4.5 Article

Copy number variations and risk for schizophrenia in 22q11.2 deletion syndrome

Related references

Note: Only part of the references are listed.
Article Genetics & Heredity

Structural variation of chromosomes in autism spectrum disorder

Christian R. Marshall et al.

AMERICAN JOURNAL OF HUMAN GENETICS (2008)

Article Multidisciplinary Sciences

Rare chromosomal deletions and duplications increase risk of schizophrenia

Jennifer L. Stone et al.

NATURE (2008)

Article Multidisciplinary Sciences

Large recurrent microdeletions associated with schizophrenia

Hreinn Stefansson et al.

NATURE (2008)

Article Genetics & Heredity

Strong association of de novo copy number mutations with sporadic schizophrenia

Bin Xu et al.

NATURE GENETICS (2008)

Article Psychiatry

Schizophrenia and 22q11.2 deletion syndrome

Anne S. Bassett et al.

Current Psychiatry Reports (2008)

Article Clinical Neurology

Association between a common haplotype in the COMT gene region and psychiatric disorders in individuals with 22q11.2DS

Elena Michaelovsky et al.

INTERNATIONAL JOURNAL OF NEUROPSYCHOPHARMACOLOGY (2008)

Article Multidisciplinary Sciences

Mapping and sequencing of structural variation from eight human genomes

Jeffrey M. Kidd et al.

NATURE (2008)

Article Biochemistry & Molecular Biology

Comparative genome hybridization suggests a role for NRXN1 and APBA2 in schizophrenia

George Kirov et al.

HUMAN MOLECULAR GENETICS (2008)

Article Biochemistry & Molecular Biology

In vivo response to high-resolution variation of Tbx1 mRNA dosage

Zhen Zhang et al.

HUMAN MOLECULAR GENETICS (2008)

Article Genetics & Heredity

Contribution of SHANK3 mutations to autism spectrum disorder

Rainald Moessner et al.

AMERICAN JOURNAL OF HUMAN GENETICS (2007)

Article Genetics & Heredity

Germ-line DNA copy number variation frequencies in a large North American population

George Zogopoulos et al.

HUMAN GENETICS (2007)

Review Biochemistry & Molecular Biology

Copy-number variation in control population cohorts

Dalila Pinto et al.

HUMAN MOLECULAR GENETICS (2007)

Article Genetics & Heredity

Genomic rearrangements and sporadic disease

James R. Lupski

NATURE GENETICS (2007)

Article Genetics & Heredity

Mapping autism risk loci using genetic linkage and chromosomal rearrangements

Peter Szatmari et al.

NATURE GENETICS (2007)

Article Genetics & Heredity

Molecular characterization of deletion breakpoints in adults with 22q11 deletion syndrome

Rosanna Weksberg et al.

HUMAN GENETICS (2007)

Article Genetics & Heredity

Evidence of linkage and association on 18p11.2 for psychosis

O. Mukherjee et al.

AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS (2006)

Article Biochemistry & Molecular Biology

Genome-wide detection of human copy number variations using high-density DNA oligonucleotide arrays

Daisuke Komura et al.

GENOME RESEARCH (2006)

Article Multidisciplinary Sciences

Global variation in copy number in the human genome

Richard Redon et al.

NATURE (2006)

Article Psychiatry

Neurocognitive profile in 22q11 deletion syndrome and schizophrenia

Eva W. C. Chow et al.

SCHIZOPHRENIA RESEARCH (2006)

Article Biochemistry & Molecular Biology

No evidence for parental imprinting of mouse 22q11 gene orthologs

Thomas M. Maynard et al.

MAMMALIAN GENOME (2006)

Article Biochemistry & Molecular Biology

Parental and chromosomal origins of microdeletion and duplication syndromes involving 7q11.23, 15q11-q13 and 22q11

N. Simon Thomas et al.

EUROPEAN JOURNAL OF HUMAN GENETICS (2006)

Article Genetics & Heredity

Clinical features of 78 adults with 22q11 deletion syndrome

AS Bassett et al.

AMERICAN JOURNAL OF MEDICAL GENETICS PART A (2005)

Review Biochemistry & Molecular Biology

Implications of human genome architecture for rearrangement-based disorders: the genomic basis of disease

CJ Shaw et al.

HUMAN MOLECULAR GENETICS (2004)

Article Biochemistry & Molecular Biology

Aberrant interchromosomal exchanges are the predominant cause of the 22q11.2 deletion

SC Saitta et al.

HUMAN MOLECULAR GENETICS (2004)

Article Pediatrics

Incidence and prevalence of the 22q11 deletion syndrome:: a population-based study in Western Sweden

S Oskarsdóttir et al.

ARCHIVES OF DISEASE IN CHILDHOOD (2004)

Article Genetics & Heredity

Detection of large-scale variation in the human genome

AJ Iafrate et al.

NATURE GENETICS (2004)

Article Psychiatry

The schizophrenia phenotype in 22q11 deletion syndrome

AS Bassett et al.

AMERICAN JOURNAL OF PSYCHIATRY (2003)