MOLGENIS catalogue

Autor Swertz, Morris, van Enckevort, David, Pang, Chao
Vydáno v J Clin Bioinforma (2015)

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

Autor Holub, Petr, Swertz, Morris, Reihs, Robert, van Enckevort, David, Müller, Heimo, Litton, Jan-Eric
Vydáno v Biopreserv Biobank (2016)

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

Autor 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.
Vydáno v Hum Mutat (2018)

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

Autor 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
Vydáno v Bioinformatics (2017)

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

Autor 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.
Vydáno v Bioinformatics (2016)

Integration of EGA secure data access into Galaxy

Autor 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
Vydáno v F1000Res (2016)

MOLGENIS research: advanced bioinformatics data software for non-bioinformaticians

Autor 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
Vydáno v Bioinformatics (2019)

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

Autor 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
Vydáno v F1000Res (2017)

Improved imputation quality of low-frequency and rare variants in European samples using the ‘Genome of The Netherlands'

Autor 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
Vydáno 2014

Recommendations for Improving the Quality of Rare Disease Registries

Autor 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
Vydáno v Int J Environ Res Public Health (2018)

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

Autor 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.
Vydáno v Nat Commun (2015)