommendations of the International Ketogenic Diet Study Group
Kossoff
1
,
Zupec‐Kania
2
,
Auvin
3
et al.
2018
Epilepsia Open
Abstract
Show
788
14
1,249
3
Get access via publisher
Add to collection
Cite
Brain somatic mutations in MTOR cause focal cortical dysplasia type II leading to intractable epilepsy
Lim
1
,
Kim
2
,
Kang
3
et al.
2015
Nat Med
Abstract
Show
568
27
520
2
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Add to collection
Cite
Early‐ and Late‐onset Complications of the Ketogenic Diet for Intractable Epilepsy
Kang
1
,
Chung
2
,
Kim
3
et al.
2004
Epilepsia
Abstract
Show
397
16
339
4
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Add to collection
Cite
Microfluidic device with brain extracellular matrix promotes structural and functional maturation of human brain organoids
Cho
1
,
Jin
2
,
An
3
et al.
2021
Nat Commun
Abstract
Show
424
3
357
0
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Add to collection
Cite
Precise detection of low-level somatic mutation in resected epilepsy brain tissue
Sim
1
,
Ko
2
,
Kim
3
et al.
2019
Acta Neuropathol
153
4
206
2
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Add to collection
Cite
Efficacy of the classic ketogenic and the modified Atkins diets in refractory childhood epilepsy
Kim
1
,
Yoon
2
,
Lee
3
et al.
2015
Epilepsia
Abstract
Show
189
13
187
2
Get access via publisher
Add to collection
Cite
Somatic Mutations in TSC1 and TSC2 Cause Focal Cortical Dysplasia
Lim
1
,
Gopalappa
2
,
Kim
3
et al.
2017
The American Journal of Human Genetics
Abstract
Show
219
14
189
0
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Cite
Frequent SLC35A2 brain mosaicism in mild malformation of cortical development with oligodendroglial hyperplasia in epilepsy (MOGHE)
Bonduelle
1
,
Hartlieb
2
,
Baldassari
3
et al.
2021
acta neuropathol commun
Abstract
Show
143
14
189
0
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Add to collection
Cite
1
2
3