Dominant NARS1 mutations causing axonal Charcot–Marie–Tooth disease expand NARS1-associated diseases is a research paper published in Brain Communications (2024). On theSindex it has a DataRank of 0. It has been cited 18 times.
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Michigan Pre-doctoral Training Program in Genetics
Grant: GM007544
National Institute of Neurological Diseases and Stroke
Grant: NS108510
National Institute of General Medical Sciences
Grant: GM136441
National Institutes of Health
Grant: R24NS098523
National Institutes of Health
Grant: R37NS054154
National Institutes of Health
Grant: 5U54NS065712
National Institutes of Health
Grant: 5R01NS105755
European Union's Horizon 2020
Grant: 779257
Solving the unsolved Rare Diseases
National Institutes of Health
Grant: 1R01NS105755-01A1
Genomic Studies in Charcot-Marie-Tooth Disease
National Institutes of Health
Grant: 1U54NS065712-01
training
National Institutes of Health
Grant: 3R37NS054154-14S1
The Genetics of the Neuromuscular Junction: Mechanisms and Disease Models
FWCI
3.62
Citation Percentile
0.9%
Citation Trend
Fields of Study
Keywords
Sustainable Development Goals
Additional file 1 of Experience of the first adult-focussed undiagnosed disease program in Australia (AHA-UDP): solving rare and puzzling genetic disorders is ageless
Additional file 1 of Experience of the first adult-focussed undiagnosed disease program in Australia (AHA-UDP): solving rare and puzzling genetic disorders is ageless
Additional file 3 of Experience of the first adult-focussed undiagnosed disease program in Australia (AHA-UDP): solving rare and puzzling genetic disorders is ageless
Additional file 2 of Experience of the first adult-focussed undiagnosed disease program in Australia (AHA-UDP): solving rare and puzzling genetic disorders is ageless
Additional file 3 of Experience of the first adult-focussed undiagnosed disease program in Australia (AHA-UDP): solving rare and puzzling genetic disorders is ageless
Additional file 2 of Experience of the first adult-focussed undiagnosed disease program in Australia (AHA-UDP): solving rare and puzzling genetic disorders is ageless