Search Results - Reedik Magi

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  1. 1

    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

    Published in Nature Communications (2021-06-01)
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  2. 2

    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

    Published in BMC Cancer (2019-06-01)
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  3. 3

    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

    Published in PLoS Genetics (2006-03-01)
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  4. 4

    Unraveling genotype–phenotype relationships in hereditary hemochromatosis through integrated biobank data analysis by Miriam Nurm, Tarmo Annilo, Sebastian May-Wilson, Anu Reigo, Reedik Mägi, Urmo Võsa, Neeme Tõnisson, Estonian Biobank Research Team, Toomas Haller

    Published in BMC Genomics (2026-03-01)
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  5. 5

    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

    Published in Scientific Reports (2024-04-01)
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  6. 6

    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

    Published in PLoS Genetics (2019-10-01)
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  7. 7

    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

    Published in Genome Medicine (2024-01-01)
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  8. 8

    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

    Published in PLoS ONE (2013-01-01)
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  9. 9

    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

    Published in Nature Communications (2024-07-01)
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  10. 10

    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

    Published in Genome Medicine (2024-05-01)
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  11. 11

    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

    Published in PLoS Genetics (2024-12-01)
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  12. 12

    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

    Published in Nature Communications (2024-11-01)
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  13. 13

    Genetic architecture of lumbar spinal stenosis by Ville Salo, Juhani Määttä, Jasmin Takala, Anni Heikkilä, FinnGen, Ene Reimann, Reedik Mägi, Estonian Biobank Research Team, Kadri Reis, Abdelrahman G. Elhanas, Anu Reigo, Priit Palta, Tõnu Esko, Ville Leinonen, Jaro Karppinen, Eeva Sliz, Johannes Kettunen

    Published in Nature Communications (2026-04-01)
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  14. 14

    Biomarker profiling by nuclear magnetic resonance spectroscopy for the prediction of all-cause mortality: an observational study of 17,345 persons. by Krista Fischer, Johannes Kettunen, Peter Würtz, Toomas Haller, Aki S Havulinna, Antti J Kangas, Pasi Soininen, Tõnu Esko, Mari-Liis Tammesoo, Reedik Mägi, Steven Smit, Aarno Palotie, Samuli Ripatti, Veikko Salomaa, Mika Ala-Korpela, Markus Perola, Andres Metspalu

    Published in PLoS Medicine (2014-02-01)
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  15. 15

    Genome-wide association study of obstructive sleep apnoea in the Million Veteran Program uncovers genetic heterogeneity by sexResearch in context by Tamar Sofer, Nuzulul Kurniansyah, Michael Murray, Yuk-Lam Ho, Erik Abner, Tõnu Esko, Jennifer E. Huffman, Kelly Cho, Peter W.F. Wilson, Daniel J. Gottlieb, Andres Metspalu, Lili Milani, Tõnu Esko, Reedik Mägi, Mari Nelis, Georgi Hudjashov

    Published in EBioMedicine (2023-04-01)
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  16. 16

    Genome-wide screen of otosclerosis in population biobanks: 27 loci and shared associations with skeletal structure by Joel T. Rämö, Tuomo Kiiskinen, Richard Seist, Kristi Krebs, Masahiro Kanai, Juha Karjalainen, Mitja Kurki, Eija Hämäläinen, Paavo Häppölä, Aki S. Havulinna, Heidi Hautakangas, FinnGen, Reedik Mägi, Priit Palta, Tõnu Esko, Andres Metspalu, Matti Pirinen, Konrad J. Karczewski, Samuli Ripatti, Lili Milani, Konstantina M. Stankovic, Antti Mäkitie, Mark J. Daly, Aarno Palotie

    Published in Nature Communications (2023-01-01)
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  17. 17

    Genome-wide risk prediction of common diseases across ancestries in one million people by Nina Mars, Sini Kerminen, Yen-Chen A. Feng, Masahiro Kanai, Kristi Läll, Laurent F. Thomas, Anne Heidi Skogholt, Pietro della Briotta Parolo, Benjamin M. Neale, Jordan W. Smoller, Maiken E. Gabrielsen, Kristian Hveem, Reedik Mägi, Koichi Matsuda, Yukinori Okada, Matti Pirinen, Aarno Palotie, Andrea Ganna, Alicia R. Martin, Samuli Ripatti

    Published in Cell Genomics (2022-04-01)
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  18. 18

    Author Correction: HLA allele-calling using multi-ancestry whole-exome sequencing from the UK Biobank identifies 129 novel associations in 11 autoimmune diseases by Guillaume Butler-Laporte, Joseph Farjoun, Tomoko Nakanishi, Tianyuan Lu, Erik Abner, Yiheng Chen, Michael Hultström, Andres Metspalu, Lili Milani, Reedik Mägi, Mari Nelis, Georgi Hudjashov, Estonian Biobank Research Team, Satoshi Yoshiji, Yann Ilboudo, Kevin Y. H. Liang, Chen-Yang Su, Julian D. S. Willett, Tõnu Esko, Sirui Zhou, Vincenzo Forgetta, Daniel Taliun, J. Brent Richards

    Published in Communications Biology (2026-04-01)
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  19. 19

    HLA allele-calling using multi-ancestry whole-exome sequencing from the UK Biobank identifies 129 novel associations in 11 autoimmune diseases by Guillaume Butler-Laporte, Joseph Farjoun, Tomoko Nakanishi, Tianyuan Lu, Erik Abner, Yiheng Chen, Michael Hultström, Andres Metspalu, Lili Milani, Reedik Mägi, Mari Nelis, Georgi Hudjashov, Estonian Biobank Research Team, Satoshi Yoshiji, Yann Ilboudo, Kevin Y. H. Liang, Chen-Yang Su, Julian D. S. Willett, Tõnu Esko, Sirui Zhou, Vincenzo Forgetta, Daniel Taliun, J. Brent Richards

    Published in Communications Biology (2023-11-01)
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  20. 20

    Coexpression network analysis in abdominal and gluteal adipose tissue reveals regulatory genetic loci for metabolic syndrome and related phenotypes. by Josine L Min, George Nicholson, Ingileif Halgrimsdottir, Kristian Almstrup, Andreas Petri, Amy Barrett, Mary Travers, Nigel W Rayner, Reedik Mägi, Fredrik H Pettersson, John Broxholme, Matt J Neville, Quin F Wills, Jane Cheeseman, GIANT Consortium, MolPAGE Consortium, Maxine Allen, Chris C Holmes, Tim D Spector, Jan Fleckner, Mark I McCarthy, Fredrik Karpe, Cecilia M Lindgren, Krina T Zondervan

    Published in PLoS Genetics (2012-01-01)
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