Harvard Catalyst Profiles

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

Albert Hofman, Ph.D., M.D.

Co-Author

This page shows the publications co-authored by Albert Hofman and Christopher Newton-Cheh.
Connection Strength

1.351
  1. 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: 0.145
  2. 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: 0.101
  3. 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: 0.058
  4. 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: 0.049
  5. 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: 0.049
  6. 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: 0.049
  7. Multi-ethnic genome-wide association study for atrial fibrillation. Nat Genet. 2018 06 11; 50(9):1225-1233.
    View in: PubMed
    Score: 0.048
  8. 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: 0.045
  9. 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: 0.045
  10. 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: 0.044
  11. A genome-wide interaction analysis of tricyclic/tetracyclic antidepressants and RR and QT intervals: a pharmacogenomics study from the Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) consortium. J Med Genet. 2017 05; 54(5):313-323.
    View in: PubMed
    Score: 0.043
  12. 52 Genetic Loci Influencing Myocardial Mass. J Am Coll Cardiol. 2016 09 27; 68(13):1435-1448.
    View in: PubMed
    Score: 0.042
  13. 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: 0.042
  14. Discovery of Genetic Variation on Chromosome 5q22 Associated with Mortality in Heart Failure. PLoS Genet. 2016 05; 12(5):e1006034.
    View in: PubMed
    Score: 0.041
  15. Rare Exome Sequence Variants in CLCN6 Reduce Blood Pressure Levels and Hypertension Risk. Circ Cardiovasc Genet. 2016 Feb; 9(1):64-70.
    View in: PubMed
    Score: 0.040
  16. 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.
    View in: PubMed
    Score: 0.036
  17. Annotation of loci from genome-wide association studies using tissue-specific quantitative interaction proteomics. Nat Methods. 2014 Aug; 11(8):868-74.
    View in: PubMed
    Score: 0.036
  18. 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: 0.033
  19. Orthostatic hypotension and novel blood pressure-associated gene variants: Genetics of Postural Hemodynamics (GPH) Consortium. Eur Heart J. 2012 Sep; 33(18):2331-41.
    View in: PubMed
    Score: 0.031
  20. 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: 0.030
  21. Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk. Nature. 2011 Sep 11; 478(7367):103-9.
    View in: PubMed
    Score: 0.030
  22. 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: 0.030
  23. 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: 0.028
  24. 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: 0.028
  25. Common variants in KCNN3 are associated with lone atrial fibrillation. Nat Genet. 2010 Mar; 42(3):240-4.
    View in: PubMed
    Score: 0.027
  26. Genome-wide association study of PR interval. Nat Genet. 2010 Feb; 42(2):153-9.
    View in: PubMed
    Score: 0.027
  27. Genetic variation in NOS1AP is associated with sudden cardiac death: evidence from the Rotterdam Study. Hum Mol Genet. 2009 Nov 01; 18(21):4213-8.
    View in: PubMed
    Score: 0.026
  28. Variants in ZFHX3 are associated with atrial fibrillation in individuals of European ancestry. Nat Genet. 2009 Aug; 41(8):879-81.
    View in: PubMed
    Score: 0.026
  29. Calcium channel blockers, NOS1AP, and heart-rate-corrected QT prolongation. Pharmacogenet Genomics. 2009 Apr; 19(4):260-6.
    View in: PubMed
    Score: 0.025
  30. Psychotropic drugs associated with corrected QT interval prolongation. J Clin Psychopharmacol. 2009 Feb; 29(1):9-15.
    View in: PubMed
    Score: 0.025
  31. A common NOS1AP genetic polymorphism is associated with increased cardiovascular mortality in users of dihydropyridine calcium channel blockers. Br J Clin Pharmacol. 2009 Jan; 67(1):61-7.
    View in: PubMed
    Score: 0.025
  32. Common variation in the NOS1AP gene is associated with reduced glucose-lowering effect and with increased mortality in users of sulfonylurea. Pharmacogenet Genomics. 2008 Jul; 18(7):591-7.
    View in: PubMed
    Score: 0.024
  33. Common NOS1AP variants are associated with a prolonged QTc interval in the Rotterdam Study. Circulation. 2007 Jul 03; 116(1):10-6.
    View in: PubMed
    Score: 0.022
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.