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2023
Mark Mosaic Loss of Chromosome Y Is Associated With Functional Outcome After Ischemic Stroke
Dorvall, Malin ; Pedersen, Annie ; Dumanski, Jan P. ; Söderholm, Martin ^LU ; Lindgren, Arne G. ^LU ; Stanne, Tara M. and Jern, Christina (2023) In Stroke 54(9). p.2434-2437
- Contribution to journal › Article
Mark Revisiting Diagnosis and Treatment of Hypertrophic Cardiomyopathy : Current Practice and Novel Perspectives
Ottaviani, Andrea ; Mansour, Davide ; Molinari, Lorenzo V. ; Galanti, Kristian ; Mantini, Cesare ; Khanji, Mohammed Y. ; Chahal, Anwar A. ; Zimarino, Marco ; Renda, Giulia and Sciarra, Luigi , et al. (2023) In Journal of Clinical Medicine 12(17).
- Contribution to journal › Scientific review
Mark Birth Weight Is Associated With Clonal Hematopoiesis of Indeterminate Potential and Cardiovascular Outcomes in Adulthood
Schuermans, Art ; Nakao, Tetsushi ; Ruan, Yunfeng ; Koyama, Satoshi ^LU ; Yu, Zhi ; Uddin, Md Mesbah ; Haidermota, Sara ; Hornsby, Whitney ; Lewandowski, Adam J. and Bick, Alexander G. , et al. (2023) In Journal of the American Heart Association 12(13).
- Contribution to journal › Article
Mark Rare-variant collapsing analyses reveal novel risk genes for arterial and venous cardiovascular diseases in the UK biobank
Zöller, Bengt ^LU ; Manderstedt, Eric ^LU ; Lind-Halldén, Christina ^LU and Halldén, Christer ^LU (2023) In Thrombosis Research 229. p.86-89
- Contribution to journal › Letter
Mark Four missense genetic variants in CUBN are associated with higher levels of eGFR in non-diabetes but not in diabetes mellitus or its subtypes : A genetic association study in Europeans
Uglebjerg, Nicoline ; Ahmadizar, Fariba ; Aly, Dina M. ^LU ; Cañadas-Garre, Marisa ; Hill, Claire ; Naber, Annemieke ; Oddsson, Asmundur ; Singh, Sunny S. ; Smyth, Laura and Trégouët, David Alexandre , et al. (2023) In Frontiers in Endocrinology 14.
- Contribution to journal › Article
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
Mark Contribution of rare and common coding variants to haematological malignancies in the UK biobank
Zöller, Bengt ^LU ; Manderstedt, Eric ^LU ; Lind-Halldén, Christina ^LU and Halldén, Christer (2023) In Leukemia Research Reports 19.
- Contribution to journal › Article
Mark HNF1B variant without hyperglycaemia as a cause of isolated profound hypomagnesaemia
Vollmer, Shobitha ; Katzman, Per ^LU and Londahl, Magnus ^LU (2023) In BMJ Case Reports 16(2).
- Contribution to journal › Article
Mark Genetically proxied impaired GIPR signaling and risk of 6 cancers
Rogers, Miranda ; Gill, Dipender ; Ahlqvist, Emma ^LU ; Robinson, Tim ; Mariosa, Daniela ; Johansson, Mattias ; Cortez Cardoso Penha, Ricardo ; Dossus, Laure ; Gunter, Marc J. and Moreno, Victor , et al. (2023) In iScience 26(6).
- Contribution to journal › Article
Mark Gene Therapy with Etranacogene Dezaparvovec for Hemophilia B
Pipe, Steven W. ; Leebeek, Frank W.G. ; Recht, Michael ; Key, Nigel S. ; Castaman, Giancarlo ; Miesbach, Wolfgang ; Lattimore, Susan ; Peerlinck, Kathelijne ; Van Der Valk, Paul and Coppens, Michiel , et al. (2023) In New England Journal of Medicine 388(8). p.706-718
- Contribution to journal › Article

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