Ning Wang

3.9k citations

164 papers · 3.1k · h-index 24

Impact in

Cellular and Molecular Neuroscience top 2%
- Genetic Neurodegenerative Diseases
- Hereditary Neurological Disorders
Biological Psychiatry top 5%

Papers in

Cellular and Molecular Neuroscience 46
- Genetic Neurodegenerative Diseases 25
- Hereditary Neurological Disorders 16
Genetics 17
- Neurogenetic and Muscular Disorders Research 16

Co-authors: Zhi‐Ying Wu (23 shared papers)Wan‐Jin Chen (50 shared papers)Hong Wei Xu (1 shared paper)Guy M. McKhann (1 shared paper)Xi Chen (1 shared paper)David M. Stern (1 shared paper)Jun Yao (1 shared paper)Casper S. Caspersen (1 shared paper)
Journals: Annals of Clinical and Translational Neurology (8 papers)Frontiers in Neurology (6 papers)Brain (5 papers)Neurological Sciences (4 papers)CNS Neuroscience & Therapeutics (4 papers)
Partner nations: China United States Taiwan

In The Last Decade

Ning Wang

146 papers receiving 3.0k citations

Peers

Countries citing papers authored by Ning Wang

Since Specialization

Citations

This map shows the geographic impact of Ning Wang's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Ning Wang with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Ning Wang more than expected).

Fields of papers citing papers by Ning Wang

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Ning Wang. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Ning Wang. The network helps show where Ning Wang may publish in the future.

Co-authors

The 25 scholars most cited alongside Ning Wang, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Ning Wang Line = papers co-authored together Ning Wang links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

Showing the 20 most-cited of 164 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	Mitochondrial Aβ: a potential focal point for neuronal metabolic dysfunction in Alzheimer's disease The FASEB Journal ·Casper S. Caspersen, Ning Wang, Jun Yao, Alexander A. Sosunov, Xi Chen, Joyce W. Lustbader, Hong Wei Xu, David M. Stern	2005	659
2	Exome sequencing identifies truncating mutations in PRRT2 that cause paroxysmal kinesigenic dyskinesia Nature Genetics ·Wan‐Jin Chen, Yu Lin, Zhi‐Qi Xiong, Wei Wei, Ni Wang, Guohe Tan, Shunling Guo, Jin He	2011	391
3	Decreased levels of serum brain-derived neurotrophic factor in drug-naïve first-episode schizophrenia: relationship to clinical phenotypes Psychopharmacology ·Da Chun Chen, Jing Wang, Bo Wang, Sheng Chang Yang, Chong Xi Zhang, You Lan Zheng, Yan Li Li, Ning Wang	2009	132
4	Biallelic Mutations in MYORG Cause Autosomal Recessive Primary Familial Brain Calcification Neuron ·Xiang‐Ping Yao, Xuewen Cheng, Chong Wang, Miao Zhao, Hui‐Zhen Su, Lu‐Lu Lai, Xiaohuan Zou, Xuejiao Chen	2018	130
5	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 Journal of Molecular Medicine ·Zhiqiang Wang, Xuejiao Chen, Shen-Xing Murong, Ning Wang, Zhi‐Ying Wu	2011	74
6	TAT-mediated delivery of neuroglobin protects against focal cerebral ischemia in mice Experimental Neurology ·Bin Cai, Yi Lin, Xie-Hua Xue, Ling Fang, Ning Wang, Zhi‐Ying Wu	2010	71
7	Clinical spectrum and genetic landscape for hereditary spastic paraplegias in China Molecular Neurodegeneration ·En‐Lin Dong, Chong Wang, Shuang Wu, Ying‐Qian Lu, Xiao-Hong Lin, Hui‐Zhen Su, Miao Zhao, Ning Wang	2018	67
8	Clinical features and mutation spectrum in Chinese patients with CADASIL : A multicenter retrospective study CNS Neuroscience & Therapeutics ·Sheng Chen, Ni Wang, Xinzhen Yin, Hanqiu Liu, Cong Lu, Qiao‐Juan Zheng, Gui‐Xian Zhao, Yongfeng Xu	2017	50
9	A common SCN5A polymorphism attenuates a severe cardiac phenotype caused by a nonsense SCN5A mutation in a Chinese family with an inherited cardiac conduction defect Journal of Medical Genetics ·Dau-Ming Niu, H W Hwang, Ning Wang, J.-Y. Wu, Jen-Chung Chien, Ru‐Chi Shieh, Y.-T. Chen +2 others	2006	44
10	Loss of function of CMPK2 causes mitochondria deficiency and brain calcification Cell Discovery ·Miao Zhao, Hui‐Zhen Su, Yi‐Heng Zeng, Yuan Sun, Yun‐Lu Li, Chong Wang, Zhiyuan Zhao, Huang Xue-jing	2022	41
11	High frequency of Machado-Joseph disease identified in Southeastern Chinese kindreds with spinocerebellar ataxia BMC Medical Genetics ·Shi‐Rui Gan, Sheng-Sheng Shi, Ning Wang, Gui‐Xian Zhao, Sheng-Tong Weng, Shen-Xing Murong, Chuanzhen Lü, Zhi‐Ying Wu +1 other	2010	38
12	Spectrum of SLC20A2 , PDGFRB , PDGFB , and XPR1 mutations in a large cohort of patients with primary familial brain calcification Human Mutation ·Xiaohuan Zou, Chong Wang, Xiang‐Ping Yao, Hui‐Zhen Su, Lu‐Lu Lai, Hai‐Ting Chen, Jinghui Lai, Yao‐Bin Liu	2019	38
13	Serum Cytokines Th1, Th2, and Th17 Expression Profiling in Active Lupus Nephritis-IV: From a Southern Chinese Han Population Mediators of Inflammation ·Keshav Raj Sigdel, Lihua Duan, Yin Wang, Weiping Hu, Ning Wang, Qingyi Sun, 刘庆燕, Xiaocong Liu	2016	37
14	Stop-gain mutations in UBAP1 cause pure autosomal-dominant spastic paraplegia Brain ·Xiang Lin, Hui‐Zhen Su, En‐Lin Dong, Xiao-Hong Lin, Miao Zhao, Can Yang, Chong Wang, Jie Wang	2019	33
15	Population Genetics and New Insight into Range of CAG Repeats of Spinocerebellar Ataxia Type 3 in the Han Chinese Population PLoS ONE ·Shi‐Rui Gan, Ni Wang, Yi Dong, Ning Wang, Zhi‐Ying Wu	2015	29
16	Significant clinical heterogeneity with similar ETFDH genotype in three Chinese patients with late-onset multiple acyl-CoA dehydrogenase deficiency Neurological Sciences ·Hong‐Xia Fu, Xinyi Liu, Zhiqiang Wang, Ming Jin, Danni Wang, Junjie He, Min-Ting Lin, Ning Wang	2016	28
17	Genetic and Clinical Profile of Chinese Patients with Autosomal Dominant Spastic Paraplegia Molecular Diagnosis & Therapy ·Miao Zhao, Yijun Chen, Mengwen Wang, Xiao-Hong Lin, En‐Lin Dong, Wan‐Jin Chen, Ning Wang, Xiang Lin +1 other	2019	28
18	Natural genetic variation determines susceptibility to aggregation or toxicity in a C. elegansmodel for polyglutamine disease BMC Biology ·Tali Gidalevitz, Ning Wang, Tanuja Deravaj, Jasmine Alexander-Floyd, Richard I. Morimoto	2013	27
19	New Insights into Genotype-phenotype Correlations in Chinese Facioscapulohumeral Muscular Dystrophy Chinese Medical Journal ·Lin Feng, Zhiqiang Wang, Min-Ting Lin, Shen-Xing Murong, Ning Wang	2015	27
20	GGC Repeat Expansion of RILPL1 is Associated with Oculopharyngodistal Myopathy Annals of Neurology ·Yi‐Heng Zeng, Kang Yang, Ganqin Du, Yi‐Kun Chen, Chun‐Yan Cao, Yusen Qiu, Jin He, Haidong Lv	2022	27

About Ning Wang

Ning Wang is a scholar working on Cellular and Molecular Neuroscience, Genetics, Molecular Biology, Neurology and Clinical Biochemistry, having authored 164 papers that have together received 3.1k indexed citations. Recurring topics across this work include Genetic Neurodegenerative Diseases (25 papers), Muscle Physiology and Disorders (22 papers), Hereditary Neurological Disorders (16 papers), Neurogenetic and Muscular Disorders Research (16 papers), Mitochondrial Function and Pathology (9 papers), Metabolism and Genetic Disorders (8 papers), RNA Research and Splicing (7 papers) and RNA modifications and cancer (6 papers). The work is most often cited by research in Cellular and Molecular Neuroscience (788 citations), Biological Psychiatry (94 citations), Clinical Biochemistry (225 citations), Neurology (248 citations) and Neurology (409 citations). Ning Wang has collaborated with scholars based in China, United States and Taiwan. Frequent co-authors include Zhi‐Ying Wu, Wan‐Jin Chen, Hong Wei Xu, Guy M. McKhann, Xi Chen, David M. Stern, Jun Yao, Casper S. Caspersen, Alexander A. Sosunov and Shi Du Yan. Their work appears in journals such as Annals of Clinical and Translational Neurology, Frontiers in Neurology, Brain, Neurological Sciences and CNS Neuroscience & Therapeutics.

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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