Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Kari M Ersland"'
Autor:
Vidar M Steen, Chirag Nepal, Kari M Ersland, Rita Holdhus, Marianne Nævdal, Siri M Ratvik, Silje Skrede, Bjarte Håvik
Publikováno v:
PLoS ONE, Vol 8, Iss 11, p e79501 (2013)
Recent meta-analyses of schizophrenia genome-wide association studies (GWASs) have identified the CUB and SUSHI multiple domains 1 (CSMD1) gene as a statistically strong risk factor. CSMD1 is a complement control-related protein suggested to inhibit
Externí odkaz:
https://doaj.org/article/d88e54d129544816924ae23e36500782
Autor:
Carla P D Fernandes, Andrea Christoforou, Sudheer Giddaluru, Kari M Ersland, Srdjan Djurovic, Manuel Mattheisen, Astri J Lundervold, Ivar Reinvang, Markus M Nöthen, Marcella Rietschel, Roel A Ophoff, Genetic Risk and Outcome of Psychosis (GROUP), Albert Hofman, André G Uitterlinden, Thomas Werge, Sven Cichon, Thomas Espeseth, Ole A Andreassen, Vidar M Steen, Stephanie Le Hellard
Publikováno v:
PLoS ONE, Vol 8, Iss 12, p e81052 (2013)
BACKGROUND:Impairments in cognitive functions are common in patients suffering from psychiatric disorders, such as schizophrenia and bipolar disorder. Cognitive traits have been proposed as useful for understanding the biological and genetic mechanis
Externí odkaz:
https://doaj.org/article/f6bade955c3c406ea0f17908b9e89b5d
Autor:
Bjarte Håvik, Franziska A Degenhardt, Stefan Johansson, Carla P D Fernandes, Anke Hinney, André Scherag, Helle Lybæk, Srdjan Djurovic, Andrea Christoforou, Kari M Ersland, Sudheer Giddaluru, Michael C O'Donovan, Michael J Owen, Nick Craddock, Thomas W Mühleisen, Manuel Mattheisen, Benno G Schimmelmann, Tobias Renner, Andreas Warnke, Beate Herpertz-Dahlmann, Judith Sinzig, Özgür Albayrak, Marcella Rietschel, Markus M Nöthen, Clive R Bramham, Thomas Werge, Johannes Hebebrand, Jan Haavik, Ole A Andreassen, Sven Cichon, Vidar M Steen, Stéphanie Le Hellard
Publikováno v:
PLoS ONE, Vol 7, Iss 4, p e35424 (2012)
Doublecortin and calmodulin like kinase 1 (DCLK1) is implicated in synaptic plasticity and neurodevelopment. Genetic variants in DCLK1 are associated with cognitive traits, specifically verbal memory and general cognition. We investigated the role of
Externí odkaz:
https://doaj.org/article/1e9c72c4001d4992b35c0bcc3e363b3c
Autor:
Kari M Ersland, Andrea Christoforou, Christine Stansberg, Thomas Espeseth, Manuel Mattheisen, Morten Mattingsdal, Gudmundur A Hardarson, Thomas Hansen, Carla P D Fernandes, Sudheer Giddaluru, René Breuer, Jana Strohmaier, Srdjan Djurovic, Markus M Nöthen, Marcella Rietschel, Astri J Lundervold, Thomas Werge, Sven Cichon, Ole A Andreassen, Ivar Reinvang, Vidar M Steen, Stephanie Le Hellard
Publikováno v:
PLoS ONE, Vol 7, Iss 2, p e31687 (2012)
BackgroundDespite its estimated high heritability, the genetic architecture leading to differences in cognitive performance remains poorly understood. Different cortical regions play important roles in normal cognitive functioning and impairment. Rec
Externí odkaz:
https://doaj.org/article/8fc382b6d0cf4619a980614c796de04e