COMT: a common susceptibility gene in bipolar disorder and schizophrenia. - Wikidata - awgldk - TriplyDB

COMT: a common susceptibility gene in bipolar disorder and schizophrenia.

COMT: a common susceptibility gene in bipolar disorder and schizophrenia.

http://www.wikidata.org/entity/Q44947666

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The genetics of bipolar disorder: genome ‘hot regions,’ genes, new potential candidates and future directions Hypomethylation of MB-COMT promoter is a major risk factor for schizophrenia and bipolar disorder COMT genetic variation confers risk for psychotic and affective disorders: a case control study From Linkage Studies to Epigenetics: What We Know and What We Need to Know in the Neurobiology of Schizophrenia Modeling complex genetic and environmental influences on comorbid bipolar disorder with tobacco use disorder.The complex global pattern of genetic variation and linkage disequilibrium at catechol-O-methyltransferase.Adolescent cannabis use, psychosis and catechol-O-methyltransferase genotype in African Americans and Caucasians Modification of depression by COMT val158met polymorphism in children exposed to early severe psychosocial deprivation Genes for schizophrenia and bipolar disorder? Implications for psychiatric nosology.Are Bipolar Disorder and Schizophrenia Neuroanatomically Distinct? An Anatomical Likelihood Meta-analysis.A selective review of multimodal fusion methods in schizophrenia.The catechol-O-methyl transferase (COMT) gene as a candidate for psychiatric phenotypes: evidence and lessons.Cognitive manic symptoms in bipolar disorder associated with polymorphisms in the DAOA and COMT genes.COMT and MAO-A polymorphisms and obsessive-compulsive disorder: a family-based association study.Genetics of stress response and stress-related disorders.Placebo-controlled adjunctive trial of pramipexole in patients with bipolar disorder: targeting cognitive dysfunction Neuroanatomical Abnormalities in Violent Individuals with and without a Diagnosis of Schizophrenia.Psychiatric outcomes in young children with a history of institutionalization.Genetics of affective (mood) disorders.Meta-analysis of genetic association studies on bipolar disorder.A gender-moderated effect of a functional COMT polymorphism on prefrontal brain morphology and function in velo-cardio-facial syndrome (22q11.2 deletion syndrome).Overlapping and distinct gray and white matter abnormalities in schizophrenia and bipolar I disorder.Associations between the COMT Val/Met polymorphism, early life stress, and personality among healthy adults No association of COMT Val158Met polymorphism with suicidal behavior or CSF monoamine metabolites in mood disorders Association between genes of Disrupted in schizophrenia 1 (DISC1) interactors and schizophrenia supports the role of the DISC1 pathway in the etiology of major mental illnesses.Evidence for single nucleotide polymorphisms and their association with bipolar disorder.Epigenetics and Neural developmental disorders: Washington DC, September 18 and 19, 2006 Association study of single nucleotide polymorphism rs165599 of COMT gene, with schizophrenia and bipolar mood disorder in the south-west of Iran.Evidence that COMT genotype and proline interact on negative-symptom outcomes in schizophrenia and bipolar disorder.Resting-state fMRI connectivity impairment in schizophrenia and bipolar disorder.Molecular genetics of the psychosis phenotype.Genetic and neurocognitive foundations of emotion abnormalities in bipolar disorder.COMT genotype increases risk for bipolar I disorder and influences neurocognitive performance.Early Adversity and Developmental Outcomes: Interaction Between Genetics, Epigenetics, and Social Experiences Across the Life Span.Working memory genetics in schizophrenia and related disorders: An RDoC perspective.Patients with bipolar disorders share similar but attenuated prospective memory impairments with patients with schizophrenia.Auditory P300 in patients with bipolar disorder and their unaffected relatives.Interaction between catechol-O-methyltransferase (COMT) Val158Met genotype and genetic vulnerability to schizophrenia during explicit processing of aversive facial stimuli.The catechol O-methyltransferase Val158Met polymorphism and herpes simplex virus type 1 infection are risk factors for cognitive impairment in bipolar disorder: additive gene-environmental effects in a complex human psychiatric disorder.Genetic susceptibility to schizophrenia: role of dopaminergic pathway gene polymorphisms.

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COMT: a common susceptibility gene in bipolar disorder and schizophrenia.

http://www.wikidata.org/entity/Q44947666

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2004年学术文章

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COMT: a common susceptibility gene in bipolar disorder and schizophrenia.

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COMT: a common susceptibility gene in bipolar disorder and schizophrenia.

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type

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COMT: a common susceptibility gene in bipolar disorder and schizophrenia.

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COMT: a common susceptibility gene in bipolar disorder and schizophrenia.

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COMT: a common susceptibility gene in bipolar disorder and schizophrenia.

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COMT: a common susceptibility gene in bipolar disorder and schizophrenia.

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American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

P1476

COMT: a common susceptibility gene in bipolar disorder and schizophrenia

@en

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Anne Pisanté

http://www.w3.org/2001/XMLSchema#string

Ariel Darvasi

http://www.w3.org/2001/XMLSchema#string

Baruch Spivak

http://www.w3.org/2001/XMLSchema#string

Benjamin Yakir

http://www.w3.org/2001/XMLSchema#string

Eilat Shinar

http://www.w3.org/2001/XMLSchema#string

Haim Y Knobler

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Ilya Reznik

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Leon Karp

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Marnina Swartz-Vanetik

http://www.w3.org/2001/XMLSchema#string

Meira Sternfeld

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P2860

A genome-wide search for schizophrenia susceptibility genes

Association studies of bipolar disorder.

Are schizophrenic and bipolar disorders related? A review of family and molecular studies.

A high-density genome scan detects evidence for a bipolar-disorder susceptibility locus on 13q32 and other potential loci on 1q32 and 18p11.2.

A highly significant association between a COMT haplotype and schizophrenia.

A combined analysis of D22S278 marker alleles in affected sib-pairs: support for a susceptibility locus for schizophrenia at chromosome 22q12. Schizophrenia Collaborative Linkage Group (Chromosome 22).

A haplotype implicated in schizophrenia susceptibility is associated with reduced COMT expression in human brain.

Low activity allele of catechol-O-methyltransferase gene associated with rapid cycling bipolar disorder.

Linkage studies suggest a possible locus for bipolar disorder near the velo-cardio-facial syndrome region on chromosome 22.

High rates of schizophrenia in adults with velo-cardio-facial syndrome.

P304

61-64

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10.1002/AJMG.B.30032

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1

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128B

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Abraham Weizman

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2004-07-01T00:00:00Z

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15211633

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bipolar disorder