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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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A distinct cognitive profile in individuals with 3q29 deletion syndrome

Journal of intellectual disability research, 2023-03, Vol.67 (3), p.216-227

2023

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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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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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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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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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Addictions Biology: Haplotype-Based Analysis for 130 Candidate Genes on a Single Array

Alcohol and alcoholism (Oxford), 2008-09, Vol.43 (5), p.505-515

2008

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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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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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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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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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Tufted angiomas in childhood: A series of 9 cases and a literature review

Anales de pediatría (Barcelona, Spain : 2003), 2015-09, Vol.83 (3), p.201-208

2015

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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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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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An Amelanotic Dysplastic Melanocytic Nevus Induced by Vemurafenib

Actas dermo-sifiliográficas (English ed.), 2014-09, Vol.105 (7), p.726-727

2014

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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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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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Angiotensin I converting enzyme polymorphism in humans with age-associated memory impairment: relationship with cognitive performance

Neuroscience letters, 2000-09, Vol.290 (3), p.177-180

2000

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Nevus melanocítico atípico amelanótico inducido por vemurafenib

Actas dermo-sifiliográficas, 2014-09, Vol.105 (7), p.726-727

2014

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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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Evaluation de la qualité de vie du nourrisson et du très jeune enfant: Validation d'un questionnaire. Étude multicentrique européenne

Archives de pédiatrie (Paris), 2000-06, Vol.7 (6), p.605-614

2000

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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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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

A distinct cognitive profile in individuals with 3q29 deletion syndrome

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

Adaptive behaviour deficits in individuals with 3q29 deletion syndrome

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

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

Addictions Biology: Haplotype-Based Analysis for 130 Candidate Genes on a Single Array

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

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

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

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

Tufted angiomas in childhood: A series of 9 cases and a literature review

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

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

An Amelanotic Dysplastic Melanocytic Nevus Induced by Vemurafenib

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

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

Angiotensin I converting enzyme polymorphism in humans with age-associated memory impairment: relationship with cognitive performance

Nevus melanocítico atípico amelanótico inducido por vemurafenib

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

Evaluation de la qualité de vie du nourrisson et du très jeune enfant: Validation d'un questionnaire. Étude multicentrique européenne

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

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