Severe acute neurotoxicity reflects absolute intra-carotid 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine dose in non-human primates by Norris, SA, White, HCB, Tanenbaum, A., Williams, EL, Cruchaga, C., Tian, L., Schmidt, RE, Perlmutter, JS

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CXCR4 involvement in neurodegenerative diseases by Bonham, Luke W., Karch, Celeste M., Fan, Chun C., Tan, Chin, Geier, Ethan G., Wang, Yunpeng, Wen, Natalie, Broce, Iris J., Li, Yi, Barkovich, Matthew J., Ferrari, Raffaele, Hardy, John, Momeni, Parastoo, Höglinger, Günter, Müller, Ulrich, Hess, Christopher P., Sugrue, Leo P., Dillon, William P., Schellenberg, Gerard D., Miller, Bruce L., Andreassen, Ole A., Dale, Anders M., Barkovich, A. James, Yokoyama, Jennifer S., Desikan, Rahul S.

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Susceptible genes and disease mechanisms identified in frontotemporal dementia and frontotemporal dementia with Amyotrophic Lateral Sclerosis by DNA-methylation and GWAS by Taskesen, E., Mishra, A., van der Sluis, S., Ferrari, R., Veldink, J. H., van Es, M. A., Smit, A. B., Posthuma, D., Pijnenburg, Y.

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Genetic variation across RNA metabolism and cell death gene networks is implicated in the semantic variant of primary progressive aphasia by Bonham, Luke W., Steele, Natasha Z. R., Karch, Celeste M., Broce, Iris, Geier, Ethan G., Wen, Natalie L., Momeni, Parastoo, Hardy, John, Miller, Zachary A., Gorno-Tempini, Maria Luisa, Hess, Christopher P., Lewis, Patrick, Miller, Bruce L., Seeley, William W., Manzoni, Claudia, Desikan, Rahul S., Baranzini, Sergio E., Ferrari, Raffaele, Yokoyama, Jennifer S.

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Pick a PACC: Comparing Domain-Specific and General Cognitive Composites in Alzheimer Disease Research by McKay, Nicole S., Millar, Peter R., Nicosia, Jessica, Aschenbrenner, Andrew J., Gordon, Brian A., Benzinger, Tammie L. S., Cruchaga, Carolos C., Schindler, Suzanne E., Morris, John C., Hassenstab, Jason

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Author Correction: Susceptible genes and disease mechanisms identified in frontotemporal dementia and frontotemporal dementia with Amyotrophic Lateral Sclerosis by DNA-methylation... by Taskesen, E., Mishra, A., van der Sluis, S., Ferrari, R., Veldink, J. H., van Es, M. A., Smit, A. B., Posthuma, D., Pijnenburg, Y.

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Suggestive synergy between genetic variants in TF and HFE as risk factors for Alzheimer's disease by Kauwe, J.S.K., Bertelsen, S., Mayo, K., Cruchaga, C., Abraham, R., Hollingworth, P., Harold, D., Owen, M.J., Williams, J., Lovestone, S., Morris, J.C., Goate, A.M.

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EMF-3 Genetic Architecture of Human Ischemic Stroke by Heitsch, L, Guilliams, K, Ford, A, Khoury, N, Connor, L, Cruchaga, C, Lee, J.-M

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The MS4A gene cluster is a key modulator of soluble TREM2 and Alzheimer's disease risk by Deming, Yuetiva, Filipello, Fabia, Cignarella, Francesca, Cantoni, Claudia, Hsu, Simon, Mikesell, Robert, Li, Zeran, Del-Aguila, Jorge L, Dube, Umber, Farias, Fabiana Geraldo, Bradley, Joseph, Budde, John, Ibanez, Laura, Fernandez, Maria Victoria, Blennow, Kaj, Zetterberg, Henrik, Heslegrave, Amanda, Johansson, Per M, Svensson, Johan, Nellgård, Bengt, Lleo, Alberto, Alcolea, Daniel, Clarimon, Jordi, Rami, Lorena, Molinuevo, José Luis, Suárez-Calvet, Marc, Morenas-Rodríguez, Estrella, Kleinberger, Gernot, Ewers, Michael, Harari, Oscar, Haass, Christian, Brett, Thomas J, Benitez, Bruno A, Karch, Celeste M, Piccio, Laura, Cruchaga, Carlos

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Stroke genetics informs drug discovery and risk prediction across ancestries by Jürgenson, Tuuli, Namba, Shinichi, Posner, Daniel C., Kamanu, Frederick K., Koido, Masaru, He, Yunye, Caro, Ilana, Krebs, Kristi, Liaw, Yi-Ching, Parodi, Livia, Bae, Hee-Joon, Chong, Michael R., Tomppo, Liisa, Akinyemi, Rufus, Roshchupkin, Gennady V., Habib, Naomi, Jee, Yon Ho, Thomassen, Jesper Qvist, Abedi, Vida, Cárcel-Márquez, Jara, Nygaard, Marianne, Yonova-Doing, Ekaterina, Knol, Maria J., Lewis, Adam J., Judy, Renae L., Amouyel, Philippe, Bakker, Mark K., Bennett, David A., Bis, Joshua C., Bordes, Constance, Børte, Sigrid, Cain, Anael, Ridker, Paul M., Cho, Kelly, Chen, Zhengming, Cruchaga, Carlos, Cole, John W., de Cid, Rafael, Ferreira, Leslie E., He, Jing, Jeon, Christina E., Jern, Christina, Kamouchi, Masahiro, Keene, Keith L., Konuma, Takahiro, Kumar, Amit, Launer, Lenore J., Lee, Keon-Joo, Li, Jiang, Li, Liming, Manichaikul, Ani, Markus, Hugh S., Meitinger, Thomas, Mitchell, Braxton D., Morisaki, Takayuki, O’Donnell, Martin J., Onland-Moret, N. Charlotte, Ovbiagele, Bruce, Peters, Annette, Rosand, Jonathan, Sabatine, Marc S., Sacco, Ralph L., Saleheen, Danish, Schmidt, Carsten O., Smith, Nicholas L., Sloane, Kelly L., Sutoh, Yoichi, Tiwari, Hemant K., Wennberg, Patrik, Wilson, Peter W. F., Yang, Qiong, Yoon, Kyungheon, Gieger, Christian, Ninomiya, Toshiharu, Grabe, Hans J., Jukema, J. Wouter, Kim, Young Jin, Chen, Pei-Hsin, Mayerhofer, Ernst, Ikram, Mohammad A., Worrall, Bradford B., Lathrop, G. Mark, Riaz, Moeen, Simonsick, Eleanor M., Kõrv, Janika, Zand, Ramin, Prasad, Kameshwar, Frikke-Schmidt, Ruth, Liman, Thomas, Ruigrok, Ynte M., Bastarache, Lisa, Damrauer, Scott M., Rotter, Jerome I., Niiranen, Teemu J., Walters, Robin G., Owolabi, Mayowa O., Huffman, Jennifer E., Kamatani, Yoichiro, Dichgans, Martin, Debette, Stephanie

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Whole exome sequencing study identifies novel rare and common Alzheimer’s-Associated variants involved in immune response and transcriptional regulation by Bis, Joshua C., Jian, Xueqiu, Kunkle, Brian W., Chen, Yuning, Hamilton-Nelson, Kara L., Bush, William S., Salerno, William J., Lancour, Daniel, Ma, Yiyi, Renton, Alan E., Marcora, Edoardo, Farrell, John J., Zhao, Yi, Qu, Liming, Ahmad, Shahzad, Amin, Najaf, Amouyel, Philippe, Beecham, Gary W., Below, Jennifer E., Campion, Dominique, Cantwell, Laura, Charbonnier, Camille, Chung, Jaeyoon, Crane, Paul K., Cruchaga, Carlos, Cupples, L. Adrienne, Dartigues, Jean-François, Debette, Stéphanie, Deleuze, Jean-François, Fulton, Lucinda, Gabriel, Stacey B., Genin, Emmanuelle, Gibbs, Richard A., Goate, Alison, Grenier-Boley, Benjamin, Gupta, Namrata, Haines, Jonathan L., Havulinna, Aki S., Helisalmi, Seppo, Hiltunen, Mikko, Howrigan, Daniel P., Ikram, M. Arfan, Kaprio, Jaakko, Konrad, Jan, Kuzma, Amanda, Lander, Eric S., Lathrop, Mark, Lehtimäki, Terho, Lin, Honghuang, Mattila, Kari, Mayeux, Richard, Muzny, Donna M., Nasser, Waleed, Neale, Benjamin, Nho, Kwangsik, Nicolas, Gaël, Patel, Devanshi, Pericak-Vance, Margaret A., Perola, Markus, Psaty, Bruce M., Quenez, Olivier, Rajabli, Farid, Redon, Richard, Reitz, Christiane, Remes, Anne M., Salomaa, Veikko, Sarnowski, Chloe, Schmidt, Helena, Schmidt, Michael, Schmidt, Reinhold, Soininen, Hilkka, Thornton, Timothy A., Tosto, Giuseppe, Tzourio, Christophe, van der Lee, Sven J., van Duijn, Cornelia M., Valladares, Otto, Vardarajan, Badri, Wang, Li-San, Wang, Weixin, Wijsman, Ellen, Wilson, Richard K., Witten, Daniela, Worley, Kim C., Zhang, Xiaoling, Bellenguez, Celine, Lambert, Jean-Charles, Kurki, Mitja I., Palotie, Aarno, Daly, Mark, Boerwinkle, Eric, Lunetta, Kathryn L., Destefano, Anita L., Dupuis, Josée, Martin, Eden R., Schellenberg, Gerard D., Seshadri, Sudha, Naj, Adam C., Fornage, Myriam, Farrer, Lindsay A.

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GWAS and colocalization analyses implicate carotid intima-media thickness and carotid plaque loci in cardiovascular outcomes by Franceschini, Nora, Giambartolomei, Claudia, de Vries, Paul S., Bis, Joshua C., Winkler, Thomas W., Graff, Misa, Kavousi, Maryam, Dale, Caroline, Hofer, Edith, van Leeuwen, Elisabeth M., Nolte, Ilja M., Lu, Lingyi, Pitkänen, Niina, Franzén, Oscar, Hwang, Shih-Jen, Musani, Solomon K., Schminke, Ulf, Palmas, Walter, Isaacs, Aaron, Correa, Adolfo, Zonderman, Alan B., Uitterlinden, André G., Wong, Andrew, Britton, Annie, Ruusalepp, Arno, Sennblad, Bengt, Hedblad, Bo, Pasaniuc, Bogdan, Penninx, Brenda W., Tzourio, Christophe, Fava, Cristiano, Baldassarre, Damiano, O’Leary, Daniel H., Tremoli, Elena, Schadt, Eric E., Ingelsson, Erik, Veglia, Fabrizio, Rivadeneira, Fernando, Beutner, Frank, Chauhan, Ganesh, Heiss, Gerardo, Snieder, Harold, Völzke, Henry, Markus, Hugh S., Deary, Ian J., Price, Jacqueline, Hopewell, Jemma C., Thiery, Joachim, Engmann, Jorgen, Rice, Kenneth, Taylor, Kent D., Dhana, Klodian, Lind, Lars, Holdt, Lesca M., Dörr, Marcus, Dichgans, Martin, Kivimaki, Mika, Melander, Olle, Raitakari, Olli, Franco, Oscar H., Rueda-Ochoa, Oscar L., Roussos, Panos, Whincup, Peter H., Giral, Philippe, Rauramaa, Rainer, Burkhardt, Ralph, Wannamethee, S. Goya, McLachlan, Stela, Trompet, Stella, Seshadri, Sudha, Kurl, Sudhir, Ring, Susan, Harris, Tamara B., Lehtimäki, Terho, Galesloot, Tessel E., Shah, Tina, Plagnol, Vincent, Rosamond, Wayne D., Post, Wendy, Zhu, Xiaofeng, Dehghan, Abbas, Seldenrijk, Adrie, Morrison, Alanna C., Hamsten, Anders, Psaty, Bruce M., Lawlor, Deborah A., Schmidt, Helena, Wilson, James F., Rotter, Jerome I., Wardlaw, Joanna M., Deanfield, John, Loeffler, Markus, Debette, Stéphanie, Humphries, Steve E., Völker, Uwe, Gudnason, Vilmundur, Hingorani, Aroon D., Björkegren, Johan L. M., Casas, Juan P., O’Donnell, Christopher J.

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A novel Alzheimer disease locus located near the gene encoding tau protein by Jun, G, Ibrahim-Verbaas, C A, Vronskaya, M, Chung, J, Naj, A C, Kunkle, B W, Wang, L-S, Bis, J C, Bellenguez, C, Harold, D, Destefano, A L, Grenier-Boley, B, Sims, R, Smith, A V, Chouraki, V, Hamilton-Nelson, K L, Ikram, M A, Fievet, N, Martin, E R, Kamatani, Y, Valladares, O, Laza, A R, Zelenika, D, 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, 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, Dartigues, J-F, Hampel, H, de Bruijn, R F A G, Tzourio, C, Pastor, P, Larson, E B, O'Donovan, M C, Montine, T J, Nalls, M A, Mead, S, Reiman, E M, Jonsson, P V, St George-Hyslop, P H, Boada, M, Passmore, P, Wendland, J R, Schmidt, R, Morgan, K, Powell, J F, Carasquillo, M, Jakobsdóttir, J, Kauwe, J S K, 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, 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 A

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Genome-wide meta-analysis for Alzheimer’s disease cerebrospinal fluid biomarkers by Jansen, Iris E., van der Lee, Sven J., Gomez-Fonseca, Duber, de Rojas, Itziar, Zettergren, Anna, Mishra, Aniket, Bellenguez, Céline, Kleineidam, Luca, Küçükali, Fahri, Tesí, Niccolo, Vromen, Ellen M., Alvarez, Ignacio, Amouyel, Philippe, Athanasiu, Lavinia, Belbin, Olivia, Bergh, Sverre, Blennow, Kaj, Blesa, Rafael, Boada, Mercè, Boland, Anne, Buerger, Katharina, Carracedo, Ángel, Chene, Geneviève, Debette, Stephanie, Deleuze, Jean-Francois, Dols-Icardo, Oriol, Dufouil, Carole, Duron, Emmanuelle, Fladby, Tormod, Frölich, Lutz, Garcia-Martinez, Maria, Gobom, Johan, Grimmer, Timo, Haapasalo, Annakaisa, Hampel, Harald, Hanon, Olivier, Hausner, Lucrezia, Heilmann-Heimbach, Stefanie, Helisalmi, Seppo, Hernández, Isabel, Herukka, Sanna-Kaisa, Holstege, Henne, Jarholm, Jonas, Koivisto, Anne M., Kornhuber, Johannes, Kuulasmaa, Teemu, Lage, Carmen, Laske, Christoph, Leinonen, Ville, Lewczuk, Piotr, Lleó, Alberto, Lopez-Garcia, Sara, Marquié, Marta, Mol, Merel O., Montrreal, Laura, Moreno, Fermin, Moreno-Grau, Sonia, Nicolas, Gael, Orellana, Adelina, Peters, Oliver, Pijnenburg, Yolande A. L., Popp, Julius, Priller, Josef, Puerta, Raquel, Quintela, Inés, Ramakers, Inez, Rodriguez-Rodriguez, Eloy, Saltvedt, Ingvild, Sanchez-Juan, Pascual, Scheltens, Philip, Scherbaum, Norbert, Schmid, Matthias, Selbæk, Geir, Shadrin, Alexey, Skoog, Ingmar, Soininen, Hilkka, Tárraga, Lluís, Tijms, Betty, Tsolaki, Magda, Van Broeckhoven, Christine, Van Dongen, Jasper, van Swieten, John C., Vandenberghe, Rik, Visser, Pieter J., Wagner, Michael, Wiltfang, Jens, Zetterberg, Henrik, Zulaica, Miren, van Duijn, Cornelia M., Engelborghs, Sebastiaan, Pastor, Pau, Hiltunen, Mikko, Ingelsson, Martin, Andreassen, Ole A., Clarimón, Jordi, Sleegers, Kristel, Ruiz, Agustín, Ramirez, Alfredo, Cruchaga, Carlos, Lambert, Jean-Charles

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Caspase-8, association with Alzheimer's Disease and functional analysis of rare variants by Rehker, Jan, Rodhe, Johanna, Nesbitt, Ryan R, Boyle, Evan A, Martin, Beth K, Lord, Jenny, Karaca, Ilker, Naj, Adam, Jessen, Frank, Helisalmi, Seppo, Soininen, Hilkka, Hiltunen, Mikko, Ramirez, Alfredo, Scherer, Martin, Farrer, Lindsay A, Haines, Jonathan L, Pericak-Vance, Margaret A, Raskind, Wendy H, Cruchaga, Carlos, Schellenberg, Gerard D, Joseph, Bertrand, Brkanac, Zoran

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Early Neurological Change After Ischemic Stroke Is Associated With 90-Day Outcome by Heitsch, Laura, Ibanez, Laura, Carrera, Caty, Binkley, Michael M., Strbian, Daniel, Tatlisumak, Turgut, Bustamante, Alejandro, Ribó, Marc, Molina, Carlos, Dávalos, Antoni, López-Cancio, Elena, Muñoz-Narbona, Lucia, Soriano-Tárraga, Carol, Giralt-Steinhauer, Eva, Obach, Victor, Slowik, Agnieszka, Pera, Joanna, Lapicka-Bodzioch, Katarzyna, Derbisz, Justyna, Sobrino, Tomás, Castillo, José, Campos, Francisco, Rodríguez-Castro, Emilio, Arias-Rivas, Susana, Segura, Tomas, Serrano-Heras, Gemma, Vives-Bauza, Cristófol, Díaz-Navarro, Rosa, Tur, Silva, Jimenez, Carmen, Martí-Fàbregas, Joan, Delgado-Mederos, Raquel, Arenillas, Juan, Krupinski, Jerzy, Cullell, Natalia, Torres-Aguila, Nuria P., Muiño, Elena, Cárcel-Márquez, Jara, Moniche, Francisco, Cabezas, Juan A., Ford, Andria L., Dhar, Rajat, Roquer, Jaume, Khatri, Pooja, Jiménez-Conde, Jordi, Fernandez-Cadenas, Israel, Montaner, Joan, Rosand, Jonathan, Cruchaga, Carlos, Lee, Jin-Moo

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Potential genetic modifiers of disease risk and age at onset in patients with frontotemporal lobar degeneration and GRN mutations: a genome-wide association study by Perkerson, Ralph B, Jenkins, Gregory D, Serie, Daniel J, Ghidoni, Roberta, Benussi, Luisa, López de Munain, Adolfo, Zulaica, Miren, Moreno, Fermin, Le Ber, Isabelle, Pasquier, Florence, Hannequin, Didier, Sánchez-Valle, Raquel, Antonell, Anna, Lladó, Albert, Parsons, Tammee M, Finch, NiCole A, Finger, Elizabeth C, Lippa, Carol F, Huey, Edward D, Neumann, Manuela, Heutink, Peter, Synofzik, Matthis, Wilke, Carlo, Slawek, Jaroslaw, Sitek, Emilia, Johannsen, Peter, Nielsen, Jørgen E, Ren, Yingxue, DeJesus-Hernandez, Mariely, Murray, Melissa E, Bieniek, Kevin F, Evers, Bret M, Richardson, Anna, Scarpini, Elio, Hardy, John, Frangipane, Francesca, Maletta, Raffaele, Anfossi, Maria, Gallo, Maura, Suh, EunRan, Lopez, Oscar L, Wong, Tsz H, van Rooij, Jeroen G J, Seelaar, Harro, Caselli, Richard J, Reiman, Eric M, Noel Sabbagh, Marwan, Kjolby, Mads, Nykjaer, Anders, Karydas, Anna M, Boxer, Adam L, Spina, Salvatore, Oblak, Adrian, Mesulam, M-Marsel, Weintraub, Sandra, Geula, Changiz, Hodges, John R, Piguet, Olivier, Irwin, David J, Trojanowski, John Q, Lee, Edward B, Josephs, Keith A, Knopman, David S, Piaceri, Irene, Bagnoli, Silvia, Sorbi, Sandro, Gearing, Marla, Beach, Thomas G, Black, Sandra E, Masellis, Mario, Rogaeva, Ekaterina, Honig, Lawrence S, Bruni, Amalia C, Snowden, Julie, Pickering-Brown, Stuart, Diehl-Schmid, Janine, Winkelmann, Juliane, Galimberti, Daniela, Graff, Caroline, Öijerstedt, Linn, Troakes, Claire, Al-Sarraj, Safa, Cruchaga, Carlos, Cairns, Nigel J, Rohrer, Jonathan D, Halliday, Glenda M, Kwok, John B, van Swieten, John C, White, Charles L, Ghetti, Bernardino, Murell, Jill R, Borroni, Barbara, Tagliavini, Fabrizio, Bigio, Eileen H, Grossman, Murray, Van Deerlin, Vivianna M, Miller, Bruce L, Dickson, Dennis W, Biernacka, Joanna M, Rademakers, Rosa

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Genome-wide analyses as part of the international FTLD-TDP whole-genome sequencing consortium reveals novel disease risk factors and increases support for immune dysfunction in FTL... by Pottier, Cyril, Ren, Yingxue, Perkerson, Ralph B., Baker, Matt, Jenkins, Gregory D., van Blitterswijk, Marka, DeJesus-Hernandez, Mariely, van Rooij, Jeroen G. J., Murray, Melissa E., Christopher, Elizabeth, McDonnell, Shannon K., Fogarty, Zachary, Batzler, Anthony, Tian, Shulan, Vicente, Cristina T., Matchett, Billie, Karydas, Anna M., Hsiung, Ging-Yuek Robin, Seelaar, Harro, Mol, Merel O., Finger, Elizabeth C., Graff, Caroline, Öijerstedt, Linn, Neumann, Manuela, Heutink, Peter, Synofzik, Matthis, Wilke, Carlo, Prudlo, Johannes, Rizzu, Patrizia, Simon-Sanchez, Javier, Edbauer, Dieter, Diehl-Schmid, Janine, Evers, Bret M., King, Andrew, Mesulam, M. Marsel, Weintraub, Sandra, Geula, Changiz, Bieniek, Kevin F., Petrucelli, Leonard, Ahern, Geoffrey L., Reiman, Eric M., Woodruff, Bryan K., Caselli, Richard J., Huey, Edward D., Farlow, Martin R., Grafman, Jordan, Mead, Simon, Grinberg, Lea T., Spina, Salvatore, Irwin, David J., Lee, Edward B., Suh, EunRan, Snowden, Julie, Mann, David, Ertekin-Taner, Nilufer, Uitti, Ryan J., Wszolek, Zbigniew K., Josephs, Keith A., Parisi, Joseph E., Knopman, David S., Petersen, Ronald C., Hodges, John R., Piguet, Olivier, Geier, Ethan G., Yokoyama, Jennifer S., Rissman, Robert A., Rogaeva, Ekaterina, Keith, Julia, Zinman, Lorne, Tartaglia, Maria Carmela, Cairns, Nigel J., Cruchaga, Carlos, Kofler, Julia, Lopez, Oscar L., Beach, Thomas G., Arzberger, Thomas, Herms, Jochen, Honig, Lawrence S., Vonsattel, Jean Paul, Halliday, Glenda M., Kwok, John B., White, Charles L., Gearing, Marla, Glass, Jonathan, Rollinson, Sara, Pickering-Brown, Stuart, Rohrer, Jonathan D., Trojanowski, John Q., Van Deerlin, Vivianna, Bigio, Eileen H., Troakes, Claire, Asmann, Yan, Miller, Bruce L., Boeve, Bradley F., Seeley, William W., Mackenzie, Ian R. A., van Swieten, John C., Dickson, Dennis W., Biernacka, Joanna M., Rademakers, Rosa

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Post‐GWAS multiomic functional investigation of the TNIP1 locus in Alzheimer's disease highlights a potential role for GPX3 by Panyard, Daniel J., Reus, Lianne M., Ali, Muhammad, Liu, Jihua, Deming, Yuetiva K., Lu, Qiongshi, Kollmorgen, Gwendlyn, Carboni, Margherita, Wild, Norbert, Visser, Pieter J., Bertram, Lars, Zetterberg, Henrik, Blennow, Kaj, Gobom, Johan, Western, Dan, Sung, Yun Ju, Carlsson, Cynthia M., Johnson, Sterling C., Asthana, Sanjay, Cruchaga, Carlos, Tijms, Betty M., Engelman, Corinne D., Snyder, Michael P.

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Frontobasal gray matter loss is associated with the TREM2 p.R47H variant by Luis, Elkin O, Ortega-Cubero, Sara, Lamet, Isabel, Razquin, Cristina, Cruchaga, Carlos, Benitez, Bruno A, Lorenzo, Elena, Irigoyen, Jaione, Pastor, Maria A, Pastor, Pau

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