PUBLICATIONS
Duong L et al.
Mutations in NRXN1 in a family multiply affected with brain disorders: NRXN1 mutations and brain disorders
American Journal of Medical Genetics. 2012 Feb 15.Kirov G et al.
De novo CNV analysis implicates specific abnormalities of postsynaptic signalling complexes in the pathogenesis of schizophrenia.
Mol. Psychyatry. 2012 Feb 15.Olsen L et al.
Copy number variations in affective disorders and meta-analysis
Psychiatric Genetics. 2011 Dec.Ripke S et al.
Genome-wide association study identifies five new schizophrenia loci
Nature Genetics. 2011 Aug 19.Steinberg S et al.
Common variants at VRK2 and TCF4 conferring risk of schizophrenia
Human Molecular Genetics. 2011 Jul 26.Hansen T et al.
At-Risk Variant in TCF7L2 for Type II Diabetes Increases Risk of Schizophrenia
Biological Psychiatry. 2011 Jul 1.Ingason A et al.
Maternally Derived Microduplications at 15q11-q13: Implication of Imprinted Genes in Psychotic Illness
The American Journal of Psychiatry. 2011 Apr 1.Ingason A et al.
A large replication study and meta-analysis in European samples provides further support for association of AHI1 markers with schizophrenia.
Human Molecular Genetics. 2010 Jan 12.Steinberg S et al.
Expanding the range of ZNF804A variants conferring risk of psychosis.
Mol Psychiatry. 2009 Sep 29. [Epub ahead of print]Ingason A et al.
Copy number variations of chromosome 16p13.1 region associated with schizophrenia.
Mol Psychiatry. 2009 Sep 29. [Epub ahead of print]Stefansson H et al.
Common variants conferring risk of schizophrenia.
Nature. 2009 Jul 1.Hansen et al.
Submikroskopiske kromosomanomalier som �rsag til skizofreni.
Ugeskrift for l�ger. 2008 Nov 10. [Epub ahead of print]Rujescu E et al.
Disruption of the neurexin 1 gene is associated with schizophrenia.
Hum Mol Genet. 2008 Oct 22. [Epub ahead of print]Stefansson H et al.
Large recurrent microdeletions associated with schizophrenia.
Nature. 2008 Jul 30 [Epub ahead of print]
