VISHNU CUDDAPAH to Child
This is a "connection" page, showing publications VISHNU CUDDAPAH has written about Child.
Connection Strength
0.150
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Rare variants in BMAL1 are associated with a neurodevelopmental syndrome. Proc Natl Acad Sci U S A. 2025 Aug 05; 122(31):e2427085122.
Score: 0.056
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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.
Score: 0.041
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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.
Score: 0.025
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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.
Score: 0.014
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Molecular and Phenotypic Characterization of the RORB-Related Disorder. Neurology. 2024 01 23; 102(2):e207945.
Score: 0.013