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- Journal Article
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- open access
Autozygome-guided exome-first study in a consanguineous cohort with early-onset retinal disease uncovers an isolated RIMS2 phenotype and a retina-enriched RIMS2 isoform
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- Journal Article
- A1
- open access
Combining a prioritization strategy and functional studies nominates 5'UTR variants underlying inherited retinal disease
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A systematic approach to characterize the contribution of 5'UTR variation to inherited retinal disease
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- Conference Paper
- C3
- open access
Whole genome sequencing delineates novel non-coding variants and candidate genes in inherited retinal diseases
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Unraveling the genetic basis of early-onset inherited retinal disease in a Saudi Arabian cohort reveals a novel RIMS2-related family
(2023) EUROPEAN JOURNAL OF HUMAN GENETICS. In European Journal of Human Genetics 31(Supplement 1). p.114-114 -
- Conference Paper
- C3
- open access
Whole genome sequencing sheds light on the dark matter of the genome in patients with inherited retinal diseases