The SOD1-mediated ALS phenotype shows a decoupling between age of symptom onset and disease duration von Opie-Martin, Sarah, Iacoangeli, Alfredo, Topp, Simon D., Abel, Olubunmi, Mayl, Keith, Mehta, Puja R., Shatunov, Aleksey, Fogh, Isabella, Bowles, Harry, Limbachiya, Naomi, Spargo, Thomas P., Al-Khleifat, Ahmad, Williams, Kelly L., Jockel-Balsarotti, Jennifer, Bali, Taha, Self, Wade, Henden, Lyndal, Nicholson, Garth A., Ticozzi, Nicola, McKenna-Yasek, Diane, Tang, Lu, Shaw, Pamela J., Chio, Adriano, Ludolph, Albert, Weishaupt, Jochen H., Landers, John E., Glass, Jonathan D., Mora, Jesus S., Robberecht, Wim, Damme, Philip Van, McLaughlin, Russell, Hardiman, Orla, van den Berg, Leonard, Veldink, Jan H., Corcia, Phillippe, Stevic, Zorica, Siddique, Nailah, Silani, Vincenzo, Blair, Ian P., Fan, Dong-sheng, Esselin, Florence, de la Cruz, Elisa, Camu, William, Basak, Nazli A., Siddique, Teepu, Miller, Timothy, Brown, Robert H., Al-Chalabi, Ammar, Shaw, Christopher E.

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TMEM106B Acts as a Modifier of Cognitive and Motor Functions in Amyotrophic Lateral Sclerosis von Manini, Arianna, Ratti, Antonia, Brusati, Alberto, Maranzano, Alessio, Fogh, Isabella, Peverelli, Silvia, Messina, Stefano, Gentilini, Davide, Verde, Federico, Poletti, Barbara, Morelli, Claudia, Silani, Vincenzo, Ticozzi, Nicola

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C9orf72 intermediate expansions of 24-30 repeats are associated with ALS von Iacoangeli, Alfredo, Al Khleifat, Ahmad, Jones, Ashley R, Sproviero, William, Shatunov, Aleksey, Opie-Martin, Sarah, Morrison, Karen E, Shaw, Pamela J, Shaw, Christopher E, Fogh, Isabella, Dobson, Richard J, Newhouse, Stephen J, Al-Chalabi, Ammar

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Author Correction: The SOD1-mediated ALS phenotype shows a decoupling between age of symptom onset and disease duration von Opie-Martin, Sarah, Iacoangeli, Alfredo, Topp, Simon D., Abel, Olubunmi, Mayl, Keith, Mehta, Puja R., Shatunov, Aleksey, Fogh, Isabella, Bowles, Harry, Limbachiya, Naomi, Spargo, Thomas P., Al-Khleifat, Ahmad, Williams, Kelly L., Jockel-Balsarotti, Jennifer, Bali, Taha, Self, Wade, Henden, Lyndal, Nicholson, Garth A., Ticozzi, Nicola, McKenna-Yasek, Diane, Tang, Lu, Shaw, Pamela J., Chio, Adriano, Ludolph, Albert, Weishaupt, Jochen H., Landers, John E., Glass, Jonathan D., Mora, Jesus S., Robberecht, Wim, Damme, Philip Van, McLaughlin, Russell, Hardiman, Orla, van den Berg, Leonard, Veldink, Jan H., Corcia, Phillippe, Stevic, Zorica, Siddique, Nailah, Silani, Vincenzo, Blair, Ian P., Fan, Dong-sheng, Esselin, Florence, de la Cruz, Elisa, Camu, William, Basak, Nazli A., Siddique, Teepu, Miller, Timothy, Brown, Robert H., Al-Chalabi, Ammar, Shaw, Christopher E.

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Genetic predisposition to increased blood cholesterol and triglyceride lipid levels and risk of Alzheimer disease: a Mendelian randomization analysis von Proitsi, Petroula, Lupton, Michelle K, Velayudhan, Latha, Newhouse, Stephen, Fogh, Isabella, Tsolaki, Magda, Daniilidou, Makrina, Pritchard, Megan, Kloszewska, Iwona, Soininen, Hilkka, Mecocci, Patrizia, Vellas, Bruno, Williams, Julie, Stewart, Robert, Sham, Pak, Lovestone, Simon, Powell, John F

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The contribution of Neanderthal introgression and natural selection to neurodegenerative diseases von Chen, Zhongbo, Reynolds, Regina H., Pardiñas, Antonio F., Gagliano Taliun, Sarah A., van Rheenen, Wouter, Lin, Kuang, Shatunov, Aleksey, Gustavsson, Emil K., Fogh, Isabella, Jones, Ashley R., Robberecht, Wim, Corcia, Philippe, Chiò, Adriano, Shaw, Pamela J., Morrison, Karen E., Veldink, Jan H., van den Berg, Leonard H., Shaw, Christopher E., Powell, John F., Silani, Vincenzo, Hardy, John A., Houlden, Henry, Owen, Michael J., Turner, Martin R., Ryten, Mina, Al-Chalabi, Ammar

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Association of the risk factor UNC13A with survival and upper motor neuron involvement in amyotrophic lateral sclerosis von Manini, Arianna, Casiraghi, Valeria, Brusati, Alberto, Maranzano, Alessio, Gentile, Francesco, Colombo, Eleonora, Bonetti, Ruggero, Peverelli, Silvia, Invernizzi, Sabrina, Gentilini, Davide, Messina, Stefano, Verde, Federico, Poletti, Barbara, Fogh, Isabella, Morelli, Claudia, Silani, Vincenzo, Ratti, Antonia, Ticozzi, Nicola

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C9ORF72 repeat expansion in a large Italian ALS cohort: evidence of a founder effect von Ratti, Antonia, Corrado, Lucia, Castellotti, Barbara, Del Bo, Roberto, Fogh, Isabella, Cereda, Cristina, Tiloca, Cinzia, D'Ascenzo, Carla, Bagarotti, Alessandra, Pensato, Viviana, Ranieri, Michela, Gagliardi, Stella, Calini, Daniela, Mazzini, Letizia, Taroni, Franco, Corti, Stefania, Ceroni, Mauro, Oggioni, Gaia D, Lin, Kuang, Powell, John F, Sorarù, Gianni, Ticozzi, Nicola, Comi, Giacomo P, D'Alfonso, Sandra, Gellera, Cinzia, Silani, Vincenzo

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Large-scale analyses of CAV1 and CAV2 suggest their expression is higher in post-mortem ALS brain tissue and affects survival von Adey, Brett N, Cooper-Knock, Johnathan, Al Khleifat, Ahmad, Fogh, Isabella, van Damme, Philip, Corcia, Philippe, Couratier, Philippe, Hardiman, Orla, McLaughlin, Russell, Gotkine, Marc, Drory, Vivian, Silani, Vincenzo, Ticozzi, Nicola, Veldink, Jan H, van den Berg, Leonard H, de Carvalho, Mamede, Pinto, Susana, Mora Pardina, Jesus S, Povedano Panades, Mónica, Andersen, Peter M, Weber, Markus, Başak, Nazli A, Shaw, Christopher E, Shaw, Pamela J, Morrison, Karen E, Landers, John E, Glass, Jonathan D, Vourc'h, Patrick, Dobson, Richard J B, Breen, Gerome, Al-Chalabi, Ammar, Jones, Ashley R, Iacoangeli, Alfredo

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Analysis of the KIFAP3 gene in amyotrophic lateral sclerosis: a multicenter survival study von van Doormaal, Perry T.C, Ticozzi, Nicola, Gellera, Cinzia, Ratti, Antonia, Taroni, Franco, Chiò, Adriano, Calvo, Andrea, Mora, Gabriele, Restagno, Gabriella, Traynor, Bryan J, Birve, Anna, Lemmens, Robin, van Es, Michael A, Saris, Christiaan G.J, Blauw, Hylke M, van Vught, Paul W.J, Groen, Ewout J.N, Corrado, Lucia, Mazzini, Letizia, Del Bo, Roberto, Corti, Stefania, Waibel, Stefan, Meyer, Thomas, Ludolph, Albert C, Goris, An, van Damme, Philip, Robberecht, Wim, Shatunov, Aleksey, Fogh, Isabella, Andersen, Peter M, D'Alfonso, Sandra, Hardiman, Orla, Cronin, Simon, Rujescu, Dan, Al-Chalabi, Ammar, Landers, John E, Silani, Vincenzo, van den Berg, Leonard H, Veldink, Jan H

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Heritability of Amyotrophic Lateral Sclerosis von Fogh, Isabella, Al-Chalabi, Ammar, Powell, John

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A genome-wide association meta-analysis identifies a novel locus at 17q11.2 associated with sporadic amyotrophic lateral sclerosis von Fogh, Isabella, Ratti, Antonia, Gellera, Cinzia, Lin, Kuang, Tiloca, Cinzia, Moskvina, Valentina, Corrado, Lucia, Sorarù, Gianni, Cereda, Cristina, Corti, Stefania, Gentilini, Davide, Calini, Daniela, Castellotti, Barbara, Mazzini, Letizia, Querin, Giorgia, Gagliardi, Stella, Del Bo, Roberto, Conforti, Francesca L, Siciliano, Gabriele, Inghilleri, Maurizio, Saccà, Francesco, Bongioanni, Paolo, Penco, Silvana, Corbo, Massimo, Sorbi, Sandro, Filosto, Massimiliano, Ferlini, Alessandra, Di Blasio, Anna M, Signorini, Stefano, Shatunov, Aleksey, Jones, Ashley, Shaw, Pamela J, Morrison, Karen E, Farmer, Anne E, Van Damme, Philip, Robberecht, Wim, Chiò, Adriano, Traynor, Bryan J, Sendtner, Michael, Melki, Judith, Meininger, Vincent, Hardiman, Orla, Andersen, Peter M, Leigh, Nigel P, Glass, Jonathan D, Overste, Daniel, Diekstra, Frank P, Veldink, Jan H, van Es, Michael A, Shaw, Christopher E, Weale, Michael E, Lewis, Cathryn M, Williams, Julie, Brown, Robert H, Landers, John E, Ticozzi, Nicola, Ceroni, Mauro, Pegoraro, Elena, Comi, Giacomo P, D'Alfonso, Sandra, van den Berg, Leonard H, Taroni, Franco, Al-Chalabi, Ammar, Powell, John, Silani, Vincenzo

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Genetic correlation between amyotrophic lateral sclerosis and schizophrenia von McLaughlin, Russell L., Schijven, Dick, van Rheenen, Wouter, van Eijk, Kristel R., O’Brien, Margaret, Kahn, René S., Ophoff, Roel A., Goris, An, Bradley, Daniel G., Al-Chalabi, Ammar, van den Berg, Leonard H., Luykx, Jurjen J., Hardiman, Orla, Veldink, Jan H.

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ATXN2 Trinucleotide Repeat Length Correlates with Risk of ALS von Sproviero, William, Shatunov, Aleksey, Stahl, Daniel, Shoai, Maryam, van Rheenen, Wouter, Jones, Ashley R, Al-Sarraj, Safa, Andersen, Peter M, Bonini, Nancy M, Conforti, Francesca L, Van Damme, Philip, Daoud, Hussein, Del Mar Amador, Maria, Fogh, Isabella, Forzan, Monica, Gaastra, Ben, Gellera, Cinzia, Gitler, Aaron D, Hardy, John, Fratta, Pietro, La Bella, Vincenzo, Le Ber, Isabelle, Van Langenhove, Tim, Lattante, Serena, Lee, Yi-Chung, Malaspina, Andrea, Meininger, Vincent, Millecamps, Stèphanie, Orrell, Richard, Rademakers, Rosa, Robberecht, Wim, Rouleau, Guy, Ross, Owen A, Salachas, Francois, Sidle, Katie, Smith, Bradley N, Soong, Bing-Wen, Sorarù, Gianni, Stevanin, Giovanni, Kabashi, Edor, Troakes, Claire, van Broeckhoven, Christine, Veldink, Jan H, van den Berg, Leonard H, Shaw, Christopher E, Powell, John F, Al-Chalabi, Ammar

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The role of TREM2 R47H as a risk factor for Alzheimer's disease, frontotemporal lobar degeneration, amyotrophic lateral sclerosis, and Parkinson's disease von Lill, Christina M, Rengmark, Aina, Pihlstrøm, Lasse, Fogh, Isabella, Shatunov, Aleksey, Sleiman, Patrick M, Wang, Li-San, Liu, Tian, Lassen, Christina F, Meissner, Esther, Alexopoulos, Panos, Calvo, Andrea, Chio, Adriano, Dizdar, Nil, Faltraco, Frank, Forsgren, Lars, Kirchheiner, Julia, Kurz, Alexander, Larsen, Jan P, Liebsch, Maria, Linder, Jan, Morrison, Karen E, Nissbrandt, Hans, Otto, Markus, Pahnke, Jens, Partch, Amanda, Restagno, Gabriella, Rujescu, Dan, Schnack, Cathrin, Shaw, Christopher E, Shaw, Pamela J, Tumani, Hayrettin, Tysnes, Ole-Bjørn, Valladares, Otto, Silani, Vincenzo, van den Berg, Leonard H, van Rheenen, Wouter, Veldink, Jan H, Lindenberger, Ulman, Steinhagen-Thiessen, Elisabeth, Teipel, Stefan, Perneczky, Robert, Hakonarson, Hakon, Hampel, Harald, von Arnim, Christine A.F, Olsen, Jørgen H, Van Deerlin, Vivianna M, Al-Chalabi, Ammar, Toft, Mathias, Ritz, Beate, Bertram, Lars

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Genome-wide Meta-analysis Finds the ACSL5-ZDHHC6 Locus Is Associated with ALS and Links Weight Loss to the Disease Genetics von Iacoangeli, Alfredo, Lin, Tian, Al Khleifat, Ahmad, Jones, Ashley R., Opie-Martin, Sarah, Coleman, Jonathan R.I., Shatunov, Aleksey, Sproviero, William, Williams, Kelly L., Garton, Fleur, Restuadi, Restuadi, Henders, Anjali K., Mather, Karen A., Needham, Merilee, Mathers, Susan, Nicholson, Garth A., Rowe, Dominic B., Henderson, Robert, McCombe, Pamela A., Pamphlett, Roger, Blair, Ian P., Schultz, David, Sachdev, Perminder S., Newhouse, Stephen J., Proitsi, Petroula, Fogh, Isabella, Ngo, Shyuan T., Dobson, Richard J.B., Wray, Naomi R., Steyn, Frederik J., Al-Chalabi, Ammar

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PON1 is a disease modifier gene in amyotrophic lateral sclerosis: association of the Q192R polymorphism with bulbar onset and reduced survival von Verde, Federico, Tiloca, Cinzia, Morelli, Claudia, Doretti, Alberto, Poletti, Barbara, Maderna, Luca, Messina, Stefano, Gentilini, Davide, Fogh, Isabella, Ratti, Antonia, Silani, Vincenzo, Ticozzi, Nicola

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The contribution of Neanderthal introgression and natural selection to neurodegenerative diseases von Chen, Zhongbo, Reynolds, Regina H, Pardiñas, Antonio F, Gagliano Taliun, Sarah A, van Rheenen, Wouter, Lin, Kuang, Shatunov, Aleksey, Gustavsson, Emil K, Fogh, Isabella, Jones, Ashley R, Robberecht, Wim, Corcia, Philippe, Chiò, Adriano, Shaw, Pamela J, Morrison, Karen E, Veldink, Jan H, van den Berg, Leonard H, Shaw, Christopher E, Powell, John F, Silani, Vincenzo, Hardy, John A, Houlden, Henry, Owen, Michael J, Turner, Martin R, Ryten, Mina, Al-Chalabi, Ammar

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The contribution of Neanderthal introgression and natural selection to neurodegenerative diseases von Chen, Zhongbo, Reynolds, Regina H, Pardinas, Antonio F, Taliun, Sarah A. Gagliano, van Rheenen, Wouter, Lin, Kuang, Shatunov, Aleksey, Gustavsson, Emil K, Fogh, Isabella, Jones, Ashley R, Robberecht, Wim, Corcia, Philippe, Chio, Adriano, Shaw, Pamela J, Morrison, Karen E, Veldink, Jan H, van den Berg, Leonard H, Shaw, Christopher E, Powell, John F, Silani, Vincenzo, Hardy, John A, Houlden, Henry, Owen, Michael J, Turner, Martin R, Ryten, Mina, Al-Chalabi, Ammar

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Computing linkage disequilibrium aware genome embeddings using autoencoders von Taş, Gizem, Westerdijk, Timo, Postma, Eric, Veldink, Jan H, Schönhuth, Alexander, Balvert, Marleen

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