Genetic correlations of polygenic disease traits: from theory to practice von van Rheenen, Wouter, Peyrot, Wouter J., Schork, Andrew J., Lee, S. Hong, Wray, Naomi R.

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Dutch population structure across space, time and GWAS design von Byrne, Ross P., van Rheenen, Wouter, van den Berg, Leonard H., Veldink, Jan H., McLaughlin, Russell L.

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Major advances in neuromuscular disorders in the past two decades von Wadman, Renske I, Rheenen, Wouter van, van der Pol, W Ludo, van den Berg, Leonard H

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Evidence for an oligogenic basis of amyotrophic lateral sclerosis von BLITTERSWIJK, Marka Van, ES, Michael A. Van, DE BAKKER, Paul I. W, VELDINK, Jan H, DEN BERG, Leonard H. Van, HENNEKAM, Eric A. M, DOOIJES, Dennis, RHEENEN, Wouter Van, MEDIC, Jelena, BOURQUE, Pierre R, SCHELHAAS, Helenius J, DER KOOI, Anneke J. Van, DE VISSER, Marianne

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Associations between lifestyle and amyotrophic lateral sclerosis stratified by C9orf72 genotype: a longitudinal, population-based, case-control study von Westeneng, Henk-Jan, van Veenhuijzen, Kevin, van der Spek, Rick A, Peters, Susan, Visser, Anne E, van Rheenen, Wouter, Veldink, Jan H, van den Berg, Leonard H

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UNC13A in amyotrophic lateral sclerosis: from genetic association to therapeutic target von Willemse, SW, Harley, P, van, Eijk RPA, Demaegd, KC, Zelina, P, Pasterkamp, RJ, van, Damme P, Ingre, C, van, Rheenen W, Veldink, JH

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Project MinE: study design and pilot analyses of a large-scale whole-genome sequencing study in amyotrophic lateral sclerosis von Wouter Van Rheenen, Pulit, Sara L, Dekker, Annelot M, Ahmad Al Khleifat, Brands, William J, Iacoangeli, Alfredo, Kenna, Kevin P, Kavak, Ersen, Kooyman, Maarten, McLaughlin, Russell L, Middelkoop, Bas, Moisse, Matthieu, Schellevis, Raymond D, Shatunov, Aleksey, Sproviero, William, Tazelaar, Gijs H P, Rick A A Van der Spek, Perry T C Van Doormaal, Van Eijk, Kristel R, Joke Van Vugt, Basak, A Nazli, Blair, Ian P, Glass, Jonathan D, Hardiman, Orla, Hide, Winston, Landers, John E, Mora, Jesus S, Morrison, Karen E, Newhouse, Stephen, Robberecht, Wim, Shaw, Christopher E, Shaw, Pamela J, Philip Van Damme, Van Es, Michael A, Wray, Naomi R, Al-Chalabi, Ammar, Leonard H Van den Berg, Veldink, Jan H

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Recessive Variants in PIGG Cause a Motor Neuropathy with Variable Conduction Block, Childhood Tremor, and Febrile Seizures: Expanding the Phenotype von Record, Christopher J., O'Connor, Antoinette, Verbeek, Nienke E., Rheenen, Wouter, Zamba Papanicolaou, Eleni, Peric, Stojan, Ligthart, Peter C., Skorupinska, Mariola, Binsbergen, Ellen, Campeau, Philippe M., Ivanovic, Vukan, Hennigan, Brian, McHugh, John C., Blake, Julian C., Murakami, Yoshiko, Laura, Matilde, Murphy, Sinéad M., Reilly, Mary M.

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Genomic signals of migration and continuity in Britain before the Anglo-Saxons von Martiniano, Rui, Caffell, Anwen, Holst, Malin, Hunter-Mann, Kurt, Montgomery, Janet, Müldner, Gundula, McLaughlin, Russell L., Teasdale, Matthew D., van Rheenen, Wouter, Veldink, Jan H., van den Berg, Leonard H., Hardiman, Orla, Carroll, Maureen, Roskams, Steve, Oxley, John, Morgan, Colleen, Thomas, Mark G., Barnes, Ian, McDonnell, Christine, Collins, Matthew J., Bradley, Daniel G.

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Autoantibody pathogenicity in a multifocal motor neuropathy induced pluripotent stem cell-derived model von Harschnitz, Oliver, van den Berg, Leonard H., Johansen, Lill Eva, Jansen, Marc D., Kling, Sandra, Vieira de Sá, Renata, Vlam, Lotte, van Rheenen, Wouter, Karst, Henk, Wierenga, Corette J., Pasterkamp, R. Jeroen, van der Pol, W. Ludo

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Whole blood transcriptome analysis in amyotrophic lateral sclerosis: A biomarker study von van Rheenen, Wouter, Diekstra, Frank P, Harschnitz, Oliver, Westeneng, Henk-Jan, van Eijk, Kristel R, Saris, Christiaan G J, Groen, Ewout J N, van Es, Michael A, Blauw, Hylke M, van Vught, Paul W J, Veldink, Jan H, van den Berg, Leonard H

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The Effect of SMN Gene Dosage on ALS Risk and Disease Severity von Moisse, Matthieu, Zwamborn, Ramona A. J., Vugt, Joke, Spek, Rick, Rheenen, Wouter, Kenna, Brendan, Van Eijk, Kristel, Kenna, Kevin, Corcia, Philippe, Couratier, Philippe, Vourc'h, Patrick, Hardiman, Orla, McLaughin, Russell, Gotkine, Marc, Drory, Vivian, Ticozzi, Nicola, Silani, Vincenzo, Carvalho, Mamede, Mora Pardina, Jesús S., Povedano, Monica, Andersen, Peter M., Weber, Markus, Başak, Nazli A., Chen, Xiao, Eberle, Michael A., Al‐Chalabi, Ammar, Shaw, Chris, Shaw, Pamela J., Morrison, Karen E., Landers, John E., Glass, Jonathan D., Robberecht, Wim, Es, Michael, Berg, Leonard, Veldink, Jan, Van Damme, Philip

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Polygenic risk score analysis for amyotrophic lateral sclerosis leveraging cognitive performance, educational attainment and schizophrenia von Restuadi, Restuadi, Garton, Fleur C, Benyamin, Beben, Lin, Tian, Williams, Kelly L, Vinkhuyzen, Anna, van Rheenen, Wouter, Zhu, Zhihong, Laing, Nigel G, Mather, Karen A, Sachdev, Perminder S, Ngo, Shyuan T, Steyn, Frederik J, Wallace, Leanne, Henders, Anjali K, Visscher, Peter M, Needham, Merrilee, Mathers, Susan, Nicholson, Garth, Rowe, Dominic B, Henderson, Robert D, McCombe, Pamela A, Pamphlett, Roger, Blair, Ian P, Wray, Naomi R, McRae, Allan F

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Circulating microRNAs in patients with intracranial aneurysms von Meeuwsen, John A L, van T Hof, Femke N G, van Rheenen, Wouter, Rinkel, Gabriel J E, Veldink, Jan H, Ruigrok, Ynte M

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UNC13A is a modifier of survival in amyotrophic lateral sclerosis von Diekstra, Frank P, van Vught, Paul W.J, van Rheenen, Wouter, Koppers, Max, Pasterkamp, R. Jeroen, van Es, Michael A, Schelhaas, Helenius J, de Visser, Marianne, Robberecht, Wim, Van Damme, Philip, Andersen, Peter M, van den Berg, Leonard H, Veldink, Jan H

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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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VAPB and C9orf72 mutations in 1 familial amyotrophic lateral sclerosis patient von van Blitterswijk, Marka, van Es, Michael A, Koppers, Max, van Rheenen, Wouter, Medic, Jelena, Schelhaas, Helenius J, van der Kooi, Anneke J, de Visser, Marianne, Veldink, Jan H, van den Berg, Leonard H

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Exome array analysis of rare and low frequency variants in amyotrophic lateral sclerosis von Dekker, Annelot M., Diekstra, Frank P., Pulit, Sara L., Tazelaar, Gijs H. P., van der Spek, Rick A., van Rheenen, Wouter, van Eijk, Kristel R., Calvo, Andrea, Brunetti, Maura, Damme, Philip Van, Robberecht, Wim, Hardiman, Orla, McLaughlin, Russell, Chiò, Adriano, Sendtner, Michael, Ludolph, Albert C., Weishaupt, Jochen H., Pardina, Jesus S. Mora, van den Berg, Leonard H., Veldink, Jan H.

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Functional characterisation of the amyotrophic lateral sclerosis risk locus GPX3/TNIP1 von Restuadi, Restuadi, Steyn, Frederik J, Kabashi, Edor, Ngo, Shyuan T, Cheng, Fei-Fei, Nabais, Marta F, Thompson, Mike J, Qi, Ting, Wu, Yang, Henders, Anjali K, Wallace, Leanne, Bye, Chris R, Turner, Bradley J, Ziser, Laura, Mathers, Susan, McCombe, Pamela A, Needham, Merrilee, Schultz, David, Kiernan, Matthew C, van Rheenen, Wouter, van den Berg, Leonard H, Veldink, Jan H, Ophoff, Roel, Gusev, Alexander, Zaitlen, Noah, McRae, Allan F, Henderson, Robert D, Wray, Naomi R, Giacomotto, Jean, Garton, Fleur C

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Large-scale screening in sporadic amyotrophic lateral sclerosis identifies genetic modifiers in C9orf72 repeat carriers von Dekker, Annelot M, Seelen, Meinie, van Doormaal, Perry T.C, van Rheenen, Wouter, Bothof, Reinoud J.P, van Riessen, Tim, Brands, William J, van der Kooi, Anneke J, de Visser, Marianne, Voermans, Nicol C, Pasterkamp, R. Jeroen, Veldink, Jan H, van den Berg, Leonard H, van Es, Michael A

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