ArticleBrain : a journal of neurology2016
High prevalence of CHCHD10 mutation in patients with frontotemporal dementia from China.
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In one paragraph
Article in Brain : a journal of neurology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.
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29citing papers in PubMed
4.7field-weighted citation impact, top 5% of its field
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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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Who cites it
29 citing papers in PubMed, 43 citations in OpenAlex.
- CHCHD2 and CHCHD10 promoted autophagic clearance of protein aggregates via GABARAPs.Autophagy · 2026Article
- Frontotemporal dementia associated CHCHD10Cell death & disease · 2026Article
- Concurrent nanotherapeutics and regulatory updates for the management of amyotrophic lateral sclerosis: a focused review for orphan drug (Tofersen).Orphanet journal of rare diseases · 2025Review
- SLP2/PHB Aggregates in ALS Mouse Models and Patients: Implications BeyondInternational journal of molecular sciences · 2025Article
- Gaps in biomedical research in frontotemporal dementia: A call for diversity and disparities focused research.Alzheimer's & dementia : the journal of the Alzheimer's Association · 2024Review
- Genetic spectrum features and diagnostic accuracy of four plasma biomarkers in 248 Chinese patients with frontotemporal dementia.Alzheimer's & dementia : the journal of the Alzheimer's Association · 2024Article
- A scoping review of the unique landscape and challenges associated with dementia in the Western Pacific region.The Lancet regional health. Western Pacific · 2024Article
- Disruption of Mitophagy Flux through the PARL-PINK1 Pathway by CHCHD10 Mutations or CHCHD10 Depletion.Cells · 2023Article
- Review
- C9orf72 expansions are the most common cause of genetic frontotemporal dementia in a Southeast Asian cohort.Annals of clinical and translational neurology · 2023Article
- Neurodegeneration-associated mitochondrial proteins, CHCHD2 and CHCHD10-what distinguishes the two?Frontiers in cell and developmental biology · 2022Review
- Amyotrophic Lateral Sclerosis: Molecular Mechanisms, Biomarkers, and Therapeutic Strategies.Antioxidants (Basel, Switzerland) · 2021Review
- Early death of ALS-linked CHCHD10-R15L transgenic mice with central nervous system, skeletal muscle, and cardiac pathology.iScience · 2021Article
- The Frequency of Genetic Mutations Associated With Behavioral Variant Frontotemporal Dementia in Chinese Han Patients.Frontiers in aging neuroscience · 2021Article
- Neuroimaging in genetic frontotemporal dementia and amyotrophic lateral sclerosis.Neurobiology of disease · 2020Review
- Intricacies of aetiology in intrafamilial degenerative disease.Brain communications · 2020Review
- Respiration Enhances TDP-43 Toxicity, but TDP-43 Retains Some Toxicity in the Absence of Respiration.Journal of molecular biology · 2019Article
- Recent advances in the genetics of frontotemporal dementia.Current genetic medicine reports · 2019Article
- A novel CHCHD10 mutation implicates a Mia40-dependent mitochondrial import deficit in ALS.EMBO molecular medicine · 2018Article
- Loss of CHCHD10-CHCHD2 complexes required for respiration underlies the pathogenicity of a CHCHD10 mutation in ALS.Human molecular genetics · 2018Article
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Authors and funding
9 authors at 4 institutions in 1 country.
Bin Jiao1 Department of Neurology, Xiangya Hospital, Central South University, Changsha 410008, China.
Tingting Xiao1 Department of Neurology, Xiangya Hospital, Central South University, Changsha 410008, China.
Lihua Hou1 Department of Neurology, Xiangya Hospital, Central South University, Changsha 410008, China.
Xiaohua Gu2 Department of Neurology, Brain Centre, Neurological Institute, Northern Jiangsu Province Hospital, Yangzhou 225001, China.
Yafang Zhou1 Department of Neurology, Xiangya Hospital, Central South University, Changsha 410008, China 3 Key Laboratory of Hunan Province in Neurodegenerative Disorders, Central South University, Changsha 410008, China.
Lin Zhou1 Department of Neurology, Xiangya Hospital, Central South University, Changsha 410008, China 3 Key Laboratory of Hunan Province in Neurodegenerative Disorders, Central South University, Changsha 410008, China.
Beisha Tang1 Department of Neurology, Xiangya Hospital, Central South University, Changsha 410008, China 3 Key Laboratory of Hunan Province in Neurodegenerative Disorders, Central South University, Changsha 410008, China 4 State Key Laboratory of Medical Genetics, Changsha 410008, China.
Jun Xu2 Department of Neurology, Brain Centre, Neurological Institute, Northern Jiangsu Province Hospital, Yangzhou 225001, China 5 Jiangsu Key Laboratory of Integrated Traditional Chinese and Western Medicine for Prevention and Treatment of Senile Diseases, School of Medicine, Yangzhou University, Yangzhou, 225001, China shenlu2505@126.com neurojun@126.com.
Lu Shen1 Department of Neurology, Xiangya Hospital, Central South University, Changsha 410008, China 3 Key Laboratory of Hunan Province in Neurodegenerative Disorders, Central South University, Changsha 410008, China 4 State Key Laboratory of Medical Genetics, Changsha 410008, China shenlu2505@126.com neurojun@126.com.
Central South University · CNXiangya Hospital Central South University · CNJiangsu Province Hospital · CNNorthern Jiangsu People's Hospital · CN
Funding
Medical Research Council G1002570
Abstract
PubMed holds no abstract for this paper.
Indexed as
Amyotrophic Lateral SclerosisDNA, MitochondrialFemaleFrontotemporal DementiaHumansMaleMitochondriaMitochondrial DiseasesMitochondrial ProteinsDNA, MitochondrialMitochondrial Proteins
Identifiers
What OpenQuestion holds
Textmetadata
Read underepoch 390
Registered trials
None linked
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.