Varaico: Literature-Extracted Genetic Variants

Gene:DBH
Variant:p.K148K
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DBH

NM_000787.4:p.K148K

Associated Papers

Dopamine beta-hydroxylase and its genetic variants in human health and disease.

Gonzalez-Lopez E et al.

Journal of Neurochemistry, 2020

Dopamine-beta-hydroxylase 19-bp insertion/deletion polymorphism affects medication overuse in patients with chronic migraine.

Barbanti P et al.

Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology, 2019

Associations between the DBH gene, plasma dopamine β-hydroxylase activity and cognitive measures in Han Chinese patients with schizophrenia.

Sun Z et al.

Schizophrenia Research, 2018

Association of Dopamine Beta-Hydroxylase Polymorphisms with Alzheimer's Disease, Parkinson's Disease and Schizophrenia: Evidence Based on Currently Available Loci.

Tang S et al.

Cellular Physiology and Biochemistry : International Journal of Experimental Cellular Physiology, Biochemistry, and Pharmacology, 2018

Analysis of dopamine beta hydroxylase gene polymorphisms in migraine.

Sezer S et al.

Clinical Neurology and Neurosurgery, 2016

Association between dopamine beta-hydroxylase 19-bp insertion/deletion polymorphism and major depressive disorder.

Zhou Y et al.

Journal of Molecular Neuroscience : Mn, 2015

Clinical features of methamphetamine-induced paranoia and preliminary genetic association with DBH-1021C→T in a Thai treatment cohort.

Kalayasiri R et al.

Addiction (abingdon, England), 2014

Polymorphisms in the aldehyde dehydrogenase 2 and dopamine β hydroxylase genes are not associated with Alzheimer's disease.

Komatsu M et al.

Journal of Neural Transmission (vienna, Austria : 1996), 2014

Association between DBH 19 bp insertion/deletion polymorphism and cognition in first-episode schizophrenic patients.

Hui L et al.

Schizophrenia Research, 2013

Association between 1603C>T polymorphism of DBH gene and bipolar disorder in a Turkish population.

Ates O et al.

Gene, 2013

Association of the dopamine β-hydroxylase 19 bp insertion/deletion polymorphism with positive symptoms but not tardive dyskinesia in schizophrenia.

Zhou N et al.

Human Psychopharmacology, 2013

Positive association between--1021TT genotype of dopamine beta hydroxylase gene and progressive behavior of injection heroin users.

Xie X et al.

Neuroscience Letters, 2013

Association of dopaminergic/GABAergic genes with attention deficit hyperactivity disorder in children.

Wang GX et al.

Molecular Medicine Reports, 2012

Association between dopamine beta hydroxylase gene polymorphism and age at onset in male schizophrenia.

Barlas IÖ et al.

Acta Neuropsychiatrica, 2012

Generational association studies of dopaminergic genes in reward deficiency syndrome (RDS) subjects: selecting appropriate phenotypes for reward dependence behaviors.

Blum K et al.

International Journal of Environmental Research and Public Health, 2011

Epigenetics in Developmental Disorder: ADHD and Endophenotypes.

Archer T et al.

Journal of Genetic Syndromes & Gene Therapy, 2011

Association study between the DAT1, DBH and DRD2 genes and cocaine dependence in a Spanish sample.

Fernàndez-Castillo N et al.

Psychiatric Genetics, 2010

Pharmacogenetics: a tool for identifying genetic factors in drug dependence and response to treatment.

Mroziewicz M et al.

Addiction Science & Clinical Practice, 2010

Variation in the nicotinic acetylcholine receptor gene cluster CHRNA5-CHRNA3-CHRNB4 and its interaction with recent tobacco use influence cognitive flexibility.

Zhang H et al.

Neuropsychopharmacology : Official Publication of the American College of Neuropsychopharmacology, 2010

Study on DBH genetic polymorphisms and plasma activity in attention deficit hyperactivity disorder patients from Eastern India.

Bhaduri N et al.

Cellular and Molecular Neurobiology, 2010

Imaging the genetics of executive function.

Greene CM et al.

Biological Psychology, 2008

The -1021 C/T DBH polymorphism is associated with neuropsychological performance among children and adolescents with ADHD.

Kieling C et al.

American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics, 2008

Polymorphisms of norepinephrine transporter and adrenergic receptor alpha1D are associated with the response to beta-blockers in dilated cardiomyopathy.

Nonen S et al.

The Pharmacogenomics Journal, 2008

Polymorphisms of dopamine-beta-hydroxylase in ADHD children.

Unknown Author

Folia Biologica, 2008

Dopaminergic genotype biases spatial attention in healthy children.

Bellgrove MA et al.

Molecular Psychiatry, 2007

Genetic polymorphisms related to delirium tremens: a systematic review.

van Munster BC et al.

Alcoholism, Clinical and Experimental Research, 2007

Polymorphisms and low plasma activity of dopamine-beta-hydroxylase in ADHD children.

Kopecková M et al.

Neuro Endocrinology Letters, 2006

Analysis of the dopamine beta hydroxylase gene in Gilles de la Tourette syndrome.

Ozbay F et al.

American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics, 2006

The cognitive genetics of attention deficit hyperactivity disorder (ADHD): sustained attention as a candidate phenotype.

Bellgrove MA et al.

Cortex; a Journal Devoted to the Study of the Nervous System and Behavior, 2006

Lack of significant association between -1021C-->T polymorphism in the dopamine beta hydroxylase gene and attention deficit hyperactivity disorder.

Bhaduri N et al.

Neuroscience Letters, 2006

DBH*444G/A polymorphism of the dopamine-beta-hydroxylase gene is associated with alcoholism but not with severe alcohol withdrawal symptoms.

Köhnke MD et al.

Journal of Neural Transmission (vienna, Austria : 1996), 2006

[Relationship between dopamine-beta-hydroxylase gene polymorphism and hypertensive disorder complicating pregnancy].

Zhu H et al.

Zhonghua Fu Chan Ke Za Zhi, 2006

Specificity of the effect of a nicotinic receptor polymorphism on individual differences in visuospatial attention.

Greenwood PM et al.

Journal of Cognitive Neuroscience, 2005

Beyond heritability: neurotransmitter genes differentially modulate visuospatial attention and working memory.

Parasuraman R et al.

Psychological Science, 2005

Analysis of polymorphisms in the dopamine beta hydroxylase gene: association with attention deficit hyperactivity disorder in Indian children.

Bhaduri N et al.

Indian Pediatrics, 2005

[Association between dopamine beta hydroxylase gene and attention deficit hyperactivity disorder complicated with disruptive behavior disorder].

Zhang HB et al.

Zhonghua Er Ke Za Zhi = Chinese Journal of Pediatrics, 2005

Human genetics of plasma dopamine beta-hydroxylase activity: applications to research in psychiatry and neurology.

Cubells JF et al.

Psychopharmacology, 2004

Dopamine beta-hydroxylase (DBH) gene and schizophrenia phenotypic variability: a genetic association study.

Yamamoto K et al.

American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics, 2003

A genotype-controlled analysis of plasma dopamine beta-hydroxylase in healthy and alcoholic subjects: evidence for alcohol-related differences in noradrenergic function.

Köhnke MD et al.

Biological Psychiatry, 2002

A polymorphism in the dopamine beta-hydroxylase gene is associated with "paranoid ideation" in patients with major depression.

Wood JG et al.

Biological Psychiatry, 2002

A quantitative-trait analysis of human plasma-dopamine beta-hydroxylase activity: evidence for a major functional polymorphism at the DBH locus.

Zabetian CP et al.

American Journal of Human Genetics, 2001

A haplotype at the DBH locus, associated with low plasma dopamine beta-hydroxylase activity, also associates with cocaine-induced paranoia.

Cubells JF et al.

Molecular Psychiatry, 2000

Dopamine beta-hydroxylase: two polymorphisms in linkage disequilibrium at the structural gene DBH associate with biochemical phenotypic variation.

Cubells JF et al.

Human Genetics, 1998

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Regarding the variants extracted from papers and shown text snippets from research papers, the following holds: "Some rights reserved. This work permits non-commercial use, distribution and reproduction in any medium, provided the original author and source are credited."