Rare de novo gain-of-function missense variants in DOT1L are associated with developmental delay and congenital anomalies is a research paper published in The American Journal of Human Genetics (2023). On theSindex it has a DataRank of 0.396. It has been cited 13 times.
Scored on demand from live citation data
Linked data & code
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
0.396
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 →National Institute for Health Research (NIHR)
Grant: NIHR203308
National Institute of Neurological Disorders and Stroke
Grant: R24 OD022005
National Institute of Neurological Disorders and Stroke
Grant: R24 OD031447
NINDS NIH HHS
Grant: U54 NS093793
Baylor College of Medicine
Grant: P50HD103555
Canadian Institutes of Health Research
Grant: PJT-178315
NICHD NIH HHS
Grant: P50 HD103525
Canadian Institutes of Health Research
Grant: unidentified
unidentified
Texas Children's Hospital
Baylor College of Medicine
Eunice Kennedy Shriver National Institute of Child Health and Human Development
Huffington Foundation
FWCI
1.28
Citation Percentile
0.8%
Citation Trend
Fields of Study
MeSH Terms
Keywords
Sustainable Development Goals