| Year |
Citation |
Score |
| 2023 |
Jain PR, Yates M, de Celis CR, Drineas P, Jahanshad N, Thompson P, Paschou P. Multiomic approach and Mendelian randomization analysis identify causal associations between blood biomarkers and subcortical brain structure volumes. Neuroimage. 284: 120466. PMID 37995919 DOI: 10.1016/j.neuroimage.2023.120466 |
0.599 |
|
| 2023 |
Jain PR, Burch M, Martinez M, Mir P, Fichna JP, Zekanowski C, Rizzo R, Tümer Z, Barta C, Yannaki E, Stamatoyannopoulos J, Drineas P, Paschou P. Can polygenic risk scores help explain disease prevalence differences around the world? A worldwide investigation. Bmc Genomic Data. 24: 70. PMID 37986041 DOI: 10.1186/s12863-023-01168-9 |
0.671 |
|
| 2023 |
Bose A, Burch M, Chowdhury A, Paschou P, Drineas P. Structure-informed clustering for population stratification in association studies. Bmc Bioinformatics. 24: 411. PMID 37907836 DOI: 10.1186/s12859-023-05511-w |
0.653 |
|
| 2023 |
Topaloudi A, Jain P, Martinez MB, Bryant JK, Reynolds G, Zagoriti Z, Lagoumintzis G, Zamba-Papanicolaou E, Tzartos J, Poulas K, Kleopa KA, Tzartos S, Georgitsi M, Drineas P, Paschou P. PheWAS and cross-disorder analysis reveal genetic architecture, pleiotropic loci and phenotypic correlations across 11 autoimmune disorders. Frontiers in Immunology. 14: 1147573. PMID 37809097 DOI: 10.3389/fimmu.2023.1147573 |
0.643 |
|
| 2023 |
Jain P, Yates M, de Celis CR, Drineas P, Jahanshad N, Thompson P, Paschou P. Multiomic approach and Mendelian randomization analysis identify causal associations between blood biomarkers and subcortical brain structure volumes. Medrxiv : the Preprint Server For Health Sciences. PMID 37066330 DOI: 10.1101/2023.03.30.23287968 |
0.601 |
|
| 2023 |
Jain P, Miller-Fleming T, Topaloudi A, Yu D, Drineas P, Georgitsi M, Yang Z, Rizzo R, Müller-Vahl KR, Tumer Z, Mol Debes N, Hartmann A, Depienne C, Worbe Y, Mir P, ... ... Paschou P, et al. Polygenic risk score-based phenome-wide association study identifies novel associations for Tourette syndrome. Translational Psychiatry. 13: 69. PMID 36823209 DOI: 10.1038/s41398-023-02341-5 |
0.66 |
|
| 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, ... ... Paschou P, 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 |
0.755 |
|
| 2022 |
Paschou P, Jin Y, Müller-Vahl K, Möller HE, Rizzo R, Hoekstra PJ, Roessner V, Mol Debes N, Worbe Y, Hartmann A, Mir P, Cath D, Neuner I, Eichele H, Zhang C, et al. Enhancing neuroimaging genetics through meta-analysis for Tourette syndrome (ENIGMA-TS): A worldwide platform for collaboration. Frontiers in Psychiatry. 13: 958688. PMID 36072455 DOI: 10.3389/fpsyt.2022.958688 |
0.641 |
|
| 2022 |
Yang Z, Paschou P, Drineas P. Reconstructing SNP allele and genotype frequencies from GWAS summary statistics. Scientific Reports. 12: 8242. PMID 35581276 DOI: 10.1038/s41598-022-12185-6 |
0.625 |
|
| 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 |
0.739 |
|
| 2021 |
Levy AM, Paschou P, Tümer Z. Candidate Genes and Pathways Associated with Gilles de la Tourette Syndrome-Where Are We? Genes. 12. PMID 34573303 DOI: 10.3390/genes12091321 |
0.427 |
|
| 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 |
0.738 |
|
| 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, ... ... Paschou P, 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 |
0.747 |
|
| 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, ... ... Paschou P, 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 |
0.736 |
|
| 2021 |
Bose A, Platt DE, Parida L, Drineas P, Paschou P. Integrating Linguistics, Social Structure, and Geography to Model Genetic Diversity within India. Molecular Biology and Evolution. PMID 33481022 DOI: 10.1093/molbev/msaa321 |
0.623 |
|
| 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, ... ... Paschou P, ... ... Paschou P, ... ... Paschou P, 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 |
0.747 |
|
| 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 |
0.72 |
|
| 2020 |
Kidd KK, Pakstis AJ, Donnelly MP, Bulbul O, Cherni L, Gurkan C, Kang L, Li H, Yun L, Paschou P, Meiklejohn KA, Haigh E, Speed WC. The distinctive geographic patterns of common pigmentation variants at the OCA2 gene. Scientific Reports. 10: 15433. PMID 32963319 DOI: 10.1038/s41598-020-72262-6 |
0.668 |
|
| 2020 |
Pagliaroli L, Vereczkei A, Padmanabhuni SS, Tarnok Z, Farkas L, Nagy P, Rizzo R, Wolanczyk T, Szymanska U, Kapisyzi M, Basha E, Koumoula A, Androutsos C, Tsironi V, Karagiannidis I, ... Paschou P, et al. Association of Genetic Variation in the 3'UTR of LHX6, IMMP2L, and AADAC With Tourette Syndrome. Frontiers in Neurology. 11: 803. PMID 32922348 DOI: 10.3389/Fneur.2020.00803 |
0.428 |
|
| 2020 |
Thompson PM, Jahanshad N, Ching CRK, Salminen LE, Thomopoulos SI, Bright J, Baune BT, Bertolín S, Bralten J, Bruin WB, Bülow R, Chen J, Chye Y, Dannlowski U, de Kovel CGF, ... ... Paschou P, et al. ENIGMA and global neuroscience: A decade of large-scale studies of the brain in health and disease across more than 40 countries. Translational Psychiatry. 10: 100. PMID 32198361 DOI: 10.1038/S41398-020-0705-1 |
0.451 |
|
| 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 |
0.738 |
|
| 2019 |
Raveane A, Aneli S, Montinaro F, Athanasiadis G, Barlera S, Birolo G, Boncoraglio G, Di Blasio AM, Di Gaetano C, Pagani L, Parolo S, Paschou P, Piazza A, Stamatoyannopoulos G, Angius A, et al. Population structure of modern-day Italians reveals patterns of ancient and archaic ancestries in Southern Europe. Science Advances. 5: eaaw3492. PMID 31517044 DOI: 10.1126/Sciadv.Aaw3492 |
0.405 |
|
| 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 |
0.789 |
|
| 2019 |
Bose A, Kalantzis V, Kontopoulou E, Elkady M, Paschou P, Drineas P. TeraPCA: a fast and scalable software package to study genetic variation in tera-scale genotypes. Bioinformatics (Oxford, England). PMID 30957838 DOI: 10.1093/Bioinformatics/Btz157 |
0.641 |
|
| 2019 |
Mufford M, Cheung J, Jahanshad N, van der Merwe C, Ding L, Groenewold N, Koen N, Chimusa ER, Dalvie S, Ramesar R, Knowles JA, Lochner C, Hibar DP, Paschou P, et al. Concordance of genetic variation that increases risk for tourette syndrome and that influences its underlying neurocircuitry. Translational Psychiatry. 9: 120. PMID 30902966 DOI: 10.1038/S41398-019-0452-3 |
0.479 |
|
| 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, ... ... Paschou P, 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 |
0.765 |
|
| 2019 |
Alexander J, Ströbel T, Georgitsi M, Hönigschnabl S, Reiner A, Fischer P, Tsifintaris M, Paschou P, Kovacs GG. Neuropathology-driven Whole-genome Sequencing Study Points to Novel Candidate Genes for Healthy Brain Aging. Alzheimer Disease and Associated Disorders. PMID 30681437 DOI: 10.1097/Wad.0000000000000294 |
0.442 |
|
| 2019 |
Paschou P. Dissecting The Etiology of Tourette Syndrome Through Large-Scale Genome, Epigenome And Transcriptome Studies and Cross-Disorder Analysis European Neuropsychopharmacology. 29: S737-S738. DOI: 10.1016/J.Euroneuro.2017.06.066 |
0.501 |
|
| 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 |
0.782 |
|
| 2019 |
Paschou P, Heiman G, Tischfield J. Genetics of Gilles De La Tourette Syndrome: Accelerating Discoveries Through Large-Scale Collaborative Efforts European Neuropsychopharmacology. 29: S736. DOI: 10.1016/J.Euroneuro.2017.06.063 |
0.502 |
|
| 2018 |
Wang S, Mandell JD, Kumar Y, Sun N, Morris MT, Arbelaez J, Nasello C, Dong S, Duhn C, Zhao X, Yang Z, Padmanabhuni SS, Yu D, King RA, Dietrich A, ... ... Paschou P, et al. De Novo Sequence and Copy Number Variants Are Strongly Associated with Tourette Disorder and Implicate Cell Polarity in Pathogenesis. Cell Reports. 25: 3544. PMID 30566877 DOI: 10.1016/j.celrep.2018.12.024 |
0.666 |
|
| 2018 |
Wang S, Mandell JD, Kumar Y, Sun N, Morris MT, Arbelaez J, Nasello C, Dong S, Duhn C, Zhao X, Yang Z, Padmanabhuni SS, Yu D, King RA, Dietrich A, ... ... Paschou P, et al. De Novo Sequence and Copy Number Variants Are Strongly Associated with Tourette Disorder and Implicate Cell Polarity in Pathogenesis. Cell Reports. 24: 3441-3454.e12. PMID 30257206 DOI: 10.1016/J.Celrep.2018.08.082 |
0.727 |
|
| 2018 |
Schrag A, Martino D, Apter A, Ball J, Bartolini E, Benaroya-Milshtein N, Buttiglione M, Cardona F, Creti R, Efstratiou A, Gariup M, Georgitsi M, Hedderly T, Heyman I, Margarit I, ... ... Paschou P, et al. European Multicentre Tics in Children Studies (EMTICS): protocol for two cohort studies to assess risk factors for tic onset and exacerbation in children and adolescents. European Child & Adolescent Psychiatry. PMID 29982875 DOI: 10.1007/S00787-018-1190-4 |
0.413 |
|
| 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, ... ... Paschou P, 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 |
0.773 |
|
| 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 |
0.725 |
|
| 2017 |
Bulbul O, Pakstis AJ, Soundararajan U, Gurkan C, Brissenden JE, Roscoe JM, Evsanaa B, Togtokh A, Paschou P, Grigorenko EL, Gurwitz D, Wootton S, Lagace R, Chang J, Speed WC, et al. Ancestry inference of 96 population samples using microhaplotypes. International Journal of Legal Medicine. PMID 29248957 DOI: 10.1007/S00414-017-1748-6 |
0.555 |
|
| 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 |
0.732 |
|
| 2017 |
Paschou P, Müller-Vahl K. Editorial: The Neurobiology and Genetics of Gilles de la Tourette Syndrome: New Avenues through Large-Scale Collaborative Projects. Frontiers in Psychiatry. 8: 197. PMID 29075205 DOI: 10.3389/Fpsyt.2017.00197 |
0.324 |
|
| 2017 |
Alexander J, Mantzaris D, Georgitsi M, Drineas P, Paschou P. Variant Ranker: a web-tool to rank genomic data according to functional significance. Bmc Bioinformatics. 18: 341. PMID 28716001 DOI: 10.1186/S12859-017-1752-3 |
0.677 |
|
| 2017 |
Liva E, Panagiotou I, Palikyras S, Parpa E, Tsilika E, Paschou P, Mystakidou K. Candidate gene investigation of spinal degenerative osteoarthritis in Greek population. The Spine Journal : Official Journal of the North American Spine Society. PMID 28662992 DOI: 10.1016/J.Spinee.2017.06.025 |
0.335 |
|
| 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, ... ... Paschou P, 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 |
0.772 |
|
| 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 |
0.798 |
|
| 2017 |
Robertson MM, Eapen V, Singer HS, Martino D, Scharf JM, Paschou P, Roessner V, Woods DW, Hariz M, Mathews CA, Črnčec R, Leckman JF. Gilles de la Tourette syndrome. Nature Reviews. Disease Primers. 3: 16097. PMID 28150698 DOI: 10.1038/nrdp.2016.97 |
0.311 |
|
| 2017 |
Pagliaroli L, Vereczkei A, Padmanabhuni SS, Paschou P, Barta C. Microrna Regulation Of Candidate Genes For Tourette Syndrome European Neuropsychopharmacology. 27: S453-S454. DOI: 10.1016/J.Euroneuro.2016.09.523 |
0.685 |
|
| 2016 |
Le Guennec K, Quenez O, Nicolas G, Wallon D, Rousseau S, Richard AC, Alexander J, Paschou P, Charbonnier C, Bellenguez C, Grenier-Boley B, Lechner D, Bihoreau MT, Olaso R, Boland A, et al. 17q21.31 duplication causes prominent tau-related dementia with increased MAPT expression. Molecular Psychiatry. PMID 27956742 DOI: 10.1038/Mp.2016.226 |
0.452 |
|
| 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 |
0.809 |
|
| 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, ... ... Paschou P, 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 |
0.808 |
|
| 2016 |
Forde NJ, Kanaan AS, Widomska J, Padmanabhuni SS, Nespoli E, Alexander J, Rodriguez Arranz JI, Fan S, Houssari R, Nawaz MS, Rizzo F, Pagliaroli L, Zilhäo NR, Aranyi T, Barta C, ... ... Paschou P, et al. TS-EUROTRAIN: A European-Wide Investigation and Training Network on the Etiology and Pathophysiology of Gilles de la Tourette Syndrome. Frontiers in Neuroscience. 10: 384. PMID 27601976 DOI: 10.3389/Fnins.2016.00384 |
0.796 |
|
| 2016 |
Georgitsi M, Willsey AJ, Mathews CA, State M, Scharf JM, Paschou P. The Genetic Etiology of Tourette Syndrome: Large-Scale Collaborative Efforts on the Precipice of Discovery. Frontiers in Neuroscience. 10: 351. PMID 27536211 DOI: 10.3389/Fnins.2016.00351 |
0.471 |
|
| 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 |
0.813 |
|
| 2016 |
Paschou P. Dissecting the genetic architecture of Tourette syndrome into subphenotypes. Neurology. PMID 27371495 DOI: 10.1212/Wnl.0000000000002934 |
0.463 |
|
| 2016 |
Alexander J, Kalev O, Mehrabian S, Traykov L, Raycheva M, Kanakis D, Drineas P, Lutz MI, Ströbel T, Penz T, Schuster M, Bock C, Ferrer I, Paschou P, Kovacs GG. Familial early-onset dementia with complex neuropathologic phenotype and genomic background. Neurobiology of Aging. 42: 199-204. PMID 27143436 DOI: 10.1016/J.Neurobiolaging.2016.03.012 |
0.693 |
|
| 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 |
0.79 |
|
| 2015 |
Zilhão NR, Padmanabhuni SS, Pagliaroli L, Barta C, Smit DJ, Cath D, Nivard MG, Baselmans BM, van Dongen J, Paschou P, Boomsma DI. Epigenome-Wide Association Study of Tic Disorders. Twin Research and Human Genetics : the Official Journal of the International Society For Twin Studies. 1-11. PMID 26499864 DOI: 10.1017/Thg.2015.72 |
0.704 |
|
| 2015 |
Bertelsen B, Stefánsson H, Riff Jensen L, Melchior L, Mol Debes N, Groth C, Skov L, Werge T, Karagiannidis I, Tarnok Z, Barta C, Nagy P, Farkas L, Brøndum-Nielsen K, Rizzo R, ... ... Paschou P, et al. Association of AADAC Deletion and Gilles de la Tourette Syndrome in a Large European Cohort. Biological Psychiatry. PMID 26444075 DOI: 10.1016/J.Biopsych.2015.08.027 |
0.455 |
|
| 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 |
0.775 |
|
| 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 |
0.775 |
|
| 2014 |
Bertelsen B, Melchior L, Jensen LR, Groth C, Glenthøj B, Rizzo R, Debes NM, Skov L, Brøndum-Nielsen K, Paschou P, Silahtaroglu A, Tümer Z. Intragenic deletions affecting two alternative transcripts of the IMMP2L gene in patients with Tourette syndrome. European Journal of Human Genetics : Ejhg. 22: 1283-9. PMID 24549057 DOI: 10.1038/Ejhg.2014.24 |
0.433 |
|
| 2014 |
Vogiatzi E, Kalogianni E, Zimmerman B, Giakoumi S, Barbieri R, Paschou P, Magoulas A, Tsaparis D, Poulakakis N, Tsigenopoulos CS. Reduced genetic variation and strong genetic population structure in the freshwater killifish Valencia letourneuxi (Valenciidae) based on nuclear and mitochondrial markers Biological Journal of the Linnean Society. 111: 334-349. DOI: 10.1111/Bij.12206 |
0.389 |
|
| 2013 |
Paschou P, Fernandez TV, Sharp F, Heiman GA, Hoekstra PJ. Genetic susceptibility and neurotransmitters in tourette syndrome International Review of Neurobiology. 112: 155-177. PMID 24295621 DOI: 10.1016/B978-0-12-411546-0.00006-8 |
0.429 |
|
| 2013 |
Karagiannidis I, Dehning S, Sandor P, Tarnok Z, Rizzo R, Wolanczyk T, Madruga-Garrido M, Hebebrand J, Nöthen MM, Lehmkuhl G, Farkas L, Nagy P, Szymanska U, Anastasiou Z, Stathias V, ... ... Paschou P, et al. Support of the histaminergic hypothesis in Tourette syndrome: association of the histamine decarboxylase gene in a large sample of families. Journal of Medical Genetics. 50: 760-4. PMID 23825391 DOI: 10.1136/Jmedgenet-2013-101637 |
0.495 |
|
| 2013 |
Hughey JR, Paschou P, Drineas P, Mastropaolo D, Lotakis DM, Navas PA, Michalodimitrakis M, Stamatoyannopoulos JA, Stamatoyannopoulos G. A European population in Minoan Bronze Age Crete. Nature Communications. 4: 1861. PMID 23673646 DOI: 10.1038/Ncomms2871 |
0.608 |
|
| 2013 |
Paschou P. The genetic basis of Gilles de la Tourette Syndrome. Neuroscience and Biobehavioral Reviews. 37: 1026-39. PMID 23333760 DOI: 10.1016/J.Neubiorev.2013.01.016 |
0.487 |
|
| 2012 |
Stathias V, Sotiris GR, Karagiannidis I, Bourikas G, Martinis G, Papazoglou D, Tavridou A, Papanas N, Maltezos E, Theodoridis M, Vargemezis V, Manolopoulos VG, Speed WC, Kidd JR, Kidd KK, ... ... Paschou P, et al. Exploring genomic structure differences and similarities between the Greek and European HapMap populations: implications for association studies. Annals of Human Genetics. 76: 472-83. PMID 23061745 DOI: 10.1111/J.1469-1809.2012.00730.X |
0.716 |
|
| 2012 |
Paschou P, Stylianopoulou E, Karagiannidis I, Rizzo R, Tarnok Z, Wolanczyk T, Hebebrand J, Nöthen MM, Lehmkuhl G, Farkas L, Nagy P, Szymanska U, Lykidis D, Androutsos C, Tsironi V, et al. Evaluation of the LIM homeobox genes LHX6 and LHX8 as candidates for Tourette syndrome. Genes, Brain, and Behavior. 11: 444-51. PMID 22435649 DOI: 10.1111/J.1601-183X.2012.00778.X |
0.509 |
|
| 2012 |
Karagiannidis I, Rizzo R, Tarnok Z, Wolanczyk T, Hebebrand J, Nöthen MM, Lehmkuhl G, Farkas L, Nagy P, Barta C, Szymanska U, Panteloglou G, Miranda DM, Feng Y, Sandor P, ... ... Paschou P, et al. Replication of association between a SLITRK1 haplotype and Tourette Syndrome in a large sample of families. Molecular Psychiatry. 17: 665-8. PMID 22083730 DOI: 10.1038/Mp.2011.151 |
0.306 |
|
| 2012 |
Donnelly MP, Paschou P, Grigorenko E, Gurwitz D, Barta C, Lu RB, Zhukova OV, Kim JJ, Siniscalco M, New M, Li H, Kajuna SL, Manolopoulos VG, Speed WC, Pakstis AJ, et al. A global view of the OCA2-HERC2 region and pigmentation. Human Genetics. 131: 683-96. PMID 22065085 DOI: 10.1007/S00439-011-1110-X |
0.642 |
|
| 2011 |
Javed A, Drineas P, Mahoney MW, Paschou P. Efficient genomewide selection of PCA-correlated tSNPs for genotype imputation. Annals of Human Genetics. 75: 707-22. PMID 21902678 DOI: 10.1111/J.1469-1809.2011.00673.X |
0.66 |
|
| 2011 |
Lewis J, Abas Z, Dadousis C, Lykidis D, Paschou P, Drineas P. Tracing cattle breeds with principal components analysis ancestry informative SNPs. Plos One. 6: e18007. PMID 21490966 DOI: 10.1371/Journal.Pone.0018007 |
0.668 |
|
| 2010 |
Paschou P, Lewis J, Javed A, Drineas P. Ancestry informative markers for fine-scale individual assignment to worldwide populations. Journal of Medical Genetics. 47: 835-47. PMID 20921023 DOI: 10.1136/Jmg.2010.078212 |
0.679 |
|
| 2010 |
Drineas P, Lewis J, Paschou P. Inferring geographic coordinates of origin for Europeans using small panels of ancestry informative markers. Plos One. 5: e11892. PMID 20805874 DOI: 10.1371/Journal.Pone.0011892 |
0.693 |
|
| 2010 |
Paschou P, Kukuvitis A, Yavropoulou MP, Dritsoula A, Giapoutzidis V, Anastasiou O, Kazakos K, Yovos JG. Genetic variation in the visfatin (PBEF1/NAMPT) gene and type 2 diabetes in the Greek population. Cytokine. 51: 25-7. PMID 20451405 DOI: 10.1016/J.Cyto.2010.04.006 |
0.449 |
|
| 2010 |
Donnelly MP, Paschou P, Grigorenko E, Gurwitz D, Mehdi SQ, Kajuna SL, Barta C, Kungulilo S, Karoma NJ, Lu RB, Zhukova OV, Kim JJ, Comas D, Siniscalco M, New M, et al. The distribution and most recent common ancestor of the 17q21 inversion in humans. American Journal of Human Genetics. 86: 161-71. PMID 20116045 DOI: 10.1016/J.Ajhg.2010.01.007 |
0.624 |
|
| 2008 |
Paschou P, Drineas P, Lewis J, Nievergelt CM, Nickerson DA, Smith JD, Ridker PM, Chasman DI, Krauss RM, Ziv E. Tracing sub-structure in the European American population with PCA-informative markers. Plos Genetics. 4: e1000114. PMID 18797516 DOI: 10.1371/Journal.Pgen.1000114 |
0.671 |
|
| 2007 |
Paschou P, Ziv E, Burchard EG, Choudhry S, Rodriguez-Cintron W, Mahoney MW, Drineas P. PCA-correlated SNPs for structure identification in worldwide human populations. Plos Genetics. 3: 1672-86. PMID 17892327 DOI: 10.1371/Journal.Pgen.0030160 |
0.653 |
|
| 2007 |
Paschou P, Mahoney MW, Javed A, Kidd JR, Pakstis AJ, Gu S, Kidd KK, Drineas P. Intra- and interpopulation genotype reconstruction from tagging SNPs. Genome Research. 17: 96-107. PMID 17151345 DOI: 10.1101/Gr.5741407 |
0.703 |
|
| 2004 |
Paschou P, Feng Y, Pakstis AJ, Speed WC, DeMille MM, Kidd JR, Jaghori B, Kurlan R, Pauls DL, Sandor P, Barr CL, Kidd KK. Indications of linkage and association of Gilles de la Tourette syndrome in two independent family samples: 17q25 is a putative susceptibility region. American Journal of Human Genetics. 75: 545-60. PMID 15303240 DOI: 10.1086/424389 |
0.609 |
|
| 2004 |
Hermann R, Bartsocas CS, Soltész G, Vazeou A, Paschou P, Bozas E, Malamitsi-Puchner A, Simell O, Knip M, Ilonen J. Genetic screening for individuals at high risk for type 1 diabetes in the general population using HLA Class II alleles as disease markers. A comparison between three European populations with variable rates of disease incidence. Diabetes/Metabolism Research and Reviews. 20: 322-9. PMID 15250035 DOI: 10.1002/Dmrr.455 |
0.619 |
|
| 2004 |
Palmatier MA, Pakstis AJ, Speed W, Paschou P, Goldman D, Odunsi A, Okonofua F, Kajuna S, Karoma N, Kungulilo S, Grigorenko E, Zhukova OV, Bonne-Tamir B, Lu RB, Parnas J, et al. COMT haplotypes suggest P2 promoter region relevance for schizophrenia. Molecular Psychiatry. 9: 859-70. PMID 15098000 DOI: 10.1038/Sj.Mp.4001496 |
0.527 |
|
| 2004 |
Paschou P, Bozas E, Dokopoulou M, Havarani B, Malamitsi-Puchner A, Ylli A, Ylli Z, Thymelli I, Gerasimidi-Vazeou A, Bartsocas CS. HLA alleles and type 1 diabetes mellitus in low disease incidence populations of Southern Europe: a comparison of Greeks and Albanians. Journal of Pediatric Endocrinology & Metabolism : Jpem. 17: 173-82. PMID 15055351 DOI: 10.1515/Jpem.2004.17.2.173 |
0.631 |
|
| 2002 |
Ilonen J, Sjöroos M, Knip M, Veijola R, Simell O, Akerblom HK, Paschou P, Bozas E, Havarani B, Malamitsi-Puchner A, Thymelli J, Vazeou A, Bartsocas CS. Estimation of genetic risk for type 1 diabetes. American Journal of Medical Genetics. 115: 30-6. PMID 12116174 DOI: 10.1002/ajmg.10341 |
0.583 |
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