Human Genome Epidemiology Literature Finder
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Records 1 - 6 (of 6 Records) |
| Query Trace: Alzheimer Disease and MS4A4A[original query] |
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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 |
| Novel late-onset Alzheimer disease loci variants associate with brain gene expression. Neurology 2012 Jul 79 (3): 221-8. Allen Mariet, Zou Fanggeng, Chai High Seng, Younkin Curtis S, Crook Julia, Pankratz V Shane, Carrasquillo Minerva M, Rowley Christopher N, Nair Asha A, Middha Sumit, Maharjan Sooraj, Nguyen Thuy, Ma Li, Malphrus Kimberly G, Palusak Ryan, Lincoln Sarah, Bisceglio Gina, Georgescu Constantin, Schultz Debra, Rakhshan Fariborz, Kolbert Christopher P, Jen Jin, Haines Jonathan L, Mayeux Richard, Pericak-Vance Margaret A, Farrer Lindsay A, Schellenberg Gerard D, Petersen Ronald C, Graff-Radford Neill R, Dickson Dennis W, Younkin Steven G, Ertekin-Taner Nilüfer, , Apostolova Liana G, Arnold Steven E, Baldwin Clinton T, Barber Robert, Barmada Michael M, Beach Thomas, Beecham Gary W, Beekly Duane, Bennett David A, Bigio Eileen H, Bird Thomas D, Blacker Deborah, Boeve Bradley F, Bowen James D, Boxer Adam, Burke James R, Buros Jacqueline, Buxbaum Joseph D, Cairns Nigel J, Cantwell Laura B, Cao Chuanhai, Carlson Chris S, Carney Regina M, Carroll Steven L, Chui Helena C, Clark David G, Corneveaux Jason, Cotman Carl W, Crane Paul K, Cruchaga Carlos, Cummings Jeffrey L, De Jager Philip L, DeCarli Charles, DeKosky Steven T, Demirci F Yesim, Diaz-Arrastia Ramon, Dick Malcolm, Dombroski Beth A, Duara Ranjan, Ellis William D, Evans Denis, Faber Kelley M, Fallon Kenneth B, Farlow Martin R, Ferris Steven, Foroud Tatiana M, Frosch Matthew, Galasko Douglas R, Gallins Paul J, Ganguli Mary, Gearing Marla, Geschwind Daniel H, Ghetti Bernardino, Gilbert John R, Gilman Sid, Giordani Bruno, Glass Jonathan D, Goate Alison M, Green Robert C, Growdon John H, Hakonarson Hakon, Hamilton Ronald L, Hardy John, Harrell Lindy E, Head Elizabeth, Honig Lawrence S, Huentelman Matthew J, Hulette Christine M, Hyman Bradley T, Jarvik Gail P, Jicha Gregory A, Jin Lee-Way, Jun Gyungah, Kamboh M Ilyas, Karlawish Jason, Karydas Anna, Kauwe John S K, Kaye Jeffrey A, Kennedy Nancy, Kim Ronald, Koo Edward H, Kowall Neil W, Kramer Patricia, Kukull Walter A, Lah James J, Larson Eric B, Levey Allan I, Lieberman Andrew P, Lopez Oscar L, Lunetta Kathryn L, Mack Wendy J, Marson Daniel C, Martin Eden R, 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, Montine Thomas J, Morris John C, Myers Amanda J, Naj Adam C, Nowotny Petra, Parisi Joseph E, Perl Daniel P, Peskind Elaine, Poon Wayne W, Potter Huntington, Quinn Joseph F, Raj Ashok, Rajbhandary Ruchita A, Raskind Murray, Reiman Eric M, Reisberg Barry, Reitz Christiane, Ringman John M, Roberson Erik D, Rogaeva Ekaterina, Rosenberg Roger N, Sano Mary, Saykin Andrew J, Schneider Julie A, Schneider Lon S, Seeley William, Shelanski Michael L, Slifer Michael A, Smith Charles D, Sonnen Joshua A, Spina Salvatore, St George-Hyslop Peter, Stern Robert A, Tanzi Rudolph E, Trojanowski John Q, Troncoso Juan C, Tsuang Debby W, Van Deerlin Vivianna M, Vardarajan Badri Narayan, Vinters Harry V, Vonsattel Jean Paul, Wang Li-San, Weintraub Sandra, Welsh-Bohmer Kathleen A, Williamson Jennifer, Woltjer Randall |
| Rare coding mutations identified by sequencing of Alzheimer disease genome-wide association studies loci. Annals of neurology 2015 Sep 78 (3): 487-98. Vardarajan Badri N, Ghani Mahdi, Kahn Amanda, Sheikh Stephanie, Sato Christine, Barral Sandra, Lee Joseph H, Cheng Rong, Reitz Christiane, Lantigua Rafael, Reyes-Dumeyer Dolly, Medrano Martin, Jimenez-Velazquez Ivonne Z, Rogaeva Ekaterina, St George-Hyslop Peter, Mayeux Richa |
| 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 |
| CpG-related SNPs in the MS4A region have a dose-dependent effect on risk of late-onset Alzheimer disease. Aging cell 2019 May e12964. Ma Yiyi, Jun Gyungah R, Chung Jaeyoon, Zhang Xiaoling, Kunkle Brian W, Naj Adam C, White Charles C, Bennett David A, De Jager Philip L, , Mayeux Richard, Haines Jonathan L, Pericak-Vance Margaret A, Schellenberg Gerard D, Farrer Lindsay A, Lunetta Kathryn |
| African Americans Have Differences in CSF Soluble TREM2 and Associated Genetic Variants. Neurology. Genetics 2021 Apr 7 (2): e571. Schindler Suzanne E, Cruchaga Carlos, Joseph Amulya, McCue Lena, Farias Fabiana H G, Wilkins Consuelo H, Deming Yuetiva, Henson Rachel L, Mikesell Robert J, Piccio Laura, Llibre-Guerra Jorge J, Moulder Krista L, Fagan Anne M, Ances Beau M, Benzinger Tammie L S, Xiong Chengjie, Holtzman David M, Morris John |
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