4.8 Article

Copy number variations of chromosome 16p13.1 region associated with schizophrenia

Related references

Note: Only part of the references are listed.
Article Biochemistry & Molecular Biology

Support for the involvement of large copy number variants in the pathogenesis of schizophrenia

George Kirov et al.

HUMAN MOLECULAR GENETICS (2009)

Article Psychiatry

Copy Number Variation and Schizophrenia

David St Clair

SCHIZOPHRENIA BULLETIN (2009)

Article Genetics & Heredity

A Genome-Wide Investigation of SNPs and CNVs in Schizophrenia

Anna C. Need et al.

PLOS GENETICS (2009)

Article Genetics & Heredity

Recurrent CNVs Disrupt Three Candidate Genes in Schizophrenia Patients

Terry Vrijenhoek et al.

AMERICAN JOURNAL OF HUMAN GENETICS (2008)

Article Multidisciplinary Sciences

Large recurrent microdeletions associated with schizophrenia

Hreinn Stefansson et al.

NATURE (2008)

Editorial Material Genetics & Heredity

Phenotypic variations on the theme of CNVs

Michael C. O'Donovan et al.

NATURE GENETICS (2008)

Article Genetics & Heredity

Strong association of de novo copy number mutations with sporadic schizophrenia

Bin Xu et al.

NATURE GENETICS (2008)

Editorial Material Neurosciences

Schizophrenia: Genome, interrupted

Rita M. Cantor et al.

NEURON (2008)

Editorial Material Medicine, General & Internal

A hot spot of genetic instability in autism

Evan E. Eichler et al.

NEW ENGLAND JOURNAL OF MEDICINE (2008)

Article Medicine, General & Internal

Recurrent rearrangements of chromosome 1q21.1 and variable pediatric phenotypes

Heather C. Mefford et al.

NEW ENGLAND JOURNAL OF MEDICINE (2008)

Letter Psychiatry

No association between the NDE1 gene and schizophrenia in the Japanese population

Shusuke Numata et al.

SCHIZOPHRENIA RESEARCH (2008)

Article Multidisciplinary Sciences

A unified genetic theory for sporadic and inherited autism

Xiaoyue Zhao et al.

PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2007)

Article Multidisciplinary Sciences

Strong association of de novo copy number mutations with autism

Jonathan Sebat et al.

SCIENCE (2007)

Article Psychiatry

Genetics of recurrent early-onset major depression (GenRED): Final genome scan report

Peter Holmans et al.

AMERICAN JOURNAL OF PSYCHIATRY (2007)

Article Psychiatry

Familiality of polarity at illness onset in bipolar affective disorder

Layla Kassem et al.

AMERICAN JOURNAL OF PSYCHIATRY (2006)

Article Genetics & Heredity

Fine-scale structural variation of the human genome

E Tuzun et al.

NATURE GENETICS (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 Genetics & Heredity

Genomic imbalances in mental retardation

M Kriek et al.

JOURNAL OF MEDICAL GENETICS (2004)

Article Biochemistry & Molecular Biology

Replication of 1q42 linkage in Finnish schizophrenia pedigrees

J Ekelund et al.

MOLECULAR PSYCHIATRY (2004)

Article Biochemistry & Molecular Biology

Evidence of susceptibility loci on 4q32 and 16p12 for bipolar disorder

JM Ekholm et al.

HUMAN MOLECULAR GENETICS (2003)

Article Psychiatry

Psychosis proneness and ADHD in young relatives of schizophrenia patients

MS Keshaven et al.

SCHIZOPHRENIA RESEARCH (2003)