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Page 1
Association of apolipoprotein E variation with cognitive impairment across multiple neurodegenerative diagnoses.
Dilliott AA, Sunderland KM, McLaughlin PM, Roberts AC, Evans EC, Abrahao A, Binns MA, Black SE, Borrie M, Casaubon LK, Dowlatshahi D, Finger E, Fischer CE, Frank A, Freedman M, Grimes D, Hassan A, Jog M, Kumar S, Kwan D, Lang AE, Mandzia J, Marras C, Masellis M, McIntyre AD, Pasternak S, Pollock BG, Rajji TK, Robinson JF, Rogaeva E, Sahlas DJ, Saposnik G, Sato C, Seitz D, Shoesmith C, Steeves T, Strother SC, Swartz RH, Tan B, Tang-Wai D, Tartaglia MC, Troyer AK, Turnbull J, Zinman L; ONDRI Investigators; Hegele RA. Dilliott AA, et al. Among authors: hegele ra. Neurobiol Aging. 2021 Sep;105:378.e1-378.e9. doi: 10.1016/j.neurobiolaging.2021.04.011. Epub 2021 Apr 24. Neurobiol Aging. 2021. PMID: 34039480
ABC transporters and sterol absorption.
Hegele RA, Robinson JF. Hegele RA, et al. Curr Drug Targets Cardiovasc Haematol Disord. 2005 Feb;5(1):31-7. doi: 10.2174/1568006053005029. Curr Drug Targets Cardiovasc Haematol Disord. 2005. PMID: 15720222 Review.
Quality assessment of microarray experiments.
Carter DE, Robinson JF, Allister EM, Huff MW, Hegele RA. Carter DE, et al. Among authors: hegele ra. Clin Biochem. 2005 Jul;38(7):639-42. doi: 10.1016/j.clinbiochem.2005.04.010. Clin Biochem. 2005. PMID: 15923000
Excess of rare variants in genes identified by genome-wide association study of hypertriglyceridemia.
Johansen CT, Wang J, Lanktree MB, Cao H, McIntyre AD, Ban MR, Martins RA, Kennedy BA, Hassell RG, Visser ME, Schwartz SM, Voight BF, Elosua R, Salomaa V, O'Donnell CJ, Dallinga-Thie GM, Anand SS, Yusuf S, Huff MW, Kathiresan S, Hegele RA. Johansen CT, et al. Among authors: hegele ra. Nat Genet. 2010 Aug;42(8):684-7. doi: 10.1038/ng.628. Epub 2010 Jul 25. Nat Genet. 2010. PMID: 20657596 Free PMC article.
An increased burden of common and rare lipid-associated risk alleles contributes to the phenotypic spectrum of hypertriglyceridemia.
Johansen CT, Wang J, Lanktree MB, McIntyre AD, Ban MR, Martins RA, Kennedy BA, Hassell RG, Visser ME, Schwartz SM, Voight BF, Elosua R, Salomaa V, O'Donnell CJ, Dallinga-Thie GM, Anand SS, Yusuf S, Huff MW, Kathiresan S, Cao H, Hegele RA. Johansen CT, et al. Among authors: hegele ra. Arterioscler Thromb Vasc Biol. 2011 Aug;31(8):1916-26. doi: 10.1161/ATVBAHA.111.226365. Epub 2011 May 19. Arterioscler Thromb Vasc Biol. 2011. PMID: 21597005 Free PMC article.
Excess of rare variants in non-genome-wide association study candidate genes in patients with hypertriglyceridemia.
Johansen CT, Wang J, McIntyre AD, Martins RA, Ban MR, Lanktree MB, Huff MW, Péterfy M, Mehrabian M, Lusis AJ, Kathiresan S, Anand SS, Yusuf S, Lee AH, Glimcher LH, Cao H, Hegele RA. Johansen CT, et al. Among authors: hegele ra. Circ Cardiovasc Genet. 2012 Feb 1;5(1):66-72. doi: 10.1161/CIRCGENETICS.111.960864. Epub 2011 Dec 1. Circ Cardiovasc Genet. 2012. PMID: 22135386 Free PMC article.
Genetic determinants of "cognitive impairment, no dementia".
Dubé JB, Johansen CT, Robinson JF, Lindsay J, Hachinski V, Hegele RA. Dubé JB, et al. Among authors: hegele ra. J Alzheimers Dis. 2013;33(3):831-40. doi: 10.3233/JAD-2012-121477. J Alzheimers Dis. 2013. PMID: 23042215
964 results