Ya Wang

ORCID

Publication Activity (10 Years)

Years Active: 2022-2024
Publications (10 Years): 7

Top Venues

Journal of human genetics

Orphanet journal of rare diseases

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

Publications

Xiaojie Yin, Qiyu Dong, Shuanglong Fan, Lina Yang, Hao Li, Yijun Jin, Mahlatsi Refiloe Laurentinah, Xiandan Chen, Aliaksei Sysa, Hezhi Fang, Jianxin Lyu, Yong-Guo Yu, Ya Wang
A novel pathogenic mitochondrial DNA variant m.4344T>C in tRNA Gln causes developmental delay. Journal of human genetics 69 (8) (2024)
Qiyu Dong, Xiaojie Yin, Shuanglong Fan, Sheng Zhong, Wenxin Yang, Keer Chen, Qian Wang, Xue Ma, Refiloe Laurentinah Mahlatsi, Yanling Yang, Jianxin Lyu, Hezhi Fang, Ya Wang
IARS2 mutations lead to Leigh syndrome with a combined oxidative phosphorylation deficiency. Orphanet journal of rare diseases 19 (1) (2024)
Qiyu Dong, Xiaojie Yin, Shuanglong Fan, Sheng Zhong, Wenxin Yang, Keer Chen, Qian Wang, Xue Ma, Refiloe Laurentinah Mahlatsi, Yanling Yang, Jianxin Lyu, Hezhi Fang, Ya Wang
IARS2 mutations lead to Leigh syndrome with a combined oxidative phosphorylation deficiency. Orphanet journal of rare diseases 19 (1) (2024)
Xiaojie Yin, Qiyu Dong, Shuanglong Fan, Lina Yang, Hao Li, Yijun Jin, Mahlatsi Refiloe Laurentinah, Xiandan Chen, Aliaksei Sysa, Hezhi Fang, Jianxin Lyu, Yong-Guo Yu, Ya Wang
A novel pathogenic mitochondrial DNA variant m.4344T>C in tRNA Gln causes developmental delay. Journal of human genetics (2024)
Xiaojie Yin, Qiyu Dong, Shuanglong Fan, Lina Yang, Hao Li, Yijun Jin, Mahlatsi Refiloe Laurentinah, Xiandan Chen, Aliaksei Sysa, Hezhi Fang, Jianxin Lyu, Yong-Guo Yu, Ya Wang
A novel pathogenic mitochondrial DNA variant m.4344T>C in tRNA Gln causes developmental delay. Journal of human genetics 69 (8) (2024)
Qiyu Dong, Xiaojie Yin, Shuanglong Fan, Sheng Zhong, Wenxin Yang, Keer Chen, Qian Wang, Xue Ma, Refiloe Laurentinah Mahlatsi, Yanling Yang, Jianxin Lyu, Hezhi Fang, Ya Wang
IARS2 mutations lead to Leigh syndrome with a combined oxidative phosphorylation deficiency. Orphanet journal of rare diseases 19 (1) (2024)
Xiyue Zhou, Xiaoting Lou, Yuwei Zhou, Yaojun Xie, Xinyu Han, Qiyu Dong, Xiaojie Ying, Mahlatsi Refiloe Laurentinah, Luyi Zhang, Zhehui Chen, Dongxiao Li, Hezhi Fang, Jianxin Lyu, Yanling Yang, Ya Wang
Novel biallelic mutations in TMEM126B cause splicing defects and lead to Leigh-like syndrome with severe complex I deficiency. Journal of human genetics (2022)

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Publication Activity (10 Years)

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Ya Wang