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Plos One|June 18, 2019
Comparison of quantitative trait loci methods: Total expression and allelic imbalance method in brain RNA-seqJesper R Gådin, Alfonso Buil, Carlo Colantuoni, et al.
Neuroimage|August 29, 2021
Differential resting-state patterns across networks are spatially associated with Comt and Trmt2a gene expression patterns in a mouse model of 22q11.2 deletionNatalia Gass, Zeru Peterson, Jonathan Reinwald, et al.
Translational Psychiatry|December 1, 2017
A mouse model of the schizophrenia-associated 1q21.1 microdeletion syndrome exhibits altered mesolimbic dopamine transmissionJacob Nielsen, Kim Fejgin, Florence Sotty, et al.
Cerebral Cortex (New York, N.Y. : 1991)|August 11, 2016
Assessing the Cognitive Translational Potential of a Mouse Model of the 22q11.2 Microdeletion SyndromeSimon Ro Nilsson, Kim Fejgin, Francois Gastambide, et al.
European Journal of Pharmacology|August 11, 2007
Lu 35-138 ((+)-(S)-3-{1-[2-(1-acetyl-2,3-dihydro-1H-indol-3-yl)ethyl]-3,6-dihydro-2H-pyridin-4-yl}-6-chloro-1H-indole), a dopamine D4 receptor antagonist and serotonin reuptake inhibitor: characterisation of its in vitro profile and pre-clinical antipsychotic potentialPeter Hertel, Michael Didriksen, Bruno Pouzet, et al.
BMC Psychiatry|September 19, 2015
The Danish 22q11 research initiativeHenriette Schmock, Anders Vangkilde, Kit Melissa Larsen, et al.
Biological Psychiatry|November 14, 2016
The Schizophrenia-Associated BRD1 Gene Regulates Behavior, Neurotransmission, and Expression of Schizophrenia Risk Enriched Gene Sets in MicePer Qvist, Jane Hvarregaard Christensen, Irina Vardya, et al.
Psychopharmacology|March 18, 2016
A mouse model of the 15q13.3 microdeletion syndrome shows prefrontal neurophysiological dysfunctions and attentional impairmentSimon R O Nilsson, Pau Celada, Kim Fejgin, et al.
Nature Neuroscience|October 28, 2016
Translating genome-wide association findings into new therapeutics for psychiatryGerome Breen, Qingqin Li, Bryan L Roth, et al.
Biological Psychiatry|October 5, 2013
A mouse model that recapitulates cardinal features of the 15q13.3 microdeletion syndrome including schizophrenia- and epilepsy-related alterationsKim Fejgin, Jacob Nielsen, Michelle R Birknow, et al.
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