Displaying all 14 Publications
Current search: 'Health', 'Journal Article' and 'Martin D. Tobin'
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Genetic landscape of chronic obstructive pulmonary disease identifies heterogeneous cell-type and phenotype associations
Phuwanat Sakornsakolpat, Dmitry Prokopenko, Maxime Lamontagne, et al.
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New genetic signals for lung function highlight pathways and chronic obstructive pulmonary disease associations across multiple ancestries
Nick Shrine, Anna L. Guyatt, A. Mesut Erzurumluoglu, et al.
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Meta-analysis of up to 622,409 individuals identifies 40 novel smoking behaviour associated genetic loci
A. Mesut Erzurumluoglu, MengZhen Liu, Victoria E. Jackson, et al.
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Exome chip meta-analysis fine maps causal variants and elucidates the genetic architecture of rare coding variants in smoking and alcohol use
David M. Brazel, Yu Jiang, Jordan M. Hughey, et al.
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Meta-analysis of exome array data identifies six novel genetic loci for lung function [version 3; referees: 2 approved]
Victoria E. Jackson, Jeanne C. Latourelle, Louise V. Wain, et al.
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Novel blood pressure locus and gene discovery using Genome-Wide Association Study and expression data sets from blood and the kidney
Louise Wain, Ahmad Vaez, Rick Jansen, et al.
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Evidence for large-scale gene-by-smoking interaction effects on pulmonary function
H. Aschard, Martin D. Tobin, D. B. Hancock, et al.
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Whole-genome sequencing coupled to imputation discovers genetic signals for anthropometric traits
Ioanna Tachmazidou, Dániel Süveges, Josine L. Min, et al.
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Novel blood pressure locus and gene discovery using GWAS and expression datasets from blood and the kidney
Louise Wain, Ahmad Vaez, Rick Jansen, et al.
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Genome-wide association analyses for lung function and chronic obstructive pulmonary disease identify new loci and potential druggable targets
Louise V. Wain, Nick Shrine, María Soler Artigas, et al.
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Genome-wide association analysis identifies novel blood pressure loci and offers biological insights into cardiovascular risk
Helen R. Warren, Evangelos Evangelou, Claudia P. Cabrera, et al.
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Trans-ancestry meta-analyses identify rare and common variants associated with blood pressure and hypertension
Praveen Surendran, Fotios Drenos, Robin Young, et al.
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Exome-wide analysis of rare coding variation identifies novel associations with COPD and airflow limitation in MOCS3, IFIT3 and SERPINA12
Victoria E. Jackson, Ioanna Ntalla, Ian Sayers, et al.
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The genetics of blood pressure regulation and its target organs from association studies in 342,415 individuals
Georg B. Ehret, Teresa Ferreira, Daniel I. Chasman, et al.