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Evangelos Vassos
Researcher at King's College London
Publications - 143
Citations - 10297
Evangelos Vassos is an academic researcher from King's College London. The author has contributed to research in topics: Schizophrenia & Population. The author has an hindex of 35, co-authored 117 publications receiving 7948 citations. Previous affiliations of Evangelos Vassos include National and Kapodistrian University of Athens & South London and Maudsley NHS Foundation Trust.
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Journal ArticleDOI
Replication Study and Meta-Analysis in European Samples Supports Association of the 3p21.1 Locus with Bipolar Disorder
Evangelos Vassos,Stacy Steinberg,Sven Cichon,Sven Cichon,Gerome Breen,Engilbert Sigurdsson,Ole A. Andreassen,Ole A. Andreassen,Srdjan Djurovic,Srdjan Djurovic,Gunnar Morken,Maria Grigoroiu-Serbanescu,Carmen C. Diaconu,Piotr M. Czerski,Joanna Hauser,Gulja Babadjanova,Lilia I. Abramova,Thomas W. Mühleisen,Markus M. Nöthen,Marcella Rietschel,Marcella Rietschel,Peter McGuffin,David St Clair,Omar Gustafsson,Omar Gustafsson,Ingrid Melle,Ingrid Melle,Olli Pietiläinen,Olli Pietiläinen,Olli Pietiläinen,M. Ruggeri,M. Ruggeri,Sarah Tosato,Thomas Werge,Roel A. Ophoff,Roel A. Ophoff,Dan Rujescu,Anders D. Børglum,Anders D. Børglum,Ole Mors,Preben Bo Mortensen,Ditte Demontis,Mads V. Hollegaard,Ruud van Winkel,Ruud van Winkel,Gunter Kenis,Marc De Hert,János Réthelyi,István Bitter,I. Alex Rubino,Vera Golimbet,Lambertus A. Kiemeney,Leonard H. van den Berg,Barbara Franke,Erik G. Jönsson,Anne Farmer,Hreinn Stefansson,Kari Stefansson,David A. Collier,David A. Collier +59 more
TL;DR: In this article, a meta-analysis of previously published data with their nonoverlapping new data confirmed genome-wide significant association (OR =.875, p = 2.68 × 10 −9 ).
Posted ContentDOI
Dynamics of Brain Structure and its Genetic Architecture over the Lifespan
Rachel M. Brouwer,Neeltje E.M. van Haren,Marta Di Forti,Leonard H. van den Berg,Brenda W.J.H. Penninx,Peter Falkai,Ingrid Agartz,Berend Malchow,Gary Donohoe,Tilo Kircher,Javier Vázquez-Bourgon,Juliane H. Fröhner,Celso Arango,Henk-Jan Westeneng,Sintia Iole Belangero,Andreas J. Forstner,Paola Dazzan,Temmuz Karali,Giovanni Abrahão Salum,Philip R. Jansen,Dirk J. Heslenfeld,René S. Kahn,Paul M. Thompson,Katrina L. Grasby,Covadonga M. Díaz-Caneja,Carol E. Franz,Svenja Caspers,Vicente Medel,Philip B. Mitchell,Arun L.W. Bokde,Stephanie H. Witt,Laura K.M. Han,William S. Kremen,Tonya White,Sophia I. Thomopoulos,Philip Shaw,John B.J. Kwok,Andreas Heinz,Erik G. Jönsson,Rhoshel K. Lenroot,Hugo G. Schnack,Gunter Schumann,Andreas Jansen,Ole A. Andreassen,Penny A. Gowland,Antoine Grigis,Jason L. Stein,Joanna Bright,Nicola J. Armstrong,Robin M. Murray,Nikita Setiaman,Janik Goltermann,Ronny Redlich,Tim Hahn,Dorret I. Boomsma,Dag Alnæs,Dennis van der Meer,Leila Nabulsi,Kang Sim,Susanne Meinert,Igor Nenadic,Jan K. Buitelaar,Jan H. Veldink,Markus M. Nöthen,Stephanie Le Hellard,Sergi Papiol,Mohammad Arfan Ikram,Nils Opel,Linda Ding,Dara M. Cannon,Kristel R. van Eijk,Daniel Keeser,Wei Wen,Frauke Nees,Margaret J. Wright,Gareth J. Barker,Ulrik Fredrik Malt,Marcos L. Santoro,Pieter J. Hoekstra,Marcella Rietschel,Catharina A. Hartman,Loes M. Olde Loohuis,Dennis van 't Ent,Katharina Wittfeld,Mayuresh S. Korgaonkar,Karen A. Mather,Bernhard T. Baune,Vidar M. Steen,Sylvane Desrivières,Hieab H.H. Adams,Roel A. Ophoff,Jalmar Teeuw,Matthew S. Panizzon,Elizabeth E.L. Buimer,Luise Poustka,Sarah J. Heany,Rodrigo A. Bressan,Bronwyn Overs,Frederike Stein,Jiyang Jiang,Katrin Amunts,Tobias Banaschewski,Sarah E. Medland,Christienne G. Damatac,Benedicto Crespo Facorro,Nicolas Crossley,Rick M. Tankard,Derek W. Morris,Clara Alloza,Elena Shumskaya,Aad van der Lugt,Yuri Milaneschi,André Zugman,Evangelos Vassos,Elisabet Blok,Julian N. Trollor,Christiane Jockwitz,Robin Bülow,Jonathan Repple,Ryan L. Muetzel,Thomas W. Mühleisen,Torbjørn Elvsåshagen,Manon H.J. Hillegers,Wiepke Cahn,Martijn G.J.C. Koevoets,Simon E. Fisher,Jacqueline Hoare,Casper L. de Mol,Udo Dannlowski,Christopher D. Whelan,Barbara Franke,Simone Ciufolini,Marieke Klein,Sonja M C de Zwarte,Erin Burke Quinlan,Dan J. Stein,Marie-Laure Paillère Martinot,Jaap Oosterlaan,Dominik Grotegerd,Henrik Walter,Jean-Luc Martinot,Nitin Gogtay,Hans J. Grabe,Erlend Bøen,Maria J. Knol,Eric Artiges,Lars T. Westlye,Michael N. Smolka,Hilleke E. Hulshoff Pol,Herta Flor,Robert Whelan,Bernd Ittermann,Katharina Dohm,Victor Ortiz-García de la Foz,Gloria Roberts,David Ames,Thomas Espeseth,Nhat Trung Doan,Perminder S. Sachdev,Jouke-Jan Hottenga,Henry Brodaty,Gennady V. Roshchupkin,Colm McDonald,Joost Janssen,Diana Tordesillas-Gutiérrez,Gustavo Sudre,Sven Cichon,Peter R. Schofield,Tianye Jia,João P.O.F.T. Guimarães,Neda Jahanshad,Emma Sprooten,Hugh Garavan,Isabella A. Breukelaar,Catherine Morgan,Janita Bralten,Axel Krug,Janice M. Fullerton,Rosa Ayesa-Arriola,Tiago Reis Marques,Herve Lemaitre,Shun Takahashi,Pedro Mario Pan,Georg Homuth,Javier González-Peñas,René C.W. Mandl,Fabian Streit,Anbupalam Thalamuthu,Shareefa Dalvie,Walter Heindel,Moji Aghajani,Sarah Hohmann,Alexander Teumer,Andrea Parolin Jackowski +193 more
TL;DR: Five genome-wide significant loci and 15 genes associated with brain structural changes are discovered in the world’s largest longitudinal imaging genetics dataset, which identifies genetic variants that alter age-dependent brain growth and atrophy throughout the authors' lives.
Journal ArticleDOI
Clinical utility gene card for: 15q13.3 microdeletion syndrome
TL;DR: Review of the analytical and clinical validity as well as of the clinical utility of DNA-based testing for microdeletions at the 15q13.3 locus in diagnostic and prenatal settings and for risk assessment in relatives is reviewed.
Journal ArticleDOI
Association of genetically proven Huntington's disease and sporadic amyotrophic lateral sclerosis in a 72-year-old woman.
Sokratis G. Papageorgiou,Alexandra Antelli,Anastasios Bonakis,Evangelos Vassos,Ioannis Zalonis,Nikolaos Kalfakis,Marios Panas +6 more
TL;DR: A case of late onset, genetically confirmed Huntington’s disease (HD) and sporadic amyotrophic lateral sclerosis (ALS) that appeared concomitantly in a 72-year-old woman that raises the question of a possible co-existence of HD with sporadic ALS.
Journal ArticleDOI
Genome-wide significant association between a 'negative mood delusions' dimension in bipolar disorder and genetic variation on chromosome 3q26.1.
Sandra Meier,Manuel Mattheisen,Manuel Mattheisen,Evangelos Vassos,Jana Strohmaier,Jens Treutlein,F Josef,René Breuer,Franziska Degenhardt,Thomas W. Mühleisen,Bertram Müller-Myhsok,Michael Steffens,Christine Schmael,Francis J. McMahon,Markus M. Nöthen,Markus M. Nöthen,Sven Cichon,Sven Cichon,Thomas G. Schulze,M. Rietschel +19 more
TL;DR: Support is provided for the hypothesis that rs9875793 is associated with BD in patients displaying ‘negative mood delusions’ symptom, such as delusions of guilt, was obtained from an European American sample (GAIN/TGEN), which included 1247 BD patients and 1434 controls.