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

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

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89 results

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Page 1
A large genome-wide association study of age-related macular degeneration highlights contributions of rare and common variants.
Fritsche LG, Igl W, Bailey JN, Grassmann F, Sengupta S, Bragg-Gresham JL, Burdon KP, Hebbring SJ, Wen C, Gorski M, Kim IK, Cho D, Zack D, Souied E, Scholl HP, Bala E, Lee KE, Hunter DJ, Sardell RJ, Mitchell P, Merriam JE, Cipriani V, Hoffman JD, Schick T, Lechanteur YT, Guymer RH, Johnson MP, Jiang Y, Stanton CM, Buitendijk GH, Zhan X, Kwong AM, Boleda A, Brooks M, Gieser L, Ratnapriya R, Branham KE, Foerster JR, Heckenlively JR, Othman MI, Vote BJ, Liang HH, Souzeau E, McAllister IL, Isaacs T, Hall J, Lake S, Mackey DA, Constable IJ, Craig JE, Kitchner TE, Yang Z, Su Z, Luo H, Chen D, Ouyang H, Flagg K, Lin D, Mao G, Ferreyra H, Stark K, von Strachwitz CN, Wolf A, Brandl C, Rudolph G, Olden M, Morrison MA, Morgan DJ, Schu M, Ahn J, Silvestri G, Tsironi EE, Park KH, Farrer LA, Orlin A, Brucker A, Li M, Curcio CA, Mohand-Saïd S, Sahel JA, Audo I, Benchaboune M, Cree AJ, Rennie CA, Goverdhan SV, Grunin M, Hagbi-Levi S, Campochiaro P, Katsanis N, Holz FG, Blond F, Blanché H, Deleuze JF, Igo RP Jr, Truitt B, Peachey NS, Meuer SM, Myers CE, Moore EL, Klein R, Hauser MA, Postel EA, Courtenay MD, Schwartz SG, Kovach JL, Scott WK, Liew G, Tan AG, Gopinath B, Merriam JC, Smith RT, Khan JC,… See abstract for full author list ➔ Fritsche LG, et al. Among authors: leveillard t. Nat Genet. 2016 Feb;48(2):134-43. doi: 10.1038/ng.3448. Epub 2015 Dec 21. Nat Genet. 2016. PMID: 26691988 Free PMC article.
Shedding light on myopia by studying complete congenital stationary night blindness.
Zeitz C, Roger JE, Audo I, Michiels C, Sánchez-Farías N, Varin J, Frederiksen H, Wilmet B, Callebert J, Gimenez ML, Bouzidi N, Blond F, Guilllonneau X, Fouquet S, Léveillard T, Smirnov V, Vincent A, Héon E, Sahel JA, Kloeckener-Gruissem B, Sennlaub F, Morgans CW, Duvoisin RM, Tkatchenko AV, Picaud S. Zeitz C, et al. Among authors: leveillard t. Prog Retin Eye Res. 2023 Mar;93:101155. doi: 10.1016/j.preteyeres.2022.101155. Epub 2023 Jan 19. Prog Retin Eye Res. 2023. PMID: 36669906 Free article. Review.
Maintaining Cone Function in Rod-Cone Dystrophies.
Sahel JA, Léveillard T. Sahel JA, et al. Among authors: leveillard t. Adv Exp Med Biol. 2018;1074:499-509. doi: 10.1007/978-3-319-75402-4_62. Adv Exp Med Biol. 2018. PMID: 29721982 Review.
Metabolic and redox signaling in the retina.
Léveillard T, Sahel JA. Léveillard T, et al. Cell Mol Life Sci. 2017 Oct;74(20):3649-3665. doi: 10.1007/s00018-016-2318-7. Epub 2016 Aug 20. Cell Mol Life Sci. 2017. PMID: 27543457 Free PMC article. Review.
Cancer metabolism of cone photoreceptors.
Léveillard T. Léveillard T. Oncotarget. 2015 Oct 20;6(32):32285-6. doi: 10.18632/oncotarget.5963. Oncotarget. 2015. PMID: 26450906 Free PMC article. No abstract available.
The Emergence of Rod-Cone Cellular Interaction.
Aït-Ali N, Léveillard T. Aït-Ali N, et al. Among authors: leveillard t. Front Genet. 2022 Aug 9;13:900849. doi: 10.3389/fgene.2022.900849. eCollection 2022. Front Genet. 2022. PMID: 36017494 Free PMC article.
CRB1 mutations in inherited retinal dystrophies.
Bujakowska K, Audo I, Mohand-Saïd S, Lancelot ME, Antonio A, Germain A, Léveillard T, Letexier M, Saraiva JP, Lonjou C, Carpentier W, Sahel JA, Bhattacharya SS, Zeitz C. Bujakowska K, et al. Among authors: leveillard t. Hum Mutat. 2012 Feb;33(2):306-15. doi: 10.1002/humu.21653. Epub 2011 Dec 27. Hum Mutat. 2012. PMID: 22065545 Free PMC article. Review.
89 results