Dominant‐negative variant in SLC1A4 causes an autosomal dominant epilepsy syndrome is a research paper published in Annals of Clinical and Translational Neurology (2023). On theSindex it has a DataRank of 0.241. It has been cited 4 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.
Base Score Contribution
0.241
From this paper's citation signal
Citation Network Contribution
0
Citation network not refreshed for this result
This paper's DataRank is currently driven only by its base citation score. Citation network data was not refreshed for this result.
Learn more about DataRank methodology →Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung
Grant: 31003A_156376
National Institutes of Health
Grant: 1U01HG010233
National Institutes of Health
Grant: 1DP5OD029630
National Human Genome Research Institute
Grant: UM1 HG006493
NIH HHS
Grant: DP5 OD029630
NHGRI NIH HHS
Grant: U01 HG007703
NINDS NIH HHS
Grant: U01 NS134356
NINDS NIH HHS
Grant: U01 NS134355
NHGRI NIH HHS
Grant: U01 HG010233
National Institutes of Health
Grant: 5R01HG000130-02
ETHICAL ISSUES ARISING FROM THE HUMAN GENOME PROJECT
National Institutes of Health
Grant: 3UM1HG006493-07S2
UW Center for Mendelian Genomics
Swiss National Science Foundation
Grant: 156376
Elucidating the role of human zinc transporters in health and disease
National Institutes of Health
Grant: 1DP5OD029630-01
Investigating the contribution of non-coding genetic variation to rare disorders
National Institutes of Health
Grant: 3U01HG010233-04S1
Pacific Northwest Undiagnosed Diseases Network Clinical Site
Burroughs Wellcome Fund
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