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ARIC Publications

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Journal Article
Liu Y, Chen S, Li Z, Morrison AC, Boerwinkle E. "ACAT: A Fast and Powerful p Value Combination Method for Rare-Variant Analysis in Sequencing Studies." Am J Hum Genet. 2019;104(3):410-421.
Chambless LE, Davis V. "Analysis of associations with change in a multivariate outcome variable when baseline is subject to measurement error." Stat Med. 2003;22(7):1041-67.
Moore CR, Jain S, Haas S, et al. "Ascertaining Framingham heart failure phenotype from inpatient electronic health record data using natural language processing: a multicentre Atherosclerosis Risk in Communities (ARIC) validation study." BMJ Open. 2021;11(6):e047356.
Chambless LE, Toole JF, Nieto JF, Rosamond W, Paton C. "Association between symptoms reported in a population questionnaire and future ischemic stroke: the ARIC study." Neuroepidemiology. 2004;23(1-2):33-7.
Peloso GM, Lange LA, Varga TV, et al. "Association of Exome Sequences With Cardiovascular Traits Among Blacks in the Jackson Heart Study." Circ Cardiovasc Genet. 2016;9(4):368-74.
Chambless LE, Shahar E, Sharrett AR, et al. "Association of transient ischemic attack/stroke symptoms assessed by standardized questionnaire and algorithm with cerebrovascular risk factors and carotid artery wall thickness. The ARIC Study, 1987-1989." Am J Epidemiol. 1996;144(9):857-66.
Stevens J, Erber-Oakkar E, Cui Z, Cai J, Virani SS, Di Angelantonio E. "Cardiovascular disease risk by assigned treatment using the 2013 and 1998 obesity guidelines." Obesity (Silver Spring). 2016;24(7):1554-60.
Yazdani A, Yazdani A. "A Causal Network Analysis of the Fatty Acid Metabolome in African-Americans Reveals a Critical Role for Palmitoleate and Margarate." OMICS. 2016;20(8):480-4.
Raina A, Zhao X, Grove ML, et al. "Cerebral white matter hyperintensities on MRI and acceleration of epigenetic aging: the atherosclerosis risk in communities study." Clin Epigenetics. 2017;9:21.
Loehr LR, Agarwal SK, Baggett C, et al. "Classification of acute decompensated heart failure: an automated algorithm compared with a physician reviewer panel: the Atherosclerosis Risk in Communities study." Circ Heart Fail. 2013;6(4):719-26.
Lemaitre RN, Johnson CO, Hesselson S, et al. "Common variation in fatty acid metabolic genes and risk of incident sudden cardiac arrest." Heart Rhythm. 2014;11(3):471-7.
Etesami M, Hoi Y, Steinman DA, et al. "Comparison of carotid plaque ulcer detection using contrast-enhanced and time-of-flight MRA techniques." AJNR Am J Neuroradiol. 2013;34(1):177-84.
Kors JA, Crow RS, Hannan PJ, Rautaharju PM, Folsom AR. "Comparison of computer-assigned Minnesota Codes with the visual standard method for new coronary heart disease events." Am J Epidemiol. 2000;151(8):790-7.
Matsushita K, Mahmoodi BK, Woodward M, et al. "Comparison of risk prediction using the CKD-EPI equation and the MDRD study equation for estimated glomerular filtration rate." JAMA. 2012;307(18):1941-51.
Chanda P, Yuhki N, Li M, et al. "Comprehensive evaluation of imputation performance in African Americans." J Hum Genet. 2012;57(7):411-21.
Liao D, Barnes RW, Chambless LE, Heiss G. "A computer algorithm to impute interrupted heart rate data for the spectral analysis of heart rate variability--the ARIC study." Comput Biomed Res. 1996;29(2):140-51.
Cuthbertson CC, Kucharska-Newton AMaria, Faurot KR, et al. "Controlling for Frailty in Pharmacoepidemiologic Studies of Older Adults: Validation of an Existing Medicare Claims-based Algorithm." Epidemiology. 2018;29(4):556-561.
"Convergent genetic and expression data implicate immunity in Alzheimer's disease." Alzheimers Dement. 2015;11(6):658-71.
Li Z, Li X, Liu Y, et al. "Dynamic Scan Procedure for Detecting Rare-Variant Association Regions in Whole-Genome Sequencing Studies." Am J Hum Genet. 2019;104(5):802-814.
Wu B, Guan W. "On Efficient and Accurate Calculation of Significance P-Values for Sequence Kernel Association Testing of Variant Set." Ann Hum Genet. 2016;80(2):123-35.
Yeung EH, Saudek CD, Jahren HA, et al. "Evaluation of a novel isotope biomarker for dietary consumption of sweets." Am J Epidemiol. 2010;172(9):1045-52.
Bare LA, Morrison AC, Rowland CM, et al. "Five common gene variants identify elevated genetic risk for coronary heart disease." Genet Med. 2007;9(10):682-9.
Lin D-Y, Zeng D, Couper D. "A general framework for integrative analysis of incomplete multiomics data." Genet Epidemiol. 2020;44(7):646-664.
Yazdani A, Yazdani A, Samiei A. "Generating a robust statistical causal structure over 13 cardiovascular disease risk factors using genomics data." J Biomed Inform. 2016;60:114-9.
Stang PE, Carson AP, Rose KM, et al. "Headache, cerebrovascular symptoms, and stroke: the Atherosclerosis Risk in Communities Study." Neurology. 2005;64(9):1573-7.
Yazdani A, Yazdani A, Samiei A. "Identification, analysis, and interpretation of a human serum metabolomics causal network in an observational study." J Biomed Inform. 2016;63:337-343.
Corona G, Rastrelli G, Silverii A, et al. "The identification of prediabetes condition with ARIC algorithm predicts long-term CV events in patients with erectile dysfunction." J Sex Med. 2013;10(4):1114-23.
Perez-Alday EAndres, Li-Pershing Y, Bender A, et al. "Importance of the heart vector origin point definition for an ECG analysis: The Atherosclerosis Risk in Communities (ARIC) study." Comput Biol Med. 2019;104:127-138.
Rebholz CM, Coresh JJ, Ballew SH, McMahon B, Whelton SP, Selvin E. "Kidney Failure and ESRD in the Atherosclerosis Risk in Communities (ARIC) Study: Comparing Ascertainment of Treated and Untreated Kidney Failure in a Cohort Study." Am J Kidney Dis. 2015;66(2):231-9.
Camplain R, Kucharska-Newton AMaria, Cuthbertson CC, Wright JD, Alonso A. "Misclassification of incident hospitalized and outpatient heart failure in administrative claims data: the Atherosclerosis Risk in Communities (ARIC) study." Pharmacoepidemiol Drug Saf. 2017;26(4):421-428.
Gogoshin G, Boerwinkle E. "New Algorithm and Software (BNOmics) for Inferring and Visualizing Bayesian Networks from Heterogeneous Big Biological and Genetic Data." J Comput Biol. 2017;24(4):340-356.
Xing C, Dupuis J. "Performance of statistical methods on CHARGE targeted sequencing data." BMC Genet. 2014;15:104.
Seplyarskiy VB, Soldatov RA, Koch E, et al. "Population sequencing data reveal a compendium of mutational processes in the human germ line." Science. 2021;373(6558):1030-1035.
Naj AC, Lin H, Vardarajan BN, et al. "Quality control and integration of genotypes from two calling pipelines for whole genome sequence data in the Alzheimer's disease sequencing project." Genomics. 2019;111(4):808-818.
Yazdani A, Yazdani A. "Rare variants analysis using penalization methods for whole genome sequence data." BMC Bioinformatics. 2015;16:405.
Ni A. "A regularized variable selection procedure in additive hazards model with stratified case-cohort design." Lifetime Data Anal. 2018;24(3):443-463.
Wei P, Cao Y, Zhang Y, Xu Z, Kwak I-Y, Boerwinkle E. "On Robust Association Testing for Quantitative Traits and Rare Variants." G3 (Bethesda). 2016;6(12):3941-3950.
"SCORE2 risk prediction algorithms: new models to estimate 10-year risk of cardiovascular disease in Europe." Eur Heart J. 2021;42(25):2439-2454.
"SCORE2-OP risk prediction algorithms: estimating incident cardiovascular event risk in older persons in four geographical risk regions." Eur Heart J. 2021;42(25):2455-2467.
Toole JF, Lefkowitz DS, Chambless LE, Wijnberg L, Paton CC, Heiss G. "Self-reported transient ischemic attack and stroke symptoms: methods and baseline prevalence. The ARIC Study, 1987-1989." Am J Epidemiol. 1996;144(9):849-56.
Wu B. "Sequence Kernel Association Test of Multiple Continuous Phenotypes." Genet Epidemiol. 2016;40(2):91-100.
Gellert KS, Rautaharju P, Snyder ML, Whitsel EA, Matsushita K, Heiss G. "Short-term repeatability of electrocardiographic Tpeak-Tend and QT intervals." J Electrocardiol. 2014;47(3):356-61.
Rautaharju PM, Prineas RJ, Zhang Z-M. "A simple procedure for estimation of the spatial QRS/T angle from the standard 12-lead electrocardiogram." J Electrocardiol. 2007;40(3):300-4.
Rodin AS, Litvinenko A, Klos K, et al. "Use of wrapper algorithms coupled with a random forests classifier for variable selection in large-scale genomic association studies." J Comput Biol. 2009;16(12):1705-18.
Schneider ALC, Pankow JS, Heiss G. "Validity and reliability of self-reported diabetes in the Atherosclerosis Risk in Communities Study." Am J Epidemiol. 2012;176(8):738-43.
Logsdon BA, Dai JY, Auer PL, et al. "A variational Bayes discrete mixture test for rare variant association." Genet Epidemiol. 2014;38(1):21-30.