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ARIC Publications

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2020
Sargurupremraj M, Suzuki H, Jian X, et al. "Cerebral small vessel disease genomics and its implications across the lifespan." Nat Commun. 2020;11(1):6285.
Sargurupremraj M, Suzuki H, Jian X, et al. "Cerebral small vessel disease genomics and its implications across the lifespan." Nat Commun. 2020;11(1):6285.
Sargurupremraj M, Suzuki H, Jian X, et al. "Cerebral small vessel disease genomics and its implications across the lifespan." Nat Commun. 2020;11(1):6285.
Sargurupremraj M, Suzuki H, Jian X, et al. "Cerebral small vessel disease genomics and its implications across the lifespan." Nat Commun. 2020;11(1):6285.
Sargurupremraj M, Suzuki H, Jian X, et al. "Cerebral small vessel disease genomics and its implications across the lifespan." Nat Commun. 2020;11(1):6285.
Sargurupremraj M, Suzuki H, Jian X, et al. "Cerebral small vessel disease genomics and its implications across the lifespan." Nat Commun. 2020;11(1):6285.
Sargurupremraj M, Suzuki H, Jian X, et al. "Cerebral small vessel disease genomics and its implications across the lifespan." Nat Commun. 2020;11(1):6285.
Sargurupremraj M, Suzuki H, Jian X, et al. "Cerebral small vessel disease genomics and its implications across the lifespan." Nat Commun. 2020;11(1):6285.
Sargurupremraj M, Suzuki H, Jian X, et al. "Cerebral small vessel disease genomics and its implications across the lifespan." Nat Commun. 2020;11(1):6285.
Sargurupremraj M, Suzuki H, Jian X, et al. "Cerebral small vessel disease genomics and its implications across the lifespan." Nat Commun. 2020;11(1):6285.
Sargurupremraj M, Suzuki H, Jian X, et al. "Cerebral small vessel disease genomics and its implications across the lifespan." Nat Commun. 2020;11(1):6285.
Sargurupremraj M, Suzuki H, Jian X, et al. "Cerebral small vessel disease genomics and its implications across the lifespan." Nat Commun. 2020;11(1):6285.
Foti K, Matsushita K, Koton S, et al. "Changes in hypertension control in a community-based population of older adults, 2011-2013 to 2016-2017." Am J Hypertens. 2020.
Sonsin-Diaz N, Gottesman RF, Fracica E, Walston J, B Windham G, Knopman DS. "Chronic Systemic Inflammation Is Associated With Symptoms of Late-Life Depression: The ARIC Study." Am J Geriatr Psychiatry. 2020;28(1):87-98.
Alonso A, Rooney MR, Chen LYee, et al. "Circulating electrolytes and the prevalence of atrial fibrillation and supraventricular ectopy: The Atherosclerosis Risk in Communities (ARIC) study." Nutr Metab Cardiovasc Dis. 2020;30(7):1121-1129.
Alonso A, Rooney MR, Chen LYee, et al. "Circulating electrolytes and the prevalence of atrial fibrillation and supraventricular ectopy: The Atherosclerosis Risk in Communities (ARIC) study." Nutr Metab Cardiovasc Dis. 2020;30(7):1121-1129.
Alonso A, Rooney MR, Chen LYee, et al. "Circulating electrolytes and the prevalence of atrial fibrillation and supraventricular ectopy: The Atherosclerosis Risk in Communities (ARIC) study." Nutr Metab Cardiovasc Dis. 2020;30(7):1121-1129.
Gore MOdette, Ayers CR, Khera A, et al. "Combining Biomarkers and Imaging for Short-Term Assessment of Cardiovascular Disease Risk in Apparently Healthy Adults." J Am Heart Assoc. 2020;9(15):e015410.
Gore MOdette, Ayers CR, Khera A, et al. "Combining Biomarkers and Imaging for Short-Term Assessment of Cardiovascular Disease Risk in Apparently Healthy Adults." J Am Heart Assoc. 2020;9(15):e015410.
Armstrong NJ, Mather KA, Sargurupremraj M, et al. "Common Genetic Variation Indicates Separate Causes for Periventricular and Deep White Matter Hyperintensities." Stroke. 2020;51(7):2111-2121.
Armstrong NJ, Mather KA, Sargurupremraj M, et al. "Common Genetic Variation Indicates Separate Causes for Periventricular and Deep White Matter Hyperintensities." Stroke. 2020;51(7):2111-2121.
Armstrong NJ, Mather KA, Sargurupremraj M, et al. "Common Genetic Variation Indicates Separate Causes for Periventricular and Deep White Matter Hyperintensities." Stroke. 2020;51(7):2111-2121.
Armstrong NJ, Mather KA, Sargurupremraj M, et al. "Common Genetic Variation Indicates Separate Causes for Periventricular and Deep White Matter Hyperintensities." Stroke. 2020;51(7):2111-2121.
Armstrong NJ, Mather KA, Sargurupremraj M, et al. "Common Genetic Variation Indicates Separate Causes for Periventricular and Deep White Matter Hyperintensities." Stroke. 2020;51(7):2111-2121.
Armstrong NJ, Mather KA, Sargurupremraj M, et al. "Common Genetic Variation Indicates Separate Causes for Periventricular and Deep White Matter Hyperintensities." Stroke. 2020;51(7):2111-2121.
Armstrong NJ, Mather KA, Sargurupremraj M, et al. "Common Genetic Variation Indicates Separate Causes for Periventricular and Deep White Matter Hyperintensities." Stroke. 2020;51(7):2111-2121.
Armstrong NJ, Mather KA, Sargurupremraj M, et al. "Common Genetic Variation Indicates Separate Causes for Periventricular and Deep White Matter Hyperintensities." Stroke. 2020;51(7):2111-2121.
Armstrong NJ, Mather KA, Sargurupremraj M, et al. "Common Genetic Variation Indicates Separate Causes for Periventricular and Deep White Matter Hyperintensities." Stroke. 2020;51(7):2111-2121.
Armstrong NJ, Mather KA, Sargurupremraj M, et al. "Common Genetic Variation Indicates Separate Causes for Periventricular and Deep White Matter Hyperintensities." Stroke. 2020;51(7):2111-2121.
Armstrong NJ, Mather KA, Sargurupremraj M, et al. "Common Genetic Variation Indicates Separate Causes for Periventricular and Deep White Matter Hyperintensities." Stroke. 2020;51(7):2111-2121.
Armstrong NJ, Mather KA, Sargurupremraj M, et al. "Common Genetic Variation Indicates Separate Causes for Periventricular and Deep White Matter Hyperintensities." Stroke. 2020;51(7):2111-2121.
Armstrong NJ, Mather KA, Sargurupremraj M, et al. "Common Genetic Variation Indicates Separate Causes for Periventricular and Deep White Matter Hyperintensities." Stroke. 2020;51(7):2111-2121.
Armstrong NJ, Mather KA, Sargurupremraj M, et al. "Common Genetic Variation Indicates Separate Causes for Periventricular and Deep White Matter Hyperintensities." Stroke. 2020;51(7):2111-2121.
Zhao D, Guallar E, Vaidya D, et al. "Cyclic Guanosine Monophosphate and Risk of Incident Heart Failure and Other Cardiovascular Events: the ARIC Study." J Am Heart Assoc. 2020;9(2):e013966.
Zhao D, Guallar E, Vaidya D, et al. "Cyclic Guanosine Monophosphate and Risk of Incident Heart Failure and Other Cardiovascular Events: the ARIC Study." J Am Heart Assoc. 2020;9(2):e013966.
Li C, Mou C, Swartz MD, Yu B, Bai Y, Tu Y. "dbMTS: A comprehensive database of putative human microRNA target site SNVs and their functional predictions." Hum Mutat. 2020;41(6):1123-1130.
Kessler MD, Loesch DP, Perry JA, et al. "De novo mutations across 1,465 diverse genomes reveal mutational insights and reductions in the Amish founder population." Proc Natl Acad Sci U S A. 2020;117(5):2560-2569.
Gigliotti JC, Tin A, Pourafshar S, et al. " Deletion Exaggerates Kidney Injury in Experimental Mouse Models and Confers the Protective Effect of Cruciferous Vegetables in Mice and Humans." J Am Soc Nephrol. 2020;31(1):102-116.
Gigliotti JC, Tin A, Pourafshar S, et al. " Deletion Exaggerates Kidney Injury in Experimental Mouse Models and Confers the Protective Effect of Cruciferous Vegetables in Mice and Humans." J Am Soc Nephrol. 2020;31(1):102-116.
Ning X, Ding N, Ballew SH, et al. "Diabetes, its duration, and the long-term risk of abdominal aortic aneurysm: The Atherosclerosis Risk in Communities (ARIC) Study." Atherosclerosis. 2020;313:137-143.
Dighe S, Zhao J, Steffen L, et al. "Diet patterns and the incidence of age-related macular degeneration in the Atherosclerosis Risk in Communities (ARIC) study." Br J Ophthalmol. 2020;104(8):1070-1076.
Xu Z, Steffen LM, Selvin E. "Diet quality, change in diet quality and risk of incident CVD and diabetes." Public Health Nutr. 2020;23(2):329-338.
Xu Z, Steffen LM, Selvin E. "Diet quality, change in diet quality and risk of incident CVD and diabetes." Public Health Nutr. 2020;23(2):329-338.
Surendran P, Feofanova EV, Lahrouchi N, et al. "Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals." Nat Genet. 2020;52(12):1314-1332.
Surendran P, Feofanova EV, Lahrouchi N, et al. "Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals." Nat Genet. 2020;52(12):1314-1332.
Surendran P, Feofanova EV, Lahrouchi N, et al. "Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals." Nat Genet. 2020;52(12):1314-1332.
Surendran P, Feofanova EV, Lahrouchi N, et al. "Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals." Nat Genet. 2020;52(12):1314-1332.
Surendran P, Feofanova EV, Lahrouchi N, et al. "Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals." Nat Genet. 2020;52(12):1314-1332.
Surendran P, Feofanova EV, Lahrouchi N, et al. "Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals." Nat Genet. 2020;52(12):1314-1332.
Surendran P, Feofanova EV, Lahrouchi N, et al. "Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals." Nat Genet. 2020;52(12):1314-1332.
Surendran P, Feofanova EV, Lahrouchi N, et al. "Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals." Nat Genet. 2020;52(12):1314-1332.
Surendran P, Feofanova EV, Lahrouchi N, et al. "Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals." Nat Genet. 2020;52(12):1314-1332.
Surendran P, Feofanova EV, Lahrouchi N, et al. "Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals." Nat Genet. 2020;52(12):1314-1332.
Surendran P, Feofanova EV, Lahrouchi N, et al. "Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals." Nat Genet. 2020;52(12):1314-1332.
Surendran P, Feofanova EV, Lahrouchi N, et al. "Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals." Nat Genet. 2020;52(12):1314-1332.
Surendran P, Feofanova EV, Lahrouchi N, et al. "Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals." Nat Genet. 2020;52(12):1314-1332.
Surendran P, Feofanova EV, Lahrouchi N, et al. "Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals." Nat Genet. 2020;52(12):1314-1332.