Generation and characterization of transgenic mice with the full-length human DMD gene. by 't Hoen, P, de Meijer, E, Boer, J, Vossen, R, Turk, R, Maatman, R, Davies, K, van Ommen, G, van Deutekom, J, den Dunnen, J

Skewed X-inactivation is common in the general female population by Shvetsova, E, Sofronova, A, Monajemi, R, Gagalova, K, Draisma, H, White, S, Santen, G, Chuva De Sousa Lopes, S, Heijmans, B, Van Meurs, J, Jansen, R, Franke, L, Kiełbasa, S, Den Dunnen, J, 'T Hoen, P, Palamara, P

Structuring research methods and data with the research object model: genomics workflows as a case study by Hettne, K, Dharuri, H, Zhao, J, Wolstencroft, K, Belhajjame, K, Soiland-Reyes, S, Mina, E, Thompson, M, Cruickshank, D, Verdes-Montenegro, L, Garrido, J, De Roure, D, Corcho, O, Klyne, G, Van Schouwen, R, 'T Hoen, P, Bechhofer, S, Goble, C, Roos, M

Transcriptome and genome sequencing uncovers functional variation in humans by Lappalainen, T, Sammeth, M, Friedländer, MR, 'T Hoen, P, Monlong, J, Rivas, M, Gonzàlez-Porta, M, Kurbatova, N, Griebel, T, Ferreira, P, Barann, M, Wieland, T, Greger, L, Van Iterson, M, Almlöf, J, Ribeca, P, Pulyakhina, I, Esser, D, Giger, T, Tikhonov, A, Sultan, M, Bertier, G, Macarthur, D, Lek, M, Lizano, E

Transcriptome and genome sequencing uncovers functional variation in humans. by Lappalainen, T, Sammeth, M, Friedländer, MR, 't Hoen, P, Monlong, J, Rivas, M, Gonzàlez-Porta, M, Kurbatova, N, Griebel, T, Ferreira, P, Barann, M, Wieland, T, Greger, L, van Iterson, M, Almlöf, J, Ribeca, P, Pulyakhina, I, Esser, D, Giger, T, Tikhonov, A, Sultan, M, Bertier, G, MacArthur, D, Lek, M, Lizano, E

Systematic identification of trans eQTLs as putative drivers of known disease associations. by Westra, H, Peters, M, Esko, T, Yaghootkar, H, Schurmann, C, Kettunen, J, Christiansen, M, Fairfax, B, Schramm, K, Powell, J, Zhernakova, A, Zhernakova, D, Veldink, J, Van den Berg, L, Karjalainen, J, Withoff, S, Uitterlinden, A, Hofman, A, Rivadeneira, F, 't Hoen, P, Reinmaa, E, Fischer, K, Nelis, M, Milani, L, Melzer, D

Autosomal genetic variation is associated with DNA methylation in regions variably escaping X-chromosome inactivation by Luijk, R, Wu, H, Ward-Caviness, C, Hannon, E, Carnero-Montoro, E, Min, J, Mandaviya, P, Müller-Nurasyid, M, Mei, H, Van Der Maarel, S, BIOS Consortium, Relton, C, Mill, J, Waldenberger, M, Bell, J, Jansen, R, Zhernakova, A, Franke, L, 'T Hoen, P, Boomsma, D, Van Duijn, C, Van Greevenbroek, M, Veldink, J, Wijmenga, C, Van Meurs, J, Daxinger, L, Slagboom, P, Van Zwet, E, Heijmans, B

The FAIR Guiding Principles for scientific data management and stewardship by Wilkinson, M, Dumontier, M, Aalbersberg, I, Appleton, G, Axton, M, Baak, A, Blomberg, N, Boiten, J, da Silva Santos, L, Bourne, P, Bouwman, J, Brookes, A, Clark, T, Crosas, M, Dillo, I, Dumon, O, Edmunds, S, Evelo, C, Finkers, R, Gonzalez-Beltran, A, Gray, A, Groth, P, Goble, C, Grethe, J, Heringa, J, 't Hoen, P, Hooft, R, Kuhn, T, Kok, R, Kok, J, Lusher, S, Martone, M, Mons, A, Packer, A, Persson, B, Rocca-Serra, P, Roos, M, van Schaik, R, Sansone, S, Schultes, E, Sengstag, T, Slater, T, Strawn, G, Swertz, M, Thompson, M, van der Lei, J, van Mulligen, E, Velterop, J, Waagmeester, A, Wittenburg, P, Wolstencroft, K, Zhao, J, Mons, B