Connection

FRITZ SEDLAZECK to Phenotype

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

0.383
  1. Long-read sequencing of 945 Han individuals identifies structural variants associated with phenotypic diversity and disease susceptibility. Nat Commun. 2025 Feb 10; 16(1):1494.
    View in: PubMed
    Score: 0.122
  2. Structural variant allelic heterogeneity in MECP2 duplication syndrome provides insight into clinical severity and variability of disease expression. Genome Med. 2024 Dec 18; 16(1):146.
    View in: PubMed
    Score: 0.121
  3. Beyond the exome: What's next in diagnostic testing for Mendelian conditions. Am J Hum Genet. 2023 08 03; 110(8):1229-1248.
    View in: PubMed
    Score: 0.028
  4. The EN-TEx resource of multi-tissue personal epigenomes?& variant-impact models. Cell. 2023 03 30; 186(7):1493-1511.e40.
    View in: PubMed
    Score: 0.027
  5. Towards accurate and reliable resolution of structural variants for clinical diagnosis. Genome Biol. 2022 03 03; 23(1):68.
    View in: PubMed
    Score: 0.025
  6. Major Impacts of Widespread Structural Variation on Gene Expression and Crop Improvement in Tomato. Cell. 2020 07 09; 182(1):145-161.e23.
    View in: PubMed
    Score: 0.022
  7. A Genocentric Approach to Discovery of Mendelian Disorders. Am J Hum Genet. 2019 11 07; 105(5):974-986.
    View in: PubMed
    Score: 0.021
  8. The genomic basis of circadian and circalunar timing adaptations in a midge. Nature. 2016 12 01; 540(7631):69-73.
    View in: PubMed
    Score: 0.017
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.