Connection

CHRIS AMOS to Sequence Deletion

This is a "connection" page, showing publications CHRIS AMOS has written about Sequence Deletion.
Connection Strength

0.844
  1. Whole-genome detection of disease-associated deletions or excess homozygosity in a case-control study of rheumatoid arthritis. Hum Mol Genet. 2013 Mar 15; 22(6):1249-61.
    View in: PubMed
    Score: 0.337
  2. Common and distinct patterns of acquired uniparental disomy and homozygous deletions between lung squamous cell carcinomas and lung adenocarcinoma. Neoplasia. 2023 11; 45:100932.
    View in: PubMed
    Score: 0.179
  3. Positional identification of microdeletions with genetic markers. Hum Hered. 2003; 56(1-3):107-18.
    View in: PubMed
    Score: 0.169
  4. An intergenic risk locus containing an enhancer deletion in 2q35 modulates breast cancer risk by deregulating IGFBP5 expression. Hum Mol Genet. 2016 09 01; 25(17):3863-3876.
    View in: PubMed
    Score: 0.108
  5. Common deletion of SMAD4 in juvenile polyposis is a mutational hotspot. Am J Hum Genet. 2002 May; 70(5):1357-62.
    View in: PubMed
    Score: 0.040
  6. Germline p53 mutations in a cohort with childhood sarcoma: sex differences in cancer risk. Am J Hum Genet. 2003 Apr; 72(4):975-83.
    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.