Publications

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2018
Evangelou E, Warren HR, Mosen-Ansorena D, Mifsud B, Pazoki R, Gao H, Ntritsos G, Dimou N, Cabrera CP, Karaman I et al..  2018.  Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits.. Nat Genet. 50(10):1412-1425.
Ligthart S, Vaez A, Võsa U, Stathopoulou MG, de Vries PS, Prins BP, van der Most PJ, Tanaka T, Naderi E, Rose LM et al..  2018.  Genome Analyses of >200,000 Individuals Identify 58 Loci for Chronic Inflammation and Highlight Pathways that Link Inflammation and Complex Disorders.. Am J Hum Genet. 103(5):691-706.
Franceschini N, Giambartolomei C, de Vries PS, Finan C, Bis JC, Huntley RP, Lovering RC, Tajuddin SM, Winkler TW, Graff M et al..  2018.  GWAS and colocalization analyses implicate carotid intima-media thickness and carotid plaque loci in cardiovascular outcomes.. Nat Commun. 9(1):5141.
Roselli C, Chaffin MD, Weng L-C, Aeschbacher S, Ahlberg G, Albert CM, Almgren P, Alonso A, Anderson CD, Aragam KG et al..  2018.  Multi-ethnic genome-wide association study for atrial fibrillation.. Nat Genet. 50(9):1225-1233.
Evangelou E, Warren HR, Mosen-Ansorena D, Mifsud B, Pazoki R, Gao H, Ntritsos G, Dimou N, Cabrera CP, Karaman I et al..  2018.  Publisher Correction: Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits.. Nat Genet. 50(12):1755.
2015
Nikpay M, Goel A, Won H-H, Hall LM, Willenborg C, Kanoni S, Saleheen D, Kyriakou T, Nelson CP, Hopewell JC et al..  2015.  A comprehensive 1,000 Genomes-based genome-wide association meta-analysis of coronary artery disease.. Nat Genet. 47(10):1121-1130.
Do R, Stitziel NO, Won H-H, Jørgensen ABerg, Duga S, Merlini PAngelica, Kiezun A, Farrall M, Goel A, Zuk O et al..  2015.  Exome sequencing identifies rare LDLR and APOA5 alleles conferring risk for myocardial infarction.. Nature. 518(7537):102-6.
Gaulton KJ, Ferreira T, Lee Y, Raimondo A, Mägi R, Reschen ME, Mahajan A, Locke A, N Rayner W, Robertson N et al..  2015.  Genetic fine mapping and genomic annotation defines causal mechanisms at type 2 diabetes susceptibility loci.. Nat Genet. 47(12):1415-25.
Wessel J, Chu AY, Willems SM, Wang S, Yaghootkar H, Brody JA, Dauriz M, Hivert M-F, Raghavan S, Lipovich L et al..  2015.  Low-frequency and rare exome chip variants associate with fasting glucose and type 2 diabetes susceptibility.. Nat Commun. 6:5897.
Huffman JE, de Vries PS, Morrison AC, Sabater-Lleal M, Kacprowski T, Auer PL, Brody JA, Chasman DI, Chen M-H, Guo X et al..  2015.  Rare and low-frequency variants and their association with plasma levels of fibrinogen, FVII, FVIII, and vWF.. Blood. 126(11):e19-29.