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A CAG repeat polymorphism of KCNN3 predicts SK3 channel function and cognitive performance in schizophrenia

KCNN3, encoding the small conductance calcium‐activated potassium channel SK3, harbours a polymorphic CAG repeat in the amino‐terminal coding region with yet unproven function. Hypothesizing that KCNN3 genotypes do not influence susceptibility to schizophrenia but modify its phenotype, we explored t...

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Published in:EMBO molecular medicine 2011-06, Vol.3 (6), p.309-319
Main Authors: Grube, Sabrina, Gerchen, Martin F., Adamcio, Bartosz, Pardo, Luis A., Martin, Sabine, Malzahn, Dörthe, Papiol, Sergi, Begemann, Martin, Ribbe, Katja, Friedrichs, Heidi, Radyushkin, Konstantin A, Müller, Michael, Benseler, Fritz, Riggert, Joachim, Falkai, Peter, Bickeböller, Heike, Nave, Klaus‐Armin, Brose, Nils, Stühmer, Walter, Ehrenreich, Hannelore
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Language:English
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Summary:KCNN3, encoding the small conductance calcium‐activated potassium channel SK3, harbours a polymorphic CAG repeat in the amino‐terminal coding region with yet unproven function. Hypothesizing that KCNN3 genotypes do not influence susceptibility to schizophrenia but modify its phenotype, we explored their contribution to specific schizophrenic symptoms. Using the Göttingen Research Association for Schizophrenia (GRAS) data collection of schizophrenic patients (n = 1074), we performed a phenotype‐based genetic association study (PGAS) of KCNN3. We show that long CAG repeats in the schizophrenic sample are specifically associated with better performance in higher cognitive tasks, comprising the capacity to discriminate, select and execute (p 
ISSN:1757-4676
1757-4684
DOI:10.1002/emmm.201100135