CHCHD10 mutations induce tissue-specific mitochondrial DNA deletions with a distinct signature is a research paper published in Human Molecular Genetics (2023). On theSindex it has a DataRank of 0. It has been cited 6 times.
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NIHR Cambridge Biomedical Research Centre
Grant: BRC-1215-20014
Alzheimer’s Society Project
Grant: AS-PG-18b-022
MRC research
Grant: MR/S035699/1
Mechanisms of oxygen toxicity in the context of mitochondrial dysfunction
Leverhulme Trust
Grant: RPG-2018-408
Medical Research Council
Grant: MR/S005021/1
MRC Strategic Award to establish an International Centre for Genomic Medicine in Neuromuscular Diseases
Medical Research Council Mitochondrial Biology Unit
Grant: MC_UU_00028/7
Mitochondrial genomics in human health and diseases. (How variation in nuclear and mitochondrial DNA causes rare mitochondrial diseases and common late-onset human disorders)
Wellcome Collaborative Award
Grant: 224486/Z/21/Z
Wellcome Principal Research Fellow
Grant: 212219/Z/18/Z
National Institute for Health Research (NIHR)
Grant: NIHR205088
Alzheimer's Society
Grant: 022
Wellcome Trust
Grant: 226653/Z/22/Z
Wellcome Trust
Grant: 224486
Cryptic single-cell mitochondrial DNA mutations in human brain aging and neurodegeneration
Wellcome Trust
Grant: 212219
Nuclear genomic control of mitochondrial DNA heteroplasmy in humans: population genetics & disease
NINDS
NIH
National Institute for Health Research (NIHR)
FWCI
0.65
Citation Percentile
0.7%
Citation Trend
Fields of Study
MeSH Terms
Keywords
Sustainable Development Goals