Sheng Yao

Long-read sequencing identified repeat expansions in the 5′UTR of the <i>NOTCH2NLC</i> gene from Chinese patients with neuronal intranuclear inclusion disease

Jianwen Deng, Muliang Gu, Yu Miao et al. · Journal of Medical Genetics · 2019 · 143 citations

Life Sciences, Genetics, Molecular Genetics +17

Impact of primary kidney disease on the effects of empagliflozin in patients with chronic kidney disease: secondary analyses of the EMPA-KIDNEY trial

PK Judge, Natalie Staplin, KJ Mayne et al. · The Lancet Diabetes & Endocrinology · 2023 · 108 citations · Full text

Medicine, Nephrology, Pharmacotherapy +11

Effects of empagliflozin on progression of chronic kidney disease: a prespecified secondary analysis from the empa-kidney trial

Natalie Staplin, Richard Haynes, PK Judge et al. · The Lancet Diabetes & Endocrinology · 2023 · 90 citations · Full text

Medicine, Pharmacology, Pharmacotherapy +14

Repeat expansion scanning of the <i>NOTCH2NLC</i> gene in patients with multiple system atrophy

Fang Pu, Yanyan Yu, Sheng Yao et al. · Annals of Clinical and Translational Neurology · 2020 · 85 citations · Full text

Life Sciences, Genetics, Neurology +17

Genetic origin of sporadic cases and RNA toxicity in neuronal intranuclear inclusion disease

Jianwen Deng, Binbin Zhou, Jiaxi Yu et al. · Journal of Medical Genetics · 2021 · 60 citations

Life Sciences, Genetics, Molecular Genetics +15