Genetics

Search results

  • 2024

    guidedNOMe-seq quantifies chromatin states at single allele resolution for hundreds of custom regions in parallel

    Schwaiger, M., Mohn, F., Bühler, M. & Kaaij, L. J. T., 29 Jul 2024, In: BMC Genomics. 25, 1, 23 p., 732.

    Research output: Contribution to journal › Article › Academic › peer-review

    Open Access
    File
  • 2022

    Rare coding variants in ten genes confer substantial risk for schizophrenia

    Apr 2022, In: Nature. 604, 7906, p. 509-516 8 p.

    Research output: Contribution to journal › Article › Academic › peer-review

  • 2020

    Exome-chip association analysis of intracranial aneurysms

    van 't Hof, F. N. G., Lai, D., van Setten, J., Bots, M. L., Vaartjes, I., Broderick, J., Woo, D., Foroud, T., Rinkel, G. J. E., de Bakker, P. I. W. & Ruigrok, Y. M., 4 Feb 2020, In: Neurology. 94, 5, p. e481-e488

    Research output: Contribution to journal › Article › Academic › peer-review

  • 2019

    Genetic and lifestyle risk factors for MRI-defined brain infarcts in a population-based setting

    29 Jan 2019, In: Neurology. 92, 5, p. E486-E503

    Research output: Contribution to journal › Article › Academic › peer-review

    Open Access
    File

  • Integrated clinical and omics approach to rare diseases: Novel genes and oligogenic inheritance in holoprosencephaly

    Kim, A., Savary, C., Dubourg, C., Carré, W., Mouden, C., Hamdi-Rozé, H., Guyodo, H., Douce, J. L., Génin, E., Campion, D., Dartigues, J. F., Deleuze, J. F., Lambert, J. C., Redon, R., Ludwig, T., Grenier-Boley, B., Letort, S., Lindenbaum, P., Meyer, V., Quenez, O., & 85 othersDina, C., Bellenguez, C., Charbonnier-Le Clézio, C., Giemza, J., Chatel, S., Férec, C., Le Marec, H., Letenneur, L., Nicolas, G., Rouault, K., Bacq, D., Boland, A., Lechner, D., Wijmenga, C., Swertz, M. A., Eline Slagboom, P., Van Ommen, G. J. B., Van Duijn, C. M., Boomsma, D. I., De Bakker, P. I. W., Bovenberg, J. A., Eline Slagboom, P., De Craen, A. J. M., Beekman, M., Hofman, A., Willemsen, G., Wolffenbuttel, B., Platteel, M., Du, Y., Chen, R., Cao, H., Cao, R., Sun, Y., Sujie Cao, J., Van Dijk, F., Neerincx, P. B. T., Deelen, P., Dijkstra, M., Byelas, G., Kanterakis, A., Bot, J., Ye, K., Lameijer, E. W., Vermaat, M., Laros, J. F. J., Den Dunnen, J. T., De Knijff, P., Karssen, L. C., Van Leeuwen, E. M., Amin, N., Koval, V., Rivadeneira, F., Estrada, K., Hehir-Kwa, J. Y., De Ligt, J., Abdellaoui, A., Hottenga, J. J., Mathijs Kattenberg, V., Van Enckevort, D., Mei, H., Santcroos, M., Van Schaik, B. D. C., Handsaker, R. E., McCarroll, S. A., Eichler, E. E., Ko, A., Sudmant, P., Francioli, L. C., Kloosterman, W. P., Nijman, I. J., Guryev, V., Pasquier, L., Flori, E., Gonzales, M., Bénéteau, C., Boute, O., Attié-Bitach, T., Roume, J., Goujon, L., Akloul, L., Odent, S., Watrin, E., Dupé, V., De Tayrac, M. & David, V., 1 Jan 2019, In: Brain. 142, 1, p. 35-49 15 p.

    Research output: Contribution to journal › Article › Academic › peer-review

    7 Citations (Scopus)

  • Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes (vol 50, pg 524, 2018): Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes (Nature Genetics, (2018), 50, 4, (524-537), 10.1038/s41588-018-0058-3)

    Jul 2019, In: Nature Genetics. 51, 7, p. 1192-1193 2 p.

    Research output: Contribution to journal › Comment/Letter to the editor › Academic › peer-review

  • Relative effects of LDL-C on ischemic stroke and coronary disease A Mendelian randomization study

    12 Mar 2019, In: Neurology. 92, 11, p. E1176-E1187

    Research output: Contribution to journal › Article › Academic › peer-review

    Open Access
    File

  • Skewed X-inactivation is common in the general female population

    1 Mar 2019, In: European Journal of Human Genetics. 27, 3, p. 455-465 11 p.

    Research output: Contribution to journal › Article › Academic › peer-review

    Open Access
    File
    7 Citations (Scopus)

  • WGS-based telomere length analysis in Dutch family trios implicates stronger maternal inheritance and a role for RRM1 gene

    1 Dec 2019, In: Scientific Reports. 9, 1, 18758.

    Research output: Contribution to journal › Article › Academic › peer-review

    Open Access
    File
  • 2018

    A comprehensive evaluation of the genetic architecture of sudden cardiac arrest

    Ashar, F. N., Mitchell, R. N., Albert, C. M., Newton-Cheh, C., Brody, J. A., Müller-Nurasyid, M., Moes, A., Meitinger, T., Mak, A., Huikuri, H., Junttila, M. J., Goyette, P., Pulit, S. L., Pazoki, R., Tanck, M. W., Blom, M. T., Zhao, X., Havulinna, A. S., Jabbari, R., Glinge, C., & 44 othersTragante, V., Escher, S. A., Chakravarti, A., Ehret, G., Coresh, J., Li, M., Prineas, R. J., Franco, O. H., Kwok, P-Y., Lumley, T., Dumas, F., McKnight, B., Rotter, J. I., Lemaitre, R. N., Heckbert, S. R., O'Donnell, C. J., Hwang, S-J., Tardif, J-C., VanDenburgh, M., Uitterlinden, A. G., Hofman, A., Stricker, B. H. C., de Bakker, P. I. W., Franks, P. W., Jansson, J-H., Asselbergs, F. W., Halushka, M. K., Maleszewski, J. J., Tfelt-Hansen, J., Engstrøm, T., Salomaa, V., Virmani, R., Kolodgie, F., Wilde, A. A. M., Tan, H. L., Bezzina, C. R., Eijgelsheim, M., Rioux, J. D., Jouven, X., Kääb, S., Psaty, B. M., Siscovick, D. S., Arking, D. E. & Sotoodehnia, N., 21 Nov 2018, In: European Heart Journal. 39, 44, p. 3961-3969 9 p.

    Research output: Contribution to journal › Article › Academic › peer-review

  • Genetic Association of Lipids and Lipid Drug Targets With Abdominal Aortic Aneurysm: A Meta-analysis

    Harrison, S. C., Holmes, M. V., Burgess, S., Asselbergs, F. W., Jones, G. T., Baas, A. F., Van't Hof, F. N., De Bakker, P. I. W., Blankensteijn, J. D., Powell, J. T., Saratzis, A., De Borst, G. J., Swerdlow, D. I., Van Der Graaf, Y., Van Rij, A. M., Carey, D. J., Elmore, J. R., Tromp, G., Kuivaniemi, H., Sayers, R. D., & 3 othersSamani, N. J., Bown, M. J. & Humphries, S. E., 1 Jan 2018, In: JAMA Cardiology. 3, 1, p. 26-33 8 p.

    Research output: Contribution to journal › Article › Academic › peer-review

    3 Citations (Scopus)

  • Genetic Susceptibility Loci for Cardiovascular Disease and Their Impact on Atherosclerotic Plaques

    van der Laan, S. W., Siemelink, M. A., Haitjema, S., Foroughi Asl, H., Perisic, L., Mokry, M., van Setten, J., Malik, R., Dichgans, M., Worrall, B. B., Samani, N. J., Schunkert, H., Erdmann, J., Hedin, U., Paulsson-Berne, G., Björkegrenn, J. L. M., de Borst, G. J., Asselbergs, F. W., den Ruijter, F. W., de Bakker, P. I. W., & 1 othersPasterkamp, G., 1 Sept 2018, In: Circ Genom Precis Med. 11, 9, e002115.

    Research output: Contribution to journal › Article › Academic › peer-review

    Open Access
    File
    1 Downloads (Pure)
  • 2017

    Erratum: Genetic loci associated with heart rate variability and their effects on cardiac disease risk

    Nolte, I. M., Munoz, M. L., Tragante, V., Amare, A. T., Jansen, R., Vaez, A., Von Der Heyde, B., Avery, C. L., Bis, J. C., Dierckx, B., van Dongen, J., Gogarten, S. M., Goyette, P., Hernesniemi, J., Huikari, V., Hwang, S-J., Jaju, D., Kerr, K. F., Kluttig, A., Krijthe, B. P., & 144 othersKumar, J., van der Laan, S. W., Lyytikäinen, L-P., Maihofer, A. X., Minassian, A., van der Most, P. J., Müller-Nurasyid, M., Nivard, M. G., Salvi, E., Stewart, J. D., Thayer, J. F., Verweij, N., Wong, A., Zabaneh, D., Zafarmand, M. H., Abdellaoui, A., Albarwani, S., Albert, C., Alonso, A., Ashar, F. N., Auvinen, J., Axelsson, T., Baker, D. G., de Bakker, P. I. W., Barcella, M., Bayoumi, R., Bieringa, R. J., Boomsma, D. I., Boucher, G., Britton, A. R., Christophersen, I. E., Dietrich, A., Ehret, G. B., Ellinor, P. T., Eskola, M., Felix, J. F., Floras, J. S., Franco, O. H., Friberg, P., Gademan, M. G. J., Geyer, M. A., Giedraitis, V., Hartman, C. A., Hemerich, D., Hofman, A., Hottenga, J-J., Huikuri, H. V., Hutri-Kähönen, N., Jouven, X., Junttila, J., Juonala, M., Kiviniemi, A. M., Kors, J. A., Kumari, M., Kuznetsova, T., Laurie, C. C., Lefrandt, J. D., Li, Y., Li, Y. R., Liao, D., Limacher, M. C., Lin, H. J., Lindgren, C. M., Lubitz, S. A., Mahajan, A., McKnight, B., Zu Schwabedissen, H. M., Milaneschi, Y., Mononen, N., Morris, A. P., Nalls, M. A., Navis, G. J., Neijts, M., Nikus, K., North, K. E., O'Connor, D. T., Ormel, J., Perz, S., Peters, A., Psaty, B. M., Raitakari, O. T., Risbrough, V. B., Sinner, M. F., Siscovick, D. S., Smit, J. H., Smith, N. L., Soliman, E. Z., Sotoodehnia, N., Staessen, J. A., Stein, P. K., Stilp, A. M., Stolarz-Skrzypek, K., Strauch, K., Sundström, J., Swenne, C. A., Syvänen, A-C., Tardif, J-C., Taylor, K. D., Teumer, A., Thornton, T. A., Tinker, L. E., Uitterlinden, A. G., van Setten, J., Voss, A., Waldenberger, M., Wilhelmsen, K. C., Willemsen, G., Wong, Q., Zhang, Z. M., Zonderman, A. B., Cusi, D., Evans, M. K., Greiser, K. H., van der Harst, P., Hassan, M., Ingelsson, E., Järvelin, M-R., Kääb, S., Kähönen, M., Kivimaki, M., Kooperberg, C., Kuh, D., Lehtimäki, T., Lind, L., Nievergelt, C. M., O'Donnell, C. J., Oldehinkel, A. J., Penninx, B. W., Reiner, A. P., Riese, H., Van Roon, A. M., Rioux, J. D., Rotter, J. I., Sofer, T., Stricker, B. H., Tiemeier, H., Vrijkotte, T. G. M., Asselbergs, F. W., Brundel, B. J. J. M., Heckbert, S. R., Whitsel, E. A., den Hoed, M., Snieder, H. & de Geus, E. J. C., 2 Aug 2017, In: Nature Communications [E]. 8, p. 16140

    Research output: Contribution to journal › Comment/Letter to the editor › Academic › peer-review

    Open Access
    File
    1 Downloads (Pure)

  • Genetic loci associated with heart rate variability and their effects on cardiac disease risk

    Nolte, I. M., Munoz, M. L., Tragante, V., Amare, A. T., Jansen, R., Vaez, A., Von Der Heyde, B., Avery, C. L., Bis, J. C., Dierckx, B., van Dongen, J., Gogarten, S. M., Goyette, P., Hernesniemi, J., Huikari, V., Hwang, S-J., Jaju, D., Kerr, K. F., Kluttig, A., Krijthe, B. P., & 144 othersKumar, J., Van Der Laan, S. W., Lyytikäinen, L-P., Maihofer, A. X., Minassian, A., van der Most, P. J., Müller-Nurasyid, M., Nivard, M. G., Salvi, E., Stewart, J. D., Thayer, J. F., Verweij, N., Wong, A., Zabaneh, D., Zafarmand, M. H., Abdellaoui, A., Albarwani, S., Albert, C., Alonso, A., Ashar, F. N., Auvinen, J., Axelsson, T., Baker, D. G., De Bakker, P. I. W., Barcella, M., Bayoumi, R., Bieringa, R. J., Boomsma, D. I., Boucher, G., Britton, A. R., Christophersen, I. E., Dietrich, A., Ehret, G. B., Ellinor, P. T., Eskola, M., Felix, J. F., Floras, J. S., Franco, O. H., Friberg, P., Gademan, M. G. J., Geyer, M. A., Giedraitis, V., Hartman, C. A., Hemerich, D., Hofman, A., Hottenga, J-J., Huikuri, H. V., Hutri-Kähönen, N., Jouven, X., Junttila, J., Juonala, M., Kiviniemi, A. M., Kors, J. A., Kumari, M., Kuznetsova, T., Laurie, C. C., Lefrandt, J. D., Li, Y., Li, Y. R., Liao, D., Limacher, M. C., Lin, H. J., Lindgren, C. M., Lubitz, S. A., Mahajan, A., McKnight, B., Meyer Zu Schwabedissen, H., Milaneschi, Y., Mononen, N., Morris, A. P., Nalls, M. A., Navis, G. J., Neijts, M., Nikus, K., North, K. E., O'Connor, D. T., Ormel, J., Perz, S., Peters, A., Psaty, B. M., Raitakari, O. T., Risbrough, V. B., Sinner, M. F., Siscovick, D. S., Smit, J. H., Smith, N. L., Soliman, E. Z., Sotoodehnia, N., Staessen, J. A., Stein, P. K., Stilp, A. M., Stolarz-Skrzypek, K., Strauch, K., Sundström, J., Swenne, C. A., Syvänen, A-C., Tardif, J-C., Taylor, K. D., Teumer, A., Thornton, T. A., Tinker, L. E., Uitterlinden, A. G., Van Setten, J., Voss, A., Waldenberger, M., Wilhelmsen, K. C., Willemsen, G., Wong, Q., Zhang, Z. M., Zonderman, A. B., Cusi, D., Evans, M. K., Greiser, K. H., van der Harst, P., Hassan, M., Ingelsson, E., Järvelin, M-R., Kääb, S., Kähönen, M., Kivimaki, M., Kooperberg, C., Kuh, D., Lehtimäki, T., Lind, L., Nievergelt, C. M., O'Donnell, C. J., Oldehinkel, A. J., Penninx, B. W., Reiner, A. P., Riese, H., Van Roon, A. M., Rioux, J. D., Rotter, J. I., Sofer, T., Stricker, B. H., Tiemeier, H., Vrijkotte, T. G. M., Asselbergs, F. W., Brundel, B. J. J. M., Heckbert, S. R., Whitsel, E. A., den Hoed, M., Snieder, H. & de Geus, E. J. C., 14 Jun 2017, In: Nature Communications [E]. 8, 15805.

    Research output: Contribution to journal › Article › Academic › peer-review

    Open Access
    File

  • Genetics of intracranial aneurysms and related diseases

    van 't Hof, F. N. G., 24 May 2017, Utrecht University. 163 p.

    Research output: Thesis › Doctoral thesis 1 (Research UU / Graduation UU)

    Open Access
    File
    3 Downloads (Pure)

  • Genetic variants associated with type 2 diabetes and adiposity and risk of intracranial and abdominal aortic aneurysms

    van 't Hof, F. N., Vaucher, J., Holmes, M. V., de Wilde, A., Baas, A. F., Blankensteijn, J. D., Hofman, A., Kiemeney, L. A., Rivadeneira, F., Uitterlinden, A. G., Vermeulen, S. H., Rinkel, G. J., de Bakker, P. I. & Ruigrok, Y. M., Jun 2017, In: European Journal of Human Genetics. 25, 6, p. 758-762 5 p.

    Research output: Contribution to journal › Article › Academic › peer-review

  • Mapping and phasing of structural variation in patient genomes using nanopore sequencing

    Cretu Stancu, M., van Roosmalen, M. J., Renkens, I., Nieboer, M. M., Middelkamp, S., de Ligt, J., Pregno, G., Giachino, D., Mandrile, G., Espejo Valle-Inclan, J., Korzelius, J., de Bruijn, E., Cuppen, E., Talkowski, M. E., Marschall, T., de Ridder, J. & Kloosterman, W. P., 6 Nov 2017, In: Nature Communications [E]. 8, 1, 1326.

    Research output: Contribution to journal › Article › Academic › peer-review

    Open Access
    File

  • Meta-Analysis of Genome-Wide Association Studies for Abdominal Aortic Aneurysm Identifies Four New Disease-Specific Risk Loci

    Jones, G. T., Tromp, G., Kuivaniemi, H., Gretarsdottir, S., Baas, A. F., Giusti, B., Strauss, E., Van't Hof, F. N. G., Webb, T. R., Erdman, R., Ritchie, M. D., Elmore, J. R., Verma, A., Pendergrass, S., Kullo, I. J., Ye, Z., Peissig, P. L., Gottesman, O., Verma, S. S., Malinowski, J., & 97 othersRasmussen-Torvik, L. J., Borthwick, K. M., Smelser, D. T., Crosslin, D. R., de Andrade, M., Ryer, E. J., McCarty, C. A., Böttinger, E. P., Pacheco, J. A., Crawford, D. C., Carrell, D. S., Gerhard, G. S., Franklin, D. P., Carey, D. J., Phillips, V. L., Williams, M. J. A., Wei, W., Blair, R., Hill, A. A., Vasudevan, T. M., Lewis, D. R., Thomson, I. A., Krysa, J., Hill, G. B., Roake, J., Merriman, T. R., Oszkinis, G., Galora, S., Saracini, C., Abbate, R., Pulli, R., Pratesi, C., Saratzis, A., Verissimo, A. R., Bumpstead, S., Badger, S. A., Clough, R. E., Cockerill, G., Hafez, H., Scott, D. J. A., Futers, T. S., Romaine, S. P. R., Bridge, K., Griffin, K. J., Bailey, M. A., Smith, A., Thompson, M. M., van Bockxmeer, F. M., Matthiasson, S. E., Thorleifsson, G., Thorsteinsdottir, U., Blankensteijn, J. D., Teijink, J. A. W., Wijmenga, C., de Graaf, J., Kiemeney, L. A., Lindholt, J. S., Hughes, A., Bradley, D. T., Stirrups, K., Golledge, J., Norman, P. E., Powell, J. T., Humphries, S. E., Hamby, S. E., Goodall, A. H., Nelson, C. P., Sakalihasan, N., Courtois, A., Ferrell, R. E., Eriksson, P., Folkersen, L., Franco-Cereceda, A., Eicher, J. D., Johnson, A. D., Betsholtz, C., Ruusalepp, A., Franzén, O., Schadt, E. E., Björkegren, J. L. M., Lipovich, L., Drolet, A. M., Verhoeven, E. L., Zeebregts, C. J., Geelkerken, R. H., van Sambeek, M. R., van Sterkenburg, S. M., de Vries, J-P., Stefansson, K., Thompson, J. R., de Bakker, P. I. W., Deloukas, P., Sayers, R. D., Harrison, S. C., van Rij, A. M., Samani, N. J. & Bown, M. J., 20 Jan 2017, In: Circulation Research. 120, 2, p. 341-353 13 p.

    Research output: Contribution to journal › Article › Academic › peer-review

    Open Access
    File

  • Missing heritability: is the gap closing? An analysis of 32 complex traits in the Lifelines Cohort Study

    Nolte, I. M., van der Most, P. J., Alizadeh, B. Z., de Bakker, P. I., Boezen, H. M., Bruinenberg, M., Franke, L., van der Harst, P., Navis, G., Postma, D. S., Rots, M. G., Stolk, R. P., Swertz, M. A., Wolffenbuttel, B. H., Wijmenga, C. & Snieder, H., 1 Jun 2017, In: European Journal of Human Genetics. 25, 7, p. 877-885 9 p.

    Research output: Contribution to journal › Article › Academic › peer-review

    Open Access

  • Negative selection in humans and fruit flies involves synergistic epistasis

    Sohail, M., Vakhrusheva, O. A., Sul, J. H., Pulit, S. L., Francioli, L. C., van den Berg, L. H., Veldink, J. H., de Bakker, P. I. W., Bazykin, G. A., Kondrashov, A. S. & Sunyaev, S. R., 5 May 2017, In: Science. 356, 6337, p. 539-542 4 p.

    Research output: Contribution to journal › Article › Academic › peer-review

  • Rare and low-frequency coding variants alter human adult height

    Marouli, E., Graff, M., Medina-Gomez, C., Lo, K. S., Wood, A. R., Kjaer, T. R., Fine, R. S., Lu, Y., Schurmann, C., Highland, H. M., Rüeger, S., Thorleifsson, G., Justice, A. E., Lamparter, D., Stirrups, K. E., Turcot, V., Young, K. L., Winkler, T. W., Esko, T., Karaderi, T., & 30 othersLocke, A. E., Masca, N. G. D., Ng, M. C. Y., Mudgal, P., Rivas, M. A., Vedantam, S., Mahajan, A., Guo, X., Abecasis, G., Aben, K. K., Adair, L. S., Alam, D. S., Albrecht, E., Allin, K. H., Allison, M., Amouyel, P., Appel, E. V., Arveiler, D., Asselbergs, F. W., Auer, P. L., Balkau, B., Bots, M. L., de Bakker, P. I. W., de Borst, G. J., de Groot, M. C. H., Kahn, R. S., Ophoff, RA., Pasterkamp, G., van der Laan, S. W. & van Setten, J., 9 Feb 2017, In: Nature. 542, 7640, p. 186-190 5 p.

    Research output: Contribution to journal › Article › Academic › peer-review

  • Reply: Poor Sensitivity and Specificity of Electrocardiographic Estimation of Myocardial Mass

    van der Harst, P. & de Bakker, P. I. W., 28 Feb 2017, In: Journal of the American College of Cardiology. 69, 8, p. 1099-1099 1 p.

    Research output: Contribution to journal › Letter › Academic › peer-review

    Open Access

  • Resetting the bar: Statistical significance in whole-genome sequencing-based association studies of global populations

    Pulit, S. L., de With, S. A. J. & de Bakker, P. I. W., 1 Feb 2017, In: Genetic Epidemiology. 41, 2, p. 145-151 7 p.

    Research output: Contribution to journal › Article › Academic › peer-review

  • The role of de novo mutations in the development of amyotrophic lateral sclerosis

    van Doormaal, P. T. C., Ticozzi, N., Weishaupt, J. H., Kenna, K. P., Diekstra, F. P., Verde, F., Andersen, P. M., Dekker, A. M., Tiloca, C., Marroquin, N., Overste, D. J., Pensato, V., Nürnberg, P., Pulit, S. L., Schellevis, R. D., Calini, D., Altmüller, J., Francioli, L. C., Muller, B., Castellotti, B., & 11 othersMotameny, S., Ratti, A., Wolf, J., Gellera, C., Ludolph, A. C., van den Berg, L. H., Kubisch, C., Landers, J. E., Veldink, J. H., Silani, V. & Volk, A. E., Nov 2017, In: Human Mutation. 38, 11, p. 1534-1541 8 p.

    Research output: Contribution to journal › Article › Academic › peer-review

  • 2016

    52 Genetic Loci Influencing Myocardial Mass

    van der Harst, P., van Setten, J., Verweij, N., Vogler, G., Franke, L., Maurano, M. T., Wang, X., Mateo Leach, I., Eijgelsheim, M., Sotoodehnia, N., Hayward, C., Sorice, R., Meirelles, O., Lyytikäinen, L-P., Polašek, O., Tanaka, T., Arking, D. E., Ulivi, S., Trompet, S., Müller-Nurasyid, M., & 140 othersSmith, A. V., Dörr, M., Kerr, K. F., Magnani, J. W., Del Greco M, F., Zhang, W., Nolte, I. M., Silva, C. T., Padmanabhan, S., Tragante Do O, V., Esko, T., Abecasis, G. R., Adriaens, M. E., Andersen, K., Barnett, P., Bis, J. C., Bodmer, R., Buckley, B. M., Campbell, H., Cannon, M. V., Chakravarti, A., Chen, L. Y., Delitala, A., Devereux, R. B., Doevendans, P. A., Dominiczak, A. F., Ferrucci, L., Ford, I., Gieger, C., Harris, T. B., Haugen, E., Heinig, M., Hernandez, D. G., Hillege, H. L., Hirschhorn, J. N., Hofman, A., Hubner, N., Hwang, S-J., Iorio, A., Kähönen, M., Kellis, M., Kolcic, I., Kooner, I. K., Kooner, J. S., Kors, J. A., Lakatta, E. G., Lage, K., Launer, L. J., Levy, D., Lundby, A., Macfarlane, P. W., May, D., Meitinger, T., Metspalu, A., Nappo, S., Naitza, S., Neph, S., Nord, A. S., Nutile, T., Okin, P. M., Olsen, J. V., Oostra, B. A., Penninger, J. M., Pennacchio, L. A., Pers, T. H., Perz, S., Peters, A., Pinto, Y. M., Pfeufer, A., Pilia, M. G., Pramstaller, P. P., Prins, B. P., Raitakari, O. T., Raychaudhuri, S., Rice, K. M., Rossin, E. J., Rotter, J. I., Schafer, S., Schlessinger, D., Schmidt, C. O., Sehmi, J., Silljé, H. H. W., Sinagra, G., Sinner, M. F., Slowikowski, K., Soliman, E. Z., Spector, T. D., Spiering, W., Stamatoyannopoulos, J. A., Stolk, R. P., Strauch, K., Tan, S-T., Tarasov, K. V., Trinh, B., Uitterlinden, A. G., van den Boogaard, M., van Duijn, C. M., van Gilst, W. H., Viikari, J. S., Visscher, P. M., Vitart, V., Völker, U., Waldenberger, M., Weichenberger, C. X., Westra, H-J., Wijmenga, C., Wolffenbuttel, B. H., Yang, J., Bezzina, C. R., Munroe, P. B., Snieder, H., Wright, A. F., Rudan, I., Boyer, L. A., Asselbergs, F. W., van Veldhuisen, D. J., Stricker, B. H., Psaty, B. M., Ciullo, M., Sanna, S., Lehtimäki, T., Wilson, J. F., Bandinelli, S., Alonso, A., Gasparini, P., Jukema, J. W., Kääb, S., Gudnason, V., Felix, S. B., Heckbert, S. R., de Boer, R. A., Newton-Cheh, C., Hicks, A. A., Chambers, J. C., Jamshidi, Y., Visel, A., Christoffels, V. M., Isaacs, A., Samani, N. J. & de Bakker, P. I. W., 27 Sept 2016, In: Journal of the American College of Cardiology. 68, 13, p. 1435-1448 14 p.

    Research output: Contribution to journal › Article › Academic › peer-review

    Open Access
    File

  • A framework for the detection of de novo mutations in family-based sequencing data

    Francioli, L. C., Cretu-Stancu, M., Garimella, K. V., Fromer, M., Kloosterman, W. P., Samocha, K. E., Neale, B. M., Daly, M. J., Banks, E., DePristo, M. A. & de Bakker, P. IW., 23 Nov 2016, In: European Journal of Human Genetics. 25, p. 227–233

    Research output: Contribution to journal › Article › Academic › peer-review

    Open Access
    File

  • A genetic risk score is associated with statin-induced low-density lipoprotein cholesterol lowering

    Leusink, M., Maitland-van der Zee, A. H., Ding, B., Drenos, F., van Iperen, E. P., Warren, H. R., Caulfield, M. J., Cupples, L. A., Cushman, M., Hingorani, A. D., Hoogeveen, R. C., Hovingh, G. K., Kumari, M., Lange, L. A., Munroe, P. B., Nyberg, F., Schreiner, P. J., Sivapalaratnam, S., de Bakker, P. I., de Boer, A., & 3 othersKeating, B. J., Asselbergs, F. W. & Onland-Moret, N. C., Apr 2016, In: Pharmacogenomics. 17, 6, p. 583-91 9 p.

    Research output: Contribution to journal › Article › Academic › peer-review

  • A high-quality human reference panel reveals the complexity and distribution of genomic structural variants

    Hehir-Kwa, J. Y., Marschall, T., Kloosterman, W. P., Francioli, L. C., Baaijens, J. A., Dijkstra, L. J., Abdellaoui, A., Koval, V., Thung, D. T., Wardenaar, R., Renkens, I., Coe, B. P., Deelen, P., De Ligt, J., Lameijer, E. W., Van Dijk, F., Hormozdiari, F., Uitterlinden, A. G., Van Duijn, C. M., Eichler, E. E., & 47 othersDe Bakker, P. I. W., Swertz, M. A., Wijmenga, C., Van Ommen, G. J. B., Slagboom, P. E., Boomsma, D. I., Schönhuth, A., Ye, K., Guryev, V., Bovenberg, J. A., De Craen, A. J. M., Beekman, M., Hofman, A., Willemsen, G., Wolffenbuttel, B., Platteel, M., Du, Y., Chen, R., Cao, H., Cao, R., Sun, Y., Cao, J. S., Neerincx, P. B. T., Dijkstra, M., Byelas, G., Kanterakis, A., Bot, J., Vermaat, M., Laros, J. F., den Dunnen, J. T., De Knijff, P., Karssen, L. C., Van Leeuwen, E. M., Amin, N., Rivadeneira, F., Estrada, K., Hottenga, J-J., Kattenberg, V. M., Van Enckevort, D., Mei, H., Santcroos, M., Van Schaik, B. D. C., Handsaker, R. E., McCarroll, S. A., Ko, A., Sudmant, P. & Nijman, I. J., 6 Oct 2016, In: Nature Communications [E]. 7, 12989.

    Research output: Contribution to journal › Article › Academic › peer-review

    Open Access
    File
    4 Citations (Scopus)

  • A reference panel of 64,976 haplotypes for genotype imputation

    McCarthy, S., Das, S., Kretzschmar, W., Delaneau, O., Wood, A. R., Teumer, A., Kang, H. M., Fuchsberger, C., Danecek, P., Sharp, K., Luo, Y., Sidore, C., Kwong, A., Timpson, N., Koskinen, S., Vrieze, S., Scott, L. J., Zhang, H., Mahajan, A., Veldink, J., & 30 othersPeters, U., Pato, C., van Duijn, C. M., Gillies, C. E., Gandin, I., Mezzavilla, M., Gilly, A., Cocca, M., Traglia, M., Angius, A., Barrett, J. C., Boomsma, D., Branham, K., Breen, G., Brummett, C. M., Busonero, F., Campbell, H., Chan, A., Chen, S., Chew, E., Collins, F. S., Corbin, L. J., Smith, G. D., Dedoussis, G., Dorr, M., Farmaki, A-E., Van den Berg, L. H., Van Rheenen, W., de Bakker, P. I. W. & Dekker, A., 22 Aug 2016, In: Nature Genetics. 48, p. 1279–1283

    Research output: Contribution to journal › Letter › Academic › peer-review

  • Correction: The Influence of Age and Sex on Genetic Associations with Adult Body Size and Shape: A Large-Scale Genome-Wide Interaction Study

    Winkler, T. W., Justice, A. E., Graff, M., Barata, L., Feitosa, M. F., Chu, S., Czajkowski, J., Esko, T., Fall, T., Kilpeläinen, T. O., Lu, Y., Mägi, R., Mihailov, E., Pers, T. H., Rüeger, S., Teumer, A., Ehret, G. B., Ferreira, T., Heard-Costa, N. L., Karjalainen, J., & 30 othersLagou, V., Mahajan, A., Neinast, M. D., Prokopenko, I., Simino, J., Teslovich, T. M., Jansen, R., Westra, H-J., White, C. C., Absher, D., Ahluwalia, T. S., Ahmad, S., Albrecht, E., Alves, A. C., Bragg-Gresham, J. L., de Craen, A. J. M., Bis, J. C., Bonnefond, A., Boucher, G., Cadby, G., Cheng, Y-C., Chiang, C. W. K., Haitjema, S., van der Laan, S. W., van Setten, J., Asselbergs, F. W., de Bakker, P. I. W., Moll, F. L., Pasterkamp, G. & den Ruijter, H. M., Jun 2016, In: PLoS Genetics. 12, 6, e1006166.

    Research output: Contribution to journal › Comment/Letter to the editor › Academic › peer-review

    Open Access
    File

  • Cystatin C and Cardiovascular Disease: A Mendelian Randomization Study

    van der Laan, S. W., Fall, T., Soumaré, A., Teumer, A., Sedaghat, S., Baumert, J., Zabaneh, D., van Setten, J., Isgum, I., Galesloot, T. E., Arpegård, J., Amouyel, P., Trompet, S., Waldenberger, M., Dörr, M., Magnusson, P. K., Giedraitis, V., Larsson, A., Morris, A. P., Felix, J. F., & 52 othersMorrison, A. C., Franceschini, N., Bis, J. C., Kavousi, M., O'Donnell, C., Drenos, F., Tragante, V., Munroe, P. B., Malik, R., Dichgans, M., Worrall, B. B., Erdmann, J., Nelson, C. P., Samani, N. J., Schunkert, H., Marchini, J., Patel, R. S., Hingorani, A. D., Lind, L., Pedersen, N. L., de Graaf, J., Kiemeney, L. A. L. M., Baumeister, S. E., Franco, O. H., Hofman, A., Uitterlinden, A. G., Koenig, W., Meisinger, C., Peters, A., Thorand, B., Jukema, J. W., Eriksen, B. O., Toft, I., Wilsgaard, T., Onland-Moret, N. C., van der Schouw, Y. T., Debette, S., Kumari, M., Svensson, P., van der Harst, P., Kivimaki, M., Keating, B. J., Sattar, N., Dehghan, A., Reiner, A. P., Ingelsson, E., den Ruijter, H. M., de Bakker, P. I. W., Pasterkamp, G., Ärnlöv, J., Holmes, M. V. & Asselbergs, F. W., 30 Aug 2016, In: Journal of the American College of Cardiology. 68, 9, p. 934-945 12 p.

    Research output: Contribution to journal › Article › Academic › peer-review

    Open Access
    File

  • Deciphering the four-letter code: The genetic basis of complex traits and common disease

    Pulit, SL., 12 Feb 2016, Utrecht University. 315 p.

    Research output: Thesis › Doctoral thesis 1 (Research UU / Graduation UU)

  • Enhancers reside in a unique epigenetic environment during early zebrafish development

    Kaaij, L. J. T., Mokry, M., Zhou, M., Musheev, M., Geeven, G., Melquiond, A. S. J., de Jesus Domingues, A. M., de Laat, W., Niehrs, C., Smith, A. D. & Ketting, R. F., 5 Jul 2016, In: Genome Biology. 17, 1, 17:146.

    Research output: Contribution to journal › Article › Academic › peer-review

    Open Access
    File

  • Extensive Association of Common Disease Variants with Regulatory Sequence

    Mokry, M., Harakalova, M., Asselbergs, F. W., de Bakker, P. I. W. & Nieuwenhuis, E. E. S., 2016, In: PLoS ONE [E]. 11, 11, e0165893.

    Research output: Contribution to journal › Article › Academic › peer-review

    Open Access
    File

  • Genetic variation in uncontrolled childhood asthma despite ICS treatment

    Leusink, M., Vijverberg, S. J. H., Koenderman, L., Raaijmakers, J. A. M., de Jongste, J. C., Sterk, P. J., Duiverman, E. J., Onland-Moret, N. C., Postma, D. S., de Boer, A., de Bakker, P. I. W., Koppelman, G. H. & Maitland-van der Zee, A. H., Apr 2016, In: The Pharmacogenomics Journal. 16, 2, p. 158-163 6 p.

    Research output: Contribution to journal › Article › Academic › peer-review

  • Genome-wide association analyses identify new risk variants and the genetic architecture of amyotrophic lateral sclerosis

    van Rheenen, W., Shatunov, A., Dekker, A. M., McLaughlin, R. L., Diekstra, F. P., Pulit, S. L., van der Spek, R. A. A., Võsa, U., de Jong, S., Robinson, M. R., Yang, J., Fogh, I., van Doormaal, P. T., Tazelaar, G. H. P., Koppers, M., Blokhuis, A. M., Sproviero, W., Jones, A. R., Kenna, K. P., van Eijk, K. R., & 30 othersHarschnitz, O., Schellevis, R. D., Brands, W. J., Medic, J., Menelaou, A., Vajda, A., Ticozzi, N., Lin, K., Rogelj, B., Vrabec, K., Ravnik-Glavač, M., Koritnik, B., Zidar, J., Leonardis, L., Grošelj, L. D., Millecamps, S., Salachas, F., Meininger, V., de Carvalho, M., Pinto, S., Mora, J. S., Rojas-García, R., Polak, M., Ophoff, R. A., Blauw, H. M., de Bakker, P. I. W., van Es, M. A., Pasterkamp, R. J., van den Berg, L. H. & Veldink, J. H., Sept 2016, In: Nature Genetics. 48, 9, p. 1043–1048

    Research output: Contribution to journal › Letter › Academic › peer-review

  • Harnessing publicly available genetic data to prioritize lipid modifying therapeutic targets for prevention of coronary heart disease based on dysglycemic risk

    Tragante, V., Asselbergs, F. W., Swerdlow, D. I., Palmer, T. M., Moore, J. H., de Bakker, P. I. W., Keating, B. J. & Holmes, M. V., 2016, In: Human Genetics. 135, 5, p. 453-67 15 p.

    Research output: Contribution to journal › Article › Academic › peer-review

    Open Access
    File

  • Loci associated with ischaemic stroke and its subtypes (SiGN): A genome-wide association study

    1 Feb 2016, In: Lancet Neurology. 15, 2, p. 174-184 11 p.

    Research output: Contribution to journal › Article › Academic › peer-review

    3 Citations (Scopus)

  • Meta-analysis of rare and common exome chip variants identifies S1PR4 and other loci influencing blood cell traits

    Pankratz, N., Schick, U. M., Zhou, Y., Zhou, W., Ahluwalia, T. S., Allende, M. L., Auer, P. L., Bork-Jensen, J., Brody, J. A., Chen, M. H., Clavo, V., Eicher, J. D., Grarup, N., Hagedorn, E. J., Hu, B., Hunker, K., Johnson, A. D., Leusink, M., Lu, Y., Lyytikainen, L. P., & 61 othersManichaikul, A., Marioni, R. E., Nalls, M. A., Pazoki, R., Smith, A. V., Van Rooij, F. J. A., Yang, M. L., Zhang, X., Zhang, Y., Asselbergs, F. W., Boerwinkle, E., Borecki, I. B., Bottinger, E. P., Cushman, M., De Bakker, P. I. W., Deary, I. J., Dong, L., Feitosa, M. F., Floyd, J. S., Franceschini, N., Franco, O. H., Garcia, M. E., Grove, M. L., Gudnason, V., Hansen, T., Harris, T. B., Hofman, A., Jackson, R. D., Jia, J., Kahonen, M., Launer, L. J., Lehtimaki, T., Liewald, D. C., Linneberg, A., Liu, Y., Loos, R. J. F., Nguyen, V. M., Numans, M. E., Pedersen, O., Psaty, B. M., Raitakari, O. T., Rich, S. S., Rivadeneira, F., Di Sant, A. M. R., Rotter, J. I., Starr, J. M., Taylor, K. D., Thuesen, B. H., Tracy, R. P., Uitterlinden, A. G., Wang, J., Wang, J., Dehghan, A., Huo, Y., Adrienne Cupples, L., Wilson, J. G., Proia, R. L., Zon, L. I., O'Donnell, C. J., Reiner, A. P. & Ganesh, S. K., 1 Aug 2016, In: Nature Genetics. 48, 8, p. 867-876 10 p.

    Research output: Contribution to journal › Article › Academic › peer-review

  • Seventeen years of statin pharmacogenetics: a systematic review

    Leusink, M., Onland-Moret, N. C., de Bakker, P., de Boer, A. & Maitland-van der Zee, A. H., 2016, In: Pharmacogenomics. 17, 2, p. 163-180 18 p.

    Research output: Contribution to journal › Literature review › peer-review

  • Shared genetic risk factors of intracranial, abdominal, and thoracic aneurysms

    van 't Hof, F. N. G., Ruigrok, Y. M., Lee, C. H., Ripke, S., Anderson, G., de Andrade, M., Baas, A. F., Blankensteijn, J. D., Böttinger, E. P., Bown, M. J., Broderick, J., Bijlenga, P., Carrell, D. S., Crawford, D. C., Crosslin, D. R., Ebeling, C., Eriksson, J. G., Fornage, M., Foroud, T., von Und Zu Fraunberg, M., & 30 othersFriedrich, C. M., Gaál, E. I., Gottesman, O., Guo, D-C., Harrison, S. C., Hernesniemi, J., Hofman, A., Inoue, I., Jääskeläinen, J. E., Jones, G. T., Kiemeney, L. A. L. M., Kivisaari, R., Ko, N., Koskinen, S., Kubo, M., Kullo, I. J., Kuivaniemi, H., Kurki, M. I., Laakso, A., Lai, D., Leal, S. M., Lehto, H., LeMaire, S. A., Low, S-K., Malinowski, J., McCarty, C. A., Milewicz, D. M., Mosley, T. H., Rinkel, G. J. E. & de Bakker, P. I. W., 1 Jul 2016, In: Journal of the American Heart Association. 5, 7, e002603.

    Research output: Contribution to journal › Article › Academic › peer-review

    Open Access
    File
    4 Citations (Scopus)

  • Trans-ancestry meta-analyses identify rare and common variants associated with blood pressure and hypertension

    Surendran, P., Drenos, F., Young, R., Warren, H., Cook, J. P., Manning, A. K., Grarup, N., Sim, X., Barnes, D. R., Witkowska, K., Staley, J. R., Tragante, V., Tukiainen, T., Yaghootkar, H., Masca, N., Freitag, D. F., Ferreira, T., Giannakopoulou, O., Tinker, A., Harakalova, M., & 30 othersMihailov, E., Liu, C., Kraja, A. T., Nielsen, S. F., Rasheed, A., Samuel, M., Zhao, W., Bonnycastle, L. L., Jackson, A. U., Narisu, N., Swift, A. J., Southam, L., Marten, J., Huyghe, J. R., Stančáková, A., Fava, C., Ohlsson, T., Matchan, A., Stirrups, K. E., Bork-Jensen, J., Gjesing, A. P., Kontto, J., Perola, M., Shaw-Hawkins, S., Havulinna, A. S., Zhang, H., Donnelly, L. A., de Bakker, P. I. W., Numans, M. E. & Asselbergs, F. W., 2016, In: Nature Genetics. 48, 10, p. 1151-1161 11 p.

    Research output: Contribution to journal › Article › Academic › peer-review

  • Transmission of human mtDNA heteroplasmy in the genome of the Netherlands families: Support for a variable-size bottleneck

    Li, M., Rothwell, R., Vermaat, M., Wachsmuth, M., Schröder, R., Laros, J. F. J., Van Oven, M., De Bakker, P. I. W., Bovenberg, J. A., Van Duijn, C. M., Van Ommen, G. J. B., Slagboom, P. E., Swertz, M. A., Wijmenga, C., Kayser, M., Boomsma, D. I., Zöllner, S., De Knijff, P., Stoneking, M., De Craen, A. J. M., & 45 othersBeekman, M., Hofman, A., Willemsen, G., Wolffenbuttel, B., Platteel, M., Du, Y., Chen, R., Cao, H., Cao, R., Sun, Y., Cao, J. S., Van Dijk, F., Neerincx, P. B. T., Deelen, P., Dijkstra, M., Byelas, G., Kanterakis, A., Bot, J., Ye, K., Lameijer, E. W., Den Dunnen, J. T., Karssen, L. C., Van Leeuwen, E. M., Amin, N., Koval, V., Rivadeneira, F., Estrada, K., Hehir-Kwa, J. Y., De Ligt, J., Abdellaoui, A., Hottenga, J. J., Kattenberg, V. M., Van Enckevort, D., Mei, H., Santcroos, M., Van Schaik, B. D. C., Handsaker, R. E., McCarroll, S. A., Eichler, E. E., Ko, A., Sudmant, P., Francioli, L. C., Kloosterman, W. P., Nijman, I. J. & Guryev, V., 1 Apr 2016, In: Genome Research. 26, 4, p. 417-426 10 p.

    Research output: Contribution to journal › Article › Academic › peer-review

    Open Access
    File
    1 Citation (Scopus)

  • Twenty-eight genetic loci associated with ST-T-wave amplitudes of the electrocardiogram

    15 May 2016, In: Human molecular genetics. 25, 10, p. 2093-2103 11 p.

    Research output: Contribution to journal › Article › Academic › peer-review

  • 2015

    Accurate and fast multiple-testing correction in eQTL studies

    Sul, J. H., Raj, T., de Jong, S., de Bakker, P. I. W., Raychaudhuri, S., Ophoff, R. A., Stranger, B. E., Eskin, E. & Han, B., 4 Jun 2015, In: American Journal of Human Genetics. 96, 6, p. 857-68 12 p.

    Research output: Contribution to journal › Article › Academic › peer-review

  • Additive and interaction effects at three amino acid positions in HLA-DQ and HLA-DR molecules drive type 1 diabetes risk

    Hu, X., Deutsch, A. J., Lenz, T. L., Onengut-Gumuscu, S., Han, B., Chen, W-M., Howson, J. M. M., Todd, J. A., de Bakker, P. I. W., Rich, S. S. & Raychaudhuri, S., Aug 2015, In: Nature Genetics. 47, 8, p. 898-905 8 p.

    Research output: Contribution to journal › Article › Academic › peer-review

  • A genome-wide association study of marginal zone lymphoma shows association to the HLA region

    Vijai, J., Wang, Z., Berndt, S. I., Skibola, C. F., Slager, S. L., de Sanjose, S., Melbye, M., Glimelius, B., Bracci, P. M., Conde, L., Birmann, B. M., Wang, S. S., Brooks-Wilson, A. R., Lan, Q., de Bakker, P. I. W., Vermeulen, R. C. H., Portlock, C., Ansell, S. M., Link, B. K., Riby, J., & 82 othersNorth, K. E., Gu, J., Hjalgrim, H., Cozen, W., Becker, N., Teras, L. R., Spinelli, J. J., Turner, J., Zhang, Y., Purdue, M. P., Giles, G. G., Kelly, R. S., Zeleniuch-Jacquotte, A., Ennas, M. G., Monnereau, A., Bertrand, K. A., Albanes, D., Lightfoot, T., Yeager, M., Chung, C. C., Burdett, L., Hutchinson, A., Lawrence, C., Montalvan, R., Liang, L., Huang, J., Ma, B., Villano, D. J., Maria, A., Corines, M., Thomas, T., Novak, A. J., Dogan, A., Liebow, M., Thompson, C. A., Witzig, T. E., Habermann, T. M., Weiner, G. J., Smith, M. T., Holly, E. A., Jackson, R. D., Tinker, L. F., Ye, Y., Adami, H-O., Smedby, K. E., De Roos, A. J., Hartge, P., Morton, L. M., Severson, R. K., Benavente, Y., Boffetta, P., Brennan, P., Foretova, L., Maynadie, M., McKay, J., Staines, A., Diver, W. R., Vajdic, C. M., Armstrong, B. K., Kricker, A., Zheng, T., Holford, T. R., Severi, G., Vineis, P., Ferri, G. M., Ricco, R., Miligi, L., Clavel, J., Giovannucci, E., Kraft, P., Virtamo, J., Smith, A., Kane, E., Roman, E., Chiu, B. C. H., Fraumeni, J. F., Wu, X., Cerhan, J. R., Offit, K., Chanock, S. J., Rothman, N. & Nieters, A., 2015, In: Nature Communications [E]. 6, 7 p., 5751.

    Research output: Contribution to journal › Article › Academic › peer-review

    Open Access
    File

  • A Large-Scale Genetic Analysis Reveals a Strong Contribution of the HLA Class II Region to Giant Cell Arteritis Susceptibility

    David Carmona, F., Mackie, S. L., Martin, J-E., Taylor, J. C., Vaglio, A., Eyre, S., Bossini-Castillo, L., Castaneda, S., Cid, M. C., Hernandez-Rodriguez, J., Prieto-Gonzalez, S., Solans, R., Ramentol-Sintas, M., Francisca Gonzalez-Escribano, M., Ortiz-Fernandez, L., Morado, I. C., Narvaez, J., Miranda-Filloy, J. A., Beretta, L., Lunardi, C., & 30 othersCimmino, M. A., Gianfreda, D., Santilli, D., Ramirez, G. A., Soriano, A., Muratore, F., Pazzola, G., Addimanda, O., Wijmenga, C., Witte, T., Schirmer, J. H., Moosig, F., Schoenau, V., Franke, A., Palm, O., Molberg, O., Diamantopoulos, A. P., Carette, S., Cuthbertson, D., Forbess, L. J., Hoffman, G. S., Khalidi, N. A., Koening, C. L., Langford, C. A., McAlear, C. A., Moreland, L., Monach, P. A., Pagnoux, C., Koeleman, B. P. C. & de Bakker, P. I. W., 2 Apr 2015, In: American Journal of Human Genetics. 96, 4, p. 565-580 16 p.

    Research output: Contribution to journal › Article › Academic › peer-review

    Open Access
    File
    1 Downloads (Pure)

  • Design and Implementation of the International Genetics and Translational Research in Transplantation Network

    Asselbergs, F., van Setten, J., de Jonge, N., Otten, HG., de Weger, RA., van de Graaf, E. A., Kluin, J. & de Bakker, P. I. W., Nov 2015, In: Transplantation. 99, 11, p. 2401-12 12 p.

    Research output: Contribution to journal › Article › Academic › peer-review

  • Fine mapping in the MHC region accounts for 18% additional genetic risk for celiac disease

    Gutierrez-Achury, J., Zhernakova, A., Pulit, S. L., Trynka, G., Hunt, K. A., Romanos, J., Raychaudhuri, S., van Heel, D. A., Wijmenga, C. & de Bakker, P. I. W., Jun 2015, In: Nature Genetics. 47, 6, p. 577-8 2 p.

    Research output: Contribution to journal › Article › Academic › peer-review