RINKI RATNA PRIYA to Humans
This is a "connection" page, showing publications RINKI RATNA PRIYA has written about Humans.
Connection Strength
0.106
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The Role of Gene Expression Regulation on Genetic Risk of Age-Related Macular Degeneration. Adv Exp Med Biol. 2023; 1415:61-66.
Score: 0.023
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Applications of Genomic Technologies in Retinal Degenerative Diseases. Adv Exp Med Biol. 2019; 1185:281-285.
Score: 0.017
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Genetic studies of age-related macular degeneration: lessons, challenges, and opportunities for disease management. Ophthalmology. 2012 Dec; 119(12):2526-36.
Score: 0.011
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Molecular Anatomy of the Developing Human Retina. Dev Cell. 2017 12 18; 43(6):763-779.e4.
Score: 0.008
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Molecular Diagnosis of Inherited Retinal Diseases in Indigenous African Populations by Whole-Exome Sequencing. Invest Ophthalmol Vis Sci. 2016 11 01; 57(14):6374-6381.
Score: 0.007
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Vision from next generation sequencing: multi-dimensional genome-wide analysis for producing gene regulatory networks underlying retinal development, aging and disease. Prog Retin Eye Res. 2015 May; 46:1-30.
Score: 0.007
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A locus for juvenile myoclonic epilepsy maps to 2q33-q36. Hum Genet. 2010 Aug; 128(2):123-30.
Score: 0.005
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Familial autosomal dominant reflex epilepsy triggered by hot water maps to 4q24-q28. Hum Genet. 2009 Nov; 126(5):677-83.
Score: 0.005
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A locus for autosomal dominant reflex epilepsy precipitated by hot water maps at chromosome 10q21.3-q22.3. Hum Genet. 2009 Jun; 125(5-6):541-9.
Score: 0.004
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Retinal transcriptome and eQTL analyses identify genes associated with age-related macular degeneration. Nat Genet. 2019 04; 51(4):606-610.
Score: 0.004
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An idiopathic epilepsy syndrome linked to 3q13.3-q21 and missense mutations in the extracellular calcium sensing receptor gene. Ann Neurol. 2008 Aug; 64(2):158-67.
Score: 0.004
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Bi-allelic Truncating Mutations in CEP78, Encoding Centrosomal Protein 78, Cause Cone-Rod Degeneration with Sensorineural Hearing Loss. Am J Hum Genet. 2016 09 01; 99(3):777-784.
Score: 0.004
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Rare and common variants in extracellular matrix gene Fibrillin 2 (FBN2) are associated with macular degeneration. Hum Mol Genet. 2014 Nov 01; 23(21):5827-37.
Score: 0.003
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Seven new loci associated with age-related macular degeneration. Nat Genet. 2013 Apr; 45(4):433-9, 439e1-2.
Score: 0.003