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John Suk

University of California, San Diego

23

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96

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Deciphering the genetic architecture and ethnographic distribution of IRD in three ethnic populations by whole genome sequence analysis.

2021 PLOS Genetics
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HTRA1 is increased in Bruch's membrane/choroid in a mouse model of L-ORD

2019 Investigative Ophthalmology & Visual Science
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Identification of the genetic determinants responsible for retinal degeneration in families of Mexican descent

2018 Ophthalmic Genetics
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Whole Genome Sequencing Revealed Mutations in Two Independent Genes as the Underlying Cause of Retinal Degeneration in an Ashkenazi Jewish Pedigree

2017 Genes
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Correction: Gustafson et al., Whole Genome Sequencing Revealed Mutations in Two Independent Genes as the Underlying Cause of Retinal Degeneration in an Ashkenazi Jewish Pedigree. Genes 2017, 8, 210

2017 Genes
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Genetic analysis of 10 pedigrees with inherited retinal degeneration by exome sequencing and phenotype-genotype association

2017 Physiological Genomics
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Whole genome sequencing revealed mutations in two independent genes as the underlying cause of retinal degeneration (RD) in an Ashkenazi Jewish Pedigree

2017 Investigative Ophthalmology & Visual Science
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Identification of a novel frame-shift deletion in the CHM gene in a consanguineous family.

2016 Investigative Ophthalmology & Visual Science
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Establishing the involvement of the novel gene AGBL5 in retinitis pigmentosa by whole genome sequencing

2016 Physiological Genomics
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Zebrafish and Mouse Models with Mutations in the Novel Gene ASRGL1 Develop Retinal Degeneration (RD) Recapitulating the Human Phenotype.

2016 Investigative Ophthalmology & Visual Science
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