Diagnostic performance of axial T2-weighted MRI sequence for exclusion of brain tumour in paediatric patients with non-localizing symptoms von Gerrish, Amy C, Malik, Luqman, Swain, Charlotte, Thomas, Adam G, Jaspan, Timothy, Dineen, Rob A

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Case 239: Cerebrotendinous Xanthomatosis von Gerrish, Amy C, Gaba, Suchi

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Brain White Matter Tracts: Functional Anatomy and Clinical Relevance von Gerrish, Amy C., BM, BS, Thomas, Adam G., MSc, MRCP, FRCR, Dineen, Robert A., FRCR, PhD

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Case 239 von Gerrish, Amy C, Gaba, Suchi

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Common schizophrenia alleles are enriched in mutation-intolerant genes and in regions under strong background selection von Pardiñas, Antonio F., Holmans, Peter, Pocklington, Andrew J., Escott-Price, Valentina, Ripke, Stephan, Carrera, Noa, Legge, Sophie E., Bishop, Sophie, Cameron, Darren, Hamshere, Marian L., Han, Jun, Hubbard, Leon, Lynham, Amy, Mantripragada, Kiran, Rees, Elliott, MacCabe, James H., McCarroll, Steven A., Baune, Bernhard T., Breen, Gerome, Byrne, Enda M., Dannlowski, Udo, Eley, Thalia C., Hayward, Caroline, Martin, Nicholas G., McIntosh, Andrew M., Plomin, Robert, Porteous, David J., Wray, Naomi R., Caballero, Armando, Geschwind, Daniel H., Huckins, Laura M., Ruderfer, Douglas M., Santiago, Enrique, Sklar, Pamela, Stahl, Eli A., Won, Hyejung, Agerbo, Esben, Als, Thomas D., Andreassen, Ole A., Bækvad-Hansen, Marie, Mortensen, Preben Bo, Pedersen, Carsten Bøcker, Børglum, Anders D., Bybjerg-Grauholm, Jonas, Djurovic, Srdjan, Durmishi, Naser, Pedersen, Marianne Giørtz, Golimbet, Vera, Grove, Jakob, Hougaard, David M., Mattheisen, Manuel, Molden, Espen, Mors, Ole, Nordentoft, Merete, Pejovic-Milovancevic, Milica, Sigurdsson, Engilbert, Silagadze, Teimuraz, Hansen, Christine Søholm, Stefansson, Kari, Stefansson, Hreinn, Steinberg, Stacy, Tosato, Sarah, Werge, Thomas, Collier, David A., Rujescu, Dan, Kirov, George, Owen, Michael J., O’Donovan, Michael C., Walters, James T. R.

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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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Common polygenic variation enhances risk prediction for Alzheimer's disease von Escott-Price, Valentina, Sims, Rebecca, Bannister, Christian, Harold, Denise, Vronskaya, Maria, Majounie, Elisa, Badarinarayan, Nandini, Morgan, Kevin, Passmore, Peter, Holmes, Clive, Powell, John, Brayne, Carol, Gill, Michael, Mead, Simon, Goate, Alison, Cruchaga, Carlos, Lambert, Jean-Charles, van Duijn, Cornelia, Maier, Wolfgang, Ramirez, Alfredo, Holmans, Peter, Jones, Lesley, Hardy, John, Seshadri, Sudha, Schellenberg, Gerard D, Amouyel, Philippe, Williams, Julie

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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

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Genetic evidence implicates the immune system and cholesterol metabolism in the aetiology of Alzheimer's disease von Jones, Lesley, Holmans, Peter A, Hamshere, Marian L, Harold, Denise, Moskvina, Valentina, Ivanov, Dobril, Pocklington, Andrew, Abraham, Richard, Hollingworth, Paul, Sims, Rebecca, Gerrish, Amy, Pahwa, Jaspreet Singh, Jones, Nicola, Stretton, Alexandra, Morgan, Angharad R, Lovestone, Simon, Powell, John, Proitsi, Petroula, Lupton, Michelle K, Brayne, Carol, Rubinsztein, David C, Gill, Michael, Lawlor, Brian, Lynch, Aoibhinn, Morgan, Kevin, Brown, Kristelle S, Passmore, Peter A, Craig, David, McGuinness, Bernadette, Todd, Stephen, Holmes, Clive, Mann, David, Smith, A David, Love, Seth, Kehoe, Patrick G, Mead, Simon, Fox, Nick, Rossor, Martin, Collinge, John, Maier, Wolfgang, Jessen, Frank, Schürmann, Britta, Heun, Reinhard, Kölsch, Heike, van den Bussche, Hendrik, Heuser, Isabella, Peters, Oliver, Kornhuber, Johannes, Wiltfang, Jens, Dichgans, Martin, Frölich, Lutz, Hampel, Harald, Hüll, Michael, Rujescu, Dan, Goate, Alison M, Kauwe, John S K, Cruchaga, Carlos, Nowotny, Petra, Morris, John C, Mayo, Kevin, Livingston, Gill, Bass, Nicholas J, Gurling, Hugh, McQuillin, Andrew, Gwilliam, Rhian, Deloukas, Panos, Al-Chalabi, Ammar, Shaw, Christopher E, Singleton, Andrew B, Guerreiro, Rita, Mühleisen, Thomas W, Nöthen, Markus M, Moebus, Susanne, Jöckel, Karl-Heinz, Klopp, Norman, Wichmann, H-Erich, Rüther, Eckhard, Carrasquillo, Minerva M, Pankratz, V Shane, Younkin, Steven G, Hardy, John, O'Donovan, Michael C, Owen, Michael J, Williams, Julie

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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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Effectiveness of nail bed repair in children with or without replacing the fingernail: NINJA multicentre randomized clinical trial von Jain, Abhilash, Greig, Aina V H, Jones, Amy, Cooper, Cushla, Davies, Loretta, Greshon, Akiko, Fletcher, Heidi, Sierakowski, Adam, Dritsaki, Melina, Nguyen, Thi Thu An, Png, May Ee, Stokes, Jamie R, Dakin, Helen, Cook, Jonathan A, Beard, David J, Gardiner, Matthew D

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Cardiovascular disease contributes to Alzheimer's disease: evidence from large-scale genome-wide association studies von Liu, Guiyou, Yao, Lifen, Liu, Jiafeng, Jiang, Yongshuai, Ma, Guoda, Chen, Zugen, Zhao, Bin, Li, Keshen

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Gene-wide analysis detects two new susceptibility genes for Alzheimer's disease von Escott-Price, Valentina, Bellenguez, Céline, Wang, Li-San, Choi, Seung-Hoan, Harold, Denise, Jones, Lesley, Holmans, Peter, Gerrish, Amy, Vedernikov, Alexey, Richards, Alexander, DeStefano, Anita L, Lambert, Jean-Charles, Ibrahim-Verbaas, Carla A, Naj, Adam C, Sims, Rebecca, Jun, Gyungah, Bis, Joshua C, Beecham, Gary W, Grenier-Boley, Benjamin, Russo, Giancarlo, Thornton-Wells, Tricia A, Denning, Nicola, Smith, Albert V, Chouraki, Vincent, Thomas, Charlene, Ikram, M Arfan, Zelenika, Diana, Vardarajan, Badri N, Kamatani, Yoichiro, Lin, Chiao-Feng, Schmidt, Helena, Kunkle, Brian, Dunstan, Melanie L, Vronskaya, Maria, Johnson, Andrew D, Ruiz, Agustin, Bihoreau, Marie-Thérèse, Reitz, Christiane, Pasquier, Florence, Hollingworth, Paul, Hanon, Olivier, Fitzpatrick, Annette L, Buxbaum, Joseph D, Campion, Dominique, Crane, Paul K, Baldwin, Clinton, Becker, Tim, Gudnason, Vilmundur, Cruchaga, Carlos, Craig, David, Amin, Najaf, Berr, Claudine, Lopez, Oscar L, De Jager, Philip L, Deramecourt, Vincent, Johnston, Janet A, Evans, Denis, Lovestone, Simon, Letenneur, Luc, Hernández, Isabel, Rubinsztein, David C, Eiriksdottir, Gudny, Sleegers, Kristel, Goate, Alison M, Fiévet, Nathalie, Huentelman, Matthew J, Gill, Michael, Brown, Kristelle, Kamboh, M Ilyas, Keller, Lina, Barberger-Gateau, Pascale, McGuinness, Bernadette, Larson, Eric B, Myers, Amanda J, Dufouil, Carole, Todd, Stephen, Wallon, David, Love, Seth, Rogaeva, Ekaterina, Gallacher, John, George-Hyslop, Peter St, Clarimon, Jordi, Lleo, Alberto, Bayer, Anthony, Tsuang, Debby W, Yu, Lei, Tsolaki, Magda, Bossù, Paola, Spalletta, Gianfranco, Proitsi, Petra, Collinge, John, Sorbi, Sandro, Garcia, Florentino Sanchez, Fox, Nick C, Hardy, John, Naranjo, Maria Candida Deniz, Bosco, Paolo, Clarke, Robert, Brayne, Carol, Galimberti, Daniela

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Quantitative Interaction Proteomics of Neurodegenerative Disease Proteins von Hosp, Fabian, Vossfeldt, Hannes, Heinig, Matthias, Vasiljevic, Djordje, Arumughan, Anup, Wyler, Emanuel, Landthaler, Markus, Hubner, Norbert, Wanker, Erich E., Lannfelt, Lars, Ingelsson, Martin, Lalowski, Maciej, Voigt, Aaron, Selbach, Matthias

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A genome-wide study shows a limited contribution of rare copy number variants to Alzheimer's disease risk von Chapman, Jade, Rees, Elliott, Harold, Denise, Ivanov, Dobril, Gerrish, Amy, Sims, Rebecca, Hollingworth, Paul, Stretton, Alexandra, Holmans, Peter, Owen, Michael J, O'Donovan, Michael C, Williams, Julie, Kirov, George

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SUCLG2 identified as both a determinator of CSF Aβ1-42 levels and an attenuator of cognitive decline in Alzheimer's disease von Ramirez, Alfredo, van der Flier, Wiesje M, Herold, Christine, Ramonet, David, Heilmann, Stefanie, Lewczuk, Piotr, Popp, Julius, Lacour, André, Drichel, Dmitriy, Louwersheimer, Eva, Kummer, Markus P, Cruchaga, Carlos, Hoffmann, Per, Teunissen, Charlotte, Holstege, Henne, Kornhuber, Johannes, Peters, Oliver, Naj, Adam C, Chouraki, Vincent, Bellenguez, Céline, Gerrish, Amy, Heun, Reiner, Frölich, Lutz, Hüll, Michael, Buscemi, Lara, Herms, Stefan, Kölsch, Heike, Scheltens, Philip, Breteler, Monique M, Rüther, Eckart, Wiltfang, Jens, Goate, Alison, Jessen, Frank, Maier, Wolfgang, Heneka, Michael T, Becker, Tim, Nöthen, Markus M

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Publisher Correction: Common schizophrenia alleles are enriched in mutation-intolerant genes and in regions under strong background selection von Pardiñas, Antonio F., Holmans, Peter, Pocklington, Andrew J., Escott-Price, Valentina, Ripke, Stephan, Carrera, Noa, Legge, Sophie E., Bishop, Sophie, Cameron, Darren, Hamshere, Marian L., Han, Jun, Hubbard, Leon, Lynham, Amy, Mantripragada, Kiran, Rees, Elliott, MacCabe, James H., McCarroll, Steven A., Baune, Bernhard T., Breen, Gerome, Byrne, Enda M., Dannlowski, Udo, Eley, Thalia C., Hayward, Caroline, Martin, Nicholas G., McIntosh, Andrew M., Plomin, Robert, Porteous, David J., Wray, Naomi R., Caballero, Armando, Geschwind, Daniel H., Huckins, Laura M., Ruderfer, Douglas M., Santiago, Enrique, Sklar, Pamela, Stahl, Eli A., Won, Hyejung, Agerbo, Esben, Als, Thomas D., Andreassen, Ole A., Bækvad-Hansen, Marie, Mortensen, Preben Bo, Pedersen, Carsten Bøcker, Børglum, Anders D., Bybjerg-Grauholm, Jonas, Djurovic, Srdjan, Durmishi, Naser, Pedersen, Marianne Giørtz, Golimbet, Vera, Grove, Jakob, Hougaard, David M., Mattheisen, Manuel, Molden, Espen, Mors, Ole, Nordentoft, Merete, Pejovic-Milovancevic, Milica, Sigurdsson, Engilbert, Silagadze, Teimuraz, Hansen, Christine Søholm, Stefansson, Kari, Stefansson, Hreinn, Steinberg, Stacy, Tosato, Sarah, Werge, Thomas, Collier, David A., Rujescu, Dan, Kirov, George, Owen, Michael J., O’Donovan, Michael C., Walters, James T. R.

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No consistent evidence for association between mtDNA variants and Alzheimer disease von HUDSON, G, SIMS, R, THOMAS, C, STRETTON, A, HOLMANS, P. A, O'DONOVAN, M. C, OWEN, M. J, WILLIAMS, J, CHINNER, P. F, HAROLD, D, CHAPMAN, J, HOLLINGWORTH, P, GERRISH, A, RUSSO, G, HAMSHERE, M, MOSKVINA, V, JONES, N

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Genetic variants influencing human aging from late-onset Alzheimer's disease (LOAD) genome-wide association studies (GWAS) von Shi, Hui, Belbin, Olivia, Medway, Christopher, Brown, Kristelle, Kalsheker, Noor, Carrasquillo, Minerva, Proitsi, Petroula, Powell, John, Lovestone, Simon, Goate, Alison, Younkin, Steven, Passmore, Peter, Morgan, Kevin

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Linking protective GAB2 variants, increased cortical GAB2 expression and decreased Alzheimer's disease pathology von Zou, Fanggeng, Belbin, Olivia, Carrasquillo, Minerva M, Culley, Oliver J, Hunter, Talisha A, Ma, Li, Bisceglio, Gina D, Allen, Mariet, Dickson, Dennis W, Graff-Radford, Neill R, Petersen, Ronald C, Morgan, Kevin, Younkin, Steven G

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