P. (Patrick) Deelen

Research

  1. 2019
  2. eQTLgen Consortium, Timmers, P. R., Mounier, N., Lall, K., Fischer, K., Ning, Z., ... Clark, D. W. (2019). Genomics of 1 million parent lifespans implicates novel pathways and common diseases and distinguishes survival chances. eLife, 8, [39856]. https://doi.org/10.7554/eLife.39856
  3. 2018
  4. 2017
  5. Pital-Zhernakova, D., Deelen, P., Vermaat, M., van Iterson, M., van Galen, M., Arindrarto, W., ... Franke, L. (2017). Identification of context-dependent expression quantitative trait loci in whole blood. Nature Genetics, 49(1), 139-145. https://doi.org/10.1038/ng.3737
  6. 2016
  7. Li, Y., Oosting, M., Smeekens, S. P., Jaeger, M., Aguirre-Gamboa, R., Le, K. T. T., ... Netea, M. G. (2016). A Functional Genomics Approach to Understand Variation in Cytokine Production in Humans. Cell, 167(4), 1099-1110. https://doi.org/10.1016/j.cell.2016.10.017
  8. Iotchkova, V., Huang, J., Morris, J. A., Jain, D., Barbieri, C., Walter, K., ... UK10K consortium (2016). Discovery and refinement of genetic loci associated with cardiometabolic risk using dense imputation maps. Nature Genetics, 48(11), 1303-1312. https://doi.org/10.1038/ng.3668
  9. Hehir-Kwa, J. Y., Marschall, T., Kloosterman, W. P., Francioli, L. C., Baaijens, J. A., Dijkstra, L. J., ... Genome Netherlands Consortium (2016). A high-quality human reference panel reveals the complexity and distribution of genomic structural variants. Nature Communications, 7, [12989]. https://doi.org/10.1038/ncomms12989
  10. Slieker, R. C., van Iterson, M., Luijk, R., Beekman, M., Zhernakova, D. V., Moed, M. H., ... BIOS Consortium (2016). Age-related accrual of methylomic variability is linked to fundamental ageing mechanisms. Genome Biology, 17, [191]. https://doi.org/10.1186/s13059-016-1053-6
  11. Hendriksen, D. (Author), Haan, M. D. (Author), [Unknown], B. (Author), Pang, C. (Author), [Unknown], J. (Author), Kelpin, F. (Author), ... Neerincx, P. (Author). (2016). joerivandervelde/molgenis: MOLGENIS v1.21.2G1. Software https://doi.org/10.5281/zenodo.155255
  12. Visschedijk, M. C., Alberts, R., Mucha, S., Deelen, P., de Jong, D. J., Pierik, M., ... Dutch Initiative on Crohn and Colitis (2016). Pooled Resequencing of 122 Ulcerative Colitis Genes in a Large Dutch Cohort Suggests Population-Specific Associations of Rare Variants in MUC2. PLoS ONE, 11(8), [e0159609]. https://doi.org/10.1371/journal.pone.0159609
  13. 2015
  14. van Leeuwen, E. M., Kanterakis, A., Deelen, P., Kattenberg, M. V., Slagboom, P. E., de Bakker, P. I. W., ... Genome Netherlands Consortium (2015). Population-specific genotype imputations using minimac or IMPUTE2. Nature protocols, 10(9), 1285-1296. https://doi.org/10.1038/nprot.2015.077
  15. Farlow, J. L., Lin, H., Sauerbeck, L., Lai, D., Koller, D. L., Pugh, E., ... FIA Study Investigators (2015). Lessons Learned from Whole Exome Sequencing in Multiplex Families Affected by a Complex Genetic Disorder, Intracranial Aneurysm. PLoS ONE, 10(3), [e0121104]. https://doi.org/10.1371/journal.pone.0121104
  16. van Leeuwen, E. M., Karssen, L. C., Deelen, J., Isaacs, A., Medina-Gomez, C., Mbarek, H., ... Genome Netherlands Consortium (2015). Genome of the Netherlands population-specific imputations identify an ABCA6 variant associated with cholesterol levels. Nature Communications, 6, [6065]. https://doi.org/10.1038/ncomms7065
  17. 2014
  18. Francioli, L. C., Menelaou, A., Pulit, S. L., Van Dijk, F., Palamara, P. F., Elbers, C. C., ... Lifelines Cohort Study (2014). Whole-genome sequence variation, population structure and demographic history of the Dutch population. Nature Genetics, 46(8), 818-825. https://doi.org/10.1038/ng.3021
  19. Boomsma, D. I., Wijmenga, C., Slagboom, E. P., Swertz, M. A., Karssen, L. C., Abdellaoui, A., ... van Duijn, C. M. (2014). The Genome of the Netherlands: design, and project goals. European Journal of Human Genetics, 22(2), 221-227. https://doi.org/10.1038/ejhg.2013.118
  20. 2013
  21. 2012
  22. 2011
  23. Szperl, A. M., Ricaño-Ponce, I., Li, J. K., Deelen, P., Kanterakis, A., Plagnol, V., ... Zheng, H. C. H. (2011). Exome sequencing in a family segregating for celiac disease. Clinical Genetics, 80(2), 138-147. https://doi.org/10.1111/j.1399-0004.2011.01714.x

ID: 453721