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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Joint sequencing of human and pathogen genomes reveals the genetics of pneumococcal meningitis von Lees, John A, Ferwerda, Bart, Kremer, Philip H.C, Wheeler, Nicole E, Serón, Mercedes Valls, Croucher, Nicholas J, Gladstone, Rebecca A, Bootsma, Hester J, Rots, Nynke Y, Wijmega-Monsuur, Alienke J, Sanders, Elisabeth A.M, Trzciński, Krzysztof, Wyllie, Anne L, Zwinderman, Aeilko H, van den Berg, Leonard H, van Rheenen, Wouter, Veldink, Jan H, Harboe, Zitta B, Lundbo, Lene F, de Groot, Lisette C.P.G.M, van Schoor, Natasja M, van der Velde, Nathalie, Ängquist, Lars H, Sørensen, Thorkild I.A, Nohr, Ellen A, Mentzer, Alexander J, Mills, Tara C, Knight, Julian C, du Plessis, Mignon, Nzenze, Susan, Weiser, Jeffrey N, Parkhill, Julian, Madhi, Shabir, Benfield, Thomas, von Gottberg, Anne, van der Ende, Arie, Brouwer, Matthijs C, Barrett, Jeffrey C, Bentley, Stephen D, van de Beek, Diederik

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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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Diagnosing primary lateral sclerosis: a clinico-pathological study von de Boer, Eva M. J., de Vries, Bálint S., Van Hecke, Wim, Mühlebner, Angelika, Vincken, Koen L., Mol, Christian P., van Rheenen, Wouter, Westeneng, Henk-Jan, Veldink, Jan H., Höglinger, Günter U., Morris, Huw R., Litvan, Irene, Raaphorst, Joost, Ticozzi, Nicola, Corcia, Philippe, Vandenberghe, Wim, Pijnenburg, Yolande A. L., Seelaar, Harro, Ingre, Caroline, Van Damme, Philip, van den Berg, Leonard H., van de Warrenburg, Bart P. C., van Es, Michael A.

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Genetic variability in sporadic amyotrophic lateral sclerosis von Van Daele, Sien Hilde, Moisse, Matthieu, van Vugt, Joke J F A, Zwamborn, Ramona A J, van der Spek, Rick, van Rheenen, Wouter, Van Eijk, Kristel, Kenna, Kevin, Corcia, Philippe, Vourc'h, Patrick, Couratier, Philippe, Hardiman, Orla, McLaughin, Russell, Gotkine, Marc, Drory, Vivian, Ticozzi, Nicola, Silani, Vincenzo, Ratti, Antonia, de Carvalho, Mamede, Mora Pardina, Jesús S, Povedano, Monica, Andersen, Peter M, Weber, Markus, Başak, Nazli A, Shaw, Chris, Shaw, Pamela J, Morrison, Karen E, Landers, John E, Glass, Jonathan D, van Es, Michael, van den Berg, Leonard H, Al-Chalabi, Ammar, Veldink, Jan, Van Damme, Philip

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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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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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30ENVIRONMENTAL FACTORS ARE OFTEN HERITABLE: DOES THIS BIAS POLYGENIC GENE-BY-ENVIRONMENT INTERACTION ANALYSES? von Peyrot, Wouter J., Keller, Matthew, van Rheenen, Wouter, Wray, Naomi, Penninx, Brenda

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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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Association Between Serum Lipids and Survival in Patients With Amyotrophic Lateral Sclerosis: A Meta-analysis and Population-Based Study von Janse van Mantgem, Mark R., van Rheenen, Wouter, Hackeng, Anemone V., van Es, Michael A., Veldink, Jan H., van den Berg, Leonard H., van Eijk, Ruben P.A.

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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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Whole genome sequencing analysis reveals post-zygotic mutation variability in monozygotic twins discordant for amyotrophic lateral sclerosis von Tazelaar, Gijs H.P., Hop, Paul J., Seelen, Meinie, van Vugt, Joke J.F.A., van Rheenen, Wouter, Kool, Lindy, van Eijk, Kristel R., Gijzen, Marleen, Dooijes, Dennis, Moisse, Matthieu, Calvo, Andrea, Moglia, Cristina, Brunetti, Maura, Canosa, Antonio, Nordin, Angelica, Pardina, Jesus S. Mora, Ravits, John, Al-Chalabi, Ammar, Chio, Adriano, McLaughlin, Russell L., Hardiman, Orla, Van Damme, Philip, de Carvalho, Mamede, Neuwirth, Christoph, Weber, Markus, Andersen, Peter M, van den Berg, Leonard H., Veldink, Jan H., van Es, Michael A.

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Distal spinal muscular atrophy featured by predominant calf muscle involvement in VRK1 associated disease – Case series and review von Demaegd, Koen, Brilstra, Eva H., Hoogendijk, Jessica E., de Bie, Charlotte I., de Pagter, Mirjam S., van Hecke, Wim, Mühlebner, Angelika, van Es, Michael A., Milone, Margherita, van Rheenen, Wouter

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Analysis of FUS, PFN2, TDP-43, and PLS3 as potential disease severity modifiers in spinal muscular atrophy von Wadman, Renske I, Jansen, Marc D, Curial, Chantall A D, Groen, Ewout J N, Stam, Marloes, Wijngaarde, Camiel A, Medic, Jelena, Sodaar, Peter, van Eijk, Kristel R, Huibers, Manon M H, van Kuik, Joyce, Lemmink, Henny H, van Rheenen, Wouter, Veldink, Jan Herman, van den Berg, Leonard H, van der Pol, W Ludo

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Distal spinal muscular atrophy featured by predominant calf muscle involvement in VRK1 associated disease - Case series and review von Demaegd, Koen, Brilstra, Eva H, Hoogendijk, Jessica E, de Bie, Charlotte I, de Pagter, Mirjam S, van Hecke, Wim, Mühlebner, Angelika, van Es, Michael A, Milone, Margherita, van Rheenen, Wouter

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NIPA1 polyalanine repeat expansions are associated with amyotrophic lateral sclerosis von BLAUW, Hylke M, RHEENEN, Wouter Van, CUPPEN, Edwin, PASTERKAMP, R. Jeroen, ROBBERECHT, Wim, LUDOLPH, Albert C, VELDINK, Jan H, DEN BERG, Leonard H. Van, KOPPERS, Max, VAN DAMME, Philip, WAIBEL, Stefan, LEMMENS, Robin, VUGHT, Paul W. J. Van, MEYER, Thomas, SCHULTE, Claudia, GASSER, Thomas

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