Connection

JOHN BELMONT to Genetic Variation

This is a "connection" page, showing publications JOHN BELMONT has written about Genetic Variation.
Connection Strength

0.729
  1. Strategic approaches to unraveling genetic causes of cardiovascular diseases. Circ Res. 2011 May 13; 108(10):1252-69.
    View in: PubMed
    Score: 0.233
  2. Postmortem genetic screening for the identification, verification, and reporting of genetic variants contributing to the sudden death of the young. Genome Res. 2016 09; 26(9):1170-7.
    View in: PubMed
    Score: 0.084
  3. Monoallelic and Biallelic Variants in EMC1 Identified in Individuals with Global Developmental Delay, Hypotonia, Scoliosis, and Cerebellar Atrophy. Am J Hum Genet. 2016 Mar 03; 98(3):562-570.
    View in: PubMed
    Score: 0.081
  4. Rare APOA5 promoter variants associated with paradoxical HDL cholesterol decrease in response to fenofibric acid therapy. J Lipid Res. 2013 Jul; 54(7):1980-7.
    View in: PubMed
    Score: 0.067
  5. NPHP4 variants are associated with pleiotropic heart malformations. Circ Res. 2012 Jun 08; 110(12):1564-74.
    View in: PubMed
    Score: 0.062
  6. Low levels of genetic divergence across geographically and linguistically diverse populations from India. PLoS Genet. 2006 Dec; 2(12):e215.
    View in: PubMed
    Score: 0.043
  7. Complex phenotypes and complex genetics: an introduction to genetic studies of complex traits. Curr Atheroscler Rep. 2005 May; 7(3):180-7.
    View in: PubMed
    Score: 0.038
  8. Large-scale comparative sequence analysis of the human and murine Bruton's tyrosine kinase loci reveals conserved regulatory domains. Genome Res. 1997 Apr; 7(4):315-29.
    View in: PubMed
    Score: 0.022
  9. Replicative mechanisms for CNV formation are error prone. Nat Genet. 2013 Nov; 45(11):1319-26.
    View in: PubMed
    Score: 0.017
  10. MCTP2 is a dosage-sensitive gene required for cardiac outflow tract development. Hum Mol Genet. 2013 Nov 01; 22(21):4339-48.
    View in: PubMed
    Score: 0.017
  11. Impact of restricted marital practices on genetic variation in an endogamous Gujarati group. Am J Phys Anthropol. 2012 Sep; 149(1):92-103.
    View in: PubMed
    Score: 0.016
  12. Clan genomics and the complex architecture of human disease. Cell. 2011 Sep 30; 147(1):32-43.
    View in: PubMed
    Score: 0.015
  13. Ancestry informative marker sets for determining continental origin and admixture proportions in common populations in America. Hum Mutat. 2009 Jan; 30(1):69-78.
    View in: PubMed
    Score: 0.012
  14. Identification and functional characterization of NODAL rare variants in heterotaxy and isolated cardiovascular malformations. Hum Mol Genet. 2009 Mar 01; 18(5):861-71.
    View in: PubMed
    Score: 0.012
  15. Mexican American ancestry-informative markers: examination of population structure and marker characteristics in European Americans, Mexican Americans, Amerindians and Asians. Hum Genet. 2004 Feb; 114(3):263-71.
    View in: PubMed
    Score: 0.009
Connection Strength

The connection strength for concepts is the sum of the scores for each matching publication.

Publication scores are based on many factors, including how long ago they were written and whether the person is a first or senior author.