ARIC Publications
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18-year change in serum intact fibroblast growth factor 23 from midlife to late life and risk of mortality: the ARIC Study." Eur J Endocrinol. 2022;187(1):39-47.
"Association of Echocardiographic Measures of Left Atrial Function and Size With Incident Dementia." JAMA. 2022;327(12):1138-1148.
"Association of Left Atrial Structure and Function With Heart Failure in Older Adults." J Am Coll Cardiol. 2022;79(16):1549-1561.
"Cardiac Structure and Function and Diabetes-Related Risk of Death or Heart Failure in Older Adults." J Am Heart Assoc. 2022;11(6):e022308.
"Changes in Serum Intact Fibroblast Growth Factor 23 Concentrations From Midlife to Late Life and Their Predictors in the Community: The ARIC Study." Mayo Clin Proc Innov Qual Outcomes. 2022;6(3):209-217.
"CKD and Risk of Incident Hospitalization With Clostridioides difficile Infection: Findings From the Atherosclerosis Risk in Communities (ARIC) Study." Am J Kidney Dis. 2022;80(2):297-299.
"Clinically Recognized Varicose Veins and Physical Function in Older Individuals: The ARIC Study." J Gerontol A Biol Sci Med Sci. 2022;77(8):1637-1643.
"Correction: Association of low-frequency and rare coding variants with information processing speed." Transl Psychiatry. 2022;12(1):88.
"Development and Validation of Prediction Models of Adverse Kidney Outcomes in the Population With and Without Diabetes." Diabetes Care. 2022;45(9):2055-2063.
"Development and Validation of Prediction Models of Adverse Kidney Outcomes in the Population With and Without Diabetes." Diabetes Care. 2022;45(9):2055-2063.
"Differences in incident and recurrent myocardial infarction among White and Black individuals aged 35 to 84: Findings from the ARIC community surveillance study." Am Heart J. 2022;253:67-75.
"Differential and shared genetic effects on kidney function between diabetic and non-diabetic individuals." Commun Biol. 2022;5(1):580.
"Differential and shared genetic effects on kidney function between diabetic and non-diabetic individuals." Commun Biol. 2022;5(1):580.
"DNA methylation signature of chronic low-grade inflammation and its role in cardio-respiratory diseases." Nat Commun. 2022;13(1):2408.
"Epigenetic and integrative cross-omics analyses of cerebral white matter hyperintensities on MRI." Brain. 2022.
"Gene-mapping study of extremes of cerebral small vessel disease reveals TRIM47 as a strong candidate." Brain. 2022;145(6):1992-2007.
"Gene-mapping study of extremes of cerebral small vessel disease reveals TRIM47 as a strong candidate." Brain. 2022;145(6):1992-2007.
"Genetic determinants of telomere length from 109,122 ancestrally diverse whole-genome sequences in TOPMed." Cell Genom. 2022;2(1).
"Genetic determinants of telomere length from 109,122 ancestrally diverse whole-genome sequences in TOPMed." Cell Genom. 2022;2(1).
"Genetic determinants of telomere length from 109,122 ancestrally diverse whole-genome sequences in TOPMed." Cell Genom. 2022;2(1).
"Genetic loci and prioritization of genes for kidney function decline derived from a meta-analysis of 62 longitudinal genome-wide association studies." Kidney Int. 2022;102(3):624-639.
"Genome-wide meta-analyses reveal novel loci for verbal short-term memory and learning." Mol Psychiatry. 2022.
"Insights From a Large-Scale Whole-Genome Sequencing Study of Systolic Blood Pressure, Diastolic Blood Pressure, and Hypertension." Hypertension. 2022;79(8):1656-1667.
"Machine Learning-Based Models Incorporating Social Determinants of Health vs Traditional Models for Predicting In-Hospital Mortality in Patients With Heart Failure." JAMA Cardiol. 2022;7(8):844-854.
"Mendelian randomization supports bidirectional causality between telomere length and clonal hematopoiesis of indeterminate potential." Sci Adv. 2022;8(14):eabl6579.
"Meta-analysis of genome-wide association studies identifies ancestry-specific associations underlying circulating total tau levels." Commun Biol. 2022;5(1):336.
"Multi-ancestry genetic study of type 2 diabetes highlights the power of diverse populations for discovery and translation." Nat Genet. 2022;54(5):560-572.
"Multi-ancestry genetic study of type 2 diabetes highlights the power of diverse populations for discovery and translation." Nat Genet. 2022;54(5):560-572.
"Multi-ancestry genetic study of type 2 diabetes highlights the power of diverse populations for discovery and translation." Nat Genet. 2022;54(5):560-572.
"Multi-ancestry genetic study of type 2 diabetes highlights the power of diverse populations for discovery and translation." Nat Genet. 2022;54(5):560-572.
"Multi-ancestry genetic study of type 2 diabetes highlights the power of diverse populations for discovery and translation." Nat Genet. 2022;54(5):560-572.
"Multi-ancestry genetic study of type 2 diabetes highlights the power of diverse populations for discovery and translation." Nat Genet. 2022;54(5):560-572.
"Multi-ancestry genetic study of type 2 diabetes highlights the power of diverse populations for discovery and translation." Nat Genet. 2022;54(5):560-572.
"Multi-ancestry genetic study of type 2 diabetes highlights the power of diverse populations for discovery and translation." Nat Genet. 2022;54(5):560-572.
"Multi-ethnic GWAS and fine-mapping of glycaemic traits identify novel loci in the PAGE Study." Diabetologia. 2022;65(3):477-489.
"New insights into the genetic etiology of Alzheimer's disease and related dementias." Nat Genet. 2022;54(4):412-436.
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