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Coding mutations in SORL1 and Alzheimer disease.
Vardarajan BN, Zhang Y, Lee JH, Cheng R, Bohm C, Ghani M, Reitz C, Reyes-Dumeyer D, Shen Y, Rogaeva E, St George-Hyslop P, Mayeux R. Vardarajan BN, et al. Among authors: cheng r. Ann Neurol. 2015 Feb;77(2):215-27. doi: 10.1002/ana.24305. Ann Neurol. 2015. PMID: 25382023 Free PMC article.
Rare coding mutations identified by sequencing of Alzheimer disease genome-wide association studies loci.
Vardarajan BN, Ghani M, Kahn A, Sheikh S, Sato C, Barral S, Lee JH, Cheng R, Reitz C, Lantigua R, Reyes-Dumeyer D, Medrano M, Jimenez-Velazquez IZ, Rogaeva E, St George-Hyslop P, Mayeux R. Vardarajan BN, et al. Among authors: cheng r. Ann Neurol. 2015 Sep;78(3):487-98. doi: 10.1002/ana.24466. Epub 2015 Jul 28. Ann Neurol. 2015. PMID: 26101835 Free PMC article.
Age-at-onset linkage analysis in Caribbean Hispanics with familial late-onset Alzheimer's disease.
Lee JH, Barral S, Cheng R, Chacon I, Santana V, Williamson J, Lantigua R, Medrano M, Jimenez-Velazquez IZ, Stern Y, Tycko B, Rogaeva E, Wakutani Y, Kawarai T, St George-Hyslop P, Mayeux R. Lee JH, et al. Among authors: cheng r. Neurogenetics. 2008 Feb;9(1):51-60. doi: 10.1007/s10048-007-0103-3. Epub 2007 Oct 17. Neurogenetics. 2008. PMID: 17940814 Free PMC article.
Meta-analysis of the association between variants in SORL1 and Alzheimer disease.
Reitz C, Cheng R, Rogaeva E, Lee JH, Tokuhiro S, Zou F, Bettens K, Sleegers K, Tan EK, Kimura R, Shibata N, Arai H, Kamboh MI, Prince JA, Maier W, Riemenschneider M, Owen M, Harold D, Hollingworth P, Cellini E, Sorbi S, Nacmias B, Takeda M, Pericak-Vance MA, Haines JL, Younkin S, Williams J, van Broeckhoven C, Farrer LA, St George-Hyslop PH, Mayeux R; Genetic and Environmental Risk in Alzheimer Disease 1 Consortium. Reitz C, et al. Among authors: cheng r. Arch Neurol. 2011 Jan;68(1):99-106. doi: 10.1001/archneurol.2010.346. Arch Neurol. 2011. PMID: 21220680 Free PMC article.
3,496 results