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Functional polymorphisms in the interleukin-6 and serotonin transporter genes, and depression and fatigue induced by interferon-α and ribavirin treatment

Molecular psychiatry, 2009-12, Vol.14 (12), p.1095-1104

2009

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Association of a polymorphism in the indoleamine- 2,3-dioxygenase gene and interferon-α-induced depression in patients with chronic hepatitis C

Molecular psychiatry, 2012-08, Vol.17 (8), p.781-789

2012

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Regulation of mRNA expression encoding chaperone and co-chaperone proteins of the glucocorticoid receptor in peripheral blood: association with depressive symptoms during pregnancy

Psychological medicine, 2012-05, Vol.42 (5), p.943-956

2012

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

Psychopharmacology, 2004-08, Vol.174 (4), p.463-476

2004

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Prodromal symptoms in adolescents with 22q11.2 deletion syndrome and schizotypal personality disorder

Schizophrenia research, 2011-06, Vol.129 (1), p.20-28

2011

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Axis I psychiatric diagnoses in adolescents and young adults with 22q11 deletion syndrome

European psychiatry, 2013-09, Vol.28 (7), p.417-422

2013

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Serotonin transporter protein (SLC6A4) allele and haplotype frequencies and linkage disequilibria in African- and European-American and Japanese populations and in alcohol-dependent subjects

Human genetics, 1997-12, Vol.101 (2), p.243-246

1997

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

Molecular psychiatry, 2000, Vol.5 (1), p.56-63

2000

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Population studies of polymorphisms of the serotonin transporter protein gene

American journal of medical genetics, 1999-02, Vol.88 (1), p.61-66

1999

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Adaptive behaviour deficits in individuals with 3q29 deletion syndrome

Journal of intellectual disability research, 2024-02, Vol.68 (2), p.113-127

2024

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Performance on the Modified Card Sorting Test and its relation to psychopathology in adolescents and young adults with 22q11.2 deletion syndrome

Journal of intellectual disability research, 2009-07, Vol.53 (7), p.665-676

2009

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Methamphetamine neurotoxicity involves vacuolation of endocytic organelles and dopamine-dependent intracellular oxidative stress

The Journal of neuroscience, 1994-04, Vol.14 (4), p.2260-2271

1994

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Dopamine β-hydroxylase : Two polymorphisms in linkage disequilibrium at the structural gene DBH associate with biochemical phenotypic variation

Human genetics, 1998-05, Vol.102 (5), p.533-540

1998

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A Quantitative-Trait Analysis of Human Plasma–Dopamine β-Hydroxylase Activity: Evidence for a Major Functional Polymorphism at the DBH Locus

American journal of human genetics, 2001-02, Vol.68 (2), p.515-522

2001

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Opiate addiction in China: current situation and treatments

Addiction (Abingdon, England), 2006-05, Vol.101 (5), p.657-665

2006

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Population genetics of a functional variant of the dopamine β-hydroxylase gene (DBH)

American journal of medical genetics, 1997-07, Vol.74 (4), p.374-379

1997

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DRD2 allele frequencies and linkage disequilibria, including the -141CIns/Del promoter polymorphism, in European-American, African-American, and Japanese subjects

Genomics (San Diego, Calif.), 1998-07, Vol.51 (1), p.21

1998

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The Structure of Linkage Disequilibrium at the DBH Locus Strongly Influences the Magnitude of Association between Diallelic Markers and Plasma Dopamine β-Hydroxylase Activity

American journal of human genetics, 2003-06, Vol.72 (6), p.1389-1400

2003

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A Transgenic Mouse Model to Study Transsynaptic Regulation of Tyrosine Hydroxylase Gene Expression

Journal of neurochemistry, 1996-07, Vol.67 (1), p.11-18

1996

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A previously undescribed intron and extensive 5' upstream sequence, but not Phox2a-mediated transactivation, are necessary for high level cell type-specific expression of the human norepinephrine transporter gene

The Journal of biological chemistry, 1999-03, Vol.274 (10), p.6507-6518

1999

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Setting Priorities for Genomic Research

Science (American Association for the Advancement of Science), 2004-06, Vol.304 (5676), p.1445-1446

2004

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Inducible cAMP Early Repressor Can Modulate Tyrosine Hydroxylase Gene Expression after Stimulation of cAMP Synthesis

The Journal of biological chemistry, 1996-10, Vol.271 (41), p.25375-25381

1996

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Diagnostic reliability of the Semi-structured Assessment for Drug Dependence and Alcoholism (SSADDA)

Drug and alcohol dependence, 2005-12, Vol.80 (3), p.303-312

2005

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Randomized clinical trial of disulfiram for cocaine dependence or abuse during buprenorphine treatment

Drug and alcohol dependence, 2014-03, Vol.136, p.36-42

2014

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Bright Light Therapy for Schizoaffective Disorder

The American journal of psychiatry, 2001-12, Vol.158 (12), p.2086-a-2087

2001

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Functional polymorphisms in the interleukin-6 and serotonin transporter genes, and depression and fatigue induced by interferon-α and ribavirin treatment

Association of a polymorphism in the indoleamine- 2,3-dioxygenase gene and interferon-α-induced depression in patients with chronic hepatitis C

Regulation of mRNA expression encoding chaperone and co-chaperone proteins of the glucocorticoid receptor in peripheral blood: association with depressive symptoms during pregnancy

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

Prodromal symptoms in adolescents with 22q11.2 deletion syndrome and schizotypal personality disorder

Axis I psychiatric diagnoses in adolescents and young adults with 22q11 deletion syndrome

Serotonin transporter protein (SLC6A4) allele and haplotype frequencies and linkage disequilibria in African- and European-American and Japanese populations and in alcohol-dependent subjects

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

Population studies of polymorphisms of the serotonin transporter protein gene

Adaptive behaviour deficits in individuals with 3q29 deletion syndrome

Performance on the Modified Card Sorting Test and its relation to psychopathology in adolescents and young adults with 22q11.2 deletion syndrome

Methamphetamine neurotoxicity involves vacuolation of endocytic organelles and dopamine-dependent intracellular oxidative stress

Dopamine β-hydroxylase : Two polymorphisms in linkage disequilibrium at the structural gene DBH associate with biochemical phenotypic variation

A Quantitative-Trait Analysis of Human Plasma–Dopamine β-Hydroxylase Activity: Evidence for a Major Functional Polymorphism at the DBH Locus

Opiate addiction in China: current situation and treatments

Population genetics of a functional variant of the dopamine β-hydroxylase gene (DBH)

DRD2 allele frequencies and linkage disequilibria, including the -141CIns/Del promoter polymorphism, in European-American, African-American, and Japanese subjects

The Structure of Linkage Disequilibrium at the DBH Locus Strongly Influences the Magnitude of Association between Diallelic Markers and Plasma Dopamine β-Hydroxylase Activity

A Transgenic Mouse Model to Study Transsynaptic Regulation of Tyrosine Hydroxylase Gene Expression

A previously undescribed intron and extensive 5' upstream sequence, but not Phox2a-mediated transactivation, are necessary for high level cell type-specific expression of the human norepinephrine transporter gene

Setting Priorities for Genomic Research

Inducible cAMP Early Repressor Can Modulate Tyrosine Hydroxylase Gene Expression after Stimulation of cAMP Synthesis

Diagnostic reliability of the Semi-structured Assessment for Drug Dependence and Alcoholism (SSADDA)

Randomized clinical trial of disulfiram for cocaine dependence or abuse during buprenorphine treatment

Bright Light Therapy for Schizoaffective Disorder

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