Harvard Catalyst Profiles

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

Calum Archibald MacRae, Ph.D., M.D.

Co-Author

This page shows the publications co-authored by Calum MacRae and Patrick Ellinor.
Connection Strength

6.260
  1. Ion channel mutations in AF: signal or noise? Heart Rhythm. 2008 Mar; 5(3):436-7.
    View in: PubMed
    Score: 0.395
  2. Genetics of atrial fibrillation. Med Clin North Am. 2008 Jan; 92(1):41-51, x.
    View in: PubMed
    Score: 0.394
  3. Cardiac sodium channel mutation in atrial fibrillation. Heart Rhythm. 2008 Jan; 5(1):99-105.
    View in: PubMed
    Score: 0.386
  4. Genetics of atrial fibrillation. Future Cardiol. 2006 Sep; 2(5):579-84.
    View in: PubMed
    Score: 0.359
  5. Potassium channel gene mutations rarely cause atrial fibrillation. BMC Med Genet. 2006 Aug 03; 7:70.
    View in: PubMed
    Score: 0.357
  6. A novel locus for dilated cardiomyopathy, diffuse myocardial fibrosis, and sudden death on chromosome 10q25-26. J Am Coll Cardiol. 2006 Jul 04; 48(1):106-11.
    View in: PubMed
    Score: 0.354
  7. C-Reactive protein in lone atrial fibrillation. Am J Cardiol. 2006 May 01; 97(9):1346-50.
    View in: PubMed
    Score: 0.348
  8. Familial aggregation in lone atrial fibrillation. Hum Genet. 2005 Nov; 118(2):179-84.
    View in: PubMed
    Score: 0.340
  9. Reduced apelin levels in lone atrial fibrillation. Eur Heart J. 2006 Jan; 27(2):222-6.
    View in: PubMed
    Score: 0.339
  10. Discordant atrial natriuretic peptide and brain natriuretic peptide levels in lone atrial fibrillation. J Am Coll Cardiol. 2005 Jan 04; 45(1):82-6.
    View in: PubMed
    Score: 0.320
  11. Genetic screening and risk assessment in hypertrophic cardiomyopathy. J Am Coll Cardiol. 2004 Dec 21; 44(12):2326-8.
    View in: PubMed
    Score: 0.319
  12. Mutations in the long QT gene, KCNQ1, are an uncommon cause of atrial fibrillation. Heart. 2004 Dec; 90(12):1487-8.
    View in: PubMed
    Score: 0.318
  13. The genetics of atrial fibrillation. J Cardiovasc Electrophysiol. 2003 Sep; 14(9):1007-9.
    View in: PubMed
    Score: 0.291
  14. Risk stratification in the long-QT syndrome. N Engl J Med. 2003 Aug 28; 349(9):908-9; author reply 908-9.
    View in: PubMed
    Score: 0.291
  15. Locus for atrial fibrillation maps to chromosome 6q14-16. Circulation. 2003 Jun 17; 107(23):2880-3.
    View in: PubMed
    Score: 0.286
  16. Genetic variation in the alternative splicing regulator RBM20 is associated with dilated cardiomyopathy. Heart Rhythm. 2012 Mar; 9(3):390-6.
    View in: PubMed
    Score: 0.128
  17. Arrhythmogenic right ventricular cardiomyopathy. Heart Fail Clin. 2010 Apr; 6(2):161-77.
    View in: PubMed
    Score: 0.115
  18. Common variants in KCNN3 are associated with lone atrial fibrillation. Nat Genet. 2010 Mar; 42(3):240-4.
    View in: PubMed
    Score: 0.114
  19. Mutation in the S3 segment of KCNQ1 results in familial lone atrial fibrillation. Heart Rhythm. 2009 Aug; 6(8):1146-53.
    View in: PubMed
    Score: 0.108
  20. Large scale replication and meta-analysis of variants on chromosome 4q25 associated with atrial fibrillation. Eur Heart J. 2009 Apr; 30(7):813-9.
    View in: PubMed
    Score: 0.106
  21. Cardiac sodium channel gene variants and sudden cardiac death in women. Circulation. 2008 Jan 01; 117(1):16-23.
    View in: PubMed
    Score: 0.098
  22. In vivo recording of adult zebrafish electrocardiogram and assessment of drug-induced QT prolongation. . 2006 Jul; 291(1):H269-73.
    View in: PubMed
    Score: 0.086
  23. Aging syndrome genes and premature coronary artery disease. BMC Med Genet. 2005 Oct 31; 6:38.
    View in: PubMed
    Score: 0.085
  24. Clinical subtypes of lone atrial fibrillation. Pacing Clin Electrophysiol. 2005 Jul; 28(7):630-8.
    View in: PubMed
    Score: 0.083
  25. miR-21 represses Pdcd4 during cardiac valvulogenesis. Development. 2013 May; 140(10):2172-80.
    View in: PubMed
    Score: 0.035
  26. Genetics and cardiovascular disease: a policy statement from the American Heart Association. Circulation. 2012 Jul 03; 126(1):142-57.
    View in: PubMed
    Score: 0.033
  27. RBM20, a gene for hereditary cardiomyopathy, regulates titin splicing. Nat Med. 2012 May; 18(5):766-73.
    View in: PubMed
    Score: 0.033
  28. ACE I/D polymorphism associated with abnormal atrial and atrioventricular conduction in lone atrial fibrillation and structural heart disease: implications for electrical remodeling. Heart Rhythm. 2009 Sep; 6(9):1327-32.
    View in: PubMed
    Score: 0.027
  29. Variants conferring risk of atrial fibrillation on chromosome 4q25. Nature. 2007 Jul 19; 448(7151):353-7.
    View in: PubMed
    Score: 0.024
  30. Myocardial blood flow and oxygen consumption in patients with Friedreich's ataxia prior to the onset of cardiomyopathy. Coron Artery Dis. 2007 Feb; 18(1):15-22.
    View in: PubMed
    Score: 0.023
  31. Mutant desmocollin-2 causes arrhythmogenic right ventricular cardiomyopathy. Am J Hum Genet. 2006 Dec; 79(6):1081-8.
    View in: PubMed
    Score: 0.023
  32. Utility of amino-terminal pro-brain natriuretic peptide, galectin-3, and apelin for the evaluation of patients with acute heart failure. J Am Coll Cardiol. 2006 Sep 19; 48(6):1217-24.
    View in: PubMed
    Score: 0.022
  33. Mutations in the desmosomal protein plakophilin-2 are common in arrhythmogenic right ventricular cardiomyopathy. Nat Genet. 2004 Nov; 36(11):1162-4.
    View in: PubMed
    Score: 0.020
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.