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Single Nucleotide Polymorphisms Associated with Coronary Heart Disease Predict Incident Ischemic Stroke in the Atherosclerosis Risk in Communities Study.
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- Cerebrovascular Diseases, 2008, v. 26, n. 4, p. 420, doi. 10.1159/000155637
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- Article
Effect of genetic clusters related to insulin resistance on neurological traits in diverse populations from the Trans‐Omics for Precision Medicine Program.
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- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2023, v. 19, p. 1, doi. 10.1002/alz.076811
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- Article
Effect of genetic clusters related to insulin resistance on neurological traits in diverse populations from the Trans‐Omics for Precision Medicine Program.
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- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2023, v. 19, p. 1, doi. 10.1002/alz.076811
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- Article
Epigenetic signatures of insulin resistance associated with Alzheimer's Disease and related traits.
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- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2022, v. 18, n. 4, p. 1, doi. 10.1002/alz.059136
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- Article
Identification of novel candidate risk genes for myelomeningocele within the glucose homeostasis/oxidative stress and folate/one‐carbon metabolism networks.
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- Molecular Genetics & Genomic Medicine, 2020, v. 8, n. 11, p. 1, doi. 10.1002/mgg3.1495
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- Article
Case growth analysis to inform local response to COVID-19 epidemic in a diverse U.S community.
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- Scientific Reports, 2022, v. 12, n. 1, p. 1, doi. 10.1038/s41598-022-20502-2
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- Article
Metabolomics Identifies Novel Blood Biomarkers of Pulmonary Function and COPD in the General Population.
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- Metabolites (2218-1989), 2019, v. 9, n. 4, p. 61, doi. 10.3390/metabo9040061
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- Article
Coronary heart disease and ischemic stroke polygenic risk scores and atherosclerotic cardiovascular disease in a diverse, population-based cohort study.
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- PLoS ONE, 2023, v. 17, n. 6, p. 1, doi. 10.1371/journal.pone.0285259
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- Article
Mutations in folate transporter genes and risk for human myelomeningocele.
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- American Journal of Medical Genetics. Part A, 2017, v. 173, n. 11, p. 2973, doi. 10.1002/ajmg.a.38472
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- Article
Maternal Hypertension and Risk for Hypospadias in Offspring.
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- American Journal of Medical Genetics. Part A, 2016, v. 170, n. 12, p. 3125, doi. 10.1002/ajmg.a.37947
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- Article
Analysis of loss-of-function variants and 20 risk factor phenotypes in 8,554 individuals identifies loci influencing chronic disease.
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- Nature Genetics, 2015, v. 47, n. 6, p. 640, doi. 10.1038/ng.3270
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- Article
Whole-genome sequence-based analysis of high-density lipoprotein cholesterol.
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- Nature Genetics, 2013, v. 45, n. 8, p. 899, doi. 10.1038/ng.2671
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- Article
Genome-wide association study of blood pressure and hypertension.
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- Nature Genetics, 2009, v. 41, n. 6, p. 677, doi. 10.1038/ng.384
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- Article
Proteomic analysis of diabetes genetic risk scores identifies complement C2 and neuropilin-2 as predictors of type 2 diabetes: the Atherosclerosis Risk in Communities (ARIC) Study.
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- Diabetologia, 2023, v. 66, n. 1, p. 105, doi. 10.1007/s00125-022-05801-7
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- Article
GEM: scalable and flexible gene–environment interaction analysis in millions of samples.
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- Bioinformatics, 2021, v. 37, n. 20, p. 3514, doi. 10.1093/bioinformatics/btab223
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- Article
Genetic susceptibility, obesity and lifetime risk of type 2 diabetes: The ARIC study and Rotterdam Study.
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- Diabetic Medicine, 2021, v. 38, n. 10, p. 1, doi. 10.1111/dme.14639
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- Article
An approach to identify gene-environment interactions and reveal new biological insight in complex traits.
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- Nature Communications, 2024, v. 15, n. 1, p. 1, doi. 10.1038/s41467-024-47806-3
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- Article
Whole-Genome Sequencing Analysis of Human Metabolome in Multi-Ethnic Populations.
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- Nature Communications, 2023, v. 14, n. 1, p. 1, doi. 10.1038/s41467-023-38800-2
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- Article
Direct Estimates of the Genomic Contributions to Blood Pressure Heritability within a Population-Based Cohort (ARIC).
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- PLoS ONE, 2015, v. 10, n. 7, p. 1, doi. 10.1371/journal.pone.0133031
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- Article
Population Genomic Analysis of 962 Whole Genome Sequences of Humans Reveals Natural Selection in Non-Coding Regions.
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- PLoS ONE, 2015, v. 10, n. 3, p. 1, doi. 10.1371/journal.pone.0121644
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- Article
Sequence Analysis of Six Blood Pressure Candidate Regions in 4,178 Individuals: The Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Targeted Sequencing Study.
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- PLoS ONE, 2014, v. 9, n. 10, p. 1, doi. 10.1371/journal.pone.0109155
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- Article
Genome-Wide Association Study of Gene by Smoking Interactions in Coronary Artery Calcification.
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- PLoS ONE, 2013, v. 8, n. 10, p. 1, doi. 10.1371/journal.pone.0074642
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- Article
Folate Metabolism Gene 5,10-Methylenetetrahydrofolate Reductase (MTHFR) Is Associated with ADHD in Myelomeningocele Patients.
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- PLoS ONE, 2012, v. 7, n. 12, p. 1, doi. 10.1371/journal.pone.0051330
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- Article
Association of NOS3 Glu298Asp SNP with hypertension and possible effect modification of dietary fat intake in the ARIC study.
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- Hypertension Research, 2010, v. 33, n. 2, p. 165, doi. 10.1038/hr.2009.198
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- Article
Maternal gene-micronutrient interactions related to one-carbon metabolism and the risk of myelomeningocele among offspring.
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- Birth Defects Research, 2017, v. 109, n. 2, p. 99, doi. 10.1002/bdra.23538
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- Article
Genetic variants in microRNA genes and targets associated with cardiovascular disease risk factors in the African-American population.
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- Human Genetics, 2018, v. 137, n. 1, p. 85, doi. 10.1007/s00439-017-1858-8
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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
Replication of the Wellcome Trust genome-wide association study of essential hypertension: the Family Blood Pressure Program.
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- European Journal of Human Genetics, 2008, v. 16, n. 12, p. 1507, doi. 10.1038/ejhg.2008.102
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- Article
The impact of data quality on the identification of complex disease genes: experience from the Family Blood Pressure Program.
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- European Journal of Human Genetics, 2006, v. 14, n. 4, p. 469, doi. 10.1038/sj.ejhg.5201582
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- Article
Identification of novel and rare variants associated with handgrip strength using whole genome sequence data from the NHLBI Trans-Omics in Precision Medicine (TOPMed) Program.
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- PLoS ONE, 2021, v. 16, n. 7, p. 1, doi. 10.1371/journal.pone.0253611
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- Article
Maternal Hypertension-Related Genotypes and Congenital Heart Defects.
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- American Journal of Hypertension, 2021, v. 34, n. 1, p. 82, doi. 10.1093/ajh/hpaa116
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- Article
Association Between SLC20A1 and Sodium-Lithium Countertransport.
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- American Journal of Hypertension, 2011, v. 24, n. 10, p. 1069, doi. 10.1038/ajh.2011.130
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- Article
Association Between NEDD4L Gene and Sodium Lithium Countertransport.
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- American Journal of Hypertension, 2011, v. 24, n. 2, p. 145, doi. 10.1038/ajh.2010.222
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- Article
Association of SLC34A2 Variation and Sodium–Lithium Countertransport Activity in Humans and Baboons.
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- American Journal of Hypertension, 2009, v. 22, n. 3, p. 288, doi. 10.1038/ajh.2008.355
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- Article
GOSR2 Lys67Arg Is Associated With Hypertension in Whites.
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- American Journal of Hypertension, 2009, v. 22, n. 2, p. 163, doi. 10.1038/ajh.2008.336
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- Article
Regional Association-based Fine-mapping for Sodium-Lithium Countertransport on Chromosome 10.
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- American Journal of Hypertension, 2008, v. 21, n. 1, p. 117, doi. 10.1038/ajh.2007.17
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- Article
Genome-Wide Linkage Study of Erythrocyte Sodium-Lithium Countertransport
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- American Journal of Hypertension, 2005, v. 18, n. 5, p. 653, doi. 10.1016/j.amjhyper.2004.11.030
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- Article
Genome scan for hypertension in nonobese African Americans: The national heart, lung, and blood institute family blood pressure program
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- American Journal of Hypertension, 2004, v. 17, n. 9, p. 834, doi. 10.1016/S0895-7061(04)00819-2
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- Article
Burden of rare deleterious variants in WNT signaling genes among 511 myelomeningocele patients.
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- PLoS ONE, 2020, v. 15, n. 9, p. 1, doi. 10.1371/journal.pone.0239083
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- Article
The impact of multiple single day blood pressure readings on cardiovascular risk estimation: The Atherosclerosis Risk in Communities study.
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- European Journal of Preventive Cardiology, 2016, v. 23, n. 14, p. 1529, doi. 10.1177/2047487316633549
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- Article
The impact of multiple single day blood pressure readings on cardiovascular risk estimation: The Atherosclerosis Risk in Communities study.
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- European Journal of Preventive Cardiology, 2016, v. 23, n. 13, p. 1529, doi. 10.1177/2047487316633549
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- Article
Inherited coding variants at the CDKN2A locus influence susceptibility to acute lymphoblastic leukaemia in children.
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- Nature Communications, 2015, v. 6, n. 6, p. 7553, doi. 10.1038/ncomms8553
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- Article
Effects of Gender-Specific Differences, Inflammatory Response, and Genetic Variation on the Associations Among Depressive Symptoms and the Risk of Major Adverse Coronary Events in Patients With Acute Coronary Syndrome.
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- Biological Research for Nursing, 2018, v. 20, n. 2, p. 168, doi. 10.1177/1099800417751662
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- Article
A polygenic risk score of atrial fibrillation improves prediction of lifetime risk for heart failure.
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- ESC Heart Failure, 2024, v. 11, n. 2, p. 1086, doi. 10.1002/ehf2.14665
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- Article
Whole-genome sequencing study of serum peptide levels: the Atherosclerosis Risk in Communities study.
- Published in:
- Human Molecular Genetics, 2017, v. 26, n. 17, p. 3442, doi. 10.1093/hmg/ddx266
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- Article
Integrative pathway genomics of lung function and airflow obstruction.
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- Human Molecular Genetics, 2015, v. 24, n. 23, p. 6836, doi. 10.1093/hmg/ddv378
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- Article
Association of genetic variation with systolic and diastolic blood pressure among African Americans: the Candidate Gene Association Resource study.
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- Human Molecular Genetics, 2011, v. 20, n. 11, p. 2273
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- Article
Combined admixture mapping and association analysis identifies a novel blood pressure genetic locus on 5p13: contributions from the CARe consortium.
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- Human Molecular Genetics, 2011, v. 20, n. 11, p. 2285, doi. 10.1093/hmg/ddr113
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- Article
Association of FMO3 Variants with Blood Pressure in the Atherosclerosis Risk in Communities Study.
- Published in:
- International Journal of Hypertension, 2019, p. 1, doi. 10.1155/2019/2137629
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- Article
Genome-Wide Association Study for Incident Myocardial Infarction and Coronary Heart Disease in Prospective Cohort Studies: The CHARGE Consortium.
- Published in:
- PLoS ONE, 2016, v. 11, n. 3, p. 1, doi. 10.1371/journal.pone.0144997
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- Article