Year |
Citation |
Score |
2023 |
Folsom AR, Tang W, Hong CP, Rosamond WD, Lane JA, Cushman M, Pankratz N. Prediction of venous thromboembolism incidence in the general adult population using two published genetic risk scores. Plos One. 18: e0280657. PMID 36716319 DOI: 10.1371/journal.pone.0280657 |
0.446 |
|
2022 |
Pankratz N, Wei P, Brody JA, Chen MH, Vries PS, Huffman JE, Stimson MR, Auer PL, Boerwinkle E, Cushman M, Maat MPM, Folsom AR, Franco OH, Gibbs RA, Haagenson KK, ... ... Tang W, et al. Whole exome sequencing of 14 389 individuals from the ESP and CHARGE consortia identifies novel rare variation associated with hemostatic factors. Human Molecular Genetics. PMID 35552711 DOI: 10.1093/hmg/ddac100 |
0.334 |
|
2022 |
Steffen BT, Pankow JS, Lutsey PL, Demmer RT, Misialek JR, Guan W, Cowan LT, Coresh J, Norby FL, Tang W. Proteomic Profiling Identifies Novel Proteins for Genetic Risk of Severe COVID-19: the Atherosclerosis Risk in Communities Study. Human Molecular Genetics. PMID 35212764 DOI: 10.1093/hmg/ddac024 |
0.314 |
|
2020 |
Maners J, Gill D, Pankratz N, Laffan MA, Wolberg AS, de Maat MPM, Ligthart S, Tang W, Ward-Caviness CK, Fornage M, Debette S, Dichgans M, McKnight B, Boerwinkle E, Smith NL, et al. A Mendelian randomization of γ' and total fibrinogen levels on venous thromboembolism and ischemic stroke. Blood. PMID 32722807 DOI: 10.1182/Blood.2019004781 |
0.329 |
|
2020 |
Hodonsky CJ, Baldassari AR, Bien SA, Raffield LM, Highland HM, Sitlani CM, Wojcik GL, Tao R, Graff M, Tang W, Thyagarajan B, Buyske S, Fornage M, Hindorff LA, Li Y, et al. Ancestry-specific associations identified in genome-wide combined-phenotype study of red blood cell traits emphasize benefits of diversity in genomics. Bmc Genomics. 21: 228. PMID 32171239 DOI: 10.1186/S12864-020-6626-9 |
0.352 |
|
2019 |
Tang W, Stimson MR, Basu S, Heckbert SR, Cushman M, Pankow JS, Folsom AR, Pankratz N. Burden of rare exome sequence variants in PROC gene is associated with venous thromboembolism: a population-based study. Journal of Thrombosis and Haemostasis : Jth. PMID 31680443 DOI: 10.1111/Jth.14676 |
0.31 |
|
2019 |
Tang W, Saratzis A, Pattee J, Smith J, Pankratz N, Leavy OC, Guan W, Dudbridge F, Pankow JS, Kitas GD, Lutsey PL, Bown MJ. Replication of Newly Identified Genetic Associations Between Abdominal Aortic Aneurysm and SMYD2, LINC00540, PCIF1/MMP9/ZNF335, and ERG. European Journal of Vascular and Endovascular Surgery : the Official Journal of the European Society For Vascular Surgery. PMID 31680049 DOI: 10.1016/J.Ejvs.2019.02.017 |
0.402 |
|
2019 |
Liang J, Cade BE, He KY, Wang H, Lee J, Sofer T, Williams S, Li R, Chen H, Gottlieb DJ, Evans DS, Guo X, Gharib SA, Hale L, Hillman DR, ... ... Tang W, et al. Sequencing Analysis at 8p23 Identifies Multiple Rare Variants in DLC1 Associated with Sleep-Related Oxyhemoglobin Saturation Level. American Journal of Human Genetics. PMID 31668705 DOI: 10.1016/J.Ajhg.2019.10.002 |
0.395 |
|
2019 |
Parikh RR, Folsom AR, Misialek JR, Rosamond WD, Chang PP, Tang W, Cushman M. Prospective study of plasma high molecular weight kininogen and prekallikrein and incidence of coronary heart disease, ischemic stroke and heart failure. Thrombosis Research. 182: 89-94. PMID 31473403 DOI: 10.1016/J.Thromres.2019.08.009 |
0.49 |
|
2019 |
Lindstrom S, Wang L, Smith EN, Gordon W, van Hylckama Vlieg A, de Andrade M, Brody JA, Pattee JW, Haessler J, Brumpton BM, Chasman DI, Suchon P, Chen MH, Turman C, Germain M, ... ... Tang W, et al. Genomic and Transcriptomic Association Studies Identify 16 Novel Susceptibility Loci for Venous Thromboembolism. Blood. PMID 31420334 DOI: 10.1182/Blood.2019000435 |
0.425 |
|
2019 |
Ward-Caviness CK, de Vries PS, Wiggins KL, Huffman JE, Yanek LR, Bielak LF, Giulianini F, Guo X, Kleber ME, Kacprowski T, Groß S, Petersman A, Davey Smith G, Hartwig FP, Bowden J, ... ... Tang W, et al. Mendelian randomization evaluation of causal effects of fibrinogen on incident coronary heart disease. Plos One. 14: e0216222. PMID 31075152 DOI: 10.1371/Journal.Pone.0216222 |
0.356 |
|
2019 |
Oyenuga AO, Folsom AR, Lutsey PL, Tang W. Association of Life's Simple 7 with reduced clinically manifest abdominal aortic aneurysm: The ARIC study. Vascular Medicine (London, England). 1358863X19829226. PMID 30898044 DOI: 10.1177/1358863X19829226 |
0.382 |
|
2019 |
Folsom AR, Tang W, Basu S, Misialek JR, Couper D, Heckbert SR, Cushman M. Plasma Concentrations of High Molecular Weight Kininogen and Prekallikrein and Venous Thromboembolism Incidence in the General Population. Thrombosis and Haemostasis. PMID 30780167 DOI: 10.1055/S-0039-1678737 |
0.372 |
|
2019 |
Lindström S, Brody JA, Turman C, Germain M, Bartz TM, Smith EN, Chen MH, Puurunen M, Chasman D, Hassler J, Pankratz N, Basu S, Guan W, Gyorgy B, Ibrahim M, ... ... Tang W, et al. A large-scale exome array analysis of venous thromboembolism. Genetic Epidemiology. PMID 30659681 DOI: 10.1002/Gepi.22187 |
0.413 |
|
2019 |
de Vries PS, Sabater-Lleal M, Huffman JE, Marten J, Song C, Pankratz N, Bartz TM, de Haan HG, Delgado GE, Eicher JD, Martinez-Perez A, Ward-Caviness CK, Brody JA, Chen MH, de Maat MPM, ... ... Tang W, et al. A genome-wide association study identifies new loci for factor VII and implicates factor VII in ischemic stroke etiology. Blood. PMID 30642921 DOI: 10.1182/Blood-2018-05-849240 |
0.383 |
|
2019 |
Maners J, Gill D, Pankratz N, Tang W, Smith NL, Morrison AC, Dehghan A, Vries PSd, Heart Cf. Abstract P106: Genetically Determined Fibrinogen, Gamma Prime Fibrinogen and Risk of Venous Thromboembolism and Ischemic Stroke: Evidence From Mendelian Randomization Circulation. 139. DOI: 10.1161/Circ.139.Suppl_1.P106 |
0.31 |
|
2018 |
Sabater-Lleal M, Huffman JE, de Vries PS, Marten J, Mastrangelo MA, Song C, Pankratz N, Ward-Caviness CK, Yanek LR, Trompet S, Delgado GE, Guo X, Bartz TM, Martinez-Perez A, Germain M, ... ... Tang W, et al. Genome-Wide Association Trans-Ethnic Meta-Analyses Identifies Novel Associations Regulating Coagulation Factor VIII and von Willebrand Factor Plasma Levels. Circulation. PMID 30586737 DOI: 10.1161/Circulationaha.118.034532 |
0.41 |
|
2018 |
Haring B, Selvin E, He X, Coresh J, Steffen LM, Folsom AR, Tang W, Rebholz CM. Adherence to the Dietary Approaches to Stop Hypertension Dietary Pattern and Risk of Abdominal Aortic Aneurysm: Results From the ARIC Study. Journal of the American Heart Association. 7: e009340. PMID 30571386 DOI: 10.1161/Jaha.118.009340 |
0.327 |
|
2018 |
Ward-Caviness CK, Huffman JE, Evertt K, Germain M, Van Dongen J, Hill WD, Jhun MA, Brody JA, Ghanbari M, Du L, Roetker NS, de Vries PS, Waldenberger M, Gieger C, Wolf P, ... ... Tang W, et al. DNA methylation age is associated with an altered hemostatic profile in a multi-ethnic meta-analysis. Blood. PMID 30042098 DOI: 10.1182/Blood-2018-02-831347 |
0.316 |
|
2018 |
Tang W, Yao L, Hoogeveen RC, Alonso A, Couper DJ, Lutsey PL, Steenson CC, Guan W, Hunter DW, Lederle FA, Folsom AR. The Association of Biomarkers of Inflammation and Extracellular Matrix Degradation With the Risk of Abdominal Aortic Aneurysm: The ARIC Study. Angiology. 3319718785278. PMID 29945457 DOI: 10.1177/0003319718785278 |
0.316 |
|
2018 |
Weng LC, Guan W, Steffen LM, Pankow JS, Pankratz N, Chen MH, Cushman M, Basu S, Folsom AR, Tang W. Pleiotropic effects of n-6 and n-3 fatty acid-related genetic variants on circulating hemostatic variables. Thrombosis Research. 168: 53-59. PMID 29902632 DOI: 10.1016/J.Thromres.2018.05.032 |
0.372 |
|
2018 |
Kocarnik JM, Richard M, Graff M, Haessler J, Bien S, Carlson C, Carty CL, Reiner AP, Avery CL, Ballantyne CM, LaCroix AZ, Assimes TL, Barbalic M, Pankratz N, Tang W, et al. Discovery, fine-mapping, and conditional analyses of genetic variants associated with C-reactive protein in multiethnic populations using the Metabochip in the Population Architecture using Genomics and Epidemiology (PAGE) study. Human Molecular Genetics. PMID 29878111 DOI: 10.1093/Hmg/Ddy211 |
0.338 |
|
2018 |
Weng LC, Roetker NS, Lutsey PL, Alonso A, Guan W, Pankow JS, Folsom AR, Steffen LM, Pankratz N, Tang W. Evaluation of the relationship between plasma lipids and abdominal aortic aneurysm: A Mendelian randomization study. Plos One. 13: e0195719. PMID 29649275 DOI: 10.1371/Journal.Pone.0195719 |
0.366 |
|
2018 |
Yao L, Folsom AR, Alonso A, Lutsey PL, Pankow JS, Guan W, Cheng S, Lederle FA, Tang W. Association of carotid atherosclerosis and stiffness with abdominal aortic aneurysm: The atherosclerosis risk in communities (ARIC) study. Atherosclerosis. 270: 110-116. PMID 29407878 DOI: 10.1016/J.Atherosclerosis.2018.01.044 |
0.308 |
|
2018 |
Lutsey PL, Rooney MR, Folsom AR, Michos ED, Alonso A, Tang W. Markers of vitamin D metabolism and incidence of clinically diagnosed abdominal aortic aneurysm: The Atherosclerosis Risk in Communities Study. Vascular Medicine (London, England). 1358863X17751258. PMID 29400142 DOI: 10.1177/1358863X17751258 |
0.35 |
|
2018 |
Jiang X, O'Reilly PF, Aschard H, Hsu YH, Richards JB, Dupuis J, Ingelsson E, Karasik D, Pilz S, Berry D, Kestenbaum B, Zheng J, Luan J, Sofianopoulou E, Streeten EA, ... ... Tang W, et al. Genome-wide association study in 79,366 European-ancestry individuals informs the genetic architecture of 25-hydroxyvitamin D levels. Nature Communications. 9: 260. PMID 29343764 DOI: 10.1038/S41467-017-02662-2 |
0.398 |
|
2018 |
Kubota Y, Folsom AR, Ballantyne CM, Tang W. Lipoprotein(a) and abdominal aortic aneurysm risk: The Atherosclerosis Risk in Communities study. Atherosclerosis. 268: 63-67. PMID 29182987 DOI: 10.1016/J.Atherosclerosis.2017.10.017 |
0.349 |
|
2018 |
Kubota Y, Folsom AR, Pankow JS, Wagenknecht LE, Tang W. Diabetes-Related Factors and Abdominal Aortic Aneurysm (AAA) Events: The Atherosclerotic Risk in Communities Study Journal of Vascular Surgery. 68: 308. DOI: 10.1016/J.Jvs.2018.05.022 |
0.302 |
|
2017 |
Kubota Y, Folsom AR, Pankow JS, Wagenknecht LE, Tang W. Diabetes-related factors and abdominal aortic aneurysm events: the Atherosclerotic Risk in Communities Study. Annals of Epidemiology. PMID 29277551 DOI: 10.1016/J.Annepidem.2017.12.003 |
0.315 |
|
2017 |
Kubota Y, Folsom AR, Matsushita K, Couper D, Tang W. Prospective study of lung function and abdominal aortic aneurysm risk: The Atherosclerosis Risk in Communities study. Atherosclerosis. PMID 29079449 DOI: 10.1016/J.Jvs.2017.11.049 |
0.328 |
|
2017 |
Folsom AR, Roetker NS, Kelley ST, Tang W, Pankratz N. Failure to replicate thrombomodulin genetic variant predictors of venous thromboembolism in African Americans. Blood. PMID 28619983 DOI: 10.1182/Blood-2017-03-771329 |
0.372 |
|
2017 |
Lindström S, Germain M, Crous-Bou M, Smith EN, Morange PE, van Hylckama Vlieg A, de Haan HG, Chasman D, Ridker P, Brody J, de Andrade M, Heit JA, Tang W, DeVivo I, Grodstein F, et al. Assessing the causal relationship between obesity and venous thromboembolism through a Mendelian Randomization study. Human Genetics. PMID 28528403 DOI: 10.1007/S00439-017-1811-X |
0.393 |
|
2017 |
Roetker NS, Armasu SM, Pankow JS, Lutsey PL, Tang W, Rosenberg MA, Palmer TM, MacLehose RF, Heckbert SR, Cushman M, de Andrade M, Folsom AR. Taller height as a risk factor for venous thromboembolism: a Mendelian randomization meta-analysis. Journal of Thrombosis and Haemostasis : Jth. PMID 28445597 DOI: 10.1111/Jth.13719 |
0.373 |
|
2017 |
de Vries PS, Sabater-Lleal M, Chasman DI, Trompet S, Ahluwalia TS, Teumer A, Kleber ME, Chen MH, Wang JJ, Attia JR, Marioni RE, Steri M, Weng LC, Pool R, Grossmann V, ... ... Tang W, et al. Comparison of HapMap and 1000 Genomes Reference Panels in a Large-Scale Genome-Wide Association Study. Plos One. 12: e0167742. PMID 28107422 DOI: 10.1371/Journal.Pone.0167742 |
0.315 |
|
2017 |
Pankow JS, Tang W, Pankratz N, Guan W, Weng LC, Cushman M, Boerwinkle E, Folsom AR. Identification of Genetic Variants Linking Protein C and Lipoprotein Metabolism: The ARIC Study (Atherosclerosis Risk in Communities). Arteriosclerosis, Thrombosis, and Vascular Biology. PMID 28082259 DOI: 10.1161/Atvbaha.116.308109 |
0.343 |
|
2017 |
Sennblad B, Basu S, Mazur J, Suchon P, Martinez-Perez A, van Hylckama Vlieg A, Truong V, Li Y, Gådin JR, Tang W, Grossman V, de Haan HG, Handin N, Silveira A, Souto JC, et al. Genome-wide association study with additional genetic and post-transcriptional analyses reveals novel regulators of plasma factor XI levels. Human Molecular Genetics. PMID 28053049 DOI: 10.1093/Hmg/Ddw401 |
0.402 |
|
2016 |
Robinson-Cohen C, Lutsey PL, Kleber ME, Nielson CM, Mitchell BD, Bis JC, Eny KM, Portas L, Eriksson J, Lorentzon M, Koller DL, Milaneschi Y, Teumer A, Pilz S, Nethander M, ... ... Tang W, et al. Genetic Variants Associated with Circulating Parathyroid Hormone. Journal of the American Society of Nephrology : Jasn. PMID 27927781 DOI: 10.1681/Asn.2016010069 |
0.399 |
|
2016 |
Tang W, Yao L, Roetker NS, Alonso A, Lutsey PL, Steenson CC, Lederle FA, Hunter DW, Bengtson LG, Guan W, Missov E, Folsom AR. Lifetime Risk and Risk Factors for Abdominal Aortic Aneurysm in a 24-Year Prospective Study: The ARIC Study (Atherosclerosis Risk in Communities). Arteriosclerosis, Thrombosis, and Vascular Biology. PMID 27834688 DOI: 10.1161/Atvbaha.116.308147 |
0.35 |
|
2016 |
Berardi C, Wassel CL, Decker PA, Larson NB, Kirsch PS, de Andrade M, Tsai MY, Pankow JS, Sale MM, Sicotte H, Tang W, Hanson NQ, McDermott MM, Criqui MH, Allison MA, et al. Elevated Levels of Adhesion Proteins Are Associated With Low Ankle-Brachial Index: Multi-Ethnic Study of Atherosclerosis. Angiology. PMID 27436494 DOI: 10.1177/0003319716659178 |
0.371 |
|
2016 |
Trégouët DA, Delluc A, Roche A, Derbois C, Olaso R, Germain M, de Andrade M, Tang W, Chasman DI, van Hylckama Vlieg A, Reitsma PH, Kabrhel C, Smith N, Morange PE. Is there still room for additional common susceptibility alleles for venous thromboembolism ? Journal of Thrombosis and Haemostasis : Jth. PMID 27326655 DOI: 10.1111/Jth.13392 |
0.383 |
|
2016 |
Larson NB, Bell EJ, Decker PA, Pike M, Wassel CL, Tsai MY, Pankow JS, Tang W, Hanson NQ, Alexander K, Zakai NA, Cushman M, Bielinski SJ. ABO blood group associations with markers of endothelial dysfunction in the Multi-Ethnic Study of Atherosclerosis. Atherosclerosis. PMID 27298014 DOI: 10.1016/J.Atherosclerosis.2016.05.049 |
0.332 |
|
2016 |
Joshi AD, Andersson C, Buch S, Stender S, Noordam R, Weng LC, Weeke PE, Auer PL, Boehm B, Chen C, Choi H, Curhan G, Denny JC, De Vivo I, Eicher JD, ... ... Tang W, et al. Four Susceptibility Loci for Gallstone Disease Identified in a Meta-analysis of Genome-wide Association Studies. Gastroenterology. PMID 27094239 DOI: 10.1053/J.Gastro.2016.04.007 |
0.427 |
|
2016 |
Pankow JS, Decker PA, Berardi C, Hanson NQ, Sale M, Tang W, Kanaya AM, Larson NB, Tsai MY, Wassel CL, Bielinski SJ. Circulating cellular adhesion molecules and risk of diabetes: the Multi-Ethnic Study of Atherosclerosis (MESA). Diabetic Medicine : a Journal of the British Diabetic Association. PMID 26937608 DOI: 10.1111/Dme.13108 |
0.3 |
|
2016 |
Folsom AR, Tang W, George KM, Heckbert SR, MacLehose RF, Cushman M, Pankow JS. Prospective study of γ' fibrinogen and incident venous thromboembolism: The Longitudinal Investigation of Thromboembolism Etiology (LITE). Thrombosis Research. 139: 44-9. PMID 26916295 DOI: 10.1016/J.Thromres.2016.01.008 |
0.383 |
|
2016 |
Larson NB, Decker PA, Wassel CL, Pankow JS, Tang W, Hanson NQ, Tsai MY, Bielinski SJ. Blood group antigen loci demonstrate multivariate genetic associations with circulating cellular adhesion protein levels in the Multi-Ethnic Study of Atherosclerosis. Human Genetics. PMID 26883866 DOI: 10.1007/S00439-016-1643-0 |
0.411 |
|
2016 |
Yao L, Folsom AR, Pankow JS, Selvin E, Michos ED, Alonso A, Tang W, Lutsey PL. Parathyroid hormone and the risk of incident hypertension: the Atherosclerosis Risk in Communities study. Journal of Hypertension. 34: 196-203. PMID 26867053 DOI: 10.1097/Hjh.0000000000000794 |
0.304 |
|
2015 |
Folsom AR, Tang W, Weng LC, Roetker NS, Cushman M, Basu S, Pankow JS. Replication of a genetic risk score for venous thromboembolism in whites but not in African Americans. Journal of Thrombosis and Haemostasis : Jth. PMID 26565658 DOI: 10.1111/Jth.13193 |
0.376 |
|
2015 |
de Vries PS, Chasman DI, Sabater-Lleal M, Chen MH, Huffman JE, Steri M, Tang W, Teumer A, Marioni RE, Grossmann V, Hottenga JJ, Trompet S, Müller-Nurasyid M, Zhao JH, Brody JA, et al. A meta-analysis of 120,246 individuals identifies 18 new loci for fibrinogen concentration. Human Molecular Genetics. PMID 26561523 DOI: 10.1093/Hmg/Ddv454 |
0.375 |
|
2015 |
Folsom AR, Alonso A, George KM, Roetker NS, Tang W, Cushman M. Prospective study of plasma D-dimer and incident venous thromboembolism: The Atherosclerosis Risk in Communities (ARIC) Study. Thrombosis Research. 136: 781-5. PMID 26337932 DOI: 10.1016/J.Thromres.2015.08.013 |
0.321 |
|
2015 |
Folsom AR, Tang W, Roetker NS, Heckbert SR, Cushman M, Pankow JS. Prospective study of circulating factor XI and incident venous thromboembolism: The Longitudinal Investigation of Thromboembolism Etiology (LITE). American Journal of Hematology. PMID 26260105 DOI: 10.1002/Ajh.24168 |
0.422 |
|
2015 |
Huffman JE, de Vries PS, Morrison AC, Sabater-Lleal M, Kacprowski T, Auer PL, Brody JA, Chasman DI, Chen MH, Guo X, Lin LA, Marioni RE, Müller-Nurasyid M, Yanek LR, Pankratz N, ... ... Tang W, et al. Rare and low-frequency variants and their association with plasma levels of fibrinogen, FVII, FVIII, and vWF. Blood. 126: e19-29. PMID 26105150 DOI: 10.1182/Blood-2015-02-624551 |
0.401 |
|
2015 |
Larson NB, Berardi C, Decker PA, Wassel CL, Kirsch PS, Pankow JS, Sale MM, de Andrade M, Sicotte H, Tang W, Hanson NQ, Tsai MY, Taylor KD, Bielinski SJ. Trans-Ethnic Meta-Analysis Identifies Common and Rare Variants Associated with Hepatocyte Growth Factor Levels in the Multi-Ethnic Study of Atherosclerosis (MESA). Annals of Human Genetics. 79: 264-74. PMID 25998175 DOI: 10.1111/Ahg.12119 |
0.444 |
|
2015 |
Tang W, Cushman M, Green D, Rich SS, Lange LA, Yang Q, Tracy RP, Tofler GH, Basu S, Wilson JG, Keating BJ, Weng LC, Taylor HA, Jacobs DR, Delaney JA, et al. Gene-centric approach identifies new and known loci for FVIII activity and VWF antigen levels in European Americans and African Americans. American Journal of Hematology. 90: 534-40. PMID 25779970 DOI: 10.1002/Ajh.24005 |
0.419 |
|
2015 |
Germain M, Chasman DI, de Haan H, Tang W, Lindström S, Weng LC, de Andrade M, de Visser MC, Wiggins KL, Suchon P, Saut N, Smadja DM, Le Gal G, van Hylckama Vlieg A, Di Narzo A, et al. Meta-analysis of 65,734 individuals identifies TSPAN15 and SLC44A2 as two susceptibility loci for venous thromboembolism. American Journal of Human Genetics. 96: 532-42. PMID 25772935 DOI: 10.1016/J.Ajhg.2015.01.019 |
0.462 |
|
2015 |
Bielinski SJ, Berardi C, Decker PA, Kirsch PS, Larson NB, Pankow JS, Sale M, de Andrade M, Sicotte H, Tang W, Hanson NQ, Wassel CL, Polak JF, Tsai MY. P-selectin and subclinical and clinical atherosclerosis: the Multi-Ethnic Study of Atherosclerosis (MESA). Atherosclerosis. 240: 3-9. PMID 25744700 DOI: 10.1016/J.Atherosclerosis.2015.02.036 |
0.327 |
|
2015 |
Berardi C, Larson NB, Decker PA, Wassel CL, Kirsch PS, Pankow JS, Sale MM, de Andrade M, Sicotte H, Tang W, Hanson NQ, Tsai MY, Chen YD, Bielinski SJ. Multi-ethnic analysis reveals soluble L-selectin may be post-transcriptionally regulated by 3'UTR polymorphism: the Multi-Ethnic Study of Atherosclerosis (MESA). Human Genetics. 134: 393-403. PMID 25576479 DOI: 10.1007/S00439-014-1527-0 |
0.449 |
|
2015 |
Weng LC, Cushman M, Pankow JS, Basu S, Boerwinkle E, Folsom AR, Tang W. A genetic association study of activated partial thromboplastin time in European Americans and African Americans: the ARIC Study. Human Molecular Genetics. 24: 2401-8. PMID 25552651 DOI: 10.1093/Hmg/Ddu732 |
0.406 |
|
2015 |
Folsom AR, Tang W, Roetker NS, Kshirsagar AV, Derebail VK, Lutsey PL, Naik R, Pankow JS, Grove ML, Basu S, Key NS, Cushman M. Prospective study of sickle cell trait and venous thromboembolism incidence. Journal of Thrombosis and Haemostasis : Jth. 13: 2-9. PMID 25393788 DOI: 10.1111/Jth.12787 |
0.319 |
|
2015 |
Lemaitre RN, King IB, Kabagambe EK, Wu JH, McKnight B, Manichaikul A, Guan W, Sun Q, Chasman DI, Foy M, Wang L, Zhu J, Siscovick DS, Tsai MY, Arnett DK, ... ... Tang W, et al. Genetic loci associated with circulating levels of very long-chain saturated fatty acids. Journal of Lipid Research. 56: 176-84. PMID 25378659 DOI: 10.1194/Jlr.M052456 |
0.367 |
|
2015 |
Li S, Miao S, Huang Y, Liu Z, Tian H, Yin X, Tang W, Steffen LM, Xi B. Fruit intake decreases risk of incident type 2 diabetes: an updated meta-analysis. Endocrine. 48: 454-60. PMID 25074631 DOI: 10.1007/S12020-014-0351-6 |
0.317 |
|
2015 |
Tang W, Bell EJ, Roetker NS, Folsom AR, Cushman M. Epidemiology of Thrombosis in Aging Blood. 126: SCI-6-SCI-6. DOI: 10.1182/Blood.V126.23.Sci-6.Sci-6 |
0.36 |
|
2014 |
Baumert J, Huang J, McKnight B, Sabater-Lleal M, Steri M, Chu AY, Trompet S, Lopez LM, Fornage M, Teumer A, Tang W, Rudnicka AR, Mälarstig A, Hottenga JJ, Kavousi M, et al. No evidence for genome-wide interactions on plasma fibrinogen by smoking, alcohol consumption and body mass index: results from meta-analyses of 80,607 subjects. Plos One. 9: e111156. PMID 25551457 DOI: 10.1371/Journal.Pone.0111156 |
0.378 |
|
2014 |
Munir MS, Weng LC, Tang W, Basu S, Pankow JS, Matijevic N, Cushman M, Boerwinkle E, Folsom AR. Genetic markers associated with plasma protein C level in African Americans: the atherosclerosis risk in communities (ARIC) study. Genetic Epidemiology. 38: 709-13. PMID 25376901 DOI: 10.1002/Gepi.21868 |
0.396 |
|
2014 |
Kraja AT, Chasman DI, North KE, Reiner AP, Yanek LR, Kilpeläinen TO, Smith JA, Dehghan A, Dupuis J, Johnson AD, Feitosa MF, Tekola-Ayele F, Chu AY, Nolte IM, Dastani Z, ... ... Tang W, et al. Pleiotropic genes for metabolic syndrome and inflammation. Molecular Genetics and Metabolism. 112: 317-38. PMID 24981077 DOI: 10.1016/J.Ymgme.2014.04.007 |
0.394 |
|
2014 |
Weng LC, Tang W, Rich SS, Smith NL, Redline S, O'Donnell CJ, Basu S, Reiner AP, Delaney JA, Tracy RP, Palmer CD, Young T, Yang Q, Folsom AR, Cushman M. A genetic association study of D-dimer levels with 50K SNPs from a candidate gene chip in four ethnic groups. Thrombosis Research. 134: 462-7. PMID 24908450 DOI: 10.1016/J.Thromres.2014.05.018 |
0.376 |
|
2014 |
Guan W, Steffen BT, Lemaitre RN, Wu JH, Tanaka T, Manichaikul A, Foy M, Rich SS, Wang L, Nettleton JA, Tang W, Gu X, Bandinelli S, King IB, McKnight B, et al. Genome-wide association study of plasma N6 polyunsaturated fatty acids within the cohorts for heart and aging research in genomic epidemiology consortium. Circulation. Cardiovascular Genetics. 7: 321-31. PMID 24823311 DOI: 10.1161/Circgenetics.113.000208 |
0.31 |
|
2014 |
Berardi C, Decker PA, Kirsch PS, de Andrade M, Tsai MY, Pankow JS, Sale MM, Sicotte H, Tang W, Hanson N, Polak JF, Bielinski SJ. Plasma and serum L-selectin and clinical and subclinical cardiovascular disease: the Multi-Ethnic Study of Atherosclerosis (MESA). Translational Research : the Journal of Laboratory and Clinical Medicine. 163: 585-92. PMID 24631064 DOI: 10.1016/J.Trsl.2014.02.001 |
0.338 |
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2014 |
Huang J, Huffman JE, Yamakuchi M, Yamkauchi M, Trompet S, Asselbergs FW, Sabater-Lleal M, Trégouët DA, Chen WM, Smith NL, Kleber ME, Shin SY, Becker DM, Tang W, Dehghan A, et al. Genome-wide association study for circulating tissue plasminogen activator levels and functional follow-up implicates endothelial STXBP5 and STX2. Arteriosclerosis, Thrombosis, and Vascular Biology. 34: 1093-101. PMID 24578379 DOI: 10.1161/Atvbaha.113.302088 |
0.405 |
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2013 |
Tang W, Morrison A, Wasserman BA, Folsom AR, Sun W, Campbell S, Kao WH, Boerwinkle E. Association of SERPINA9 gene variants with carotid artery atherosclerosis: the Atherosclerosis Risk in Communities (ARIC) Carotid MRI Study. International Journal of Molecular Epidemiology and Genetics. 4: 258-67. PMID 24319541 |
0.31 |
|
2013 |
Folsom AR, Pankow JS, Li X, Duprez DA, Jacobs DR, Klein R, Klein B, Tang W, Wong TY, Cotch MF, Taylor KD, Rich SS, Hall JL, Post WS, Rotter JI. No association of 9p21 with arterial elasticity and retinal microvascular findings. Atherosclerosis. 230: 301-3. PMID 24075760 DOI: 10.1016/J.Atherosclerosis.2013.07.049 |
0.366 |
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2013 |
Sabater-Lleal M, Huang J, Chasman D, Naitza S, Dehghan A, Johnson AD, Teumer A, Reiner AP, Folkersen L, Basu S, Rudnicka AR, Trompet S, Mälarstig A, Baumert J, Bis JC, ... ... Tang W, et al. Multiethnic meta-analysis of genome-wide association studies in >100 000 subjects identifies 23 fibrinogen-associated Loci but no strong evidence of a causal association between circulating fibrinogen and cardiovascular disease. Circulation. 128: 1310-24. PMID 23969696 DOI: 10.1161/Circulationaha.113.002251 |
0.432 |
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2013 |
Tang W, Teichert M, Chasman DI, Heit JA, Morange PE, Li G, Pankratz N, Leebeek FW, Paré G, de Andrade M, Tzourio C, Psaty BM, Basu S, Ruiter R, Rose L, et al. A genome-wide association study for venous thromboembolism: the extended cohorts for heart and aging research in genomic epidemiology (CHARGE) consortium. Genetic Epidemiology. 37: 512-21. PMID 23650146 DOI: 10.1002/Gepi.21731 |
0.43 |
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2013 |
Wu JH, Lemaitre RN, Manichaikul A, Guan W, Tanaka T, Foy M, Kabagambe EK, Djousse L, Siscovick D, Fretts AM, Johnson C, King IB, Psaty BM, McKnight B, Rich SS, ... ... Tang W, et al. Genome-wide association study identifies novel loci associated with concentrations of four plasma phospholipid fatty acids in the de novo lipogenesis pathway: results from the Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) consortium. Circulation. Cardiovascular Genetics. 6: 171-83. PMID 23362303 DOI: 10.1161/Circgenetics.112.964619 |
0.372 |
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2013 |
Yu B, Barbalic M, Brautbar A, Nambi V, Hoogeveen RC, Tang W, Mosley TH, Rotter JI, deFilippi CR, O'Donnell CJ, Kathiresan S, Rice K, Heckbert SR, Ballantyne CM, Psaty BM, et al. Association of genome-wide variation with highly sensitive cardiac troponin-T levels in European Americans and Blacks: a meta-analysis from atherosclerosis risk in communities and cardiovascular health studies. Circulation. Cardiovascular Genetics. 6: 82-8. PMID 23247143 DOI: 10.1161/Circgenetics.112.963058 |
0.342 |
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2012 |
Huang J, Sabater-Lleal M, Asselbergs FW, Tregouet D, Shin SY, Ding J, Baumert J, Oudot-Mellakh T, Folkersen L, Johnson AD, Smith NL, Williams SM, Ikram MA, Kleber ME, Becker DM, ... ... Tang W, et al. Genome-wide association study for circulating levels of PAI-1 provides novel insights into its regulation. Blood. 120: 4873-81. PMID 22990020 DOI: 10.1182/Blood-2012-06-436188 |
0.419 |
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2012 |
Folsom AR, Nambi V, Pankow JS, Tang W, Farbakhsh K, Yamagishi K, Boerwinkle E. Effect of 9p21 genetic variation on coronary heart disease is not modified by other risk markers. The Atherosclerosis Risk in Communities (ARIC) Study. Atherosclerosis. 224: 435-9. PMID 22935634 DOI: 10.1016/J.Atherosclerosis.2012.08.007 |
0.396 |
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2012 |
Tang W, Schwienbacher C, Lopez LM, Ben-Shlomo Y, Oudot-Mellakh T, Johnson AD, Samani NJ, Basu S, Gögele M, Davies G, Lowe GD, Tregouet DA, Tan A, Pankow JS, Tenesa A, et al. Genetic associations for activated partial thromboplastin time and prothrombin time, their gene expression profiles, and risk of coronary artery disease. American Journal of Human Genetics. 91: 152-62. PMID 22703881 DOI: 10.1016/J.Ajhg.2012.05.009 |
0.422 |
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2012 |
Qayyum R, Snively BM, Ziv E, Nalls MA, Liu Y, Tang W, Yanek LR, Lange L, Evans MK, Ganesh S, Austin MA, Lettre G, Becker DM, Zonderman AB, Singleton AB, et al. A meta-analysis and genome-wide association study of platelet count and mean platelet volume in african americans. Plos Genetics. 8: e1002491. PMID 22423221 DOI: 10.1371/Journal.Pgen.1002491 |
0.358 |
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2012 |
Smith NL, Heit JA, Tang W, Teichert M, Chasman DI, Morange PE. Genetic variation in F3 (tissue factor) and the risk of incident venous thrombosis: meta-analysis of eight studies. Journal of Thrombosis and Haemostasis : Jth. 10: 719-22. PMID 22340074 DOI: 10.1111/J.1538-7836.2012.04665.X |
0.346 |
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2012 |
Xi B, Tang W, Wang Q. Polymorphism near the ATP2B1 gene is associated with hypertension risk in East Asians: a meta-analysis involving 15 909 cases and 18 529 controls. Blood Pressure. 21: 134-8. PMID 22229515 DOI: 10.3109/08037051.2012.632845 |
0.419 |
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2012 |
Lutsey PL, Rasmussen-Torvik LJ, Pankow JS, Alonso A, Smolenski DJ, Tang W, Coresh J, Volcik KA, Ballantyne CM, Boerwinkle E, Folsom AR. Relation of lipid gene scores to longitudinal trends in lipid levels and incidence of abnormal lipid levels among individuals of European ancestry: the Atherosclerosis Risk in Communities (ARIC) study. Circulation. Cardiovascular Genetics. 5: 73-80. PMID 22057756 DOI: 10.1161/Circgenetics.111.959619 |
0.321 |
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2012 |
Alonso A, Tang W, Agarwal SK, Soliman EZ, Chamberlain AM, Folsom AR. Hemostatic markers are associated with the risk and prognosis of atrial fibrillation: the ARIC study. International Journal of Cardiology. 155: 217-22. PMID 20965585 DOI: 10.1016/J.Ijcard.2010.09.051 |
0.391 |
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2011 |
Gieger C, Radhakrishnan A, Cvejic A, Tang W, Porcu E, Pistis G, Serbanovic-Canic J, Elling U, Goodall AH, Labrune Y, Lopez LM, Mägi R, Meacham S, Okada Y, Pirastu N, ... ... Tang WH, et al. New gene functions in megakaryopoiesis and platelet formation. Nature. 480: 201-8. PMID 22139419 DOI: 10.1038/Nature10659 |
0.307 |
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2011 |
Lemaitre RN, Tanaka T, Tang W, Manichaikul A, Foy M, Kabagambe EK, Nettleton JA, King IB, Weng LC, Bhattacharya S, Bandinelli S, Bis JC, Rich SS, Jacobs DR, Cherubini A, et al. Genetic loci associated with plasma phospholipid n-3 fatty acids: a meta-analysis of genome-wide association studies from the CHARGE Consortium. Plos Genetics. 7: e1002193. PMID 21829377 DOI: 10.1371/Journal.Pgen.1002193 |
0.391 |
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2011 |
Taylor KC, Lange LA, Zabaneh D, Lange E, Keating BJ, Tang W, Smith NL, Delaney JA, Kumari M, Hingorani A, North KE, Kivimaki M, Tracy RP, O'Donnell CJ, Folsom AR, et al. A gene-centric association scan for Coagulation Factor VII levels in European and African Americans: the Candidate Gene Association Resource (CARe) Consortium. Human Molecular Genetics. 20: 3525-34. PMID 21676895 DOI: 10.1093/Hmg/Ddr264 |
0.433 |
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2011 |
Lutsey PL, Cushman M, Heckbert SR, Tang W, Folsom AR. Longer legs are associated with greater risk of incident venous thromboembolism independent of total body height. The Longitudinal Study of Thromboembolism Etiology (LITE). Thrombosis and Haemostasis. 106: 113-20. PMID 21655679 DOI: 10.1160/Th11-02-0100 |
0.376 |
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2011 |
Shimbo D, Muntner P, Mann D, Barr RG, Tang W, Post W, Lima J, Burke G, Bluemke D, Shea S. Association of left ventricular hypertrophy with incident hypertension: the multi-ethnic study of atherosclerosis. American Journal of Epidemiology. 173: 898-905. PMID 21422061 DOI: 10.1093/Aje/Kwq509 |
0.335 |
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2011 |
Campos M, Sun W, Yu F, Barbalic M, Tang W, Chambless LE, Wu KK, Ballantyne C, Folsom AR, Boerwinkle E, Dong JF. Genetic determinants of plasma von Willebrand factor antigen levels: a target gene SNP and haplotype analysis of ARIC cohort. Blood. 117: 5224-30. PMID 21343614 DOI: 10.1182/Blood-2010-08-300152 |
0.379 |
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2011 |
Lynch AI, Tang W, Shi G, Devereux RB, Eckfeldt JH, Arnett DK. Epistatic effects of ACE I/D and AGT gene variants on left ventricular mass in hypertensive patients: the HyperGEN study. Journal of Human Hypertension. 26: 133-40. PMID 21248783 DOI: 10.1038/Jhh.2010.131 |
0.348 |
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2011 |
Smith NL, Rice KM, Bovill EG, Cushman M, Bis JC, McKnight B, Lumley T, Glazer NL, van Hylckama Vlieg A, Tang W, Dehghan A, Strachan DP, O'Donnell CJ, Rotter JI, Heckbert SR, et al. Genetic variation associated with plasma von Willebrand factor levels and the risk of incident venous thrombosis. Blood. 117: 6007-11. PMID 21163921 DOI: 10.1182/Blood-2010-10-315473 |
0.462 |
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2011 |
Lo KS, Wilson JG, Lange LA, Folsom AR, Galarneau G, Ganesh SK, Grant SF, Keating BJ, McCarroll SA, Mohler ER, O'Donnell CJ, Palmas W, Tang W, Tracy RP, Reiner AP, et al. Genetic association analysis highlights new loci that modulate hematological trait variation in Caucasians and African Americans. Human Genetics. 129: 307-17. PMID 21153663 DOI: 10.1007/S00439-010-0925-1 |
0.41 |
|
2011 |
Wassel CL, Lange LA, Keating BJ, Taylor KC, Johnson AD, Palmer C, Ho LA, Smith NL, Lange EM, Li Y, Yang Q, Delaney JA, Tang W, Tofler G, Redline S, et al. Association of genomic loci from a cardiovascular gene SNP array with fibrinogen levels in European Americans and African-Americans from six cohort studies: the Candidate Gene Association Resource (CARe). Blood. 117: 268-75. PMID 20978265 DOI: 10.1182/Blood-2010-06-289546 |
0.44 |
|
2010 |
van Loon JE, Leebeek FW, Deckers JW, Dippel DW, Poldermans D, Strachan DP, Tang W, O'Donnell CJ, Smith NL, de Maat MP. Effect of genetic variations in syntaxin-binding protein-5 and syntaxin-2 on von Willebrand factor concentration and cardiovascular risk. Circulation. Cardiovascular Genetics. 3: 507-12. PMID 21156930 DOI: 10.1161/Circgenetics.110.957407 |
0.42 |
|
2010 |
Tang W, Basu S, Kong X, Pankow JS, Aleksic N, Tan A, Cushman M, Boerwinkle E, Folsom AR. Genome-wide association study identifies novel loci for plasma levels of protein C: the ARIC study. Blood. 116: 5032-6. PMID 20802025 DOI: 10.1182/Blood-2010-05-283739 |
0.396 |
|
2010 |
Smith NL, Chen MH, Dehghan A, Strachan DP, Basu S, Soranzo N, Hayward C, Rudan I, Sabater-Lleal M, Bis JC, de Maat MP, Rumley A, Kong X, Yang Q, Williams FM, ... ... Tang W, et al. Novel associations of multiple genetic loci with plasma levels of factor VII, factor VIII, and von Willebrand factor: The CHARGE (Cohorts for Heart and Aging Research in Genome Epidemiology) Consortium. Circulation. 121: 1382-92. PMID 20231535 DOI: 10.1161/Circulationaha.109.869156 |
0.384 |
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2010 |
Tang W, Apostol G, Schreiner PJ, Jacobs DR, Boerwinkle E, Fornage M. Associations of lipoprotein lipase gene polymorphisms with longitudinal plasma lipid trends in young adults: The Coronary Artery Risk Development in Young Adults (CARDIA) study. Circulation. Cardiovascular Genetics. 3: 179-86. PMID 20150529 DOI: 10.1161/Circgenetics.109.913426 |
0.411 |
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2010 |
Tang W, Cushman M, Basu S, Green D, Reiner AP, Delaney JA, Lange LA, Smith NL, Tracy RP, Wilson JG, Tofler G, Yang Q, Keating BJ, Taylor H, Jacobs D, et al. Gene-Centric Approach Identifies New and Known Loci for Factor VIII Activity and Von Willebrand Factor Antigen In the Candidate Gene Association Resource (CARe) Consortium Blood. 116: 806-806. DOI: 10.1182/Blood.V116.21.806.806 |
0.421 |
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2010 |
Tang W, Cushman M, Schwienbacher C, López LM, Ben-Shlomo Y, Basu S, Gögele M, Davies G, Lowe G, Pankow JS, Tenesa A, Volpato C, Rumley A, Gow A, Minelli C, et al. Genome-Wide Association Study Identifies Multiple Genetic Loci for Activated Partial Thromboplastin Time and Prothrombin Time Blood. 116: 4222-4222. DOI: 10.1182/Blood.V116.21.4222.4222 |
0.398 |
|
2009 |
Dehghan A, Yang Q, Peters A, Basu S, Bis JC, Rudnicka AR, Kavousi M, Chen MH, Baumert J, Lowe GD, McKnight B, Tang W, de Maat M, Larson MG, Eyhermendy S, et al. Association of novel genetic Loci with circulating fibrinogen levels: a genome-wide association study in 6 population-based cohorts. Circulation. Cardiovascular Genetics. 2: 125-33. PMID 20031576 DOI: 10.1161/Circgenetics.108.825224 |
0.391 |
|
2009 |
Tsai AK, Li N, Hanson NQ, Tsai MY, Tang W. Associations of genetic polymorphisms of arachidonate 5-lipoxygenase-activating protein with risk of coronary artery disease in a European-American population. Atherosclerosis. 207: 487-91. PMID 19596330 DOI: 10.1016/J.Atherosclerosis.2009.06.018 |
0.433 |
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2009 |
Arnett DK, Devereux RB, Rao DC, Li N, Tang W, Kraemer R, Claas SA, Leon JM, Broeckel U. Novel genetic variants contributing to left ventricular hypertrophy: the HyperGEN study. Journal of Hypertension. 27: 1585-93. PMID 19593212 DOI: 10.1097/Hjh.0B013E32832Be612 |
0.34 |
|
2009 |
Arnett DK, Li N, Tang W, Rao DC, Devereux RB, Claas SA, Kraemer R, Broeckel U. Genome-wide association study identifies single-nucleotide polymorphism in KCNB1 associated with left ventricular mass in humans: the HyperGEN Study. Bmc Medical Genetics. 10: 43. PMID 19454037 DOI: 10.1186/1471-2350-10-43 |
0.394 |
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2008 |
Kraja AT, Huang P, Tang W, Hunt SC, North KE, Lewis CE, Devereux RB, de Simone G, Arnett DK, Rice T, Rao DC. QTLs of factors of the metabolic syndrome and echocardiographic phenotypes: the hypertension genetic epidemiology network study. Bmc Medical Genetics. 9: 103. PMID 19038053 DOI: 10.1186/1471-2350-9-103 |
0.337 |
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2008 |
Huang P, Kraja AT, Tang W, Hunt SC, North KE, Lewis CE, Devereux RB, de Simone G, Arnett DK, Rice T, Rao DC. Factor relationships of metabolic syndrome and echocardiographic phenotypes in the HyperGEN study. Journal of Hypertension. 26: 1360-6. PMID 18551011 DOI: 10.1097/Hjh.0B013E3282Ffdc80 |
0.36 |
|
2008 |
Djoussé L, Kochar J, Hunt SC, North KE, Gu CC, Tang W, Arnett DK, Devereux RB. Relation of albuminuria to left ventricular mass (from the HyperGEN Study). The American Journal of Cardiology. 101: 212-6. PMID 18178409 DOI: 10.1016/J.Amjcard.2007.07.065 |
0.317 |
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2007 |
de Simone G, Tang W, Devereux RB, Hunt SC, Kitzman DW, Rao D, Arnett DK. Assessment of the interaction of heritability of volume load and left ventricular mass: the HyperGEN offspring study. Journal of Hypertension. 25: 1397-402. PMID 17563561 DOI: 10.1097/Hjh.0B013E328126851E |
0.333 |
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2007 |
Bella JN, Tang W, Kraja A, Rao DC, Hunt SC, Miller MB, Palmieri V, Roman MJ, Kitzman DW, Oberman A, Devereux RB, Arnett DK. Genome-wide linkage mapping for valve calcification susceptibility loci in hypertensive sibships: the Hypertension Genetic Epidemiology Network Study. Hypertension. 49: 453-60. PMID 17224468 DOI: 10.1161/01.Hyp.0000256957.10242.75 |
0.328 |
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2006 |
Kraja AT, Borecki IB, North K, Tang W, Myers RH, Hopkins PN, Arnett D, Corbett J, Adelman A, Province MA. Longitudinal and age trends of metabolic syndrome and its risk factors: the Family Heart Study. Nutrition & Metabolism. 3: 41. PMID 17147796 DOI: 10.1186/1743-7075-3-41 |
0.304 |
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2006 |
Bielinski SJ, Tang W, Pankow JS, Miller MB, Mosley TH, Boerwinkle E, Olshen RA, Curb JD, Jaquish CE, Rao DC, Weder A, Arnett DK. Genome-wide linkage scans for loci affecting total cholesterol, HDL-C, and triglycerides: the Family Blood Pressure Program. Human Genetics. 120: 371-80. PMID 16868761 DOI: 10.1007/S00439-006-0223-0 |
0.323 |
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2006 |
Tang W, Arnett DK, Province MA, Lewis CE, North K, Carr JJ, Pankow JS, Hopkins PN, Devereux RB, Wilk JB, Wagenknecht L. Racial differences in the association of coronary calcified plaque with left ventricular hypertrophy: the National Heart, Lung, and Blood Institute Family Heart Study and Hypertension Genetic Epidemiology Network. The American Journal of Cardiology. 97: 1441-8. PMID 16679080 DOI: 10.1016/J.Amjcard.2005.11.076 |
0.331 |
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2006 |
Tang W, Hong Y, Province MA, Rich SS, Hopkins PN, Arnett DK, Pankow JS, Miller MB, Eckfeldt JH. Familial clustering for features of the metabolic syndrome: the National Heart, Lung, and Blood Institute (NHLBI) Family Heart Study. Diabetes Care. 29: 631-6. PMID 16505518 DOI: 10.2337/Diacare.29.03.06.Dc05-0679 |
0.347 |
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2005 |
Tang W, Arnett DK, Devereux RB, Panagiotou D, Province MA, Miller MB, de Simone G, Gu C, Ferrell RE. Identification of a novel 5-base pair deletion in calcineurin B (PPP3R1) promoter region and its association with left ventricular hypertrophy. American Heart Journal. 150: 845-51. PMID 16209992 DOI: 10.1016/J.Ahj.2004.12.004 |
0.362 |
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2003 |
Tang W, Miller MB, Rich SS, North KE, Pankow JS, Borecki IB, Myers RH, Hopkins PN, Leppert M, Arnett DK. Linkage analysis of a composite factor for the multiple metabolic syndrome: the National Heart, Lung, and Blood Institute Family Heart Study. Diabetes. 52: 2840-7. PMID 14578304 DOI: 10.2337/Diabetes.52.11.2840 |
0.349 |
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2002 |
Tang W, Arnett DK, Devereux RB, Atwood LD, Kitzman DW, Rao DC. Linkage of left ventricular early diastolic peak filling velocity to chromosome 5 in hypertensive African Americans: the HyperGEN echocardiography study. American Journal of Hypertension. 15: 621-7. PMID 12118910 DOI: 10.1016/S0895-7061(02)02943-6 |
0.301 |
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