A sedimentary overlap assemblage links Australia to northwestern Laurentia at 1.6 Ga von Verbaas, J., Thorkelson, D.J., Crowley, J., Davis, W.J., Foster, D.A., Gibson, H.D., Marshall, D.D., Milidragovic, D.

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First evidence of uhp metamorphism within the Seve Nappe Complex of central Sweden von Majka, J, Janak, M, Gee, D.G, van Roermund, H.L.M, Verbaas, J

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A genome-wide association meta-analysis of plasma Aβ peptides concentrations in the elderly von Chouraki, V, De Bruijn, R F A G, Chapuis, J, Bis, J C, Reitz, C, Schraen, S, Ibrahim-Verbaas, C A, Grenier-Boley, B, Delay, C, Rogers, R, Demiautte, F, Mounier, A, Fitzpatrick, A L, Berr, C, Dartigues, J-F, Uitterlinden, A G, Hofman, A, Breteler, M, Becker, J T, Lathrop, M, Schupf, N, Alpérovitch, A, Mayeux, R, van Duijn, C M, Buée, L, Amouyel, P, Lopez, O L, Ikram, M A, Tzourio, C, Lambert, J-C

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Identification of novel risk loci and causal insights for sporadic Creutzfeldt-Jakob disease: a genome-wide association study von Jones, Emma, Hummerich, Holger, Viré, Emmanuelle, Uphill, James, Dimitriadis, Athanasios, Speedy, Helen, Campbell, Tracy, Norsworthy, Penny, Quinn, Liam, Whitfield, Jerome, Linehan, Jacqueline, Jaunmuktane, Zane, Brandner, Sebastian, Jat, Parmjit, Nihat, Akin, How Mok, Tze, Ahmed, Parvin, Collins, Steven, Stehmann, Christiane, Sarros, Shannon, Kovacs, Gabor G, Geschwind, Michael D, Golubjatnikov, Aili, Frontzek, Karl, Budka, Herbert, Aguzzi, Adriano, Karamujić-Čomić, Hata, van der Lee, Sven J, Ibrahim-Verbaas, Carla A, van Duijn, Cornelia M, Sikorska, Beata, Golanska, Ewa, Liberski, Pawel P, Calero, Miguel, Calero, Olga, Sanchez-Juan, Pascual, Salas, Antonio, Martinón-Torres, Federico, Bouaziz-Amar, Elodie, Haïk, Stéphane, Laplanche, Jean-Louis, Brandel, Jean-Phillipe, Amouyel, Phillipe, Lambert, Jean-Charles, Parchi, Piero, Bartoletti-Stella, Anna, Capellari, Sabina, Poleggi, Anna, Ladogana, Anna, Pocchiari, Maurizio, Aneli, Serena, Matullo, Giuseppe, Knight, Richard, Zafar, Saima, Zerr, Inga, Booth, Stephanie, Coulthart, Michael B, Jansen, Gerard H, Glisic, Katie, Blevins, Janis, Gambetti, Pierluigi, Safar, Jiri, Appleby, Brian, Collinge, John, Mead, Simon

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Genetic contributions to variation in general cognitive function: a meta-analysis of genome-wide association studies in the CHARGE consortium (N=53 949) von Davies, G, Armstrong, N, Bis, J C, Bressler, J, Chouraki, V, Ibrahim-Verbaas, C A, Lahti, J, van der Lee, S J, Le Hellard, S, Liu, T, Marioni, R E, Oldmeadow, C, Smith, A V, Smith, J A, Thomson, R, Vitart, V, Wang, J, Zgaga, L, Boxall, R, Hill, W D, Liewald, D C, Luciano, M, Adams, H, Ames, D, Amin, N, Amouyel, P, Becker, J T, Berr, C, Bertram, L, Buckley, B M, Campbell, H, Corley, J, De Jager, P L, Dufouil, C, Eriksson, J G, Espeseth, T, Faul, J D, Ford, I, Gottesman, R F, Gudnason, V, Harris, T B, Heiss, G, Hofman, A, Holliday, E G, Huffman, J, Kardia, S L R, Knopman, D S, Lambert, J-C, Lee, T, Li, S-C, Lopez, O L, Lundervold, A J, Lundqvist, A, Mather, K A, Mirza, S S, Oostra, B A, Palotie, A, Papenberg, G, Pattie, A, Petrovic, K, Polasek, O, Psaty, B M, Redmond, P, Reppermund, S, Rotter, J I, Schuur, M, Schofield, P W, van Swieten, J C, Trompet, S, Uitterlinden, A G, Weinstein, G, Widen, E, Windham, B G, Jukema, J W, Wright, A F, Wright, M J, Yang, Q, Attia, J R, Bennett, D A, Brodaty, H, de Craen, A J M, Hayward, C, Ikram, M A, Lindenberger, U, Porteous, D J, Räikkönen, K, Reinvang, I, Rudan, I, Sachdev, P S, Schofield, P R, Srikanth, V, Starr, J M, Turner, S T, Weir, D R, Wilson, J F, van Duijn, C, Launer, L, Fitzpatrick, A L, Seshadri, S, Mosley, T H

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Human prion diseases in the Netherlands (1998-2009): clinical, genetic and molecular aspects von Jansen, Casper, Parchi, Piero, Capellari, Sabina, Ibrahim-Verbaas, Carla A, Schuur, Maaike, Strammiello, Rosaria, Corrado, Patrizia, Bishop, Matthew T, van Gool, Willem A, Verbeek, Marcel M, Baas, Frank, van Saane, Wesley, Spliet, Wim G M, Jansen, Gerard H, van Duijn, Cornelia M, Rozemuller, Annemieke J M

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The effect of surface OH-population on the photocatalytic activity of rare earth-doped P25-TiO2 in methylene blue degradation von Du, P., Bueno-López, A., Verbaas, M., Almeida, A.R., Makkee, M., Moulijn, J.A., Mul, G.

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GWAS for executive function and processing speed suggests involvement of the CADM2 gene von Ibrahim-Verbaas, C A, Bressler, J, Schuur, M, Davies, G, Trompet, S, Smith, J A, Liu, Y, Vitart, V, Petrovic, K, Polasek, O, Zgaga, L, Fawns-Ritchie, C, Hoffmann, P, Karjalainen, J, Lahti, J, Llewellyn, D J, Schmidt, C O, Mather, K A, Chouraki, V, Resnick, S M, Rose, L M, Oldmeadow, C, Stewart, M, deJager, P L, Harris, T B, Liewald, D C, Amin, N, Coker, L H, Stegle, O, Lopez, O L, Teumer, A, Ford, I, Karbalai, N, Becker, J T, Jonsdottir, M K, Au, R, Fehrmann, R S N, Herms, S, Nalls, M, Yaffe, K, Lohman, K, van Swieten, J C, Kardia, S L R, Knopman, D S, Meeks, W M, Heiss, G, Holliday, E G, Tanaka, T, Stott, D J, Wang, J, Ridker, P, Pattie, A, Starr, J M, Hocking, L J, Armstrong, N J, McLachlan, S, Shulman, J M, Eiriksdottir, G, Scott, R J, Kochan, N A, Palotie, A, Hsieh, Y-C, Penman, A, Gottesman, R F, Yu, L, Beiser, A, Garcia, M, Rotter, J I, Slagboom, P E, Westendorp, R G J, Buckley, B M, Wolf, P A, Uitterlinden, A G, Grabe, H J, Bandinelli, S, Chasman, D I, Grodstein, F, Räikkönen, K, Porteous, D J, Price, J F, Sachdev, P S, Ferrucci, L, Attia, J R, Rudan, I, Hayward, C, Wright, A F, Wilson, J F, Cichon, S, Schmidt, H, Ding, J, de Craen, A J M, Fornage, M, Bennett, D A, Deary, I J, Ikram, M A, Launer, L J, Fitzpatrick, A L, Seshadri, S, van Duijn, C M, Mosley, T H

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Rare Functional Variant in TM2D3 is Associated with Late-Onset Alzheimer's Disease von Jakobsdottir, Johanna, van der Lee, Sven J, Bis, Joshua C, Chouraki, Vincent, Li-Kroeger, David, Yamamoto, Shinya, Grove, Megan L, Naj, Adam, Vronskaya, Maria, Salazar, Jose L, DeStefano, Anita L, Brody, Jennifer A, Smith, Albert V, Amin, Najaf, Sims, Rebecca, Ibrahim-Verbaas, Carla A, Choi, Seung-Hoan, Satizabal, Claudia L, Lopez, Oscar L, Beiser, Alexa, Ikram, M Arfan, Garcia, Melissa E, Hayward, Caroline, Varga, Tibor V, Ripatti, Samuli, Franks, Paul W, Hallmans, Göran, Rolandsson, Olov, Jansson, Jan-Håkon, Porteous, David J, Salomaa, Veikko, Eiriksdottir, Gudny, Rice, Kenneth M, Bellen, Hugo J, Levy, Daniel, Uitterlinden, Andre G, Emilsson, Valur, Rotter, Jerome I, Aspelund, Thor, O'Donnell, Christopher J, Fitzpatrick, Annette L, Launer, Lenore J, Hofman, Albert, Wang, Li-San, Williams, Julie, Schellenberg, Gerard D, Boerwinkle, Eric, Psaty, Bruce M, Seshadri, Sudha, Shulman, Joshua M, Gudnason, Vilmundur, van Duijn, Cornelia M

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Multilocus Genetic Risk Score Associates With Ischemic Stroke in Case-Control and Prospective Cohort Studies von MALIK, Rainer, BEVAN, Steve, DE STEFANO, Anita L, FORNAGE, Myriam, PSATY, Bruce M, IKRAM, M. Arfan, LAUNER, Lenore J, VAN DUIJN, Cornelia M, SHARMA, Pankaj, MITCHELL, Braxton D, ROSAND, Jonathan, MESCHIA, James F, NALLS, Michael A, LEVI, Christopher, ROTHWELL, Peter M, SUDLOW, Cathie, MARKUS, Hugh S, SESHADRI, Sudha, DICHGANS, Martin, HOLLIDAY, Elizabeth G, DEVAN, William J, CHENG, Yu-Ching, IBRAHIM-VERBAAS, Carla A, VERHAAREN, Benjamin F. J, BIS, Joshua C, JOON, Aron Y

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Variant of TREM2 Associated with the Risk of Alzheimer's Disease von Jonsson, Thorlakur, Stefansson, Hreinn, Steinberg, Stacy, Jonsdottir, Ingileif, Jonsson, Palmi V, Snaedal, Jon, Bjornsson, Sigurbjorn, Huttenlocher, Johanna, Levey, Allan I, Lah, James J, Rujescu, Dan, Hampel, Harald, Giegling, Ina, Andreassen, Ole A, Engedal, Knut, Ulstein, Ingun, Djurovic, Srdjan, Ibrahim-Verbaas, Carla, Hofman, Albert, Ikram, M. Arfan, van Duijn, Cornelia M, Thorsteinsdottir, Unnur, Kong, Augustine, Stefansson, Kari

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Multiethnic Genome-Wide Association Study of Cerebral White Matter Hyperintensities on MRI von Verhaaren, Benjamin F.J, Debette, Stéphanie, Bis, Joshua C, Smith, Jennifer A, Ikram, M Kamran, Adams, Hieab H, Beecham, Ashley H, Rajan, Kumar B, Lopez, Lorna M, Barral, Sandra, van Buchem, Mark A, van der Grond, Jeroen, Smith, Albert V, Hegenscheid, Katrin, Aggarwal, Neelum T, de Andrade, Mariza, Atkinson, Elizabeth J, Beekman, Marian, Beiser, Alexa S, Blanton, Susan H, Boerwinkle, Eric, Brickman, Adam M, Bryan, R Nick, Chauhan, Ganesh, Chen, Christopher P.L.H, Chouraki, Vincent, de Craen, Anton J.M, Crivello, Fabrice, Deary, Ian J, Deelen, Joris, De Jager, Philip L, Dufouil, Carole, Elkind, Mitchell S.V, Evans, Denis A, Freudenberger, Paul, Gottesman, Rebecca F, Gunason, Vilmundur, Habes, Mohamad, Heckbert, Susan R, Heiss, Gerardo, Hilal, Saima, Hofer, Edith, Hofman, Albert, Knopman, David S, Lewis, Cora E, Liao, Jiemin, Liewald, David C.M, Luciano, Michelle, van der Lugt, Aad, Martinez, Oliver O, Mayeux, Richard, Mazoyer, Bernard, Nalls, Mike, Nauck, Matthias, Niessen, Wiro J, Oostra, Ben A, Psaty, Bruce M, Rice, Kenneth M, Rotter, Jerome I, von Sarnowski, Bettina, Schmidt, Helena, Schreiner, Pamela J, Schuur, Maaike, Sidney, Stephen S, Sigurdsson, Sigurdur, Slagboom, P Eline, Stott, David J.M, van Swieten, John C, Teumer, Alexander, Töglhofer, Anna Maria, Traylor, Matthew, Trompet, Stella, Turner, Stephen T, Tzourio, Christophe, Uh, Hae-Won, Uitterlinden, André G, Vernooij, Meike W, Wang, Jing J, Wong, Tien Y, Wardlaw, Joanna M, Windham, B Gwen, Wittfeld, Katharina, Wolf, Christiane, Wright, Clinton B, Yang, Qiong, Zhao, Wei, Zijdenbos, Alex, Jukema, J Wouter, Sacco, Ralph L, Kardia, Sharon L.R, Mosley, Thomas H, Longstreth, W T, DeCarli, Charles C, van Duijn, Cornelia M, Schmidt, Reinhold, Launer, Lenore J, Grabe, Hans J, Seshadri, Sudha S, Ikram, M Arfan, Fornage, Myriam

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Discovery by the Epistasis Project of an epistatic interaction between the GSTM3 gene and the HHEX/IDE/KIF11 locus in the risk of Alzheimer's disease von Bullock, James M, Medway, Christopher, Cortina-Borja, Mario, Turton, James C, Prince, Jonathan A, Ibrahim-Verbaas, Carla A, Schuur, Maaike, Breteler, Monique M, van Duijn, Cornelia M, Kehoe, Patrick G, Barber, Rachel, Coto, Eliecer, Alvarez, Victoria, Deloukas, Panos, Hammond, Naomi, Combarros, Onofre, Mateo, Ignacio, Warden, Donald R, Lehmann, Michael G, Belbin, Olivia, Brown, Kristelle, Wilcock, Gordon K, Heun, Reinhard, Kölsch, Heike, Smith, A. David, Lehmann, Donald J, Morgan, Kevin

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Middle Paleolithic complex technology and a Neandertal tar-backed tool from the Dutch North Sea von Niekus, Marcel J. L. Th, Kozowyk, Paul R. B., Langejans, Geeske H. J., Ngan-Tillard, Dominique, van Keulen, Henk, van der Plicht, Johannes, Cohen, Kim M., van Wingerden, Willy, van Os, Bertil, Smit, Bjørn I., Amkreutz, Luc W. S. W., Johansen, Lykke, Verbaas, Annemieke, Dusseldorp, Gerrit L.

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Assessing the genetic overlap between BMI and cognitive function von Marioni, R E, Yang, J, Dykiert, D, Mõttus, R, Campbell, A, Davies, G, Hayward, C, Porteous, D J, Visscher, P M, Deary, I J

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Predicting Stroke Through Genetic Risk Functions The CHARGE Risk Score Project von IBRAHIM-VERBAAS, Carla A, FORNAGE, Myriam, KATHIRESAN, Sekar, EHRET, Georg B, FOX, Caroline S, MALIK, Rainer, DICHGANS, Martin, SCHMIDT, Helena, LAHTI, Jari, HECKBERT, Susan R, LUMLEY, Thomas, RICE, Kenneth, BIS, Joshua C, ROTTER, Jerome I, TAYLOR, Kent D, FOLSOM, Aaron R, BOERWINKLE, Eric, ROSAMOND, Wayne D, SHAHAR, Eyal, GOTTESMAN, Rebecca F, KOUDSTAAL, Peter J, AMIN, Najaf, WIEBERDINK, Renske G, SEUNG HOAN CHOI, DEHGHAN, Abbas, HOFMAN, Albert, UITTERLINDEN, André G, DESTEFANO, Anita L, DEBETTE, Stephanie, LUTING XUE, BEISER, Alexa, WOLF, Philip A, DECARLI, Charles, IKRAM, M. Arfan, PSATY, Bruce M, SESHADRI, Sudha, MOSLEY, Thomas H, LONGSTRETH, W. T, VAN DUIJN, Cornelia M, LAUNER, Lenore J, MEIGS, James B, RAO, Madhu, NALLS, Mike, FONTES, Joao D, O'DONNELL, Christopher J

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Rifting of western Laurentia at 1.38 Ga: The Hart River sills of Yukon, Canada von Verbaas, Jacob, Thorkelson, Derek J., Milidragovic, Dejan, Crowley, James L., Foster, David, Daniel Gibson, H., Marshall, Daniel D.

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Convergent genetic and expression data implicate immunity in Alzheimer's disease von Jones, Lesley, Wang, Li-San, Choi, Seung-Hoan, Vedernikov, Alexey, Escott-Price, Valentina, Richards, Alexander, Naj, Adam C., Sims, Rebecca, Gerrish, Amy, Jun, Gyungah, Beecham, Gary W., Grenier-Boley, Benjamin, Smith, Albert V., Chouraki, Vincent, Thomas, Charlene, Zelenika, Diana, Vardarajan, Badri N., Kamatani, Yoichiro, Bihoreau, Marie-Thérèse, Reitz, Christiane, Pasquier, Florence, Hanon, Olivier, Buxbaum, Joseph D., Campion, Dominique, Crane, Paul K., Gudnason, Vilmundur, Cruchaga, Carlos, Craig, David, Berr, Claudine, Lopez, Oscar L., De Jager, Philip L., Deramecourt, Vincent, Evans, Denis, Tárraga, Lluís, Sleegers, Kristel, Gill, Michael, Emilsson, Valur, Keller, Lina, Barberger-Gateau, Pascale, McGuinness, Bernadette, Larson, Eric B., Myers, Amanda J., Dufouil, Carole, Todd, Stephen, Love, Seth, Kehoe, Pat, Rogaeva, Ekaterina, Gallacher, John, Tsuang, Debby W., Yu, Lei, Sorbi, Sandro, Fox, Nick, Hardy, John, Deniz Naranjo, Maria Candida, Clarke, Robert, Mancuso, Michelangelo, Mecocci, Patrizia, del Zompo, Maria, Maier, Wolfgang, Pilotto, Alberto, Bullido, Maria, Caffarra, Paolo, Gilbert, John R., Mayhaus, Manuel, Lannfelt, Lars, Pichler, Sabrina, Ingelsson, Martin, Beekly, Duane, Valladares, Otto, Coto, Eliecer, Hamilton-Nelson, Kara L., Owen, Michael J., Faber, Kelley M., O'Donovan, Michael C., Soininen, Hilkka, Mead, Simon, de Bruijn, Renee F.A.G., Rotter, Jerome I., Brice, Alexis, Morgan, Kevin, Foroud, Tatiana M., Hannequin, Didier, Powell, John F., Nalls, Michael A., Ritchie, Karen, Riemenschneider, Matthias, Boada, Mercè, Hiltunen, Mikko, Pastor, Pau, Mayeux, Richard, Graff, Caroline, Psaty, Bruce M., Haines, Jonathan L., Lathrop, Mark, Pericak-Vance, Margaret A., Launer, Lenore J., Farrer, Lindsay A., van Duijn, Cornelia M., Williams, Julie, Holmans, Peter A.

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Common variants at 12q14 and 12q24 are associated with hippocampal volume von Bis, Joshua C, DeCarli, Charles, Smith, Albert Vernon, van der Lijn, Fedde, Crivello, Fabrice, Fornage, Myriam, Debette, Stephanie, Shulman, Joshua M, Schmidt, Helena, Srikanth, Velandai, Schuur, Maaike, Yu, Lei, Choi, Seung-Hoan, Sigurdsson, Sigurdur, Verhaaren, Benjamin F J, DeStefano, Anita L, Lambert, Jean-Charles, Jack, Jr, Clifford R, Struchalin, Maksim, Stankovich, Jim, Ibrahim-Verbaas, Carla A, Fleischman, Debra, Zijdenbos, Alex, den Heijer, Tom, Mazoyer, Bernard, Coker, Laura H, Enzinger, Christian, Danoy, Patrick, Amin, Najaf, Arfanakis, Konstantinos, van Buchem, Mark A, de Bruijn, Renée F A G, Beiser, Alexa, Dufouil, Carole, Huang, Juebin, Cavalieri, Margherita, Thomson, Russell, Niessen, Wiro J, Chibnik, Lori B, Gislason, Gauti K, Hofman, Albert, Pikula, Aleksandra, Amouyel, Philippe, Freeman, Kevin B, Phan, Thanh G, Oostra, Ben A, Stein, Jason L, Medland, Sarah E, Vasquez, Alejandro Arias, Hibar, Derrek P, Wright, Margaret J, Franke, Barbara, Martin, Nicholas G, Thompson, Paul M, Nalls, Michael A, Uitterlinden, Andre G, Au, Rhoda, Elbaz, Alexis, Beare, Richard J, van Swieten, John C, Lopez, Oscar L, Harris, Tamara B, Chouraki, Vincent, Breteler, Monique M B, De Jager, Philip L, Becker, James T, Vernooij, Meike W, Knopman, David, Fazekas, Franz, Wolf, Philip A, van der Lugt, Aad, Gudnason, Vilmundur, Longstreth, Jr, W T, Brown, Matthew A, Bennett, David A, van Duijn, Cornelia M, Mosley, Thomas H, Schmidt, Reinhold, Tzourio, Christophe, Launer, Lenore J, Ikram, M Arfan, Seshadri, Sudha

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Molecular genetic aetiology of general cognitive function is enriched in evolutionarily conserved regions von Hill, W D, Davies, G, Harris, S E, Hagenaars, S P, Liewald, D C, Penke, L, Gale, C R, Deary, I J

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