Enrichment of SARM1 alleles encoding variants with constitutively hyperactive NADase in patients with ALS and other motor nerve disorders by Gilley, Jonathan, Jackson, Oscar, Pipis, Menelaos, Estiar, Mehrdad A, Al-Chalabi, Ammar, Danzi, Matt C, van Eijk, Kristel R, Goutman, Stephen A, Harms, Matthew B, Houlden, Henry, Iacoangeli, Alfredo, Kaye, Julia, Lima, Leandro, Ravits, John, Rouleau, Guy A, Schüle, Rebecca, Xu, Jishu, Züchner, Stephan, Cooper-Knock, Johnathan, Gan-Or, Ziv, Reilly, Mary M, Coleman, Michael P

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Genetic analysis of DNA methylation and gene expression levels in whole blood of healthy human subjects by van Eijk, Kristel R, de Jong, Simone, Boks, Marco P M, Langeveld, Terry, Colas, Fabrice, Veldink, Jan H, de Kovel, Carolien G F, Janson, Esther, Strengman, Eric, Langfelder, Peter, Kahn, René S, van den Berg, Leonard H, Horvath, Steve, Ophoff, Roel A

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Whole blood transcriptome analysis in amyotrophic lateral sclerosis: A biomarker study by 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 Distinct Traits of the UNC13A Polymorphism in Amyotrophic Lateral Sclerosis by Tan, Harold H. G., Westeneng, Henk‐Jan, Burgh, Hannelore K., Es, Michael A., Bakker, Leonhard A., Veenhuijzen, Kevin, Eijk, Kristel R., Eijk, Ruben P. A., Veldink, Jan H., Berg, Leonard H.

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Characterization of genome-methylome interactions in 22 nuclear pedigrees by Plongthongkum, Nongluk, van Eijk, Kristel R, de Jong, Simone, Wang, Tina, Sul, Jae Hoon, Boks, Marco P M, Kahn, René S, Fung, Ho-Lim, Ophoff, Roel A, Zhang, Kun

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Pharmacogenetic interactions in amyotrophic lateral sclerosis: a step closer to a cure? by van Eijk, Ruben P. A., Eijkemans, Marinus J. C., Nikolakopoulos, Stavros, Jansen, Marc D., Westeneng, Henk-Jan, van Eijk, Kristel R., van der Spek, Rick A. A., van Vugt, Joke J. F. A., Piepers, Sanne, Groeneveld, Geert-Jan, Veldink, Jan H., van den Berg, Leonard H., van Es, Michael A.

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Childhood maltreatment mediates the effect of the genetic background on psychosis risk in young adults by Marchi, Mattia, Elkrief, Laurent, Alkema, Anne, van Gastel, Willemijn, Schubart, Chris D., van Eijk, Kristel R., Luykx, Jurjen J., Branje, Susan, Mastrotheodoros, Stefanos, Galeazzi, Gian M., van Os, Jim, Cecil, Charlotte A., Conrod, Patricia J., Boks, Marco P.

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Exome array analysis of rare and low frequency variants in amyotrophic lateral sclerosis by 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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Expression QTL analysis of top loci from GWAS meta-analysis highlights additional schizophrenia candidate genes by DE JONG, Simone, VAN EIJK, Kristel R, OPHOFF, Roel A, ZEEGERS, Dave W. L. H, STRENGMAN, Eric, JANSON, Esther, VELDINK, Jan H, VAN DEN BERG, Leonard H, CAHN, Wiepke, KAHN, René S, BOKS, Marco P. M

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Genetic variants associated with longitudinal changes in brain structure across the lifespan by Schnack, Hugo G., Jahanshad, Neda, Thomopoulos, Sophia I., Sprooten, Emma, Gogtay, Nitin, Whelan, Christopher D., Alloza, Clara, Artiges, Eric, Blok, Elisabet, Bright, Joanna K., Buimer, Elizabeth E. L., Cannon, Dara M., Ciufolini, Simone, Crossley, Nicolas A., Damatac, Christienne G., de Mol, Casper L., de Zwarte, Sonja M. C., Díaz-Caneja, Covadonga M., Doan, Nhat Trung, Dohm, Katharina, Fröhner, Juliane H., Goltermann, Janik, Grigis, Antoine, Han, Laura K. M., Hartman, Catharina A., Heindel, Walter, Janssen, Joost, Jiang, Jiyang, Jockwitz, Christiane, Lenroot, Rhoshel K., Mandl, René C. W., Medel, Vicente, de la Foz, Víctor Ortiz-García, Overs, Bronwyn J., Paillère Martinot, Marie-Laure, Repple, Jonathan, Roberts, Gloria, Setiaman, Nikita, Shumskaya, Elena, Wen, Wei, Westeneng, Henk-Jan, Wittfeld, Katharina, Zugman, Andre, Armstrong, Nicola J., Davies, Gail, Di Forti, Marta, Ding, Linda, Donohoe, Gary, Forstner, Andreas J., Guimaraes, Joao P. O. F. T., Knol, Maria J., Kwok, John B. J., Milaneschi, Yuri, Morris, Derek W., Rietschel, Marcella, Streit, Fabian, van ‘t Ent, Dennis, van der Meer, Dennis, van Eijk, Kristel R., Vázquez-Bourgon, Javier, Witt, Stephanie H., Agartz, Ingrid, Ames, David, Amunts, Katrin, Arango, Celso, Baune, Bernhard T., Belangero, Sintia I., Bokde, Arun L. W., Boomsma, Dorret I., Bressan, Rodrigo A., Brodaty, Henry, Cahn, Wiepke, Caspers, Svenja, Cox, Simon R., Fisher, Simon E., Flor, Herta, Grabe, Hans J., Hoekstra, Pieter J., Jackowski, Andrea P., Jansen, Andreas, Jönsson, Erik G., Kahn, Rene S., Kircher, Tilo, Krug, Axel, Lemaitre, Herve, Martinot, Jean-Luc, McDonald, Colm, Nenadić, Igor, Pan, Pedro M., Penninx, Brenda W. J. H., Poustka, Luise, Schofield, Peter R., Schumann, Gunter, Sim, Kang, Trollor, Julian N., Veldink, Jan H., Westlye, Lars T., Whelan, Robert, Medland, Sarah E., Thompson, Paul M.

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The role of rare compound heterozygous events in autism spectrum disorder by Lin, Bochao Danae, Colas, Fabrice, Nijman, Isaac J., Medic, Jelena, Brands, William, Parr, Jeremy R., van Eijk, Kristel R., Klauck, Sabine M., Chiocchetti, Andreas G., Freitag, Christine M., Maestrini, Elena, Bacchelli, Elena, Coon, Hilary, Vicente, Astrid, Oliveira, Guiomar, Pagnamenta, Alistair T., Gallagher, Louise, Ennis, Sean, Anney, Richard, Bourgeron, Thomas, Luykx, Jurjen J., Vorstman, Jacob

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Project MinE: study design and pilot analyses of a large-scale whole-genome sequencing study in amyotrophic lateral sclerosis by 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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Phenome-wide and genome-wide analyses of quality of life in schizophrenia - ERRATUM by Pazoki, Raha, Lin, Bochao Danae, van Eijk, Kristel R, Schijven, Dick, de Zwarte, Sonja, Guloksuz, Sinan, Luykx, Jurjen J

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Cross-reactive probes on Illumina DNA methylation arrays: a large study on ALS shows that a cautionary approach is warranted in interpreting epigenome-wide association studies by Hop, Paul J, Zwamborn, Ramona A J, Hannon, Eilis J, Dekker, Annelot M, van Eijk, Kristel R, Walker, Emma M, Iacoangeli, Alfredo, Jones, Ashley R, Shatunov, Aleksey, Khleifat, Ahmad Al, Opie-Martin, Sarah, Shaw, Christopher E, Morrison, Karen E, Shaw, Pamela J, McLaughlin, Russell L, Hardiman, Orla, Al-Chalabi, Ammar, Van Den Berg, Leonard H, Mill, Jonathan, Veldink, Jan H

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Phenome-wide and genome-wide analyses of quality of life in schizophrenia by Pazoki, Raha, Lin, Bochao Danae, van Eijk, Kristel R., Schijven, Dick, de Zwarte, Sonja, Guloksuz, Sinan, Luykx, Jurjen J.

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Genetic vulnerability to schizophrenia is associated with cannabis use patterns during adolescence by Hiemstra, Marieke, Nelemans, Stefanie A., Branje, Susan, van Eijk, Kristel R., Hottenga, Jouke-Jan, Vinkers, Christiaan H., van Lier, Pol, Meeus, Wim, Boks, Marco P.

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Polygenic risk, familial liability and stress reactivity in psychosis: an experience sampling study by Schick, Anita, van Winkel, Ruud, Lin, Bochao D., Luykx, Jurjen J., de Zwarte, Sonja M.C., van Eijk, Kristel R., Myin-Germeys, Inez, Reininghaus, Ulrich

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Increased paternal age and the influence on burden of genomic copy number variation in the general population by Buizer-Voskamp, Jacobine E., Blauw, Hylke M., Boks, Marco P. M., van Eijk, Kristel R., Veldink, Jan H., Hennekam, Eric A. M., Vorstman, Jacob A. S., Mulder, Flip, Tiemeier, Henning, Uitterlinden, André G., Kiemeney, Lambertus A., van den Berg, Leonard H., Kahn, René S., Sabatti, Chiara, Ophoff, Roel A.

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Association of preceding psychosis risk states and non‐psychotic mental disorders with incidence of clinical psychosis in the general population: a prospective study in the NEMESIS... by Guloksuz, Sinan, Pries, Lotta‐Katrin, Have, Margreet, Graaf, Ron, Dorsselaer, Saskia, Klingenberg, Boris, Bak, Maarten, Lin, Bochao D., Eijk, Kristel R., Delespaul, Philippe, Amelsvoort, Therese, Luykx, Jurjen J., Rutten, Bart P.F., Os, Jim

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Integrative genetic analysis illuminates ALS heritability and identifies risk genes by Megat, Salim, Mora, Natalia, Sanogo, Jason, Roman, Olga, Catanese, Alberto, Alami, Najwa Ouali, Freischmidt, Axel, Mingaj, Xhuljana, De Calbiac, Hortense, Muratet, François, Dirrig-Grosch, Sylvie, Dieterle, Stéphane, Van Bakel, Nick, Müller, Kathrin, Sieverding, Kirsten, Weishaupt, Jochen, Andersen, Peter Munch, Weber, Markus, Neuwirth, Christoph, Margelisch, Markus, Sommacal, Andreas, Van Eijk, Kristel R., Veldink, Jan H., Lautrette, Géraldine, Couratier, Philippe, Camuzat, Agnès, Le Ber, Isabelle, Grassano, Maurizio, Chio, Adriano, Boeckers, Tobias, Ludolph, Albert C., Roselli, Francesco, Yilmazer-Hanke, Deniz, Millecamps, Stéphanie, Kabashi, Edor, Storkebaum, Erik, Sellier, Chantal, Dupuis, Luc

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