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Published Manuscripts

Over 3,000 articles have been published with the help of ARIC research.

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Displaying 1401 - 1500 of 3014

Publication Year: 2016
Zanoni, P, Global, Lipids. Rare variant in scavenger receptor BI raises HDL cholesterol and increases risk of coronary heart disease.. Science. 2016-03-11; 351(6278): 1166-71 doi: 10.1126/science.aad3517. PMID: 26965621; PMCID: PMC4889017.Pubmed : MS# U0272
Verweij, N, Van, Der. Twenty-eight genetic loci associated with ST-T-wave amplitudes of the electrocardiogram.. Hum Mol Genet. 2016-03-8; 25(10): 2093-2103 . PMID: 26962151; PMCID: PMC5062578.Pubmed : MS# U0271
Marioni, RE, Deary, IJ. Assessing the genetic overlap between BMI and cognitive function.. Mol Psychiatry. 2016-02-9; 21(10): 1477-82 doi: 10.1038/mp.2015.205. PMID: 26857597; PMCID: PMC4863955.Pubmed : MS# U0270
Zubair, N, Carty, CL. Fine-mapping of lipid regions in global populations discovers ethnic-specific signals and refines previously identified lipid loci.. Hum Mol Genet. 2016-12-15; 25(24): 5500-5512 doi: 10.1093/hmg/ddw358. PMID: 28426890; PMCID: PMC5721937.Pubmed : MS# U0120
Yoneyama, S, North, KE. Generalization and fine mapping of European ancestry-based central adiposity variants in African ancestry populations.. Int J Obes (Lond). 2016-11-21; 41(2): 324-331 doi: 10.1038/ijo.2016.207. PMID: 27867202; PMCID: PMC5296276.Pubmed : MS# U0117
Winkler, TW, Loos, RJ. Correction: The Influence of Age and Sex on Genetic Associations with Adult Body Size and Shape: A Large-Scale Genome-Wide Interaction Study.. PLoS Genet. 2016-06-29; 12(6): e1006166 doi: 10.1371/journal.pgen.1006166. PMID: 27355579; PMCID: PMC4927064.Pubmed : MS# U0116
Shah, AM, Solomon, SD. Contemporary Assessment of Left Ventricular Diastolic Function in Older Adults: The Atherosclerosis Risk in Communities Study.. Circulation. 2016-12-7; 135(5): 426-439 doi: 10.1161/CIRCULATIONAHA.116.024825. PMID: 27927714; PMCID: PMC5285443.Pubmed : MS# U0107
Robinson-Cohen, C, Kestenbaum, B. Genetic Variants Associated with Circulating Parathyroid Hormone.. J Am Soc Nephrol. 2016-12-7; 28(5): 1553-1565 doi: 10.1681/ASN.2016010069. PMID: 27927781; PMCID: PMC5407713.Pubmed : MS# U0103
Offenbacher, S, North, KE. Genome-wide association study of biologically informed periodontal complex traits offers novel insights into the genetic basis of periodontal disease.. Hum Mol Genet. 2016-03-8; 25(10): 2113-2129 . PMID: 26962152; PMCID: PMC5062586.Pubmed : MS# U0101
Morelli, T, Offenbacher, S. Derivation and Validation of the Periodontal and Tooth Profile Classification System for Patient Stratification.. J Periodontol. 2016-09-13; 88(2): 153-165 doi: 10.1902/jop.2016.160379. PMID: 27620653; PMCID: PMC5288277.Pubmed : MS# U0096
Lu, Y, Loos, RJ. New loci for body fat percentage reveal link between adiposity and cardiometabolic disease risk.. Nat Commun. 2016-02-1; 7(): 10495 doi: 10.1038/ncomms10495. PMID: 26833246; PMCID: PMC4740398.Pubmed : MS# U0093
Liu, C, Levy, D. A DNA methylation biomarker of alcohol consumption.. Mol Psychiatry. 2016-11-15; 23(2): 422-433 doi: 10.1038/mp.2016.192. PMID: 27843151; PMCID: PMC5575985.Pubmed : MS# U0092
Liu, X, Boerwinkle, E. The performance of deleteriousness prediction scores for rare non-protein-changing single nucleotide variants in human genes.. J Med Genet. 2016-12-20; 54(2): 134-144 doi: 10.1136/jmedgenet-2016-104369. PMID: 27999115; PMCID: PMC5736365.Pubmed : MS# U0091
Hinney, A, Hebebrand, J. Evidence for three genetic loci involved in both anorexia nervosa risk and variation of body mass index.. Mol Psychiatry. 2016-05-17; 22(2): 192-201 doi: 10.1038/mp.2016.71. PMID: 27184124; PMCID: PMC5114162.Pubmed : MS# U0083
Gregson, JM, EPIC-CVD, consortium. Genetic invalidation of Lp-PLA(2) as a therapeutic target: Large-scale study of five functional Lp-PLA(2)-lowering alleles.. Eur J Prev Cardiol. 2016-12-8; 24(5): 492-504 doi: 10.1177/2047487316682186. PMID: 27940953; PMCID: PMC5460752.Pubmed : MS# U0080
Gogoshin, G, Rodin, AS. New Algorithm and Software (BNOmics) for Inferring and Visualizing Bayesian Networks from Heterogeneous Big Biological and Genetic Data.. J Comput Biol. 2016-09-28; 24(4): 340-356 doi: 10.1089/cmb.2016.0100. PMID: 27681505; PMCID: PMC5372779.Pubmed : MS# U0077
Direk, N, Sullivan, PF. An Analysis of Two Genome-wide Association Meta-analyses Identifies a New Locus for Broad Depression Phenotype.. Biol Psychiatry. 2016-12-8; 82(5): 322-329 doi: 10.1016/j.biopsych.2016.11.013. PMID: 28049566; PMCID: PMC5462867.Pubmed : MS# U0076
Avery, CL, North, KE. Fine mapping of QT interval regions in global populations refines previously identified QT interval loci and identifies signals unique to African and Hispanic descent populations.. Heart Rhythm. 2016-12-14; 14(4): 572-580 doi: 10.1016/j.hrthm.2016.12.021. PMID: 27988371; PMCID: PMC5448160.Pubmed : MS# U0069
Wei, P, Pan, W. On Robust Association Testing for Quantitative Traits and Rare Variants.. G3 (Bethesda). 2016-12-7; 6(12): 3941-3950 doi: 10.1534/g3.116.035485. PMID: 27678522; PMCID: PMC5144964.Pubmed : MS# U0066
Ried, JS, Loos, RJ. A principal component meta-analysis on multiple anthropometric traits identifies novel loci for body shape.. Nat Commun. 2016-11-23; 7(): 13357 doi: 10.1038/ncomms13357. PMID: 27876822; PMCID: PMC5114527.Pubmed : MS# U0065
Ligthart, S, Dehghan, A. DNA methylation signatures of chronic low-grade inflammation are associated with complex diseases.. Genome Biol. 2016-12-12; 17(1): 255 . PMID: 27955697; PMCID: PMC5151130.Pubmed : MS# U0062
Khera, AV, Kathiresan, S. Genetic Risk, Adherence to a Healthy Lifestyle, and Coronary Disease.. N Engl J Med. 2016-11-13; 375(24): 2349-2358 . PMID: 27959714; PMCID: PMC5338864.Pubmed : MS# U0061
Hill, WD, Deary, IJ. Molecular genetic aetiology of general cognitive function is enriched in evolutionarily conserved regions.. Transl Psychiatry. 2016-12-13; 6(12): e980 doi: 10.1038/tp.2016.246. PMID: 27959336; PMCID: PMC5290340.Pubmed : MS# U0060
Dong, J, Chen, H. Genome-Wide Association Analysis of the Sense of Smell in U.S. Older Adults: Identification of Novel Risk Loci in African-Americans and European-Americans.. Mol Neurobiol. 2016-11-23; 54(10): 8021-8032 doi: 10.1007/s12035-016-0282-8. PMID: 27878761; PMCID: PMC5441979.Pubmed : MS# U0059
Adams, HH, Thompson, PM. Novel genetic loci underlying human intracranial volume identified through genome-wide association.. Nat Neurosci. 2016-10-3; 19(12): 1569-1582 doi: 10.1038/nn.4398. PMID: 27694991; PMCID: PMC5227112.Pubmed : MS# U0058
Evans, DS, Sotoodehnia, N. Fine-mapping, novel loci identification, and SNP association transferability in a genome-wide association study of QRS duration in African Americans.. Hum Mol Genet. 2016-08-29; 25(19): 4350-4368 doi: 10.1093/hmg/ddw284. PMID: 27577874; PMCID: PMC5291202.Pubmed : MS# U0055CARE.
Joehanes, R, London, SJ. Epigenetic Signatures of Cigarette Smoking.. Circ Cardiovasc Genet. 2016-09-20; 9(5): 436-447 . PMID: 27651444; PMCID: PMC5267325.Pubmed : MS# U0055
Neurology, Working, Neurology, Working. Identification of additional risk loci for stroke and small vessel disease: a meta-analysis of genome-wide association studies.. Lancet Neurol. 2016-04-7; 15(7): 695-707 doi: 10.1016/S1474-4422(16)00102-2. PMID: 27068588; PMCID: PMC4943223.Pubmed : MS# U0053
Demirkan, A, Räikkönen, K. Somatic, positive and negative domains of the Center for Epidemiological Studies Depression (CES-D) scale: a meta-analysis of genome-wide association studies.. Psychol Med. 2016-03-21; 46(8): 1613-23 doi: 10.1017/S0033291715002081. PMID: 26997408; PMCID: PMC5812462.Pubmed : MS# U0052
Cheng, YC, Mitchell, BD. Genome-Wide Association Analysis of Young-Onset Stroke Identifies a Locus on Chromosome 10q25 Near HABP2.. Stroke. 2016-01-5; 47(2): 307-16 doi: 10.1161/STROKEAHA.115.011328. PMID: 26732560; PMCID: PMC4729659.Pubmed : MS# U0051
Liu, C, Chasman, DI. Meta-analysis identifies common and rare variants influencing blood pressure and overlapping with metabolic trait loci.. Nat Genet. 2016-09-12; 48(10): 1162-70 doi: 10.1038/ng.3660. PMID: 27618448; PMCID: PMC5320952.Pubmed : MS# U0049
Huang, Z, Yu, F. A hybrid computational strategy to address WGS variant analysis in >5000 samples.. BMC Bioinformatics. 2016-09-10; 17(1): 361 doi: 10.1186/s12859-016-1211-6. PMID: 27612449; PMCID: PMC5018196.Pubmed : MS# U0048
Yazdani, A, Boerwinkle, E. Identification, analysis, and interpretation of a human serum metabolomics causal network in an observational study.. J Biomed Inform. 2016-08-31; 63(): 337-343 doi: 10.1016/j.jbi.2016.08.017. PMID: 27592308; PMCID: .Pubmed : MS# U0047
Yazdani, A, Boerwinkle, E. 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 doi: 10.1089/omi.2016.0071. PMID: 27501297; PMCID: PMC4982951.Pubmed : MS# U0046
Peloso, GM, Kathiresan, S. Association of Exome Sequences With Cardiovascular Traits Among Blacks in the Jackson Heart Study.. Circ Cardiovasc Genet. 2016-07-15; 9(4): 368-74 doi: 10.1161/CIRCGENETICS.116.001410. PMID: 27422940; PMCID: PMC4988917.Pubmed : MS# U0045
Yazdani, A, Boerwinkle, E. Identification of Rare Variants in Metabolites of the Carnitine Pathway by Whole Genome Sequencing Analysis.. Genet Epidemiol. 2016-06-3; 40(6): 486-91 doi: 10.1002/gepi.21980. PMID: 27256581; PMCID: PMC5609480.Pubmed : MS# U0044
Willems, SM, Meigs, JB. Association of the IGF1 gene with fasting insulin levels.. Eur J Hum Genet. 2016-02-10; 24(9): 1337-43 doi: 10.1038/ejhg.2016.4. PMID: 26860063; PMCID: PMC4989214.Pubmed : MS# U0043
Chami, N, Lettre, G. Exome Genotyping Identifies Pleiotropic Variants Associated with Red Blood Cell Traits.. Am J Hum Genet. 2016-06-23; 99(1): 8-21 doi: 10.1016/j.ajhg.2016.05.007. PMID: 27346685; PMCID: PMC5005438.Pubmed : MS# U0042
Yazdani, A, Boerwinkle, E. A causal network analysis in an observational study identifies metabolomics pathways influencing plasma triglyceride levels.. Metabolomics. 2016-05-11; 12(6): 104 . PMID: 27330524; PMCID: PMC4869741.Pubmed : MS# U0041
Scott, RA, Waterworth, DM. A genomic approach to therapeutic target validation identifies a glucose-lowering GLP1R variant protective for coronary heart disease.. Sci Transl Med. 2016-06-1; 8(341): 341ra76 doi: 10.1126/scitranslmed.aad3744. PMID: 27252175; PMCID: PMC5219001.Pubmed : MS# U0040
Sung, YJ, Cupples, LA. An Empirical Comparison of Joint and Stratified Frameworks for Studying G × E Interactions: Systolic Blood Pressure and Smoking in the CHARGE Gene-Lifestyle Interactions Working Group.. Genet Epidemiol. 2016-05-27; 40(5): 404-15 doi: 10.1002/gepi.21978. PMID: 27230302; PMCID: PMC4911246.Pubmed : MS# U0039
Mirzaa, GM, Dobyns, WB. Association of MTOR Mutations With Developmental Brain Disorders, Including Megalencephaly, Focal Cortical Dysplasia, and Pigmentary Mosaicism.. JAMA Neurol. 2016-07-1; 73(7): 836-845 doi: 10.1001/jamaneurol.2016.0363. PMID: 27159400; PMCID: PMC4979321.Pubmed : MS# U0038
Smith, JG, Smith, NL. Discovery of Genetic Variation on Chromosome 5q22 Associated with Mortality in Heart Failure.. PLoS Genet. 2016-05-5; 12(5): e1006034 doi: 10.1371/journal.pgen.1006034. PMID: 27149122; PMCID: PMC4858216.Pubmed : MS# U0037
Khera, AV, Kathiresan, S. Diagnostic Yield and Clinical Utility of Sequencing Familial Hypercholesterolemia Genes in Patients With Severe Hypercholesterolemia.. J Am Coll Cardiol. 2016-04-3; 67(22): 2578-89 doi: 10.1016/j.jacc.2016.03.520. PMID: 27050191; PMCID: PMC5405769.Pubmed : MS# U0036
Harel, T, Lupski, JR. Monoallelic and Biallelic Variants in EMC1 Identified in Individuals with Global Developmental Delay, Hypotonia, Scoliosis, and Cerebellar Atrophy.. Am J Hum Genet. 2016-03-3; 98(3): 562-570 doi: 10.1016/j.ajhg.2016.01.011. PMID: 26942288; PMCID: PMC4800043.Pubmed : MS# U0035
Pattaro, C, Fox, CS. Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function.. Nat Commun. 2016-01-21; 7(): 10023 doi: 10.1038/ncomms10023. PMID: 26831199; PMCID: PMC4735748.Pubmed : MS# U0033
Yazdani, A, Boerwinkle, E. Generating a robust statistical causal structure over 13 cardiovascular disease risk factors using genomics data.. J Biomed Inform. 2016-01-28; 60(): 114-9 doi: 10.1016/j.jbi.2016.01.012. PMID: 26827624; PMCID: PMC4886234.Pubmed : MS# U0032
Lalani, SR, Yang, Y. Recurrent Muscle Weakness with Rhabdomyolysis, Metabolic Crises, and Cardiac Arrhythmia Due to Bi-allelic TANGO2 Mutations.. Am J Hum Genet. 2016-01-21; 98(2): 347-57 doi: 10.1016/j.ajhg.2015.12.008. PMID: 26805781; PMCID: PMC4746334.Pubmed : MS# U0031
Huang, J, Han, S. FLAGS: A Flexible and Adaptive Association Test for Gene Sets Using Summary Statistics.. Genetics. 2016-01-15; 202(3): 919-29 doi: 10.1534/genetics.115.185009. PMID: 26773050; PMCID: PMC4788129.Pubmed : MS# U0030
Bayram, Y, Lupski, JR. Molecular etiology of arthrogryposis in multiple families of mostly Turkish origin.. J Clin Invest. 2016-01-11; 126(2): 762-78 doi: 10.1172/JCI84457. PMID: 26752647; PMCID: PMC4731160.Pubmed : MS# U0029
White, J, Sutton, VR. POGZ truncating alleles cause syndromic intellectual disability.. Genome Med. 2016-01-6; 8(1): 3 doi: 10.1186/s13073-015-0253-0. PMID: 26739615; PMCID: PMC4702300.Pubmed : MS# U0028
Liu, X, Boerwinkle, E. dbNSFP v3.0: A One-Stop Database of Functional Predictions and Annotations for Human Nonsynonymous and Splice-Site SNVs.. Hum Mutat. 2016-01-5; 37(3): 235-41 doi: 10.1002/humu.22932. PMID: 26555599; PMCID: PMC4752381.Pubmed : MS# U0023
Rosenthal, EA, Jarvik, GP. Association Between Absolute Neutrophil Count and Variation at TCIRG1: The NHLBI Exome Sequencing Project.. Genet Epidemiol. 2016-05-27; 40(6): 470-4 doi: 10.1002/gepi.21976. PMID: 27229898; PMCID: PMC5079157.Pubmed : MS# U0021ESP.
Roberts, JD, Marcus, GM. Genetic Investigation Into the Differential Risk of Atrial Fibrillation Among Black and White Individuals.. JAMA Cardiol. 2016-07-1; 1(4): 442-50 doi: 10.1001/jamacardio.2016.1185. PMID: 27438321; PMCID: PMC5395094.Pubmed : MS# U0021
Klimentidis, YC, Allison, DB. The Genetic Contribution of West-African Ancestry to Protection against Central Obesity in African-American Men but Not Women: Results from the ARIC and MESA Studies.. Front Genet. 2016-06-1; 7(): 89 doi: 10.3389/fgene.2016.00089. PMID: 27313598; PMCID: PMC4888933.Pubmed : MS# U0020
Kan, M, Leal, SM. Rare variant associations with waist-to-hip ratio in European-American and African-American women from the NHLBI-Exome Sequencing Project.. Eur J Hum Genet. 2016-01-13; 24(8): 1181-7 doi: 10.1038/ejhg.2015.272. PMID: 26757982; PMCID: PMC4970686.Pubmed : MS# U0019ESP.
Rhee, EP, Gerszten, RE. An exome array study of the plasma metabolome.. Nat Commun. 2016-07-25; 7(): 12360 doi: 10.1038/ncomms12360. PMID: 27453504; PMCID: PMC4962516.Pubmed : MS# U0019
Natriuretic, Peptides, Di, Angelantonio. Natriuretic peptides and integrated risk assessment for cardiovascular disease: an individual-participant-data meta-analysis.. Lancet Diabetes Endocrinol. 2016-09-3; 4(10): 840-9 doi: 10.1016/S2213-8587(16)30196-6. PMID: 27599814; PMCID: PMC5035346.Pubmed : MS# U0017
Global, BMI, Hu, FB. Body-mass index and all-cause mortality: individual-participant-data meta-analysis of 239 prospective studies in four continents.. Lancet. 2016-07-13; 388(10046): 776-86 doi: 10.1016/S0140-6736(16)30175-1. PMID: 27423262; PMCID: PMC4995441.Pubmed : MS# U0004ERFC.
Kubota, Y, Folsom, AR. Lung function, respiratory symptoms and venous thromboembolism risk: the Atherosclerosis Risk in Communities Study.. J Thromb Haemost. 2016-11-8; 14(12): 2394-2401 doi: 10.1111/jth.13525. PMID: 27696765; PMCID: PMC5378065.Pubmed : MS# 1295
van, Leeuwen, van, Duijn. Meta-analysis of 49 549 individuals imputed with the 1000 Genomes Project reveals an exonic damaging variant in ANGPTL4 determining fasting TG levels.. J Med Genet. 2016-04-1; 53(7): 441-9 doi: 10.1136/jmedgenet-2015-103439. PMID: 27036123; PMCID: PMC4941146.Pubmed : MS# 1190
Cushman, M, Folsom, AR. Body size measures, hemostatic and inflammatory markers and risk of venous thrombosis: The Longitudinal Investigation of Thromboembolism Etiology.. Thromb Res. 2016-06-15; 144(): 127-32 doi: 10.1016/j.thromres.2016.06.012. PMID: 27328432; PMCID: PMC4980192.Pubmed : MS# 1082
Publication Year: 2015
Gross, AL, Bandeen-Roche, K. Application of Latent Variable Methods to the Study of Cognitive Decline When Tests Change over Time.. Epidemiology. 2015-11; 26(6): 878-87 doi: 10.1097/EDE.0000000000000379. PMID: 26414855; PMCID: PMC4819068.Pubmed : MS# 2215
Bis, JC, Arnett, D. Drug-Gene Interactions of Antihypertensive Medications and Risk of Incident Cardiovascular Disease: A Pharmacogenomics Study from the CHARGE Consortium.. PLoS One. 2015-10-30; 10(10): e0140496 doi: 10.1371/journal.pone.0140496. PMID: 26516778; PMCID: PMC4627813.Pubmed : MS# 1870
Yu, B, CHARGE, Consortium. Rare Exome Sequence Variants in CLCN6 Reduce Blood Pressure Levels and Hypertension Risk.. Circ Cardiovasc Genet. 2015-12-11; 9(1): 64-70 doi: 10.1161/CIRCGENETICS.115.001215. PMID: 26658788; PMCID: PMC4771070.Pubmed : MS# 2068B
Kucharska-Newton, AM, Chambless, L. Identification of Heart Failure Events in Medicare Claims: The Atherosclerosis Risk in Communities (ARIC) Study.. J Card Fail. 2015-07-23; 22(1): 48-55 doi: 10.1016/j.cardfail.2015.07.013. PMID: 26211720; PMCID: PMC4706484.Pubmed : MS# 1528
Luciano, M, CHARGE, Consortium. Structural Brain MRI Trait Polygenic Score Prediction of Cognitive Abilities.. Twin Res Hum Genet. 2015-10-2; 18(6): 738-45 doi: 10.1017/thg.2015.71. PMID: 26427786; PMCID: PMC4747328.Pubmed : MS# U0002
Teumer, A, Köttgen, A. Genome-wide Association Studies Identify Genetic Loci Associated With Albuminuria in Diabetes.. Diabetes. 2015-12-2; 65(3): 803-17 doi: 10.2337/db15-1313. PMID: 26631737; PMCID: PMC4764151.Pubmed : MS# 1379O
Gonçalves, A, Solomon, SD. Alcohol consumption and risk of heart failure: the Atherosclerosis Risk in Communities Study.. Eur Heart J. 2015-01-19; 36(15): 939-45 doi: 10.1093/eurheartj/ehu514. PMID: 25602025; PMCID: PMC4481602.Pubmed : MS# 2247
Gonçalves, A, Solomon, SD. Relationship between alcohol consumption and cardiac structure and function in the elderly: the Atherosclerosis Risk In Communities Study.. Circ Cardiovasc Imaging. 2015-06; 8(6): doi: 10.1161/CIRCIMAGING.114.002846. PMID: 26015266; PMCID: PMC4458702.Pubmed : MS# 2231
Schultheiss, UT, Köttgen, A. A genetic risk score for thyroid peroxidase antibodies associates with clinical thyroid disease in community-based populations.. J Clin Endocrinol Metab. 2015-02-26; 100(5): E799-807 doi: 10.1210/jc.2014-4352. PMID: 25719932; PMCID: PMC4422885.Pubmed : MS# U0273
Dearborn, JL, Gottesman, RF. Obesity, Insulin Resistance, and Incident Small Vessel Disease on Magnetic Resonance Imaging: Atherosclerosis Risk in Communities Study.. Stroke. 2015-10-8; 46(11): 3131-6 doi: 10.1161/STROKEAHA.115.010060. PMID: 26451022; PMCID: PMC4624467.Pubmed : MS# 1902B
Daya, N, Grams, ME. Kidney Function and Fracture Risk: The Atherosclerosis Risk in Communities (ARIC) Study.. Am J Kidney Dis. 2015-08-4; 67(2): 218-226 doi: 10.1053/j.ajkd.2015.06.020. PMID: 26250781; PMCID: PMC4724513.Pubmed : MS# 2371
Camplain, R, Heiss, G. Smoking Behaviors and Arterial Stiffness Measured by Pulse Wave Velocity in Older Adults: The Atherosclerosis Risk in Communities (ARIC) Study.. Am J Hypertens. 2015-12-10; 29(11): 1268-1275 doi: 10.1093/ajh/hpv189. PMID: 26657706; PMCID: PMC5055735.Pubmed : MS# 2320
de, Vries, Dehghan, A. A meta-analysis of 120 246 individuals identifies 18 new loci for fibrinogen concentration.. Hum Mol Genet. 2015-11-10; 25(2): 358-70 doi: 10.1093/hmg/ddv454. PMID: 26561523; PMCID: PMC4715256.Pubmed : MS# 1383E
Folsom, AR, Appiah, D. Lack of association of plasma factor XI with incident stroke and coronary heart disease: The Atherosclerosis Risk in Communities (ARIC) Study.. Atherosclerosis. 2015-09-10; 243(1): 181-5 doi: 10.1016/j.atherosclerosis.2015.09.015. PMID: 26386215; PMCID: PMC4620543.Pubmed : MS# 2456E
Folsom, AR, Pankow, JS. Prospective study of circulating factor XI and incident venous thromboembolism: The Longitudinal Investigation of Thromboembolism Etiology (LITE).. Am J Hematol. 2015-11; 90(11): 1047-51 doi: 10.1002/ajh.24168. PMID: 26260105; PMCID: PMC4618026.Pubmed : MS# 2456B
Wu, B, Pankow, JS. Statistical methods for association tests of multiple continuous traits in genome-wide association studies.. Ann Hum Genet. 2015-04-7; 79(4): 282-93 doi: 10.1111/ahg.12110. PMID: 25857693; PMCID: PMC4474745.Pubmed : MS# 2416B
Rebholz, CM, Coresh, J. Change in Multiple Filtration Markers and Subsequent Risk of Cardiovascular Disease and Mortality.. Clin J Am Soc Nephrol. 2015-03-30; 10(6): 941-8 doi: 10.2215/CJN.10101014. PMID: 25825481; PMCID: PMC4455217.Pubmed : MS# 2225B
Day, FR, Murray, A. Large-scale genomic analyses link reproductive aging to hypothalamic signaling, breast cancer susceptibility and BRCA1-mediated DNA repair.. Nat Genet. 2015-09-28; 47(11): 1294-1303 doi: 10.1038/ng.3412. PMID: 26414677; PMCID: PMC4661791.Pubmed : MS# 2163C
Lunetta, KL, Perry, JR. Rare coding variants and X-linked loci associated with age at menarche.. Nat Commun. 2015-08-4; 6(): 7756 doi: 10.1038/ncomms8756. PMID: 26239645; PMCID: PMC4538850.Pubmed : MS# 2163B
Bower, JK, Selvin, E. N-Terminal Pro-Brain Natriuretic Peptide (NT-proBNP) and Risk of Hypertension in the Atherosclerosis Risk in Communities (ARIC) Study.. Am J Hypertens. 2015-03-16; 28(10): 1262-6 doi: 10.1093/ajh/hpv026. PMID: 25783741; PMCID: PMC4580540.Pubmed : MS# 2133B
McEvoy, JW, Selvin, E. High-Sensitivity Cardiac Troponin T and Risk of Hypertension.. Circulation. 2015-07-7; 132(9): 825-33 doi: 10.1161/CIRCULATIONAHA.114.014364. PMID: 26152706; PMCID: PMC4558242.Pubmed : MS# 2128B
Yu, B, Boerwinkle, E. Association of Rare Loss-Of-Function Alleles in HAL, Serum Histidine: Levels and Incident Coronary Heart Disease.. Circ Cardiovasc Genet. 2015-01-8; 8(2): 351-5 doi: 10.1161/CIRCGENETICS.114.000697. PMID: 25575548; PMCID: PMC4406800.Pubmed : MS# 2084B
Davies, G, Deary, IJ. Genetic contributions to variation in general cognitive function: a meta-analysis of genome-wide association studies in the CHARGE consortium (N=53949).. Mol Psychiatry. 2015-02-3; 20(2): 183-92 doi: 10.1038/mp.2014.188. PMID: 25644384; PMCID: PMC4356746.Pubmed : MS# 2080B
James, MT, CKD, Prognosis. A Meta-analysis of the Association of Estimated GFR, Albuminuria, Diabetes Mellitus, and Hypertension With Acute Kidney Injury.. Am J Kidney Dis. 2015-05-11; 66(4): 602-12 doi: 10.1053/j.ajkd.2015.02.338. PMID: 25975964; PMCID: PMC4594211.Pubmed : MS# 1944D
Greenberg, KI, Grams, ME. Plasma Urate and Risk of a Hospital Stay with AKI: The Atherosclerosis Risk in Communities Study.. Clin J Am Soc Nephrol. 2015-02-25; 10(5): 776-83 doi: 10.2215/CJN.05870614. PMID: 25717072; PMCID: PMC4422233.Pubmed : MS# 1944C
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