| Year |
Citation |
Score |
| 2023 |
Tsetsos F, Topaloudi A, Jain P, Yang Z, Yu D, Kolovos P, Tumer Z, Rizzo R, Hartmann A, Depienne C, Worbe Y, Müller-Vahl KR, Cath DC, Boomsma DI, Wolanczyk T, et al. Genome-wide Association Study points to novel locus for Gilles de la Tourette Syndrome. Biological Psychiatry. PMID 36738982 DOI: 10.1016/j.biopsych.2023.01.023 |
0.662 |
|
| 2021 |
Tsekmekidou X, Tsetsos F, Koufakis T, Georgitsi M, Papanas N, Papazoglou D, Roumeliotis A, Panagoutsos S, Thodis E, Theodoridis M, Passadakis P, Maltezos E, Paschou P, Kotsa K. Variants in clock genes could be associated with lower risk of type 2 diabetes in an elderly Greek population. Maturitas. 152: 20-25. PMID 34674804 DOI: 10.1016/j.maturitas.2021.07.004 |
0.643 |
|
| 2021 |
Roumeliotis A, Roumeliotis S, Tsetsos F, Georgitsi M, Georgianos PI, Stamou A, Vasilakou A, Kotsa K, Tsekmekidou X, Paschou P, Panagoutsos S, Liakopoulos V. Oxidative Stress Genes in Diabetes Mellitus Type 2: Association with Diabetic Kidney Disease. Oxidative Medicine and Cellular Longevity. 2021: 2531062. PMID 34545296 DOI: 10.1155/2021/2531062 |
0.636 |
|
| 2021 |
Topaloudi A, Zagoriti Z, Flint AC, Martinez MB, Yang Z, Tsetsos F, Christou YP, Lagoumintzis G, Yannaki E, Zamba-Papanicolaou E, Tzartos J, Tsekmekidou X, Kotsa K, Maltezos E, Papanas N, et al. Myasthenia gravis genome-wide association study implicates AGRN as a risk locus. Journal of Medical Genetics. PMID 34400559 DOI: 10.1136/jmedgenet-2021-107953 |
0.638 |
|
| 2021 |
Yang Z, Wu H, Lee PH, Tsetsos F, Davis LK, Yu D, Lee SH, Dalsgaard S, Haavik J, Barta C, Zayats T, Eapen V, Wray NR, Devlin B, Daly M, et al. Investigating Shared Genetic Basis Across Tourette Syndrome and Comorbid Neurodevelopmental Disorders Along the Impulsivity-Compulsivity Spectrum. Biological Psychiatry. PMID 33714545 DOI: 10.1016/j.biopsych.2020.12.028 |
0.642 |
|
| 2021 |
Tsetsos F, Yu D, Sul JH, Huang AY, Illmann C, Osiecki L, Darrow SM, Hirschtritt ME, Greenberg E, Muller-Vahl KR, Stuhrmann M, Dion Y, Rouleau GA, Aschauer H, Stamenkovic M, ... ... Tsetsos F, ... ... Tsetsos F, et al. Synaptic processes and immune-related pathways implicated in Tourette syndrome. Translational Psychiatry. 11: 56. PMID 33462189 DOI: 10.1038/s41398-020-01082-z |
0.647 |
|
| 2020 |
Tsetsos F, Roumeliotis A, Tsekmekidou X, Alexouda S, Roumeliotis S, Theodoridis M, Thodis E, Panagoutsos S, Papanas N, Papazoglou D, Kotsa K, Yovos JG, Maltezos E, Passadakis P, Paschou P, et al. Genetic variation in , a gene coding for an NLRP3 inflammasome-associated protein, alters the genetic risk for diabetic nephropathy in the context of type 2 diabetes mellitus. Diabetes & Vascular Disease Research. 17: 1479164120970892. PMID 33164551 DOI: 10.1177/1479164120970892 |
0.609 |
|
| 2019 |
Tsekmekidou X, Tsetsos F, Koufakis T, Karras SN, Georgitsi M, Papanas N, Papazoglou D, Roumeliotis A, Panagoutsos S, Thodis E, Theodoridis M, Pasadakis P, Maltezos E, Paschou P, Kotsa K. Association between CUBN gene variants, type 2 diabetes and vitamin D concentrations in an elderly Greek population. The Journal of Steroid Biochemistry and Molecular Biology. 105549. PMID 31770575 DOI: 10.1016/J.Jsbmb.2019.105549 |
0.639 |
|
| 2019 |
Drineas P, Tsetsos F, Plantinga A, Lazaridis I, Yannaki E, Razou A, Kanaki K, Michalodimitrakis M, Perez-Jimenez F, De Silvestro G, Renda MC, Stamatoyannopoulos JA, Kidd KK, Browning BL, Paschou P, et al. Genetic history of the population of Crete. Annals of Human Genetics. PMID 31192450 DOI: 10.1111/Ahg.12328 |
0.677 |
|
| 2019 |
Yu D, Sul JH, Tsetsos F, Nawaz MS, Huang AY, Zelaya I, Illmann C, Osiecki L, Darrow SM, Hirschtritt ME, Greenberg E, Muller-Vahl KR, Stuhrmann M, Dion Y, Rouleau G, et al. Interrogating the Genetic Determinants of Tourette's Syndrome and Other Tic Disorders Through Genome-Wide Association Studies. The American Journal of Psychiatry. 176: 217-227. PMID 30818990 DOI: 10.1176/Appi.Ajp.2018.18070857 |
0.693 |
|
| 2019 |
Roumeliotis A, Roumeliotis S, Tsetsos F, Theodoridis M, Kantartzi K, Manolopoulos V, Pasadakis P, Panagoutsos S. Sp033Diabetic Nephropathy Genes In The Greek Population Nephrology Dialysis Transplantation. 34. DOI: 10.1093/Ndt/Gfz103.Sp033 |
0.37 |
|
| 2019 |
Yang Z, Wu H, Lee P, Tsetsos F, Davis L, Yu D, Lee SH, Dalsgaard S, Haavik J, Barta C, Zayats T, Corfield E, Eapen V, Wray NR, Devlin B. 89 Cross-Disorder Meta-Analysis Of Genomewide Association Studies Sheds Light Into Potentially Shared Neurobiology Across Adhd, Asd, Ocd, And Ts European Neuropsychopharmacology. 29. DOI: 10.1016/J.Euroneuro.2019.07.230 |
0.405 |
|
| 2019 |
Scharf J, Yu D, Huang A, Tsetsos F, Paschou P, Coppola G, Mathews C. Collaborative Genome-Wide Association and Copy Number Variation Analysis of Tourette Syndrome European Neuropsychopharmacology. 29. DOI: 10.1016/J.Euroneuro.2017.06.064 |
0.696 |
|
| 2018 |
Anttila V, Bulik-Sullivan B, Finucane HK, Walters RK, Bras J, Duncan L, Escott-Price V, Falcone GJ, Gormley P, Malik R, Patsopoulos NA, Ripke S, Wei Z, Yu D, ... ... Tsetsos F, et al. Analysis of shared heritability in common disorders of the brain. Science (New York, N.Y.). 360. PMID 29930110 DOI: 10.1126/Science.Aap8757 |
0.683 |
|
| 2018 |
Tsekmekidou XA, Kotsa KD, Tsetsos FS, Didangelos TP, Georgitsi MA, Roumeliotis AK, Panagoutsos SA, Thodis ED, Theodoridis MT, Papanas NP, Papazoglou DA, Pasadakis PS, Eustratios MS, Paschou PI, Yovos JG. Assessment of association between lipoxygenase genes variants in elderly Greek population and type 2 diabetes mellitus. Diabetes & Vascular Disease Research. 1479164118756241. PMID 29392977 DOI: 10.1177/1479164118756241 |
0.618 |
|
| 2017 |
Roumeliotis AK, Roumeliotis SK, Panagoutsos SA, Tsetsos F, Georgitsi M, Manolopoulos V, Paschou P, Passadakis PS. Association of ALOX12 gene polymorphism with all-cause and cardiovascular mortality in diabetic nephropathy. International Urology and Nephrology. PMID 29196930 DOI: 10.1007/S11255-017-1755-Z |
0.63 |
|
| 2017 |
Huang AY, Yu D, Davis LK, Sul JH, Tsetsos F, Ramensky V, Zelaya I, Ramos EM, Osiecki L, Chen JA, McGrath LM, Illmann C, Sandor P, Barr CL, Grados M, et al. Rare Copy Number Variants in NRXN1 and CNTN6 Increase Risk for Tourette Syndrome. Neuron. 94: 1101-1111.e7. PMID 28641109 DOI: 10.1016/J.Neuron.2017.06.010 |
0.684 |
|
| 2017 |
Stamatoyannopoulos G, Bose A, Teodosiadis A, Tsetsos F, Plantinga A, Psatha N, Zogas N, Yannaki E, Zalloua P, Kidd KK, Browning BL, Stamatoyannopoulos J, Paschou P, Drineas P. Genetics of the peloponnesean populations and the theory of extinction of the medieval peloponnesean Greeks. European Journal of Human Genetics : Ejhg. PMID 28272534 DOI: 10.1038/Ejhg.2017.18 |
0.691 |
|
| 2016 |
Padmanabhuni SS, Houssari R, Esserlind AL, Olesen J, Werge TM, Hansen TF, Bertelsen B, Tsetsos F, Paschou P, Tümer Z. Investigation of SNP rs2060546 Immediately Upstream to NTN4 in a Danish Gilles de la Tourette Syndrome Cohort. Frontiers in Neuroscience. 10: 531. PMID 27920664 DOI: 10.3389/Fnins.2016.00531 |
0.761 |
|
| 2016 |
Alexander J, Potamianou H, Xing J, Deng L, Karagiannidis I, Tsetsos F, Drineas P, Tarnok Z, Rizzo R, Wolanczyk T, Farkas L, Nagy P, Szymanska U, Androutsos C, Tsironi V, et al. Targeted Re-Sequencing Approach of Candidate Genes Implicates Rare Potentially Functional Variants in Tourette Syndrome Etiology. Frontiers in Neuroscience. 10: 428. PMID 27708560 DOI: 10.3389/Fnins.2016.00428 |
0.716 |
|
| 2016 |
Zai G, Alberry B, Arloth J, Bánlaki Z, Bares C, Boot E, Camilo C, Chadha K, Chen Q, Cole CB, Cost KT, Crow M, Ekpor I, Fischer SB, Flatau L, ... ... Tsetsos F, et al. Rapporteur summaries of plenary, symposia, and oral sessions from the XXIIIrd World Congress of Psychiatric Genetics Meeting in Toronto, Canada, 16-20 October 2015. Psychiatric Genetics. PMID 27606929 DOI: 10.1097/Ypg.0000000000000148 |
0.37 |
|
| 2016 |
Tsetsos F, Padmanabhuni SS, Alexander J, Karagiannidis I, Tsifintaris M, Topaloudi A, Mantzaris D, Georgitsi M, Drineas P, Paschou P. Meta-Analysis of Tourette Syndrome and Attention Deficit Hyperactivity Disorder Provides Support for a Shared Genetic Basis. Frontiers in Neuroscience. 10: 340. PMID 27499730 DOI: 10.3389/Fnins.2016.00340 |
0.784 |
|
| 2016 |
Karagiannidis I, Tsetsos F, Padmanabhuni SS, Alexander J, Georgitsi M, Paschou P. The Genetics of Gilles de la Tourette Syndrome: a Common Aetiological Basis with Comorbid Disorders? Current Behavioral Neuroscience Reports. 3: 218-231. DOI: 10.1007/S40473-016-0088-Z |
0.752 |
|
| 2014 |
Paschou P, Yu D, Gerber G, Evans P, Tsetsos F, Davis LK, Karagiannidis I, Chaponis J, Gamazon E, Mueller-Vahl K, Stuhrmann M, Schloegelhofer M, Stamenkovic M, Hebebrand J, Noethen M, et al. Genetic association signal near NTN4 in Tourette syndrome. Annals of Neurology. 76: 310-5. PMID 25042818 DOI: 10.1002/Ana.24215 |
0.69 |
|
| 2014 |
Paschou P, Drineas P, Yannaki E, Razou A, Kanaki K, Tsetsos F, Padmanabhuni SS, Michalodimitrakis M, Renda MC, Pavlovic S, Anagnostopoulos A, Stamatoyannopoulos JA, Kidd KK, Stamatoyannopoulos G. Maritime route of colonization of Europe. Proceedings of the National Academy of Sciences of the United States of America. 111: 9211-6. PMID 24927591 DOI: 10.1073/Pnas.1320811111 |
0.736 |
|
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