Selected publications

  • Ganna A, Reilly M, de Faire U, Pedersen N, Magnusson P, Ingelsson E. Risk Prediction Measures for Case-Cohort and Nested Case-Control Designs: An Application to Cardiovascular Disease. Am J Epidemiol. 2012.

  • Berndt SI*, Gustafsson S*, Mägi R*, Ganna A*, Wheeler E, [>300 authors], Scherag A, McCarthy MI*, Speliotes EK*, North KE*, Loos RJ*, Ingelsson E*. Genome-Wide Meta-Analysis Identifies 11 New Loci for Anthropometric Traits and Provides Insights into Genetic Architecture. Nat Genet. 2013.

  • Ganna A, Magnusson PK, Pedersen NL, de Faire U, Reilly M, Arnlöv J, Sundström J, Hamsten A, Ingelsson E. Multilocus Genetic Risk Scores for Coronary Heart Disease Prediction. Arterioscler Thromb Vasc Biol. 2013.

  • Ganna A, Salihovic S, Sundström J, Broeckling CD, Hedman ÅK, Magnusson PKE, Pedersen NL, Larsson A, Siegbahn A, Zilmer M, Prenni J, Ärnlöv J,  Lind L, Fall T, Ingelsson E. Large-scale Metabolomic Profiling Identifies Novel Biomarkers for Incident Coronary Heart Disease. PLoS Genet. 2014.

  • Ganna A, Ingelsson E. Five-year mortality predictors: A prospective study of ~500,000 UK Biobank participants. Lancet. 2015.

  • Ganna A*, Genovese G*, Howrigan DP, Byrnes A, Kurki MI, […], Neale BM. Ultra-rare disruptive and damaging mutations influence educational attainment in the general population. Nat Neuroscience. 2016.

  • Ganna A, Satterstrom KF, Zekavat SM, […], Neale BM. Quantifying the impact of rare and ultra-rare coding variation across the phenotypic spectrum. Am J Hum Genet. 2018.

  • Zekavat SM, Ruotsalainen S, Handsaker RE, […] Ganna A*, Ripatti S*, Kathiresan S*, Natarajan P*. Deep coverage whole genome sequences and plasma lipoprotein(a) in individuals of European and African ancestries. Nat Communications. 2018.


Complete List of Published Work available at: http://www.ncbi.nlm.nih.gov/pubmed/?term=andrea+ganna