Mutations in potassium channel kcnd3 cause spinocerebellar ataxia type 19 by Duarri, Anna, Jezierska, Justyna, Fokkens, Michiel, Meijer, Michel, Schelhaas, Helenius J., den Dunnen, Wilfred F. A., van Dijk, Freerk, Verschuuren-Bemelmans, Corien, Hageman, Gerard, van de Vlies, Pieter, Küsters, Benno, van de Warrenburg, Bart P., Kremer, Berry, Wijmenga, Cisca, Sinke, Richard J., Swertz, Morris A., Kampinga, Harm H., Boddeke, Erik, Verbeek, Dineke S.

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Feasibility of predicting allele specific expression from DNA sequencing using machine learning by Zhang, Zhenhua, van Dijk, Freerk, de Klein, Niek, van Gijn, Mariëlle E, Franke, Lude H, Sinke, Richard J, Swertz, Morris A, van der Velde, K Joeri

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Deleterious alleles in the human genome are on average younger than neutral alleles of the same frequency by Kiezun, Adam, Pulit, Sara L, Francioli, Laurent C, van Dijk, Freerk, Swertz, Morris, Boomsma, Dorret I, van Duijn, Cornelia M, Slagboom, P Eline, van Ommen, G J B, Wijmenga, Cisca, de Bakker, Paul I W, Sunyaev, Shamil R

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Cohort Profile: LifeLines, a three-generation cohort study and biobank by Scholtens, Salome, Smidt, Nynke, Swertz, Morris A, Bakker, Stephan J L, Dotinga, Aafje, Vonk, Judith M, van Dijk, Freerk, van Zon, Sander K R, Wijmenga, Cisca, Wolffenbuttel, Bruce H R, Stolk, Ronald P

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Meta-GWAS and Meta-Analysis of Exome Array Studies Do Not Reveal Genetic Determinants of Serum Hepcidin by Galesloot, Tessel E, Verweij, Niek, Traglia, Michela, Barbieri, Caterina, van Dijk, Freerk, Geurts-Moespot, Anneke J, Girelli, Domenico, Kiemeney, Lambertus A L M, Sweep, Fred C G J, Swertz, Morris A, van der Meer, Peter, Camaschella, Clara, Toniolo, Daniela, Vermeulen, Sita H, van der Harst, Pim, Swinkels, Dorine W

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Optical genome mapping identifies a germline retrotransposon insertion in SMARCB1 in two siblings with atypical teratoid rhabdoid tumors by Sabatella, Mariangela, Mantere, Tuomo, Waanders, Esmé, Neveling, Kornelia, Mensenkamp, Arjen R, Dijk, Freerk, Hehir‐Kwa, Jayne Y, Derks, Ronnie, Kwint, Michael, O'Gorman, Luke, Tropa Martins, Madalena, Gidding, Corrie EM, Lequin, Maarten H, Küsters, Benno, Wesseling, Pieter, Nelen, Marcel, Biegel, Jacklyn A, Hoischen, Alexander, Jongmans, Marjolijn C, Kuiper, Roland P

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Minimal residual disease (MRD) detection in acute lymphoblastic leukaemia based on fusion genes and genomic deletions: towards MRD for all by Kuiper, Roland P., Hoogeveen, Patricia G., Bladergroen, Reno, Dijk, Freerk, Sonneveld, Edwin, Leeuwen, Frank N., Boer, Judith, Sergeeva, Irina, Feitsma, Harma, Boer, Monique L., Velden, Vincent H. J.

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Improved imputation quality of low-frequency and rare variants in European samples using the 'Genome of The Netherlands' by Deelen, Patrick, Menelaou, Androniki, van Leeuwen, Elisabeth M, Kanterakis, Alexandros, van Dijk, Freerk, Medina-Gomez, Carolina, Francioli, Laurent C, Hottenga, Jouke Jan, Karssen, Lennart C, Estrada, Karol, Kreiner-Møller, Eskil, Rivadeneira, Fernando, van Setten, Jessica, Gutierrez-Achury, Javier, Westra, Harm-Jan, Franke, Lude, van Enckevort, David, Dijkstra, Martijn, Byelas, Heorhiy, van Duijn, Cornelia M, de Bakker, Paul I W, Wijmenga, Cisca, Swertz, Morris A

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NIPTeR: an R package for fast and accurate trisomy prediction in non-invasive prenatal testing by Johansson, Lennart F, de Weerd, Hendrik A, de Boer, Eddy N, van Dijk, Freerk, Te Meerman, Gerard J, Sijmons, Rolf H, Sikkema-Raddatz, Birgit, Swertz, Morris A

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A pipeline‐friendly software tool for genome diagnostics to prioritize genes by matching patient symptoms to literature by Velde, K. Joeri, Hoek, Sander, Dijk, Freerk, Hendriksen, Dennis, Diemen, Cleo C., Johansson, Lennart F., Abbott, Kristin M., Deelen, Patrick, Sikkema‐Raddatz, Birgit, Swertz, Morris A.

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Genetic and environmental influences interact with age and sex in shaping the human methylome by van Dongen, Jenny, Nivard, Michel G., Willemsen, Gonneke, Hottenga, Jouke-Jan, Helmer, Quinta, Dolan, Conor V., Ehli, Erik A., Davies, Gareth E., van Iterson, Maarten, Breeze, Charles E., Beck, Stephan, Suchiman, H. Eka, Jansen, Rick, van Meurs, Joyce B., Heijmans, Bastiaan T., Slagboom, P. Eline, Boomsma, Dorret I.

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Controlling bias and inflation in epigenome- and transcriptome-wide association studies using the empirical null distribution by van Iterson, Maarten, van Zwet, Erik W, Heijmans, Bastiaan T

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DNA Methylation Analysis Identifies Loci for Blood Pressure Regulation by Richard, Melissa A., Huan, Tianxiao, Ligthart, Symen, Gondalia, Rahul, Jhun, Min A., Brody, Jennifer A., Irvin, Marguerite R., Montasser, May E., Jia, Yucheng, Syme, Catriona, Salfati, Elias L., Boerwinkle, Eric, Guan, Weihua, Mosley, Thomas H., Bressler, Jan, Morrison, Alanna C., Liu, Chunyu, Mendelson, Michael M., Uitterlinden, André G., van Meurs, Joyce B., ’t Hoen, Peter A.C., van Meurs, Joyce, Isaacs, Aaron, Franke, Lude, Boomsma, Dorret I., Pool, René, Hottenga, Jouke J., van Greevenbroek, Marleen M.J., Stehouwer, Coen D.A., Wijmenga, Cisca, Zhernakova, Alexandra, Slagboom, P. Eline, Beekman, Marian, Deelen, Joris, van Heemst, Diana, Veldink, Jan H., van den Berg, Leonard H., van Duijn, Cornelia M., Hofman, Albert, Uitterlinden, André G., Jhamai, P. Mila, Verbiest, Michael, Suchiman, H. Eka D., Verkerk, Marijn, van der Breggen, Ruud, van Rooij, Jeroen, Lakenberg, Nico, Mei, Hailiang, van Iterson, Maarten, van Galen, Michiel, Bot, Jan, Nooren, Irene, Moed, Matthijs, Vermaat, Martijn, Zhernakova, Dasha V., Luijk, René, Bonder, Marc Jan, van Dijk, Freerk, Arindrarto, Wibowo, Kielbasa, Szymon M., Swertz, Morris A., van Zwet, Erik W., Franco, Oscar H., Zhang, Guosheng, Li, Yun, Stewart, James D., Bis, Joshua C., Psaty, Bruce M., Chen, Yii-Der Ida, Kardia, Sharon L.R., Zhao, Wei, Absher, Devin, Aslibekyan, Stella, Starr, John M., McRae, Allan F., Schwartz, Joel D., Vokonas, Pantel S., Menni, Cristina, Spector, Tim D., Shuldiner, Alan, Damcott, Coleen M., Rotter, Jerome I., Palmas, Walter, Liu, Yongmei, Paus, Tomáš, Horvath, Steve, O’Connell, Jeffrey R., Guo, Xiuqing, Pausova, Zdenka, Assimes, Themistocles L., Sotoodehnia, Nona, Smith, Jennifer A., Arnett, Donna K., Deary, Ian J., Baccarelli, Andrea A., Bell, Jordana T., Whitsel, Eric, Dehghan, Abbas, Levy, Daniel, Fornage, Myriam

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Mendelian randomization integrating GWAS and eQTL data reveals genetic determinants of complex and clinical traits by Porcu, Eleonora, Rüeger, Sina, Lepik, Kaido, Santoni, Federico A., Reymond, Alexandre, Kutalik, Zoltán

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Genome-wide study of DNA methylation shows alterations in metabolic, inflammatory, and cholesterol pathways in ALS by Hop, Paul J, Zwamborn, Ramona A J, Hannon, Eilis, Shireby, Gemma L, Nabais, Marta F, Walker, Emma M, van Rheenen, Wouter, van Vugt, Joke J F A, Dekker, Annelot M, Westeneng, Henk-Jan, Tazelaar, Gijs H P, van Eijk, Kristel R, Moisse, Matthieu, Baird, Denis, Al Khleifat, Ahmad, Iacoangeli, Alfredo, Ticozzi, Nicola, Ratti, Antonia, Cooper-Knock, Jonathan, Morrison, Karen E, Shaw, Pamela J, Basak, A Nazli, Chiò, Adriano, Calvo, Andrea, Moglia, Cristina, Canosa, Antonio, Brunetti, Maura, Grassano, Maurizio, Gotkine, Marc, Lerner, Yossef, Zabari, Michal, Vourc'h, Patrick, Corcia, Philippe, Couratier, Philippe, Mora Pardina, Jesus S, Salas, Teresa, Dion, Patrick, Ross, Jay P, Henderson, Robert D, Mathers, Susan, McCombe, Pamela A, Needham, Merrilee, Nicholson, Garth, Rowe, Dominic B, Pamphlett, Roger, Mather, Karen A, Sachdev, Perminder S, Furlong, Sarah, Garton, Fleur C, Henders, Anjali K, Lin, Tian, Ngo, Shyuan T, Steyn, Frederik J, Wallace, Leanne, Williams, Kelly L, Neto, Miguel Mitne, Cauchi, Ruben J, Blair, Ian P, Kiernan, Matthew C, Drory, Vivian, Povedano, Monica, de Carvalho, Mamede, Pinto, Susana, Weber, Markus, Rouleau, Guy A, Silani, Vincenzo, Landers, John E, Shaw, Christopher E, Andersen, Peter M, McRae, Allan F, van Es, Michael A, Pasterkamp, R Jeroen, Wray, Naomi R, McLaughlin, Russell L, Hardiman, Orla, Kenna, Kevin P, Tsai, Ellen, Runz, Heiko, Al-Chalabi, Ammar, van den Berg, Leonard H, Van Damme, Philip, Mill, Jonathan, Veldink, Jan H

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Skewed X-inactivation is common in the general female population by Shvetsova, Ekaterina, Sofronova, Alina, Monajemi, Ramin, Gagalova, Kristina, Draisma, Harmen H M, White, Stefan J, Santen, Gijs W E, Chuva de Sousa Lopes, Susana M, Heijmans, Bastiaan T, van Meurs, Joyce, Jansen, Rick, Franke, Lude, Kiełbasa, Szymon M, den Dunnen, Johan T, 't Hoen, Peter A C

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Genetics, Lifestyle, and Low-Density Lipoprotein Cholesterol in Young and Apparently Healthy Women by Balder, Jan-Willem, Rimbert, Antoine, Zhang, Xiang, Viel, Martijn, Kanninga, Roan, van Dijk, Freerk, Lansberg, Peter, Sinke, Richard, Kuivenhoven, Jan Albert

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A Novel Germline PAX5 Single Exon Deletion in a Paediatric Patient with B-Cell Leukaemia by van Engelen, Nienke, Roest, Merel A., van Dijk, Freerk, Sonneveld, Edwin, Bladergroen, Reno, van Reijmersdal, Simon, van der Velden, Vincent H.J., Hoogeveen, Patricia G., Kors, W.A., Waanders, Esme, Kuiper, Roland P., Jongmans, Marjolijn C.J.

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Epigenome-wide Association Study of Attention-Deficit/Hyperactivity Disorder Symptoms in Adults by van Dongen, Jenny, Zilhão, Nuno R., Sugden, Karen, Heijmans, Bastiaan T., ’t Hoen, Peter A.C., van Meurs, Joyce, Isaacs, Aaron, Jansen, Rick, Franke, Lude, Boomsma, Dorret I., Pool, René, van Dongen, Jenny, Hottenga, Jouke J., van Greevenbroek, Marleen M.J., Stehouwer, Coen D.A., van der Kallen, Carla J.H., Schalkwijk, Casper G., Wijmenga, Cisca, Zhernakova, Sasha, Tigchelaar, Ettje F., Slagboom, P. Eline, Beekman, Marian, Deelen, Joris, van Heemst, Diana, Veldink, Jan H., van den Berg, Leonard H., van Duijn, Cornelia M., Hofman, Bert A., Uitterlinden, André G., van Meurs, Joyce, Jhamai, P. Mila, Verbiest, Michael, Suchiman, H. Eka D., Verkerk, Marijn, van der Breggen, Ruud, van Rooij, Jeroen, Lakenberg, Nico, Mei, Hailiang, van Iterson, Maarten, van Galen, Michiel, Bot, Jan, Zhernakova, Dasha V., Hof, Peter van ’t, Deelen, Patrick, Nooren, Irene, Heijmans, Bastiaan T., Moed, Matthijs, Franke, Lude, Vermaat, Martijn, Luijk, René, Bonder, Marc Jan, van Dijk, Freerk, Arindrarto, Wibowo, Kielbasa, Szymon M., Swertz, Morris A., van Zwet, Erik. W., Hoen, Peter-Bram ’t, Heijmans, Bastiaan T., Hannon, Eilis J., Mill, Jonathan, Caspi, Avshalom, Agnew-Blais, Jessica, Arseneault, Louise, Corcoran, David L., Moffitt, Terrie E., Poulton, Richie, Franke, Barbara, Boomsma, Dorret I.

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Improving Phenotypic Prediction by Combining Genetic and Epigenetic Associations by Shah, Sonia, Bonder, Marc J., Marioni, Riccardo E., Zhu, Zhihong, McRae, Allan F., Zhernakova, Alexandra, Harris, Sarah E., Liewald, Dave, Henders, Anjali K., Mendelson, Michael M., Liu, Chunyu, Joehanes, Roby, Liang, Liming, Heijmans, Bastiaan T., ’t Hoen, Peter A.C., van Meurs, Joyce, Isaacs, Aaron, Jansen, Rick, Franke, Lude, Boomsma, Dorret I., Pool, René, van Dongen, Jenny, Hottenga, Jouke J., van Greevenbroek, Marleen M.J., Stehouwer, Coen D.A., van der Kallen, Carla J.H., Schalkwijk, Casper G., Wijmenga, Cisca, Zhernakova, Sasha, Tigchelaar, Ettje F., Slagboom, P. Eline, Beekman, Marian, Deelen, Joris, van Heemst, Diana, Veldink, Jan H., van den Berg, Leonard H., van Duijn, Cornelia M., Hofman, Bert A., Uitterlinden, André G., Jhamai, P. Mila, Verbiest, Michael, Suchiman, H. Eka D., Verkerk, Marijn, van der Breggen, Ruud, van Rooij, Jeroen, Lakenberg, Nico, Mei, Hailiang, van Iterson, Maarten, van Galen, Michiel, Bot, Jan, van ’t Hof, Peter, Deelen, Patrick, Nooren, Irene, Moed, Matthijs, Vermaat, Martijn, Zhernakova, Dasha V., Luijk, René, Bonder, Marc Jan, van Dijk, Freerk, Arindrarto, Wibowo, Kielbasa, Szymon M., Swertz, Morris A., van Zwet, Erik W., Levy, Daniel, Martin, Nicholas G., Starr, John M., Wijmenga, Cisca, Wray, Naomi R., Yang, Jian, Montgomery, Grant W., Franke, Lude, Deary, Ian J., Visscher, Peter M.

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