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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
An examination of polygenic score risk prediction in individuals with first-episode psychosis
Evangelos Vassos,Marta Di Forti,Jonathan R. I. Coleman,Conrad Iyegbe,Diana Prata,Diana Prata,Jack Euesden,Paul F. O'Reilly,Charles Curtis,Charles Curtis,Anna Kolliakou,Hamel Patel,Hamel Patel,Stephen Newhouse,Stephen Newhouse,Matthew Traylor,Oleysa Ajnakina,Valeria Mondelli,Valeria Mondelli,Tiago Reis Marques,Poonam Gardner-Sood,Katherine J. Aitchison,Katherine J. Aitchison,John Powell,Zerrin Atakan,Kathryn Greenwood,Shubulade Smith,Shubulade Smith,Khalida Ismail,Carmine M. Pariante,Fiona Gaughran,Paola Dazzan,Paola Dazzan,Hugh S. Markus,Anthony S. David,Cathryn M. Lewis,Robin M. Murray,Gerome Breen,Gerome Breen +38 more
TL;DR: Polygenic risk scores was a powerful predictor of case-control status in a European sample of patients with FEP, even though a large proportion did not have an established diagnosis of schizophrenia at the time of assessment.
Journal ArticleDOI
Systematic meta-analyses and field synopsis of genetic association studies of violence and aggression
TL;DR: Current evidence does not support the use of such genes to predict dangerousness or as markers for therapeutic interventions, and no association between any polymorphism analyzed and aggression is found.
Journal ArticleDOI
Expanding the range of ZNF804A variants conferring risk of psychosis
Stacy Steinberg,Ole Mors,Anders D. Børglum,Anders D. Børglum,Omar Gustafsson,Omar Gustafsson,Thomas Werge,Preben Bo Mortensen,Ole A. Andreassen,Engilbert Sigurdsson,Thorgeir E. Thorgeirsson,Yvonne Böttcher,Pall I. Olason,Roel A. Ophoff,Roel A. Ophoff,Sven Cichon,Iris H Gudjonsdottir,Olli Pietiläinen,Olli Pietiläinen,Mette Nyegaard,Annamari Tuulio-Henriksson,Andres Ingason,Thomas Hansen,Lavinia Athanasiu,Jaana Suvisaari,Jan-Erik Lönnqvist,Tiina Paunio,Annette M. Hartmann,Gesche Jürgens,Merete Nordentoft,David M. Hougaard,Bent Nørgaard-Pedersen,René Breuer,H.-J. Möller,Ina Giegling,Birte Glenthøj,Henrik B. Rasmussen,M. Mattheisen,István Bitter,János Réthelyi,Thordur Sigmundsson,Ragnheidur Fossdal,Unnur Thorsteinsdottir,Unnur Thorsteinsdottir,Mirella Ruggeri,Sarah Tosato,Eric Strengman,Lambertus A. Kiemeney,Ingrid Melle,Srdjan Djurovic,Lilia I. Abramova,Kaleda Vg,Muriel Walshe,Elvira Bramon,Evangelos Vassos,Tao Li,Tao Li,Gillian Fraser,Neil Walker,Timothea Toulopoulou,J. Yoon,Nelson B. Freimer,Rita M. Cantor,Robin M. Murray,Augustine Kong,Vera Golimbet,Erik G. Jönsson,Lars Terenius,Ingrid Agartz,Hannes Petursson,Markus M. Nöthen,M. Rietschel,Leena Peltonen,Leena Peltonen,Dan Rujescu,David A. Collier,David A. Collier,Hreinn Stefansson,D St Clair,Kari Stefansson,Kari Stefansson +80 more
TL;DR: As it has been proposed that variants such as rs1344706[T]—common and with low relative risk—may also serve to identify regions harboring less common, higher-risk susceptibility alleles, ZNF804A is searched for large copy number variants (CNVs) in psychosis patients and patients with other psychiatric disorders and 39 481 controls.
Journal ArticleDOI
Prospects for using risk scores in polygenic medicine.
TL;DR: The potential for translation to clinical use of polygenic risk scores that combine thousands of variants show some predictive ability across a range of complex traits and diseases, including neuropsychiatric disorders is considered.
Journal ArticleDOI
Penetrance for copy number variants associated with schizophrenia
Evangelos Vassos,David A. Collier,Simon Holden,Christine Patch,Dan Rujescu,David St Clair,Cathryn M. Lewis +6 more
TL;DR: Although CNVs are still far from being clinically useful or relevant to genetic counselling for specific disorders, their detection may hold an important clinical value in predicting negative developmental outcomes.