MOLGENIS catalogue

by Swertz, Morris, van Enckevort, David, Pang, Chao
Published in J Clin Bioinforma (2015)

BBMRI-ERIC Directory: 515 Biobanks with Over 60 Million Biological Samples

by Holub, Petr, Swertz, Morris, Reihs, Robert, van Enckevort, David, Müller, Heimo, Litton, Jan-Eric
Published in Biopreserv Biobank (2016)

MECP2 variation in Rett syndrome—An overview of current coverage of genetic and phenotype data within existing databases

by Townend, Gillian S., Ehrhart, Friederike, van Kranen, Henk J., Wilkinson, Mark, Jacobsen, Annika, Roos, Marco, Willighagen, Egon L., van Enckevort, David, Evelo, Chris T., Curfs, Leopold M. G.
Published in Hum Mutat (2018)

BiobankUniverse: automatic matchmaking between datasets for biobank data discovery and integration

by Pang, Chao, Kelpin, Fleur, van Enckevort, David, Eklund, Niina, Silander, Kaisa, Hendriksen, Dennis, de Haan, Mark, Jetten, Jonathan, de Boer, Tommy, Charbon, Bart, Holub, Petr, Hillege, Hans, Swertz, Morris A
Published in Bioinformatics (2017)

MOLGENIS/connect: a system for semi-automatic integration of heterogeneous phenotype data with applications in biobanks

by Pang, Chao, van Enckevort, David, de Haan, Mark, Kelpin, Fleur, Jetten, Jonathan, Hendriksen, Dennis, de Boer, Tommy, Charbon, Bart, Winder, Erwin, van der Velde, K. Joeri, Doiron, Dany, Fortier, Isabel, Hillege, Hans, Swertz, Morris A.
Published in Bioinformatics (2016)

Integration of EGA secure data access into Galaxy

by Hoogstrate, Youri, Zhang, Chao, Senf, Alexander, Bijlard, Jochem, Hiltemann, Saskia, van Enckevort, David, Repo, Susanna, Heringa, Jaap, Jenster, Guido, Fijneman, Remond J.A., Boiten, Jan-Willem, A. Meijer, Gerrit, Stubbs, Andrew, Rambla, Jordi, Spalding, Dylan, Abeln, Sanne
Published in F1000Res (2016)

MOLGENIS research: advanced bioinformatics data software for non-bioinformaticians

by van der Velde, K Joeri, Imhann, Floris, Charbon, Bart, Pang, Chao, van Enckevort, David, Slofstra, Mariska, Barbieri, Ruggero, Alberts, Rudi, Hendriksen, Dennis, Kelpin, Fleur, de Haan, Mark, de Boer, Tommy, Haakma, Sido, Stroomberg, Connor, Scholtens, Salome, van de Geijn, Gert-Jan, Festen, Eleonora A M, Weersma, Rinse K, Swertz, Morris A
Published in Bioinformatics (2019)

Systematically linking tranSMART, Galaxy and EGA for reusing human translational research data

by Zhang, Chao, Bijlard, Jochem, Staiger, Christine, Scollen, Serena, van Enckevort, David, Hoogstrate, Youri, Senf, Alexander, Hiltemann, Saskia, Repo, Susanna, Pipping, Wibo, Bierkens, Mariska, Payralbe, Stefan, Stringer, Bas, Heringa, Jaap, Stubbs, Andrew, Bonino Da Silva Santos, Luiz Olavo, Belien, Jeroen, Weistra, Ward, Azevedo, Rita, van Bochove, Kees, Meijer, Gerrit, Boiten, Jan-Willem, Rambla, Jordi, Fijneman, Remond, Spalding, J. Dylan, Abeln, Sanne
Published in F1000Res (2017)

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
Published 2014

Recommendations for Improving the Quality of Rare Disease Registries

by Kodra, Yllka, Weinbach, Jérôme, Posada-de-la-Paz, Manuel, Coi, Alessio, Lemonnier, S. Lydie, van Enckevort, David, Roos, Marco, Jacobsen, Annika, Cornet, Ronald, Ahmed, S. Faisal, Bros-Facer, Virginie, Popa, Veronica, Van Meel, Marieke, Renault, Daniel, von Gizycki, Rainald, Santoro, Michele, Landais, Paul, Torreri, Paola, Carta, Claudio, Mascalzoni, Deborah, Gainotti, Sabina, Lopez, Estrella, Ambrosini, Anna, Müller, Heimo, Reis, Robert, Bianchi, Fabrizio, Rubinstein, Yaffa R., Lochmüller, Hanns, Taruscio, Domenica
Published in Int J Environ Res Public Health (2018)

Genome of the Netherlands population-specific imputations identify an ABCA6 variant associated with cholesterol levels

by van Leeuwen, Elisabeth M., Karssen, Lennart C., Deelen, Joris, Isaacs, Aaron, Medina-Gomez, Carolina, Mbarek, Hamdi, Kanterakis, Alexandros, Trompet, Stella, Postmus, Iris, Verweij, Niek, van Enckevort, David J., Huffman, Jennifer E., White, Charles C., Feitosa, Mary F., Bartz, Traci M., Manichaikul, Ani, Joshi, Peter K., Peloso, Gina M., Deelen, Patrick, van Dijk, Freerk, Willemsen, Gonneke, de Geus, Eco J., Milaneschi, Yuri, Penninx, Brenda W.J.H., Francioli, Laurent C., Menelaou, Androniki, Pulit, Sara L., Rivadeneira, Fernando, Hofman, Albert, Oostra, Ben A., Franco, Oscar H., Leach, Irene Mateo, Beekman, Marian, de Craen, Anton J.M., Uh, Hae-Won, Trochet, Holly, Hocking, Lynne J., Porteous, David J., Sattar, Naveed, Packard, Chris J., Buckley, Brendan M., Brody, Jennifer A., Bis, Joshua C., Rotter, Jerome I., Mychaleckyj, Josyf C., Campbell, Harry, Duan, Qing, Lange, Leslie A., Wilson, James F., Hayward, Caroline, Polasek, Ozren, Vitart, Veronique, Rudan, Igor, Wright, Alan F., Rich, Stephen S., Psaty, Bruce M., Borecki, Ingrid B., Kearney, Patricia M., Stott, David J., Adrienne Cupples, L., Jukema, J. Wouter, van der Harst, Pim, Sijbrands, Eric J., Hottenga, Jouke-Jan, Uitterlinden, Andre G., Swertz, Morris A., van Ommen, Gert-Jan B., de Bakker, Paul I.W., Eline Slagboom, P., Boomsma, Dorret I., Wijmenga, Cisca, van Duijn, Cornelia M.
Published in Nat Commun (2015)