T

Taosheng Huang

The Centre for Health (New Zealand)

ORCID: 0000-0001-6601-6687

190 papers and 7.8k citations.

PubIndex Score97Top 3%How it's scored

190Publications

7.8kTotal Citations

First publication: 1997First senior author: 2003

Top publicationsby citations

Biparental Inheritance of Mitochondrial DNA in Humans

Shiyu Luo, Taosheng Huang, C. Alexander Valencia et al.|Proceedings of the National Academy of Sciences|2018

Cited by 451

Different <i>TBX5</i> interactions in heart and limb defined by Holt–Oram syndrome mutations

Craig T. Basson, Christine E. Seidman, Mitsuhiro Kamisago et al.|Proceedings of the National Academy of Sciences|1999

Cited by 365

A deafness-associated tRNA<sup>His</sup>mutation alters the mitochondrial function, ROS production and membrane potential

Shasha Gong, Min‐Xin Guan, Huawei Li et al.|Nucleic Acids Research|2014

Cited by 114

The exome sequencing identified the mutation in YARS2 encoding the mitochondrial tyrosyl-tRNA synthetase as a nuclear modifier for the phenotypic manifestation of Leber's hereditary optic neuropathy-associated mitochondrial DNA mutation

Pingping Jiang, Min‐Xin Guan, Xiaoling Liu et al.|Human Molecular Genetics|2015

Cited by 103

PRICKLE3 linked to ATPase biogenesis manifested Leber’s hereditary optic neuropathy

Jialing Yu, Min‐Xin Guan, Xiaoyang Liang et al.|Journal of Clinical Investigation|2020

Cited by 63

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