K
Kaleda Vg
Researcher at Russian Academy
Publications - 116
Citations - 3061
Kaleda Vg is an academic researcher from Russian Academy. The author has contributed to research in topics: Schizophrenia & Psychosis. The author has an hindex of 17, co-authored 115 publications receiving 2808 citations. Previous affiliations of Kaleda Vg include University of Massachusetts Medical School & University of Copenhagen.
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Journal ArticleDOI
Common variants conferring risk of schizophrenia
Hreinn Stefansson,Hreinn Stefansson,Roel A. Ophoff,Roel A. Ophoff,Roel A. Ophoff,Stacy Steinberg,Stacy Steinberg,Ole A. Andreassen,Sven Cichon,Dan Rujescu,Thomas Werge,Olli Pietilainen,Ole Mors,Preben Bo Mortensen,Engilbert Sigurdsson,Omar Gustafsson,Mette Nyegaard,Annamari Tuulio-Henriksson,Andres Ingason,Thomas Hansen,Jaana Suvisaari,Jouko Lönnqvist,Tiina Paunio,Anders D. Børglum,Anders D. Børglum,Annette M. Hartmann,Anders Fink-Jensen,Merete Nordentoft,David M. Hougaard,Bent Nørgaard-Pedersen,Yvonne Böttcher,Jes Olesen,René Breuer,Hans-Jürgen Möller,Ina Giegling,Henrik B. Rasmussen,Sally Timm,Manuel Mattheisen,István Bitter,János Réthelyi,Brynja B. Magnusdottir,Thordur Sigmundsson,Pall I. Olason,Gisli Masson,Jeffrey R. Gulcher,Magnús Haraldsson,Ragnheidur Fossdal,Thorgeir E. Thorgeirsson,Unnur Thorsteinsdottir,Unnur Thorsteinsdottir,Mirella Ruggeri,Sarah Tosato,Barbara Franke,Eric Strengman,Lambertus A. Kiemeney,Ingrid Melle,Srdjan Djurovic,Lilia I. Abramova,Kaleda Vg,Julio Sanjuán,Rosa de Frutos,Elvira Bramon,Evangelos Vassos,Gillian Fraser,Ulrich Ettinger,Marco Picchioni,Nicholas Walker,T. Toulopoulou,Anna C. Need,Dongliang Ge,Joeng Lim Yoon,Kevin V. Shianna,Nelson B. Freimer,Rita M. Cantor,Robin M. Murray,Augustine Kong,Vera Golimbet,Angel Carracedo,Celso Arango,Javier Costas,Erik G. Jönsson,Lars Terenius,Ingrid Agartz,Hannes Petursson,Markus M. Nöthen,Marcella Rietschel,Paul M. Matthews,Pierandrea Muglia,Leena Peltonen,David St Clair,David Goldstein,Kari Stefansson,Kari Stefansson,David A. Collier,David A. Collier +94 more
TL;DR: Findings implicating the MHC region are consistent with an immune component to schizophrenia risk, whereas the association with NRGN and TCF4 points to perturbation of pathways involved in brain development, memory and cognition.
Journal ArticleDOI
Common variants at VRK2 and TCF4 conferring risk of schizophrenia
Stacy Steinberg,Simone de Jong,Ole A. Andreassen,Thomas Werge,Anders D. Børglum,Ole Mors,Preben Bo Mortensen,Omar Gustafsson,Omar Gustafsson,Javier Costas,Olli Pietilainen,Ditte Demontis,Sergi Papiol,Johanna Huttenlocher,Manuel Mattheisen,René Breuer,Evangelos Vassos,Ina Giegling,Gillian Fraser,Nicholas Walker,Annamari Tuulio-Henriksson,Jaana Suvisaari,Jouko Lönnqvist,Tiina Paunio,Ingrid Agartz,Ingrid Melle,Srdjan Djurovic,Eric Strengman,Gesche Jürgens,Birte Glenthøj,Lars Terenius,David M. Hougaard,Torben F. Ørntoft,Carsten Wiuf,Michael Didriksen,Mads V. Hollegaard,Merete Nordentoft,Ruud van Winkel,Gunter Kenis,Lilia I. Abramova,Kaleda Vg,Manuel Arrojo,Julio Sanjuán,Celso Arango,Swetlana Sperling,Moritz J. Rossner,Michele Ribolsi,Valentina Magni,Alberto Siracusano,Claus Christiansen,Lambertus A. Kiemeney,Jan H. Veldink,Leonard H. van den Berg,Andres Ingason,Pierandrea Muglia,Robin M. Murray,Markus M. Nöthen,Engilbert Sigurdsson,Hannes Petursson,Unnur Thorsteinsdottir,Augustine Kong,I. Alex Rubino,Marc De Hert,János Réthelyi,István Bitter,Erik G. Jönsson,Vera Golimbet,Angel Carracedo,Hannelore Ehrenreich,Nicholas John Craddock,Michael John Owen,Michael Conlon O'Donovan,Mirella Ruggeri,Sarah Tosato,Leena Peltonen,Roel A. Ophoff,David A. Collier,David St Clair,Marcella Rietschel,Sven Cichon,Hreinn Stefansson,Dan Rujescu,Kari Stefansson +82 more
TL;DR: An expanded set of variants in the major histocompatibility complex region, near neurogranin (NRGN) and in an intron of transcription factor 4 (TCF4), and two novel variants showing genome-wide significant association are 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
Association between genetic variation in a region on chromosome 11 and schizophrenia in large samples from Europe
Marcella Rietschel,Manuel Mattheisen,Franziska Degenhardt,R. S. Kahn,Don H. Linszen,Jim van Os,D. Wiersma,Richard Bruggeman,W. Cahn,L. de Haan,Lydia Krabbendam,Inez Myin-Germeys,Thomas W. Mühleisen,Peter Kirsch,Christine Esslinger,Stefan Herms,Ditte Demontis,Michael Steffens,Jana Strohmaier,Britta Haenisch,René Breuer,Piotr M. Czerski,Ina Giegling,Eric Strengman,Christine Schmael,Ole Mors,Preben Bo Mortensen,David M. Hougaard,Torben F. Ørntoft,Pawel Kapelski,Lutz Priebe,F. B. Basmanav,Andreas J. Forstner,Peter Hoffmann,Sandra Meier,J. Nikitopoulos,Susanne Moebus,Michael Alexander,Rainald Mössner,Heinz Erich Wichmann,Stefan Schreiber,F. Rivandeneira,F. Rivandeneira,Albert Hofman,A.G. Uitterlinden,A.G. Uitterlinden,Thomas F. Wienker,Johannes Schumacher,Joanna Hauser,Wolfgang Maier,Rita M. Cantor,Susanne Erk,Susanne Erk,Thomas G. Schulze,Thomas G. Schulze,Hreinn Stefansson,Hreinn Stefansson,Stacy Steinberg,Omar Gustafsson,Engilbert Sigurdsson,H. Petursson,Augustine Kong,K. Stefansson,Olli Pietiläinen,Annamari Tuulio-Henriksson,Tiina Paunio,Jan-Erik Lönnqvist,Jaana Suvisaari,Leena Peltonen,M. Ruggeri,Sarah Tosato,Muriel Walshe,Robin M. Murray,D. A. Collier,David St Clair,Thomas Hansen,Andrés Ingason,K. D. Jakobsen,L. Duong,Thomas Werge,I. Melle,Ole A. Andreassen,Srdjan Djurovic,István Bitter,János Réthelyi,Lilia I. Abramova,Kaleda Vg,Vera Golimbet,Erik G. Jönsson,Lars Terenius,Ingrid Agartz,Ruud van Winkel,G. Kenis,Marc De Hert,Jan H. Veldink,Carsten Wiuf,Michael Didriksen,Nicholas John Craddock,Michael John Owen,Michael Conlon O'Donovan,Anders D. Børglum,Anders D. Børglum,Dan Rujescu,Henrik Walter,Henrik Walter,Andreas Meyer-Lindenberg,Markus M. Nöthen +106 more
TL;DR: In this article, the authors performed a genome-wide association study (GWAS) of 1169 clinically well characterized and ethnically homogeneous SCZ patients from a confined area of Western Europe (464 from Germany, 705 from The Netherlands) and 3714 ethnically matched controls (1272 and 2442, respectively).
Journal ArticleDOI
MicroRNA in schizophrenia: genetic and expression analysis of miR-130b (22q11).
TL;DR: A first attempt to carry out a genetic study coupled with gene expression analysis of microRNA in human neuropsychiatric pathology revealing no statistically significant association of any of the miR-130b allelic variants with schizophrenia is carried out.