Identification of Deep-Intronic Splice Mutations in a Large Cohort of Patients With Inherited Retinal Diseases is a research paper published in Frontiers in Genetics (2021). On theSindex it has a DataRank of 0. It has been cited 69 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.
National Eye Institute
Grant: EY022356
National Eye Institute
Grant: EY018571
National Eye Institute
Grant: EY002520
NEI NIH HHS
Grant: R01 EY022356
NEI NIH HHS
Grant: R01 EY018571
NEI NIH HHS
Grant: P30 EY002520
NEI NIH HHS
Grant: R01 EY009076
NIH HHS
Grant: S10 OD023469
National Institutes of Health
Grant: 5R01EY018571-03
Genetics of Early Onset Retinal Diseases
National Institutes of Health
Grant: 1S10OD023469-01
High Throughput Genomic Sequencer at BCM Core Facility
National Institutes of Health
Grant: 5P30EY002520-40
P30 - Core Grant for Vision Research
National Institutes of Health
Grant: 5R01EY022356-07
Molecular Basis of Human Visual System Disorders
National Institutes of Health
Grant: 2R01EY009076-21
MEASURES OF HUMAN RECEPTOR AND POST RECEPTOR ACTIVITY
FWCI
9.07
Citation Percentile
1.0%
Citation Trend
Fields of Study
Keywords
Sustainable Development Goals
Additional file 2 of Combining a prioritization strategy and functional studies nominates 5’UTR variants underlying inherited retinal disease
Additional file 2 of Combining a prioritization strategy and functional studies nominates 5’UTR variants underlying inherited retinal disease
Additional file 3 of Combining a prioritization strategy and functional studies nominates 5’UTR variants underlying inherited retinal disease
Additional file 3 of Combining a prioritization strategy and functional studies nominates 5’UTR variants underlying inherited retinal disease
Additional file 1 of Combining a prioritization strategy and functional studies nominates 5’UTR variants underlying inherited retinal disease
Additional file 1 of Combining a prioritization strategy and functional studies nominates 5’UTR variants underlying inherited retinal disease
Additional file 6 of Intronic position +9 and −9 are potentially splicing sites boundary from intronic variants analysis of whole exome sequencing data
Additional file 6 of Intronic position +9 and −9 are potentially splicing sites boundary from intronic variants analysis of whole exome sequencing data
Additional file 2 of Intronic position +9 and −9 are potentially splicing sites boundary from intronic variants analysis of whole exome sequencing data
Additional file 5 of Intronic position +9 and −9 are potentially splicing sites boundary from intronic variants analysis of whole exome sequencing data
Additional file 1 of Intronic position +9 and −9 are potentially splicing sites boundary from intronic variants analysis of whole exome sequencing data
Additional file 1 of Intronic position +9 and −9 are potentially splicing sites boundary from intronic variants analysis of whole exome sequencing data
Additional file 4 of Intronic position +9 and −9 are potentially splicing sites boundary from intronic variants analysis of whole exome sequencing data
Additional file 4 of Intronic position +9 and −9 are potentially splicing sites boundary from intronic variants analysis of whole exome sequencing data
Additional file 2 of Intronic position +9 and −9 are potentially splicing sites boundary from intronic variants analysis of whole exome sequencing data
Additional file 5 of Intronic position +9 and −9 are potentially splicing sites boundary from intronic variants analysis of whole exome sequencing data
Additional file 3 of Intronic position +9 and −9 are potentially splicing sites boundary from intronic variants analysis of whole exome sequencing data
Additional file 3 of Intronic position +9 and −9 are potentially splicing sites boundary from intronic variants analysis of whole exome sequencing data