Ran Mo

Statistics

Publications

Citations

124

H-Index

Active since

2020

Affiliations

Peking University First Hospital(Current)

Peking University

Nanjing Medical University

Beijing Children’s Hospital

Capital Medical University

Ran Mo is an author at Peking University First Hospital specializing in mutation analysis, sterol regulatory element-binding proteins, and inherited endocrine syndromes.

ORCID

Publications per year

2020–2025

Publications

Mutations in SREBF1, Encoding Sterol Regulatory Element Binding Transcription Factor 1, Cause Autosomal-Dominant IFAP Syndrome

Huijun Wang, Aytaj Humbatova, Yuanxiang Liu et al. · The American Journal of Human Genetics · 2020 · 61 citations · Full text

Life Sciences, Genetics, Molecular Genetics +9

Empagliflozin-Pretreated MSC-Derived Exosomes Enhance Angiogenesis and Wound Healing via PTEN/AKT/VEGF Pathway

Zihao Bai, Yan Qiu, Yanqing Zhu et al. · International Journal of Nanomedicine · 2025 · 22 citations · Full text

Medicine, Cell Biology, Molecular Medicine +17

Somatic frameshift mutation in PIK3CA causes CLOVES syndrome by provoking PI3K/AKT/mTOR pathway

Wei Yan, Bin Zhang, Huijun Wang et al. · Hereditas · 2021 · 17 citations · Full text

Medicine, Dermatology, Molecular Genetics +17

Investigation of Nagashima‐type palmoplantar keratoderma in China: A cross‐sectional study of 234 patients

Juan Liu, Zhiming Chen, Linghan Hu et al. · The Journal of Dermatology · 2022 · 13 citations

Medicine, Dermatology, Genetics +12

<scp>KRT5</scp> mutation regulate melanin metabolism through notch signalling pathway between keratinocytes and melanocytes

Weixue Jia, Yuanyuan Zhang, Xue Wang et al. · Experimental Dermatology · 2023 · 11 citations

Life Sciences, Dermatology, Genetics +14

1–5 of 5