Ole Birger Vesterager Pedersen

Ole Birger Vesterager Pedersen

    Member of:

    • Clinical immunology

    ORCID: 0000-0003-2312-5976

    Publication year:
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    41 - 50 out of 155Page size: 10
    1. 2023
    2. Published

      An atlas of genetic determinants of forearm fracture

      Nethander, M., Movérare-Skrtic, S., Kämpe, A., Coward, E., Reimann, E., Grahnemo, L., Borbély, É., Helyes, Z., Funck-Brentano, T., Cohen-Solal, M., Tuukkanen, J., Koskela, A., Wu, J., Li, L., Lu, T., Gabrielsen, M. E., Mägi, R., Hoff, M., Lerner, U. H., Henning, P. & 15 others, Ullum, H., Erikstrup, C., Brunak, Søren, Langhammer, A., Tuomi, T., Oddsson, A., Stefansson, K., Pettersson-Kymmer, U., Ostrowski, Sisse Rye, Pedersen, Ole Birger Vesterager, Styrkarsdottir, U., Mäkitie, O., Hveem, K., Richards, J. B. & Ohlsson, C., 2023, In: Nature Genetics. 55, 11, p. 1820-1830 11 p.

      Research output: Contribution to journal › Journal article › Research › peer-review

    3. Published

      Developmental language disorder – a comprehensive study of more than 46,000 individuals

      Nudel, R., Christensen, Rikke Vang, Kalnak, N., Schwinn, M., Banasik, Karina, Dinh, K. M., Erikstrup, C., Pedersen, Ole Birger Vesterager, Burgdorf, Kristoffer Sølvsten, Ullum, H., Ostrowski, Sisse Rye, Hansen, Thomas Folkmann, Werge, Thomas & DBDS Genomic Consortium, D. G. C., 2023, In: Psychiatry Research. 323, 9 p., 115171.

      Research output: Contribution to journal › Journal article › Research › peer-review

    4. Published

      Deficit of homozygosity among 1.52 million individuals and genetic causes of recessive lethality

      Oddsson, A., Sulem, P., Sveinbjornsson, G., Arnadottir, G. A., Steinthorsdottir, V., Halldorsson, G. H., Atlason, B. A., Oskarsson, G. R., Helgason, H., Nielsen, H. S., Westergaard, D., Karjalainen, J. M., Katrinardottir, H., Fridriksdottir, R., Jensson, B. O., Tragante, V., Ferkingstad, E., Jonsson, H., Gudjonsson, S. A., Beyter, D. & 31 others, Moore, K. H. S., Thordardottir, H. B., Kristmundsdottir, S., Stefansson, O. A., Rantapää-Dahlqvist, S., Sonderby, I. E., Didriksen, Maria, Stridh, P., Haavik, J., Tryggvadottir, L., Frei, O., Walters, G. B., Kockum, I., Hjalgrim, Henrik, Olafsdottir, T. A., Selbaek, G., Nyegaard, M., Erikstrup, C., Brodersen, T., Saevarsdottir, S., Olsson, T., Nielsen, K. R., Hansen, Thomas Folkmann, Brunak, Søren, Jacobsen, R. L., Brunak, Søren, Banasik, Karina, Askling, J., Pedersen, Ole Birger Vesterager, Ostrowski, Sisse Rye & DBDS Genomic Consortium, D. G. C., 2023, In: Nature Communications. 14, 15 p., 3453.

      Research output: Contribution to journal › Journal article › Research › peer-review

    5. Published

      Cluster headache polygenetic risk and known functional variants of CYP3A4 are not associated with treatment response

      DBDS Genomic Consortium, D. G. C., 2023, In: European Journal of Neurology. 30, 5, p. 1425-1434 10 p.

      Research output: Contribution to journal › Journal article › Research › peer-review

    6. Published

      Genome-wide association meta-analysis identifies risk loci for abdominal aortic aneurysm and highlights PCSK9 as a therapeutic target

      Roychowdhury, T., Klarin, D., Levin, M. G., Spin, J. M., Rhee, Y. H., Deng, A., Headley, C. A., Tsao, N. L., Gellatly, C., Zuber, V., Shen, F., Hornsby, W. E., Laursen, I. H., Verma, S. S., Locke, A. E., Einarsson, G., Thorleifsson, G., Graham, S. E., Dikilitas, O., Pattee, J. W. & 74 others, Judy, R. L., Pauls-Verges, F., Nielsen, J. B., Wolford, B. N., Brumpton, B. M., Dilmé, J., Peypoch, O., Juscafresa, L. C., Edwards, T. L., Li, D., Banasik, Karina, Brunak, Søren, Jacobsen, Rikke Vita Borre, Garcia-Barrio, M. T., Zhang, J., Rasmussen, L. M., Lee, R., Handa, A., Wanhainen, A., Mani, K., Lindholt, J. S., Obel, L. M., Strauss, E., Oszkinis, G., Nelson, C. P., Saxby, K. L., van Herwaarden, J. A., van der Laan, S. W., van Setten, J., Camacho, M., Davis, F. M., Wasikowski, R., Tsoi, L. C., Gudjonsson, J. E., Eliason, J. L., Coleman, D. M., Henke, P. K., Ganesh, S. K., Chen, Y. E., Guan, W., Pankow, J. S., Pankratz, N., Pedersen, Ole Birger Vesterager, Erikstrup, C., Tang, W., Hveem, K., Gudbjartsson, D., Gretarsdottir, S., Thorsteinsdottir, U., Holm, H., Stefansson, K., Ferreira, M. A., Baras, A., Kullo, I. J., Ritchie, M. D., Christensen, Alex Hørby, Iversen, Kasper, Eldrup, Nikolaj, Sillesen, Henrik, Ostrowski, Sisse Rye, Bundgård, Henning, Ullum, H., Burgess, S., Gill, D., Gallagher, K., Sabater-Lleal, M., Dudbridge, F., Samani, N. J., Surakka, I., Jones, G. T., Bown, M. J., Tsao, P. S., Willer, C. J. & Damrauer, S. M., 2023, In: Nature Genetics. 55, p. 1831–1842 13 p.

      Research output: Contribution to journal › Journal article › Research › peer-review

    7. Published

      COVID-19 illness severity and 2-year prevalence of physical symptoms: an observational study in Iceland, Sweden, Norway and Denmark

      Shen, Q., Joyce, E. E., Ebrahimi, O. V., Didriksen, M., Lovik, A., Sævarsdóttir, K. S., Magnúsdóttir, I., Mikkelsen, D. H., Unnarsdóttir, A. B., Hauksdóttir, A., Hoffart, A., Kähler, A. K., Thórdardóttir, E. B., Eythórsson, E., Frans, E. M., Tómasson, G., Ask, H., Hardardóttir, H., Jakobsdóttir, J., Lehto, K. & 12 others, Lu, L., Andreassen, O. A., Sullivan, P. F., Pálsson, R., Erikstrup, C., Ostrowski, Sisse Rye, Werge, Thomas, Aspelund, T., Pedersen, Ole Birger Vesterager, Johnson, S. U., Fang, F. & Valdimarsdóttir, U. A., 2023, In: The Lancet Regional Health - Europe. 35, 12 p., 100756.

      Research output: Contribution to journal › Journal article › Research › peer-review

    8. Published

      Deep integrative models for large-scale human genomics

      Sigurdsson, Arnór Ingi, Louloudis, Ioannis, Banasik, Karina, Westergaard, David, Winther, Ole, Lund, O., Ostrowski, Sisse Rye, Erikstrup, C., Pedersen, Ole Birger Vesterager, Nyegaard, Mette, Brunak, Søren, Vilhjálmsson, B. & Rasmussen, Simon, 2023, In: Nucleic Acids Symposium Series. 51, 12, 16 p.

      Research output: Contribution to journal › Journal article › Research › peer-review

    9. Published

      Complex effects of sequence variants on lipid levels and coronary artery disease

      Snaebjarnarson, A. S., Helgadottir, A., Arnadottir, G. A., Ivarsdottir, E. V., Thorleifsson, G., Ferkingstad, E., Einarsson, G., Sveinbjornsson, G., Thorgeirsson, T. E., Ulfarsson, M. O., Halldorsson, B. V., Olafsson, I., Erikstrup, C., Pedersen, O. B., Nyegaard, M., Bruun, M. T., Ullum, H., Brunak, S., Iversen, K. K., Christensen, A. H. & 14 others, Olesen, Morten Steen Salling, Ghouse, Jonas, Banasik, Karina, Knowlton, K. U., Arnar, D. O., Thorgeirsson, G., Nadauld, L., Ostrowski, Sisse Rye, Bundgård, Henning, Holm, H., Sulem, P., Stefansson, K., Gudbjartsson, D. F. & DBDS Genomic Consortium, D. G. C., 2023, In: Cell. 186, 19, p. 4085-4099.e15

      Research output: Contribution to journal › Journal article › Research › peer-review

    10. Published

      Genetic effects on the timing of parturition and links to fetal birth weight: [Inkl. Correction]

      Solé-Navais, P., Flatley, C., Steinthorsdottir, V., Vaudel, M., Juodakis, J., Chen, J., Laisk, T., LaBella, A. L., Westergaard, D., Bacelis, J., Brumpton, B., Skotte, L., Borges, M. C., Helgeland, Ø., Mahajan, A., Wielscher, M., Lin, F., Briggs, C., Wang, C. A., Moen, G. H. & 33 others, Beaumont, R. N., Bradfield, J. P., Abraham, A., Thorleifsson, G., Gabrielsen, M. E., Ostrowski, Sisse Rye, Modzelewska, D., Nohr, E. A., Hypponen, E., Srivastava, A., Talbot, O., Allard, C., Williams, S. M., Menon, R., Shields, B. M., Sveinbjornsson, G., Xu, H., Melbye, M., Lowe, W., Bouchard, L., Oken, E., Pedersen, Ole Birger Vesterager, Gudbjartsson, D. F., Erikstrup, C., Sørensen, E., McCarthy, M. I., Lie, R. T., Ullum, H., Nyegaard, Mette, Nielsen, Henriette Svarre, Early Growth Genetics Consortium, E. G. G. C., Estonian Biobank Research Team, E. B. R. T. & Danish Blood Donor Study Genomic Consortium, D. B. D. S. G. C., 2023, In: Nature Genetics. 55, p. 559–567

      Research output: Contribution to journal › Journal article › Research › peer-review

    11. Published

      Pregnancy-Associated Bleeding and Genetics: Five Sequence Variants in the Myometrium and Progesterone Signaling Pathway are associated with postpartum hemorrhage

      Westergaard, D., Steinthorsdottir, V., Stefansdottir, L., Rohde, P. D., Wu, X., Geller, F., Tyrmi, J., Havulinna, A. S., Navais, P. S., Flatley, C., Ostrowski, S. R., Pedersen, O. B., Erikstrup, C., Sørensen, E., Mikkelsen, C., Brun, M. T., Jensen, B. A., Brodersen, T., Ullum, H., Magnus, P. & 8 others, Andreassen, O. A., Njolstad, P. R., Krebs, Lone, Hansen, Thomas Folkmann, Banasik, Karina, Brunak, Søren, Nielsen, Henriette Svarre & FinnGen, F., 2023, medRxiv, 51 p. (medRxiv).

      Research output: Working paper › Preprint › Research

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    ID: 14608282