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2018
Mark Genome-wide analysis yields new loci associating with aortic valve stenosis
Helgadottir, Anna ; Thorleifsson, Gudmar ; Gretarsdottir, Solveig ; Stefansson, Olafur A. ; Tragante, Vinicius ; Thorolfsdottir, Rosa B. ; Jonsdottir, Ingileif ; Bjornsson, Thorsteinn ; Steinthorsdottir, Valgerdur and Verweij, Niek , et al. (2018) In Nature Communications 9(1).
- Contribution to journal › Article
2017
Mark Whole-genome sequencing identifies rare genotypes in COMP and CHADL associated with high risk of hip osteoarthritis
Styrkarsdottir, Unnur ; Helgason, Hannes ; Sigurdsson, Asgeir ; Norddahl, Gudmundur L. ^LU ; Agustsdottir, Arna B. ; Reynard, Louise N. ; Villalvilla, Amanda ; Halldorsson, Gisli H. ; Jonasdottir, Aslaug and Magnusdottir, Audur , et al. (2017) In Nature Genetics 49(5). p.801-805
- Contribution to journal › Article
2014
Mark Meta-analysis in more than 17,900 cases of ischemic stroke reveals a novel association at 12q24.12
Kilarski, Laura L. ; Achterberg, Sefanja ; Devan, William J. ; Traylor, Matthew ; Malik, Rainer ; Lindgren, Arne ^LU ; Pare, Guillame ; Sharma, Pankaj ; Slowik, Agniesczka and Thijs, Vincent , et al. (2014) In Neurology 83(8). p.678-685
- Contribution to journal › Article
2013
Mark The Role of Adiposity in Cardiometabolic Traits: A Mendelian Randomization Analysis
Fall, Tove ; Hagg, Sara ; Maegi, Reedik ; Ploner, Alexander ; Fischer, Krista ; Horikoshi, Momoko ; Sarin, Antti-Pekka ; Thorleifsson, Gudmar ; Ladenvall, Claes ^LU and Kals, Mart , et al. (2013) In PLoS Medicine 10(6).
- Contribution to journal › Article
2012
Mark Genome-wide association study identifies a variant in HDAC9 associated with large vessel ischemic stroke
Bellenguez, Celine ; Bevan, Steve ; Gschwendtner, Andreas ; Spencer, Chris C. A. ; Burgess, Annette I. ; Pirinen, Matti ; Jackson, Caroline A. ; Traylor, Matthew ; Strange, Amy and Su, Zhan , et al. (2012) In Nature Genetics 44(3). p.141-328
- Contribution to journal › Article
Mark Genetic risk factors for ischaemic stroke and its subtypes (the METASTROKE Collaboration): a meta-analysis of genome-wide association studies
Traylor, Matthew ; Farrall, Martin ; Holliday, Elizabeth G. ; Sudlow, Cathie ; Hopewell, Jemma C. ; Cheng, Yu-Ching ; Fomage, Myriam ; Ikram, M. Arfan ; Malik, Rainer and Bevan, Steve , et al. (2012) In Lancet Neurology 11(11). p.951-962
- Contribution to journal › Article
Mark Apolipoprotein(a) Genetic Sequence Variants Associated With Systemic Atherosclerosis and Coronary Atherosclerotic Burden But Not With Venous Thromboembolism
Helgadottir, Anna ; Gretarsdottir, Solveig ; Thorleifsson, Gudmar ; Holm, Hilma ; Patel, Riyaz S. ; Gudnason, Thorarinn ; Jones, Gregory T. ; van Rij, Andre M. ; Eapen, Danny J. and Baas, Annette F. , et al. (2012) In Journal of the American College of Cardiology 60(8). p.722-729
- Contribution to journal › Article
2011
Mark Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease
Schunkert, Heribert ; Koenig, Inke R. ; Kathiresan, Sekar ; Reilly, Muredach P. ; Assimes, Themistocles L. ; Holm, Hilma ; Preuss, Michael ; Stewart, Alexandre F. R. ; Barbalic, Maja and Gieger, Christian , et al. (2011) In Nature Genetics 43(4). p.153-333
- Contribution to journal › Article
2010
Mark Genome-wide association study identifies a sequence variant within the DAB2IP gene conferring susceptibility to abdominal aortic aneurysm
Gretarsdottir, Solveig ; Baas, Annette F. ; Thorleifsson, Gudmar ; Holm, Hilma ; den Heijer, Martin ; de Vries, Jean-Paul P. M. ; Kranendonk, Steef E. ; Zeebregts, Clark J. A. M. ; van Sterkenburg, Steven M. and Geelkerken, Robert H. , et al. (2010) In Nature Genetics 42(8). p.71-692
- Contribution to journal › Article
2008
Mark The same sequence variant on 9p21 associates with myocardial infarction, abdominal aortic aneurysm and intracranial aneurysm
Helgadottir, Anna ; Thorleifsson, Gudmar ; Magnusson, Kristinn P. ; Gretarsdottir, Solveig ; Steinthorsdottir, Valgerdur ; Manolescu, Andrei ; Jones, Gregory T. ; Rinkel, Gabriel J. E. ; Blankensteijn, Jan D. and Ronkainen, Antti , et al. (2008) In Nature Genetics 40(2). p.217-224
- Contribution to journal › Article

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