meta-analysis | Q815382 |
scholarly article | Q13442814 |
P50 | author | Michael Marmot | Q1928530 |
Renate B. Schnabel | Q21264509 | ||
Daniel S Evans | Q88964145 | ||
Steven A Lubitz | Q88968134 | ||
Rajat Deo | Q90604867 | ||
Solomon K Musani | Q114270645 | ||
Martina Müller-Nurasyid | Q28805353 | ||
Nona Sotoodehnia | Q30225548 | ||
Arne Pfeufer | Q30225573 | ||
Alan B. Zonderman | Q37368449 | ||
Alvaro Alonso | Q39964242 | ||
Reena Mehra | Q42877389 | ||
Elsayed Z. Soliman | Q55153694 | ||
Michele K. Evans | Q55426351 | ||
Patrick T Ellinor | Q57775928 | ||
Jared W Magnani | Q57776581 | ||
Susan Redline | Q64755281 | ||
Yongmei Liu | Q67422669 | ||
Kathleen F. Kerr | Q76350439 | ||
Jan Gustav Smith | Q81044315 | ||
Susan R Heckbert | Q88077554 | ||
P2093 | author name string | Cameron Palmer | |
Dina N Paltoo | |||
Ervin R Fox | |||
Candidate-gene Association Resource (CARe) Consortium | |||
Yan A Meng | |||
P2860 | cites work | Sensitive detection of chromosomal segments of distinct ancestry in admixed populations | Q21563344 |
The genetic structure and history of Africans and African Americans | Q22065887 | ||
Methods for high-density admixture mapping of disease genes | Q22337164 | ||
Genetic variation in SCN10A influences cardiac conduction | Q24294598 | ||
MYH9 is a major-effect risk gene for focal segmental glomerulosclerosis | Q24643421 | ||
A common MYBPC3 (cardiac myosin binding protein C) variant associated with cardiomyopathies in South Asia | Q24645034 | ||
PLINK: a tool set for whole-genome association and population-based linkage analyses | Q24677407 | ||
A haplotype map of the human genome | Q24679827 | ||
Principal components analysis corrects for stratification in genome-wide association studies | Q27860975 | ||
Genetic analysis of African populations: human evolution and complex disease | Q28216772 | ||
Genomic control for association studies | Q29547213 | ||
Integrated detection and population-genetic analysis of SNPs and copy number variation | Q29614584 | ||
Genotype imputation | Q29614590 | ||
Estimation of the multiple testing burden for genomewide association studies of nearly all common variants | Q29614917 | ||
The Atherosclerosis Risk in Communities (ARIC) Study: design and objectives. The ARIC investigators | Q29614947 | ||
Multi-Ethnic Study of Atherosclerosis: objectives and design | Q29615490 | ||
Candidate gene association resource (CARe): design, methods, and proof of concept | Q30432077 | ||
Statistical tests for detection of misspecified relationships by use of genome-screen data | Q30587143 | ||
Variant of SCN5A sodium channel implicated in risk of cardiac arrhythmia | Q33148058 | ||
Heritability of cardiovascular and personality traits in 6,148 Sardinians | Q33255344 | ||
Genome-wide association study of electrocardiographic and heart rate variability traits: the Framingham Heart Study | Q33300817 | ||
Concept, design and implementation of a cardiovascular gene-centric 50 k SNP array for large-scale genomic association studies | Q33381588 | ||
GWAF: an R package for genome-wide association analyses with family data | Q33521158 | ||
Genome-wide association study of PR interval | Q33772170 | ||
Genome-wide association studies in diverse populations | Q34817128 | ||
Genome-wide association study of electrocardiographic conduction measures in an isolated founder population: Kosrae | Q37169876 | ||
Ethnic distribution of ECG predictors of atrial fibrillation and its impact on understanding the ethnic distribution of ischemic stroke in the Atherosclerosis Risk in Communities (ARIC) study | Q37199773 | ||
Integrated genotype calling and association analysis of SNPs, common copy number polymorphisms and rare CNVs | Q37373867 | ||
Long-term outcomes in individuals with prolonged PR interval or first-degree atrioventricular block | Q37396589 | ||
The familial aggregation of obstructive sleep apnea. | Q48823823 | ||
Several common variants modulate heart rate, PR interval and QRS duration | Q57309310 | ||
Genetic factors in the electrocardiogram and heart rate of twins reared apart and together | Q69950887 | ||
Variability of heart rate, P-R, QRS and Q-T durations in twins | Q70646096 | ||
Toward resolution of cardiovascular health disparities in African Americans: design and methods of the Jackson Heart Study | Q81557872 | ||
P275 | copyright license | Creative Commons CC0 License | Q6938433 |
P6216 | copyright status | copyrighted, dedicated to the public domain by copyright holder | Q88088423 |
P433 | issue | 2 | |
P921 | main subject | genome-wide association study | Q1098876 |
P304 | page(s) | e1001304 | |
P577 | publication date | 2011-02-10 | |
P1433 | published in | PLOS Genetics | Q1893441 |
P1476 | title | Genome-wide association studies of the PR interval in African Americans | |
P478 | volume | 7 |
Q37232148 | A SCN10A SNP biases human pain sensitivity |
Q41126903 | A TBX5 3'UTR variant increases the risk of congenital heart disease in the Han Chinese population |
Q30370146 | A common SCN5A variant is associated with PR interval and atrial fibrillation among African Americans |
Q37679987 | A common genetic variant within SCN10A modulates cardiac SCN5A expression |
Q39007031 | Animal models of RLS phenotypes |
Q37330585 | Attitudes toward Genetic Testing for Hypertension among African American Women and Girls |
Q47720327 | Cardiac Arrhythmias Related to Sodium Channel Dysfunction. |
Q26995980 | Cardiovascular genomics |
Q36638837 | Channelopathy-related SCN10A gene variants predict cerebellar dysfunction in multiple sclerosis |
Q37688211 | Common SCN10A variants modulate PR interval and heart rate response during atrial fibrillation. |
Q36091692 | Common Variants in the TBX5 Gene Associated with Atrial Fibrillation in a Chinese Han Population |
Q57258989 | Common and Rare Coding Genetic Variation Underlying the Electrocardiographic PR Interval |
Q37976147 | Common genetic variation modulating cardiac ECG parameters and susceptibility to sudden cardiac death. |
Q36512658 | Comparison of the performance of two commercial genome-wide association study genotyping platforms in Han Chinese samples |
Q45262771 | Development and Function of the Cardiac Conduction System in Health and Disease |
Q24305930 | Dissection of a quantitative trait locus for PR interval duration identifies Tnni3k as a novel modulator of cardiac conduction |
Q88636796 | Effects of obesity on the association between common variations in the TBX5 gene and matrix metalloproteinase 9 levels in Taiwanese |
Q26852051 | Emerging directions in the genetics of atrial fibrillation |
Q35234780 | Evidence of heterogeneity by race/ethnicity in genetic determinants of QT interval |
Q38644720 | Fifteen Genetic Loci Associated With the Electrocardiographic P Wave |
Q34388513 | Fine-mapping and initial characterization of QT interval loci in African Americans |
Q40505706 | Fine-mapping, novel loci identification, and SNP association transferability in a genome-wide association study of QRS duration in African Americans |
Q38109952 | First-degree AV block-an entirely benign finding or a potentially curable cause of cardiac disease? |
Q49606348 | GAREM1 regulates the PR interval on electrocardiograms. |
Q47131418 | GWAS of the electrocardiographic QT interval in Hispanics/Latinos generalizes previously identified loci and identifies population-specific signals |
Q37096305 | Generalization of variants identified by genome-wide association studies for electrocardiographic traits in African Americans |
Q37406362 | Genetic Variants Associated With Atrial Fibrillation and PR Interval Following Cardiac Surgery |
Q34076355 | Genetic determinants of P wave duration and PR segment |
Q34297198 | Genetic loci associated with atrial fibrillation: relation to left atrial structure in the Framingham Heart Study |
Q38324392 | Genetic variation in T-box binding element functionally affects SCN5A/SCN10A enhancer |
Q61980338 | Genetics of Restless Legs Syndrome (RLS) |
Q38169914 | Genetics of sudden cardiac death caused by ventricular arrhythmias |
Q35565624 | Genome-wide association studies in Africans and African Americans: expanding the framework of the genomics of human traits and disease |
Q46927520 | Genome-wide association study of PR interval in Hispanics/Latinos identifies novel locus at ID2. |
Q33638413 | Genome-wide identification of expression quantitative trait loci (eQTLs) in human heart |
Q64880518 | Genomic approaches for the elucidation of genes and gene networks underlying cardiovascular traits. |
Q36136132 | Genotype imputation of Metabochip SNPs using a study-specific reference panel of ~4,000 haplotypes in African Americans from the Women's Health Initiative |
Q28709065 | Impact of ancestry and common genetic variants on QT interval in African Americans |
Q40239547 | Investigating the Genetic Architecture of the PR Interval Using Clinical Phenotypes |
Q36599424 | Loss of the transcription factor Meis1 prevents sympathetic neurons target-field innervation and increases susceptibility to sudden cardiac death |
Q24300388 | Mutations in SCN10A are responsible for a large fraction of cases of Brugada syndrome |
Q30416016 | Novel loci associated with PR interval in a genome-wide association study of 10 African American cohorts |
Q33768883 | OccuPeak: ChIP-Seq peak calling based on internal background modelling |
Q37086627 | Playing with heart and soul…and genomes: sports implications and applications of personal genomics |
Q90569575 | Prevalence of first-degree atrioventricular block and the associated risk factors: a cross-sectional study in rural Northeast China |
Q37699206 | Recent genetic discoveries implicating ion channels in human cardiovascular diseases |
Q37227359 | Reference ranges of PR duration and P-wave indices in individuals free of cardiovascular disease: the Multi-Ethnic Study of Atherosclerosis (MESA). |
Q57398487 | Replication of Associations with Electrocardio-graphic Traits in African Americans from Clinical and Epidemiologic Studies |
Q64096963 | SLMAP3 isoform modulates cardiac gene expression and function |
Q28655342 | Sequencing of SCN5A identifies rare and common variants associated with cardiac conduction: Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium |
Q36133874 | Sequential Binding of MEIS1 and NKX2-5 on the Popdc2 Gene: A Mechanism for Spatiotemporal Regulation of Enhancers during Cardiogenesis |
Q36068330 | TBX5 drives Scn5a expression to regulate cardiac conduction system function |
Q38585131 | The cardiac sodium channel gene SCN5A and its gene product NaV1.5: Role in physiology and pathophysiology. |
Q26770904 | The formation and function of the cardiac conduction system |
Q36273824 | Towards a phenome-wide catalog of human clinical traits impacted by genetic ancestry. |
Q42182352 | Two new targeted alleles for the comprehensive analysis of Meis1 functions in the mouse. |
Q37364440 | Variants in the SCN5A Promoter Associated With Various Arrhythmia Phenotypes |
Q49963136 | [EXPRESS] A variant in the SCN10A enhancer may affect human mechanical pain sensitivity. |
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