Publications by authors named "Han-I Lin"

Claim this Profile
I
Intraarterial microbubble delivery enhances focused ultrasound induced blood brain barrier opening in the murine substantia nigra.
Hsun Li, Yung-Han Lee, Xiao Zen, Mei-Wei Huang, Chia-Wei Liu, Han-I Lin, Chin-Hsien Lin

Sci Rep· November 2025

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
C
Compound heterozygous TMEM67 biallelic variants including a novel frameshift mutation in two Filipino adolescent siblings with Joubert syndrome.
Khloe L Kruzette Solijon, Roi O Engkong, Barbra Charina V Cavan, Leslee Y Ong, Yi-Hsuan Chen, Han-I Lin, Chin-Hsien Lin

J Neural Transm (Vienna)· May 2025

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
L
Low Efficiency of Homology-Independent Targeted Integration for CRISPR/Cas9 Correction in the Vicinity of the c.919-2A>G Variant.
Chang-Han Ho, Cheng-Yu Tsai, Chi-Chieh Chang, Chin-Ju Hu, Cheng-Yen Huang, Pei-Hsuan Lin, Chin-Hsien Lin, Han-I Lin

Int J Mol Sci· May 2025

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
R
Recognizing familial Huntington's disease in an Asian cohort: Insights from the Philippines.
Jao Jarro B Garcia, Gilbert J Cabataña, Iris Ditan, Karl Josef Niño J Separa, Ida Ingrid Rocha-Tulagan, Han-I Lin, Chin-Hsien Lin

eNeurologicalSci· March 2025

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
P
Phenotypic Heterogeneity in Patients with Mutations in the Mitochondrial Complex I Assembly Gene NDUFAF5.
Pin-Shiuan Chen, Ni-Chung Lee, Chieh-Ju Sung, Ya-Wen Liu, Wen-Chin Weng, Han-I Lin, Chin-Hsien Lin

Mov Disord· December 2023

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
C
Clinical Characteristics, Genetic Features, and Long-Term Outcome of Wilson's Disease in a Taiwanese Population: An 11-Year Follow-Up Study.
Sung-Pin Fan, Yih-Chih Kuo, Ni-Chung Lee, Yin-Hsiu Chien, Wuh-Liang Hwu, Han-I Lin, Huey-Ling Chen, Chin-Hsien Lin

J Mov Disord· May 2023

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
A
A novel C19orf12 frameshift mutation in a MPAN pedigree impairs mitochondrial function and connectivity leading to neurodegeneration.
Huan-Yun Chen, Han-I Lin, Chia-Lang Hsu, Pei-Lung Chen, Cheng-Yen Huang, Chin-Hsien Lin

Parkinsonism Relat Disord· April 2023

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
G
Genetic analysis of IMPDH2 gene in Taiwanese patients with isolated or combined dystonia.
Pin-Shiuan Chen, Meng-Chen Wu, Chun-Hwei Tai, Yung-Yee Chang, Min-Yu Lan, Han-I Lin, Chin-Hsien Lin

Parkinsonism Relat Disord· February 2023

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
G
Generation of a human induced pluripotent stem cell line NTUHi002-A from a patient with aceruloplasminemia harboring a homozygous splicing mutation c.607+1 delG in CP gene.
Chih-Hsin Ou-Yang, Han-I Lin, Chin-Hsien Lin

Stem Cell Res· August 2022

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
C
Craniocervical dystonia with levodopa-responsive parkinsonism co-segregating with a pathogenic ANO3 mutation in a Taiwanese family.
Ming-Che Kuo, Han-I Lin, Chin-Hsien Lin

Parkinsonism Relat Disord· May 2019

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
R
Reprogramming of a human induced pluripotent stem cell (iPSC) line (IBMSi012-A) from an early-onset Parkinson's disease patient harboring a homozygous p.D331Y mutation in the PLA2G6 gene.
Yu-Che Cheng, Han-I Lin, Shih-Han Syu, Huai-En Lu, Ching-Ying Huang, Chin-Hsien Lin

Stem Cell Res· May 2019

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
G
Generation of induced pluripotent stem cells (IBMSi011-A) from a patient with Parkinson's disease carrying LRRK2 p.I1371V mutation.
Han-I Lin, Yu-Che Cheng, Hui-Wen Ko, Cheng-Hao Wen, Huai-En Lu, Chin-Hsien Lin

Stem Cell Res· May 2019

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
P
PDE8B mutation is not associated with Parkinson's disease in a Taiwanese population.
Tian-Sin Fan, Ruey-Meei Wu, Han-I Lin, Chieh Cheng, Chin-Hsien Lin

Neurobiol Aging· November 2018

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
C
Catechol-O-methyltransferase (COMT) genetic variants are associated with cognitive decline in patients with Parkinson's disease.
Chin-Hsien Lin, Jun-Yu Fan, Han-I Lin, Chia-Wen Chang, Yih-Ru Wu

Parkinsonism Relat Disord· May 2018

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
G
Generation of 2 induced pluripotent stem cell lines derived from patients with Parkinson's disease carrying LRRK2 G2385R variant.
Yu-Che Cheng, Ching-Ying Huang, Ming-Ching Ho, Yu-Hung Hsu, Shih-Han Syu, Han-I Lin, Chin-Hsien Lin

Stem Cell Res· April 2018

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
G
Generation of induced pluripotent stem cells from a patient with Parkinson's disease carrying LRRK2 p.I2012T mutation.
Chin-Hsien Lin, Yu-Che Cheng, Han-I Lin, Ming-Ching Ho, Yu-Hung Hsu

Stem Cell Res· December 2017

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
D
Depression and Catechol-O-methyltransferase (COMT) genetic variants are associated with pain in Parkinson's disease.
Chin-Hsien Lin, K Ray Chaudhuri, Jun-Yu Fan, Chia-I Ko, Alexandra Rizos, Han-I Lin

Sci Rep· July 2017

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
L
Lack of RAB39B mutations in early-onset and familial Parkinson's disease in a Taiwanese cohort.
Hsien-Han Lin, Ruey-Meei Wu, Han-I Lin, Meng-Ling Chen, Chun-Hwei Tai, Chin-Hsien Lin

Neurobiol Aging· February 2017

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
A
A limb-girdle myopathy phenotype of RUNX2 mutation in a patient with cleidocranial dysplasia: a case study and literature review.
Sung-Ju Hsueh, Ni-Chung Lee, Shu-Hua Yang, Han-I Lin, Chin-Hsien Lin

BMC Neurol· January 2017

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
L
Lovastatin protects neurite degeneration in LRRK2-G2019S parkinsonism through activating the Akt/Nrf pathway and inhibiting GSK3β activity.
Chin-Hsien Lin, Han-I Lin, Meng-Ling Chen, Tzu-Ting Lai, Li-Ping Cao

Hum Mol Genet· May 2016

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
V
Vitamin D receptor genetic variants and Parkinson's disease in a Taiwanese population.
Chin-Hsien Lin, Kai-Hsiang Chen, Meng-Ling Chen, Han-I Lin, Ruey-Meei Wu

Neurobiol Aging· May 2014

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
L
Lack of c9orf72 repeat expansion in taiwanese patients with mixed neurodegenerative disorders.
Chin-Hsien Lin, Ta-Fu Chen, Ming-Jang Chiu, Han-I Lin, Ruey-Meei Wu

Front Neurol· May 2014

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
T
The p.L302P mutation in the lysosomal enzyme gene SMPD1 is a risk factor for Parkinson disease.
Ruey-Meei Wu, Chin-Hsien Lin, Han-I Lin

Neurology· January 2014

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis