Combined linkage and association analysis identifies rare and low frequency variants for blood pressure at 1q31

No abstract is available for this paper.

• Publication year

  2018

• Venue

  European Journal of Human Genetics

• Publication date

  2018-09-27

• Fields of study

  Biology, Medicine

• Identifiers
  DOI 10.1038/s41431-018-0277-1PMID 30262922PMCID PMC6336803
• External record

  Open on Semantic Scholar

• Source metadata

  Semantic Scholar, PubMed

• No claims are published for this paper.

• No concepts are published for this paper.

• Identifying Rare Variant Associations in Admixed Populations

  2019cited by this paper
• Sequencing Analysis at 8p23 Identifies Multiple Rare Variants in DLC1 Associated with Sleep-Related Oxyhemoglobin Saturation Level.

  2019cited by this paper
• Rare variants in fox-1 homolog A (RBFOX1) are associated with lower blood pressure

  2017cited by this paper
• Trans-ancestry meta-analyses identify rare and common variants associated with blood pressure and hypertension

  2016cited by this paper
• The genetics of blood pressure regulation and its target organs from association studies in 342,415 individuals

  2016cited by this paper
• Genome-wide association analyses using electronic health records identify new loci influencing blood pressure variation

  2016cited by this paper
• Pappa2 is linked to salt-sensitive hypertension in Dahl S rats.

  2016cited by this paper
• Meta-analysis identifies common and rare variants influencing blood pressure and overlapping with metabolic trait loci

  2016cited by this paper
• Rare and low-frequency coding variants alter human adult height

  2016cited by this paper
• Variants in angiopoietin-2 (ANGPT2) contribute to variation in nocturnal oxyhaemoglobin saturation level.

  2016cited by this paper
• A statistical approach for rare-variant association testing in affected sibships.

  2015cited by this paper
• The Genotype-Tissue Expression (GTEx) pilot analysis: Multitissue gene regulation in humans

  2015cited by this paper
• Faculty Opinions recommendation of Human genomics. The Genotype-Tissue Expression (GTEx) pilot analysis: multitissue gene regulation in humans.

  2015cited by this paper
• Meta-analysis of correlated traits via summary statistics from GWASs with an application in hypertension.

  2015cited by this paper
• STRING v10: protein–protein interaction networks, integrated over the tree of life

  2014cited by this paper
• Characterization of biological pathways associated with a 1.37 Mbp genomic region protective of hypertension in Dahl S rats.

  2014cited by this paper
• Genome-wide association analysis of blood-pressure traits in African-ancestry individuals reveals common associated genes in African and non-African populations.

  2013cited by this paper
• Genes for blood pressure: an opportunity to understand hypertension.

  2013cited by this paper
• Sequence Kernel Association Test for Quantitative Traits in Family Samples

  2013cited by this paper
• Lifetime risks of cardiovascular disease.

  2012cited by this paper
• Optimal tests for rare variant effects in sequencing association studies.

  2012cited by this paper
• A comparative risk assessment of burden of disease and injury attributable to 67 risk factors and risk factor clusters in 21 regions, 1990-2010: a systematic analysis for the Global Burden of Disease Study 2010.

  2012cited by this paper
• Meta-analysis of genome-wide association studies identifies common variants associated with blood pressure variation in east Asians

  2011cited by this paper
• Genetic Variants in Novel Pathways Influence Blood Pressure and Cardiovascular Disease Risk

  2011cited by this paper
• A general framework for detecting disease associations with rare variants in sequencing studies.

  2011cited by this paper
• Detecting rare and common variants for complex traits: sibpair and odds ratio weighted sum statistics (SPWSS, ORWSS)

  2011cited by this paper
• Pooled Association Tests for Rare Variants in Exon-Resequencing Studies

  2010cited by this paper
• Pooled association tests for rare variants in exon-resequencing studies.

  2010cited by this paper
• Detecting rare variants for complex traits using family and unrelated data

  2010cited by this paper
• Genome-Wide Association Studies: Contribution of Genomics to Understanding Blood Pressure and Essential Hypertension

  2010cited by this paper
• A Groupwise Association Test for Rare Mutations Using a Weighted Sum Statistic

  2009cited by this paper
• Faculty Opinions recommendation of Genome-wide association study identifies eight loci associated with blood pressure.

  2009cited by this paper
• Genome-wide association study of blood pressure and hypertension

  2009cited by this paper
• Methods for detecting associations with rare variants for common diseases: application to analysis of sequence data.

  2008cited by this paper
• Combined Genome Scans for Body Stature in 6,602 European Twins: Evidence for Common Caucasian Loci

  2007cited by this paper
• Multiple genes for essential-hypertension susceptibility on chromosome 1q.

  2007cited by this paper
• An updated meta-analysis of genome scans for hypertension and blood pressure in the NHLBI Family Blood Pressure Program (FBPP).

  2006cited by this paper
• A review of the 'Statistical Analysis for Genetic Epidemiology' (SAGE) software package

  2004cited by this paper
• Genome scan linkage results for longitudinal systolic blood pressure phenotypes in subjects from the Framingham Heart Study

  2003cited by this paper
• Biochemical and clinical aspects of the human flavin-containing monooxygenase form 3 (FMO3) related to trimethylaminuria.

  2003cited by this paper
• A meta-analysis of genome-wide linkage scans for hypertension: the National Heart, Lung and Blood Institute Family Blood Pressure Program.

  2003cited by this paper
• Genome-wide mapping of human loci for essential hypertension.

  2003cited by this paper
• The Seventh Report of the Joint National Committee on Prevention, Detection, Evaluation, and Treatment of High Blood Pressure: the JNC 7 report.

  2003cited by this paper
• Genome Scans for Blood Pressure and Hypertension: The National Heart, Lung, and Blood Institute Family Heart Study*

  2002cited by this paper
• Genome Scan Among Nigerians Linking Blood Pressure to Chromosomes 2, 3, and 19

  2002cited by this paper
• Merlin—rapid analysis of dense genetic maps using sparse gene flow trees

  2002cited by this paper
• Molecular Mechanisms of Human Hypertension

  2001cited by this paper
• Genome‐wide scan of predisposing loci for increased diastolic blood pressure in Finnish siblings

  2000cited by this paper
• Genetic heterogeneity and penetrance analysis of the BRCA1 and BRCA2 genes in breast cancer families. The Breast Cancer Linkage Consortium.

  1998cited by this paper
• Mutations of the flavin-containing monooxygenase gene (FMO3) cause trimethylaminuria, a defect in detoxication.

  1998cited by this paper
• Molecular Genetics of Human Blood Pressure Variation

  1996cited by this paper
• Genetic dissection of complex traits: guidelines for interpreting and reporting linkage results

  1995cited by this paper
• Analysis of Human Genetic Linkage

  1985cited by this paper
• Sequential tests for the detection of linkage.

  1955cited by this paper

• Hypertension as a Novel Link for Shared Heritability in Age at Menarche and Cardiometabolic Traits.

  2023cites this paper
• Rare coding variants in RCN3 are associated with blood pressure

  2022influential citation
• Targeted Genome Sequencing Identifies Multiple Rare Variants in Caveolin-1 Associated with Obstructive Sleep Apnea.

  2022cites this paper
• Identifying Rare Variant Associations in Admixed Populations

  2019cites this paper
• Sequencing Analysis at 8p23 Identifies Multiple Rare Variants in DLC1 Associated with Sleep-Related Oxyhemoglobin Saturation Level.

  2019cites this paper