LDpred2: better, faster, stronger von Privé, Florian, Arbel, Julyan, Vilhjálmsson, Bjarni J

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Portability of 245 polygenic scores when derived from the UK Biobank and applied to 9 ancestry groups from the same cohort von Privé, Florian, Aschard, Hugues, Carmi, Shai, Folkersen, Lasse, Hoggart, Clive, O’Reilly, Paul F., Vilhjálmsson, Bjarni J.

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Adjusting for Heritable Covariates Can Bias Effect Estimates in Genome-Wide Association Studies von Aschard, Hugues, Vilhjálmsson, Bjarni J., Joshi, Amit D., Price, Alkes L., Kraft, Peter

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Maximizing the Power of Principal-Component Analysis of Correlated Phenotypes in Genome-wide Association Studies von Aschard, Hugues, Vilhjálmsson, Bjarni J., Greliche, Nicolas, Morange, Pierre-Emmanuel, Trégouët, David-Alexandre, Kraft, Peter

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Conditions under which genome-wide association studies will be positively misleading von Platt, Alexander, Vilhjálmsson, Bjarni J, Nordborg, Magnus

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Towards fair and clinically relevant polygenic predictions von Vilhjálmsson, Bjarni Jóhann

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Genetic architecture of skin and eye color in an African-European admixed population von Beleza, Sandra, Johnson, Nicholas A, Candille, Sophie I, Absher, Devin M, Coram, Marc A, Lopes, Jailson, Campos, Joana, Araújo, Isabel Inês, Anderson, Tovi M, Vilhjálmsson, Bjarni J, Nordborg, Magnus, Correia E Silva, António, Shriver, Mark D, Rocha, Jorge, Barsh, Gregory S, Tang, Hua

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Large uncertainty in individual polygenic risk score estimation impacts PRS-based risk stratification von Ding, Yi, Hou, Kangcheng, Burch, Kathryn S., Lapinska, Sandra, Privé, Florian, Vilhjálmsson, Bjarni, Sankararaman, Sriram, Pasaniuc, Bogdan

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Identifying and correcting for misspecifications in GWAS summary statistics and polygenic scores von Privé, Florian, Arbel, Julyan, Aschard, Hugues, Vilhjálmsson, Bjarni J.

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DNA methylation in Arabidopsis has a genetic basis and shows evidence of local adaptation von Dubin, Manu J, Zhang, Pei, Meng, Dazhe, Remigereau, Marie-Stanislas, Osborne, Edward J, Paolo Casale, Francesco, Drewe, Philipp, Kahles, André, Jean, Geraldine, Vilhjálmsson, Bjarni, Jagoda, Joanna, Irez, Selen, Voronin, Viktor, Song, Qiang, Long, Quan, Rätsch, Gunnar, Stegle, Oliver, Clark, Richard M, Nordborg, Magnus

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Multitrait GWAS to connect disease variants and biological mechanisms von Julienne, Hanna, Laville, Vincent, McCaw, Zachary R., He, Zihuai, Guillemot, Vincent, Lasry, Carla, Ziyatdinov, Andrey, Nerin, Cyril, Vaysse, Amaury, Lechat, Pierre, Menager, Herve, Le Goff, Wilfried, Dube, Marie-Pierre, Kraft, Peter, Ionita-Laza, Iuliana, Vilhjalmsson, Bjarni J., Aschard, Hugues

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Inferring disease architecture and predictive ability with LDpred2-auto von Privé, Florian, Albiñana, Clara, Arbel, Julyan, Pasaniuc, Bogdan, Vilhjálmsson, Bjarni J.

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Harnessing the Power of Population Cohorts to Study the Relationship Between Endocrine-Metabolic Disorders and Depression von Jespersen, Anders, Yilmaz, Zeynep, Vilhjálmsson, Bjarni J.

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ADuLT: An efficient and robust time-to-event GWAS von Pedersen, Emil M., Agerbo, Esben, Plana-Ripoll, Oleguer, Steinbach, Jette, Krebs, Morten D., Hougaard, David M., Werge, Thomas, Nordentoft, Merete, Børglum, Anders D., Musliner, Katherine L., Ganna, Andrea, Schork, Andrew J., Mortensen, Preben B., McGrath, John J., Privé, Florian, Vilhjálmsson, Bjarni J.

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Portability of 245 polygenic scores when derived from the UK Biobank and applied to 9 ancestry groups from the same cohort von Privé, Florian, Aschard, Hugues, Carmi, Shai, Folkersen, Lasse, Hoggart, Clive, O’Reilly, Paul F., Vilhjálmsson, Bjarni J.

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Leveraging both individual-level genetic data and GWAS summary statistics increases polygenic prediction von Albiñana, Clara, Grove, Jakob, McGrath, John J., Agerbo, Esben, Wray, Naomi R., Bulik, Cynthia M., Nordentoft, Merete, Hougaard, David M., Werge, Thomas, Børglum, Anders D., Mortensen, Preben Bo, Privé, Florian, Vilhjálmsson, Bjarni J.

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Accounting for age of onset and family history improves power in genome-wide association studies von Pedersen, Emil M., Agerbo, Esben, Plana-Ripoll, Oleguer, Grove, Jakob, Dreier, Julie W., Musliner, Katherine L., Bækvad-Hansen, Marie, Athanasiadis, Georgios, Schork, Andrew, Bybjerg-Grauholm, Jonas, Hougaard, David M., Werge, Thomas, Nordentoft, Merete, Mors, Ole, Dalsgaard, Søren, Christensen, Jakob, Børglum, Anders D., Mortensen, Preben B., McGrath, John J., Privé, Florian, Vilhjálmsson, Bjarni J.

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Genetic liability estimated from large-scale family data improves genetic prediction, risk score profiling, and gene mapping for major depression von Dybdahl Krebs, Morten, Georgii Hellberg, Kajsa-Lotta, Lundberg, Mischa, Appadurai, Vivek, Ohlsson, Henrik, Pedersen, Emil, Steinbach, Jette, Matthews, Jamie, Border, Richard, LaBianca, Sonja, Calle, Xabier, Meijsen, Joeri J., Ingason, Andrés, Buil, Alfonso, Vilhjálmsson, Bjarni J., Flint, Jonathan, Bacanu, Silviu-Alin, Cai, Na, Dahl, Andy, Zaitlen, Noah, Werge, Thomas, Kendler, Kenneth S., Schork, Andrew J.

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Interplay of polygenic liability with birth-related, somatic, and psychosocial factors in anorexia nervosa risk: a nationwide study von Papini, Natalie M., Presseller, Emily, Bulik, Cynthia M., Holde, Katrine, Larsen, Janne T., Thornton, Laura M., Albiñana, Clara, Vilhjálmsson, Bjarni J., Mortensen, Preben B., Yilmaz, Zeynep, Petersen, Liselotte V.

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Polygenic risk score, psychosocial environment and the risk of attention-deficit/hyperactivity disorder von Østergaard, Søren D., Trabjerg, Betina B., Als, Thomas D., Climent, Clara Albiñana, Privé, Florian, Vilhjálmsson, Bjarni Jóhann, Bækvad-Hansen, Marie, Bybjerg-Grauholm, Jonas, Hougaard, David M., Nordentoft, Merete, Werge, Thomas, Demontis, Ditte, Mortensen, Preben B., Børglum, Anders D., Mors, Ole, Agerbo, Esben

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