Stefan Stender

Integrative common and rare variant analyses provide insights into the genetic architecture of liver cirrhosis

DBDS Genomic Consortium, D. G. C., 2024, (E-pub ahead of print) In: Nature Genetics. 18 p.

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

A rare genetic variant in the manganese transporter SLC30A10 and elevated liver enzymes in the general population

Seidelin, A. S., Nordestgaard, Børge, Tybjærg-Hansen, Anne, Yaghootkar, H. & Stender, Stefan, 2022, In: Hepatology International. 16, 3, p. 702-711

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

Coffee intake protects against symptomatic gallstone disease in the general population: a Mendelian randomization study

Nordestgaard, A. T., Stender, Stefan, Nordestgaard, Børge & Tybjærg-Hansen, Anne, 2020, In: Journal of Internal Medicine. 287, 1, p. 42-53

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Prevalence and Risk Factors of Moderate-to-Severe Hepatic Steatosis in Human Immunodeficiency Virus Infection: The Copenhagen Co-morbidity Liver Study

Kirkegaard-Klitbo, D. M., Fuchs, A., Stender, Stefan, Sigvardsen, P. E., Kühl, J. T., Kofoed, Klaus Fuglsang, Køber, Lars Valeur, Nordestgaard, Børge, Bendtsen, Flemming, Mocroft, A., Lundgren, Jens, Nielsen, Susanne Dam & Benfield, Thomas, 2020, In: The Journal of Infectious Diseases. 222, 8, p. 1353-1362

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

The Effect of Overweight and Obesity on Liver Biochemical Markers in Children and Adolescents

Johansen, M. J., Gade, J., Stender, Stefan, Frithioff-Bojsoe, C., Lund, M. A., Chabanova, E., Thomsen, Henrik S., Pedersen, Oluf Borbye, Fonvig, C. E., Hansen, Torben & Holm, Jens-Christian, 2020, In: Journal of Clinical Endocrinology & Metabolism. 105, 2, p. 430-442 13 p.

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

HMG-coenzyme A reductase inhibition, type 2 diabetes, and bodyweight: evidence from genetic analysis and randomised trials

Swerdlow, D. I., Preiss, D., Kuchenbaecker, K. B., Holmes, M. V., Engmann, J. E. L., Shah, T., Sofat, R., Stender, S., Johnson, P. C. D., Scott, R. A., Leusink, M., Verweij, N., Sharp, S. J., Guo, Y., Giambartolomei, C., Chung, C., Peasey, A., Amuzu, A., Li, K., Palmen, J. & 113 others, Howard, P., Cooper, J. A., Drenos, F., Li, Y. R., Lowe, G., Gallacher, J., Stewart, M. C. W., Tzoulaki, I., Buxbaum, S. G., van der A, D. L., Forouhi, N. G., Onland-Moret, N. C., van der Schouw, Y. T., Schnabel, R. B., Hubacek, J. A., Kubinova, R., Baceviciene, M., Tamosiunas, A., Pajak, A., Topor-Madry, R., Stepaniak, U., Malyutina, S., Baldassarre, D., Sennblad, B., Tremoli, E., de Faire, U., Veglia, F., Ford, I., Jukema, J. W., Westendorp, Rudi GJ, de Borst, G. J., de Jong, P. A., Algra, A., Spiering, W., Maitland-van der Zee, A. H., Klungel, O. H., de Boer, A., Doevendans, P. A., Eaton, C. B., Robinson, J. G., Duggan, D., Kjekshus, J., Downs, J. R., Gotto, A. M., Keech, A. C., Marchioli, R., Tognoni, G., Sever, P. S., Poulter, N. R., Waters, D. D., Pedersen, T. R., Amarenco, P., Nakamura, H., McMurray, J. J. V., Lewsey, J. D., Chasman, D. I., Ridker, P. M., Maggioni, A. P., Tavazzi, L., Ray, K. K., Seshasai, S. R. K., Manson, J. E., Price, J. F., Whincup, P. H., Morris, R. W., Lawlor, D. A., Smith, G. D., Ben-Shlomo, Y., Schreiner, P. J., Fornage, M., Siscovick, D. S., Cushman, M., Kumari, M., Wareham, N. J., Verschuren, W. M. M., Redline, S., Patel, S. R., Whittaker, J. C., Hamsten, A., Delaney, J. A., Dale, C., Gaunt, T. R., Wong, A., Kuh, D., Hardy, R., Kathiresan, S., Castillo, B. A., van der Harst, P., Brunner, E. J., Tybjærg-Hansen, Anne, Marmot, M. G., Krauss, R. M., Tsai, M., Coresh, J., Hoogeveen, R. C., Psaty, B. M., Lange, L. A., Hakonarson, H., Dudbridge, F., Humphries, S. E., Talmud, P. J., Kivimäki, M., Timpson, N. J., Langenberg, C., Asselbergs, F. W., Voevoda, M., Bobak, M., Pikhart, H., Wilson, J. G., Reiner, A. P., Keating, B. J., Hingorani, A. D. & Sattar, N., 24 Jan 2015, In: Lancet. 385, 9965, p. 351-361 11 p.

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

Exome-wide association study identifies a TM6SF2 variant that confers susceptibility to nonalcoholic fatty liver disease

Kozlitina, J., Smagris, E., Stender, Stefan, Nordestgaard, Børge, Zhou, H. H., Tybjærg-Hansen, Anne, Vogt, T. F., Hobbs, H. H. & Cohen, J. C., Apr 2014, In: Nature Genetics. 46, 4, p. 352-356 5 p.

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

Elevated body mass index as a causal risk factor for symptomatic gallstone disease: A Mendelian randomization study

Stender, Stefan, Nordestgaard, B. G. & Tybjærg-Hansen, Anne, 2013, In: Hepatology. 58, 6, p. 2133–2141

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

Extreme Bilirubin Levels as a Causal Risk Factor for Symptomatic Gallstone Disease

Stender, Stefan, Frikke-Schmidt, Ruth, Nordestgaard, Børge & Tybjærg-Hansen, Anne, 2013, In: Annals of Internal Medicine. 173, 13, p. 1222-1228 7 p.

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

Low-density lipoprotein cholesterol and the risk of cancer: a mendelian randomization study

Benn, Marianne, Tybjærg-Hansen, Anne, Stender, Stefan, Frikke-Schmidt, Ruth, Nordestgaard, Børge & Benn, M., 16 Mar 2011, In: National Cancer Institute. Journal (Print). 103, 6, p. 508-19 12 p.

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