Treffer 1 - 20 von 37 für Suche 'KUNKLE, JAMES R', Suchdauer: 1,53s Treffer weiter einschränken
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    Novel Alzheimer Disease Risk Loci and Pathways in African American Individuals Using the African Genome Resources Panel: A Meta-analysis von Kunkle, Brian W, Schmidt, Michael, Klein, Hans-Ulrich, Naj, Adam C, Hamilton-Nelson, Kara L, Larson, Eric B, Evans, Denis A, De Jager, Phil L, Crane, Paul K, Buxbaum, Joe D, Ertekin-Taner, Nilufer, Barnes, Lisa L, Fallin, M. Daniele, Manly, Jennifer J, Go, Rodney C. P, Obisesan, Thomas O, Kamboh, M. Ilyas, Bennett, David A, Hall, Kathleen S, Goate, Alison M, Foroud, Tatiana M, Martin, Eden R, Wang, Li-San, Byrd, Goldie S, Farrer, Lindsay A, Haines, Jonathan L, Schellenberg, Gerard D, Mayeux, Richard, Pericak-Vance, Margaret A, Reitz, Christiane, Graff-Radford, Neill R, Martinez, Izri, Ayodele, Temitope, Logue, Mark W, Cantwell, Laura B, Jean-Francois, Melissa, Kuzma, Amanda B, Adams, L.D, Vance, Jeffery M, Cuccaro, Michael L, Chung, Jaeyoon, Mez, Jesse, Lunetta, Kathryn L, Jun, Gyungah R, Lopez, Oscar L, Hendrie, Hugh C, Reiman, Eric M, Kowall, Neil W, Leverenz, James B, Small, Scott A, Levey, Allan I, Golde, Todd E, Saykin, Andrew J, Starks, Takiyah D, Albert, Marilyn S, Hyman, Bradley T, Petersen, Ronald C, Sano, Mary, Wisniewski, Thomas, Vassar, Robert, Kaye, Jeffrey A, Henderson, Victor W, DeCarli, Charles, LaFerla, Frank M, Brewer, James B, Miller, Bruce L, Swerdlow, Russell H, Van Eldik, Linda J, Paulson, Henry L, Trojanowski, John Q, Chui, Helena C, Rosenberg, Roger N, Craft, Suzanne, Grabowski, Thomas J, Asthana, Sanjay, Morris, John C, Strittmatter, Stephen M, Kukull, Walter A

    Veröffentlicht in JAMA neurology

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    New insights into the genetic etiology of Alzheimer’s disease and related dementias von Holmans, Peter A., de Rojas, Itziar, Bis, Joshua C., Alarcón-Martín, Emilio, Alcolea, Daniel, Alegret, Montserrat, Alvarez, Ignacio, Álvarez, Victoria, Antúnez, Carmen, Arosio, Beatrice, Athanasiu, Lavinia, Banaj, Nerisa, Below, Jennifer E., Benussi, Luisa, Bossù, Paola, Burholt, Vanessa, Calero, Miguel, Cervera-Carles, Laura, Chen, Hung-Hsin, Custodero, Carlo, de Paiva Lopes, Katia, DeStefano, Anita, Dichgans, Martin, Diehl-Schmid, Janine, Duron, Emmanuelle, Dufouil, Carole, Espinosa, Ana, Nielsen, Sune Fallgaard, Fenoglio, Chiara, Ferrari, Raffaele, Fox, Nick C., Frank-García, Ana, Galimberti, Daniela, Grande, Giulia, Green, Emma, Grünblatt, Edna, Grunin, Michelle, Gudnason, Vilmundur, Hampel, Harald, Hausner, Lucrezia, Hulsman, Marc, Kivipelto, Miia, Kornhuber, Johannes, Kuzma, Amanda B., Launer, Lenore, Ma, Yiyi, Maier, Wolfgang, Montes, Angel Martín, Masullo, Carlo, Mendoza, Silvia, Moebus, Susanne, Morgan, Kevin, Muchnik, Carolina, Mukherjee, Shubhabrata, Nacmias, Benedetta, Ngandu, Tiia, Nicolas, Gael, Nordestgaard, Børge G., Ortega, Gemma, Paolo, Caffarra, Papenberg, Goran, Peloso, Gina, Pérez-Cordón, Alba, Pérez-Tur, Jordi, Pineda, Juan A., Pisanu, Claudia, Polak, Thomas, Quintela, Inés, Rábano, Alberto, Reinders, Marcel J. T., Riedel-Heller, Steffi, Rubino, Elisa, Rujescu, Dan, Sanabria, Ángela, Sánchez-Valle, Raquel, Satizabal, Claudia L., Scarpini, Elio, Scheltens, Philip, Schmid, Matthias, Schneider, Anja, Serrano, Manuel, Solomon, Alina, Song, Yeunjoo, Spalletta, Gianfranco, Squassina, Alessio, Stordal, Eystein, Tartan, Juan Pablo, Tárraga, Lluís, Thomas, Tegos, Tosto, Giuseppe, Wallon, David, Wang, Li-San, Weinhold, Leonie, Wiltfang, Jens, Zare, Habil, Farrer, Lindsay A., Psaty, Bruce M., Williams, Julie, Frikke-Schmidt, Ruth, Deleuze, Jean-François

    Veröffentlicht in Nature genetics

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    Rare coding variants in PLCG2, ABI3, and TREM2 implicate microglial-mediated innate immunity in Alzheimer's disease von Badarinarayan, Nandini, Bis, Joshua C, Heilmann-Heimbach, Stefanie, Sleegers, Kristel, Vronskaya, Maria, White, Charles C, Hamilton-Nelson, Kara L, Choi, Seung-Hoan, Forstner, Andreas J, Bacq, Delphine, Brody, Jennifer A, Wolters, Frank J, Fornage, Myriam, Majounie, Elisa, Wallon, David, Lupton, Michelle K, Jian, Xueqiu, Mukherjee, Shubhabrata, Solfrizzi, Vincenzo, Allen, Mariet, Cupples, L Adrienne, Giegling, Ina, Giedraitis, Vilmantas, Wang, Xue, Mecocci, Patrizia, Eiriksdottir, Gudny, Chen, Yuning, Frosch, Matthew P, Huebinger, Ryan M, Morris, John, Sotolongo-Grau, Oscar, Katz, Mindy J, Braddel, Amy, Chapman, Jade, Hill, Matt, Vellas, Bruno, Soininen, Hilkka, Hughes, Joseph T, Mayhaus, Manuel, Maletta, Raffaele Giovanni, Carrell, David, Pilotto, Alberto, Fox, Nick C, Arnold, Steven E, Becker, James T, Burke, James R, Carlsson, Cynthia M, Clark, David G, Cribbs, David H, Duara, Ranjan, Evans, Denis A, Fallon, Kenneth B, Farlow, Martin R, Foroud, Tatiana M, Galasko, Douglas R, Jin, Lee-Way, Lah, James J, Levey, Allan I, Lieberman, Andrew P, McKee, Ann C, Morris, John C, Paulson, Henry L, Peskind, Elaine, Quinn, Joseph F, Raskind, Murray, Spina, Salvatore, Swerdlow, Russell H, Van Eldik, Linda J, Vinters, Harry V, Vonsattel, Jean Paul, De Deyn, Peter P, Concari, Letizia, Brice, Alexis, Dubois, Bruno, Tschanz, JoAnn, Fitzpatrick, Annette L, Kukull, Walter A, Bullido, María J, Coto, Eliecer, Reiman, Eric M, Gallo, Maura, Scarpini, Elio, Tsuang, Debby W, Bonuccelli, Ubaldo, Rubinsztein, David C, Bras, Jose, Guerreiro, Rita, Lovestone, Simon, Owen, Michael J, Cruchaga, Carlos, Powell, John, De Jager, Philip L, Rujescu, Dan, Ortega-Cubero, Sara, Ikram, M Arfan, Mayeux, Richard, Deleuze, Jean-François, Amin, Najaf, Amouyel, Philippe, van Duijn, Cornelia M

    Veröffentlicht in Nature genetics

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    Genetic and lifestyle risk factors for MRI-defined brain infarcts in a population-based setting von Bis, Joshua C, Smith, Albert Vernon, Saba, Yasaman, Luciano, Michelle, Bastin, Mark E, Lemmens, Robin, Ames, David, Chong, Elizabeth, van der Lugt, Aad, Jimenez-Conde, Jordi, Rundek, Tatjana, Arnett, Donna K, Jern, Christina, Johnson, Julie A, Benavente, Oscar R, Geerlings, Mirjam I, Tzourio, Christophe, Sachdev, Perminder S, Markus, Hugh S, Seshadri, Sudha, Anderson, Christopher D, de Bakker, Paul IW, Engström, Gunnar, Kissela, Brett M, Pera, Joanna, Soriano-Tárraga, Carolina, Stanne, Tara, Nyquist, Paul, Drazyk, Anna, Markus, Hugh, Chasman, Daniel, Elkind, Mitchell, Bijlenga, Philippe, Yue, Suo, Mateen, Farrah, Meschia, James, Pare, Guillaume, Klijn, Karin, Kamatani, Yoichiro, Tregouet, David, Carrera, Caty, Ruigrok, Ynte, Sargurupremraj, Murali, Liebeskind, David, Tan, Rhea, Broderick, Joseph, Sale, Michele, Konrad, Jan, Nordestgaard, Børge G, Psaty, Bruce M, Benn, Marianne, Farrall, Martin, Nalls, Mike, Oliveira, Sofia A, Becker, James T, Carlsson, Cynthia M, Carney, Regina M, Crocco, Elizabeth A, Faber, Kelley M, Farlow, Martin R, Farrer, Lindsay A, Gearing, Marla, Gilbert, John R, Hamilton-Nelson, Kara L, Haroutunian, Vahram, Huebinger, Ryan M, Kukull, Walter A, Lah, James J, Li, Ge, Lunetta, Kathryn L, Mack, Wendy J, Manly, Jennifer J, Masliah, Eliezer, Miller, Carol A, Pierce, Aimee, Potter, Huntington, Raj, Ashok, Sano, Mary, Spina, Salvatore, Tanzi, Rudolph E, Vinters, Harry V, Yu, Chang-En, Yu, Lei, Liu, Yongmei, Johnson, Andrew D, deStefano, Anita L, van Buchem, Mark A, Boerwinkle, Eric, de Craen, Anton J.M, Ibrahim-Verbaas, Carla A, Oostra, Ben A, Cupples, L Adrienne, Meisinger, Christa, Nambi, Vijay, Halperin, Eran, Orru, Marco, Ernst, Florian, Chilukoti, Ravi Kumar, Wilson, James F, Gudnason, Vilmundur

    Veröffentlicht in Neurology

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    Rarity of the Alzheimer Disease–Protective APP A673T Variant in the United States von Wang, Li-San, Kunkle, Brian W, Cruchaga, Carlos, Zetterberg, Henrik, Kukull, Walter A, Norton, Maria C, Munger, Ronald G, Corcoran, Christopher D, Lin, Chiao-Feng, Dombroski, Beth A, Cantwell, Laura B, Partch, Amanda, Valladares, Otto, Green, Robert C, Goate, Alison M, Foroud, Tatiana M, Behrens, Timothy W, Haines, Jonathan L, Farrer, Lindsay A, Pericak-Vance, Margaret A, Mayeux, Richard, Albert, Marilyn S, Albin, Roger L, Apostolova, Liana G, Beach, Thomas G, Becker, James T, Beekly, Duane, Bennett, David A, Blacker, Deborah, Boeve, Bradley F, Bowen, James D, Boxer, Adam, Burke, James R, Cairns, Nigel J, Cao, Chuanhai, Carlson, Chris S, Carroll, Steven L, Cribbs, David H, DeKosky, Steven T, Dickson, Dennis W, Ertekin-Taner, Nilufer, Fallon, Kenneth B, Farlow, Martin R, Frosch, Matthew P, Galasko, Douglas R, Geschwind, Daniel H, Gilbert, John R, Glass, Jonathan D, Graff-Radford, Neill R, Growdon, John H, Hamilton, Ronald L, Harrell, Lindy E, Head, Elizabeth, Honig, Lawrence S, Hyman, Bradley T, Jarvik, Gail P, Jicha, Gregory A, Jin, Lee-Way, Jun, Gyungah, Kamboh, M. Ilyas, Kaye, Jeffrey A, Kowall, Neil W, Kramer, Joel H, Kramer, Patricia, Leverenz, James B, Levey, Allan I, Li, Ge, Marson, Daniel C, Martin, Eden R, Martiniuk, Frank, Masliah, Eliezer, McDavid, Andrew N, Mesulam, M. Marsel, Miller, Joshua W, Morris, John C, Murrell, Jill R, Perry, William, Peskind, Elaine, Petersen, Ronald C, Pierce, Aimee, Potter, Huntington, Quinn, Joseph F, Reisberg, Barry, Reitz, Christiane, Rosenberg, Roger N, Sano, Mary, Saykin, Andrew J, Schneider, Lon S, Seeley, William W, Sonnen, Joshua A, Spina, Salvatore, Trojanowski, John Q, Tsuang, Debby W, Van Eldik, Linda J, Vardarajan, Badri N, Vonsattel, Jean Paul, Weintraub, Sandra, Welsh-Bohmer, Kathleen A, Wishnek, Sarah, Yu, Lei

    Veröffentlicht in JAMA neurology

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