The role of rare variants in systolic blood pressure: analysis of ExomeChip data in HyperGEN African Americans

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The role of rare variants in systolic blood pressure: analysis of ExomeChip data in HyperGEN African Americans is …
instance of (P31):
scholarly articleQ13442814

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P356DOI10.1159/000375373
P932PMC publication ID4374048
P698PubMed publication ID25765051

P50authorDonna K ArnettQ88878357
Steven C HuntQ89298880
Khanh-Dung H NguyenQ130279531
P2093author name stringDabeeru C Rao
Aravinda Chakravarti
Yun Ju Sung
Jacob Basson
Nuo Cheng
Priyanka Nandakumar
Victor G Dávila-Román
P2860cites workFinding the missing heritability of complex diseasesQ22122198
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NHLBI family blood pressure program: methodology and recruitment in the HyperGEN network. Hypertension genetic epidemiology networkQ40750706
Differential confounding of rare and common variants in spatially structured populationsQ42054812
Analysis of rare variant population structure in Europeans explains differential stratification of gene-based tests.Q42796366
High plasma hemopexin activity is an independent risk factor for late graft failure in renal transplant recipientsQ43165361
Increased transient receptor potential canonical type 3 channels in vasculature from hypertensive rats.Q46231212
Major quantitative trait locus for resting heart rate maps to a region on chromosome 4.Q48016968
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Genetic variants in novel pathways influence blood pressure and cardiovascular disease riskQ24630394
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Genome-wide association study of blood pressure and hypertensionQ28943443
Genome-wide association study of blood pressure extremes identifies variant near UMOD associated with hypertensionQ29417122
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Non-synonymous single-nucleotide polymorphisms associated with blood pressure and hypertension.Q30385528
Genome-wide association analysis of blood-pressure traits in African-ancestry individuals reveals common associated genes in African and non-African populationsQ30414381
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Effects of long-term averaging of quantitative blood pressure traits on the detection of genetic associationsQ33858783
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Common genetic variants in ANK2 modulate QT interval: results from the KORA studyQ34089732
Effect of population stratification analysis on false-positive rates for common and rare variantsQ34176552
Rare and low frequency variant stratification in the UK population: description and impact on association tests.Q34306378
Multiple rare variants in NPC1L1 associated with reduced sterol absorption and plasma low-density lipoprotein levelsQ34478587
The genomic basis of the Williams-Beuren syndromeQ34601047
Novel loci associated with increased risk of sudden cardiac death in the context of coronary artery diseaseQ34672534
Meta-analysis of genome-wide association studies identifies common variants associated with blood pressure variation in east AsiansQ35172107
Genome-wide association study identifies six new loci influencing pulse pressure and mean arterial pressureQ36241862
Sequence kernel association test for quantitative traits in family samplesQ36812083
Uric acid level and elevated blood pressure in US adolescents: National Health and Nutrition Examination Survey, 1999-2006.Q36979391
Genome-wide association studies: potential next steps on a genetic journeyQ37292893
Gene-centric meta-analysis in 87,736 individuals of European ancestry identifies multiple blood-pressure-related lociQ37634121
P433issue1
P407language of work or nameEnglishQ1860
P921main subjectsystoleQ496359
P304page(s)20-27
P577publication date2015-01-01
P1433published inHuman HeredityQ15755116
P1476titleThe role of rare variants in systolic blood pressure: analysis of ExomeChip data in HyperGEN African Americans
P478volume79

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cites work (P2860)
Q52370685Advances in the Genetics of Hypertension: The Effect of Rare Variants.
Q56917541Whole exome analyses to examine the impact of rare variants on left ventricular traits in African American participants from the HyperGEN and GENOA studies

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