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Christopher Joseph O'Donnell, M.D.

Co-Author

This page shows the publications co-authored by Christopher O'Donnell and Christopher Newton-Cheh.
  1. Common genetic variation in KCNH2 is associated with QT interval duration: the Framingham Heart Study. Circulation. 2007 Sep 04; 116(10):1128-36.
    View in: PubMed
    Score: 0.351
  2. QT interval is a heritable quantitative trait with evidence of linkage to chromosome 3 in a genome-wide linkage analysis: The Framingham Heart Study. Heart Rhythm. 2005 Mar; 2(3):277-84.
    View in: PubMed
    Score: 0.296
  3. On the significance of linkage studies of complex traits. Am J Hum Genet. 2004 Jul; 75(1):151-2; author reply 152-4.
    View in: PubMed
    Score: 0.282
  4. Sex differences and genetic associations with myocardial infarction. JAMA. 2004 Jun 23; 291(24):3008-10.
    View in: PubMed
    Score: 0.282
  5. Genetic association study of QT interval highlights role for calcium signaling pathways in myocardial repolarization. Nat Genet. 2014 Aug; 46(8):826-36.
    View in: PubMed
    Score: 0.141
  6. Resequencing and clinical associations of the 9p21.3 region: a comprehensive investigation in the Framingham heart study. Circulation. 2013 Feb 19; 127(7):799-810.
    View in: PubMed
    Score: 0.127
  7. QT interval and long-term mortality risk in the Framingham Heart Study. Ann Noninvasive Electrocardiol. 2012 Oct; 17(4):340-8.
    View in: PubMed
    Score: 0.124
  8. 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.
    View in: PubMed
    Score: 0.112
  9. Genome-wide association analysis identifies multiple loci related to resting heart rate. Hum Mol Genet. 2010 Oct 01; 19(19):3885-94.
    View in: PubMed
    Score: 0.107
  10. Genome-wide association study identifies eight loci associated with blood pressure. Nat Genet. 2009 Jun; 41(6):666-76.
    View in: PubMed
    Score: 0.099
  11. Common variants at ten loci influence QT interval duration in the QTGEN Study. Nat Genet. 2009 Apr; 41(4):399-406.
    View in: PubMed
    Score: 0.098
  12. Genome-wide association study of electrocardiographic and heart rate variability traits: the Framingham Heart Study. BMC Med Genet. 2007 Sep 19; 8 Suppl 1:S7.
    View in: PubMed
    Score: 0.088
  13. Clinical and genetic correlates of aldosterone-to-renin ratio and relations to blood pressure in a community sample. Hypertension. 2007 Apr; 49(4):846-56.
    View in: PubMed
    Score: 0.085
  14. 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: 0.057
  15. 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: 0.055
  16. 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: 0.048
  17. 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: 0.048
  18. A comprehensive evaluation of the genetic architecture of sudden cardiac arrest. Eur Heart J. 2018 11 21; 39(44):3961-3969.
    View in: PubMed
    Score: 0.048
  19. 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: 0.047
  20. Common Coding Variants in SCN10A Are Associated With the Nav1.8 Late Current and Cardiac Conduction. Circ Genom Precis Med. 2018 05; 11(5):e001663.
    View in: PubMed
    Score: 0.046
  21. Pharmacogenomics study of thiazide diuretics and QT interval in multi-ethnic populations: the cohorts for heart and aging research in genomic epidemiology. Pharmacogenomics J. 2018 04; 18(2):215-226.
    View in: PubMed
    Score: 0.044
  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: 0.041
  23. 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.
    View in: PubMed
    Score: 0.041
  24. Sequencing of SCN5A identifies rare and common variants associated with cardiac conduction: Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium. Circ Cardiovasc Genet. 2014 Jun; 7(3):365-73.
    View in: PubMed
    Score: 0.035
  25. Assessing the phenotypic effects in the general population of rare variants in genes for a dominant Mendelian form of diabetes. Nat Genet. 2013 Nov; 45(11):1380-5.
    View in: PubMed
    Score: 0.034
  26. Common genetic variation at the IL1RL1 locus regulates IL-33/ST2 signaling. J Clin Invest. 2013 Oct; 123(10):4208-18.
    View in: PubMed
    Score: 0.033
  27. Silencing of the Drosophila ortholog of SOX5 in heart leads to cardiac dysfunction as detected by optical coherence tomography. Hum Mol Genet. 2013 Sep 15; 22(18):3798-806.
    View in: PubMed
    Score: 0.033
  28. Identification of heart rate-associated loci and their effects on cardiac conduction and rhythm disorders. Nat Genet. 2013 Jun; 45(6):621-31.
    View in: PubMed
    Score: 0.032
  29. Burden of rare sarcomere gene variants in the Framingham and Jackson Heart Study cohorts. Am J Hum Genet. 2012 Sep 07; 91(3):513-9.
    View in: PubMed
    Score: 0.031
  30. Development and application of a longitudinal electrocardiogram repository: the Framingham Heart Study. J Electrocardiol. 2012 Nov-Dec; 45(6):673-6.
    View in: PubMed
    Score: 0.031
  31. A meta-analysis of genome-wide association studies of the electrocardiographic early repolarization pattern. Heart Rhythm. 2012 Oct; 9(10):1627-34.
    View in: PubMed
    Score: 0.031
  32. Plasma HDL cholesterol and risk of myocardial infarction: a mendelian randomisation study. Lancet. 2012 Aug 11; 380(9841):572-80.
    View in: PubMed
    Score: 0.030
  33. A common variant near the KCNJ2 gene is associated with T-peak to T-end interval. Heart Rhythm. 2012 Jul; 9(7):1099-103.
    View in: PubMed
    Score: 0.030
  34. Genome-wide association study identifies six new loci influencing pulse pressure and mean arterial pressure. Nat Genet. 2011 Sep 11; 43(10):1005-11.
    View in: PubMed
    Score: 0.029
  35. Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk. Nature. 2011 Sep 11; 478(7367):103-9.
    View in: PubMed
    Score: 0.029
  36. Relation of visceral adiposity to circulating natriuretic peptides in ambulatory individuals. Am J Cardiol. 2011 Oct 01; 108(7):979-84.
    View in: PubMed
    Score: 0.029
  37. Identification of a sudden cardiac death susceptibility locus at 2q24.2 through genome-wide association in European ancestry individuals. PLoS Genet. 2011 Jun; 7(6):e1002158.
    View in: PubMed
    Score: 0.029
  38. The early repolarization pattern in the general population: clinical correlates and heritability. J Am Coll Cardiol. 2011 May 31; 57(22):2284-9.
    View in: PubMed
    Score: 0.028
  39. Common variants in 22 loci are associated with QRS duration and cardiac ventricular conduction. Nat Genet. 2010 Dec; 42(12):1068-76.
    View in: PubMed
    Score: 0.027
  40. Genome-wide association of echocardiographic dimensions, brachial artery endothelial function and treadmill exercise responses in the Framingham Heart Study. BMC Med Genet. 2007 Sep 19; 8 Suppl 1:S2.
    View in: PubMed
    Score: 0.022
  41. Framingham Heart Study 100K project: genome-wide associations for cardiovascular disease outcomes. BMC Med Genet. 2007 Sep 19; 8 Suppl 1:S5.
    View in: PubMed
    Score: 0.022
  42. Heritability, linkage, and genetic associations of exercise treadmill test responses. Circulation. 2007 Jun 12; 115(23):2917-24.
    View in: PubMed
    Score: 0.022
  43. Vascular stiffness and genetic variation at the endothelial nitric oxide synthase locus: the Framingham Heart study. Hypertension. 2007 Jun; 49(6):1285-90.
    View in: PubMed
    Score: 0.021
  44. The Framingham Heart Study 100K SNP genome-wide association study resource: overview of 17 phenotype working group reports. BMC Med Genet. 2007; 8 Suppl 1:S1.
    View in: PubMed
    Score: 0.021
  45. A common genetic variant in the NOS1 regulator NOS1AP modulates cardiac repolarization. Nat Genet. 2006 Jun; 38(6):644-51.
    View in: PubMed
    Score: 0.020
  46. Contribution of clinical correlates and 13 C-reactive protein gene polymorphisms to interindividual variability in serum C-reactive protein level. Circulation. 2006 Mar 21; 113(11):1415-23.
    View in: PubMed
    Score: 0.020
  47. Common genetic variation at the endothelial nitric oxide synthase locus and relations to brachial artery vasodilator function in the community. Circulation. 2005 Sep 06; 112(10):1419-27.
    View in: PubMed
    Score: 0.019
Connection Strength
The connection strength for co-authors is the sum of the scores for each of their shared publications.

Publication scores are based on many factors, including how long ago they were written and whether the person is a first or senior author.
Funded by the NIH National Center for Advancing Translational Sciences through its Clinical and Translational Science Awards Program, grant number UL1TR002541.