Connection

RYAN DHINDSA to Phenotype

This is a "connection" page, showing publications RYAN DHINDSA has written about Phenotype.
Connection Strength

0.187
  1. Identification of a missense variant in SPDL1 associated with idiopathic pulmonary fibrosis. Commun Biol. 2021 03 23; 4(1):392.
    View in: PubMed
    Score: 0.091
  2. Disease prediction with multi-omics and biomarkers empowers case-control genetic discoveries in the UK Biobank. Nat Genet. 2024 Sep; 56(9):1821-1831.
    View in: PubMed
    Score: 0.029
  3. Phenome-wide identification of therapeutic genetic targets, leveraging knowledge graphs, graph neural networks, and UK Biobank data. Sci Adv. 2024 May 10; 10(19):eadj1424.
    View in: PubMed
    Score: 0.028
  4. Rare variant contribution to human disease in 281,104 UK Biobank exomes. Nature. 2021 09; 597(7877):527-532.
    View in: PubMed
    Score: 0.023
  5. Whole-exome sequencing in undiagnosed genetic diseases: interpreting 119 trios. Genet Med. 2015 Oct; 17(10):774-81.
    View in: PubMed
    Score: 0.015
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.