P. (Patrick) Deelen

P. (Patrick) Deelen
p.deelen umcg.nl


  1. 2020
  2. Consortium for the study of genetic associations of celiac disease in Latin-America, Ricaño-Ponce, I., Gutierrez-Achury, J., Costa, A. F., Deelen, P., Kurilshikov, A., ... Wijmenga, C. (2020). Immunochip meta-analysis in European and Argentinian populations identifies two novel genetic loci associated with celiac disease. EJHG, 28(3), 313-323. https://doi.org/10.1038/s41431-019-0520-4
  3. BIOS Consortium, Ouwens, K. G., Jansen, R., Nivard, M. G., van Dongen, J., Frieser, M. J., ... Franke, L. (2020). A characterization of cis- and trans-heritability of RNA-Seq-based gene expression. European Journal of Human Genetics, 28(2), 253-263. https://doi.org/10.1038/s41431-019-0511-5
  4. Hauer, A. J., Kleinloog, R., Giuliani, F., Rinkel, G. J. E., de Kort, G. A., van der Sprenkel, J. W. B., ... Klijn, C. J. M. (2020). RNA-Sequencing Highlights Inflammation and Impaired Integrity of the Vascular Wall in Brain Arteriovenous Malformations. Stroke, 51(1), 268-274. https://doi.org/10.1161/STROKEAHA.119.025657
  5. 2019
  6. Clark, D. W., Okada, Y., Moore, K. H. S., Mason, D., Pirastu, N., Gandin, I., ... Wilson, J. F. (2019). Associations of autozygosity with a broad range of human phenotypes. Nature Communications, 10(1), [4957]. https://doi.org/10.1038/s41467-019-12283-6
  7. BIOS Consortium, van Dongen, J., Zilhao, N. R., Sugden, K., Hannon, E. J., Mill, J., ... Boomsma, D. (2019). Epigenome-wide Association Study of Attention-Deficit/Hyperactivity Disorder Symptoms in Adults. Biological Psychiatry, 86(8), 599-607. https://doi.org/10.1016/j.biopsych.2019.02.016
  8. 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
  9. FREX Consortium, GoNL Consortium, Kim, A., Savary, C., Dubourg, C., Carre, W., ... David, V. (2019). Integrated clinical and omics approach to rare diseases: novel genes and oligogenic inheritance in holoprosencephaly. Brain, 142(1), 35-49. https://doi.org/10.1093/brain/awy290
  10. 2018
  11. 2017
  12. 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
  13. 2016
  14. 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
  15. 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
  16. 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
  17. 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
  18. Hendriksen, D. (Author), Haan, M. D. (Author), Charbon, 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
  19. 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
  20. 2015
  21. 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
  22. 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
  23. 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
  24. 2014
  25. 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
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