Harvard Catalyst Profiles

Contact, publication, and social network information about Harvard faculty and fellows.

Dan Chasman, Ph.D.

Co-Author

This page shows the publications co-authored by Dan Chasman and Paul Ridker.
Connection Strength

19.856
  1. Genetic determinants of statin-induced low-density lipoprotein cholesterol reduction: the Justification for the Use of Statins in Prevention: an Intervention Trial Evaluating Rosuvastatin (JUPITER) trial. Circ Cardiovasc Genet. 2012 Apr 01; 5(2):257-64.
    View in: PubMed
    Score: 0.508
  2. Kinesin-like protein 6 (KIF6) polymorphism and the efficacy of rosuvastatin in primary prevention. Circ Cardiovasc Genet. 2011 Jun; 4(3):312-7.
    View in: PubMed
    Score: 0.479
  3. Forty-three loci associated with plasma lipoprotein size, concentration, and cholesterol content in genome-wide analysis. PLoS Genet. 2009 Nov; 5(11):e1000730.
    View in: PubMed
    Score: 0.435
  4. Polymorphism in the CETP gene region, HDL cholesterol, and risk of future myocardial infarction: Genomewide analysis among 18 245 initially healthy women from the Women's Genome Health Study. Circ Cardiovasc Genet. 2009 Feb; 2(1):26-33.
    View in: PubMed
    Score: 0.411
  5. Population-based genomewide genetic analysis of common clinical chemistry analytes. Clin Chem. 2009 Jan; 55(1):39-51.
    View in: PubMed
    Score: 0.406
  6. Genetic loci associated with plasma concentration of low-density lipoprotein cholesterol, high-density lipoprotein cholesterol, triglycerides, apolipoprotein A1, and Apolipoprotein B among 6382 white women in genome-wide analysis with replication. Circ Cardiovasc Genet. 2008 Oct; 1(1):21-30.
    View in: PubMed
    Score: 0.402
  7. Polymorphism in the apolipoprotein(a) gene, plasma lipoprotein(a), cardiovascular disease, and low-dose aspirin therapy. Atherosclerosis. 2009 Apr; 203(2):371-6.
    View in: PubMed
    Score: 0.397
  8. Loci related to metabolic-syndrome pathways including LEPR,HNF1A, IL6R, and GCKR associate with plasma C-reactive protein: the Women's Genome Health Study. Am J Hum Genet. 2008 May; 82(5):1185-92.
    View in: PubMed
    Score: 0.390
  9. Qualitative and quantitative effects of APOE genetic variation on plasma C-reactive protein, LDL-cholesterol, and apoE protein. Genes Immun. 2006 Apr; 7(3):211-9.
    View in: PubMed
    Score: 0.338
  10. Pharmacogenetics: the outlook for genetic testing in statin therapy. Nat Clin Pract Cardiovasc Med. 2005 Jan; 2(1):2-3.
    View in: PubMed
    Score: 0.310
  11. Pharmacogenetic study of statin therapy and cholesterol reduction. JAMA. 2004 Jun 16; 291(23):2821-7.
    View in: PubMed
    Score: 0.298
  12. Phenotypic and Genotypic Associations Between Migraine and Lipoprotein Subtractions. Neurology. 2021 Oct 11.
    View in: PubMed
    Score: 0.248
  13. Association Between Hemostatic Profile and Migraine: A Mendelian Randomization Analysis. Neurology. 2021 05 18; 96(20):e2481-e2487.
    View in: PubMed
    Score: 0.239
  14. Association of Genetic Variants With Migraine Subclassified by Clinical Symptoms in Adult Females. Front Neurol. 2020; 11:617472.
    View in: PubMed
    Score: 0.237
  15. Hypothyroidism and Kidney Function: A Mendelian Randomization Study. Thyroid. 2020 03; 30(3):365-379.
    View in: PubMed
    Score: 0.221
  16. COMT and Alpha-Tocopherol Effects in Cancer Prevention: Gene-Supplement Interactions in Two Randomized Clinical Trials. J Natl Cancer Inst. 2019 07 01; 111(7):684-694.
    View in: PubMed
    Score: 0.212
  17. Assessment of the Relationship Between Genetic Determinants of Thyroid Function and Atrial Fibrillation: A Mendelian Randomization Study. JAMA Cardiol. 2019 02 01; 4(2):144-152.
    View in: PubMed
    Score: 0.206
  18. Gene-Based Elevated Triglycerides and Type 2 Diabetes Mellitus Risk in the Women's Genome Health Study. Arterioscler Thromb Vasc Biol. 2019 01; 39(1):97-106.
    View in: PubMed
    Score: 0.204
  19. Family History of MI, Smoking, and Risk of Periodontal Disease. J Dent Res. 2018 09; 97(10):1106-1113.
    View in: PubMed
    Score: 0.197
  20. A Large-Scale Multi-ancestry Genome-wide Study Accounting for Smoking Behavior Identifies Multiple Significant Loci for Blood Pressure. Am J Hum Genet. 2018 03 01; 102(3):375-400.
    View in: PubMed
    Score: 0.192
  21. Adiposity and Genetic Factors in Relation to Triglycerides and Triglyceride-Rich Lipoproteins in the Women's Genome Health Study. Clin Chem. 2018 01; 64(1):231-241.
    View in: PubMed
    Score: 0.189
  22. Meta-analysis identifies common and rare variants influencing blood pressure and overlapping with metabolic trait loci. Nat Genet. 2016 10; 48(10):1162-70.
    View in: PubMed
    Score: 0.174
  23. Catechol-O-methyltransferase association with hemoglobin A1c. Metabolism. 2016 07; 65(7):961-967.
    View in: PubMed
    Score: 0.169
  24. Are Genetic Tests for Atherosclerosis Ready for Routine Clinical Use? Circ Res. 2016 Feb 19; 118(4):607-19.
    View in: PubMed
    Score: 0.168
  25. Differential Genetic Effects on Statin-Induced Changes Across Low-Density Lipoprotein-Related Measures. Circ Cardiovasc Genet. 2015 Oct; 8(5):688-95.
    View in: PubMed
    Score: 0.162
  26. Correction: Selectivity in Genetic Association with Sub-classified Migraine in Women. PLoS Genet. 2015 Jun; 11(6):e1005330.
    View in: PubMed
    Score: 0.160
  27. Cardiovascular risks associated with incident and prevalent periodontal disease. J Clin Periodontol. 2015 Jan; 42(1):21-8.
    View in: PubMed
    Score: 0.155
  28. Genome-wide meta-analysis identifies six novel loci associated with habitual coffee consumption. Mol Psychiatry. 2015 May; 20(5):647-656.
    View in: PubMed
    Score: 0.152
  29. Polymorphisms in catechol-O-methyltransferase modify treatment effects of aspirin on risk of cardiovascular disease. Arterioscler Thromb Vasc Biol. 2014 Sep; 34(9):2160-7.
    View in: PubMed
    Score: 0.150
  30. Plasma levels of the proinflammatory chitin-binding glycoprotein YKL-40, variation in the chitinase 3-like 1 gene (CHI3L1), and incident cardiovascular events. J Am Heart Assoc. 2014 Jun 23; 3(3):e000897.
    View in: PubMed
    Score: 0.149
  31. Selectivity in genetic association with sub-classified migraine in women. PLoS Genet. 2014 May; 10(5):e1004366.
    View in: PubMed
    Score: 0.149
  32. Catechol-O-methyltransferase Associated Risk of Cardiovascular Disease Is Modified by Treatment with Vitamin E. J Altern Complement Med. 2014 May; 20(5):A3.
    View in: PubMed
    Score: 0.148
  33. Lack of association between SLCO1B1 polymorphisms and clinical myalgia following rosuvastatin therapy. Am Heart J. 2013 Jun; 165(6):1008-14.
    View in: PubMed
    Score: 0.137
  34. Genetic variation of fifteen folate metabolic pathway associated gene loci and the risk of incident head and neck carcinoma: the Women's Genome Health Study. Clin Chim Acta. 2013 Mar 15; 418:33-6.
    View in: PubMed
    Score: 0.135
  35. Genome-wide association study evaluating lipoprotein-associated phospholipase A2 mass and activity at baseline and after rosuvastatin therapy. Circ Cardiovasc Genet. 2012 Dec; 5(6):676-85.
    View in: PubMed
    Score: 0.133
  36. Integration of genome-wide association studies with biological knowledge identifies six novel genes related to kidney function. Hum Mol Genet. 2012 Dec 15; 21(24):5329-43.
    View in: PubMed
    Score: 0.132
  37. Pharmacogenetic determinants of statin-induced reductions in C-reactive protein. Circ Cardiovasc Genet. 2012 Feb 01; 5(1):58-65.
    View in: PubMed
    Score: 0.126
  38. Genome-wide association study reveals three susceptibility loci for common migraine in the general population. Nat Genet. 2011 Jun 12; 43(7):695-8.
    View in: PubMed
    Score: 0.121
  39. Genetic variants of 11 telomere-pathway gene loci and the risk of incident type 2 diabetes mellitus: the Women's Genome Health Study. Atherosclerosis. 2011 Sep; 218(1):144-6.
    View in: PubMed
    Score: 0.121
  40. Genome-wide association analysis of soluble ICAM-1 concentration reveals novel associations at the NFKBIK, PNPLA3, RELA, and SH2B3 loci. PLoS Genet. 2011 Apr; 7(4):e1001374.
    View in: PubMed
    Score: 0.120
  41. Meta-analysis of genome-wide association studies in >80 000 subjects identifies multiple loci for C-reactive protein levels. Circulation. 2011 Feb 22; 123(7):731-8.
    View in: PubMed
    Score: 0.118
  42. Discovery and replication of novel blood pressure genetic loci in the Women's Genome Health Study. J Hypertens. 2011 Jan; 29(1):62-9.
    View in: PubMed
    Score: 0.117
  43. Mitochondrial uncoupling protein gene cluster variation (UCP2-UCP3) and the risk of incident type 2 diabetes mellitus: the Women's Genome Health Study. Atherosclerosis. 2011 Jan; 214(1):107-9.
    View in: PubMed
    Score: 0.116
  44. Genetic variants in eleven telomere-associated genes and the risk of incident cardio/cerebrovascular disease: The Women's Genome Health Study. Clin Chim Acta. 2011 Jan 14; 412(1-2):199-202.
    View in: PubMed
    Score: 0.116
  45. On the use of variance per genotype as a tool to identify quantitative trait interaction effects: a report from the Women's Genome Health Study. PLoS Genet. 2010 Jun 17; 6(6):e1000981.
    View in: PubMed
    Score: 0.113
  46. Association between a literature-based genetic risk score and cardiovascular events in women. JAMA. 2010 Feb 17; 303(7):631-7.
    View in: PubMed
    Score: 0.111
  47. Genome-wide association studies identify loci associated with age at menarche and age at natural menopause. Nat Genet. 2009 Jun; 41(6):724-8.
    View in: PubMed
    Score: 0.105
  48. Novel associations of CPS1, MUT, NOX4, and DPEP1 with plasma homocysteine in a healthy population: a genome-wide evaluation of 13 974 participants in the Women's Genome Health Study. Circ Cardiovasc Genet. 2009 Apr; 2(2):142-50.
    View in: PubMed
    Score: 0.104
  49. Novel loci, including those related to Crohn disease, psoriasis, and inflammation, identified in a genome-wide association study of fibrinogen in 17 686 women: the Women's Genome Health Study. Circ Cardiovasc Genet. 2009 Apr; 2(2):134-41.
    View in: PubMed
    Score: 0.103
  50. Cardiovascular disease risk prediction with and without knowledge of genetic variation at chromosome 9p21.3. Ann Intern Med. 2009 Jan 20; 150(2):65-72.
    View in: PubMed
    Score: 0.103
  51. Novel association of HK1 with glycated hemoglobin in a non-diabetic population: a genome-wide evaluation of 14,618 participants in the Women's Genome Health Study. PLoS Genet. 2008 Dec; 4(12):e1000312.
    View in: PubMed
    Score: 0.102
  52. Novel association of ABO histo-blood group antigen with soluble ICAM-1: results of a genome-wide association study of 6,578 women. PLoS Genet. 2008 Jul 04; 4(7):e1000118.
    View in: PubMed
    Score: 0.099
  53. A kinesin family member 6 variant is associated with coronary heart disease in the Women's Health Study. J Am Coll Cardiol. 2008 Jan 29; 51(4):444-8.
    View in: PubMed
    Score: 0.096
  54. Rationale, design, and methodology of the Women's Genome Health Study: a genome-wide association study of more than 25,000 initially healthy american women. Clin Chem. 2008 Feb; 54(2):249-55.
    View in: PubMed
    Score: 0.095
  55. Purinergic receptor P2Y, G-protein coupled, 12 gene variants and risk of incident ischemic stroke, myocardial infarction, and venous thromboembolism. Atherosclerosis. 2008 Apr; 197(2):694-9.
    View in: PubMed
    Score: 0.093
  56. Influence of genetic variation in the C-reactive protein gene on the inflammatory response during and after acute coronary ischemia. Ann Hum Genet. 2006 Nov; 70(Pt 6):705-16.
    View in: PubMed
    Score: 0.088
  57. Tryptophanyl-tRNA synthetase gene polymorphisms and risk of incident myocardial infarction. Atherosclerosis. 2005 Jul; 181(1):137-41.
    View in: PubMed
    Score: 0.078
  58. The genomics of heart failure: design and rationale of the HERMES consortium. ESC Heart Fail. 2021 Sep 03.
    View in: PubMed
    Score: 0.062
  59. Genetic insights into biological mechanisms governing human ovarian ageing. Nature. 2021 08; 596(7872):393-397.
    View in: PubMed
    Score: 0.061
  60. Sugar-Sweetened Beverage Consumption May Modify Associations Between Genetic Variants in the CHREBP (Carbohydrate Responsive Element Binding Protein) Locus and HDL-C (High-Density Lipoprotein Cholesterol) and Triglyceride Concentrations. Circ Genom Precis Med. 2021 08; 14(4):e003288.
    View in: PubMed
    Score: 0.061
  61. The trans-ancestral genomic architecture of glycemic traits. Nat Genet. 2021 06; 53(6):840-860.
    View in: PubMed
    Score: 0.060
  62. Publisher Correction: Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals. Nat Genet. 2021 May; 53(5):762.
    View in: PubMed
    Score: 0.060
  63. Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals. Nat Genet. 2020 12; 52(12):1314-1332.
    View in: PubMed
    Score: 0.058
  64. Genetic loci associated with prevalent and incident myocardial infarction and coronary heart disease in the Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium. PLoS One. 2020; 15(11):e0230035.
    View in: PubMed
    Score: 0.058
  65. Association of the Mediterranean Diet With Onset of Diabetes in the Women's Health Study. JAMA Netw Open. 2020 11 02; 3(11):e2025466.
    View in: PubMed
    Score: 0.058
  66. Genetic Studies of Leptin Concentrations Implicate Leptin in the Regulation of Early Adiposity. Diabetes. 2020 12; 69(12):2806-2818.
    View in: PubMed
    Score: 0.057
  67. Role of Rare and Low-Frequency Variants in Gene-Alcohol Interactions on Plasma Lipid Levels. Circ Genom Precis Med. 2020 08; 13(4):e002772.
    View in: PubMed
    Score: 0.056
  68. Smoking-by-genotype interaction in type 2 diabetes risk and fasting glucose. PLoS One. 2020; 15(5):e0230815.
    View in: PubMed
    Score: 0.056
  69. Mendelian randomization analysis does not support causal associations of birth weight with hypertension risk and blood pressure in adulthood. Eur J Epidemiol. 2020 Jul; 35(7):685-697.
    View in: PubMed
    Score: 0.056
  70. Gene-educational attainment interactions in a multi-ancestry genome-wide meta-analysis identify novel blood pressure loci. Mol Psychiatry. 2021 06; 26(6):2111-2125.
    View in: PubMed
    Score: 0.056
  71. Additive and Multiplicative Interactions Between Genetic Risk Score and Family History and Lifestyle in Relation to Risk of Type 2 Diabetes. Am J Epidemiol. 2020 05 05; 189(5):445-460.
    View in: PubMed
    Score: 0.056
  72. Genome-wide association and Mendelian randomisation analysis provide insights into the pathogenesis of heart failure. Nat Commun. 2020 01 09; 11(1):163.
    View in: PubMed
    Score: 0.055
  73. Catechol-O-Methyltransferase and Cardiovascular Disease: MESA. J Am Heart Assoc. 2019 12 17; 8(24):e014986.
    View in: PubMed
    Score: 0.055
  74. Genomic and transcriptomic association studies identify 16 novel susceptibility loci for venous thromboembolism. Blood. 2019 11 07; 134(19):1645-1657.
    View in: PubMed
    Score: 0.054
  75. Genetic variation at the coronary artery disease risk locus GUCY1A3 modifies cardiovascular disease prevention effects of aspirin. Eur Heart J. 2019 11 01; 40(41):3385-3392.
    View in: PubMed
    Score: 0.054
  76. Associations of autozygosity with a broad range of human phenotypes. Nat Commun. 2019 10 31; 10(1):4957.
    View in: PubMed
    Score: 0.054
  77. Phenome-wide association analysis of LDL-cholesterol lowering genetic variants in PCSK9. BMC Cardiovasc Disord. 2019 10 29; 19(1):240.
    View in: PubMed
    Score: 0.054
  78. Genome-wide association and epidemiological analyses reveal common genetic origins between uterine leiomyomata and endometriosis. Nat Commun. 2019 10 24; 10(1):4857.
    View in: PubMed
    Score: 0.054
  79. Exome-Derived Adiponectin-Associated Variants Implicate Obesity and Lipid Biology. Am J Hum Genet. 2019 Sep 05; 105(3):670-671.
    View in: PubMed
    Score: 0.054
  80. Association of Birth Weight With Type 2 Diabetes and Glycemic Traits: A Mendelian Randomization Study. JAMA Netw Open. 2019 09 04; 2(9):e1910915.
    View in: PubMed
    Score: 0.054
  81. A multi-ancestry genome-wide study incorporating gene-smoking interactions identifies multiple new loci for pulse pressure and mean arterial pressure. Hum Mol Genet. 2019 08 01; 28(15):2615-2633.
    View in: PubMed
    Score: 0.053
  82. Quality of dietary fat and genetic risk of type 2 diabetes: individual participant data meta-analysis. BMJ. 2019 07 25; 366:l4292.
    View in: PubMed
    Score: 0.053
  83. Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity. Nat Genet. 2019 Jul; 51(7):1191-1192.
    View in: PubMed
    Score: 0.053
  84. Publisher Correction: Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes. Nat Genet. 2019 Jul; 51(7):1192-1193.
    View in: PubMed
    Score: 0.053
  85. Genome-wide analysis of dental caries and periodontitis combining clinical and self-reported data. Nat Commun. 2019 06 24; 10(1):2773.
    View in: PubMed
    Score: 0.053
  86. COMT Effects on Vitamin E and Colorectal Cancer, in-vitro and in Two Randomized Trials (P15-005-19). Curr Dev Nutr. 2019 Jun; 3(Suppl 1).
    View in: PubMed
    Score: 0.053
  87. Exome-Derived Adiponectin-Associated Variants Implicate Obesity and Lipid Biology. Am J Hum Genet. 2019 07 03; 105(1):15-28.
    View in: PubMed
    Score: 0.053
  88. Group IIA Secretory Phospholipase A2, Vascular Inflammation, and Incident Cardiovascular Disease. Arterioscler Thromb Vasc Biol. 2019 06; 39(6):1182-1190.
    View in: PubMed
    Score: 0.053
  89. Multiancestry Genome-Wide Association Study of Lipid Levels Incorporating Gene-Alcohol Interactions. Am J Epidemiol. 2019 06 01; 188(6):1033-1054.
    View in: PubMed
    Score: 0.053
  90. A catalog of genetic loci associated with kidney function from analyses of a million individuals. Nat Genet. 2019 06; 51(6):957-972.
    View in: PubMed
    Score: 0.053
  91. Mendelian randomization evaluation of causal effects of fibrinogen on incident coronary heart disease. PLoS One. 2019; 14(5):e0216222.
    View in: PubMed
    Score: 0.052
  92. Multi-ancestry genome-wide gene-smoking interaction study of 387,272 individuals identifies new loci associated with serum lipids. Nat Genet. 2019 04; 51(4):636-648.
    View in: PubMed
    Score: 0.052
  93. Protein-coding variants implicate novel genes related to lipid homeostasis contributing to body-fat distribution. Nat Genet. 2019 03; 51(3):452-469.
    View in: PubMed
    Score: 0.052
  94. Multi-ancestry study of blood lipid levels identifies four loci interacting with physical activity. Nat Commun. 2019 01 22; 10(1):376.
    View in: PubMed
    Score: 0.051
  95. A large-scale exome array analysis of venous thromboembolism. Genet Epidemiol. 2019 06; 43(4):449-457.
    View in: PubMed
    Score: 0.051
  96. Associations of Mitochondrial and Nuclear Mitochondrial Variants and Genes with Seven Metabolic Traits. Am J Hum Genet. 2019 01 03; 104(1):112-138.
    View in: PubMed
    Score: 0.051
  97. Trans-ethnic association study of blood pressure determinants in over 750,000 individuals. Nat Genet. 2019 01; 51(1):51-62.
    View in: PubMed
    Score: 0.051
  98. Assessment of Risk Factors and Biomarkers Associated With Risk of Cardiovascular Disease Among Women Consuming a Mediterranean Diet. JAMA Netw Open. 2018 12 07; 1(8):e185708.
    View in: PubMed
    Score: 0.051
  99. Publisher Correction: Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits. Nat Genet. 2018 12; 50(12):1755.
    View in: PubMed
    Score: 0.051
  100. Genome Analyses of >200,000 Individuals Identify 58 Loci for Chronic Inflammation and Highlight Pathways that Link Inflammation and Complex Disorders. Am J Hum Genet. 2018 11 01; 103(5):691-706.
    View in: PubMed
    Score: 0.051
  101. Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits. Nat Genet. 2018 10; 50(10):1412-1425.
    View in: PubMed
    Score: 0.050
  102. Genome-wide meta-analysis of macronutrient intake of 91,114 European ancestry participants from the cohorts for heart and aging research in genomic epidemiology consortium. Mol Psychiatry. 2019 12; 24(12):1920-1932.
    View in: PubMed
    Score: 0.049
  103. Novel genetic associations for blood pressure identified via gene-alcohol interaction in up to 570K individuals across multiple ancestries. PLoS One. 2018; 13(6):e0198166.
    View in: PubMed
    Score: 0.049
  104. Multi-ethnic genome-wide association study for atrial fibrillation. Nat Genet. 2018 06 11; 50(9):1225-1233.
    View in: PubMed
    Score: 0.049
  105. Correction to: Assessing the causal relationship between obesity and venous thromboembolism through a Mendelian Randomization study. Hum Genet. 2018 05; 137(5):429.
    View in: PubMed
    Score: 0.049
  106. Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity. Nat Genet. 2018 05; 50(5):765-766.
    View in: PubMed
    Score: 0.049
  107. Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity. Nat Genet. 2018 05; 50(5):766-767.
    View in: PubMed
    Score: 0.049
  108. Homocysteine, B Vitamins, MTHFR Genotype, and Incident Age-related Macular Degeneration. Ophthalmol Retina. 2018 May; 2(5):508-510.
    View in: PubMed
    Score: 0.049
  109. Analysis of predicted loss-of-function variants in UK Biobank identifies variants protective for disease. Nat Commun. 2018 04 24; 9(1):1613.
    View in: PubMed
    Score: 0.049
  110. Gene Variation of Endoplasmic Reticulum Aminopeptidases 1 and 2, and Risk of Blood Pressure Progression and Incident Hypertension among 17,255 Initially Healthy Women. Int J Genomics. 2018; 2018:2308585.
    View in: PubMed
    Score: 0.049
  111. Refining the accuracy of validated target identification through coding variant fine-mapping in type 2 diabetes. Nat Genet. 2018 04; 50(4):559-571.
    View in: PubMed
    Score: 0.049
  112. Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes. Nat Genet. 2018 04; 50(4):524-537.
    View in: PubMed
    Score: 0.048
  113. Association between Vitamin D Genetic Risk Score and Cancer Risk in a Large Cohort of U.S. Women. Nutrients. 2018 Jan 09; 10(1).
    View in: PubMed
    Score: 0.048
  114. Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity. Nat Genet. 2018 01; 50(1):26-41.
    View in: PubMed
    Score: 0.048
  115. A common missense variant of LILRB5 is associated with statin intolerance and myalgia. Eur Heart J. 2017 12 21; 38(48):3569-3575.
    View in: PubMed
    Score: 0.048
  116. Genome-wide association meta-analysis of fish and EPA+DHA consumption in 17 US and European cohorts. PLoS One. 2017; 12(12):e0186456.
    View in: PubMed
    Score: 0.048
  117. Residual Risk of Atherosclerotic Cardiovascular Events in Relation to Reductions in Very-Low-Density Lipoproteins. J Am Heart Assoc. 2017 Dec 09; 6(12).
    View in: PubMed
    Score: 0.047
  118. Exome-wide association study of plasma lipids in >300,000 individuals. Nat Genet. 2017 Dec; 49(12):1758-1766.
    View in: PubMed
    Score: 0.047
  119. Genome-wide meta-analysis associates HLA-DQA1/DRB1 and LPA and lifestyle factors with human longevity. Nat Commun. 2017 10 13; 8(1):910.
    View in: PubMed
    Score: 0.047
  120. New Blood Pressure-Associated Loci Identified in Meta-Analyses of 475?000 Individuals. Circ Cardiovasc Genet. 2017 Oct; 10(5).
    View in: PubMed
    Score: 0.047
  121. Impact of common genetic determinants of Hemoglobin A1c on type 2 diabetes risk and diagnosis in ancestrally diverse populations: A transethnic genome-wide meta-analysis. PLoS Med. 2017 Sep; 14(9):e1002383.
    View in: PubMed
    Score: 0.047
  122. Analysis of potential protein-modifying variants in 9000 endometriosis patients and 150000 controls of European ancestry. Sci Rep. 2017 09 12; 7(1):11380.
    View in: PubMed
    Score: 0.047
  123. Correction: Genome-wide physical activity interactions in adiposity - A meta-analysis of 200,452 adults. PLoS Genet. 2017 Aug; 13(8):e1006972.
    View in: PubMed
    Score: 0.047
  124. CKM Glu83Gly Is Associated With Blunted Creatine Kinase Variation, but Not With Myalgia. Circ Cardiovasc Genet. 2017 Aug; 10(4).
    View in: PubMed
    Score: 0.046
  125. Erratum: Large-scale analyses of common and rare variants identify 12 new loci associated with atrial fibrillation. Nat Genet. 2017 07 27; 49(8):1286.
    View in: PubMed
    Score: 0.046
  126. Novel Blood Pressure Locus and Gene Discovery Using Genome-Wide Association Study and Expression Data Sets From Blood and the Kidney. Hypertension. 2017 Jul 24.
    View in: PubMed
    Score: 0.046
  127. Atherogenic Lipoprotein Determinants of Cardiovascular Disease and Residual Risk Among Individuals With Low Low-Density Lipoprotein Cholesterol. J Am Heart Assoc. 2017 Jul 21; 6(7).
    View in: PubMed
    Score: 0.046
  128. Ranking and characterization of established BMI and lipid associated loci as candidates for gene-environment interactions. PLoS Genet. 2017 Jun; 13(6):e1006812.
    View in: PubMed
    Score: 0.046
  129. Corrigendum: 1000 Genomes-based meta-analysis identifies 10 novel loci for kidney function. Sci Rep. 2017 05 26; 7:46835.
    View in: PubMed
    Score: 0.046
  130. Meta-analysis identifies five novel loci associated with endometriosis highlighting key genes involved in hormone metabolism. Nat Commun. 2017 05 24; 8:15539.
    View in: PubMed
    Score: 0.046
  131. Assessing the causal relationship between obesity and venous thromboembolism through a Mendelian Randomization study. Hum Genet. 2017 07; 136(7):897-902.
    View in: PubMed
    Score: 0.046
  132. 1000 Genomes-based meta-analysis identifies 10 novel loci for kidney function. Sci Rep. 2017 04 28; 7:45040.
    View in: PubMed
    Score: 0.046
  133. Genome-wide physical activity interactions in adiposity - A meta-analysis of 200,452 adults. PLoS Genet. 2017 Apr; 13(4):e1006528.
    View in: PubMed
    Score: 0.045
  134. Genome-wide meta-analysis of 241,258 adults accounting for smoking behaviour identifies novel loci for obesity traits. Nat Commun. 2017 04 26; 8:14977.
    View in: PubMed
    Score: 0.045
  135. Genomic analyses identify hundreds of variants associated with age at menarche and support a role for puberty timing in cancer risk. Nat Genet. 2017 Jun; 49(6):834-841.
    View in: PubMed
    Score: 0.045
  136. Large-scale analyses of common and rare variants identify 12 new loci associated with atrial fibrillation. Nat Genet. 2017 Jun; 49(6):946-952.
    View in: PubMed
    Score: 0.045
  137. Investigating methotrexate toxicity within a randomized double-blinded, placebo-controlled trial: Rationale and design of the Cardiovascular Inflammation Reduction Trial-Adverse Events (CIRT-AE) Study. Semin Arthritis Rheum. 2017 08; 47(1):133-142.
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    Score: 0.045
  138. Discordance between Circulating Atherogenic Cholesterol Mass and Lipoprotein Particle Concentration in Relation to Future Coronary Events in Women. Clin Chem. 2017 04; 63(4):870-879.
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    Score: 0.045
  139. Rare and low-frequency coding variants alter human adult height. Nature. 2017 02 09; 542(7640):186-190.
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    Score: 0.045
  140. Comparison of HapMap and 1000 Genomes Reference Panels in a Large-Scale Genome-Wide Association Study. PLoS One. 2017; 12(1):e0167742.
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    Score: 0.045
  141. Genome-wide Trans-ethnic Meta-analysis Identifies Seven Genetic Loci Influencing Erythrocyte Traits and a Role for RBPMS in Erythropoiesis. Am J Hum Genet. 2017 Jan 05; 100(1):51-63.
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    Score: 0.044
  142. SOS2 and ACP1 Loci Identified through Large-Scale Exome Chip Analysis Regulate Kidney Development and Function. J Am Soc Nephrol. 2017 Mar; 28(3):981-994.
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    Score: 0.044
  143. PCSK9 genetic variants and risk of type 2 diabetes: a mendelian randomisation study. Lancet Diabetes Endocrinol. 2017 02; 5(2):97-105.
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    Score: 0.044
  144. KLB is associated with alcohol drinking, and its gene product ß-Klotho is necessary for FGF21 regulation of alcohol preference. Proc Natl Acad Sci U S A. 2016 12 13; 113(50):14372-14377.
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    Score: 0.044
  145. A principal component meta-analysis on multiple anthropometric traits identifies novel loci for body shape. Nat Commun. 2016 11 23; 7:13357.
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    Score: 0.044
  146. Genetic Risk, Adherence to a Healthy Lifestyle, and Coronary Disease. N Engl J Med. 2016 12 15; 375(24):2349-2358.
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    Score: 0.044
  147. Genome-wide analysis identifies 12 loci influencing human reproductive behavior. Nat Genet. 2016 12; 48(12):1462-1472.
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    Score: 0.044
  148. Corrigendum: Meta-analysis of 375,000 individuals identifies 38 susceptibility loci for migraine. Nat Genet. 2016 09 28; 48(10):1296.
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    Score: 0.044
  149. The genetics of blood pressure regulation and its target organs from association studies in 342,415 individuals. Nat Genet. 2016 10; 48(10):1171-1184.
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    Score: 0.044
  150. Meta-analysis of genome-wide association studies of HDL cholesterol response to statins. J Med Genet. 2016 12; 53(12):835-845.
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    Score: 0.043
  151. 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; 12(6):e1006166.
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    Score: 0.043
  152. Meta-analysis of 375,000 individuals identifies 38 susceptibility loci for migraine. Nat Genet. 2016 08; 48(8):856-66.
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    Score: 0.043
  153. Endophenotype Network Models: Common Core of Complex Diseases. Sci Rep. 2016 06 09; 6:27414.
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    Score: 0.043
  154. 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 07; 40(5):404-15.
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    Score: 0.043
  155. Physical and neurobehavioral determinants of reproductive onset and success. Nat Genet. 2016 06; 48(6):617-623.
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    Score: 0.042
  156. Four Susceptibility Loci for Gallstone Disease Identified in a Meta-analysis of Genome-Wide Association Studies. Gastroenterology. 2016 Aug; 151(2):351-363.e28.
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    Score: 0.042
  157. Genome-Wide Association Study for Incident Myocardial Infarction and Coronary Heart Disease in Prospective Cohort Studies: The CHARGE Consortium. PLoS One. 2016; 11(3):e0144997.
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    Score: 0.042
  158. Genome-wide meta-analysis uncovers novel loci influencing circulating leptin levels. Nat Commun. 2016 Feb 01; 7:10494.
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    Score: 0.042
  159. Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function. Nat Commun. 2016 Jan 21; 7:10023.
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    Score: 0.042
  160. Interaction of methylation-related genetic variants with circulating fatty acids on plasma lipids: a meta-analysis of 7 studies and methylation analysis of 3 studies in the Cohorts for Heart and Aging Research in Genomic Epidemiology consortium. Am J Clin Nutr. 2016 Feb; 103(2):567-78.
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    Score: 0.042
  161. Genome-wide association analysis identifies TXNRD2, ATXN2 and FOXC1 as susceptibility loci for primary open-angle glaucoma. Nat Genet. 2016 Feb; 48(2):189-94.
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    Score: 0.042
  162. Corrigendum: Rare coding variants and X-linked loci associated with age at menarche. Nat Commun. 2015 Dec 17; 6:10257.
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    Score: 0.041
  163. A meta-analysis of 120 246 individuals identifies 18 new loci for fibrinogen concentration. Hum Mol Genet. 2016 Jan 15; 25(2):358-70.
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    Score: 0.041
  164. Identifying Novel Gene Variants in Coronary Artery Disease and Shared Genes With Several Cardiovascular Risk Factors. Circ Res. 2016 Jan 08; 118(1):83-94.
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    Score: 0.041
  165. The Influence of Age and Sex on Genetic Associations with Adult Body Size and Shape: A Large-Scale Genome-Wide Interaction Study. PLoS Genet. 2015 Oct; 11(10):e1005378.
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    Score: 0.041
  166. Large-scale genomic analyses link reproductive aging to hypothalamic signaling, breast cancer susceptibility and BRCA1-mediated DNA repair. Nat Genet. 2015 Nov; 47(11):1294-1303.
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    Score: 0.041
  167. Whole-genome sequencing identifies EN1 as a determinant of bone density and fracture. Nature. 2015 Oct 01; 526(7571):112-7.
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    Score: 0.041
  168. A comprehensive 1,000 Genomes-based genome-wide association meta-analysis of coronary artery disease. Nat Genet. 2015 Oct; 47(10):1121-1130.
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    Score: 0.041
  169. Rare, low frequency and common coding variants in CHRNA5 and their contribution to nicotine dependence in European and African Americans. Mol Psychiatry. 2016 May; 21(5):601-7.
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  170. Rare coding variants and X-linked loci associated with age at menarche. Nat Commun. 2015 Aug 04; 6:7756.
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    Score: 0.040
  171. Directional dominance on stature and cognition in diverse human populations. Nature. 2015 Jul 23; 523(7561):459-462.
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    Score: 0.040
  172. Rare and low-frequency variants and their association with plasma levels of fibrinogen, FVII, FVIII, and vWF. Blood. 2015 Sep 10; 126(11):e19-29.
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  173. Using genetics to test the causal relationship of total adiposity and periodontitis: Mendelian randomization analyses in the Gene-Lifestyle Interactions and Dental Endpoints (GLIDE) Consortium. Int J Epidemiol. 2015 Apr; 44(2):638-50.
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  174. A multivariate genome-wide association analysis of 10 LDL subfractions, and their response to statin treatment, in 1868 Caucasians. PLoS One. 2015; 10(4):e0120758.
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    Score: 0.040
  175. GWAS for executive function and processing speed suggests involvement of the CADM2 gene. Mol Psychiatry. 2016 Feb; 21(2):189-197.
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  176. Polygenic Overlap Between C-Reactive Protein, Plasma Lipids, and Alzheimer Disease. Circulation. 2015 Jun 09; 131(23):2061-2069.
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  177. Dietary fatty acids modulate associations between genetic variants and circulating fatty acids in plasma and erythrocyte membranes: Meta-analysis of nine studies in the CHARGE consortium. Mol Nutr Food Res. 2015 Jul; 59(7):1373-83.
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  178. Meta-analysis of 65,734 individuals identifies TSPAN15 and SLC44A2 as two susceptibility loci for venous thromboembolism. Am J Hum Genet. 2015 Apr 02; 96(4):532-42.
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  179. Is the adiposity-associated FTO gene variant related to all-cause mortality independent of adiposity? Meta-analysis of data from 169,551 Caucasian adults. Obes Rev. 2015 Apr; 16(4):327-340.
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  180. Genetic risk, coronary heart disease events, and the clinical benefit of statin therapy: an analysis of primary and secondary prevention trials. Lancet. 2015 Jun 06; 385(9984):2264-2271.
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  181. New genetic loci link adipose and insulin biology to body fat distribution. Nature. 2015 Feb 12; 518(7538):187-196.
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  182. Genetic studies of body mass index yield new insights for obesity biology. Nature. 2015 Feb 12; 518(7538):197-206.
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    Score: 0.039
  183. Efficient Bayesian mixed-model analysis increases association power in large cohorts. Nat Genet. 2015 Mar; 47(3):284-90.
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  184. Low-frequency and rare exome chip variants associate with fasting glucose and type 2 diabetes susceptibility. Nat Commun. 2015 Jan 29; 6:5897.
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  185. 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. 2014; 9(12):e111156.
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    Score: 0.039
  186. Vitamin D-associated genetic variation and risk of breast cancer in the breast and prostate cancer cohort consortium (BPC3). Cancer Epidemiol Biomarkers Prev. 2015 Mar; 24(3):627-30.
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  187. Genome-wide association study of kidney function decline in individuals of European descent. Kidney Int. 2015 May; 87(5):1017-29.
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  188. Genetic loci associated with circulating phospholipid trans fatty acids: a meta-analysis of genome-wide association studies from the CHARGE Consortium. Am J Clin Nutr. 2015 Feb; 101(2):398-406.
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  189. Genome-wide studies of verbal declarative memory in nondemented older people: the Cohorts for Heart and Aging Research in Genomic Epidemiology consortium. Biol Psychiatry. 2015 Apr 15; 77(8):749-63.
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  190. Inactivating mutations in NPC1L1 and protection from coronary heart disease. N Engl J Med. 2014 Nov 27; 371(22):2072-82.
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  191. Genetic loci associated with circulating levels of very long-chain saturated fatty acids. J Lipid Res. 2015 Jan; 56(1):176-84.
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    Score: 0.038
  192. Pharmacogenetic meta-analysis of genome-wide association studies of LDL cholesterol response to statins. Nat Commun. 2014 Oct 28; 5:5068.
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    Score: 0.038
  193. Defining the role of common variation in the genomic and biological architecture of adult human height. Nat Genet. 2014 Nov; 46(11):1173-86.
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    Score: 0.038
  194. HMG-coenzyme A reductase inhibition, type 2 diabetes, and bodyweight: evidence from genetic analysis and randomised trials. Lancet. 2015 Jan 24; 385(9965):351-61.
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    Score: 0.038
  195. FTO genetic variants, dietary intake and body mass index: insights from 177,330 individuals. Hum Mol Genet. 2014 Dec 20; 23(25):6961-72.
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  196. Parent-of-origin-specific allelic associations among 106 genomic loci for age at menarche. Nature. 2014 Oct 02; 514(7520):92-97.
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  197. Effects of long-term averaging of quantitative blood pressure traits on the detection of genetic associations. Am J Hum Genet. 2014 Jul 03; 95(1):49-65.
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  198. Gene-age interactions in blood pressure regulation: a large-scale investigation with the CHARGE, Global BPgen, and ICBP Consortia. Am J Hum Genet. 2014 Jul 03; 95(1):24-38.
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  199. Gene variations of ROCKs and risk of ischaemic stroke: the Women's Genome Health Study. Clin Sci (Lond). 2014 Jun; 126(12):829-835.
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    Score: 0.037
  200. Pleiotropic genes for metabolic syndrome and inflammation. Mol Genet Metab. 2014 Aug; 112(4):317-38.
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    Score: 0.037
  201. Association of cyclooxygenase-2 genetic variant with cardiovascular disease. Eur Heart J. 2014 Sep 01; 35(33):2242-8a.
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    Score: 0.037
  202. Common genetic variations in the vitamin D pathway in relation to blood pressure. Am J Hypertens. 2014 Nov; 27(11):1387-95.
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    Score: 0.037
  203. Fried food consumption, genetic risk, and body mass index: gene-diet interaction analysis in three US cohort studies. BMJ. 2014 Mar 19; 348:g1610.
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    Score: 0.037
  204. DNA mismatch repair gene MSH6 implicated in determining age at natural menopause. Hum Mol Genet. 2014 May 01; 23(9):2490-7.
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    Score: 0.036
  205. Common variants associated with plasma triglycerides and risk for coronary artery disease. Nat Genet. 2013 Nov; 45(11):1345-52.
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    Score: 0.036
  206. Discovery and refinement of loci associated with lipid levels. Nat Genet. 2013 Nov; 45(11):1274-1283.
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    Score: 0.036
  207. Cholesteryl ester transfer protein polymorphisms, statin use, and their impact on cholesterol levels and cardiovascular events. Clin Pharmacol Ther. 2014 Mar; 95(3):314-20.
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    Score: 0.036
  208. Common variants in Mendelian kidney disease genes and their association with renal function. J Am Soc Nephrol. 2013 Dec; 24(12):2105-17.
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    Score: 0.035
  209. A statin-dependent QTL for GATM expression is associated with statin-induced myopathy. Nature. 2013 Oct 17; 502(7471):377-80.
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    Score: 0.035
  210. 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. 2013 Sep 17; 128(12):1310-24.
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  211. Genome-wide association analysis of blood-pressure traits in African-ancestry individuals reveals common associated genes in African and non-African populations. Am J Hum Genet. 2013 Sep 05; 93(3):545-54.
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    Score: 0.035
  212. Gene × physical activity interactions in obesity: combined analysis of 111,421 individuals of European ancestry. PLoS Genet. 2013; 9(7):e1003607.
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    Score: 0.035
  213. Common genetic loci influencing plasma homocysteine concentrations and their effect on risk of coronary artery disease. Am J Clin Nutr. 2013 Sep; 98(3):668-76.
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    Score: 0.035
  214. Genome-wide meta-analysis identifies new susceptibility loci for migraine. Nat Genet. 2013 Aug; 45(8):912-917.
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    Score: 0.035
  215. Sex-stratified genome-wide association studies including 270,000 individuals show sexual dimorphism in genetic loci for anthropometric traits. PLoS Genet. 2013 Jun; 9(6):e1003500.
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    Score: 0.035
  216. A genome-wide association study for venous thromboembolism: the extended cohorts for heart and aging research in genomic epidemiology (CHARGE) consortium. Genet Epidemiol. 2013 Jul; 37(5):512-521.
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    Score: 0.035
  217. Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture. Nat Genet. 2013 May; 45(5):501-12.
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    Score: 0.034
  218. Association of adiposity genetic variants with menarche timing in 92,105 women of European descent. Am J Epidemiol. 2013 Aug 01; 178(3):451-60.
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    Score: 0.034
  219. Novel genetic markers improve measures of atrial fibrillation risk prediction. Eur Heart J. 2013 Aug; 34(29):2243-51.
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    Score: 0.034
  220. Novel locus including FGF21 is associated with dietary macronutrient intake. Hum Mol Genet. 2013 May 01; 22(9):1895-902.
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    Score: 0.034
  221. A genome-wide association study of early menopause and the combined impact of identified variants. Hum Mol Genet. 2013 Apr 01; 22(7):1465-72.
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    Score: 0.034
  222. Loci influencing blood pressure identified using a cardiovascular gene-centric array. Hum Mol Genet. 2013 Apr 15; 22(8):1663-78.
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    Score: 0.034
  223. Prospective evaluation of B-type natriuretic peptide concentrations and the risk of type 2 diabetes in women. Clin Chem. 2013 Mar; 59(3):557-65.
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    Score: 0.034
  224. Lipoprotein(a), polymorphisms in the LPA gene, and incident venous thromboembolism among 21483 women. J Thromb Haemost. 2013 Jan; 11(1):205-8.
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    Score: 0.034
  225. Genome-wide association analyses identify 18 new loci associated with serum urate concentrations. Nat Genet. 2013 Feb; 45(2):145-54.
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    Score: 0.034
  226. Genome-wide linkage and association analyses implicate FASN in predisposition to Uterine Leiomyomata. Am J Hum Genet. 2012 Oct 05; 91(4):621-8.
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    Score: 0.033
  227. Sugar-sweetened beverages and genetic risk of obesity. N Engl J Med. 2012 Oct 11; 367(15):1387-96.
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    Score: 0.033
  228. FTO genotype is associated with phenotypic variability of body mass index. Nature. 2012 Oct 11; 490(7419):267-72.
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    Score: 0.033
  229. A meta-analysis of genome-wide association studies of breast cancer identifies two novel susceptibility loci at 6q14 and 20q11. Hum Mol Genet. 2012 Dec 15; 21(24):5373-84.
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    Score: 0.033
  230. A genome-wide analysis of 'Bounty' descendants implicates several novel variants in migraine susceptibility. Neurogenetics. 2012 Aug; 13(3):261-6.
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    Score: 0.032
  231. An X chromosome association scan of the Norfolk Island genetic isolate provides evidence for a novel migraine susceptibility locus at Xq12. PLoS One. 2012; 7(5):e37903.
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    Score: 0.032
  232. Meta-analysis identifies six new susceptibility loci for atrial fibrillation. Nat Genet. 2012 Apr 29; 44(6):670-5.
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    Score: 0.032
  233. Genome-wide meta-analysis identifies 56 bone mineral density loci and reveals 14 loci associated with risk of fracture. Nat Genet. 2012 Apr 15; 44(5):491-501.
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    Score: 0.032
  234. Genome-wide association and functional follow-up reveals new loci for kidney function. PLoS Genet. 2012; 8(3):e1002584.
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    Score: 0.032
  235. Novel loci for adiponectin levels and their influence on type 2 diabetes and metabolic traits: a multi-ethnic meta-analysis of 45,891 individuals. PLoS Genet. 2012; 8(3):e1002607.
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    Score: 0.032
  236. Reproductive aging-associated common genetic variants and the risk of breast cancer. Breast Cancer Res. 2012 Mar 20; 14(2):R54.
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  237. Interleukin-6 receptor pathways in coronary heart disease: a collaborative meta-analysis of 82 studies. Lancet. 2012 Mar 31; 379(9822):1205-13.
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    Score: 0.032
  238. Meta-analyses identify 13 loci associated with age at menopause and highlight DNA repair and immune pathways. Nat Genet. 2012 Jan 22; 44(3):260-8.
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  239. Rosuvastatin, proprotein convertase subtilisin/kexin type 9 concentrations, and LDL cholesterol response: the JUPITER trial. Clin Chem. 2012 Jan; 58(1):183-9.
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    Score: 0.031
  240. Physical activity attenuates the influence of FTO variants on obesity risk: a meta-analysis of 218,166 adults and 19,268 children. PLoS Med. 2011 Nov; 8(11):e1001116.
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    Score: 0.031
  241. Association of variation at the ABO locus with circulating levels of soluble intercellular adhesion molecule-1, soluble P-selectin, and soluble E-selectin: a meta-analysis. Circ Cardiovasc Genet. 2011 Dec; 4(6):681-6.
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  242. Genome-wide association study identifies six new loci influencing pulse pressure and mean arterial pressure. Nat Genet. 2011 Sep 11; 43(10):1005-11.
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    Score: 0.031
  243. Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk. Nature. 2011 Sep 11; 478(7367):103-9.
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  244. Genetic determinants of cardiovascular events among women with migraine: a genome-wide association study. PLoS One. 2011; 6(7):e22106.
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  245. Association of hypertension drug target genes with blood pressure and hypertension in 86,588 individuals. Hypertension. 2011 May; 57(5):903-10.
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  246. Association of genetic variation with systolic and diastolic blood pressure among African Americans: the Candidate Gene Association Resource study. Hum Mol Genet. 2011 Jun 01; 20(11):2273-84.
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  247. Lifestyle interaction with fat mass and obesity-associated (FTO) genotype and risk of obesity in apparently healthy U.S. women. Diabetes Care. 2011 Mar; 34(3):675-80.
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  248. Physical activity modifies the effect of LPL, LIPC, and CETP polymorphisms on HDL-C levels and the risk of myocardial infarction in women of European ancestry. Circ Cardiovasc Genet. 2011 Feb; 4(1):74-80.
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  249. Islet amyloid polypeptide gene variation (IAPP) and the risk of incident type 2 diabetes mellitus: the Women's Genome Health Study. Clin Chim Acta. 2011 Apr 11; 412(9-10):785-7.
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  250. Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies. Nat Genet. 2010 Dec; 42(12):1077-85.
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  251. The fat-mass and obesity-associated (FTO) gene, physical activity, and risk of incident cardiovascular events in white women. Am Heart J. 2010 Dec; 160(6):1163-9.
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  252. Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution. Nat Genet. 2010 Nov; 42(11):949-60.
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    Score: 0.029
  253. Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index. Nat Genet. 2010 Nov; 42(11):937-48.
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    Score: 0.029
  254. Multiple genetic loci influence serum urate levels and their relationship with gout and cardiovascular disease risk factors. Circ Cardiovasc Genet. 2010 Dec; 3(6):523-30.
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  255. Hundreds of variants clustered in genomic loci and biological pathways affect human height. Nature. 2010 Oct 14; 467(7317):832-8.
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  256. A large-scale candidate gene association study of age at menarche and age at natural menopause. Hum Genet. 2010 Nov; 128(5):515-27.
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  257. Biological, clinical and population relevance of 95 loci for blood lipids. Nature. 2010 Aug 05; 466(7307):707-13.
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    Score: 0.029
  258. Genetic variants at 2q24 are associated with susceptibility to type 2 diabetes. Hum Mol Genet. 2010 Jul 01; 19(13):2706-15.
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    Score: 0.028
  259. New loci associated with kidney function and chronic kidney disease. Nat Genet. 2010 May; 42(5):376-84.
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    Score: 0.028
  260. Genome-wide association of lipid-lowering response to statins in combined study populations. PLoS One. 2010 Mar 22; 5(3):e9763.
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  261. Genome-wide association study identifies variants at the IL18-BCO2 locus associated with interleukin-18 levels. Arterioscler Thromb Vasc Biol. 2010 Apr; 30(4):885-90.
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  262. Multiple loci associated with indices of renal function and chronic kidney disease. Nat Genet. 2009 Jun; 41(6):712-7.
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  263. Population analysis of large copy number variants and hotspots of human genetic disease. Am J Hum Genet. 2009 Feb; 84(2):148-61.
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  264. GOSR2 Lys67Arg is associated with hypertension in whites. Am J Hypertens. 2009 Feb; 22(2):163-8.
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  265. Tracing sub-structure in the European American population with PCA-informative markers. PLoS Genet. 2008 Jul 04; 4(7):e1000114.
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  266. Polymorphisms of the HNF1A gene encoding hepatocyte nuclear factor-1 alpha are associated with C-reactive protein. Am J Hum Genet. 2008 May; 82(5):1193-201.
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  267. Lack of association between genetic variation in 9 innate immunity genes and baseline CRP levels. Ann Hum Genet. 2006 Sep; 70(Pt 5):574-86.
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  268. Lack of Association Between Genetic Variation in 9 Innate Immunity Genes and Baseline CRP Levels. Ann Hum Genet. 2006 Sep; 70(5):574-586.
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  269. Association of common CRP gene variants with CRP levels and cardiovascular events. Ann Hum Genet. 2005 Nov; 69(Pt 6):623-38.
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Funded by the NIH National Center for Advancing Translational Sciences through its Clinical and Translational Science Awards Program, grant number UL1TR002541.