Hongying Ma

Gain-of-Function Mutations in SCN11A Cause Familial Episodic Pain

X ZHANG, Jingmin Wen, Wei Yang et al. · The American Journal of Human Genetics · 2013 · 189 citations · Full text

Pain Disorders, Health Sciences, Genetic Disorder +7

Excision repair cross complementation group 1 polymorphisms and lung cancer risk: a meta-analysis.

Chao Cao, Yanmei Zhang, Ran Wang et al. · PubMed · 2011 · 25 citations

Discovery of pyrazolones as novel carboxylesterase 2 inhibitors that potently inhibit the adipogenesis in cells

Xing‐Kai Qian, Jing Zhang, Pei‐Fang Song et al. · Bioorganic & Medicinal Chemistry · 2021 · 20 citations · Full text

Biochemistry, Medicine, Rational Drug Design +6

The Origin of a Coastal Indigenous Horse Breed in China Revealed by Genome-Wide SNP Data

Hongying Ma, Sheng Wang, Guorong Zeng et al. · Genes · 2019 · 17 citations · Full text

A <i><scp>PRRT</scp>2</i> variant in a Chinese family with paroxysmal kinesigenic dyskinesia and benign familial infantile seizures results in loss of interaction with <i><scp>STX</scp>1B</i>

Hongying Ma, Shenglei Feng, Xuejun Deng et al. · Epilepsia · 2018 · 12 citations · Full text