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Whole-Exome Sequencing and hiPSC Cardiomyocyte Models Identify MYRIP , TRAPPC11 , and SLC27A6 of Potential Importance to Left Ventricular Hypertrophy in an African Ancestry Population.
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- Frontiers in Genetics, 2021, v. 11, p. N.PAG, doi. 10.3389/fgene.2021.588452
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- Article
Genome-wide association study in Han Chinese identifies four new susceptibility loci for coronary artery disease.
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- Nature Genetics, 2012, v. 44, n. 8, p. 890, doi. 10.1038/ng.2337
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- Article
Admixture mapping for hypertension loci with genome-scan markers.
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- Nature Genetics, 2005, v. 37, n. 2, p. 177, doi. 10.1038/ng1510
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- Article
A Gene-Based Analysis of Variants in the Serum/Glucocorticoid Regulated Kinase (SGK) Genes with Blood Pressure Responses to Sodium Intake: The GenSalt Study.
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- PLoS ONE, 2014, v. 9, n. 5, p. 1, doi. 10.1371/journal.pone.0098432
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- Article
Genome-Wide Detection of Allele Specific Copy Number Variation Associated with Insulin Resistance in African Americans from the HyperGEN Study.
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- PLoS ONE, 2011, v. 6, n. 8, p. 1, doi. 10.1371/journal.pone.0024052
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- Article
Gene Expression and Functional Studies of the Optic Nerve Head Astrocyte Transcriptome from Normal African Americans and Caucasian Americans Donors.
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- PLoS ONE, 2008, v. 3, n. 8, p. 1, doi. 10.1371/journal.pone.0002847
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- Article
Genome-wide distribution of ancestry in Mexican Americans.
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- Human Genetics, 2008, v. 124, n. 3, p. 207, doi. 10.1007/s00439-008-0541-5
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- Article
An investigation of genome-wide associations of hypertension with microsatellite markers in the family blood pressure program (FBPP).
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- Human Genetics, 2007, v. 121, n. 5, p. 577, doi. 10.1007/s00439-007-0349-8
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- Article
Machine learning models for predicting blood pressure phenotypes by combining multiple polygenic risk scores.
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- Scientific Reports, 2024, v. 14, n. 1, p. 1, doi. 10.1038/s41598-024-62945-9
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- Article
Random forest fishing: a novel approach to identifying organic group of risk factors in genome-wide association studies.
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- European Journal of Human Genetics, 2014, v. 22, n. 2, p. 254, doi. 10.1038/ejhg.2013.109
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- Article
Pathway-based genome-wide association analysis of coronary heart disease identifies biologically important gene sets.
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- European Journal of Human Genetics, 2012, v. 20, n. 11, p. 1168, doi. 10.1038/ejhg.2012.66
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- Article
Characterization of autosomal copy-number variation in African Americans: the HyperGEN Study.
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- European Journal of Human Genetics, 2011, v. 19, n. 12, p. 1271, doi. 10.1038/ejhg.2011.115
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- Article
Variable set enrichment analysis in genome-wide association studies.
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- European Journal of Human Genetics, 2011, v. 19, n. 8, p. 893, doi. 10.1038/ejhg.2011.46
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- Article
Associations Between Genetic Variants of the Natriuretic Peptide System and Blood Pressure Response to Dietary Sodium Intervention: The GenSalt Study.
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- American Journal of Hypertension, 2016, v. 29, n. 3, p. 397, doi. 10.1093/ajh/hpv129
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- Article
Common Genetic Variants in the Endothelial System Predict Blood Pressure Response to Sodium Intake: The GenSalt Study.
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- American Journal of Hypertension, 2013, v. 26, n. 5, p. 643, doi. 10.1093/ajh/hps099
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- Article
Five Blood Pressure Loci Identified by an Updated Genome-Wide Linkage Scan: Meta-Analysis of the Family Blood Pressure Program.
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- American Journal of Hypertension, 2011, v. 24, n. 3, p. 347, doi. 10.1038/ajh.2010.238
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- Article
Association of Genetic Variants in the Apelin–APJ System and ACE2 With Blood Pressure Responses to Potassium Supplementation: The GenSalt Study.
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- American Journal of Hypertension, 2010, v. 23, n. 6, p. 606, doi. 10.1038/ajh.2010.36
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- Article
Heritability of Blood Pressure Responses to Cold Pressor Test in a Chinese Population.
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- American Journal of Hypertension, 2009, v. 22, n. 10, p. 1096, doi. 10.1038/ajh.2009.139
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- Article
Novel Genetic Variants in the α-Adducin and Guanine Nucleotide Binding Protein β-Polypeptide 3 Genes and Salt Sensitivity of Blood Pressure.
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- American Journal of Hypertension, 2009, v. 22, n. 9, p. 985, doi. 10.1038/ajh.2009.118
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- Article
The Association of Cell Cycle Checkpoint 2 Variants and Kidney Function: Findings of the Family Blood Pressure Program and the Atherosclerosis Risk in Communities Study.
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- American Journal of Hypertension, 2009, v. 22, n. 5, p. 552, doi. 10.1038/ajh.2009.41
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- Article
Measuring Marker Information Content by the Ambiguity of Block Boundaries Observed in Dense SNP Data.
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- Annals of Human Genetics, 2007, v. 71, n. 1, p. 127, doi. 10.1111/j.1469-1809.2006.00315.x
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- Article
Genome-wide joint SNP and CNV analysis of aortic root diameter in African Americans: the HyperGEN study.
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- BMC Medical Genomics, 2011, v. 4, n. 1, p. 1, doi. 10.1186/1755-8794-4-4
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- Article
THE CANTILEVER STRIP PLATE OF VARYING THICKNESS AND THE CENTRE OF SHEAR.
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- Quarterly Journal of Mechanics & Applied Mathematics, 2002, v. 55, n. 1, p. 29, doi. 10.1093/qjmam/55.1.29
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- Article
ATRAID regulates the action of nitrogen-containing bisphosphonates on bone.
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- Science Translational Medicine, 2020, v. 12, n. 544, p. 1, doi. 10.1126/scitranslmed.aav9166
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- Article
A variable fold‐change threshold determines significance for expression microarrays.
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- FASEB Journal, 2003, v. 17, n. 2, p. 321, doi. 10.1096/fj.02-0351fje
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- Article
Tissue-specific DNA methylation is conserved across human, mouse, and rat, and driven by primary sequence conservation.
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- BMC Genomics, 2017, v. 18, p. 1, doi. 10.1186/s12864-017-4115-6
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- Article
Association of Comorbidity Burden With Abnormal Cardiac Mechanics: Findings From the HyperGEN Study.
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- Journal of the American Heart Association, 2014, v. 3, n. 3, p. 1, doi. 10.1161/JAHA.113.000631
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- Article
Genome-wideassociation study in Chineseidentifies novel loci for blood pressure and hypertension.
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- Human Molecular Genetics, 2015, v. 24, n. 3, p. 865, doi. 10.1093/hmg/ddu478
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- Article
Genotype-by-Sex Interaction on Fasting Insulin Concentration.
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- Diabetes, 2007, v. 56, n. 1, p. 137, doi. 10.2337/db06-0624
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- Article
Multi-omics insights into the biological mechanisms underlying statistical gene-by-lifestyle interactions with smoking and alcohol consumption.
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- Frontiers in Genetics, 2022, v. 13, p. 1, doi. 10.3389/fgene.2022.954713
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- Article
Enrichment analysis of genetic association in genes and pathways by aggregating signals from both rare and common variants.
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- BMC Proceedings, 2011, v. 5, n. Suppl 9, p. 1, doi. 10.1186/1753-6561-5-S9-S52
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- Article
Genetic association analysis of coronary heart disease by profiling gene-environment interaction based on latent components in longitudinal endophenotypes.
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- BMC Proceedings, 2009, v. 3, p. 1, doi. 10.1186/1753-6561-3-S7-S86
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- Article
Combining least absolute shrinkage and selection operator (LASSO) and principal-components analysis for detection of gene-gene interactions in genome-wide association studies.
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- BMC Proceedings, 2009, v. 3, p. 1, doi. 10.1186/1753-6561-3-S7-S62
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- Article
Genome-wide association analysis of Framingham Heart Study data for the Genetics Analysis Workshop 16: effects due to medication use.
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- BMC Proceedings, 2009, v. 3, p. 1, doi. 10.1186/1753-6561-3-S7-S52
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- Article
Comparison between single-marker analysis using Merlin and multi-marker analysis using LASSO for Framingham simulated data.
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- BMC Proceedings, 2009, v. 3, p. 1, doi. 10.1186/1753-6561-3-S7-S27
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- Article
A Custom Correlation Coefficient (CCC) Approach for Fast Identification of Multi-SNP Association Patterns in Genome-Wide SNPs Data.
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- Genetic Epidemiology, 2014, v. 38, n. 7, p. 610, doi. 10.1002/gepi.21833
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- Article
A Whole-Genome Simulator Capable of Modeling High-Order Epistasis for Complex Disease.
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- Genetic Epidemiology, 2013, v. 37, n. 7, p. 686, doi. 10.1002/gepi.21761
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- Article
Genotype Imputation for African Americans Using Data From Hap Map Phase II Versus 1000 Genomes Projects.
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- Genetic Epidemiology, 2012, v. 36, n. 5, p. 508, doi. 10.1002/gepi.21647
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- Article
Mining gold dust under the genome wide significance level: a two-stage approach to analysis of GWAS.
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- Genetic Epidemiology, 2011, v. 35, n. 2, p. 111, doi. 10.1002/gepi.20556
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- Article
Enhanced detection of genetic association of hypertensive heart disease by analysis of latent phenotypes.
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- Genetic Epidemiology, 2008, v. 32, n. 6, p. 528, doi. 10.1002/gepi.20326
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- Article
On transferability of genome-wide tagSNPs.
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- Genetic Epidemiology, 2008, v. 32, n. 2, p. 89, doi. 10.1002/gepi.20269
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- Article
Comprehensive linkage and linkage heterogeneity analysis of 4344 sibling pairs affected with hypertension from the Family Blood Pressure Program.
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- Genetic Epidemiology, 2007, v. 31, n. 3, p. 195, doi. 10.1002/gepi.20202
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- Article
Global transmission/disequilibrium tests based on haplotype sharing in multiple candidate genes.
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- Genetic Epidemiology, 2005, v. 29, n. 4, p. 323, doi. 10.1002/gepi.20102
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- Article
Genetic association mapping under founder heterogeneity via weighted haplotype similarity analysis in candidate genes.
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- Genetic Epidemiology, 2004, v. 27, n. 3, p. 182, doi. 10.1002/gepi.20022
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- Article
Haplotype Association Analysis of AGT Variants with Hypertension-Related Traits: The HyperGEN Study.
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- Human Heredity, 2005, v. 60, n. 3, p. 164, doi. 10.1159/000090118
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- Article
Power Loss for Linkage Analysis due to the Dichotomization of Trichotomous Phenotypes.
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- Human Heredity, 2004, v. 57, n. 1, p. 21, doi. 10.1159/000077386
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- Article
Admixture Mapping of Quantitative Trait Loci for BMI in African Americans: Evidence for Loci on Chromosomes 3q, 5q, and 15q.
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- Obesity (19307381), 2009, v. 17, n. 6, p. 1226, doi. 10.1038/oby.2009.24
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- Article
Association and interaction of PPAR-complex gene variants with latent traits of left ventricular diastolic function.
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- BMC Medical Genetics, 2010, v. 11, p. 65, doi. 10.1186/1471-2350-11-65
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- Article