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

Co-Author

This page shows the publications co-authored by Calum MacRae and Craig Basson.
Connection Strength

0.247
  1. Genetic heterogeneity of familial atrial myxoma syndromes (Carney complex). Am J Cardiol. 1997 Apr 01; 79(7):994-5.
    View in: PubMed
    Score: 0.043
  2. New understandings in the genetics of congenital heart disease. Curr Opin Pediatr. 1996 Oct; 8(5):505-11.
    View in: PubMed
    Score: 0.041
  3. Identification, characterization, and chromosomal localization of the human homolog (hES) of ES/130. Genomics. 1996 Aug 01; 35(3):628-31.
    View in: PubMed
    Score: 0.041
  4. Familial Hypertrophic cardiomyopathy with Wolff-Parkinson-White syndrome maps to a locus on chromosome 7q3. J Clin Invest. 1995 Sep; 96(3):1216-20.
    View in: PubMed
    Score: 0.038
  5. Genetic heterogeneity of heart-hand syndromes. Circulation. 1995 Mar 01; 91(5):1326-9.
    View in: PubMed
    Score: 0.037
  6. Mutant desmocollin-2 causes arrhythmogenic right ventricular cardiomyopathy. Am J Hum Genet. 2006 Dec; 79(6):1081-8.
    View in: PubMed
    Score: 0.021
  7. 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: 0.018
  8. A gene defect that causes conduction system disease and dilated cardiomyopathy maps to chromosome 1p1-1q1. Nat Genet. 1994 Aug; 7(4):546-51.
    View in: PubMed
    Score: 0.009
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.