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

Year Number of Results
2003 1
2006 2
2007 2
2008 4
2009 5
2010 10
2011 8
2012 9
2013 2
2014 4
2015 3
2016 5
2017 6
2018 2
2019 6
2020 6
2021 4
2022 7
2023 1
2024 1

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81 results

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Page 1
Multitrait analysis of glaucoma identifies new risk loci and enables polygenic prediction of disease susceptibility and progression.
Craig JE, Han X, Qassim A, Hassall M, Cooke Bailey JN, Kinzy TG, Khawaja AP, An J, Marshall H, Gharahkhani P, Igo RP Jr, Graham SL, Healey PR, Ong JS, Zhou T, Siggs O, Law MH, Souzeau E, Ridge B, Hysi PG, Burdon KP, Mills RA, Landers J, Ruddle JB, Agar A, Galanopoulos A, White AJR, Willoughby CE, Andrew NH, Best S, Vincent AL, Goldberg I, Radford-Smith G, Martin NG, Montgomery GW, Vitart V, Hoehn R, Wojciechowski R, Jonas JB, Aung T, Pasquale LR, Cree AJ, Sivaprasad S, Vallabh NA; NEIGHBORHOOD consortium; UK Biobank Eye and Vision Consortium; Viswanathan AC, Pasutto F, Haines JL, Klaver CCW, van Duijn CM, Casson RJ, Foster PJ, Khaw PT, Hammond CJ, Mackey DA, Mitchell P, Lotery AJ, Wiggs JL, Hewitt AW, MacGregor S. Craig JE, et al. Among authors: ruddle jb. Nat Genet. 2020 Feb;52(2):160-166. doi: 10.1038/s41588-019-0556-y. Epub 2020 Jan 20. Nat Genet. 2020. PMID: 31959993 Free PMC article.
Optical coherence tomography in paediatric clinical practice.
Maccora KA, Sheth S, Ruddle JB. Maccora KA, et al. Among authors: ruddle jb. Clin Exp Optom. 2019 May;102(3):300-308. doi: 10.1111/cxo.12909. Epub 2019 Apr 15. Clin Exp Optom. 2019. PMID: 30983019 Free article. Review.
Genetic isolates in ophthalmic diseases.
Sherwin JC, Hewitt AW, Ruddle JB, Mackey DA. Sherwin JC, et al. Among authors: ruddle jb. Ophthalmic Genet. 2008 Dec;29(4):149-61. doi: 10.1080/13816810802334341. Ophthalmic Genet. 2008. PMID: 19005985 Review.
Pseudoexfoliation syndrome: more than meets the eye.
Ruddle JB, Mackey DA. Ruddle JB, et al. Clin Exp Ophthalmol. 2010 Jul;38(5):437-8. doi: 10.1111/j.1442-9071.2010.02323.x. Clin Exp Ophthalmol. 2010. PMID: 20649612 No abstract available.
Is the disease risk and penetrance in Leber hereditary optic neuropathy actually low?
Mackey DA, Ong JS, MacGregor S, Whiteman DC, Craig JE, Lopez Sanchez MIG, Kearns LS, Staffieri SE, Clarke L, McGuinness MB, Meteoukki W, Samuel S, Ruddle JB, Chen C, Fraser CL, Harrison J, Howell N, Hewitt AW. Mackey DA, et al. Among authors: ruddle jb. Am J Hum Genet. 2023 Jan 5;110(1):170-176. doi: 10.1016/j.ajhg.2022.11.014. Epub 2022 Dec 23. Am J Hum Genet. 2023. PMID: 36565701 Free PMC article.
Pathogenic genetic variants identified in Australian families with paediatric cataract.
Jones JL, McComish BJ, Staffieri SE, Souzeau E, Kearns LS, Elder JE, Charlesworth JC, Mackey DA, Ruddle JB, Taranath D, Pater J, Casey T, Craig JE, Burdon KP. Jones JL, et al. Among authors: ruddle jb. BMJ Open Ophthalmol. 2022 Aug;7(1):e001064. doi: 10.1136/bmjophth-2022-001064. BMJ Open Ophthalmol. 2022. PMID: 36161833 Free PMC article.
Mutations in SPATA13/ASEF2 cause primary angle closure glaucoma.
Waseem NH, Low S, Shah AZ, Avisetti D, Ostergaard P, Simpson M, Niemiec KA, Martin-Martin B, Aldehlawi H, Usman S, Lee PS, Khawaja AP, Ruddle JB, Shah A, Sackey E, Day A, Jiang Y, Swinfield G, Viswanathan A, Alfano G, Chakarova C, Cordell HJ, Garway-Heath DF, Khaw PT, Bhattacharya SS, Waseem A, Foster PJ. Waseem NH, et al. Among authors: ruddle jb. PLoS Genet. 2020 Apr 27;16(4):e1008721. doi: 10.1371/journal.pgen.1008721. eCollection 2020 Apr. PLoS Genet. 2020. PMID: 32339198 Free PMC article.
81 results