The Polygenic Nature and Complex Genetic Architecture of Specific Learning Disorder de réir Marianthi Georgitsi, Iasonas Dermitzakis, Evgenia Soumelidou, Eleni Bonti

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Meta-analysis of Tourette Syndrome and Attention Deficit Hyperactivity Disorder provides support for a shared genetic basis de réir Fotis Tsetsos, Shanmukha Sampath Padmanabhuni, John Alexander, Iordanis Karagiannidis, Margaritis Tsifintaris, Apostolia Topaloudi, Dimitrios Mantzaris, Marianthi Georgitsi, Marianthi Georgitsi, Petros Drineas, Peristera Paschou

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Variant Ranker: a web-tool to rank genomic data according to functional significance de réir John Alexander, Dimitris Mantzaris, Marianthi Georgitsi, Petros Drineas, Peristera Paschou

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The genetic etiology of Tourette Syndrome: Large-scale collaborative efforts on the precipice of discovery de réir Marianthi Georgitsi, Jeremy Willsey, Carol A Mathews, Matthew State, Jeremiah Scharf, Peristera Paschou

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Genetics of Myasthenia Gravis: A Case-Control Association Study in the Hellenic Population de réir Zoi Zagoriti, Marianthi Georgitsi, Olga Giannakopoulou, Fotios Ntellos, Socrates J. Tzartos, George P. Patrinos, Konstantinos Poulas

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Clinical Profiles and Socio-Demographic Characteristics of Adults with Specific Learning Disorder in Northern Greece de réir Eleni Bonti, Sofia Giannoglou, Marianthi Georgitsi, Maria Sofologi, Georgia-Nektaria Porfyri, Artemis Mousioni, Anastasia Konsta, Paraskevi Tatsiopoulou, Afroditi Kamari, Sofia Vavetsi, Ioannis Diakogiannis

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PheWAS and cross-disorder analysis reveal genetic architecture, pleiotropic loci and phenotypic correlations across 11 autoimmune disorders de réir Apostolia Topaloudi, Pritesh Jain, Melanie B. Martinez, Josephine K. Bryant, Grace Reynolds, Grace Reynolds, Zoi Zagoriti, George Lagoumintzis, Eleni Zamba-Papanicolaou, John Tzartos, Konstantinos Poulas, Kleopas A. Kleopa, Socrates Tzartos, Socrates Tzartos, Marianthi Georgitsi, Petros Drineas, Peristera Paschou

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Polygenic risk score-based phenome-wide association study identifies novel associations for Tourette syndrome de réir Pritesh Jain, Tyne Miller-Fleming, Apostolia Topaloudi, Dongmei Yu, Petros Drineas, Marianthi Georgitsi, Zhiyu Yang, Renata Rizzo, Kirsten R. Müller-Vahl, Zeynep Tumer, Nanette Mol Debes, Andreas Hartmann, Christel Depienne, Yulia Worbe, Pablo Mir, Danielle C. Cath, Dorret I. Boomsma, Veit Roessner, Tomasz Wolanczyk, Piotr Janik, Natalia Szejko, Cezary Zekanowski, Csaba Barta, Zsofia Nemoda, Zsanett Tarnok, Joseph D. Buxbaum, Dorothy Grice, Jeffrey Glennon, Hreinn Stefansson, Bastian Hengerer, Noa Benaroya-Milshtein, Francesco Cardona, Tammy Hedderly, Isobel Heyman, Chaim Huyser, Astrid Morer, Norbert Mueller, Alexander Munchau, Kerstin J. Plessen, Cesare Porcelli, Susanne Walitza, Anette Schrag, Davide Martino, The Psychiatric Genomics Consortium Tourette Syndrome Working Group (PGC-TS), The EMTICS collaborative group, Andrea Dietrich, The TS-EUROTRAIN Network, Carol A. Mathews, Jeremiah M. Scharf, Pieter J. Hoekstra, Lea K. Davis, Peristera Paschou

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