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Page 1
Establishing risk of vision loss in Leber hereditary optic neuropathy.
Lopez Sanchez MIG, Kearns LS, Staffieri SE, Clarke L, McGuinness MB, Meteoukki W, Samuel S, Ruddle JB, Chen C, Fraser CL, Harrison J, Hewitt AW, Howell N, Mackey DA. Lopez Sanchez MIG, et al. Among authors: clarke l. Am J Hum Genet. 2021 Nov 4;108(11):2159-2170. doi: 10.1016/j.ajhg.2021.09.015. Epub 2021 Oct 19. Am J Hum Genet. 2021. PMID: 34670133 Free PMC article.
Development of a Modular Automated System for Maintenance and Differentiation of Adherent Human Pluripotent Stem Cells.
Crombie DE, Daniszewski M, Liang HH, Kulkarni T, Li F, Lidgerwood GE, Conquest A, Hernández D, Hung SS, Gill KP, De Smit E, Kearns LS, Clarke L, Sluch VM, Chamling X, Zack DJ, Wong RCB, Hewitt AW, Pébay A. Crombie DE, et al. Among authors: clarke l. SLAS Discov. 2017 Sep;22(8):1016-1025. doi: 10.1177/2472555217696797. Epub 2017 Mar 13. SLAS Discov. 2017. PMID: 28287872 Free article.
Mitochondrial replacement in an iPSC model of Leber's hereditary optic neuropathy.
Wong RCB, Lim SY, Hung SSC, Jackson S, Khan S, Van Bergen NJ, De Smit E, Liang HH, Kearns LS, Clarke L, Mackey DA, Hewitt AW, Trounce IA, Pébay A. Wong RCB, et al. Among authors: clarke l. Aging (Albany NY). 2017 Apr;9(4):1341-1350. doi: 10.18632/aging.101231. Aging (Albany NY). 2017. PMID: 28455970 Free PMC article.
Longitudinal expression profiling of CD4+ and CD8+ cells in patients with active to quiescent giant cell arteritis.
De Smit E, Lukowski SW, Anderson L, Senabouth A, Dauyey K, Song S, Wyse B, Wheeler L, Chen CY, Cao K, Wong Ten Yuen A, Shuey N, Clarke L, Lopez Sanchez I, Hung SSC, Pébay A, Mackey DA, Brown MA, Hewitt AW, Powell JE. De Smit E, et al. Among authors: clarke l. BMC Med Genomics. 2018 Jul 23;11(1):61. doi: 10.1186/s12920-018-0376-4. BMC Med Genomics. 2018. PMID: 30037347 Free PMC article.
Single-cell eQTL mapping identifies cell type-specific genetic control of autoimmune disease.
Yazar S, Alquicira-Hernandez J, Wing K, Senabouth A, Gordon MG, Andersen S, Lu Q, Rowson A, Taylor TRP, Clarke L, Maccora K, Chen C, Cook AL, Ye CJ, Fairfax KA, Hewitt AW, Powell JE. Yazar S, et al. Among authors: clarke l. Science. 2022 Apr 8;376(6589):eabf3041. doi: 10.1126/science.abf3041. Epub 2022 Apr 8. Science. 2022. PMID: 35389779
Transcriptomic and proteomic retinal pigment epithelium signatures of age-related macular degeneration.
Senabouth A, Daniszewski M, Lidgerwood GE, Liang HH, Hernández D, Mirzaei M, Keenan SN, Zhang R, Han X, Neavin D, Rooney L, Lopez Sanchez MIG, Gulluyan L, Paulo JA, Clarke L, Kearns LS, Gnanasambandapillai V, Chan CL, Nguyen U, Steinmann AM, McCloy RA, Farbehi N, Gupta VK, Mackey DA, Bylsma G, Verma N, MacGregor S, Watt MJ, Guymer RH, Powell JE, Hewitt AW, Pébay A. Senabouth A, et al. Among authors: clarke l. Nat Commun. 2022 Jul 26;13(1):4233. doi: 10.1038/s41467-022-31707-4. Nat Commun. 2022. PMID: 35882847 Free PMC article.
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: clarke l. 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.
Retinal ganglion cell-specific genetic regulation in primary open-angle glaucoma.
Daniszewski M, Senabouth A, Liang HH, Han X, Lidgerwood GE, Hernández D, Sivakumaran P, Clarke JE, Lim SY, Lees JG, Rooney L, Gulluyan L, Souzeau E, Graham SL, Chan CL, Nguyen U, Farbehi N, Gnanasambandapillai V, McCloy RA, Clarke L, Kearns LS, Mackey DA, Craig JE, MacGregor S, Powell JE, Pébay A, Hewitt AW. Daniszewski M, et al. Among authors: clarke l, clarke je. Cell Genom. 2022 Jun 8;2(6):100142. doi: 10.1016/j.xgen.2022.100142. eCollection 2022 Jun 8. Cell Genom. 2022. PMID: 36778138 Free PMC article.
1,418 results