Peristera Paschou - Publications

Affiliations: 
Department of Molecular Biology and Genetics, Democritus University of Thrace 
Area:
Population Genetics, Genetic Epidemiology, Complex disorders, Psychiatric genetics

65 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
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  0.72
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  1
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  0.68
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  0.72
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  0.72
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  1
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  1
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  0.72
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  0.72
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  0.72
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  0.72
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  0.72
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  0.72
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  0.72
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  0.48
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  0.68
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  0.72
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  1
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  0.72
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  1
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  0.72
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  0.72
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  1
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  1
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  1
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  1
2016 Paschou P. Dissecting the genetic architecture of Tourette syndrome into subphenotypes. Neurology. PMID 27371495 DOI: 10.1212/Wnl.0000000000002934  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
2014 Paschou P, Hoekstra PJ, Heiman GA. Genetics of Tourette Syndrome Movement Disorders: Genetics and Models: Second Edition. 713-731. DOI: 10.1016/B978-0-12-405195-9.00045-7  1
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  1
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  1
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  1
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  1
2013 Rickards H, Paschou P, Rizzo R, Stern JS. A brief history of the European Society for the Study of Tourette Syndrome. Behavioural Neurology. 27: 3-5. PMID 23187138 DOI: 10.3233/Ben-120287  1
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  1
2012 Iordanidou M, Paraskakis E, Tavridou A, Paschou P, Chatzimichael A, Manolopoulos VG. G894T polymorphism of eNOS gene is a predictor of response to combination of inhaled corticosteroids with long-lasting β2-agonists in asthmatic children. Pharmacogenomics. 13: 1363-72. PMID 22966886 DOI: 10.2217/Pgs.12.120  1
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  1
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  1
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  1
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  1
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  1
2011 Müller-Vahl KR, Cath DC, Cavanna AE, Dehning S, Porta M, Robertson MM, Visser-Vandewalle V, Androutsos C, Aschauer H, Baird G, Bos-Veneman N, Brambilla A, Cardona F, Czernecki V, Eapter A, ... ... Paschou P, et al. European clinical guidelines for Tourette syndrome and other tic disorders. Part IV: Deep brain stimulation European Child and Adolescent Psychiatry. 20: 209-217. PMID 21445726 DOI: 10.1007/s00787-011-0166-4  0.32
2011 Verdellen C, Van De Griendt J, Hartmann A, Murphy T, Androutsos C, Aschauer H, Baird G, Bos-Veneman N, Brambilla A, Cardona F, Cath DC, Cavanna AE, Czernecki V, Dehning S, Eapter A, ... ... Paschou P, et al. European clinical guidelines for Tourette syndrome and other tic disorders. Part III: Behavioural and psychosocial interventions European Child and Adolescent Psychiatry. 20: 197-207. PMID 21445725 DOI: 10.1007/s00787-011-0167-3  0.32
2011 Roessner V, Plessen KJ, Rothenberger A, Ludolph AG, Rizzo R, Skov L, Strand G, Stern JS, Termine C, Hoekstra PJ. European clinical guidelines for Tourette syndrome and other tic disorders. Part II: pharmacological treatment. European Child & Adolescent Psychiatry. 20: 173-96. PMID 21445724 DOI: 10.1007/s00787-011-0163-7  0.32
2011 Cath DC, Hedderly T, Ludolph AG, Stern JS, Murphy T, Hartmann A, Czernecki V, Robertson MM, Martino D, Munchau A, Rizzo R. European clinical guidelines for Tourette syndrome and other tic disorders. Part I: assessment. European Child & Adolescent Psychiatry. 20: 155-71. PMID 21445723 DOI: 10.1007/S00787-011-0164-6  0.32
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  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
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  0.64
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  1
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  1
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  0.64
2001 Paschou P. Prevention of type 1 diabetes mellitus Archives of Hellenic Medicine. 18: 566-574.  1
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