Systematic assessment of the contribution of structural variants to inherited retinal diseases is a research paper published in Human Molecular Genetics (2023). On theSindex it has a DataRank of 0. It has been cited 10 times.
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National Eye Institute
Grant: EY022356
Fighting Blindness Canada
Grant: RG1302
NEI NIH HHS
Grant: R01 EY018571
Fighting Blindness Canada
Grant: RG9801
NEI NIH HHS
Grant: P30 EY002520
Fighting Blindness Canada
Grant: RG0202
Fighting Blindness Canada
Grant: RG1001
NIH HHS
Grant: S10 OD023469
National Eye Institute
Grant: EY09076
NEI NIH HHS
Grant: P30 EY010572
Fighting Blindness Canada
Grant: PR1901
NEI NIH HHS
Grant: R01 EY022356
NEI NIH HHS
Grant: R01 EY030499
Fighting Blindness Canada
Grant: RG0505
National Eye Institute
Grant: EY030499
Fighting Blindness Canada
Grant: SP2002
National Eye Institute
Grant: EY002520
National Eye Institute
Grant: EY018571
NEI NIH HHS
Grant: R01 EY009076
Fighting Blindness Canada
Grant: RG0802
National Institutes of Health
Grant: 5R01EY018571-03
Genetics of Early Onset Retinal Diseases
National Institutes of Health
Grant: 3P30EY010572-20S1
OPHTHALMOLOGY CORE FACILITY
National Institutes of Health
Grant: 1S10OD023469-01
High Throughput Genomic Sequencer at BCM Core Facility
National Institutes of Health
Grant: 5R01EY022356-07
Molecular Basis of Human Visual System Disorders
National Institutes of Health
Grant: 1R01EY030499-01
Antisense therapy for the treatment of visual loss in Usher syndrome
National Institutes of Health
Grant: 2R01EY009076-21
MEASURES OF HUMAN RECEPTOR AND POST RECEPTOR ACTIVITY
FWCI
2.41
Citation Percentile
0.9%
Citation Trend
Fields of Study
MeSH Terms
Keywords
Sustainable Development Goals