Yunting Lin

ORCID

Publication Activity (10 Years)

Years Active: 2019-2024
Publications (10 Years): 11

Top Venues

Metabolic brain disease

Clinical genetics

Calcified tissue international

Journal of clinical research in pediatric endocrinology

Central South University (PHD)

This page only lists publications with an associated author ORCID identifier.

Education History

Central South University Sep 01 2010 - Jun 02 2015

China

PHD :: The State Key Laboratory of Medical Genetics & School of Life Sciences

Central South University Sep 01 2006 - Jun 25 2010

China

BSC :: School of biological science and technology (renamed as School of Life Sciences)

Publications

Taolin Li, Yonglan Huang, Chunyan Tao, Xi Yin, Xueying Su, Yongxian Shao, Cuili Liang, Minyan Jiang, Yanna Cai, Yunting Lin, Chunhua Zeng, Xiaoyuan Zhao, Li Liu, Wen Zhang
Biochemical and molecular analysis of pediatric patients with metachromatic leukodystrophy in South China: functional characterization of five novel ARSA variants. Metabolic brain disease 39 (5) (2024)
Taolin Li, Yonglan Huang, Chunyan Tao, Xi Yin, Xueying Su, Yongxian Shao, Cuili Liang, Minyan Jiang, Yanna Cai, Yunting Lin, Chunhua Zeng, Xiaoyuan Zhao, Li Liu, Wen Zhang
Biochemical and molecular analysis of pediatric patients with metachromatic leukodystrophy in South China: functional characterization of five novel ARSA variants. Metabolic brain disease (2024)
Taolin Li, Yonglan Huang, Chunyan Tao, Xi Yin, Xueying Su, Yongxian Shao, Cuili Liang, Minyan Jiang, Yanna Cai, Yunting Lin, Chunhua Zeng, Xiaoyuan Zhao, Li Liu, Wen Zhang
Biochemical and molecular analysis of pediatric patients with metachromatic leukodystrophy in South China: functional characterization of five novel ARSA variants. Metabolic brain disease 39 (5) (2024)
Zhikun Lu, Wen Zhang, Xiaojian Mao, Duan Li, Xiaodan Chen, Li Liu, Yunting Lin
The third case of Marbach-Rustad progeroid syndrome caused by a de novo LEMD2 variant. Clinical genetics (2023)
Jian Ma, Ye Zhang, Xiaoxiao Ding, Zhijiang Liang, Chaoxiang Yang, Zhi Deng, Hui He, Zhihong Guan, Chunhua Zeng, Yunting Lin, Xianqiong Luo
Co-occurrence of Spondyloepiphyseal Dysplasia and X-Linked Hypophosphatemia in a Three-Generation Chinese Family. Calcified tissue international (2023)
Yunting Lin, Wen Zhang, Duan Li, Xiaodan Chen, Zhikun Lu, Xiaojing Li, Xiuzhen Li
The first Chinese case of Siddiqi syndrome caused by a homozygous FITM2 variant. Clinical genetics 102 (3) (2022)
Yunting Lin, Wen Zhang, Xinjiang Huang, Ling Su, Yanna Cai, Cuili Liang, Min Rao, Li Liu, Chunhua Zeng
Two De Novo Mosaic Variants Within the Same Site of PHEX Gene in a Girl with X-Linked Hypophosphatemic Rickets. Calcified tissue international (2021)
Yunting Lin, Chunhua Zeng, Xiaodan Chen, Taolin Li, Huazhen Liu, Hongsheng Liu, Hao Hu, Li Liu
Chinese family with Blau syndrome: Mutated NOD2 allele transmitted from the father with de novo somatic and germ line mosaicism. The Journal of dermatology 47 (11) (2020)
Aijing Xu, Yunting Lin, Huiying Sheng, Jing Cheng, Huifen Mei, Tzer Hwu Ting, Chunhua Zeng, Cuili Liang, Wen Zhang, Cuiling Li, Xiuzhen Li, Li Liu
Molecular diagnosis of maturity-onset diabetes of the young in a cohort of Chinese children. Pediatric diabetes 21 (3) (2020)
Aijing Xu, Jing Cheng, Huiying Sheng, Zhe Wen, Yunting Lin, Zhihong Zhou, Chunhua Zeng, Yongxian Shao, Cuiling Li, Xiuzhen Li
Clinical Management and Gene Mutation Analysis of Children with Congenital Hyperinsulinism in South China Journal of clinical research in pediatric endocrinology 11 (4) (2019)
Yunting Lin, Chunhua Zeng, Zhikun Lu, Ruizhu Lin, Li Liu
A novel homozygous splice-site variant of NCAPD2 gene identified in two siblings with primary microcephaly: The second case report. Clinical genetics 96 (1) (2019)

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Publication Activity (10 Years)

Top Topics

Top Venues

Yunting Lin