Torben Hansen

Torben Hansen

Professor

Member of:

    ORCID: 0000-0001-8748-3831

    Publication year:
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    41 - 50 out of 679Page size: 10
    1. 2023
    2. Published

      Genetic insights into resting heart rate and its role in cardiovascular disease

      van de Vegte, Y. J., Eppinga, R. N., van der Ende, M. Y., Hagemeijer, Y. P., Mahendran, Y., Salfati, E., Smith, A. V., Tan, V. Y., Arking, D. E., Ntalla, I., Appel, E. V., Schurmann, C., Brody, J. A., Rueedi, R., Polasek, O., Sveinbjornsson, G., Lecoeur, C., Ladenvall, C., Zhao, J. H., Isaacs, A. & 31 others, Wang, L., Luan, J., Hwang, S. J., Mononen, N., Auro, K., Jackson, A. U., Bielak, L. F., Zeng, L., Shah, N., Nethander, M., Campbell, A., Rankinen, T., Pechlivanis, S., Qi, L., Zhao, W., Rizzi, F., Tanaka, T., Robino, A., Cocca, M., Lange, L., Müller-Nurasyid, M., Roselli, C., Zhang, W., Kleber, M. E., Witte, D. R., Linneberg, Allan René, Lind, L., Hansen, Torben, Grarup, Niels, Loos, Ruth & DCCT/EDIC Research Group, D. R. G., 2023, In: Nature Communications. 14, 4646.

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

    3. Published

      Genetics of Plasma Bilirubin and Associations between Bilirubin and Cardiometabolic Risk Profiles in Danish Children and Adolescents

      Ullah, A., Stankevic, Evelina, Holm, L. A., Stinson, Sara, Juel, H. B., Fonvig, Cilius Esmann, Lund, M. A. V., Trier, C., pjx571, pjx571, Ängquist, Lars, Jonsson, Anna Elisabet, Pedersen, Oluf Borbye, Grarup, Niels, Holm, Jens-Christian & Hansen, Torben, 2023, In: Antioxidants. 12, 8, 1613.

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

    4. Published

      Genetics of metabolic traits in Greenlanders

      Thuesen, Anne Cathrine Baun, Lepola, Mette Andersen & Hansen, Torben, 2023, In: Danish Medical Journal. 70, 12, 9 p., A05230332.

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

    5. Published

      Genome-wide association study and functional characterization identifies candidate genes for insulin-stimulated glucose uptake

      Williamson, A., Norris, D. M., Yin, X., Broadaway, K. A., Moxley, A. H., Vadlamudi, S., Wilson, E. P., Jackson, A. U., Ahuja, V., Andersen, M. K., Arzumanyan, Z., Bonnycastle, L. L., Bornstein, S. R., Bretschneider, M. P., Buchanan, T. A., Chang, Y-C., Chuang, L-M., Chung, R-H., Clausen, T. D., Damm, P. & 31 others, Delgado, G. E., de Mello, V. D., Dupuis, J., Dwivedi, O. P., Erdos, M. R., Silva, L. F., Frayling, T. M., Gieger, C., Goodarzi, M. O., Guo, X., Gustafsson, S., Hakaste, L., Hammar, U., Hatem, G., Herrmann, S., Højlund, K., Horn, K., Jonsson, Anna Elisabet, Kovacs, P., Linneberg, Allan René, Mathiesen, Elisabeth, Friis, Carsten, Stinson, Sara, Suleman, Sufyan, Vistisen, D., Witte, D. R., Hansen, Torben, Lind, L., Schwarz, Peter, Grarup, Niels & Meta-Analysis of Glucose and Insulin-related Traits Consortium (MAGIC), M. O. G. A. I. T. C. (., 2023, In: Nature Genetics. 55, 6, p. 973-983 11 p.

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

    6. Published

      Genome-wide association study of placental weight identifies distinct and shared genetic influences between placental and fetal growth

      Beaumont, R. N., Flatley, C., Vaudel, M., Wu, X., Chen, J., Moen, G. H., Skotte, L., Helgeland, Ø., Solé-Navais, P., Banasik, K., Albiñana, C., Ronkainen, J., Fadista, J., Stinson, S. E., Trajanoska, K., Wang, C. A., Westergaard, D., Srinivasan, S., Sánchez-Soriano, C., Bilbao, J. R. & 68 others, Allard, C., Groleau, M., Kuulasmaa, T., Leirer, D. J., White, F., Jacques, P. É., Cheng, H., Hao, K., Andreassen, O. A., Åsvold, B. O., Atalay, M., Bhatta, L., Bouchard, L., Brumpton, B. M., Brunak, Søren, Bybjerg-Grauholm, J., Ebbing, C., Elliott, P., pjx571, pjx571, Erikstrup, C., Estarlich, M., Franks, S., Gaillard, R., Geller, F., Grove, J., Hougaard, D. M., Kajantie, E., Morgen, C. S., Nohr, E. A., Nyegaard, Mette, Palmer, C. N. A., Pedersen, Ole Birger Vesterager, Rivadeneira, F., Sebert, S., Shields, B. M., Stoltenberg, C., Surakka, I., Thørner, L. W., Ullum, H., Vaarasmaki, M., Vilhjalmsson, B. J., Willer, C. J., Lakka, T. A., Gybel-Brask, D., Bustamante, M., Hansen, Torben, Pearson, E. R., Reynolds, R. M., Ostrowski, Sisse Rye, Pennell, C. E., Jaddoe, V. W. V., Felix, J. F., Hattersley, A. T., Melbye, M., Lawlor, D. A., Hveem, K., Werge, Thomas, Nielsen, Henriette Svarre, Magnus, P., Evans, D. M., Jacobsson, B., Järvelin, M. R., Zhang, G., Hivert, M. F., Johansson, S., Freathy, R. M., Feenstra, B. & Njølstad, P. R., 2023, In: Nature Genetics. 55, 11, p. 1807-1819 13 p.

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

    7. Published

      High Plasma Levels of Soluble Lectin-like Oxidized Low-Density Lipoprotein Receptor-1 Are Associated With Inflammation and Cardiometabolic Risk Profiles in Pediatric Overweight and Obesity

      Stinson, Sara, Jonsson, Anna Elisabet, Lepola, Mette Andersen, Lund, Morten Asp Vonsild, Holm, L. A., Fonvig, Cilius Esmann, Huang, Yun, Stankevic, Evelina, Juel, H. B., Ängquist, Lars, Sørensen, Thorkild I.A., Ongstad, E. L., Gaddipati, R., Grimsby, J., Rhodes, C. J., Pedersen, Oluf Borbye, Christiansen, M., Holm, Jens-Christian & Hansen, Torben, 2023, In: Journal of the American Heart Association. 12, 3, p. 538-544 22 p., e8145.

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

    8. Published

      Identification of genetic variants associated with a wide spectrum of phenotypes clinically diagnosed as Sanfilippo and Morquio syndromes using whole genome sequencing

      Gul, Rutaba, Firasat, S., Schubert, Mikkel, Ullah, A., Peña Lozano, Elionora, Thuesen, Anne Cathrine Baun, Gjesing, A. P., Hussain, M., Tufail, M., Saqib, M., Afshan, K. & Hansen, Torben, 2023, In: Frontiers in Genetics. 14, 14 p., 1254909.

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

    9. Published

      Identification of pathogenic GCK variants in patients with common type 2 diabetes can lead to discontinuation of pharmacological treatment

      Thuesen, Anne Cathrine Baun, Jensen, Rasmus Tanderup, Maagensen, H., Kristiansen, M. R., Sørensen, H. T., Vaag, Allan, Beck-Nielsen, H., Pedersen, Oluf Borbye, Grarup, Niels, Nielsen, J. S., Rungby, Jørgen, Gjesing, A. P., Storgaard, H., Vilsbøll, Tina & Hansen, Torben, 2023, In: Molecular Genetics and Metabolism Reports. 35, 8 p., 100972.

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

    10. Published

      Identifying the genetic causes of phenotypically diagnosed Pakistani mucopolysaccharidoses patients by whole genome sequencing

      Gul, Rutaba, Firasat, S., Schubert, Mikkel, Ullah, A., Peña, E., Thuesen, Anne Cathrine Baun, Hussain, M., Stæger, Frederik Filip Vinggaard, Gjesing, A. P., Albrechtsen, Anders & Hansen, Torben, 2023, In: Frontiers in Genetics. 14, 13 p., 1128850.

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

    11. Published

      Low birthweight is associated with a higher incidence of type 2 diabetes over two decades independent of adult BMI and genetic predisposition

      Wibaek, R., Andersen, G. S., Linneberg, Allan René, Hansen, Torben, Grarup, Niels, Thuesen, Anne Cathrine Baun, Jensen, Rasmus Tanderup, Wells, J. C. K., Pilgaard, Kasper Ascanius, Brøns, C., Vistisen, D. & Vaag, Allan, 2023, In: Diabetologia. 66, p. 1669–1679 11 p.

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

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    ID: 33351878