| Analysis of shared heritability in common disorders of the brain Brainstorm Consortium, V Anttila, B Bulik-Sullivan, HK Finucane, ... Science 360 (6395), eaap8757, 2018 | 1123 | 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 | 173 | 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 | 150 | 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 | 142 | 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 | 91 | 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 | 67 | 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 | 57 | 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 | 36 | 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 | 36 | 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 | 30 | 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 | 25 | 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 | 25 | 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 | 18 | 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 | 17 | 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 | 14 | 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 | 9 | 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 | 9 | 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 | 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 | 8 | 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 | 7 | 2018 |
Peristera PaschouProfessor, Department of Biological Sciences, Purdue UniversityVerified email at purdue.edu
