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Marcus R. Munafo et al.
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Jacqueline MacArthur et al.
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Mohammad H. Forouzanfar et al.
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Wenguang Feng et al.
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Yasunori Miyamoto et al.
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Rare and low-frequency coding variants alter human adult height
Eirini Marouli et al.
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Helen R. Warren et al.
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WebGestalt 2017: a more comprehensive, powerful, flexible and interactive gene set enrichment analysis toolkit
Jing Wang et al.
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Cardiovascular effects of exogenous adrenomedullin and CGRP in Ramp and Calcrl deficient mice
J. B. Pawlak et al.
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Elevated Plasma Transforming Growth Factor β1 Levels Predict the Development of Hypertension in Normotensives: The 14-Year Follow-Up Study
Erika Nakao et al.
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An Expanded View of Complex Traits: From Polygenic to Omnigenic
Evan A. Boyle et al.
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PhenoScanner: a database of human genotype-phenotype associations
James R. Staley et al.
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Worldwide Exposures to Cardiovascular Risk Factors and Associated Health Effects Current Knowledge and Data Gaps
Ioanna Tzoulaki et al.
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John Michael Gaziano et al.
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Mohammad H. Forouzanfar et al.
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Chunyu Liu et al.
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Trans-ancestry meta-analyses identify rare and common variants associated with blood pressure and hypertension
Praveen Surendran et al.
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Evaluating the contribution of genetics and familial shared environment to common disease using the UK Biobank
Maria Munoz 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 et al.
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A reference panel of 64,976 haplotypes for genotype imputation
Shane McCarthy et al.
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Relaxin in paraventricular nucleus contributes to sympathetic overdrive and hypertension via PI3K-Akt pathway
Hai-Jian Sun et al.
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Anthony D. Schmitt et al.
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Reecha Sofat et al.
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Polymorphisms in VEGFA gene affect the antihypertensive responses to enalapril
G. H. Oliveira-Paula et al.
EUROPEAN JOURNAL OF CLINICAL PHARMACOLOGY (2015)
Adrenal cortex tissue homeostasis and zonation: A WNT perspective
Coralie Drelon et al.
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A global reference for human genetic variation
David M. Altshuler et al.
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LD Score regression distinguishes confounding from polygenicity in genome-wide association studies
Brendan K. Bulik-Sullivan et al.
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Efficient Bayesian mixed-model analysis increases association power in large cohorts
Po-Ru Loh et al.
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Jian Zhou et al.
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Pregnancy, Primary Aldosteronism, and Adrenal CTNNB1 Mutations
Ada E. D. Teo et al.
NEW ENGLAND JOURNAL OF MEDICINE (2015)
Exploring hypertension genome-wide association studies findings and impact on pathophysiology, pathways, and pharmacogenetics
Claudia P. Cabrera et al.
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DisGeNET: a discovery platform for the dynamical exploration of human diseases and their genes
Janet Pinero et al.
DATABASE-THE JOURNAL OF BIOLOGICAL DATABASES AND CURATION (2015)
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Cathie Sudlow et al.
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Novel insights into the genetics of smoking behaviour, lung function, and chronic obstructive pulmonary disease (UK BiLEVE): a genetic association study in UK Biobank
Louise V. Wain et al.
LANCET RESPIRATORY MEDICINE (2015)
Cohort Profile: Estonian Biobank of the Estonian Genome Center, University of Tartu
Liis Leitsalu et al.
INTERNATIONAL JOURNAL OF EPIDEMIOLOGY (2015)
A 3D Map of the Human Genome at Kilobase Resolution Reveals Principles of Chromatin Looping
Suhas S. P. Rao et al.
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Paul Elliott et al.
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Blood pressure-lowering treatment based on cardiovascular risk: a meta-analysis of individual patient data
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Georg B. Ehret et al.
EUROPEAN HEART JOURNAL (2013)
Meta-analysis methods for genome-wide association studies and beyond
Evangelos Evangelou et al.
NATURE REVIEWS GENETICS (2013)
GCTA: A Tool for Genome-wide Complex Trait Analysis
Jian Yang et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2011)
The Wnt/beta-catenin pathway in adrenocortical development and cancer
Abeer El Wakil et al.
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Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk
Georg B. Ehret et al.
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Louise V. Wain et al.
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METAL: fast and efficient meta-analysis of genomewide association scans
Cristen J. Willer et al.
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Kirk P. Conrad
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Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis
Benjamin F. Voight et al.
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Prevalence of primary hyperaldosteronism in resistant hypertension: a retrospective observational study
Stella Douma et al.
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Heterogeneity in Meta-Analyses of Genome-Wide Association Investigations
John P. A. Ioannidis et al.
PLOS ONE (2007)
PLINK: A tool set for whole-genome association and population-based linkage analyses
Shaun Purcell et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2007)
A prospective study of the prevalence of primary aldosteronism in 1,125 hypertensive patients
Gian Paolo Rossi et al.
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY (2006)
Adjusting for treatment effects in studies of quantitative traits: antihypertensive therapy and systolic blood pressure
MD Tobin et al.
STATISTICS IN MEDICINE (2005)
Signal-crosstalk between Rho/ROCK and c-Jun NH2-terminal kinase mediates migration of vascular smooth muscle cells stimulated by angiotensin II
H Ohtsu et al.
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Mutations of β-catenin in adrenocortical tumors:: Activation of the wnt signaling pathway is a frequent event in both benign and malignant adrenocortical tumors
F Tissier et al.
CANCER RESEARCH (2005)
Hyperaldosteronism among with resistant black and white subjects hypertension
DA Calhoun et al.
HYPERTENSION (2002)
Heterozygous germline mutations in BMPR2, encoding a TGF-beta receptor, cause familial primary pulmonary hypertension
KB Lane et al.
NATURE GENETICS (2000)
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