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2019
Mark Roadmap for a precision-medicine initiative in the Nordic region
Njølstad, Pål Rasmus ; Andreassen, Ole Andreas ; Brunak, Søren ; Børglum, Anders D. ; Dillner, Joakim ^LU ; Esko, Tõnu ; Franks, Paul W. ^LU ; Freimer, Nelson ; Groop, Leif ^LU and Heimer, Hakon , et al. (2019) In Nature Genetics
- Contribution to journal › Debate/Note/Editorial
2017
Mark Systematic Evaluation of Pleiotropy Identifies 6 Further Loci Associated With Coronary Artery Disease
Webb, Thomas R. ; Erdmann, Jeanette ; Stirrups, Kathleen E. ; Stitziel, Nathan O. ; Masca, Nicholas G D ; Jansen, Henning ; Kanoni, Stavroula ; Nelson, Christopher P ; Ferrario, Paola G. and König, Inke R. , et al. (2017) In Journal of the American College of Cardiology 69(7). p.823-836
- Contribution to journal › Article
2016
Mark Coding variation in ANGPTL4, LPL, and SVEP1 and the risk of coronary disease
Stitziel, Nathan O. ; Stirrups, Kathleen E. ; Masca, Nicholas G D ; Erdmann, Jeanette ; Ferrario, Paola G. ; König, Inke R. ; Weeke, Peter E. ; Webb, Thomas R. ; Auer, Paul L. and Schick, Ursula M. , et al. (2016) In New England Journal of Medicine 374(12). p.1134-1144
- Contribution to journal › Article
2015
Mark Genetic risk, coronary heart disease events, and the clinical benefit of statin therapy: an analysis of primary and secondary prevention trials.
Mega, Jessica L ; Stitziel, Nathan O ; Smith, Gustav ^LU ; Chasman, Daniel I ; Caulfield, Mark J ; Devlin, James J ; Nordio, Francesco ; Hyde, Craig L ; Cannon, Christopher P and Sacks, Frank M , et al. (2015) In The Lancet 385(9984). p.2264-2271
- Contribution to journal › Article
Mark Association of exome sequences with plasma C-reactive protein levels in >9000 participants.
Schick, Ursula M ; Auer, Paul L ; Bis, Joshua C ; Lin, Honghuang ; Wei, Peng ; Pankratz, Nathan ; Lange, Leslie A ; Brody, Jennifer ; Stitziel, Nathan O and Kim, Daniel S , et al. (2015) In Human Molecular Genetics 24(2). p.559-571
- Contribution to journal › Article
2014
Mark Distribution and Medical Impact of Loss-of-Function Variants in the Finnish Founder Population.
Lim, Elaine T ; Würtz, Peter ; Havulinna, Aki S ; Palta, Priit ; Tukiainen, Taru ; Rehnström, Karola ; Esko, Tõnu ; Mägi, Reedik ; Inouye, Michael and Lappalainen, Tuuli , et al. (2014) In PLoS Genetics 10(7).
- Contribution to journal › Article
Mark Loss-of-Function Mutations in APOC3, Triglycerides, and Coronary Disease
Crosby, Jacy ; Peloso, Gina M. ; Auer, Paul L. ; Crosslin, David R. ; Stitziel, Nathan O. ; Lange, Leslie A. ; Lu, Yingchang ; Tang, Zheng-zheng ; Zhang, He and Hindy, George ^LU , et al. (2014) In New England Journal of Medicine 371(1). p.22-31
- Contribution to journal › Article
Mark Association of low-frequency and rare coding-sequence variants with blood lipids and coronary heart disease in 56,000 whites and blacks.
Peloso, Gina M ; Auer, Paul L ; Bis, Joshua C ; Voorman, Arend ; Morrison, Alanna C ; Stitziel, Nathan O ; Brody, Jennifer A ; Khetarpal, Sumeet A ; Crosby, Jacy R and Fornage, Myriam , et al. (2014) In American Journal of Human Genetics 94(2). p.223-232
- Contribution to journal › Article
2013
Mark Exome Sequencing and Directed Clinical Phenotyping Diagnose Cholesterol Ester Storage Disease Presenting as Autosomal Recessive Hypercholesterolemia.
Stitziel, Nathan O ; Fouchier, Sigrid W ; Sjouke, Barbara ; Peloso, Gina M ; Moscoso, Alessa M ; Auer, Paul L ; Goel, Anuj ; Gigante, Bruna ; Barnes, Timothy A and Melander, Olle ^LU , et al. (2013) In Arteriosclerosis, Thrombosis and Vascular Biology 33(12). p.2909-2914
- Contribution to journal › Article

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