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About the database ScholarIQanswers from OpenAlex & ORCID
How has Syuan‐Yu Hong's publication output changed over time?
ScholarIQpublication output · 2018–2023
Output grew50% over the shown period — from 2 works in 2018 to 3 in 2023.
2
2
1
3
3
20182019202020212023
What are the most-cited papers on Syuan‐Yu Hong?
ScholarIQmost cited works
A Wide Spectrum of Genetic Disorders Causing Severe Childhood Epilepsy in Taiwan: A Case Series of Ultrarare Genetic Cause and Novel Mutation Analysis in a Pilot Study
Syuan‐Yu Hong, Jiann‐Jou Yang, Shuan‐Yow Li, Inn‐Chi Lee
Journal of Personalized Medicine. 202027 CitationsOPEN ACCESS
Epilepsy and Neurodevelopmental Outcomes in Children With Etiologically Diagnosed Central Nervous System Infections: A Retrospective Cohort Study
Chien‐Heng Lin, Wei‐De Lin, I‐Ching Chou, Inn‐Chi Lee, Syuan‐Yu Hong
Frontiers in Neurology. 201924 CitationsOPEN ACCESS
Genetic Testing in Children with Developmental and Epileptic Encephalopathies: A Review of Advances in Epilepsy Genomics
Yu‐Tzu Chang, Syuan‐Yu Hong, Wei‐De Lin, Chien‐Heng Lin, Sheng‐Shing Lin, Fuu‐Jen Tsai, I‐Ching Chou
Children. 202322 CitationsOPEN ACCESS
Heterogeneous neurodevelopmental disorders in children with Kawasaki disease: what is new today?
Chien‐Heng Lin, Wei‐De Lin, I‐Ching Chou, Inn‐Chi Lee, Syuan‐Yu Hong
BMC Pediatrics. 201921 CitationsOPEN ACCESS
NAXE gene mutation-related progressive encephalopathy
Li-Wei Chiu, Sheng‐Shing Lin, Chieh‐Ho Chen, Chien‐Heng Lin, Ni‐Chung Lee, Syuan‐Yu Hong, I‐Ching Chou, Chien-Lin Lin, Pei‐Yu Yang
Medicine. 202120 CitationsOPEN ACCESS
Related on ScholarIQ
China Medical University
Institution
A Wide Spectrum of Genetic Disorders Causing Severe Childhood Epilepsy in Taiwan: A Case Series of Ultrarare Genetic Cause and Novel Mutation Analysis in a Pilot Study
Paper
Epilepsy and Neurodevelopmental Outcomes in Children With Etiologically Diagnosed Central Nervous System Infections: A Retrospective Cohort Study
Paper
Genetic Testing in Children with Developmental and Epileptic Encephalopathies: A Review of Advances in Epilepsy Genomics
Paper
Heterogeneous neurodevelopmental disorders in children with Kawasaki disease: what is new today?
Paper
NAXE gene mutation-related progressive encephalopathy
Paper