Connection

HUGO BELLEN to Mammals

This is a "connection" page, showing publications HUGO BELLEN has written about Mammals.
Connection Strength

0.489
  1. De novo variants in FRYL are associated with developmental delay, intellectual disability, and dysmorphic features. Am J Hum Genet. 2024 04 04; 111(4):742-760.
    View in: PubMed
    Score: 0.204
  2. Integrating non-mammalian model organisms in the diagnosis of rare genetic diseases in humans. Nat Rev Genet. 2024 Jan; 25(1):46-60.
    View in: PubMed
    Score: 0.195
  3. SPTSSA variants alter sphingolipid synthesis and cause a complex hereditary spastic paraplegia. Brain. 2023 04 19; 146(4):1420-1435.
    View in: PubMed
    Score: 0.048
  4. Using Drosophila to study mechanisms of hereditary hearing loss. Dis Model Mech. 2018 05 31; 11(6).
    View in: PubMed
    Score: 0.034
  5. pavarotti encodes a kinesin-like protein required to organize the central spindle and contractile ring for cytokinesis. Genes Dev. 1998 May 15; 12(10):1483-94.
    View in: PubMed
    Score: 0.009
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.