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Anand Swaroop
Researcher at National Institutes of Health
Publications - 528
Citations - 53580
Anand Swaroop is an academic researcher from National Institutes of Health. The author has contributed to research in topics: Retinitis pigmentosa & Retinal degeneration. The author has an hindex of 89, co-authored 508 publications receiving 43170 citations. Previous affiliations of Anand Swaroop include Vision-Sciences, Inc. & Yale University.
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Journal ArticleDOI
A New 2–Base Pair Deletion in the RPGR Gene in a Black Family With X-Linked Retinitis Pigmentosa
TL;DR: A 2-base pair deletion in exon 13 of the RPGR gene that creates a frameshift was found to segregate with the retinal disease in affected males and the carrier state in female heterozygotes in this family.
Journal ArticleDOI
Integration of genomics and transcriptomics predicts diabetic retinopathy susceptibility genes
Andrew D Skol,Segun Jung,Ana Marija Sokovic,Siquan Chen,Sarah Fazal,Olukayode A. Sosina,Olukayode A. Sosina,Poulami P Borkar,Amy Y. Lin,Maria Sverdlov,Dingcai Cao,Anand Swaroop,Ionut Bebu,Dcct,Barbara E. Stranger,Michael A. Grassi +15 more
TL;DR: Estimation of genetic association with gene expression implicated FLCN as a disease gene for diabetic retinopathy and Mendelian randomization confirmed a direct positive effect of increased F LCN expression on Retinopathy.
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Nonsyndromic Early-Onset Cone-Rod Dystrophy and Limb-Girdle Muscular Dystrophy in a Consanguineous Israeli Family are Caused by Two Independent yet Linked Mutations in ALMS1 and DYSF.
Csilla H. Lazar,Csilla H. Lazar,Adva Kimchi,Prasanthi Namburi,Mousumi Mutsuddi,Lina Zelinger,Lina Zelinger,Avigail Beryozkin,Shiran Ben-Simhon,Alexey Obolensky,Ziva Ben-Neriah,Zohar Argov,Eli Pikarsky,Yakov Fellig,Devorah Marks-Ohana,Rinki Ratnapriya,Eyal Banin,Dror Sharon,Anand Swaroop +18 more
TL;DR: This study implicates ALMS1 as a nonsyndromic retinal disease gene and suggests a potential role of variants in interacting cilia genes in modifying clinical phenotypes in consanguineous families.
Journal ArticleDOI
Origin of mutations in two families with X-linked chronic granulomatous disease.
TL;DR: The mothers of the affected boys must have received a paternal X chromosome carrying a new mutation, consistent with the maternal grandmothers' normal NBT tests, and the results of the NBT and DNA marker testing were in complete agreement.
Journal ArticleDOI
No CFH or ARMS2 Interaction With Omega-3 Fatty Acids, Low Versus High Zinc, or β-Carotene Versus Lutein and Zeaxanthin on Progression of Age-Related Macular Degeneration in the Age-Related Eye Disease Study 2: Age-Related Eye Disease Study 2 Report No. 18
Freekje van Asten,Chi-Yang Chiu,Elvira Agrón,Traci E Clemons,Rinki Ratnapriya,Anand Swaroop,Michael L. Klein,Ruzong Fan,Emily Y. Chew +8 more
TL;DR: CFH and ARMS2 risk alleles do not modify the response to the AREDS2 nutrient supplements with respect to the progression to late AMD (GA and neovascular AMD).