Genetic variation in CACNA1C affects brain circuitries related to mental illness (Q35764284)

10 August 2017

Genetic variation in CACNA1C affects brain circuitries related to mental illness (English)

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10 August 2017

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Joseph H Callicott

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Daniel R. Weinberger

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object named as

Daniel R Weinberger

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10 August 2017

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Venkata S Mattay

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Richard E Straub

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Bhaskar Kolachana

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Kristin L Bigos

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Radhakrishna Vakkalanka

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Thomas M Hyde

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Barbara K Lipska

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Joel E Kleinman

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10 August 2017

language of work or name

English

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publication date

1 September 2010

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939-945

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describes a project that uses

10 August 2017

limma

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22 June 2022

https://europepmc.org/article/PMC/3282053

based on heuristic

inferred from PubMed Central ID database lookup

cites work

Effects of the CACNA1C risk allele for bipolar disorder on cerebral gray matter volume in healthy individuals

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Elevated amygdala activity to sad facial expressions: a state marker of bipolar but not unipolar depression

2 October 2017

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

2 October 2017

1 reference

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Common polygenic variation contributes to risk of schizophrenia and bipolar disorder

2 October 2017

1 reference

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2 October 2017

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Common genetic variants on 5p14.1 associate with autism spectrum disorders

2 October 2017

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Association of common variants in NPPA and NPPB with circulating natriuretic peptides and blood pressure

2 October 2017

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2 October 2017

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Evidence that altered amygdala activity in schizophrenia is related to clinical state and not genetic risk

2 October 2017

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2 October 2017

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

2 October 2017

1 reference

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Whole-genome association study of bipolar disorder

2 October 2017

1 reference

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2 October 2017

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Epistasis between catechol-O-methyltransferase and type II metabotropic glutamate receptor 3 genes on working memory brain function

2 October 2017

1 reference

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2 October 2017

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A genome-wide association study implicates diacylglycerol kinase eta (DGKH) and several other genes in the etiology of bipolar disorder

2 October 2017

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Electrical activity in early neuronal development

2 October 2017

1 reference

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Intermediate phenotypes and genetic mechanisms of psychiatric disorders

2 October 2017

1 reference

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Linear models and empirical bayes methods for assessing differential expression in microarray experiments

2 October 2017

1 reference

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Neural mechanisms of genetic risk for impulsivity and violence in humans

2 October 2017

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Risk and resilience markers in bipolar disorder: brain responses to emotional challenge in bipolar patients and their healthy siblings

2 October 2017

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Variation in DISC1 affects hippocampal structure and function and increases risk for schizophrenia

2 October 2017

1 reference

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A susceptibility gene for affective disorders and the response of the human amygdala

2 October 2017

1 reference

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Ca(V)1.2 calcium channel dysfunction causes a multisystem disorder including arrhythmia and autism

2 October 2017

1 reference

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An automated method for neuroanatomic and cytoarchitectonic atlas-based interrogation of fMRI data sets

2 October 2017

1 reference

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Serotonin transporter genetic variation and the response of the human amygdala

2 October 2017

1 reference

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Effect of COMT Val108/158 Met genotype on frontal lobe function and risk for schizophrenia

2 October 2017

1 reference

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Genetic variants associated with Lp(a) lipoprotein level and coronary disease.

2 October 2017

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Nimodipine monotherapy and carbamazepine augmentation in patients with refractory recurrent affective illness.

12 July 2018

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Open trial of a calcium antagonist, nimodipine, in acute mania

12 July 2018

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Functional imaging of emotional memory in bipolar disorder and schizophrenia.

12 July 2018

1 reference

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Prefrontal-hippocampal coupling during memory processing is modulated by COMT val158met genotype.

25 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3282053

Expression of DISC1 binding partners is reduced in schizophrenia and associated with DISC1 SNPs.

25 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3282053

Brain-derived neurotrophic factor val66met polymorphism affects human memory-related hippocampal activity and predicts memory performance.

25 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3282053

Abnormal fMRI response of the dorsolateral prefrontal cortex in cognitively intact siblings of patients with schizophrenia.

25 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3282053

Relative risk of attention deficits in siblings of patients with schizophrenia.

25 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3282053

A further study of a possible locus for schizophrenia on the X chromosome

25 September 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/20819988

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1001/ARCHGENPSYCHIATRY.2010.96

1 reference

10 August 2017

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10 August 2017

1 reference