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Hui Lin · SciRah

Researcher profile · Semantic Scholar

Hui Lin

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Hui Lin — researcher profile on SciRah

h-index: 11
Works: 25
Citations: 365

Most-cited papers

A deletion mutation in the βA1/A3 crystallin gene (CRYBA1/A3) is associated with autosomal dominant congenital nuclear cataract in a Chinese family
Yanhua Qi, Hong-yan Jia, Shang-zhi Huang, Hui Lin +7 more
2003Human Genetics74 citations
Semantic Scholar
Mutation analysis of 73 southern Chinese Wilson's disease patients: identification of 10 novel mutations and its clinical correlation
Li-Hua Wang, Ye-Qing Huang, Xuan Shang, Quan-Xi Su +6 more
2011Journal of Human Genetics49 citations
Semantic Scholar
A substitution of arginine to lysine at the COOH-terminus of MIP caused a different binocular phenotype in a congenital cataract family.
Hui Lin, J. Hejtmancik, Yanhua Qi
2007Molecular Vision42 citations
Semantic Scholar
Autosomal-Dominant Cerulean Cataract in a Chinese Family Associated with Gene Conversion Mutation in Beta-B2-Crystallin
Li Wang, Hui Lin, Jing-zhi Gu, Hong Su +2 more
2009Ophthalmic Research25 citations
Semantic Scholar
Macular corneal dystrophy in a Chinese family related with novel mutations of CHST6
X. Dang, Qing-Guo Zhu, Li Wang, Hong Su +7 more
2009Molecular Vision20 citations
Semantic Scholar
Exome sequencing in multiplex families with left-sided cardiac defects has high yield for disease gene discovery
David M. Gordon, D. Cunningham, Gloria A Zender, Patrick J. Lawrence +14 more
2022PLoS Genetics19 citations Open access
Semantic Scholar
An atypical phenotype of Reis-Bücklers corneal dystrophy caused by the G623D mutation in TGFBI
Dandan Li, Yanhua Qi, Li Wang, Hui Lin +2 more
2008Molecular Vision19 citations
Semantic Scholar
The Arg233Lys AQP0 Mutation Disturbs Aquaporin0-Calmodulin Interaction Causing Polymorphic Congenital Cataract
Shanshan Hu, Bin-Bin Wang, Yanhua Qi, Hui Lin
2012PLoS ONE18 citations Open access
Semantic Scholar
A Novel MIP Gene Mutation Analysis in a Chinese Family Affected with Congenital Progressive Punctate Cataract
Xuchen Ding, Nan Zhou, Hui Lin, Jian-Jun Chen +4 more
2014PLoS ONE17 citations Open access
Semantic Scholar
A new congenital nuclear cataract caused by a missense mutation in the gammaD-crystallin gene (CRYGD) in a Chinese family.
Jing-zhi Gu, Yanhua Qi, Li Wang, Jin Wang +5 more
2005Molecular Vision16 citations
Semantic Scholar
A novel mutation I522N within the TGFBI gene caused lattice corneal dystrophy I
Chunmei Zhang, Guang Zeng, Hui Lin, Dandan Li +3 more
2009Molecular Vision13 citations
Semantic Scholar
A novel PITX2 mutation in a Chinese family with Axenfeld-Rieger syndrome
Dandan Li, Qing-Guo Zhu, Hui Lin, Nan Zhou +1 more
2008Molecular Vision11 citations
Semantic Scholar
A new locus for inherited nuclear cataract mapped to the long arm of chromosome 1.
Li Wang, Hui Lin, Yan-Wei Shen, Shang-zhi Huang +3 more
2007Molecular Vision10 citations
Semantic Scholar
[Autosomal dominant congenital nuclear cataract caused by a deletion mutation in the beta A1-crystallin gene].
Yan-hua Qi, Hong-yan Jia, Shang-zhi Huang, Hui Lin +4 more
2003Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics8 citations
Semantic Scholar
[Analysis of TGFBI gene mutation in a Chinese family with atypical Reis-Buckler corneal dystrophy].
Dandan Li, Yan-hua Qi, Qing Han, Hui Lin +2 more
2009Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics5 citations
Semantic Scholar
Two novel FBN1 mutations associated with ectopia lentis and marfanoid habitus in two Chinese families
Liming Zhao, Ting Liang, Jianzhen Xu, Hui Lin +2 more
2009Molecular Vision4 citations
Semantic Scholar
[A research on TGFBI gene mutations in Chinese families with corneal dystrophies].
Yan-hua Qi, Hong-Dan He, Y. Li, Hui Lin +3 more
2006Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics4 citations
Semantic Scholar
Pre-Implantation Genetic Testing for Aneuploidy on a Semiconductor Based Next-Generation Sequencing Platform.
Cheng-Ming Xu, Riqing Wei, Hui Lin, Leiyu Deng +9 more
2022Journal of Visualized Experiments3 citations
Semantic Scholar
[Autosomal dominant congenital golden crystal nuclear cataract caused by a missense mutation in gammaD crystallin gene (CRYGD) in a Chinese family].
Jing-zhi Gu, Yan-hua Qi, Hui Lin, Xiang Li +3 more
2006[Zhonghua yan ke za zhi] Chinese journal of ophthalmology3 citations
Semantic Scholar
[TGFBI gene mutation analysis in a Chinese family with Thiel-Behnke corneal dystrophy].
Yan-hua Qi, Hong-Dan He, Y. Li, Li Wang +4 more
2007[Zhonghua yan ke za zhi] Chinese journal of ophthalmology2 citations
Semantic Scholar
[Mutation analysis of FOXL2 in Chinese patients with blepharophimosis-ptosis-epicanthus inversus syndrome].
Yan-hua Qi, Y. Li, Hui Lin, Hong-yan Jia +4 more
2006[Zhonghua yan ke za zhi] Chinese journal of ophthalmology1 citations
Semantic Scholar
[Gene mapping of a pedigree with autosomal dominant congenital cataract].
Yan-hua Qi, Hong-yan Jia, Shang-zhi Huang, Hui Lin +4 more
2004[Zhonghua yan ke za zhi] Chinese journal of ophthalmology1 citations
Semantic Scholar
[A novel missense mutation in MIP gene resulted in polymorphic cataract].
Hui Lin, Li Wang, Nan Zhou, Hong Su +2 more
2008Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics0 citations
Semantic Scholar
Four Novel Mutations in FOXL2 Gene Are Detected in Chinese Patients With Blepharophimosis-Ptosis-Epicanthus Inversus Syndrome
Yanhua Qi, Hui Lin, Nan Zhou, Y. Li +2 more
20070 citations
Semantic Scholar
Mutation analysis of FOXL2 in Chinese patients with blepharophimosis-ptosis-epicanthus inversus syndrome
Yan-hua Qi, Y. Li, Hui Lin, Hong-yan Jia +4 more
20060 citations
Semantic Scholar

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Dandan Li — researcher profile on SciRah

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Y. Li — researcher profile on SciRah

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Liming Zhao — researcher profile on SciRah