Connection

CHAD SHAW to Genetic Testing

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

0.826
  1. Clinical exome sequencing efficacy and phenotypic expansions involving non-isolated congenital anomalies of kidney and urinary tract (CAKUT+). Eur J Hum Genet. 2025 Dec; 33(12):1606-1615.
    View in: PubMed
    Score: 0.143
  2. Non-isolated tetralogy of fallot (TOF+): exome sequencing efficacy and phenotypic expansions. Eur J Hum Genet. 2026 Mar; 34(3):333-339.
    View in: PubMed
    Score: 0.142
  3. 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: 0.131
  4. Clinical genome sequencing: Three years' experience at a tertiary children's hospital. Genet Med. 2023 10; 25(10):100916.
    View in: PubMed
    Score: 0.122
  5. Reanalysis of Clinical Exome Sequencing Data. N Engl J Med. 2019 06 20; 380(25):2478-2480.
    View in: PubMed
    Score: 0.093
  6. Copy number variant and runs of homozygosity detection by microarrays enabled more precise molecular diagnoses in 11,020 clinical exome cases. Genome Med. 2019 05 17; 11(1):30.
    View in: PubMed
    Score: 0.092
  7. Molecular diagnostic experience of whole-exome sequencing in adult patients. Genet Med. 2016 07; 18(7):678-85.
    View in: PubMed
    Score: 0.073
  8. Clinical exome sequencing efficacy and phenotypic expansions involving anomalous pulmonary venous return. Eur J Hum Genet. 2023 12; 31(12):1430-1439.
    View in: PubMed
    Score: 0.031
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.