Treffer 1 - 20 von 124 für Suche 'Larson, Kathleen G.', Suchdauer: 1,69s Treffer weiter einschränken
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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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    Multiple independent variants at the TERT locus are associated with telomere length and risks of breast and ovarian cancer von Edwards, Stacey L, Lawrenson, Kate, Woods, Nicholas, French, Juliet D, Bolla, Manjeet K, Dennis, Joe, Vincent, Daniel, Rossing, Mary Anne, Doherty, Jennifer A, Larson, Melissa C, Fridley, Brooke L, Peto, Julian, Braaf, Linde M, Andrulis, Irene L, Moysich, Kirsten B, Brenner, Hermann, Brauch, Hiltrud, Hillemanns, Peter, Butzow, Ralf, Bogdanova, Natalia V, Pelttari, Liisa M, Heitz, Florian, Matsuo, Keitaro, du Bois, Andreas, Wu, Anna H, Harter, Philipp, Blot, William, Hosono, Satoyo, Hamann, Ute, Kjaer, Susanne Krüger, Shen, Chen-Yang, Brown, Judith, Luben, Robert, Flyger, Henrik, Vachon, Celine, Gibson, Lorna, Fletcher, Olivia, Poole, Elizabeth M, Tworoger, Shelley S, Bandera, Elisa V, Li, Jingmei, Wauters, Els, Kiemeney, Lambertus A, Hoatlin, Maureen, Zamora, M Pilar, Cook, Linda S, Brooks-Wilson, Angela, Cybulski, Cezary, Henderson, Brian E, Schumacher, Fredrick, Engelholm, Svend Aage, Gore, Martin, Tsimiklis, Helen, Martens, John W M, Flanagan, James M, Whittemore, Alice S, McGuire, Valerie, Gao, Yu-Tang, McLaughlin, John R, Beckmann, Matthias W, Peissel, Bernard, Ashworth, Alan, Ko, Yon-Dschun, Kupryjanczyk, Jolanta, Rzepecka, Iwona K, Hartikainen, Jaana M, Deming-Halverson, Sandra, Lophatananon, Artitaya, Iwata, Hiroji, McKay, James, Piedmonte, Marion, Neuhausen, Susan L, Szabo, Csilla I, Godwin, Andrew K, Campbell, Ian, Rookus, Matti A, Frost, Debra, Fineberg, Elena, Barwell, Julian, Davidson, Rosemarie, Buecher, Bruno, Faivre, Laurence, Caron, Olivier, Giraud, Sophie, Byrski, Tomasz, Bonanni, Bernardo, Giannini, Giuseppe, Dolcetti, Riccardo, Salani, Ritu, Kaulich, Daphne Gschwantler, Laitman, Yael, Jensen, Uffe Birk, Ejlertsen, Bent, Foretova, Lenka, Kuchenbaecker, Karoline B, Cunningham, Julie M, Monteiro, Alvaro N A, Gayther, Simon A, Berchuck, Andrew, Dunning, Alison M

    Veröffentlicht in Nature genetics

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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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