Ning Wang
Shihezi University(CN)Qingdao University(CN)Hebei Medical University(CN)Fujian Medical University(CN)Johns Hopkins University(US)Harbin Medical University(CN)Northeast Agricultural University(CN)Chinese University of Hong Kong(HK)Dalian Medical University(CN)Chinese Academy of Sciences(CN)Johns Hopkins Medicine(US)University of Chicago(US)Second Hospital of Hebei Medical University(CN)Second Affiliated Hospital of Dalian Medical University(CN)Institute of Oceanology(CN)Huzhou Central Hospital(CN)Hebei Meteorological Bureau(CN)Second Affiliated Hospital of Zhengzhou University(CN)National Center for Chronic and Noncommunicable Disease Control and Prevention(CN)Affiliated Hospital of Qingdao University(CN)Zhejiang Hospital(CN)First Affiliated Hospital of Fujian Medical University(CN)Hebei University of Chinese Medicine(CN)Shanghai First People's Hospital(CN)First Affiliated Hospital of Shihezi University Medical College(CN)Education Department of Heilongjiang Province(CN)Affiliated Hospital of Hebei University(CN)Ministry of Agriculture and Rural Affairs(CN)Qilu Hospital of Shandong University(CN)Hebei Science and Technology Department(CN)University of Hong Kong(HK)
Publications by Year
Research Areas
Genetic Neurodegenerative Diseases, Mitochondrial Function and Pathology, Muscle Physiology and Disorders, Neurogenetic and Muscular Disorders Research, Hereditary Neurological Disorders
Most-Cited Works
- → Mitochondrial Aβ: a potential focal point for neuronal metabolic dysfunction in Alzheimer's disease(2005)731 cited
- → Exome sequencing identifies truncating mutations in PRRT2 that cause paroxysmal kinesigenic dyskinesia(2011)477 cited
- → Biallelic Mutations in MYORG Cause Autosomal Recessive Primary Familial Brain Calcification(2018)154 cited
- → Decreased levels of serum brain-derived neurotrophic factor in drug-naïve first-episode schizophrenia: relationship to clinical phenotypes(2009)135 cited
- → Molecular analysis of 51 unrelated pedigrees with late-onset multiple acyl-CoA dehydrogenation deficiency (MADD) in southern China confirmed the most common ETFDH mutation and high carrier frequency of c.250G>A(2011)98 cited
- → TAT-mediated delivery of neuroglobin protects against focal cerebral ischemia in mice(2010)78 cited