The mechanistic role of alpha-synuclein in the nucleus: impaired nuclear function caused by familial Parkinson’s disease SNCA mutations is a research paper published in Human Molecular Genetics (2020). On theSindex it has a DataRank of 0. It has been cited 76 times.
Scored on demand from live citation data
DataRank reads this dataset's downstream impact straight off the citation graph — no black box, no proprietary weighting. How is this computed?
FAIR checklist signals are shown for context only and do not affect DataRank scoring.
We only score data papers we can read in full — never from an abstract alone.
National Institutes of Health
Grant: R01 NS085011
National Institute of Neurological Disorders and Stroke
Grant: R01 NS113548-01A1
NINDS NIH HHS
Grant: RF1 NS113548
National Institutes of Health
Grant: 1RF1NS113548-01A1
Lewy body neuropathologies and SNCA gene: variants expression and splicing
National Institutes of Health
Grant: 5R01NS085011-03
Lewy body neuropathologies and SNCA gene: variants expression and splicing
Fields of Study
MeSH Terms
Keywords