Iordanis Karagiannidis
Alexandroupoli, ESYE11, Greece
Last Updated: 09/26/2026
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Found 9 publications
Association of Genetic Variation in the 3'UTR of LHX6, IMMP2L, and AADAC With Tourette Syndrome.
Journal: Frontiers in neurology
Published: April 23, 2020
Targeted Re-Sequencing Approach of Candidate Genes Implicates Rare Potentially Functional Variants in Tourette Syndrome Etiology.
Journal: Frontiers in neuroscience
Published: March 31, 2016
Meta-Analysis of Tourette Syndrome and Attention Deficit Hyperactivity Disorder Provides Support for a Shared Genetic Basis.
Journal: Frontiers in neuroscience
Published: March 31, 2016
Association of AADAC Deletion and Gilles de la Tourette Syndrome in a Large European Cohort.
Journal: Biological psychiatry
Published: January 29, 2015
Genetic association signal near NTN4 in Tourette syndrome.
Journal: Annals of neurology
Published: March 04, 2014
Support of the histaminergic hypothesis in Tourette syndrome: association of the histamine decarboxylase gene in a large sample of families.
Journal: Journal of medical genetics
Published: July 05, 2013
Exploring genomic structure differences and similarities between the Greek and European HapMap populations: implications for association studies.
Journal: Annals of human genetics
Published: October 16, 2012
Evaluation of the LIM homeobox genes LHX6 and LHX8 as candidates for Tourette syndrome.
Journal: Genes, brain, and behavior
Published: March 23, 2012
Replication of association between a SLITRK1 haplotype and Tourette Syndrome in a large sample of families.
Journal: Molecular psychiatry
Published: November 16, 2011
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Last Updated: 09/26/2026