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2025
Mark Rare MTNR1B variants causing diminished MT2 signalling associate with elevated HbA_1c levels but not with type 2 diabetes
Sørensen, Kimmie V. ; Justesen, Johanne M. ; Ängquist, Lars ; Bork-Jensen, Jette ; Hartmann, Bolette ; Jørgensen, Niklas R. ; Rungby, Jørgen ; Sørensen, Henrik T. ; Vaag, Allan ^LU and Nielsen, Jens S. , et al. (2025) In Diabetologia 68(5). p.1016-1030
- Contribution to journal › Article
2024
Mark Analyses of 1236 genotyped primary ciliary dyskinesia individuals identify regional clusters of distinct DNA variants and significant genotype–phenotype correlations
Raidt, J. ; Hansen, C.R. ^LU and Omran, H. (2024) In European Respiratory Journal 64(2).
- Contribution to journal › Article
2023
Mark Aggregation tests identify new gene associations with breast cancer in populations with diverse ancestry
Mueller, S.H. ; Augustinsson, A. ^LU ; Olsson, H. ^LU and Kuchenbaecker, Karoline B. (2023) In Genome Medicine 15(1).
- Contribution to journal › Article

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