Genome-wide association meta-analysis of neuropathologic features of Alzheimer's disease and related dementias von Beecham, Gary W, Hamilton, Kara, Naj, Adam C, Martin, Eden R, Huentelman, Matt, Myers, Amanda J, Corneveaux, Jason J, Hardy, John, Vonsattel, Jean-Paul, Younkin, Steven G, Bennett, David A, De Jager, Philip L, Larson, Eric B, Crane, Paul K, Kamboh, M Ilyas, Kofler, Julia K, Mash, Deborah C, Duque, Linda, Gilbert, John R, Gwirtsman, Harry, Buxbaum, Joseph D, Kramer, Patricia, Dickson, Dennis W, Farrer, Lindsay A, Frosch, Matthew P, Ghetti, Bernardino, Haines, Jonathan L, Hyman, Bradley T, Kukull, Walter A, Mayeux, Richard P, Pericak-Vance, Margaret A, Schneider, Julie A, Trojanowski, John Q, Reiman, Eric M, Schellenberg, Gerard D, Montine, Thomas J

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Ancestral risk modification for multiple sclerosis susceptibility detected across the Major Histocompatibility Complex in a multi-ethnic population von Beecham, Ashley H, Amezcua, Lilyana, Chinea, Angel, Manrique, Clara P, Gomez, Lissette, Martinez, Andrea, Beecham, Gary W, Patsopoulos, Nikolaos A, Chitnis, Tanuja, Weiner, Howard L, De Jager, Philip L, Burchard, Esteban G, Lund, Brett T, Fitzgerald, Kathryn C, Calabresi, Peter A, Delgado, Silvia R, Oksenberg, Jorge R, McCauley, Jacob L

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A locus at 19q13.31 significantly reduces the ApoE ε4 risk for Alzheimer's Disease in African Ancestry von Rajabli, Farid, Beecham, Gary W, Hendrie, Hugh C, Baiyewu, Olusegun, Ogunniyi, Adesola, Gao, Sujuan, Kushch, Nicholas A, Lipkin-Vasquez, Marina, Hamilton-Nelson, Kara L, Young, Juan I, Dykxhoorn, Derek M, Nuytemans, Karen, Kunkle, Brian W, Wang, Liyong, Jin, Fulai, Liu, Xiaoxiao, Feliciano-Astacio, Briseida E, Schellenberg, Gerard D, Dalgard, Clifton L, Griswold, Anthony J, Byrd, Goldie S, Reitz, Christiane, Cuccaro, Michael L, Haines, Jonathan L, Pericak-Vance, Margaret A, Vance, Jeffery M

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Coronary collateralization shows sex and racial-ethnic differences in obstructive artery disease patients von Liu, Zhi, Pericak-Vance, Margaret A, Goldschmidt-Clermont, Pascal, Seo, David, Wang, Liyong, Rundek, Tatjana, Beecham, Gary W

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Properties of global‐ and local‐ancestry adjustments in genetic association tests in admixed populations von Martin, Eden R., Tunc, Ilker, Liu, Zhi, Slifer, Susan H., Beecham, Ashley H., Beecham, Gary W.

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Genome-wide Association Study Implicates a Chromosome 12 Risk Locus for Late-Onset Alzheimer Disease von Beecham, Gary W., Martin, Eden R., Li, Yi-Ju, Slifer, Michael A., Gilbert, John R., Haines, Jonathan L., Pericak-Vance, Margaret A.

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Meta-analysis of Parkinson's Disease: Identification of a novel locus, RIT2 von Pankratz, Nathan, Beecham, Gary W., DeStefano, Anita L., Dawson, Ted M., Doheny, Kimberly F., Factor, Stewart A., Hamza, Taye H., Hung, Albert Y., Hyman, Bradley T., Ivinson, Adrian J., Krainc, Dmitri, Latourelle, Jeanne C., Clark, Lorraine N., Marder, Karen, Martin, Eden R., Mayeux, Richard, Ross, Owen A., Scherzer, Clemens R., Simon, David K., Tanner, Caroline, Vance, Jeffery M., Wszolek, Zbigniew K., Zabetian, Cyrus P., Myers, Richard H., Payami, Haydeh, Scott, William K., Foroud, Tatiana

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Genome‐Wide Association Study Confirms SNPs in SNCA and the MAPT Region as Common Risk Factors for Parkinson Disease von Edwards, Todd L., Scott, William K., Almonte, Cherylyn, Burt, Amber, Powell, Eric H., Beecham, Gary W., Wang, Liyong, Züchner, Stephan, Konidari, Ioanna, Wang, Gaofeng, Singer, Carlos, Nahab, Fatta, Scott, Burton, Stajich, Jeffrey M., Pericak‐Vance, Margaret, Haines, Jonathan, Vance, Jeffery M., Martin, Eden R.

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Notch activation induces endothelial cell senescence and pro-inflammatory response: Implication of Notch signaling in atherosclerosis von Liu, Zhao-Jun, Tan, Yurong, Beecham, Gary W, Seo, David M, Tian, Runxia, Li, Yan, Vazquez-Padron, Roberto I, Pericak-Vance, Margaret, Vance, Jeffery M, Goldschmidt-Clermont, Pascal J, Livingstone, Alan S, Velazquez, Omaida C

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Late-onset vs nonmendelian early-onset Alzheimer disease: A distinction without a difference? von Reitz, Christiane, Rogaeva, Ekaterina, Beecham, Gary W.

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Dementia revealed: novel chromosome 6 locus for late-onset Alzheimer disease provides genetic evidence for folate-pathway abnormalities von Naj, Adam C, Beecham, Gary W, Martin, Eden R, Gallins, Paul J, Powell, Eric H, Konidari, Ioanna, Whitehead, Patrice L, Cai, Guiqing, Haroutunian, Vahram, Scott, William K, Vance, Jeffery M, Slifer, Michael A, Gwirtsman, Harry E, Gilbert, John R, Haines, Jonathan L, Buxbaum, Joseph D, Pericak-Vance, Margaret A

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Identifying consensus disease pathways in Parkinson's disease using an integrative systems biology approach von Edwards, Yvonne J K, Beecham, Gary W, Scott, William K, Khuri, Sawsan, Bademci, Guney, Tekin, Demet, Martin, Eden R, Jiang, Zhijie, Mash, Deborah C, ffrench-Mullen, Jarlath, Pericak-Vance, Margaret A, Tsinoremas, Nicholas, Vance, Jeffery M

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Comparison of three targeted enrichment strategies on the SOLiD sequencing platform von Hedges, Dale J, Guettouche, Toumy, Yang, Shan, Bademci, Guney, Diaz, Ashley, Andersen, Ashley, Hulme, William F, Linker, Sara, Mehta, Arpit, Edwards, Yvonne J K, Beecham, Gary W, Martin, Eden R, Pericak-Vance, Margaret A, Zuchner, Stephan, Vance, Jeffery M, Gilbert, John R

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Disentangling the genetic underpinnings of neuropsychiatric symptoms in Alzheimer's disease in the Alzheimer's Disease Sequencing Project: Study design and methodology von Ray, Nicholas R., Kumar, Ajneesh, Zaman, Andrew, Rosario, Pamela, Mena, Pedro R., Manoochehri, Masood, Stein, Colin, De Vito, Alyssa N., Sweet, Robert A., Hohman, Timothy J., Cuccaro, Michael L., Beecham, Gary W., Huey, Edward D., Reitz, Christiane

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Haplotype-specific modulation of a SOX10/CREB response element at the Charcot-Marie-Tooth disease type 4C locus SH3TC2 von Brewer, Megan Hwa, Ma, Ki Hwan, Beecham, Gary W, Gopinath, Chetna, Baas, Frank, Choi, Byung-Ok, Reilly, Mary M, Shy, Michael E, Züchner, Stephan, Svaren, John, Antonellis, Anthony

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Meta-analysis of 74,046 individuals identifies 11 new susceptibility loci for Alzheimer's disease von Lambert, Jean-Charles, Ibrahim-Verbaas, Carla A, Naj, Adam C, Sims, Rebecca, Bellenguez, Céline, DeStefano, Anita L, Bis, Joshua C, Grenier-Boley, Benjamin, Russo, Giancarlo, Thornton-Wells, Tricia A, Chouraki, Vincent, Zelenika, Diana, Vardarajan, Badri N, Lin, Chiao-Feng, Gerrish, Amy, Schmidt, Helena, Pasquier, Florence, Hollingworth, Paul, Ramirez, Alfredo, Fitzpatrick, Annette L, Buxbaum, Joseph D, Crane, Paul K, Gudnason, Vilmundur, Cruchaga, Carlos, Craig, David, Amin, Najaf, De Jager, Philip L, Deramecourt, Vincent, Johnston, Janet A, Letenneur, Luc, Morón, Francisco J, Kamboh, M Ilyas, Keller, Lina, Barberger-Gateau, Pascale, McGuinness, Bernadette, Larson, Eric B, Green, Robert, Dufouil, Carole, Wallon, David, Love, Seth, St George-Hyslop, Peter, Clarimon, Jordi, Lleo, Alberto, Tsuang, Debby W, Yu, Lei, Bossù, Paola, Proitsi, Petroula, Sorbi, Sandro, Hardy, John, Naranjo, Maria Candida Deniz, Clarke, Robert, Brayne, Carol, Galimberti, Daniela, Mancuso, Michelangelo, Matthews, Fiona, Hampel, Harald, Pilotto, Alberto, Panza, Francesco, Caffarra, Paolo, Gilbert, John R, Mayhaus, Manuel, Lannfelt, Lars, Pichler, Sabrina, Carrasquillo, Minerva M, Alvarez, Victoria, Valladares, Otto, Younkin, Steven G, Coto, Eliecer, Razquin, Cristina, Pastor, Pau, Mateo, Ignacio, O'Donovan, Michael C, Cantwell, Laura B, Blacker, Deborah, Mosley, Thomas H, Bennett, David A, Harris, Tamara B, Holmes, Clive, Passmore, Peter, Montine, Thomas J, Bettens, Karolien, Rotter, Jerome I, Brice, Alexis, Morgan, Kevin, Lunetta, Kathryn L, Kauwe, John S K, Boerwinkle, Eric, Hiltunen, Mikko, Rujescu, Dan, Mayeux, Richard, Hofman, Albert, Graff, Caroline, Psaty, Bruce M, Farrer, Lindsay A, van Duijn, Cornelia M, Van Broeckhoven, Christine, Moskvina, Valentina, Seshadri, Sudha, Williams, Julie, Amouyel, Philippe

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The executive prominent / memory prominent spectrum in Alzheimer’s disease is highly heritable von Mez, Jesse, MD MS, Mukherjee, Shubhabrata, PhD, Thornton, Timothy, PhD, Fardo, David W., PhD, Trittschuh, Emily, PhD, Sutti, Sheila, MS, Sherva, Richard, PhD, Kauwe, John S., PhD, Naj, Adam C., PhD, Beecham, Gary W., PhD, Gross, Alden, PhD, Saykin, Andrew J., PsyD, Green, Robert C., MD MPH, Crane, Paul K., MD MPH

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Exome sequencing identifies rare damaging variants in ATP8B4 and ABCA1 as risk factors for Alzheimer’s disease von Holstege, Henne, Hulsman, Marc, Charbonnier, Camille, Grenier-Boley, Benjamin, Quenez, Olivier, Grozeva, Detelina, van Rooij, Jeroen G. J., Sims, Rebecca, Ahmad, Shahzad, Amin, Najaf, Norsworthy, Penny J., Dols-Icardo, Oriol, Hummerich, Holger, Kawalia, Amit, Amouyel, Philippe, Beecham, Gary W., Berr, Claudine, Bis, Joshua C., Boland, Anne, Bossù, Paola, Bouwman, Femke, Bras, Jose, Campion, Dominique, Cochran, J. Nicholas, Dartigues, Jean-François, Debette, Stéphanie, Deleuze, Jean-François, Denning, Nicola, DeStefano, Anita L., Farrer, Lindsay A., Fox, Nick C., Galimberti, Daniela, Gille, Johan J. P., Le Guen, Yann, Guerreiro, Rita, Haines, Jonathan L., Holmes, Clive, Ikram, M. Arfan, Ikram, M. Kamran, Jansen, Iris E., Kraaij, Robert, Lathrop, Marc, Lemstra, Afina W., Lleó, Alberto, Luckcuck, Lauren, Mannens, Marcel M. A. M., Marshall, Rachel, Martin, Eden R., Masullo, Carlo, Mayeux, Richard, Mecocci, Patrizia, Meggy, Alun, Mol, Merel O., Morgan, Kevin, Myers, Richard M., Nacmias, Benedetta, Naj, Adam C., Napolioni, Valerio, Pasquier, Florence, Pastor, Pau, Pericak-Vance, Margaret A., Raybould, Rachel, Redon, Richard, Reinders, Marcel J. T., Riedel-Heller, Steffi G., Rivadeneira, Fernando, Rousseau, Stéphane, Ryan, Natalie S., Saad, Salha, Sanchez-Juan, Pascual, Schellenberg, Gerard D., Scheltens, Philip, Schott, Jonathan M., Seripa, Davide, Seshadri, Sudha, Sie, Daoud, Sistermans, Erik A., Spalletta, Gianfranco, Tesi, Niccolo’, Tijms, Betty, Uitterlinden, André G., van der Lee, Sven J., Visser, Pieter Jelle, Wagner, Michael, Wallon, David, Wang, Li-San, Zarea, Aline, Clarimon, Jordi, van Swieten, John C., Greicius, Michael D., Yokoyama, Jennifer S., Hardy, John, Ramirez, Alfredo, Mead, Simon, van der Flier, Wiesje M., van Duijn, Cornelia M., Williams, Julie, Nicolas, Gaël, Bellenguez, Céline, Lambert, Jean-Charles

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Ancestral origin of ApoE ε4 Alzheimer disease risk in Puerto Rican and African American populations von Rajabli, Farid, Feliciano, Briseida E, Celis, Katrina, Hamilton-Nelson, Kara L, Whitehead, Patrice L, Adams, Larry D, Bussies, Parker L, Manrique, Clara P, Rodriguez, Alejandra, Rodriguez, Vanessa, Starks, Takiyah, Byfield, Grace E, Sierra Lopez, Carolina B, McCauley, Jacob L, Acosta, Heriberto, Chinea, Angel, Kunkle, Brian W, Reitz, Christiane, Farrer, Lindsay A, Schellenberg, Gerard D, Vardarajan, Badri N, Vance, Jeffery M, Cuccaro, Michael L, Martin, Eden R, Haines, Jonathan L, Byrd, Goldie S, Beecham, Gary W, Pericak-Vance, Margaret A

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The Puerto Rico Alzheimer Disease Initiative (PRADI): A Multisource Ascertainment Approach von Feliciano-Astacio, Briseida E, Celis, Katrina, Ramos, Jairo, Rajabli, Farid, Adams, Larry Deon, Rodriguez, Alejandra, Rodriguez, Vanessa, Bussies, Parker L, Sierra, Carolina, Manrique, Patricia, Mena, Pedro R, Grana, Antonella, Prough, Michael, Hamilton-Nelson, Kara L, Feliciano, Nereida, Chinea, Angel, Acosta, Heriberto, McCauley, Jacob L, Vance, Jeffery M, Beecham, Gary W, Pericak-Vance, Margaret A, Cuccaro, Michael L

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