Connection

VISHNU CUDDAPAH to Child

This is a "connection" page, showing publications VISHNU CUDDAPAH has written about Child.
Connection Strength

0.150
  1. Rare variants in BMAL1 are associated with a neurodevelopmental syndrome. Proc Natl Acad Sci U S A. 2025 Aug 05; 122(31):e2427085122.
    View in: PubMed
    Score: 0.056
  2. Understanding the phenotypic spectrum of ASXL-related disease: Ten cases and a review of the literature. Am J Med Genet A. 2021 06; 185(6):1700-1711.
    View in: PubMed
    Score: 0.041
  3. Methyl-CpG-binding protein 2 (MECP2) mutation type is associated with disease severity in Rett syndrome. J Med Genet. 2014 Mar; 51(3):152-8.
    View in: PubMed
    Score: 0.025
  4. Functional and pharmacological investigation of novel and de novo KCND3 variants identified in patients with neurodevelopmental disorders. J Hum Genet. 2026 Apr; 71(4):187-193.
    View in: PubMed
    Score: 0.014
  5. Molecular and Phenotypic Characterization of the RORB-Related Disorder. Neurology. 2024 01 23; 102(2):e207945.
    View in: PubMed
    Score: 0.013
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.