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The rare TREM2 R47H variant exerts only a modest effect on Alzheimer disease risk.
Hooli BV, Parrado AR, Mullin K, Yip WK, Liu T, Roehr JT, Qiao D, Jessen F, Peters O, Becker T, Ramirez A, Lange C, Bertram L, Tanzi RE. Hooli BV, et al. Among authors: lange c. Neurology. 2014 Oct 7;83(15):1353-8. doi: 10.1212/WNL.0000000000000855. Epub 2014 Sep 3. Neurology. 2014. PMID: 25186855 Free PMC article.
Family-based association between Alzheimer's disease and variants in UBQLN1.
Bertram L, Hiltunen M, Parkinson M, Ingelsson M, Lange C, Ramasamy K, Mullin K, Menon R, Sampson AJ, Hsiao MY, Elliott KJ, Velicelebi G, Moscarillo T, Hyman BT, Wagner SL, Becker KD, Blacker D, Tanzi RE. Bertram L, et al. Among authors: lange c. N Engl J Med. 2005 Mar 3;352(9):884-94. doi: 10.1056/NEJMoa042765. N Engl J Med. 2005. PMID: 15745979 Free article.
Exploring candidate gene associations with neuropsychological performance.
McQueen MB, Bertram L, Lange C, Becker KD, Albert MS, Tanzi RE, Blacker D. McQueen MB, et al. Among authors: lange c. Am J Med Genet B Neuropsychiatr Genet. 2007 Dec 5;144B(8):987-91. doi: 10.1002/ajmg.b.30500. Am J Med Genet B Neuropsychiatr Genet. 2007. PMID: 17579348
Genome-wide association analysis reveals putative Alzheimer's disease susceptibility loci in addition to APOE.
Bertram L, Lange C, Mullin K, Parkinson M, Hsiao M, Hogan MF, Schjeide BM, Hooli B, Divito J, Ionita I, Jiang H, Laird N, Moscarillo T, Ohlsen KL, Elliott K, Wang X, Hu-Lince D, Ryder M, Murphy A, Wagner SL, Blacker D, Becker KD, Tanzi RE. Bertram L, et al. Among authors: lange c. Am J Hum Genet. 2008 Nov;83(5):623-32. doi: 10.1016/j.ajhg.2008.10.008. Epub 2008 Oct 30. Am J Hum Genet. 2008. PMID: 18976728 Free PMC article.
2,884 results