Yanyan Peng

Mutations in SLC25A46, encoding a UGO1-like protein, cause an optic atrophy spectrum disorder

Alexander J. Abrams, Robert B. Hufnagel, Adriana Rebelo et al. · Nature Genetics · 2015 · 200 citations · Full text

Somatic Variant, Mendelian Disorder, Genetic Disorder +7

A deafness-associated tRNA^Hismutation alters the mitochondrial function, ROS production and membrane potential

Shasha Gong, Yanyan Peng, Pingping Jiang et al. · Nucleic Acids Research · 2014 · 113 citations · Full text

Mitochondrial Trnahis Mutation, Genetics, Molecular Biology +20

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, Xiaofen Jin, Yanyan Peng et al. · Human Molecular Genetics · 2015 · 103 citations · Full text

Loss of SLC25A46 causes neurodegeneration by affecting mitochondrial dynamics and energy production in mice

Zhuo Li, Yanyan Peng, Robert B. Hufnagel et al. · Human Molecular Genetics · 2017 · 59 citations · Full text

Mitophagy, Cell Death, Mitochondrial Fission +16

A Hypertension-Associated tRNA^Ala Mutation Alters tRNA Metabolism and Mitochondrial Function

Pingping Jiang, Meng Wang, Ling Xue et al. · Molecular and Cellular Biology · 2016 · 58 citations · Full text

→ G Mutation, Genetics, Molecular Biology +16