Human Genome Epidemiology Literature Finder
Records 1 - 15 (of 15 Records) |
Query Trace: EXOC3L2[original query] |
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Genome-wide analysis of genetic loci associated with Alzheimer disease.
JAMA 2010 May 303 (18): 1832-40. Seshadri Sudha, Fitzpatrick Annette L, Ikram M Arfan, DeStefano Anita L, Gudnason Vilmundur, Boada Merce, Bis Joshua C, Smith Albert V, Carassquillo Minerva M, Lambert Jean Charles, Harold Denise, Schrijvers Elisabeth M C, Ramirez-Lorca Reposo, Debette Stephanie, Longstreth W T, Janssens A Cecile J W, Pankratz V Shane, Dartigues Jean François, Hollingworth Paul, Aspelund Thor, Hernandez Isabel, Beiser Alexa, Kuller Lewis H, Koudstaal Peter J, Dickson Dennis W, Tzourio Christophe, Abraham Richard, Antunez Carmen, Du Yangchun, Rotter Jerome I, Aulchenko Yurii S, Harris Tamara B, Petersen Ronald C, Berr Claudine, Owen Michael J, Lopez-Arrieta Jesus, Varadarajan Badri N, Becker James T, Rivadeneira Fernando, Nalls Michael A, Graff-Radford Neill R, Campion Dominique, Auerbach Sanford, Rice Kenneth, Hofman Albert, Jonsson Palmi V, Schmidt Helena, Lathrop Mark, Mosley Thomas H, Au Rhoda, Psaty Bruce M, Uitterlinden Andre G, Farrer Lindsay A, Lumley Thomas, Ruiz Agustin, Williams Julie, Amouyel Philippe, Younkin Steve G, Wolf Philip A, Launer Lenore J, Lopez Oscar L, van Duijn Cornelia M, Breteler Monique M B, , , |
Investigation of 15 of the top candidate genes for late-onset Alzheimer's disease. Human genetics 2011 Mar 129 (3): 273-82. Belbin Olivia, Carrasquillo Minerva M, Crump Michael, Culley Oliver J, Hunter Talisha A, Ma Li, Bisceglio Gina, Zou Fanggeng, Allen Mariet, Dickson Dennis W, Graff-Radford Neill R, Petersen Ronald C, Morgan Kevin, Younkin Steven |
Common variants at MS4A4/MS4A6E, CD2AP, CD33 and EPHA1 are associated with late-onset Alzheimer's disease.
Nature genetics 2011 May 43 (5): 436-41. Naj Adam C, Jun Gyungah, Beecham Gary W, Wang Li-San, Vardarajan Badri Narayan, Buros Jacqueline, Gallins Paul J, Buxbaum Joseph D, Jarvik Gail P, Crane Paul K, Larson Eric B, Bird Thomas D, Boeve Bradley F, Graff-Radford Neill R, De Jager Philip L, Evans Denis, Schneider Julie A, Carrasquillo Minerva M, Ertekin-Taner Nilufer, Younkin Steven G, Cruchaga Carlos, Kauwe John S K, Nowotny Petra, Kramer Patricia, Hardy John, Huentelman Matthew J, Myers Amanda J, Barmada Michael M, Demirci F Yesim, Baldwin Clinton T, Green Robert C, Rogaeva Ekaterina, St George-Hyslop Peter, Arnold Steven E, Barber Robert, Beach Thomas, Bigio Eileen H, Bowen James D, Boxer Adam, Burke James R, Cairns Nigel J, Carlson Chris S, Carney Regina M, Carroll Steven L, Chui Helena C, Clark David G, Corneveaux Jason, Cotman Carl W, Cummings Jeffrey L, DeCarli Charles, DeKosky Steven T, Diaz-Arrastia Ramon, Dick Malcolm, Dickson Dennis W, Ellis William G, 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, Gilman Sid, Giordani Bruno, 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, Johnson Nancy, Karlawish Jason, Karydas Anna, Kaye Jeffrey A, Kim Ronald, Koo Edward H, Kowall Neil W, Lah James J, Levey Allan I, Lieberman Andrew P, Lopez Oscar L, Mack Wendy J, Marson Daniel C, 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, Parisi Joseph E, Perl Daniel P, Peskind Elaine, Petersen Ronald C, Poon Wayne W, Quinn Joseph F, Rajbhandary Ruchita A, Raskind Murray, Reisberg Barry, Ringman John M, Roberson Erik D, Rosenberg Roger N, Sano Mary, Schneider Lon S, Seeley William, Shelanski Michael L, Slifer Michael A, Smith Charles D, Sonnen Joshua A, Spina Salvatore, Stern Robert A, Tanzi Rudolph E, Trojanowski John Q, Troncoso Juan C, Van Deerlin Vivianna M, Vinters Harry V, Vonsattel Jean Paul, Weintraub Sandra, Welsh-Bohmer Kathleen A, Williamson Jennifer, Woltjer Randall L, Cantwell Laura B, Dombroski Beth A, Beekly Duane, Lunetta Kathryn L, Martin Eden R, Kamboh M Ilyas, Saykin Andrew J, Reiman Eric M, 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, Haines Jonathan L, Mayeux Richard, Pericak-Vance Margaret A, Farrer Lindsay A, Schellenberg Gerard |
Genome-wide association of familial late-onset Alzheimer's disease replicates BIN1 and CLU and nominates CUGBP2 in interaction with APOE.
PLoS genetics 2011 Feb 7 (2): e1001308. Wijsman Ellen M, Pankratz Nathan D, Choi Yoonha, Rothstein Joseph H, Faber Kelley M, Cheng Rong, Lee Joseph H, Bird Thomas D, Bennett David A, Diaz-Arrastia Ramon, Goate Alison M, Farlow Martin, Ghetti Bernardino, Sweet Robert A, Foroud Tatiana M, Mayeux Richard, |
Replication of BIN1 association with Alzheimer's disease and evaluation of genetic interactions. Journal of Alzheimer's disease : JAD 2011 24 (4): 751-8. Carrasquillo Minerva M, Belbin Olivia, Hunter Talisha A, Ma Li, Bisceglio Gina D, Zou Fanggeng, Crook Julia E, Pankratz V Shane, Sando Sigrid B, Aasly Jan O, Barcikowska Maria, Wszolek Zbigniew K, Dickson Dennis W, Graff-Radford Neill R, Petersen Ronald C, Morgan Kevin, Younkin Steven |
Genetics of late-onset Alzheimer's disease: update from the alzgene database and analysis of shared pathways. International journal of Alzheimer's disease 2011 2011 . Olgiati P, Politis AM, Papadimitriou GN, De Ronchi D, Serretti A |
Evidence of the association of BIN1 and PICALM with the AD risk in contrasting European populations. Neurobiology of aging 2011 Apr 32 (4): 756.e11-5. Lambert Jean-Charles, Zelenika Diana, Hiltunen Mikko, Chouraki Vincent, Combarros Onofre, Bullido Maria J, Tognoni Gloria, Fiévet Nathalie, Boland Anne, Arosio Beatrice, Coto Eliecer, Del Zompo Maria, Mateo Ignacio, Frank-Garcia Ana, Helisalmi Seppo, Porcellini Elisa, Pilotto Alberto, Forti Paola, Ferri Raffaele, Delepine Marc, Scarpini Elio, Siciliano Gabriele, Solfrizzi Vincenzo, Sorbi Sandro, Spalletta Gianfranco, Ravaglia Giovanni, Valdivieso Fernando, Alvarez Victoria, Bosco Paolo, Mancuso Michelangelo, Panza Francesco, Nacmias Benedetta, Bossù Paola, Piccardi Paola, Annoni Giorgio, Seripa Davide, Galimberti Daniela, Licastro Federico, Lathrop Mark, Soininen Hilkka, Amouyel Philip |
Lack of association between rs597668 polymorphism near EXOC3L2 and late-onset Alzheimer's disease in Han Chinese. Neuroscience letters 2012 Apr 513 (2): 174-7. Liu Qiu-Yan, Miao Dan, Yu Jin-Tai, Xing Yao-Yao, Zhong Xiao-Ling, Wu Zhong-Chen, Zhang Qun, Tan L |
Alzheimer's disease: genetic polymorphisms and rate of decline. Dementia and geriatric cognitive disorders 2012 33 (2-3): 84-9. Schmidt Christian, Wolff Martin, von Ahsen Nicolas, Zerr In |
Association between EXOC3L2 rs597668 polymorphism and Alzheimer's disease. CNS neuroscience & therapeutics 2013 Oct 19 (10): 834-9. Shang Hong, Fu Jin, Zhang Xue-Mei, Song Rong-Rong, Wang Wei-Z |
CR1 is potentially associated with rate of decline in sporadic Alzheimer's disease. Journal of clinical neuroscience : official journal of the Neurosurgical Society of Australasia 2014 Oct 21 (10): 1705-8. Schmidt Christian, Wolff Martin, von Ahsen Nicolas, Lange Katharina, Friede Tim, Zerr In |
Gene-based aggregate SNP associations between candidate AD genes and cognitive decline. Age (Dordrecht, Netherlands) 2016 Apr 38 (2): 41. Nettiksimmons Jasmine, Tranah Gregory, Evans Daniel S, Yokoyama Jennifer S, Yaffe Kristi |
EXOC3L2 rs597668 variant contributes to Alzheimer's disease susceptibility in Asian population. Oncotarget 2017 Mar 8 (12): 20086-20091. Wu Qing-Jian, Sun Shu-Yin, Yan Cheng-Jun, Cheng Zi-Cui, Yang Ming-Feng, Li Zi-Fei, Cheng Hou-Wen, Fang Ti-K |
A minor allele of the haplotype located in the 19q13 loci is associated with a decreased risk of hyper-LDL-cholesterolemia, and a balanced diet and high protein intake can reduce the risk. Lipids in health and disease 2020 Jul 19 (1): 178. Park Sunmin, Kang Su |
Comparison of risk allele frequencies of single nucleotide polymorphisms associated with age-related macular degeneration in different ethnic groups. BMC ophthalmology 2021 2 21 (1): 97. Shin Hyun-Tae, Yoon Byung Woo, Seo Je Hy |
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- Page last updated:Apr 22, 2024
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