Peristera Paschou
Peristera Paschou
Professor, Department of Biological Sciences, Purdue University
Verified email at - Homepage
Cited by
Cited by
Analysis of shared heritability in common disorders of the brain
Brainstorm Consortium, V Anttila, B Bulik-Sullivan, HK Finucane, ...
Science 360 (6395), eaap8757, 2018
Genomic relationships, novel loci, and pleiotropic mechanisms across eight psychiatric disorders
PH Lee, V Anttila, H Won, YCA Feng, J Rosenthal, Z Zhu, EM Tucker-Drob, ...
Cell 179 (7), 1469-1482. e11, 2019
European clinical guidelines for Tourette syndrome and other tic disorders. Part II: pharmacological treatment
V Roessner, KJ Plessen, A Rothenberger, AG Ludolph, R Rizzo, L Skov, ...
European child & adolescent psychiatry 20, 173-196, 2011
ENIGMA and global neuroscience: A decade of large-scale studies of the brain in health and disease across more than 40 countries
PM Thompson, N Jahanshad, CRK Ching, LE Salminen, SI Thomopoulos, ...
Translational psychiatry 10 (1), 100, 2020
Gilles de la Tourette syndrome
MM Robertson, V Eapen, HS Singer, D Martino, JM Scharf, P Paschou, ...
Nature reviews Disease primers 3 (1), 1-20, 2017
PCA-correlated SNPs for structure identification in worldwide human populations
P Paschou, E Ziv, EG Burchard, S Choudhry, W Rodriguez-Cintron, ...
PLoS genetics 3 (9), e160, 2007
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
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
A global view of the OCA2-HERC2 region and pigmentation
MP Donnelly, P Paschou, E Grigorenko, D Gurwitz, C Barta, RB Lu, ...
Human genetics 131, 683-696, 2012
The genetic basis of Gilles de la Tourette Syndrome
P Paschou
Neuroscience & Biobehavioral Reviews 37 (6), 1026-1039, 2013
Estimation of genetic risk for type 1 diabetes
J Ilonen, M Sjöroos, M Knip, R Veijola, O Simell, HK Åkerblom, P Paschou, ...
American journal of medical genetics 115 (1), 30-36, 2002
Support of the histaminergic hypothesis in Tourette syndrome: association of the histamine decarboxylase gene in a large sample of families
I Karagiannidis, S Dehning, P Sandor, Z Tarnok, R Rizzo, T Wolanczyk, ...
Journal of medical genetics 50 (11), 760-764, 2013
De novo sequence and copy number variants are strongly associated with tourette disorder and implicate cell polarity in pathogenesis
S Wang, JD Mandell, Y Kumar, N Sun, MT Morris, J Arbelaez, C Nasello, ...
Cell reports 24 (13), 3441-3454. e12, 2018
Ancestry informative markers for fine-scale individual assignment to worldwide populations
P Paschou, J Lewis, A Javed, P Drineas
Journal of Medical Genetics 47 (12), 835-847, 2010
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
COMT haplotypes suggest P2 promoter region relevance for schizophrenia
MA Palmatier, AJ Pakstis, W Speed, P Paschou, D Goldman, A Odunsi, ...
Molecular psychiatry 9 (9), 859-870, 2004
Indications of linkage and association of Gilles de la Tourette syndrome in two independent family samples: 17q25 is a putative susceptibility region
P Paschou, Y Feng, AJ Pakstis, WC Speed, MM DeMille, JR Kidd, ...
The American Journal of Human Genetics 75 (4), 545-560, 2004
Intragenic deletions affecting two alternative transcripts of the IMMP2L gene in patients with Tourette syndrome
B Bertelsen, L Melchior, LR Jensen, C Groth, B Glenthøj, R Rizzo, ...
European Journal of Human Genetics 22 (11), 1283-1289, 2014
The distribution and most recent common ancestor of the 17q21 inversion in humans
MP Donnelly, P Paschou, E Grigorenko, D Gurwitz, SQ Mehdi, ...
The American Journal of Human Genetics 86 (2), 161-171, 2010
Replication of association between a SLITRK1 haplotype and Tourette Syndrome in a large sample of families
I Karagiannidis, R Rizzo, Z Tarnok, T Wolanczyk, J Hebebrand, ...
Molecular psychiatry 17 (7), 665-668, 2012
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