HuGE Literature Finder
Records 1-15
Association Between Common Variants in RBFOX1, an RNA-Binding Protein, and Brain Amyloidosis in Early and Preclinical Alzheimer Disease.
JAMA neurology 2020 Jun . Raghavan Neha S, Dumitrescu Logan, Mormino Elizabeth, Mahoney Emily R, Lee Annie J, Gao Yizhe, Bilgel Murat, Goldstein David, Harrison Theresa, Engelman Corinne D, Saykin Andrew J, Whelan Christopher D, Liu Jimmy Z, Jagust William, Albert Marilyn, Johnson Sterling C, Yang Hyun-Sik, Johnson Keith, Aisen Paul, Resnick Susan M, Sperling Reisa, De Jager Philip L, Schneider Julie, Bennett David A, Schrag Matthew, Vardarajan Badri, Hohman Timothy J, Mayeux Richard, |
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Analysis of Whole-Exome Sequencing Data for Alzheimer Disease Stratified by APOE Genotype.
JAMA neurology 2019 Jun . Ma Yiyi, Jun Gyungah R, Zhang Xiaoling, Chung Jaeyoon, Naj Adam C, Chen Yuning, Bellenguez Celine, Hamilton-Nelson Kara, Martin Eden R, Kunkle Brian W, Bis Joshua C, Debette Stéphanie, DeStefano Anita L, Fornage Myriam, Nicolas Gaël, van Duijn Cornelia, Bennett David A, De Jager Philip L, Mayeux Richard, Haines Jonathan L, Pericak-Vance Margaret A, Seshadri Sudha, Lambert Jean-Charles, Schellenberg Gerard D, Lunetta Kathryn L, Farrer Lindsay A, |
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Investigation of Genetic Variants Associated with Alzheimer Disease in Parkinson Disease Cognition.
Journal of Parkinson's disease 2016 Jan . Barrett Matthew J, Koeppel Alexander F, Flanigan Joseph L, Turner Stephen D, Worrall Bradford |
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A novel Alzheimer disease locus located near the gene encoding tau protein.
Molecular psychiatry 2015 Mar . Jun G, Ibrahim-Verbaas C A, Vronskaya M, Lambert J-C, Chung J, Naj A C, Kunkle B W, Wang L-S, Bis J C, Bellenguez C, Harold D, Lunetta K L, Destefano A L, Grenier-Boley B, Sims R, Beecham G W, Smith A V, Chouraki V, Hamilton-Nelson K L, Ikram M A, Fievet N, Denning N, Martin E R, Schmidt H, Kamatani Y, Dunstan M L, Valladares O, Laza A R, Zelenika D, Ramirez A, Foroud T M, Choi S-H, Boland A, Becker T, Kukull W A, van der Lee S J, Pasquier F, Cruchaga C, Beekly D, Fitzpatrick A L, Hanon O, Gill M, Barber R, Gudnason V, Campion D, Love S, Bennett D A, Amin N, Berr C, Tsolaki Magda, Buxbaum J D, Lopez O L, Deramecourt V, Fox N C, Cantwell L B, Tárraga L, Dufouil C, Hardy J, Crane P K, Eiriksdottir G, Hannequin D, Clarke R, Evans D, Mosley T H, Letenneur L, Brayne C, Maier W, De Jager P, Emilsson V, Dartigues J-F, Hampel H, Kamboh M I, de Bruijn R F A G, Tzourio C, Pastor P, Larson E B, Rotter J I, O'Donovan M C, Montine T J, Nalls M A, Mead S, Reiman E M, Jonsson P V, Holmes C, St George-Hyslop P H, Boada M, Passmore P, Wendland J R, Schmidt R, Morgan K, Winslow A R, Powell J F, Carasquillo M, Younkin S G, Jakobsdóttir J, Kauwe J S K, Wilhelmsen K C, Rujescu D, Nöthen M M, Hofman A, Jones L, , Haines J L, Psaty B M, Van Broeckhoven C, Holmans P, Launer L J, Mayeux R, Lathrop M, Goate A M, Escott-Price V, Seshadri S, Pericak-Vance M A, Amouyel P, Williams J, van Duijn C M, Schellenberg G D, Farrer L |
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Effects of multiple genetic loci on age at onset in late-onset Alzheimer disease: a genome-wide association study.
JAMA neurology 2014 Nov 71 (11): 1394-404. Naj Adam C, Jun Gyungah, Reitz Christiane, Kunkle Brian W, Perry William, Park Yo Son, Beecham Gary W, Rajbhandary Ruchita A, Hamilton-Nelson Kara L, Wang Li-San, Kauwe John S K, Huentelman Matthew J, Myers Amanda J, Bird Thomas D, Boeve Bradley F, Baldwin Clinton T, Jarvik Gail P, Crane Paul K, Rogaeva Ekaterina, Barmada M Michael, Demirci F Yesim, Cruchaga Carlos, Kramer Patricia L, Ertekin-Taner Nilufer, Hardy John, Graff-Radford Neill R, Green Robert C, Larson Eric B, St George-Hyslop Peter H, Buxbaum Joseph D, Evans Denis A, Schneider Julie A, Lunetta Kathryn L, Kamboh M Ilyas, Saykin Andrew J, Reiman Eric M, De Jager Philip L, Bennett David A, Morris John C, Montine Thomas J, Goate Alison M, Blacker Deborah, Tsuang Debby W, Hakonarson Hakon, Kukull Walter A, Foroud Tatiana M, Martin Eden R, Haines Jonathan L, Mayeux Richard P, Farrer Lindsay A, Schellenberg Gerard D, Pericak-Vance Margaret A, , Albert Marilyn S, Albin Roger L, Apostolova Liana G, Arnold Steven E, Barber Robert, Barnes Lisa L, Beach Thomas G, Becker James T, Beekly Duane, Bigio Eileen H, Bowen James D, Boxer Adam, Burke James R, Cairns Nigel J, Cantwell Laura B, Cao Chuanhai, Carlson Chris S, Carney Regina M, Carrasquillo Minerva M, Carroll Steven L, Chui Helena C, Clark David G, Corneveaux Jason, Cribbs David H, Crocco Elizabeth A, DeCarli Charles, DeKosky Steven T, Dick Malcolm, Dickson Dennis W, Duara Ranjan, Faber Kelley M, Fallon Kenneth B, Farlow Martin R, Ferris Steven, Frosch Matthew P, Galasko Douglas R, Ganguli Mary, Gearing Marla, Geschwind Daniel H, Ghetti Bernardino, Gilbert John R, Glass Jonathan D, Growdon John H, Hamilton Ronald L, Harrell Lindy E, Head Elizabeth, Honig Lawrence S, Hulette Christine M, Hyman Bradley T, Jicha Gregory A, Jin Lee-Way, Karydas Anna, Kaye Jeffrey A, Kim Ronald, Koo Edward H, Kowall Neil W, Kramer Joel H, LaFerla Frank M, Lah James J, Leverenz James B, Levey Allan I, Li Ge, Lieberman Andrew P, Lin Chiao-Feng, Lopez Oscar L, Lyketsos Constantine G, Mack Wendy J, Martiniuk Frank, Mash Deborah C, Masliah Eliezer, McCormick Wayne C, McCurry Susan M, McDavid Andrew N, McKee Ann C, Mesulam Marsel, Miller Bruce L, Miller Carol A, Miller Joshua W, Murrell Jill R, Olichney John M, Pankratz Vernon S, Parisi Joseph E, Paulson Henry L, Peskind Elaine, Petersen Ronald C, Pierce Aimee, Poon Wayne W, Potter Huntington, Quinn Joseph F, Raj Ashok, Raskind Murray, Reisberg Barry, Ringman John M, Roberson Erik D, Rosen Howard J, Rosenberg Roger N, Sano Mary, Schneider Lon S, Seeley William W, Smith Amanda G, Sonnen Joshua A, Spina Salvatore, Stern Robert A, Tanzi Rudolph E, Thornton-Wells Tricia A, Trojanowski John Q, Troncoso Juan C, Valladares Otto, Van Deerlin Vivianna M, Van Eldik Linda J, Vardarajan Badri N, Vinters Harry V, Vonsattel Jean Paul, Weintraub Sandra, Welsh-Bohmer Kathleen A, Williamson Jennifer, Wishnek Sarah, Woltjer Randall L, Wright Clinton B, Younkin Steven G, Yu Chang-En, Yu L |
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The rare TREM2 R47H variant exerts only a modest effect on Alzheimer disease risk.
Neurology 2014 Oct 83 (15): 1353-8. Hooli Basavaraj V, Parrado Antonio R, Mullin Kristina, Yip Wai-Ki, Liu Tian, Roehr Johannes T, Qiao Dandi, Jessen Frank, Peters Oliver, Becker Tim, Ramirez Alfredo, Lange Christoph, Bertram Lars, Tanzi Rudolph |
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Apolipoprotein ?4-allele as a significant risk factor for conversion from mild cognitive impairment to Alzheimer's disease: a meta-analysis of prospective studies.
Journal of molecular neuroscience : MN 2013 Jun 50 (2): 257-63. Fei Ma, Jianhua Wa |
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Variants in the ATP-binding cassette transporter (ABCA7), apolipoprotein E ?4,and the risk of late-onset Alzheimer disease in African Americans.
JAMA 2013 Apr 309 (14): 1483-92. Reitz Christiane, Jun Gyungah, Naj Adam, Rajbhandary Ruchita, Vardarajan Badri Narayan, Wang Li-San, Valladares Otto, Lin Chiao-Feng, Larson Eric B, Graff-Radford Neill R, Evans Denis, De Jager Philip L, Crane Paul K, Buxbaum Joseph D, Murrell Jill R, Raj Towfique, Ertekin-Taner Nilufer, Logue Mark, Baldwin Clinton T, Green Robert C, Barnes Lisa L, Cantwell Laura B, Fallin M Daniele, Go Rodney C P, Griffith Patrick, Obisesan Thomas O, Manly Jennifer J, Lunetta Kathryn L, Kamboh M Ilyas, Lopez Oscar L, Bennett David A, Hendrie Hugh, Hall Kathleen S, Goate Alison M, Byrd Goldie S, Kukull Walter A, Foroud Tatiana M, Haines Jonathan L, Farrer Lindsay A, Pericak-Vance Margaret A, Schellenberg Gerard D, Mayeux Richard, |
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Multiple loci influencing hippocampal degeneration identified by genome scan.
Annals of neurology 2012 Jul 72 (1): 65-75. Melville Scott A, Buros Jacqueline, Parrado Antonio R, Vardarajan Badri, Logue Mark W, Shen Li, Risacher Shannon L, Kim Sungeun, Jun Gyungah, DeCarli Charles, Lunetta Kathryn L, Baldwin Clinton T, Saykin Andrew J, Farrer Lindsay A, |
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Genome-wide and gene-based association implicates FRMD6 in Alzheimer disease.
Human mutation 2011 Dec . Hong MG, Reynolds CA, Feldman AL, Kallin M, Lambert JC, Amouyel P, Ingelsson E, Pedersen NL, Prince JA |
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Meta-analysis confirms CR1, CLU, and PICALM as alzheimer disease risk loci and reveals interactions with APOE genotypes.
Archives of neurology 2010 Dec 67 (12): 1473-84. Jun Gyungah, Naj Adam C, Beecham Gary W, Wang Li-San, Buros Jacqueline, Gallins Paul J, Buxbaum Joseph D, Ertekin-Taner Nilufer, Fallin M Daniele, Friedland Robert, Inzelberg Rivka, Kramer Patricia, Rogaeva Ekaterina, St George-Hyslop Peter, , Cantwell Laura B, Dombroski Beth A, Saykin Andrew J, Reiman Eric M, Bennett David A, Morris John C, Lunetta Kathryn L, Martin Eden R, Montine Thomas J, Goate Alison M, Blacker Deborah, Tsuang Debby W, Beekly Duane, Cupples L Adrienne, Hakonarson Hakon, Kukull Walter, Foroud Tatiana M, Haines Jonathan, Mayeux Richard, Farrer Lindsay A, Pericak-Vance Margaret A, Schellenberg Gerard |
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[Influence of APOE gene polymorphisms on interferon-beta treatment response in multiple sclerosis.]
Neurologia (Barcelona, Spain) 2010 Nov . Guerrero AL, Tejero MA, Gutiérrez F, Martín-Polo J, Iglesias F, Laherran E, Martín-Serradilla JI, Merino S |
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Apolipoprotein E promoter polymorphisms and risk of Alzheimer's disease: evidence from meta-analysis.
Journal of Alzheimer's disease : JAD 2010 19 (4): 1283-94. Xin Xiao-Yu, Ding Jian-Qing, Chen Sheng- |
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Association study and meta-analysis of Alzheimer's disease risk and presenilin-1 intronic polymorphism.
Brain research 2007 Sep 1170 119-28. Rodríguez-Manotas Miguel, Amorín-Díaz Manuel, Cañizares-Hernández Francisco, Ruíz-Espejo Francisco, Martínez-Vidal Salvadora, González-Sarmiento Rogelio, Martínez-Hernández Pedro, Cabezas-Herrera Ju |
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APOE-[epsilon]2 allele associated with higher prevalence of sporadic Parkinson disease.
Neurology 2004 Jun 62 (12): 2198-202. Huang Xuemei, Chen Peter C, Poole Charl |
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- Page last updated:Jan 19, 2021
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