ERIC BOERWINKLE to Humans
This is a "connection" page, showing publications ERIC BOERWINKLE has written about Humans.
Connection Strength
4.984
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COVID-19 infection history as a risk factor for early pregnancy loss: results from the electronic health record-based Southeast Texas COVID and Pregnancy Cohort Study. BMC Med. 2025 May 09; 23(1):274.
Score: 0.024
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Design and Framework of a Technology-Based Closed-Loop Referral Project for Care Coordination of Social Determinants of Health. Popul Health Manag. 2024 12; 27(6):390-396.
Score: 0.023
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Baseline characteristics of SARS-CoV-2 vaccine non-responders in a large population-based sample. PLoS One. 2024; 19(5):e0303420.
Score: 0.022
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Prozone masks elevated SARS-CoV-2 antibody level measurements. PLoS One. 2024; 19(3):e0301232.
Score: 0.022
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Social determinants of health predict readmission following COVID-19 hospitalization: a health information exchange-based retrospective cohort study. Front Public Health. 2024; 12:1352240.
Score: 0.022
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Long-term immune response to SARS-CoV-2 infection and vaccination in children and adolescents. Pediatr Res. 2024 07; 96(2):525-534.
Score: 0.022
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Antibody Duration After Infection From SARS-CoV-2 in the Texas Coronavirus Antibody Response Survey. J Infect Dis. 2023 01 11; 227(2):193-201.
Score: 0.021
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Case growth analysis to inform local response to COVID-19 epidemic in a diverse U.S community. Sci Rep. 2022 10 04; 12(1):16217.
Score: 0.020
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Methodology to estimate natural- and vaccine-induced antibodies to SARS-CoV-2 in a large geographic region. PLoS One. 2022; 17(9):e0273694.
Score: 0.020
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Comparison of Persistent Symptoms Following SARS-CoV-2 Infection by Antibody Status in Nonhospitalized Children and Adolescents. Pediatr Infect Dis J. 2022 10 01; 41(10):e409-e417.
Score: 0.020
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Examining Social Vulnerability and the Association With COVID-19 Incidence in Harris County, Texas. Front Public Health. 2021; 9:798085.
Score: 0.019
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Strategies to Estimate Prevalence of SARS-CoV-2 Antibodies in a Texas Vulnerable Population: Results From Phase I of the Texas Coronavirus Antibody Response Survey. Front Public Health. 2021; 9:753487.
Score: 0.019
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Exome sequence association study of levels and longitudinal change of cardiovascular risk factor phenotypes in European Americans and African Americans from the Atherosclerosis Risk in Communities Study. Genet Epidemiol. 2021 09; 45(6):651-663.
Score: 0.018
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Leveraging a health information exchange for analyses of COVID-19 outcomes including an example application using smoking history and mortality. PLoS One. 2021; 16(6):e0247235.
Score: 0.018
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muCNV: Genotyping Structural Variants for Population-level Sequencing. Bioinformatics. 2021 08 04; 37(14):2055?2057.
Score: 0.018
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Innovation in Genomic Data Sharing at the NIH. N Engl J Med. 2019 Jun 06; 380(23):2192-2195.
Score: 0.016
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A generalized weighted quantile sum approach for analyzing correlated data in the presence of interactions. Biom J. 2019 07; 61(4):934-954.
Score: 0.016
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Serum Metabolomics and Incidence of Atrial Fibrillation (from the Atherosclerosis Risk in Communities Study). Am J Cardiol. 2019 06 15; 123(12):1955-1961.
Score: 0.016
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Sequence-Based Analysis of Lipid-Related Metabolites in a Multiethnic Study. Genetics. 2018 06; 209(2):607-616.
Score: 0.015
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Prospective Study of Epigenetic Age Acceleration and Incidence of Cardiovascular Disease Outcomes in the ARIC Study (Atherosclerosis Risk in Communities). Circ Genom Precis Med. 2018 03; 11(3):e001937.
Score: 0.015
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Metabolomics and cognition in African American adults in midlife: the atherosclerosis risk in communities study. Transl Psychiatry. 2017 07 18; 7(7):e1173.
Score: 0.014
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The diagnosis of autism and autism spectrum disorder in low- and middle-income countries: Experience from Jamaica. Autism. 2017 07; 21(5):564-572.
Score: 0.014
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Practical Approaches for Whole-Genome Sequence Analysis of Heart- and Blood-Related Traits. Am J Hum Genet. 2017 02 02; 100(2):205-215.
Score: 0.014
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The performance of deleteriousness prediction scores for rare non-protein-changing single nucleotide variants in human genes. J Med Genet. 2017 02; 54(2):134-144.
Score: 0.013
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Whole genome sequence analysis of serum amino acid levels. Genome Biol. 2016 11 24; 17(1):237.
Score: 0.013
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Role of Metabolic Genes in Blood Aluminum Concentrations of Jamaican Children with and without Autism Spectrum Disorder. Int J Environ Res Public Health. 2016 11 08; 13(11).
Score: 0.013
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Genetic variants associated with risk of Alzheimer's disease contribute to cognitive change in midlife: The Atherosclerosis Risk in Communities Study. Am J Med Genet B Neuropsychiatr Genet. 2017 Apr; 174(3):269-282.
Score: 0.013
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Concentrations of Polychlorinated Biphenyls and Organochlorine Pesticides in Umbilical Cord Blood Serum of Newborns in Kingston, Jamaica. Int J Environ Res Public Health. 2016 10 21; 13(10).
Score: 0.013
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Identification, analysis, and interpretation of a human serum metabolomics causal network in an observational study. J Biomed Inform. 2016 10; 63:337-343.
Score: 0.013
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Loss-of-function variants influence the human serum metabolome. Sci Adv. 2016 08; 2(8):e1600800.
Score: 0.013
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A Causal Network Analysis of the Fatty Acid Metabolome in African-Americans Reveals a Critical Role for Palmitoleate and Margarate. OMICS. 2016 08; 20(8):480-4.
Score: 0.013
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Identification of Rare Variants in Metabolites of the Carnitine Pathway by Whole Genome Sequencing Analysis. Genet Epidemiol. 2016 09; 40(6):486-91.
Score: 0.013
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Associations Between the Serum Metabolome and All-Cause Mortality Among African Americans in the Atherosclerosis Risk in Communities (ARIC) Study. Am J Epidemiol. 2016 Apr 01; 183(7):650-6.
Score: 0.013
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Generating a robust statistical causal structure over 13 cardiovascular disease risk factors using genomics data. J Biomed Inform. 2016 Apr; 60:114-9.
Score: 0.013
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dbNSFP v3.0: A One-Stop Database of Functional Predictions and Annotations for Human Nonsynonymous and Splice-Site SNVs. Hum Mutat. 2016 Mar; 37(3):235-41.
Score: 0.013
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Rare variants analysis using penalization methods for whole genome sequence data. BMC Bioinformatics. 2015 Dec 04; 16:405.
Score: 0.013
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Metabolomics and Incidence of Atrial Fibrillation in African Americans: The Atherosclerosis Risk in Communities (ARIC) Study. PLoS One. 2015; 10(11):e0142610.
Score: 0.012
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WGSA: an annotation pipeline for human genome sequencing studies. J Med Genet. 2016 Feb; 53(2):111-2.
Score: 0.012
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Sequence variation in telomerase reverse transcriptase (TERT) as a determinant of risk of cardiovascular disease: the Atherosclerosis Risk in Communities (ARIC) study. BMC Med Genet. 2015 Jul 23; 16:52.
Score: 0.012
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Analysis of loss-of-function variants and 20 risk factor phenotypes in 8,554 individuals identifies loci influencing chronic disease. Nat Genet. 2015 Jun; 47(6):640-2.
Score: 0.012
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Concentration of lead, mercury, cadmium, aluminum, arsenic and manganese in umbilical cord blood of Jamaican newborns. Int J Environ Res Public Health. 2015 Apr 23; 12(5):4481-501.
Score: 0.012
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Population genomic analysis of 962 whole genome sequences of humans reveals natural selection in non-coding regions. PLoS One. 2015; 10(3):e0121644.
Score: 0.012
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Roger et al. respond to "future of population studies". Am J Epidemiol. 2015 Mar 15; 181(6):372-3.
Score: 0.012
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Strategic transformation of population studies: recommendations of the working group on epidemiology and population sciences from the National Heart, Lung, and Blood Advisory Council and Board of External Experts. Am J Epidemiol. 2015 Mar 15; 181(6):363-8.
Score: 0.012
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Coronary heart disease and genetic variants with low phospholipase A2 activity. N Engl J Med. 2015 Jan 15; 372(3):295-6.
Score: 0.012
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Factors associated with blood lead concentrations of children in Jamaica. J Environ Sci Health A Tox Hazard Subst Environ Eng. 2015; 50(6):529-39.
Score: 0.012
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Prospective associations of coronary heart disease loci in African Americans using the MetaboChip: the PAGE study. PLoS One. 2014; 9(12):e113203.
Score: 0.012
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Blood lead concentrations in Jamaican children with and without autism spectrum disorder. Int J Environ Res Public Health. 2014 Dec 23; 12(1):83-105.
Score: 0.012
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Transethnic meta-analysis suggests genetic variation in the HEME pathway influences potassium response in patients treated with hydrochlorothiazide. Pharmacogenomics J. 2015 Apr; 15(2):153-7.
Score: 0.012
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Blood manganese concentrations in Jamaican children with and without autism spectrum disorders. Environ Health. 2014 Aug 23; 13:69.
Score: 0.011
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Role of metabolic genes in blood arsenic concentrations of Jamaican children with and without autism spectrum disorder. Int J Environ Res Public Health. 2014 Aug 06; 11(8):7874-95.
Score: 0.011
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Serum metabolomic profiling and incident CKD among African Americans. Clin J Am Soc Nephrol. 2014 Aug 07; 9(8):1410-7.
Score: 0.011
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Medium-term variability of the human serum metabolome in the Atherosclerosis Risk in Communities (ARIC) study. OMICS. 2014 Jun; 18(6):364-73.
Score: 0.011
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Following-up genome-wide association study signals: lessons learned from Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium Targeted Sequencing Study. Circ Cardiovasc Genet. 2014 Jun; 7(3):332-4.
Score: 0.011
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Essential hypertension vs. secondary hypertension among children. Am J Hypertens. 2015 Jan; 28(1):73-80.
Score: 0.011
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Human metabolome associates with dietary intake habits among African Americans in the atherosclerosis risk in communities study. Am J Epidemiol. 2014 Jun 15; 179(12):1424-33.
Score: 0.011
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Metabolomic patterns and alcohol consumption in African Americans in the Atherosclerosis Risk in Communities Study. Am J Clin Nutr. 2014 Jun; 99(6):1470-8.
Score: 0.011
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Genetic determinants influencing human serum metabolome among African Americans. PLoS Genet. 2014 Mar; 10(3):e1004212.
Score: 0.011
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Launching genomics into the cloud: deployment of Mercury, a next generation sequence analysis pipeline. BMC Bioinformatics. 2014 Jan 29; 15:30.
Score: 0.011
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Interaction between the NOS3 gene and obesity as a determinant of risk of type 2 diabetes: the Atherosclerosis Risk in Communities study. PLoS One. 2013; 8(11):e79466.
Score: 0.011
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APOE modulates the correlation between triglycerides, cholesterol, and CHD through pleiotropy, and gene-by-gene interactions. Genetics. 2013 Dec; 195(4):1397-405.
Score: 0.011
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Genome-wide association study of a heart failure related metabolomic profile among African Americans in the Atherosclerosis Risk in Communities (ARIC) study. Genet Epidemiol. 2013 Dec; 37(8):840-5.
Score: 0.011
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Best practices and joint calling of the HumanExome BeadChip: the CHARGE Consortium. PLoS One. 2013; 8(7):e68095.
Score: 0.011
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dbNSFP v2.0: a database of human non-synonymous SNVs and their functional predictions and annotations. Hum Mutat. 2013 Sep; 34(9):E2393-402.
Score: 0.011
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Metabolomics and incident hypertension among blacks: the atherosclerosis risk in communities study. Hypertension. 2013 Aug; 62(2):398-403.
Score: 0.011
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Genome-wide association analyses suggest NELL1 influences adverse metabolic response to HCTZ in African Americans. Pharmacogenomics J. 2014 Feb; 14(1):35-40.
Score: 0.010
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Response to genomic association analysis identifies multiple loci influencing antihypertensive response to an angiotensin II receptor blocker. Hypertension. 2013 Jan; 61(1):e6.
Score: 0.010
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Fat mass and obesity gene and cognitive decline: the Atherosclerosis Risk in Communities Study. Neurology. 2013 Jan 01; 80(1):92-9.
Score: 0.010
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Maternal and paternal age are jointly associated with childhood autism in Jamaica. J Autism Dev Disord. 2012 Sep; 42(9):1928-38.
Score: 0.010
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Effect of 9p21 genetic variation on coronary heart disease is not modified by other risk markers. The Atherosclerosis Risk in Communities (ARIC) Study. Atherosclerosis. 2012 Oct; 224(2):435-9.
Score: 0.010
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The role of drinking water sources, consumption of vegetables and seafood in relation to blood arsenic concentrations of Jamaican children with and without Autism Spectrum Disorders. Sci Total Environ. 2012 Sep 01; 433:362-70.
Score: 0.010
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Genomic association analysis identifies multiple loci influencing antihypertensive response to an angiotensin II receptor blocker. Hypertension. 2012 Jun; 59(6):1204-11.
Score: 0.010
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Seafood consumption and blood mercury concentrations in Jamaican children with and without autism spectrum disorders. Neurotox Res. 2013 Jan; 23(1):22-38.
Score: 0.010
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Translational genomics is not a spectator sport: a call to action. Genet Epidemiol. 2012 Feb; 36(2):85-7.
Score: 0.010
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Systems biology data analysis methodology in pharmacogenomics. Pharmacogenomics. 2011 Sep; 12(9):1349-60.
Score: 0.009
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Genome-wide association analysis of incident coronary heart disease (CHD) in African Americans: a short report. PLoS Genet. 2011 Aug; 7(8):e1002199.
Score: 0.009
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dbNSFP: a lightweight database of human nonsynonymous SNPs and their functional predictions. Hum Mutat. 2011 Aug; 32(8):894-9.
Score: 0.009
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Association of glycemic index and glycemic load with risk of incident coronary heart disease among Whites and African Americans with and without type 2 diabetes: the Atherosclerosis Risk in Communities study. Ann Epidemiol. 2010 Aug; 20(8):610-6.
Score: 0.009
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Transcription factor 7-like 2 (TCF7L2) polymorphism and context-specific risk of impaired fasting glucose in African American and Caucasian adults: the atherosclerosis risk in communities (ARIC) study. Diabetes Metab Res Rev. 2010 Jul; 26(5):371-7.
Score: 0.009
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Risk of type 2 diabetes and obesity is differentially associated with variation in FTO in whites and African-Americans in the ARIC study. PLoS One. 2010 May 20; 5(5):e10521.
Score: 0.009
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Associations between dietary patterns and flow cytometry-measured biomarkers of inflammation and cellular activation in the Atherosclerosis Risk in Communities (ARIC) Carotid Artery MRI Study. Atherosclerosis. 2010 Sep; 212(1):260-7.
Score: 0.009
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Intercellular adhesion molecule-1 G241R polymorphism predicts risk of incident ischemic stroke: Atherosclerosis Risk in Communities study. Stroke. 2010 May; 41(5):1038-40.
Score: 0.008
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A weighted false discovery rate control procedure reveals alleles at FOXA2 that influence fasting glucose levels. Am J Hum Genet. 2010 Mar 12; 86(3):440-6.
Score: 0.008
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MMP2 genetic variation is associated with measures of fibrous cap thickness: The Atherosclerosis Risk in Communities Carotid MRI Study. Atherosclerosis. 2010 May; 210(1):188-93.
Score: 0.008
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Association of NOS3 Glu298Asp SNP with hypertension and possible effect modification of dietary fat intake in the ARIC study. Hypertens Res. 2010 Feb; 33(2):165-9.
Score: 0.008
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Genetic variants identified in a European genome-wide association study that were found to predict incident coronary heart disease in the atherosclerosis risk in communities study. Am J Epidemiol. 2010 Jan 01; 171(1):14-23.
Score: 0.008
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Estimating population genetic parameters and comparing model goodness-of-fit using DNA sequences with error. Genome Res. 2010 Jan; 20(1):101-9.
Score: 0.008
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Use of wrapper algorithms coupled with a random forests classifier for variable selection in large-scale genomic association studies. J Comput Biol. 2009 Dec; 16(12):1705-18.
Score: 0.008
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Kininogen gene (KNG) variation has a consistent effect on aldosterone response to antihypertensive drug therapy: the GERA study. Physiol Genomics. 2009 Sep 09; 39(1):56-60.
Score: 0.008
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Coronary heart disease risk, aspirin use, and apolipoprotein(a) 4399Met allele in the Atherosclerosis Risk in Communities (ARIC) study. Thromb Haemost. 2009 Jul; 102(1):179-80.
Score: 0.008
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Ala54Thr polymorphism of the fatty acid binding protein 2 gene and saturated fat intake in relation to lipid levels and insulin resistance: the Coronary Artery Risk Development in Young Adults (CARDIA) study. Metabolism. 2009 Sep; 58(9):1222-8.
Score: 0.008
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The INSIG2 rs7566605 genetic variant does not play a major role in obesity in a sample of 24,722 individuals from four cohorts. BMC Med Genet. 2009 Jun 12; 10:56.
Score: 0.008
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Correlates of carotid plaque presence and composition as measured by MRI: the Atherosclerosis Risk in Communities Study. Circ Cardiovasc Imaging. 2009 Jul; 2(4):314-22.
Score: 0.008
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SELP and SELPLG genetic variation is associated with cell surface measures of SELP and SELPLG: the Atherosclerosis Risk in Communities Carotid MRI Study. Clin Chem. 2009 Jun; 55(6):1076-82.
Score: 0.008
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Impact of adding a single allele in the 9p21 locus to traditional risk factors on reclassification of coronary heart disease risk and implications for lipid-modifying therapy in the Atherosclerosis Risk in Communities study. Circ Cardiovasc Genet. 2009 Jun; 2(3):279-85.
Score: 0.008
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Inflammatory protein levels and depression screening after coronary stenting predict major adverse coronary events. Biol Res Nurs. 2009 Oct; 11(2):163-73.
Score: 0.008
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GOSR2 Lys67Arg is associated with hypertension in whites. Am J Hypertens. 2009 Feb; 22(2):163-8.
Score: 0.008
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Risk factor correlates of platelet and leukocyte markers assessed by flow cytometry in a population-based sample. Atherosclerosis. 2009 Jul; 205(1):272-8.
Score: 0.008
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Variation in ANGPTL4 and risk of coronary heart disease: the Atherosclerosis Risk in Communities Study. Metabolism. 2008 Nov; 57(11):1591-6.
Score: 0.008
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Transcription factor 7-like 2 (TCF7L2) polymorphism and context-specific risk of type 2 diabetes in African American and Caucasian adults: the Atherosclerosis Risk in Communities study. Diabetes. 2009 Jan; 58(1):285-9.
Score: 0.008
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Single nucleotide polymorphisms associated with coronary heart disease predict incident ischemic stroke in the atherosclerosis risk in communities study. Cerebrovasc Dis. 2008; 26(4):420-4.
Score: 0.008
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Carbohydrate intake modifies associations between ANGPTL4[E40K] genotype and HDL-cholesterol concentrations in White men from the Atherosclerosis Risk in Communities (ARIC) study. Atherosclerosis. 2009 Mar; 203(1):214-20.
Score: 0.007
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Peroxisome proliferator-activated receptor [alpha] genetic variation interacts with n-6 and long-chain n-3 fatty acid intake to affect total cholesterol and LDL-cholesterol concentrations in the Atherosclerosis Risk in Communities Study. Am J Clin Nutr. 2008 Jun; 87(6):1926-31.
Score: 0.007
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Atherosclerosis Risk in Communities (ARIC) Carotid MRI flow cytometry study of monocyte and platelet markers: intraindividual variability and reliability. Clin Chem. 2008 Aug; 54(8):1363-71.
Score: 0.007
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TCF7L2 single nucleotide polymorphisms, cardiovascular disease and all-cause mortality: the Atherosclerosis Risk in Communities (ARIC) study. Diabetologia. 2008 Jun; 51(6):968-70.
Score: 0.007
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Association of the complement factor H Y402H polymorphism with cardiovascular disease is dependent upon hypertension status: The ARIC study. Am J Hypertens. 2008 May; 21(5):533-8.
Score: 0.007
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Variation in TCF7L2 and increased risk of colon cancer: the Atherosclerosis Risk in Communities (ARIC) Study. Diabetes Care. 2008 May; 31(5):905-9.
Score: 0.007
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Sequence variation in proprotein convertase subtilisin/kexin type 9 serine protease gene, low LDL cholesterol, and cancer incidence. Cancer Epidemiol Biomarkers Prev. 2007 Nov; 16(11):2455-8.
Score: 0.007
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Five common gene variants identify elevated genetic risk for coronary heart disease. Genet Med. 2007 Oct; 9(10):682-9.
Score: 0.007
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Relationship of alcohol consumption and type of alcoholic beverage consumed with plasma lipid levels: differences between Whites and African Americans of the ARIC study. Ann Epidemiol. 2008 Feb; 18(2):101-7.
Score: 0.007
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Interaction effects of high-density lipoprotein metabolism gene variation and alcohol consumption on coronary heart disease risk: the atherosclerosis risk in communities study. J Stud Alcohol Drugs. 2007 Jul; 68(4):485-92.
Score: 0.007
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Personalized medicine for high blood pressure. Hypertension. 2007 Jul; 50(1):1-5.
Score: 0.007
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Prediction of coronary heart disease risk using a genetic risk score: the Atherosclerosis Risk in Communities Study. Am J Epidemiol. 2007 Jul 01; 166(1):28-35.
Score: 0.007
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Specific P-selectin and P-selectin glycoprotein ligand-1 genotypes/haplotypes are associated with risk of incident CHD and ischemic stroke: the Atherosclerosis Risk in Communities (ARIC) study. Atherosclerosis. 2007 Nov; 195(1):e76-82.
Score: 0.007
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Increased risk of incident stroke associated with the cyclooxygenase 2 (COX-2) G-765C polymorphism in African-Americans: the Atherosclerosis Risk in Communities Study. Atherosclerosis. 2008 Feb; 196(2):926-30.
Score: 0.007
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Explaining the unexplained admixture mapping signals via rare variants: the HCHS/SOL. Hum Mol Genet. 2026 Sep 25; 35(20).
Score: 0.007
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Measuring marker information content by the ambiguity of block boundaries observed in dense SNP data. Ann Hum Genet. 2007 Jan; 71(Pt 1):127-40.
Score: 0.007
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Metabolites Associated With Long-Term Risk of Peripheral Artery Disease: The ARIC Study. Arterioscler Thromb Vasc Biol. 2026 Oct; 46(10):e324549.
Score: 0.007
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SeqBoard: a genomics-based data dashboard for comprehensive wastewater virome monitoring. J Am Med Inform Assoc. 2026 Aug 01; 33(8):1446-1456.
Score: 0.007
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Proteomic Signatures of 3-Year Progression From Impaired Fasting Glucose to Diabetes: The Atherosclerosis Risk in Communities (ARIC) Study. Diabetes Care. 2026 Aug 01; 49(8):1490-1497.
Score: 0.007
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Temporal Alignment of Wastewater Signals with Clinical Indicators of Respiratory Illness Postpandemic, Texas, USA. Emerg Infect Dis. 2026 Aug; 32(13):43-52.
Score: 0.007
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Mosaic loss of Y chromosome associates with lung function, emphysema, and epigenetic aging. Am J Respir Crit Care Med. 2026 07 01; 212(7):1483-1494.
Score: 0.007
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Alzheimer's disease proteome-wide association study implicates adaptive immunity and identifies risk genes LILRB1 and SIRPA. Sci Transl Med. 2026 Jul; 18(856):eadx4852.
Score: 0.007
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Longitudinal genomic surveillance of SARS-CoV-2 in a university microcosm reflects global evolutionary trends. Microbiol Spectr. 2026 Jul 07; 14(7):e0086026.
Score: 0.006
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Statewide multi-year wastewater sequencing reveals dual origins of HIV-1 signal. Nat Commun. 2026 Jun 11; 17(1).
Score: 0.006
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Apolipoprotein E polymorphisms predict low density lipoprotein cholesterol levels and carotid artery wall thickness but not incident coronary heart disease in 12,491 ARIC study participants. Am J Epidemiol. 2006 Aug 15; 164(4):342-8.
Score: 0.006
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Co-occurring clonal hematopoiesis exhibits strong selection and high leukemia risk. Nat Commun. 2026 May 21; 17(1).
Score: 0.006
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Population-Based Analysis of Rare Genetic Variants in Sudden Cardiac Arrest. JACC Clin Electrophysiol. 2026 08; 12(8):1819-1829.
Score: 0.006
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Detection, persistence, and rising prevalence of oncogenic viruses revealed by wastewater metagenomics. Appl Environ Microbiol. 2026 06 17; 92(6):e0054726.
Score: 0.006
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Admixture-informed polygenic risk reporting using the ePRS framework. Nat Commun. 2026 Apr 30; 17(1).
Score: 0.006
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Gestational diabetes and risk of type 2 diabetes: exploring the role of the gut microbiome in the Hispanic Community Health Study/Study of Latinos (HCHS/SOL). Diabetologia. 2026 Aug; 69(8):2225-2239.
Score: 0.006
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Plasma metabolomic profiles associated with cardiovascular disease in type 2 diabetes from the Trans-Omics for Precision Medicine (TOPMed) program. Atherosclerosis. 2026 Jun; 417:120758.
Score: 0.006
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Whole genome sequencing analysis of over 3500 individuals dementia-free over 85 years old. J Alzheimers Dis. 2026 06; 111(4):1772-1782.
Score: 0.006
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An integrated germline and somatic genomic model for coronary artery disease. Nat Commun. 2026 Mar 26; 17(1).
Score: 0.006
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Epigenome-wide association study of blood proteome in the Atherosclerosis Risk in Communities study. HGG Adv. 2026 Apr 09; 7(2):100585.
Score: 0.006
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DNA methylation is associated with von Willebrand factor and coagulation factor VIII plasma levels: the atherosclerosis risk in communities study. Clin Epigenetics. 2026 Mar 02; 18(1).
Score: 0.006
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Comparison of variant callers using 60?532 multi-ancestry whole genome sequences. Brief Bioinform. 2026 Mar 01; 27(2).
Score: 0.006
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Intracoronary Imaging and Transcriptomic Characteristics Before and After Maximum Lipid-Lowering Therapy: YELLOW-III Study of Evolocumab and Maximum Statin Therapy in Chronic Coronary Disease. JACC Cardiovasc Imaging. 2026 Apr; 19(4):516-534.
Score: 0.006
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Proteomic Profiling of Pulmonary Function and Cardiovascular Disease Risk in the Atherosclerosis Risk in Communities Study. J Am Heart Assoc. 2026 03 03; 15(5):e043281.
Score: 0.006
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Novel Plasma Proteomic Markers and Risk of Venous Thromboembolism. Circulation. 2026 Mar 17; 153(11):810-825.
Score: 0.006
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Genetic Architecture of N-Terminal Pro-B-Type Natriuretic Peptide in a Multiancestry Study Population. Circ Genom Precis Med. 2026 Feb; 19(1):e005130.
Score: 0.006
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Proteomic Signatures of Cardiac Dysfunction Among People With Diabetes: The Atherosclerosis Risk in Communities Study. Circ Heart Fail. 2026 Mar; 19(3):e013171.
Score: 0.006
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Metabolome contribution to sex differences in the link between alcohol consumption and type 2 diabetes: a prospective analysis in the Hispanic Community Health Study/Study of Latinos. Am J Clin Nutr. 2026 Mar; 123(3):101203.
Score: 0.006
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Circulating metabolites, genetics and lifestyle factors in relation to future risk of type 2 diabetes. Nat Med. 2026 Feb; 32(2):660-670.
Score: 0.006
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Genome-wide gene by sleepiness interaction analysis for sleep apnea. Sleep. 2026 Jan 13; 49(1).
Score: 0.006
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Fibrinogen-associated plasma metabolites and implications for coagulation, inflammation, and vascular diseases. J Thromb Haemost. 2026 04; 24(4):1523-1541.
Score: 0.006
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cellSTAAR: incorporating single-cell-sequencing-based functional data to boost power in rare variant association testing of noncoding regions. Nat Methods. 2026 Feb; 23(2):338-349.
Score: 0.006
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Epigenome-wide association study meta-analysis of BMI in African Americans. HGG Adv. 2026 Jan 15; 7(1):100552.
Score: 0.006
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Epigenome-wide association study of nuclear DNA methylation in relation to mitochondrial heteroplasmy. Nat Commun. 2025 Dec 02; 16(1):10962.
Score: 0.006
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Lipoprotein-associated phospholipase A2, high-sensitivity C-reactive protein, and risk for incident ischemic stroke in middle-aged men and women in the Atherosclerosis Risk in Communities (ARIC) study. Arch Intern Med. 2005 Nov 28; 165(21):2479-84.
Score: 0.006
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Genome-wide gene-sleep interaction study identifies novel lipid loci in 732,564 participants. Atherosclerosis. 2026 Jan; 412:120603.
Score: 0.006
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Association of metabolomics measurements with blood cell phenotypes. Blood Cells Mol Dis. 2026 Mar; 117:102966.
Score: 0.006
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Genetic determinants and genomic consequences of non-leukemogenic somatic point mutations. Nat Commun. 2025 Oct 16; 16(1):9194.
Score: 0.006
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Association of genetic scores related to insulin resistance with neurological outcomes in ancestrally diverse cohorts from the Trans-Omics for Precision Medicine (TOPMed) program. Commun Biol. 2025 Sep 24; 8(1):1352.
Score: 0.006
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WNK1 kinase polymorphism and blood pressure response to a thiazide diuretic. Hypertension. 2005 Oct; 46(4):758-65.
Score: 0.006
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Score: 0.002
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Apolipoprotein E genotype and incident ischemic stroke: the Atherosclerosis Risk in Communities Study. Stroke. 2005 Nov; 36(11):2484-6.
Score: 0.002
-
A novel quantitative trait locus on chromosome 1 with pleiotropic effects on HDL-cholesterol and LDL particle size in hypertensive sibships. Am J Hypertens. 2005 Aug; 18(8):1084-90.
Score: 0.002
-
Genomic loci with pleiotropic effects on coronary artery calcification. Atherosclerosis. 2006 Apr; 185(2):340-6.
Score: 0.002
-
Pharmacogenetic association of the angiotensin-converting enzyme insertion/deletion polymorphism on blood pressure and cardiovascular risk in relation to antihypertensive treatment: the Genetics of Hypertension-Associated Treatment (GenHAT) study. Circulation. 2005 Jun 28; 111(25):3374-83.
Score: 0.002
-
Apolipoprotein E and progression of chronic kidney disease. JAMA. 2005 Jun 15; 293(23):2892-9.
Score: 0.002
-
Polymorphisms within the C-reactive protein (CRP) promoter region are associated with plasma CRP levels. Am J Hum Genet. 2005 Jul; 77(1):64-77.
Score: 0.002
-
An entropy-based statistic for genomewide association studies. Am J Hum Genet. 2005 Jul; 77(1):27-40.
Score: 0.002
-
Genome-wide linkage study of erythrocyte sodium-lithium countertransport. Am J Hypertens. 2005 May; 18(5 Pt 1):653-6.
Score: 0.002
-
Plasma MCP-1 level and risk for peripheral arterial disease and incident coronary heart disease: Atherosclerosis Risk in Communities study. Atherosclerosis. 2005 Dec; 183(2):301-7.
Score: 0.001
-
Autosomal genome scan for loci linked to blood pressure levels and trends since childhood: the Bogalusa Heart Study. Hypertension. 2005 May; 45(5):954-9.
Score: 0.001
-
Linkage analysis of plasma ApoE in three ethnic groups: multiple genes with context-dependent effects. Ann Hum Genet. 2005 Mar; 69(Pt 2):157-67.
Score: 0.001
-
Genome-wide linkage scans for fasting glucose, insulin, and insulin resistance in the National Heart, Lung, and Blood Institute Family Blood Pressure Program: evidence of linkages to chromosome 7q36 and 19q13 from meta-analysis. Diabetes. 2005 Mar; 54(3):909-14.
Score: 0.001
-
Lack of agreement between office and ambulatory blood pressure responses to hydrochlorothiazide. Am J Hypertens. 2005 Mar; 18(3):398-402.
Score: 0.001
-
Interactive effects between polymorphisms in the beta-adrenergic receptors and longitudinal changes in obesity. Obes Res. 2005 Mar; 13(3):519-26.
Score: 0.001
-
Genomic susceptibility loci for brain atrophy in hypertensive sibships from the GENOA study. Hypertension. 2005 Apr; 45(4):793-8.
Score: 0.001
-
APOE genotype and cognitive decline in a middle-aged cohort. Neurology. 2005 Jan 25; 64(2):268-76.
Score: 0.001
-
Pleiotropic genetic effects contribute to the correlation between HDL cholesterol, triglycerides, and LDL particle size in hypertensive sibships. Am J Hypertens. 2005 Jan; 18(1):99-103.
Score: 0.001
-
Ethnicity and human genetic linkage maps. Am J Hum Genet. 2005 Feb; 76(2):276-90.
Score: 0.001
-
Genetic structure, self-identified race/ethnicity, and confounding in case-control association studies. Am J Hum Genet. 2005 Feb; 76(2):268-75.
Score: 0.001
-
APOA5 polymorphisms influence plasma triglycerides in young, healthy African Americans and whites of the CARDIA Study. J Lipid Res. 2005 Mar; 46(3):564-71.
Score: 0.001
-
An autosomal genomic scan for loci linked to type 2 diabetes in northern Han Chinese. J Mol Med (Berl). 2005 Mar; 83(3):209-15.
Score: 0.001
-
Q192R polymorphism of the paraoxanase 1 gene and its association with serum lipoprotein variables and carotid artery intima-media thickness in young adults from a biracial community. The Bogalusa Heart Study. Atherosclerosis. 2004 Nov; 177(1):167-74.
Score: 0.001
-
Evidence for non-additive influence of single nucleotide polymorphisms within the apolipoprotein E gene. Ann Hum Genet. 2004 Nov; 68(Pt 6):521-35.
Score: 0.001
-
Gender-specific influence of NO synthase gene on blood pressure since childhood: the Bogalusa Heart Study. Hypertension. 2004 Nov; 44(5):668-73.
Score: 0.001
-
Lack of association between lipoprotein(a) and coronary artery calcification in the Genetic Epidemiology Network of Arteriopathy (GENOA) study. Mayo Clin Proc. 2004 Oct; 79(10):1258-63.
Score: 0.001
-
The beta(2)-adrenergic receptor Arg16-gly polymorphism and interactions involving beta(2)- and beta(3)-adrenergic receptor polymorphisms are associated with variations in longitudinal serum lipid profiles: the Bogalusa Heart Study. Metabolism. 2004 Sep; 53(9):1184-91.
Score: 0.001
-
Low-density lipoprotein particle size and coronary atherosclerosis in subjects belonging to hypertensive sibships. Am J Hypertens. 2004 Sep; 17(9):845-51.
Score: 0.001
-
Imputing gene-treatment interactions when the genotype distribution is unknown using case-only and putative placebo analyses--a new method for the Genetics of Hypertension Associated Treatment (GenHAT) study. Stat Med. 2004 Aug 15; 23(15):2413-27.
Score: 0.001
-
Genetics of ultrasonographic carotid atherosclerosis. Arterioscler Thromb Vasc Biol. 2004 Sep; 24(9):1567-77.
Score: 0.001
-
Multivariate linkage analysis of blood pressure and body mass index. Genet Epidemiol. 2004 Jul; 27(1):64-73.
Score: 0.001
-
Nitric oxide synthase gene polymorphism (G894T) influences arterial stiffness in adults: The Bogalusa Heart Study. Am J Hypertens. 2004 Jul; 17(7):553-9.
Score: 0.001
-
Ethnic and sex differences in the prevalence, treatment, and control of dyslipidemia among hypertensive adults in the GENOA study. Arch Intern Med. 2004 Jun 28; 164(12):1313-8.
Score: 0.001
-
Familial aggregation of hypertension treatment and control in the Genetic Epidemiology Network of Arteriopathy (GENOA) study. Am J Med. 2004 May 15; 116(10):676-81.
Score: 0.001
-
The effects of scale: variation in the APOA1/C3/A4/A5 gene cluster. Hum Genet. 2004 Jun; 115(1):36-56.
Score: 0.001
-
An autosomal genome scan for loci influencing longitudinal burden of body mass index from childhood to young adulthood in white sibships: The Bogalusa Heart Study. Int J Obes Relat Metab Disord. 2004 Apr; 28(4):462-9.
Score: 0.001
-
Positional identification of hypertension susceptibility genes on chromosome 2. Hypertension. 2004 Feb; 43(2):477-82.
Score: 0.001
-
Polymorphism of the soluble epoxide hydrolase is associated with coronary artery calcification in African-American subjects: The Coronary Artery Risk Development in Young Adults (CARDIA) study. Circulation. 2004 Jan 27; 109(3):335-9.
Score: 0.001
-
Heritability of leukoaraiosis in hypertensive sibships. Hypertension. 2004 Feb; 43(2):483-7.
Score: 0.001
-
The role of the genetics of sodium lithium countertransport in the determination of blood pressure variability in the population at large. Prog Clin Biol Res. 1984; 165:479-507.
Score: 0.001
-
Ethnic differences in peripheral arterial disease in the NHLBI Genetic Epidemiology Network of Arteriopathy (GENOA) study. Vasc Med. 2003 Nov; 8(4):237-42.
Score: 0.001
-
The variable number of tandem repeat polymorphism of platelet glycoprotein Ibalpha and risk of coronary heart disease. Blood. 2004 Feb 01; 103(3):963-5.
Score: 0.001
-
From vulnerable plaque to vulnerable patient: a call for new definitions and risk assessment strategies: Part II. Circulation. 2003 Oct 14; 108(15):1772-8.
Score: 0.001
-
From vulnerable plaque to vulnerable patient: a call for new definitions and risk assessment strategies: Part I. Circulation. 2003 Oct 07; 108(14):1664-72.
Score: 0.001
-
Interaction effect of Serine447Stop variant of the lipoprotein lipase gene and C-514T variant of the hepatic lipase gene on serum triglyceride levels in young adults: the Bogalusa Heart Study. Metabolism. 2003 Oct; 52(10):1337-42.
Score: 0.001
-
Relation of C-reactive protein and fibrinogen to coronary artery calcium in subjects with systemic hypertension. Am J Cardiol. 2003 Jul 01; 92(1):56-8.
Score: 0.001
-
Hepatic lipase promoter C-514T polymorphism influences serial changes in HDL cholesterol levels since childhood: the Bogalusa Heart Study. Atherosclerosis. 2003 Jul; 169(1):175-82.
Score: 0.001
-
R219K polymorphism of the ABCA1 gene and its modulation of the variations in serum high-density lipoprotein cholesterol and triglycerides related to age and adiposity in white versus black young adults. The Bogalusa heart study. Metabolism. 2003 Jul; 52(7):930-4.
Score: 0.001
-
Pro12Ala of the peroxisome proliferator-activated receptor-gamma2 gene is associated with lower serum insulin levels in nonobese African Americans: the Atherosclerosis Risk in Communities Study. Diabetes. 2003 Jun; 52(6):1568-72.
Score: 0.001
-
Diagnostic tools in linkage analysis for quantitative traits. Genet Epidemiol. 2003 May; 24(4):302-8.
Score: 0.001
-
The peroxisome proliferator-activated receptor-gamma2 gene polymorphism (Pro12Ala) beneficially influences insulin resistance and its tracking from childhood to adulthood: the Bogalusa Heart Study. Diabetes. 2003 May; 52(5):1265-9.
Score: 0.001
-
Risk of atherosclerosis: interaction of smoking and glutathione S-transferase genes. Epidemiology. 2003 May; 14(3):321-7.
Score: 0.001
-
Evaluating the context-dependent effect of family history of stroke in a genome scan for hypertension. Stroke. 2003 May; 34(5):1170-5.
Score: 0.001
-
Combined analysis of genomewide scans for adult height: results from the NHLBI Family Blood Pressure Program. Eur J Hum Genet. 2003 Mar; 11(3):271-4.
Score: 0.001
-
A meta-analysis of genome-wide linkage scans for hypertension: the National Heart, Lung and Blood Institute Family Blood Pressure Program. Am J Hypertens. 2003 Feb; 16(2):144-7.
Score: 0.001
-
Beta(2)-adrenergic receptor polymorphism and nitric oxide-dependent forearm blood flow responses to isoproterenol in humans. J Physiol. 2003 Jan 15; 546(Pt 2):583-9.
Score: 0.001
-
Relationship of blood pressure measures with coronary artery calcification. Med Sci Monit. 2002 Dec; 8(12):CR775-81.
Score: 0.001
-
Screening for primary aldosteronism: implications of an increased plasma aldosterone/renin ratio. Clin Chem. 2002 Nov; 48(11):1919-23.
Score: 0.001
-
Reproducibility of blood pressure response to hydrochlorothiazide. J Clin Hypertens (Greenwich). 2002 Nov-Dec; 4(6):408-12.
Score: 0.001
-
Contributions of 18 additional DNA sequence variations in the gene encoding apolipoprotein E to explaining variation in quantitative measures of lipid metabolism. Am J Hum Genet. 2002 Sep; 71(3):501-17.
Score: 0.001
-
Heritability of coronary artery calcium quantity measured by electron beam computed tomography in asymptomatic adults. Circulation. 2002 Jul 16; 106(3):304-8.
Score: 0.001
-
Influence of the beta2-adrenergic receptor Arg16Gly polymorphism on longitudinal changes in obesity from childhood through young adulthood in a biracial cohort: the Bogalusa Heart Study. Int J Obes Relat Metab Disord. 2002 Jul; 26(7):928-37.
Score: 0.001
-
Sequence polymorphism at the human apolipoprotein AII gene ( APOA2): unexpected deficit of variation in an African-American sample. Hum Genet. 2002 Jul; 111(1):75-87.
Score: 0.001
-
Predictors of antihypertensive response to a standard dose of hydrochlorothiazide for essential hypertension. Kidney Int. 2002 Mar; 61(3):1047-55.
Score: 0.001
-
Autosomal genome-wide scan for coronary artery calcification loci in sibships at high risk for hypertension. Arterioscler Thromb Vasc Biol. 2002 Mar 01; 22(3):418-23.
Score: 0.001
-
Factor XIIIA Val34Leu polymorphism does not predict risk of coronary heart disease: The Atherosclerosis Risk in Communities (ARIC) Study. Arterioscler Thromb Vasc Biol. 2002 Feb 01; 22(2):348-52.
Score: 0.001
-
SNP43 of CAPN10 and the risk of type 2 Diabetes in African-Americans: the Atherosclerosis Risk in Communities Study. Diabetes. 2002 Jan; 51(1):231-7.
Score: 0.001
-
Pharmacogenetic approaches to hypertension therapy: design and rationale for the Genetics of Hypertension Associated Treatment (GenHAT) study. Pharmacogenomics J. 2002; 2(5):309-17.
Score: 0.001
-
Influence of lipoprotein lipase serine 447 stop polymorphism on tracking of triglycerides and HDL cholesterol from childhood to adulthood and familial risk of coronary artery disease: the Bogalusa heart study. Atherosclerosis. 2001 Dec; 159(2):367-73.
Score: 0.001
-
Combined effects of endothelial nitric oxide synthase gene polymorphism (G894T) and insulin resistance status on blood pressure and familial risk of hypertension in young adults: the Bogalusa Heart Study. Am J Hypertens. 2001 Oct; 14(10):1046-52.
Score: 0.001
-
Validity of the aldosterone-renin ratio used to screen for primary aldosteronism. Mayo Clin Proc. 2001 Sep; 76(9):877-82.
Score: 0.001
-
The Ser(447)-Stop polymorphism of lipoprotein lipase is associated with variation in longitudinal serum high-density lipoprotein-cholesterol profiles: the Bogalusa Heart Study. Metabolism. 2001 Aug; 50(8):894-904.
Score: 0.001
-
Gender- and age-dependent relationships between the E-selectin S128R polymorphism and coronary artery calcification. J Mol Med (Berl). 2001 Jul; 79(7):390-8.
Score: 0.001
-
Genome-wide linkage analysis reveals evidence of multiple regions that influence variation in plasma lipid and apolipoprotein levels associated with risk of coronary heart disease. Arterioscler Thromb Vasc Biol. 2001 Jun; 21(6):971-8.
Score: 0.001
-
Familial thoracic aortic aneurysms and dissections: genetic heterogeneity with a major locus mapping to 5q13-14. Circulation. 2001 May 22; 103(20):2461-8.
Score: 0.001
-
G-protein beta3 subunit and alpha-adducin polymorphisms and risk of subclinical and clinical stroke. Stroke. 2001 Apr; 32(4):822-9.
Score: 0.001
-
Beta-fibrinogen gene -455G/A polymorphism and coronary heart disease incidence: the Atherosclerosis Risk in Communities (ARIC) Study. Ann Epidemiol. 2001 Apr; 11(3):166-70.
Score: 0.001
-
High-throughput multiplex SNP genotyping with MALDI-TOF mass spectrometry: practice, problems and promise. Hum Mutat. 2001 Apr; 17(4):296-304.
Score: 0.001
-
Thrombomodulin Ala455Val polymorphism and risk of coronary heart disease. Circulation. 2001 Mar 13; 103(10):1386-9.
Score: 0.001
-
Metabolic and lifestyle determinants of postprandial lipemia differ from those of fasting triglycerides: The Atherosclerosis Risk In Communities (ARIC) study. Arterioscler Thromb Vasc Biol. 2001 Feb; 21(2):275-81.
Score: 0.001
-
Linkage of hypertension to chromosome 2q14-q23 in Chinese families. J Hypertens. 2001 Jan; 19(1):55-61.
Score: 0.001
-
Population structure in admixed populations: effect of admixture dynamics on the pattern of linkage disequilibrium. Am J Hum Genet. 2001 Jan; 68(1):198-207.
Score: 0.001
-
Cladistic structure within the human Lipoprotein lipase gene and its implications for phenotypic association studies. Genetics. 2000 Nov; 156(3):1259-75.
Score: 0.001
-
Platelet Pl(A2) allele and incidence of coronary heart disease: results from the Atherosclerosis Risk In Communities (ARIC) Study. Circulation. 2000 Oct 17; 102(16):1901-5.
Score: 0.001
-
Genetic variation in the gene encoding calpain-10 is associated with type 2 diabetes mellitus. Nat Genet. 2000 Oct; 26(2):163-75.
Score: 0.001
-
Sequence diversity and large-scale typing of SNPs in the human apolipoprotein E gene. Genome Res. 2000 Oct; 10(10):1532-45.
Score: 0.001
-
Apolipoprotein E variation at the sequence haplotype level: implications for the origin and maintenance of a major human polymorphism. Am J Hum Genet. 2000 Oct; 67(4):881-900.
Score: 0.001
-
Lack of association of the angiotensinogen-6 polymorphism with blood pressure levels in the comprehensive NHLBI Family Blood Pressure Program. National Heart, Lung and Blood Institute. J Hypertens. 2000 Jul; 18(7):867-76.
Score: 0.001
-
Sequence variation within the neuropeptide Y gene and obesity in Mexican Americans. Obes Res. 2000 May; 8(3):219-26.
Score: 0.001
-
Glutathione S-transferase genotype as a susceptibility factor in smoking-related coronary heart disease. Atherosclerosis. 2000 Apr; 149(2):451-62.
Score: 0.001
-
Recombinational and mutational hotspots within the human lipoprotein lipase gene. Am J Hum Genet. 2000 Jan; 66(1):69-83.
Score: 0.001
-
Analysis of lipoprotein lipase haplotypes reveals associations not apparent from analysis of the constituent loci. Ann Hum Genet. 1999 Nov; 63(Pt 6):499-510.
Score: 0.001
-
Context-dependent associations of the ACE I/D polymorphism with blood pressure. Hypertension. 1999 Oct; 34(4 Pt 2):773-8.
Score: 0.001
-
Variants of the insulin receptor substrate-1 and fatty acid binding protein 2 genes and the risk of type 2 diabetes, obesity, and hyperinsulinemia in African-Americans: the Atherosclerosis Risk in Communities Study. Diabetes. 1999 Sep; 48(9):1868-72.
Score: 0.001
-
Apolipoprotein E affects serial changes in total and low-density lipoprotein cholesterol in adolescent girls: Project HeartBeat! Metabolism. 1999 Mar; 48(3):285-90.
Score: 0.001
-
Linkage analysis of candidate obesity genes among the Mexican-American population of Starr County, Texas. Genet Epidemiol. 1999; 16(4):397-411.
Score: 0.001
-
Haplotype structure and population genetic inferences from nucleotide-sequence variation in human lipoprotein lipase. Am J Hum Genet. 1998 Aug; 63(2):595-612.
Score: 0.001
-
DNA sequence diversity in a 9.7-kb region of the human lipoprotein lipase gene. Nat Genet. 1998 Jul; 19(3):233-40.
Score: 0.001
-
The Asn9 variant of lipoprotein lipase is associated with the -93G promoter mutation and an increased risk of coronary artery disease. The Regress Study Group. Clin Genet. 1998 Jan; 53(1):27-33.
Score: 0.001
-
Genetic variant showing a positive interaction with beta-blocking agents with a beneficial influence on lipoprotein lipase activity, HDL cholesterol, and triglyceride levels in coronary artery disease patients. The Ser447-stop substitution in the lipoprotein lipase gene. REGRESS Study Group. Circulation. 1997 Jun 17; 95(12):2628-35.
Score: 0.001
-
Comparison of model-free linkage mapping strategies for the study of a complex trait. Genet Epidemiol. 1997; 14(6):743-8.
Score: 0.001
-
OB gene not linked to human obesity in Mexican American affected sib pairs from Starr County, Texas. Hum Genet. 1996 Nov; 98(5):590-5.
Score: 0.001
-
Guidelines of the National Heart, Lung, and Blood Institute Working Group on Blood Drawing, Processing, and Storage for Genetic Studies. Am J Epidemiol. 1996 Sep 01; 144(5):437-41.
Score: 0.001
-
The GENNID Study. A resource for mapping the genes that cause NIDDM. Diabetes Care. 1996 Aug; 19(8):864-72.
Score: 0.001
-
A genome-wide search for human non-insulin-dependent (type 2) diabetes genes reveals a major susceptibility locus on chromosome 2. Nat Genet. 1996 Jun; 13(2):161-6.
Score: 0.001
-
A novel measure of genetic distance for highly polymorphic tandem repeat loci. Mol Biol Evol. 1995 Sep; 12(5):914-20.
Score: 0.001
-
Effect of apolipoprotein E polymorphism on fasting retinyl palmitate level. Biochem Mol Med. 1995 Aug; 55(2):156-7.
Score: 0.001
-
No association between plasma lipoprotein(a) concentrations and the presence or absence of coronary atherosclerosis in African-Americans. Arterioscler Thromb Vasc Biol. 1995 Jul; 15(7):850-5.
Score: 0.001
-
Sequence polymorphisms in the apo(a) gene associated with specific levels of Lp(a) in plasma. Hum Mol Genet. 1995 Feb; 4(2):173-81.
Score: 0.001
-
Comparative analysis of the apo(a) gene, apo(a) glycoprotein, and plasma concentrations of Lp(a) in three ethnic groups. Evidence for no common "null" allele at the apo(a) locus. J Clin Invest. 1994 Jun; 93(6):2526-34.
Score: 0.001
-
Apolipoprotein E genotype and lipid transport: insight into the role of the epsilon 4 allele. Atherosclerosis. 1994 Mar; 106(1):119-21.
Score: 0.001
-
The relation of lipoprotein[a] concentrations and apolipoprotein[a] phenotypes with asymptomatic atherosclerosis in subjects of the Atherosclerosis Risk in Communities (ARIC) Study. Arterioscler Thromb. 1993 Nov; 13(11):1558-66.
Score: 0.001
-
Relation of plasma lipoprotein(a) to infarct artery patency in survivors of myocardial infarction. Circulation. 1993 Sep; 88(3):935-40.
Score: 0.001
-
Plasma lipid, lipoprotein cholesterol, and apoprotein distributions in selected US communities. The Atherosclerosis Risk in Communities (ARIC) Study. Arterioscler Thromb. 1993 Aug; 13(8):1139-58.
Score: 0.001
-
Apo(a) isoforms predict risk for coronary heart disease. A study in six populations. Arterioscler Thromb. 1992 Oct; 12(10):1214-26.
Score: 0.001
-
Anticipation in myotonic dystrophy. I. Statistical verification based on clinical and haplotype findings. Neurology. 1992 Oct; 42(10):1871-7.
Score: 0.001
-
Anticipation in myotonic dystrophy. II. Complex relationships between clinical findings and structure of the GCT repeat. Neurology. 1992 Oct; 42(10):1877-83.
Score: 0.001
-
Apolipoprotein(a) phenotypes, Lp(a) concentration and plasma lipid levels in relation to coronary heart disease in a Chinese population: evidence for the role of the apo(a) gene in coronary heart disease. J Clin Invest. 1992 Mar; 89(3):1040-6.
Score: 0.001
-
Multivariate genetic analysis of high density lipoprotein particles. Atherosclerosis. 1992 Feb; 92(2-3):219-27.
Score: 0.001
-
Dietary intake and gene variation influence the response of plasma lipids to dietary intervention. Genet Epidemiol. 1992; 9(4):249-60.
Score: 0.001
-
The apolipoprotein E polymorphism: a comparison of allele frequencies and effects in nine populations. Am J Hum Genet. 1991 Aug; 49(2):338-49.
Score: 0.001
-
Molecular basis of apolipoprotein (a) isoform size heterogeneity as revealed by pulsed-field gel electrophoresis. J Clin Invest. 1991 Jun; 87(6):2153-61.
Score: 0.001
-
Effects of the apolipoprotein(a) size polymorphism on the lipoprotein(a) concentration in 7 ethnic groups. Hum Genet. 1991 Apr; 86(6):607-14.
Score: 0.001
-
Frequency and effects of apolipoprotein E polymorphism in Mexican-American NIDDM subjects. Diabetes. 1991 Mar; 40(3):334-7.
Score: 0.001
-
Study of the sequence tagged site (STS) in the beginning of human apo A4 gene region. Nucleic Acids Res. 1990 Sep 25; 18(18):5576.
Score: 0.001
-
Frequency and effects of the apolipoprotein A-IV polymorphism. Clin Genet. 1990 Jun; 37(6):435-41.
Score: 0.001
-
Relation of serum lipoprotein(a) concentration and apolipoprotein(a) phenotype to coronary heart disease in patients with familial hypercholesterolemia. N Engl J Med. 1990 May 24; 322(21):1494-9.
Score: 0.001
-
Frequency and effect of human apolipoprotein A-IV polymorphism on lipid and lipoprotein levels in an Icelandic population. Hum Genet. 1990 Mar; 84(4):344-6.
Score: 0.001
-
Variation in concentration of lipids, lipoprotein lipids, and apolipoproteins A-I and B in plasma from healthy women. Clin Chem. 1990 Feb; 36(2):207-10.
Score: 0.001
-
Genetic variation at the apolipoprotein gene loci contribute to response of plasma lipids to dietary change. Genet Epidemiol. 1990; 7(4):261-75.
Score: 0.001
-
Two distinct truncated apolipoprotein B species in a kindred with hypobetalipoproteinemia. Arteriosclerosis. 1989 Nov-Dec; 9(6):856-68.
Score: 0.001
-
Human apolipoprotein A-IV polymorphism: frequency and effect on lipid and lipoprotein levels. Hum Genet. 1988 Aug; 79(4):368-72.
Score: 0.000
-
Linkage of the Wilson disease gene to chromosome 13 in North-American pedigrees. Am J Hum Genet. 1988 Jun; 42(6):825-9.
Score: 0.000
-
Sodium-lithium countertransport in ambulatory hypertensive and normotensive patients. Hypertension. 1987 Jan; 9(1):24-34.
Score: 0.000
-
Lithium ion transport by erythrocytes of randomly selected blood donors and manic-depressive patients: lack of association with affective illness. Am J Psychiatry. 1986 Apr; 143(4):457-62.
Score: 0.000
-
A statistical analysis of spot variation using the two-dimensional polyacrylamide gel electrophoresis. Comput Biomed Res. 1986 Feb; 19(1):90-102.
Score: 0.000
-
Genetics of primary hypertension. Clin Exp Hypertens A. 1986; 8(4-5):623-51.
Score: 0.000
-
Sodium-lithium countertransport and blood pressure in healthy blood donors. Hypertension. 1985 Nov-Dec; 7(6 Pt 1):955-62.
Score: 0.000
-
Strategies for elucidating the phenotypic and genetic heterogeneity of a chronic disease with a complex etiology. Prog Clin Biol Res. 1985; 194:39-66.
Score: 0.000