VISHNU CUDDAPAH to Humans
This is a "connection" page, showing publications VISHNU CUDDAPAH has written about Humans.
Connection Strength
0.207
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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: 0.025
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A recurrent de novo splice site variant involving DNM1 exon 10a causes developmental and epileptic encephalopathy through a dominant-negative mechanism. Am J Hum Genet. 2022 12 01; 109(12):2253-2269.
Score: 0.021
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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: 0.018
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Regulation of the Blood-Brain Barrier by Circadian Rhythms and Sleep. Trends Neurosci. 2019 07; 42(7):500-510.
Score: 0.016
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Hemispherectomy for Hemimegalencephaly Due to Tuberous Sclerosis and a Review of the Literature. Pediatr Neurol. 2015 Nov; 53(5):452-5.
Score: 0.012
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A neurocentric perspective on glioma invasion. Nat Rev Neurosci. 2014 Jul; 15(7):455-65.
Score: 0.011
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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: 0.011
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Bradykinin-induced chemotaxis of human gliomas requires the activation of KCa3.1 and ClC-3. J Neurosci. 2013 Jan 23; 33(4):1427-40.
Score: 0.010
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Calcium entry via TRPC1 channels activates chloride currents in human glioma cells. Cell Calcium. 2013 Mar; 53(3):187-94.
Score: 0.010
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Kinase activation of ClC-3 accelerates cytoplasmic condensation during mitotic cell rounding. Am J Physiol Cell Physiol. 2012 Feb 01; 302(3):C527-38.
Score: 0.010
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Ion channels and transporters [corrected] in cancer. 2. Ion channels and the control of cancer cell migration. Am J Physiol Cell Physiol. 2011 Sep; 301(3):C541-9.
Score: 0.009
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Molecular interaction and functional regulation of ClC-3 by Ca2+/calmodulin-dependent protein kinase II (CaMKII) in human malignant glioma. J Biol Chem. 2010 Apr 09; 285(15):11188-96.
Score: 0.008
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Delayed auditory feedback effects during reading and conversation tasks: gender differences in fluent adults. J Fluency Disord. 2008 Dec; 33(4):291-305.
Score: 0.008
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Genetic testing for familial epilepsies: Diagnostic yield and genetic findings. Epilepsia. 2026 Jun; 67(6):3048-3057.
Score: 0.006
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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: 0.006
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Haploinsufficiency of ITSN1 is associated with a substantial increased risk of Parkinson's disease. Cell Rep. 2025 Mar 25; 44(3):115355.
Score: 0.006
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Molecular and Phenotypic Characterization of the RORB-Related Disorder. Neurology. 2024 01 23; 102(2):e207945.
Score: 0.006
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Genotype-phenotype specificity in Menke-Hennekam syndrome caused by missense variants in exon 30 or 31 of CREBBP. Am J Med Genet A. 2019 06; 179(6):1058-1062.
Score: 0.004
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The role of glial-specific Kir4.1 in normal and pathological states of the CNS. Acta Neuropathol. 2016 07; 132(1):1-21.
Score: 0.003
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Differential role of IK and BK potassium channels as mediators of intrinsic and extrinsic apoptotic cell death. Am J Physiol Cell Physiol. 2012 Nov 15; 303(10):C1070-8.
Score: 0.003
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With-No-Lysine Kinase 3 (WNK3) stimulates glioma invasion by regulating cell volume. Am J Physiol Cell Physiol. 2011 Nov; 301(5):C1150-60.
Score: 0.002