| Analysis of shared heritability in common disorders of the brain Brainstorm Consortium, V Anttila, B Bulik-Sullivan, HK Finucane, ... Science 360 (6395), eaap8757, 2018 | 1545 | 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 | 1199 | 2019 |
| Analysis of shared heritability in common disorders of the brain Brainstorm Consortium Science (New York, NY) 360 (6395), eaap8757, 2018 | 716 | 2018 |
| 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 | 573 | 2020 |
| 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 | 555 | 2011 |
| 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 | 434 | 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 | 363 | 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 | 338 | 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 | 197 | 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 | 169 | 2012 |
| The genetic basis of Gilles de la Tourette Syndrome P Paschou Neuroscience & Biobehavioral Reviews 37 (6), 1026-1039, 2013 | 135 | 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 | 133 | 2018 |
| 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 | 130 | 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 | 127 | 2002 |
| 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 | 116 | 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 | 107 | 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 | 98 | 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 | 96 | 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 | 95 | 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 | 87 | 2010 |
Petros DrineasProfessor, Computer Science Department, Purdue UniversityVerificeret mail på purdue.edu
