Associated Papers
SLITRK1-mediated noradrenergic projection suppression in the neonatal prefrontal cortex.
Hatayama M et al.
Communications Biology, 2022
Candidate Genes and Pathways Associated with Gilles de la Tourette Syndrome-Where Are We?
Levy AM et al.
Genes, 2021
Biallelic loss-of-function variants in RBL2 in siblings with a neurodevelopmental disorder.
Brunet T et al.
Annals of Clinical and Translational Neurology, 2020
32105419 (PubMed )
Supplement: ACN3-7-390-s001.docx
Synaptic organizer: Slitrks and type IIa receptor protein tyrosine phosphatases.
Won SY et al.
Current Opinion in Structural Biology, 2019
Association of Rare Genetic Variants in Opioid Receptors with Tourette Syndrome.
Depienne C et al.
Tremor and Other Hyperkinetic Movements (new York, N.y.), 2019
Integrated genomic analyses of de novo pathways underlying atypical meningiomas.
Harmancı AS et al.
Nature Communications, 2017
28195122 (PubMed )
Supplement: ncomms14433-s3.xlsx › Table_S2D
Targeted Re-Sequencing Approach of Candidate Genes Implicates Rare Potentially Functional Variants in Tourette Syndrome Etiology.
Alexander J et al.
Frontiers in Neuroscience, 2016
Slitrk Missense Mutations Associated with Neuropsychiatric Disorders Distinctively Impair Slitrk Trafficking and Synapse Formation.
Kang H et al.
Frontiers in Molecular Neuroscience, 2016
Characterization of SLITRK1 variation in obsessive-compulsive disorder.
Ozomaro U et al.
Plos One, 2013
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