Connection

LINYAN MENG to Genetic Diseases, Inborn

This is a "connection" page, showing publications LINYAN MENG has written about Genetic Diseases, Inborn.
Connection Strength

1.081
  1. Use of Exome Sequencing for Infants in Intensive Care Units: Ascertainment of Severe Single-Gene Disorders and Effect on Medical Management. JAMA Pediatr. 2017 12 04; 171(12):e173438.
    View in: PubMed
    Score: 0.448
  2. Gene-targeting pharmaceuticals for single-gene disorders. Hum Mol Genet. 2016 Apr 15; 25(R1):R18-26.
    View in: PubMed
    Score: 0.390
  3. Reanalysis of Clinical Exome Sequencing Data. N Engl J Med. 2019 06 20; 380(25):2478-2480.
    View in: PubMed
    Score: 0.125
  4. Clinical exome sequencing for fetuses with ultrasound abnormalities and a suspected Mendelian disorder. Genome Med. 2018 09 28; 10(1):74.
    View in: PubMed
    Score: 0.118
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.