Követés
Iordanis Karagiannidis
Iordanis Karagiannidis
E-mail megerősítve itt: mbg.duth.gr
Cím
Hivatkozott rá
Hivatkozott rá
Év
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
1192018
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
1182013
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
812012
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
722014
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
502016
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, 202929, 2016
402016
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
302016
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
222012
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
182019
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
172020
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
152020
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
152016
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
122013
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
102012
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
82023
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
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Cikkek 1–16