Connection

Bradley Schulte to Deafness

This is a "connection" page, showing publications Bradley Schulte has written about Deafness.
Connection Strength

0.227
  1. Whole exome sequencing in adult-onset hearing loss reveals a high load of predicted pathogenic variants in known deafness-associated genes and identifies new candidate genes. BMC Med Genomics. 2018 Sep 04; 11(1):77.
    View in: PubMed
    Score: 0.146
  2. Translational and interdisciplinary insights into presbyacusis: A multidimensional disease. Hear Res. 2021 03 15; 402:108109.
    View in: PubMed
    Score: 0.042
  3. Mutation of the Na-K-Cl co-transporter gene Slc12a2 results in deafness in mice. Hum Mol Genet. 1999 Aug; 8(8):1579-84.
    View in: PubMed
    Score: 0.039
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.