Fotis Tsetsos
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Analysis of shared heritability in common disorders of the brain
Brainstorm Consortium, V Anttila, B Bulik-Sullivan, HK Finucane, ...
Science 360 (6395), eaap8757, 2018
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
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
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
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 architecture of 11 major psychiatric disorders at biobehavioral, functional genomic and molecular genetic levels of analysis
AD Grotzinger, TT Mallard, WA Akingbuwa, HF Ip, MJ Adams, CM Lewis, ...
Nature genetics 54 (5), 548-559, 2022
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
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 90 (5), 317-327, 2021
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
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), 56, 2021
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), 120, 2019
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
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, 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, 218-231, 2016
Elevated common variant genetic risk for tourette syndrome in a densely-affected pedigree
M Halvorsen, J Szatkiewicz, P Mudgal, D Yu, AE Nordsletten, ...
Molecular psychiatry 26 (12), 7522-7529, 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
Association of rs11780592 polymorphism in the human soluble epoxide hydrolase gene (EPHX2) with oxidized LDL and mortality in patients with diabetic chronic kidney disease
S Roumeliotis, A Roumeliotis, A Stamou, S Panagoutsos, ...
Oxidative medicine and cellular longevity 2021, 1-8, 2021
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
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
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