Lista de obras - Marianne Bernadette van den Bree

16p11.2 Locus modulates response to satiety before the onset of obesity.

artículo científico publicado en 2015

1q21.1 distal copy number variants are associated with cerebral and cognitive alterations in humans

artículo científico publicado en 2021

A family based study implicates solute carrier family 1-member 3 (SLC1A3) gene in attention-deficit/hyperactivity disorder

artículo científico publicado en 2005

A feasibility study of short message service text messaging as a surveillance tool for alcohol consumption and vehicle for interventions in university students

artículo científico publicado en 2013

A neurogenetic model for the study of schizophrenia spectrum disorders: the International 22q11.2 Deletion Syndrome Brain Behavior Consortium

artículo científico publicado en 2017

A systematic review of the relationships between family functioning, pubertal timing and adolescent substance use.

artículo científico

A twin study on sensation seeking, risk taking behavior and marijuana use.

artículo científico publicado en 2001

ASD Diagnosis in Adults: Phenotype and Genotype Findings from a Clinically-derived Cohort

Adolescent clinical outcomes for young people with attention-deficit hyperactivity disorder

artículo científico publicado en 2010

Agreement between maternal report and antenatal records for a range of pre and peri-natal factors: the influence of maternal and child characteristics.

artículo científico publicado en 2006

Alcohol misuse in bipolar disorder. A systematic review and meta-analysis of comorbidity rates.

artículo científico publicado en 2013

Are obsessive-compulsive symptom dimensions familial in nonclinical individuals?

artículo científico publicado en 2009

Association of Copy Number Variation of the 15q11.2 BP1-BP2 Region With Cortical and Subcortical Morphology and Cognition

artículo científico publicado en 2019

Association of the CHRNA5-A3-B4 Gene Cluster With Heaviness of Smoking: A Meta-Analysis ⬇️

artículo científico publicado el 9 de noviembre de 2011

Association of the dopamine D4 receptor gene 7-repeat allele with neuropsychological test performance of children with ADHD.

artículo científico publicado en 2004

Associations between maternal older age, family environment and parent and child wellbeing in families using assisted reproductive techniques to conceive.

artículo científico publicado en 2009

Attention deficit hyperactivity disorder symptoms as antecedents of later psychotic outcomes in 22q11.2 deletion syndrome

scientific article published on 07 August 2018

Candidate gene analysis of the Price Foundation anorexia nervosa affected relative pair dataset.

artículo científico publicado en 2003

Candidate genes for anorexia nervosa in the 1p33-36 linkage region: serotonin 1D and delta opioid receptor loci exhibit significant association to anorexia nervosa.

artículo científico publicado en 2003

Catechol O-methyltransferase gene variant and birth weight predict early-onset antisocial behavior in children with attention-deficit/hyperactivity disorder

artículo científico publicado en 2005

Childhood cognitive development in 22q11.2 deletion syndrome: case-control study.

artículo científico publicado en 2017

Cis- and trans- loci influence expression of the schizophrenia susceptibility gene DTNBP1.

artículo científico publicado en 2008

Combining research approaches to advance our understanding of drug addiction.

artículo científico publicado en 2005

Conduct problems in children and adolescents: a twin study.

artículo científico publicado en 2004

Defective processing speed and nonclinical psychotic experiences in children: longitudinal analyses in a large birth cohort

artículo científico publicado en 2013

Development of a short instrument for the measurement of self-aggression. Preliminary results in female migraine patients.

artículo científico publicado en 1989

Developmental coordination disorder, psychopathology and IQ in 22q11.2 deletion syndrome.

artículo científico publicado en 2018

Diet and personality: associations in a population-based sample.

artículo científico publicado en 2006

Do intrauterine or genetic influences explain the foetal origins of chronic disease? A novel experimental method for disentangling effects.

artículo científico publicado en 2007

Effects of low birth weight, maternal smoking in pregnancy and social class on the phenotypic manifestation of Attention Deficit Hyperactivity Disorder and associated antisocial behaviour: investigation in a clinical sample

artículo científico publicado en 2007

Efficacy of mood stabilisers in the treatment of impulsive or repetitive aggression: systematic review and meta-analysis.

artículo científico publicado en 2011

Enhanced maternal origin of the 22q11.2 deletion in velocardiofacial and DiGeorge syndromes

artículo científico publicado en 2013

Environmental transmission of DSM-IV substance use disdorders in adoptive and step families

artículo científico publicado en 2000

Epilepsy and seizures in young people with 22q11.2 deletion syndrome: Prevalence and links with other neurodevelopmental disorders

artículo científico publicado en 2019

Examining differences in psychological adjustment problems among children conceived by assisted reproductive technologies

Exploring the indirect effects of catechol-O-methyltransferase (COMT) genotype on psychotic experiences through cognitive function and anxiety disorders in a large birth cohort of children.

artículo científico publicado en 2014

Extension of a Typology of Alcohol Dependence Based on Relative Genetic and Environmental Loading ⬇️

artículo científico publicado el 1 de octubre de 1998

Familial predictors of obsessive-compulsive symptom dimensions (contamination/cleaning and symmetry/ordering) in a nonclinical sample.

artículo científico publicado en 2012

Familial transmission of depression and antisocial behavior symptoms: disentangling the contribution of inherited and environmental factors and testing the mediating role of parenting.

artículo científico publicado en 2010

Follow-up of genetic linkage findings on chromosome 16p13: evidence of association of N-methyl-D aspartate glutamate receptor 2A gene polymorphism with ADHD.

artículo científico publicado en 2004

From Men to Mice: CHRNA5/CHRNA3, Smoking Behavior and Disease ⬇️

artículo científico publicado el 27 de abril de 2012

Further evidence for high rates of schizophrenia in 22q11.2 deletion syndrome.

artículo científico publicado en 2014

Genetic analysis of diagnostic systems of alcoholism in males.

artículo científico publicado en 1998

Genetic and environmental influences on drug use and abuse/dependence in male and female twins.

artículo científico publicado en 1998

Genetic influences in antisocial personality and drug use disorders.

artículo científico publicado en 1998

Genetic regulation of hemodynamic variables during dynamic exercise. The MCV twin study.

artículo científico publicado en 1996

Indicators of genetic and environmental influence in alcohol-dependent individuals.

artículo científico publicado en 1996

Indicators of genetic and environmental influences in drug abusing individuals

scientific article published on 01 May 1996

Large-scale mapping of cortical alterations in 22q11.2 deletion syndrome: Convergence with idiopathic psychosis and effects of deletion size

artículo científico publicado en 2018

Linkage disequilibrium mapping provides further evidence of a gene for reading disability on chromosome 6p21.3-22.

artículo científico publicado en 2003

Mental health and behavioural problems in children with XXYY: a comparison with intellectual disabilities

artículo científico publicado en 2019

Mental health problems in young people with experiences of homelessness and the relationship with health service use: a follow-up study.

artículo científico publicado en 2014

Molecular genetic contribution to the developmental course of attention-deficit hyperactivity disorder.

artículo científico publicado en 2008

NRSF/REST lies at the intersection between epigenetic regulation, miRNA-mediated gene control and neurodevelopmental pathways associated with Intellectual disability (ID) and Schizophrenia

artículo científico publicado en 2022

No evidence of association between Catechol-O-Methyltransferase (COMT) Val158Met genotype and performance on neuropsychological tasks in children with ADHD: a case-control study

artículo científico publicado en 2004

No evidence of association between HLA-DRB1 and attention deficit hyperactivity disorder

artículo científico publicado en 2003

Predictors of antisocial behaviour in children with attention deficit hyperactivity disorder.

artículo científico publicado en 2006

Predictors of smoking development in a population-based sample of adolescents: a prospective study.

artículo científico publicado en 2004

Prenatal smoking might not cause attention-deficit/hyperactivity disorder: evidence from a novel design

artículo científico publicado en 2009

Promoting Measured Genes and Measured Environments: On the Importance of Careful Statistical Analyses and Biological Relevance—Reply

article

Psychiatric disorders from childhood to adulthood in 22q11.2 deletion syndrome: results from the International Consortium on Brain and Behavior in 22q11.2 Deletion Syndrome

artículo científico publicado en 2014

Psychopathology among young homeless people: longitudinal mental health outcomes for different subgroups.

artículo científico publicado en 2015

Psychopathology and cognition in children with 22q11.2 deletion syndrome

artículo científico publicado en 2013

Psychopathology in young people experiencing homelessness: a systematic review

article

Psychopathy trait scores in adolescents with childhood ADHD: the contribution of genotypes affecting MAOA, 5HTT and COMT activity.

artículo científico publicado en 2009

Psychopathy traits in adolescents with childhood attention-deficit hyperactivity disorder

artículo científico publicado en 2009

Rare Genome-Wide Copy Number Variation and Expression of Schizophrenia in 22q11.2 Deletion Syndrome

artículo científico publicado en 2017

Relaxation training in school classes does not reduce headache complaints.

artículo científico publicado en 1990

Resemblances of parents and twins in sports participation and heart rate

artículo científico publicado en 1989

Response to letter to editor: "Knowing when and how to use epilepsy screening questionnaires"

artículo científico publicado en 2020

Response to: Testing the Association Between Smoking in Pregnancy and Attention-Deficit/Hyperactivity Disorder in a Novel Design

artículo científico publicado en 2010

Risk factors predicting changes in marijuana involvement in teenagers

artículo científico publicado en 2005

Sleep problems and associations with psychopathology and cognition in young people with 22q11.2 deletion syndrome (22q11.2DS)

scientific article published on 30 May 2019

Subthreshold Psychosis in 22q11.2 Deletion Syndrome: Multisite Naturalistic Study

artículo científico publicado en 2017

Subtypes of alcohol-dependent men: a typology based on relative genetic and environmental loading

artículo científico publicado en 1996

Testing for gene x environment interaction effects in attention deficit hyperactivity disorder and associated antisocial behavior.

artículo científico publicado en 2008

The Cardiff Study of all Wales and North West of England Twins (CaStANET): a longitudinal research program of child and adolescent development.

artículo científico publicado en 2007

The Developmental Relationship Between Depressive Symptoms in Adolescence and Harmful Drinking in Emerging Adulthood: The Role of Peers and Parents

artículo científico publicado en 2015

The Moderating Effects of Pubertal Timing on the Longitudinal Associations Between Parent-Child Relationship Quality and Adolescent Substance Use.

artículo científico publicado en 2010

The association between conduct problems and the initiation and progression of marijuana use during adolescence: a genetic analysis across time

artículo científico publicado en 2007

The clinical presentation of attention deficit-hyperactivity disorder (ADHD) in children with 22q11.2 deletion syndrome.

artículo científico publicado en 2015

The future of psychiatric genetics

scientific article published on 01 January 2003

The internet is parents' main source of information about psychiatric manifestations of 22q11.2 deletion syndrome (22q11.2DS).

artículo científico publicado en 2013

The mediating role of deviant peers on the link between depressed mood and harmful drinking

artículo científico publicado en 2015

The relationship between childhood depressive symptoms and problem alcohol use in early adolescence: findings from a large longitudinal population-based study.

artículo científico publicado en 2012

Variance of IQ is partially dependent on deletion type among 1,427 22q11.2 deletion syndrome subjects

artículo científico publicado en 2018

Lista de obras de Marianne Bernadette van den Bree

16p11.2 Locus modulates response to satiety before the onset of obesity.

1q21.1 distal copy number variants are associated with cerebral and cognitive alterations in humans

A family based study implicates solute carrier family 1-member 3 (SLC1A3) gene in attention-deficit/hyperactivity disorder

A feasibility study of short message service text messaging as a surveillance tool for alcohol consumption and vehicle for interventions in university students

A neurogenetic model for the study of schizophrenia spectrum disorders: the International 22q11.2 Deletion Syndrome Brain Behavior Consortium

A systematic review of the relationships between family functioning, pubertal timing and adolescent substance use.

A twin study on sensation seeking, risk taking behavior and marijuana use.

ASD Diagnosis in Adults: Phenotype and Genotype Findings from a Clinically-derived Cohort

Adolescent clinical outcomes for young people with attention-deficit hyperactivity disorder

Agreement between maternal report and antenatal records for a range of pre and peri-natal factors: the influence of maternal and child characteristics.

Alcohol misuse in bipolar disorder. A systematic review and meta-analysis of comorbidity rates.

Are obsessive-compulsive symptom dimensions familial in nonclinical individuals?

Association of Copy Number Variation of the 15q11.2 BP1-BP2 Region With Cortical and Subcortical Morphology and Cognition

Association of the CHRNA5-A3-B4 Gene Cluster With Heaviness of Smoking: A Meta-Analysis ⬇️

Association of the dopamine D4 receptor gene 7-repeat allele with neuropsychological test performance of children with ADHD.

Associations between maternal older age, family environment and parent and child wellbeing in families using assisted reproductive techniques to conceive.

Attention deficit hyperactivity disorder symptoms as antecedents of later psychotic outcomes in 22q11.2 deletion syndrome

Candidate gene analysis of the Price Foundation anorexia nervosa affected relative pair dataset.

Candidate genes for anorexia nervosa in the 1p33-36 linkage region: serotonin 1D and delta opioid receptor loci exhibit significant association to anorexia nervosa.

Catechol O-methyltransferase gene variant and birth weight predict early-onset antisocial behavior in children with attention-deficit/hyperactivity disorder

Childhood cognitive development in 22q11.2 deletion syndrome: case-control study.

Cis- and trans- loci influence expression of the schizophrenia susceptibility gene DTNBP1.

Combining research approaches to advance our understanding of drug addiction.

Conduct problems in children and adolescents: a twin study.

Defective processing speed and nonclinical psychotic experiences in children: longitudinal analyses in a large birth cohort

Development of a short instrument for the measurement of self-aggression. Preliminary results in female migraine patients.

Developmental coordination disorder, psychopathology and IQ in 22q11.2 deletion syndrome.

Diet and personality: associations in a population-based sample.

Do intrauterine or genetic influences explain the foetal origins of chronic disease? A novel experimental method for disentangling effects.

Effects of low birth weight, maternal smoking in pregnancy and social class on the phenotypic manifestation of Attention Deficit Hyperactivity Disorder and associated antisocial behaviour: investigation in a clinical sample

Efficacy of mood stabilisers in the treatment of impulsive or repetitive aggression: systematic review and meta-analysis.

Enhanced maternal origin of the 22q11.2 deletion in velocardiofacial and DiGeorge syndromes

Environmental transmission of DSM-IV substance use disdorders in adoptive and step families

Epilepsy and seizures in young people with 22q11.2 deletion syndrome: Prevalence and links with other neurodevelopmental disorders

Examining differences in psychological adjustment problems among children conceived by assisted reproductive technologies

Exploring the indirect effects of catechol-O-methyltransferase (COMT) genotype on psychotic experiences through cognitive function and anxiety disorders in a large birth cohort of children.

Extension of a Typology of Alcohol Dependence Based on Relative Genetic and Environmental Loading ⬇️

Familial predictors of obsessive-compulsive symptom dimensions (contamination/cleaning and symmetry/ordering) in a nonclinical sample.

Familial transmission of depression and antisocial behavior symptoms: disentangling the contribution of inherited and environmental factors and testing the mediating role of parenting.

Follow-up of genetic linkage findings on chromosome 16p13: evidence of association of N-methyl-D aspartate glutamate receptor 2A gene polymorphism with ADHD.

From Men to Mice: CHRNA5/CHRNA3, Smoking Behavior and Disease ⬇️

Further evidence for high rates of schizophrenia in 22q11.2 deletion syndrome.

Genetic analysis of diagnostic systems of alcoholism in males.

Genetic and environmental influences on drug use and abuse/dependence in male and female twins.

Genetic influences in antisocial personality and drug use disorders.

Genetic regulation of hemodynamic variables during dynamic exercise. The MCV twin study.

Indicators of genetic and environmental influence in alcohol-dependent individuals.

Indicators of genetic and environmental influences in drug abusing individuals

Large-scale mapping of cortical alterations in 22q11.2 deletion syndrome: Convergence with idiopathic psychosis and effects of deletion size

Linkage disequilibrium mapping provides further evidence of a gene for reading disability on chromosome 6p21.3-22.

Mental health and behavioural problems in children with XXYY: a comparison with intellectual disabilities

Mental health problems in young people with experiences of homelessness and the relationship with health service use: a follow-up study.

Molecular genetic contribution to the developmental course of attention-deficit hyperactivity disorder.

NRSF/REST lies at the intersection between epigenetic regulation, miRNA-mediated gene control and neurodevelopmental pathways associated with Intellectual disability (ID) and Schizophrenia

No evidence of association between Catechol-O-Methyltransferase (COMT) Val158Met genotype and performance on neuropsychological tasks in children with ADHD: a case-control study

No evidence of association between HLA-DRB1 and attention deficit hyperactivity disorder

Predictors of antisocial behaviour in children with attention deficit hyperactivity disorder.

Predictors of smoking development in a population-based sample of adolescents: a prospective study.

Prenatal smoking might not cause attention-deficit/hyperactivity disorder: evidence from a novel design

Promoting Measured Genes and Measured Environments: On the Importance of Careful Statistical Analyses and Biological Relevance—Reply

Psychiatric disorders from childhood to adulthood in 22q11.2 deletion syndrome: results from the International Consortium on Brain and Behavior in 22q11.2 Deletion Syndrome

Psychopathology among young homeless people: longitudinal mental health outcomes for different subgroups.

Psychopathology and cognition in children with 22q11.2 deletion syndrome

Psychopathology in young people experiencing homelessness: a systematic review

Psychopathy trait scores in adolescents with childhood ADHD: the contribution of genotypes affecting MAOA, 5HTT and COMT activity.

Psychopathy traits in adolescents with childhood attention-deficit hyperactivity disorder

Rare Genome-Wide Copy Number Variation and Expression of Schizophrenia in 22q11.2 Deletion Syndrome

Relaxation training in school classes does not reduce headache complaints.

Resemblances of parents and twins in sports participation and heart rate

Response to letter to editor: "Knowing when and how to use epilepsy screening questionnaires"

Response to: Testing the Association Between Smoking in Pregnancy and Attention-Deficit/Hyperactivity Disorder in a Novel Design

Risk factors predicting changes in marijuana involvement in teenagers

Sleep problems and associations with psychopathology and cognition in young people with 22q11.2 deletion syndrome (22q11.2DS)

Subthreshold Psychosis in 22q11.2 Deletion Syndrome: Multisite Naturalistic Study

Subtypes of alcohol-dependent men: a typology based on relative genetic and environmental loading

Testing for gene x environment interaction effects in attention deficit hyperactivity disorder and associated antisocial behavior.

The Cardiff Study of all Wales and North West of England Twins (CaStANET): a longitudinal research program of child and adolescent development.

The Developmental Relationship Between Depressive Symptoms in Adolescence and Harmful Drinking in Emerging Adulthood: The Role of Peers and Parents

The Moderating Effects of Pubertal Timing on the Longitudinal Associations Between Parent-Child Relationship Quality and Adolescent Substance Use.