David Westergaard

David Westergaard

Assistant Professor

ORCID: 0000-0003-0128-8432

Publication year:
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11 - 15 out of 15Page size: 10
  1. 2023
  2. 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

  3. Published

    The genetic basis of endometriosis and comorbidity with other pain and inflammatory conditions

    Rahmioglu, N., Mortlock, S., Ghiasi, M., Møller, P. L., Stefansdottir, L., Galarneau, G., Turman, C., Danning, R., Law, M. H., Sapkota, Y., Christofidou, P., Skarp, S., Giri, A., Banasik, K., Krassowski, M., Lepamets, M., Marciniak, B., Nõukas, M., Perro, D., Sliz, E. & 35 others, Sobalska-Kwapis, M., Thorleifsson, G., Topbas-Selcuki, N. F., Vitonis, A., Westergaard, David, Arnadottir, R., Burgdorf, Kristoffer Sølvsten, Campbell, A., Cheuk, C. S. K., Clementi, C., Cook, J., De Vivo, I., DiVasta, A., Dorien, O., Donoghue, J. F., Edwards, T., Fontanillas, P., Fung, J. N., Geirsson, R. T., Girling, J. E., Harkki, P., Harris, H. R., Healey, M., Heikinheimo, O., Holdsworth-Carson, S., Hostettler, I. C., Houlden, H., Houshdaran, S., Schork, A. J., Nyegaard, M., DBDS Genomic Consortium, D. G. C., FinnGen Study, F. S., FinnGen Endometriosis Taskforce, F. E. T., Celmatix Research Team, C. R. T. & 23andMe Research Team, 2. R. T., 2023, In: Nature Genetics. 55, 3, p. 423-436 14 p.

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

  4. 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

  5. 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

  6. 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: 130783904