Global genetic diversity of human apolipoproteins and effects on cardiovascular disease risk [S] by Yitian Zhou, Reedik Mägi, Lili Milani, Volker M. Lauschke

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Parents of early‐maturing girls die younger by Peeter Hõrak, Markus Valge, Krista Fischer, Reedik Mägi, Tanel Kaart

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Genetic variants in humanin nuclear isoform gene regions show no association with coronary artery disease by Mall Eltermaa, Maili Jakobson, Meeme Utt, Sulev Kõks, Reedik Mägi, Joel Starkopf

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Genome-wide association study identifies five risk loci for pernicious anemia by Triin Laisk, Maarja Lepamets, Mariann Koel, Erik Abner, Estonian Biobank Research Team, Reedik Mägi

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Polygenic prediction of breast cancer: comparison of genetic predictors and implications for risk stratification by Kristi Läll, Maarja Lepamets, Marili Palover, Tõnu Esko, Andres Metspalu, Neeme Tõnisson, Peeter Padrik, Reedik Mägi, Krista Fischer

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An evaluation of the performance of tag SNPs derived from HapMap in a Caucasian population. by Alexandre Montpetit, Mari Nelis, Philippe Laflamme, Reedik Magi, Xiayi Ke, Maido Remm, Lon Cardon, Thomas J Hudson, Andres Metspalu

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Genetic determinants of plasma protein levels in the Estonian population by Anette Kalnapenkis, Maarja Jõeloo, Kaido Lepik, Viktorija Kukuškina, Mart Kals, Kaur Alasoo, Estonian Biobank Research Team, Reedik Mägi, Tõnu Esko, Urmo Võsa

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Advancing our understanding of genetic risk factors and potential personalized strategies for pelvic organ prolapse by Natàlia Pujol-Gualdo, Kristi Läll, Maarja Lepamets, Estonian Biobank Research Team, Henna-Riikka Rossi, Riikka K. Arffman, Terhi T. Piltonen, Reedik Mägi, Triin Laisk

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Causal relationships between obesity and the leading causes of death in women and men. by Jenny C Censin, Sanne A E Peters, Jonas Bovijn, Teresa Ferreira, Sara L Pulit, Reedik Mägi, Anubha Mahajan, Michael V Holmes, Cecilia M Lindgren

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Genomic architecture and prediction of censored time-to-event phenotypes with a Bayesian genome-wide analysis by Sven E. Ojavee, Athanasios Kousathanas, Daniel Trejo Banos, Etienne J. Orliac, Marion Patxot, Kristi Läll, Reedik Mägi, Krista Fischer, Zoltan Kutalik, Matthew R. Robinson

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Rare copy-number variants as modulators of common disease susceptibility by Chiara Auwerx, Maarja Jõeloo, Marie C. Sadler, Nicolò Tesio, Sven Ojavee, Charlie J. Clark, Reedik Mägi, Estonian Biobank Research Team, Alexandre Reymond, Zoltán Kutalik

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Contribution of 32 GWAS-identified common variants to severe obesity in European adults referred for bariatric surgery. by Reedik Mägi, Sean Manning, Ahmed Yousseif, Andrea Pucci, Ferruccio Santini, Efthimia Karra, Giorgia Querci, Caterina Pelosini, Mark I McCarthy, Cecilia M Lindgren, Rachel L Batterham

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Polygenic risk scores as a marker for epilepsy risk across lifetime and after unspecified seizure events by Henrike O. Heyne, Fanny-Dhelia Pajuste, Julian Wanner, Jennifer I. Daniel Onwuchekwa, Reedik Mägi, Aarno Palotie, FinnGen, Estonian Biobank research team, Reetta Kälviainen, Mark J. Daly

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DNA methylation changes in endometrium and correlation with gene expression during the transition from pre-receptive to receptive phase by Viktorija Kukushkina, Vijayachitra Modhukur, Marina Suhorutšenko, Maire Peters, Reedik Mägi, Nilufer Rahmioglu, Agne Velthut-Meikas, Signe Altmäe, Francisco J. Esteban, Jaak Vilo, Krina Zondervan, Andres Salumets, Triin Laisk-Podar

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Variability of polygenic prediction for body mass index in Africa by Tinashe Chikowore, Kristi Läll, Lisa K. Micklesfield, Zane Lombard, Julia H. Goedecke, Segun Fatumo, Shane A. Norris, Reedik Magi, Michele Ramsay, Paul W. Franks, Guillaume Pare, Andrew P. Morris

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Disentangling the consequences of type 2 diabetes on targeted metabolite profiles using causal inference and interaction QTL analyses. by Ozvan Bocher, Archit Singh, Yue Huang, Urmo Võsa, Ene Reimann, Ana Arruda, Andrei Barysenska, Anastassia Kolde, Nigel W Rayner, Estonian Biobank research team, Tõnu Esko, Reedik Mägi, Eleftheria Zeggini

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Probabilistic inference of the genetic architecture underlying functional enrichment of complex traits by Marion Patxot, Daniel Trejo Banos, Athanasios Kousathanas, Etienne J. Orliac, Sven E. Ojavee, Gerhard Moser, Alexander Holloway, Julia Sidorenko, Zoltan Kutalik, Reedik Mägi, Peter M. Visscher, Lars Rönnegård, Matthew R. Robinson

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Genome-wide meta-analysis conducted in three large biobanks expands the genetic landscape of lumbar disc herniations by Ville Salo, Juhani Määttä, Eeva Sliz, FinnGen, Ene Reimann, Reedik Mägi, Estonian Biobank Research Team, Kadri Reis, Abdelrahman G. Elhanas, Anu Reigo, Priit Palta, Tõnu Esko, Jaro Karppinen, Johannes Kettunen

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Improved polygenic prediction by Bayesian multiple regression on summary statistics by Luke R. Lloyd-Jones, Jian Zeng, Julia Sidorenko, Loïc Yengo, Gerhard Moser, Kathryn E. Kemper, Huanwei Wang, Zhili Zheng, Reedik Magi, Tõnu Esko, Andres Metspalu, Naomi R. Wray, Michael E. Goddard, Jian Yang, Peter M. Visscher

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Omics-informed CNV calls reduce false-positive rates and improve power for CNV-trait associations by Maarja Lepamets, Chiara Auwerx, Margit Nõukas, Annique Claringbould, Eleonora Porcu, Mart Kals, Tuuli Jürgenson, Andrew Paul Morris, Urmo Võsa, Murielle Bochud, Silvia Stringhini, Cisca Wijmenga, Lude Franke, Hedi Peterson, Jaak Vilo, Kaido Lepik, Reedik Mägi, Zoltán Kutalik

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