ArticleCell discovery2021
TMEM151A variants cause paroxysmal kinesigenic dyskinesia.
Erratum issuedOpen access · goldAbstract readLetter
In one paragraph
Article in Cell discovery, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 16 papers.
0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
4.7field-weighted citation impact, top 5% of its field
What it found
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
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Who cites it
16 citing papers in PubMed, 36 citations in OpenAlex.
- Functional Characterization and Pathogenicity Classification of PRRT2 Splice Variants in PRRT2-Related Disorders.Annals of clinical and translational neurology · 2025Article
- Pediatric Genetic Dystonias: Current Diagnostic Approaches and Treatment Options.Life (Basel, Switzerland) · 2025Review
- Paroxysmal Kinesigenic Dyskinesia: Genetics and Pathophysiological Mechanisms.Neuroscience bulletin · 2024Review
- A new genetic diagnosis strategy for paroxysmal kinesigenic dyskinesia: Targeted high-throughput detection of PRRT2 gene c.649 locus.Molecular genetics & genomic medicine · 2024Article
- Identification of a de novo CACNA1B variant and a start-loss ADRA2B variant in paroxysmal kinesigenic dyskinesia.Heliyon · 2024Article
- An Electroencephalography Profile of Paroxysmal Kinesigenic Dyskinesia.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2024Article
- Genetic and phenotypic analyses of PRRT2 positive and negative paroxysmal kinesigenic dyskinesia.Therapeutic advances in neurological disorders · 2024Article
- TMEM151A variants associated with paroxysmal kinesigenic dyskinesia.Human genetics · 2023Article
- Translating Genetic Discovery into a Mechanistic Understanding of Pediatric Movement Disorders: Lessons from Genetic Dystonias and Related Disorders.Advanced genetics (Hoboken, N.J.) · 2023Article
- Two Cases ofMovement disorders clinical practice · 2023Article
- Genetic Links to Episodic Movement Disorders: Current Insights.The application of clinical genetics · 2023Review
- Aberrant Neuregulin 1/ErbB Signaling in Charcot-Marie-Tooth Type 4D Disease.Molecular and cellular biology · 2022Article
- De Novo Mutation in TMEM151A and Paroxysmal Kinesigenic Dyskinesia.Movement disorders : official journal of the Movement Disorder Society · 2022Article
- Paroxysmal Kinesigenic Dyskinesia Caused by 16p11.2 Microdeletion and Related Clinical Features.Neurology. Genetics · 2022Article
- Screening of theFrontiers in neurology · 2022Article
- Author Correction: TMEM151A variants cause paroxysmal kinesigenic dyskinesia.Cell discovery · 2021Article
Corrections and comments
- Erratum issued
Authors and funding
11 authors at 6 institutions in 1 country.
Hong-Fu Li *Department of Neurology and Research Center of Neurology in Second Affiliated Hospital, Zhejiang University School of Medicine, and Key Laboratory of Medical Neurobiology of Zhejiang Province, Hangzhou, Zhejiang, China.
Yu-Lan Chen *Department of Neurology and Research Center of Neurology in Second Affiliated Hospital, Zhejiang University School of Medicine, and Key Laboratory of Medical Neurobiology of Zhejiang Province, Hangzhou, Zhejiang, China.
Ling Zhuang *Institute of Neuroscience and State Key Laboratory of Neuroscience, CAS Center for Excellence in Brain Science and Intelligence Technology, Chinese Academy of Sciences, Shanghai, China.
Dian-Fu ChenDepartment of Neurology and Research Center of Neurology in Second Affiliated Hospital, Zhejiang University School of Medicine, and Key Laboratory of Medical Neurobiology of Zhejiang Province, Hangzhou, Zhejiang, China.
Hua-Zhen KeDepartment of Neurology and Research Center of Neurology in Second Affiliated Hospital, Zhejiang University School of Medicine, and Key Laboratory of Medical Neurobiology of Zhejiang Province, Hangzhou, Zhejiang, China.
Wen-Jiao LuoDepartment of Neurology and Research Center of Neurology in Second Affiliated Hospital, Zhejiang University School of Medicine, and Key Laboratory of Medical Neurobiology of Zhejiang Province, Hangzhou, Zhejiang, China.
Gong-Lu LiuDepartment of Neurology, Huashan Hospital, Shanghai Medical College, Fudan University, Shanghai, China.
Sheng-Nan WuLaboratory for Molecular Diagnostics, Shanghai Children's Hospital, Shanghai Jiao Tong University, Shanghai, China.
Wen-Hao ZhouDepartment of Neonatology, Children's Hospital, Fudan University, Shanghai, China.
Zhi-Qi XiongInstitute of Neuroscience and State Key Laboratory of Neuroscience, CAS Center for Excellence in Brain Science and Intelligence Technology, Chinese Academy of Sciences, Shanghai, China. xiongzhiqi@ion.ac.cn.
Zhi-Ying WuDepartment of Neurology and Research Center of Neurology in Second Affiliated Hospital, Zhejiang University School of Medicine, and Key Laboratory of Medical Neurobiology of Zhejiang Province, Hangzhou, Zhejiang, China. zhiyingwu@zju.edu.cn.ORCID http://orcid.org/0000-0003-2106-572X
Second Affiliated Hospital of Zhejiang University · CNCenter for Excellence in Brain Science and Intelligence Technology · CNChildren's Hospital of Fudan University · CNChinese Academy of Sciences · CNFudan University · CNShanghai Jiao Tong University · CN
Funding
National Natural Science Foundation of China (National Science Foundation of China) 81330025National Natural Science Foundation of China (National Science Foundation of China) 81500973Zhejiang University (ZJU) 188020-193810101/089
Abstract
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