Connection

JOHN BELMONT to Genetic Testing

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

1.146
  1. Runs of homozygosity and parental relatedness. Genet Med. 2013 Sep; 15(9):753-4.
    View in: PubMed
    Score: 0.278
  2. Array-based DNA diagnostics: let the revolution begin. Annu Rev Med. 2008; 59:113-29.
    View in: PubMed
    Score: 0.187
  3. SNP genotyping to screen for a common deletion in CHARGE syndrome. BMC Med Genet. 2005 Feb 14; 6:8.
    View in: PubMed
    Score: 0.154
  4. The impact of clinical genome sequencing in a global population with suspected rare genetic disease. Am J Hum Genet. 2024 07 11; 111(7):1271-1281.
    View in: PubMed
    Score: 0.146
  5. 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: 0.085
  6. The ethics of conducting molecular autopsies in cases of sudden death in the young. Genome Res. 2016 09; 26(9):1165-9.
    View in: PubMed
    Score: 0.085
  7. Points to Consider: Ethical, Legal, and Psychosocial Implications of Genetic Testing in Children and Adolescents. Am J Hum Genet. 2015 Jul 02; 97(1):6-21.
    View in: PubMed
    Score: 0.079
  8. The Expansion of Genetic Testing in Cardiovascular Medicine: Preparing the Cardiology Community for the Changing Landscape. Curr Cardiol Rep. 2024 03; 26(3):135-146.
    View in: PubMed
    Score: 0.036
  9. A Diagnosis for All Rare Genetic Diseases: The Horizon and the Next Frontiers. Cell. 2019 03 21; 177(1):32-37.
    View in: PubMed
    Score: 0.025
  10. Copy-number variants in clinical genome sequencing: deployment and interpretation for rare and undiagnosed disease. Genet Med. 2019 05; 21(5):1121-1130.
    View in: PubMed
    Score: 0.025
  11. Toward clinical genomics in everyday medicine: perspectives and recommendations. Expert Rev Mol Diagn. 2016; 16(5):521-32.
    View in: PubMed
    Score: 0.021
  12. SHROOM3 is a novel candidate for heterotaxy identified by whole exome sequencing. Genome Biol. 2011 Sep 21; 12(9):R91.
    View in: PubMed
    Score: 0.015
  13. A genomewide single-nucleotide-polymorphism panel for Mexican American admixture mapping. Am J Hum Genet. 2007 Jun; 80(6):1014-23.
    View in: PubMed
    Score: 0.011
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.