2 research outputs found
Correction: The Influence of Age and Sex on Genetic Associations with Adult Body Size and Shape: A Large-Scale Genome-Wide Interaction Study.
- Author
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- T. Wilsgaard (3474971)
- U. de Faire (7605206)
- U. Gyllensten (7612145)
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- W. L. McArdle (7609397)
- W. Maerz (7646285)
- W. R. Scott (7785866)
- W. Zhang (820655)
- Y-C. Cheng (7785698)
- Y-D. I. Chen (7737380)
- Y-M. Gu (7785785)
- Y-P. Liu (7785839)
- Y. J. Sung (7785731)
- Y. Liu (543492)
- Y. Lu (1469287)
- Z. Kutalik (7626725)
- Z. Wang (70993)
- Ă . Johansson (7670804)
- Publication venue
- Publication date
- 29/06/2016
- Field of study
The arcOGEN Consortium should be listed as an author of this article. They contributed to the genome-wide association study results presented in this work. They should be listed in the author byline at position 292 and affiliated with The Arthritis Research UK Osteoarthritis Genetics Consortium. They should also be included in the footnote designating consortia which is underneath the author affiliation list in the PDF version of the article, and in the S2 Text. Please view the correct S2 Text below, containing correct consortia members. S2 Text. Consortia members and extended acknowledgments.
https://doi.org/10.1371/journal.pgen.1006166.s001
(DOCX) [This corrects the article DOI: 10.1371/journal.pgen.1005378.]
Trans-ancestry meta-analyses identify rare and common variants associated with blood pressure and hypertension
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- A. A. Majumder (7652774)
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- A. Linneberg (3444095)
- A. M. Yiorkas (7652675)
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- M. J. Caulfield (7602383)
- M. J. Neville (7652672)
- M. Laakso (7609358)
- M. MĂŒller-Nurasyid (7626752)
- M. Perola (7605860)
- M. R. Jarvelin (7611464)
- M. Samuel (3483809)
- M. Tomaszewski (7602446)
- M. Traylor (7652726)
- M. Uria-Nickelsen (7652711)
- M. Uusitupa (7626860)
- N. Grarup (7627439)
- N. J. Samani (7591811)
- N. J. Wareham (7608962)
- N. Masca (7652639)
- N. Narisu (7609415)
- N. Poulter (7611311)
- N. R. Robertson (7647422)
- N. Sattar (7608890)
- N. Soranzo (7608857)
- N. Verweij (7652687)
- N. W. Rayner (7626794)
- O. Giannakopoulou (7652642)
- O. L. Holmen (7626680)
- O. Melander (7602683)
- O. Pedersen (7627493)
- O. Polasek (7609424)
- O. Rolandsson (7652735)
- P. Amouyel (7605287)
- P. B. Munroe (7602386)
- P. Deloukas (7603691)
- P. Elliott (1293702)
- P. Frossard (7605893)
- P. I. de Bakker (7626020)
- P. Jousilahti (7611407)
- P. Komulainen (4753311)
- P. Sever (7602536)
- P. Surendran (7652621)
- P. van der Harst (7594607)
- P. van der Meer (7652741)
- P. W. Franks (7605191)
- R. A. de Boer (7594610)
- R. A. Scott (2840021)
- R. Chowdhury (7646300)
- R. Marioni (7652705)
- R. MĂ€gi (7609376)
- R. Rauramaa (7626923)
- R. S. Vasan (7626878)
- R. Young (7646078)
- S. Blankenberg (7603658)
- S. Burgess (4176619)
- S. E. Harris (7620116)
- S. F. Nielsen (7646099)
- S. Franks (7351091)
- S. Kathiresan (7606013)
- S. M. Willems (7647404)
- S. MÀnnistö (7626749)
- S. Padmanabhan (637530)
- S. Ripatti (7606073)
- S. Shaw-Hawkins (7602380)
- S. Trompet (7625936)
- T. A. Lakka (7626731)
- T. D. Spector (7608968)
- T. Esko (7626638)
- T. F. Vogt (7652723)
- T. Ferreira (3480845)
- T. Hansen (3919604)
- T. Ohlsson (7652660)
- T. Skaaby (7652765)
- T. Tukiainen (7652633)
- T. Tuomi (7611443)
- T. V. Varga (7652696)
- V. Salomaa (7605350)
- V. Tragante (7625963)
- W. Lieb (7412738)
- W. Zhang (820655)
- W. Zhao (696097)
- X. Sim (7626824)
- Publication venue
- Publication date
- 12/09/2016
- Field of study
High blood pressure is a major risk factor for cardiovascular disease and premature death. However, there is limited knowledge on specific causal genes and pathways. To better understand the genetics of blood pressure, we genotyped 242,296 rare, low-frequency and common genetic variants in up to 192,763 individuals and used âŒ155,063 samples for independent replication. We identified 30 new blood pressure- or hypertension-associated genetic regions in the general population, including 3 rare missense variants in RBM47, COL21A1 and RRAS with larger effects (>1.5 mm Hg/allele) than common variants. Multiple rare nonsense and missense variant associations were found in A2ML1, and a low-frequency nonsense variant in ENPEP was identified. Our data extend the spectrum of allelic variation underlying blood pressure traits and hypertension, provide new insights into the pathophysiology of hypertension and indicate new targets for clinical intervention