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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2002 1
2003 5
2004 2
2005 6
2006 6
2007 3
2008 4
2009 2
2010 6
2011 7
2012 8
2013 3
2014 5
2015 6
2016 8
2017 8
2018 9
2019 8
2020 7
2021 3
2022 2
2023 2
2024 3

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103 results

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Page 1
A multi-cohort genome-wide association study in African ancestry individuals reveals risk loci for primary open-angle glaucoma.
Verma SS, Gudiseva HV, Chavali VRM, Salowe RJ, Bradford Y, Guare L, Lucas A, Collins DW, Vrathasha V, Nair RM, Rathi S, Zhao B, He J, Lee R, Zenebe-Gete S, Bowman AS, McHugh CP, Zody MC, Pistilli M, Khachatryan N, Daniel E, Murphy W, Henderer J; Regeneron Genetics Center; Kinzy TG, Iyengar SK, Peachey NS; VA Million Veteran Program; Taylor KD, Guo X, Chen YI, Zangwill L, Girkin C, Ayyagari R, Liebmann J, Chuka-Okosa CM, Williams SE, Akafo S, Budenz DL, Olawoye OO, Ramsay M, Ashaye A, Akpa OM, Aung T, Wiggs JL, Ross AG, Cui QN, Addis V, Lehman A, Miller-Ellis E, Sankar PS, Williams SM, Ying GS, Cooke Bailey J, Rotter JI, Weinreb R, Khor CC, Hauser MA, Ritchie MD, O'Brien JM. Verma SS, et al. Among authors: ayyagari r. Cell. 2024 Jan 18;187(2):464-480.e10. doi: 10.1016/j.cell.2023.12.006. Cell. 2024. PMID: 38242088
Reticular Pseudodrusen in Late-Onset Retinal Degeneration.
Borooah S, Papastavrou V, Lando L, Han J, Lin JH, Ayyagari R, Dhillon B, Browning AC. Borooah S, et al. Among authors: ayyagari r. Ophthalmol Retina. 2021 Oct;5(10):1043-1051. doi: 10.1016/j.oret.2020.12.012. Epub 2020 Dec 22. Ophthalmol Retina. 2021. PMID: 33352318 Free PMC article.
Mouse Choroid Proteome Revisited: Focus on Aging.
Garland D, Harnly J, Ayyagari R. Garland D, et al. Among authors: ayyagari r. Adv Exp Med Biol. 2023;1415:359-363. doi: 10.1007/978-3-031-27681-1_52. Adv Exp Med Biol. 2023. PMID: 37440057
Whole genome sequencing data of multiple individuals of Pakistani descent.
Khan SY, Ali M, Lee MW, Ma Z, Biswas P, Khan AA, Naeem MA, Riazuddin S, Riazuddin S, Ayyagari R, Hejtmancik JF, Riazuddin SA. Khan SY, et al. Among authors: ayyagari r. Sci Data. 2020 Oct 13;7(1):350. doi: 10.1038/s41597-020-00664-2. Sci Data. 2020. PMID: 33051442 Free PMC article.
Phenotypic variability associated with the D226N allele of IMPDH1.
Ali S, Khan SY, Naeem MA, Khan SN, Husnain T, Riazuddin S, Ayyagari R, Riazuddin S, Hejtmancik JF, Riazuddin SA. Ali S, et al. Among authors: ayyagari r. Ophthalmology. 2015 Feb;122(2):429-31. doi: 10.1016/j.ophtha.2014.07.057. Epub 2014 Nov 13. Ophthalmology. 2015. PMID: 25439607 No abstract available.
A mutation in IFT43 causes non-syndromic recessive retinal degeneration.
Biswas P, Duncan JL, Ali M, Matsui H, Naeem MA, Raghavendra PB, Frazer KA, Arts HH, Riazuddin S, Akram J, Hejtmancik JF, Riazuddin SA, Ayyagari R. Biswas P, et al. Among authors: ayyagari r. Hum Mol Genet. 2017 Dec 1;26(23):4741-4751. doi: 10.1093/hmg/ddx356. Hum Mol Genet. 2017. PMID: 28973684 Free PMC article.
103 results