Fotis Tsetsos
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Analysis of shared heritability in common disorders of the brain
V Anttila, B Bulik-Sullivan, HK Finucane, RK Walters, J Bras, L Duncan, ...
Science 360 (6395), 2018
Rare copy number variants in NRXN1 and CNTN6 increase risk for Tourette syndrome
AY Huang, D Yu, LK Davis, JH Sul, F Tsetsos, V Ramensky, I Zelaya, ...
Neuron 94 (6), 1101-1111. e7, 2017
Interrogating the genetic determinants of Tourette’s syndrome and other tic disorders through genome-wide association studies
D Yu, JH Sul, F Tsetsos, MS Nawaz, AY Huang, I Zelaya, C Illmann, ...
American Journal of Psychiatry 176 (3), 217-227, 2019
Maritime route of colonization of Europe
P Paschou, P Drineas, E Yannaki, A Razou, K Kanaki, F Tsetsos, ...
Proceedings of the National Academy of Sciences 111 (25), 9211-9216, 2014
Genetic correlations among psychiatric and immune‐related phenotypes based on genome‐wide association data
DS Tylee, J Sun, JL Hess, MA Tahir, E Sharma, R Malik, BB Worrall, ...
American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 177 …, 2018
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
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
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
Genetics of the peloponnesean populations and the theory of extinction of the medieval peloponnesean Greeks
G Stamatoyannopoulos, A Bose, A Teodosiadis, F Tsetsos, A Plantinga, ...
European Journal of Human Genetics 25 (5), 637-645, 2017
Concordance of genetic variation that increases risk for tourette syndrome and that influences its underlying neurocircuitry
M Mufford, J Cheung, N Jahanshad, C Van Der Merwe, L Ding, ...
Translational psychiatry 9 (1), 1-10, 2019
Association of ALOX12 gene polymorphism with all-cause and cardiovascular mortality in diabetic nephropathy
AK Roumeliotis, SK Roumeliotis, SA Panagoutsos, F Tsetsos, M Georgitsi, ...
International urology and nephrology 50 (2), 321-329, 2018
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 (3), 218-231, 2016
Investigation of SNP rs2060546 immediately upstream to NTN4 in a Danish Gilles de la Tourette syndrome cohort
SS Padmanabhuni, R Houssari, AL Esserlind, J Olesen, TM Werge, ...
Frontiers in neuroscience 10, 531, 2016
Synaptic processes and immune-related pathways implicated in Tourette syndrome
F Tsetsos, D Yu, JH Sul, AY Huang, C Illmann, L Osiecki, SM Darrow, ...
Translational psychiatry 11 (1), 1-12, 2021
Cross-disorder GWAS meta-analysis for attention deficit/hyperactivity disorder, autism spectrum disorder, obsessive compulsive disorder, and Tourette syndrome
Z Yang, H Wu, PH Lee, F Tsetsos, LK Davis, D Yu, SH Lee, S Dalsgaard, ...
bioRxiv, 770222, 2019
Assessment of association between lipoxygenase genes variants in elderly Greek population and type 2 diabetes mellitus
XA Tsekmekidou, KD Kotsa, FS Tsetsos, TP Didangelos, MA Georgitsi, ...
Diabetes and Vascular Disease Research 15 (4), 340-343, 2018
Investigating shared genetic basis across tourette syndrome and comorbid neurodevelopmental disorders along the impulsivity-compulsivity spectrum
Z Yang, H Wu, PH Lee, F Tsetsos, LK Davis, D Yu, SH Lee, S Dalsgaard, ...
Biological psychiatry, 2021
Rapporteur Summaries of Plenary, Symposia, and Oral sessions from the XXIIIrd World Congress of Psychiatric Genetics Meeting in Toronto, Canada, October 16-20, 2015
G Zai, B Alberry, J Arloth, Z Bánlaki, C Bares, E Boot, C Camilo, K Chadha, ...
Psychiatric genetics 26 (6), 229, 2016
Association between CUBN gene variants, type 2 diabetes and vitamin D concentrations in an elderly Greek population
X Tsekmekidou, F Tsetsos, T Koufakis, SN Karras, M Georgitsi, ...
The Journal of steroid biochemistry and molecular biology 198, 105549, 2020
Genetic variation in CARD8, a gene coding for an NLRP3 inflammasome-associated protein, alters the genetic risk for diabetic nephropathy in the context of type 2 …
F Tsetsos, A Roumeliotis, X Tsekmekidou, S Alexouda, S Roumeliotis, ...
Diabetes and Vascular Disease Research 17 (6), 1479164120970892, 2020
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