Identification of a CACNA2D4 deletion in late onset bipolar disorder patients and implications for the involvement of voltage-dependent calcium channels in psychiatric disorders

Psychotic Manifestations in a Patient with Mental Retardation and a 6.2 Megabase Deletion at the Distal Short Arm of Chromosome 12

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Genome-wide Association Study Identifies Genetic Variation in Neurocan as a Susceptibility Factor for Bipolar Disorder

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Genome-Wide Analysis Shows Increased Frequency of Copy Number Variation Deletions in Dutch Schizophrenia Patients

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The CACNA1C and ANK3 risk alleles impact on affective personality traits and startle reactivity but not on cognition or gating in healthy males

(2011) Panos Roussos et al.   BIPOLAR DISORDERS

The association of genetic variation in CACNA1C with structure and function of a frontotemporal system

(2011) Fei Wang et al.   BIPOLAR DISORDERS

Analysis of genetic deletions and duplications in the University College London bipolar disorder case control sample

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The size and burden of mental disorders and other disorders of the brain in Europe 2010

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Initial evidence for the role of CACNA1C on subcortical brain morphology in patients with bipolar disorder

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Genome-wide survey implicates the influence of copy number variants (CNVs) in the development of early-onset bipolar disorder

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The impact of the CACNA1C gene polymorphism on frontolimbic function in bipolar disorder

(2011) J Jogia et al.   MOLECULAR PSYCHIATRY

De novo CNV analysis implicates specific abnormalities of postsynaptic signalling complexes in the pathogenesis of schizophrenia

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Duplications of the neuropeptide receptor gene VIPR2 confer significant risk for schizophrenia

(2011) Vladimir Vacic et al.   NATURE

Large-scale genome-wide association analysis of bipolar disorder identifies a new susceptibility locus near ODZ4

(2011)   NATURE GENETICS

High Frequencies of De Novo CNVs in Bipolar Disorder and Schizophrenia

(2011) Dheeraj Malhotra et al.   NEURON

The Effects of CACNA1C Gene Polymorphism on Spatial Working Memory in Both Healthy Controls and Patients with Schizophrenia or Bipolar Disorder

(2011) Qiumei Zhang et al.   NEUROPSYCHOPHARMACOLOGY

Structural and functional differences between L-type calcium channels: crucial issues for future selective targeting

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Genome-Wide Association of Bipolar Disorder Suggests an Enrichment of Replicable Associations in Regions near Genes

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L-type calcium channels and psychiatric disorders: A brief review

(2010) Francesco Casamassima et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS

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(2010) Detelina Grozeva   ARCHIVES OF GENERAL PSYCHIATRY

Genetic Variation in CACNA1C Affects Brain Circuitries Related to Mental Illness

(2010) Kristin L. Bigos et al.   ARCHIVES OF GENERAL PSYCHIATRY

Brain Function in Carriers of a Genome-wide Supported Bipolar Disorder Variant

(2010) Susanne Erk et al.   ARCHIVES OF GENERAL PSYCHIATRY

Genetic Variation in CACNA1C, a Gene Associated with Bipolar Disorder, Influences Brainstem Rather than Gray Matter Volume in Healthy Individuals

(2010) Barbara Franke et al.   BIOLOGICAL PSYCHIATRY

1.39 Mb inherited interstitial deletion in 12p13.33 associated with developmental delay

(2010) Ahmed T. Abdelmoity et al.   European Journal of Medical Genetics

A genome-wide association study of bipolar disorder in Norwegian individuals, followed by replication in Icelandic sample

(2010) Srdjan Djurovic et al.   JOURNAL OF AFFECTIVE DISORDERS

Meta-analysis of genome-wide association data of bipolar disorder and major depressive disorder

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Genome-wide association study of bipolar I disorder in the Han Chinese population

(2010) M T M Lee et al.   MOLECULAR PSYCHIATRY

CACNA1C (rs1006737) is associated with schizophrenia

(2010) M Nyegaard et al.   MOLECULAR PSYCHIATRY

The CACNA1C risk variant for bipolar disorder influences limbic activity

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Genome-wide association study of CNVs in 16,000 cases of eight common diseases and 3,000 shared controls

(2010)   NATURE

Functional impact of global rare copy number variation in autism spectrum disorders

(2010) Dalila Pinto et al.   NATURE

Understanding variable expressivity in microdeletion syndromes

(2010) Joris A Veltman et al.   NATURE GENETICS

A recurrent 16p12.1 microdeletion supports a two-hit model for severe developmental delay

(2010) Santhosh Girirajan et al.   NATURE GENETICS

Effects of a CACNA1C genotype on attention networks in healthy individuals

(2010) M. Thimm et al.   PSYCHOLOGICAL MEDICINE

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

(2009) George Kirov et al.   HUMAN MOLECULAR GENETICS

Common genetic determinants of schizophrenia and bipolar disorder in Swedish families: a population-based study

(2009) Paul Lichtenstein et al.   LANCET

Genome-wide association study of bipolar disorder in European American and African American individuals

(2009) E N Smith et al.   MOLECULAR PSYCHIATRY

The bipolar disorder risk allele at CACNA1C also confers risk of recurrent major depression and of schizophrenia

(2009) E K Green et al.   MOLECULAR PSYCHIATRY

Effect of CACNA1C rs1006737 on neural correlates of verbal fluency in healthy individuals

(2009) Axel Krug et al.   NEUROIMAGE

Genome-wide association and meta-analysis of bipolar disorder in individuals of European ancestry

(2009) L. J. Scott et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

Structural Variation of Chromosomes in Autism Spectrum Disorder

(2008) Christian R. Marshall et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Recurrent CNVs Disrupt Three Candidate Genes in Schizophrenia Patients

(2008) Terry Vrijenhoek et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Singleton deletions throughout the genome increase risk of bipolar disorder

(2008) D Zhang et al.   MOLECULAR PSYCHIATRY

Whole-genome association study of bipolar disorder

(2008) P Sklar et al.   MOLECULAR PSYCHIATRY

Genome-wide association for major depressive disorder: a possible role for the presynaptic protein piccolo

(2008) P F Sullivan et al.   MOLECULAR PSYCHIATRY

Rare chromosomal deletions and duplications increase risk of schizophrenia

(2008) Jennifer L. Stone et al.   NATURE

Large recurrent microdeletions associated with schizophrenia

(2008) Hreinn Stefansson et al.   NATURE

Strong association of de novo copy number mutations with sporadic schizophrenia

(2008) Bin Xu et al.   NATURE GENETICS

Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder

(2008) Manuel A R Ferreira et al.   NATURE GENETICS

Rare Structural Variants Disrupt Multiple Genes in Neurodevelopmental Pathways in Schizophrenia

(2008) T. Walsh et al.   SCIENCE