Publications | Lund University Publications

11 – 20 of 1982

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2025
Mark Meta-analysis of uveal melanoma genome-wide association studies identifies novel risk loci and population effect size heterogeneity
Mies, Georgia ; Tsao, Noah L. ; Houy, Alexandre ; Coupland, Sarah E. ; Kalirai, Helen ; Försti, Asta ^LU ; Hemminki, Kari ^LU ; Thomsen, Hauke ^LU ; Stern, Marc Henri and Shields, Carol L. , et al. (2025) In Human Genetics and Genomics Advances 6(3).
- Contribution to journal › Article
Mark Twin pair analysis uncovers links between DNA methylation, mitochondrial DNA quantity and obesity
Heikkinen, Aino ; Esser, Vivienne F.C. ; Lee, Seung Hyuk T. ; Lundgren, Sara ; Hakkarainen, Antti ; Lundbom, Jesper ; Kuula, Juho ; Groop, Per Henrik ; Heinonen, Sini and Villicaña, Sergio , et al. (2025) In Nature Communications 16(1).
- Contribution to journal › Article
Mark Deficiency of Peptidylglycine-alpha-amidating Monooxygenase, a Cause of Sarcopenic Diabetes Mellitus
Giontella, Alice ^LU ; Åkerlund, Mikael ^LU ; Bronton, Kevin ^LU ; Fava, Cristiano ^LU ; Lotta, Luca A. ; Baras, Aris ; Overton, John D. ; Jones, Marcus ; Bergmann, Andreas and Kaufmann, Paul , et al. (2025) In Journal of Clinical Endocrinology and Metabolism 110(3). p.820-829
- Contribution to journal › Article
Mark Precision Omics Initiative Sweden (PROMISE) will integrate research with healthcare
Kämpe, Anders ; Gudmundsson, Sanna ; Walsh, Colum P ; Lindblad-Toh, Kerstin ^LU ; Johansson, Åsa ; Clareborn, Anna ; Ameur, Adam ; Edsjö, Anders ^LU ; Fioretos, Thoas ^LU and Ehrencrona, Hans ^LU , et al. (2025) In Nature Medicine
- Contribution to journal › Letter
Mark TREM2 risk variants and associated endophenotypes in alzheimer’s disease
Dijkstra, Janna I.R. ; Vermunt, Lisa ; Venkatraghavan, Vikram ; Ozhegov, Georgii ; Coomans, Emma M. ^LU ; Ossenkoppele, Rik ^LU ; van de Giessen, Elsmarieke ; Hulsman, Marc ; de Geus, Christa M. and van der Flier, Wiesje M. , et al. (2025) In Alzheimer's Research and Therapy 17(1).
- Contribution to journal › Article
Mark Whole genome sequencing in early onset advanced heart failure
Linnér, Erik ^LU ; Czuba, Tomasz ^LU ; Gidlöf, Olof ^LU ; Lundgren, Jakob ^LU ; Bollano, Entela ; Hellberg, Maria ; Celik, Selvi ^LU ; Pimpalwar, Neha ^LU ; Rentzsch, Philipp ^LU and Martorella, Molly ^LU , et al. (2025) In Scientific Reports 15(1).
- Contribution to journal › Article
Mark TOR1AIP2 as a candidate gene for dystonia-hemichorea/hemiballism
Kafantari, Efthymia ^LU ; Hernandez, Victoria J. ; Necpál, Ján ; Leonidou, Marina ; Baureder, Regina ^LU ; Hedberg-Oldfors, Carola ^LU ; Jech, Robert ; Zech, Michael ; Schwartz, Thomas U. and Puschmann, Andreas ^LU (2025) In Parkinsonism and Related Disorders 134.
- Contribution to journal › Article
2024
Mark Gustavson syndrome is caused by an in-frame deletion in RBMX associated with potentially disturbed SH3 domain interactions
Johansson, Josefin ; Lidéus, Sarah ; Frykholm, Carina ; Gunnarsson, Cecilia ; Mihalic, Filip ; Gudmundsson, Sanna ; Ekvall, Sara ; Molin, Anna Maja ; Pham, Mai and Vihinen, Mauno ^LU , et al. (2024) In European Journal of Human Genetics 32(3). p.333-341
- Contribution to journal › Article
Mark KnockoffHybrid : A knockoff framework for hybrid analysis of trio and population designs in genome-wide association studies
Yang, Yi ; Wang, Qi ; Wang, Chen ; Buxbaum, Joseph and Ionita-Laza, Iuliana ^LU (2024) In American Journal of Human Genetics 111(7). p.1448-1461
- Contribution to journal › Article
Mark Frontiers in congenital disorders of glycosylation consortium, a cross-sectional study report at year 5 of 280 individuals in the natural history cohort
Lam, Christina ; Eklund, E.A. ^LU and Morava, E. (2024) In Molecular Genetics and Metabolism 142(4).
- Contribution to journal › Article

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