| Support of the histaminergic hypothesis in Tourette syndrome: association of the histamine decarboxylase gene in a large sample of families I Karagiannidis, S Dehning, P Sandor, Z Tarnok, R Rizzo, T Wolanczyk, ... Journal of medical genetics 50 (11), 760-764, 2013 | 113 | 2013 |
| De novo sequence and copy number variants are strongly associated with tourette disorder and implicate cell polarity in pathogenesis S Wang, JD Mandell, Y Kumar, N Sun, MT Morris, J Arbelaez, C Nasello, ... Cell reports 24 (13), 3441-3454. e12, 2018 | 99 | 2018 |
| Replication of association between a SLITRK1 haplotype and Tourette Syndrome in a large sample of families I Karagiannidis, R Rizzo, Z Tarnok, T Wolanczyk, J Hebebrand, ... Molecular psychiatry 17 (7), 665-668, 2012 | 76 | 2012 |
| Genetic association signal near NTN4 in Tourette syndrome P Paschou, D Yu, G Gerber, P Evans, F Tsetsos, LK Davis, I Karagiannidis, ... Annals of neurology 76 (2), 310-315, 2014 | 59 | 2014 |
| Association of AADAC deletion and Gilles de la Tourette syndrome in a large European cohort B Bertelsen, H Stefánsson, LR Jensen, L Melchior, NM Debes, C Groth, ... Biological psychiatry 79 (5), 383-391, 2016 | 40 | 2016 |
| Meta-analysis of tourette syndrome and attention deficit hyperactivity disorder provides support for a shared genetic basis F Tsetsos, SS Padmanabhuni, J Alexander, I Karagiannidis, M Tsifintaris, ... Frontiers in neuroscience 10, 340, 2016 | 37 | 2016 |
| Targeted re-sequencing approach of candidate genes implicates rare potentially functional variants in Tourette syndrome etiology J Alexander, H Potamianou, J Xing, L Deng, I Karagiannidis, F Tsetsos, ... Frontiers in neuroscience 10, 428, 2016 | 25 | 2016 |
| Evaluation of the LIM homeobox genes LHX6 and LHX8 as candidates for Tourette syndrome P Paschou, E Stylianopoulou, I Karagiannidis, R Rizzo, Z Tarnok, ... Genes, Brain and Behavior 11 (4), 444-451, 2012 | 21 | 2012 |
| Antibodies to neuronal surface proteins in Tourette Syndrome: Lack of evidence in a European paediatric cohort V Baglioni, E Coutinho, DA Menassa, MP Giannoccaro, L Jacobson, ... Brain, Behavior, and Immunity 81, 665-669, 2019 | 17 | 2019 |
| The genetics of Gilles de la Tourette syndrome: a common aetiological basis with comorbid disorders? I Karagiannidis, F Tsetsos, SS Padmanabhuni, J Alexander, M Georgitsi, ... Current Behavioral Neuroscience Reports 3, 218-231, 2016 | 14 | 2016 |
| Anti‐dopamine D2 receptor antibodies in chronic tic disorders F Addabbo, V Baglioni, A Schrag, MJ Schwarz, A Dietrich, PJ Hoekstra, ... Developmental Medicine & Child Neurology 62 (10), 1205-1212, 2020 | 12 | 2020 |
| Association of Genetic Variation in the 3'UTR of LHX6, IMMP2L, and AADAC With Tourette Syndrome L Pagliaroli, A Vereczkei, SS Padmanabhuni, Z Tarnok, L Farkas, P Nagy, ... Frontiers in Neurology 11, 803, 2020 | 12 | 2020 |
| Selected rapporteur summaries from the XX world congress of psychiatric genetics, Hamburg, Germany, october 14–18, 2012 H Anderson‐Schmidt, O Beltcheva, MD Brandon, EM Byrne, EJ Diehl, ... American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 162 …, 2013 | 12 | 2013 |
| Exploring genomic structure differences and similarities between the Greek and European HapMap populations: implications for association studies V Stathias, GR Sotiris, I Karagiannidis, G Bourikas, G Martinis, ... Annals of human genetics 76 (6), 472-483, 2012 | 10 | 2012 |
| Genome-wide Association Study points to novel locus for Gilles de la Tourette Syndrome F Tsetsos, A Topaloudi, P Jain, Z Yang, D Yu, P Kolovos, Z Tumer, ... Biological psychiatry, 2023 | | 2023 |
| The genetic basis of Gilles de la Tourette syndrome in populations of european ancestry I Karagiannidis Δημοκρίτειο Πανεπιστήμιο Θράκης (ΔΠΘ). Σχολή Επιστημών Υγείας. Τμήμα …, 2017 | | 2017 |
