A. Arias-Vasquez

发表

Common genetic variants influence human subcortical brain structures

Thomas E. Nichols, Robert W. Williams, Benjamin S. Aribisala, 2015, Nature.

ENIGMA and the individual: Predicting factors that affect the brain in 35 countries worldwide

Anders M. Dale, Paul M. Thompson, et al., 2017, NeuroImage.

Association of the Alzheimer's gene SORL1 with hippocampal volume in young, healthy adults.

B. Franke, J. Veltman, G. Fernández, 2011, The American journal of psychiatry.

The genetic architecture of the human cerebral cortex

Anders M. Dale, Robert C. Green, Shannon L. Risacher, 2020, Science.

The genetic architecture of the human cerebral cortex

Anders M. Dale, Robert C. Green, Shannon L. Risacher, 2020, Science.

Meta-analysis of the BDNF Val66Met polymorphism in major depressive disorder: effects of gender and ethnicity

B. Franke, J. Buitelaar, A. Arias-Vasquez, 2010, Molecular Psychiatry.

Human subcortical brain asymmetries in 15,847 people worldwide reveal effects of age and sex

Dan J Stein, Benjamin S. Aribisala, Nora C. Vetter, 2016, Brain Imaging and Behavior.

A genomewide screen for late-onset Alzheimer disease in a genetically isolated Dutch population.

K. Sleegers, C. V. van Duijn, P. Heutink, 2007, American journal of human genetics.

Novel genetic loci underlying human intracranial volume identified through genome-wide association

Benjamin S Aribisala, Wiro J Niessen, Peter Kochunov, 2016, Nature Neuroscience.

&agr;-Adducin Polymorphism, Atherosclerosis, and Cardiovascular and Cerebrovascular Risk

A. Hofman, J. Witteman, A. Isaacs, 2006, Stroke.

Genetic influences on schizophrenia and subcortical brain volumes: large-scale proof-of-concept and roadmap for future studies

Anbupalam Thalamuthu, Thomas E. Nichols, Manuel Mattheisen, 2016, Nature Neuroscience.

Patterns of Gray Matter Abnormalities in Schizophrenia Based on an International Mega-analysis.

Jiayu Chen, Lei Wang, Jingyu Liu, 2015, Schizophrenia bulletin.

Sparse parallel independent component analysis and its application to identify linked genomic and gray matter alterations underlying working memory impairment in attention-deficit/hyperactivity disorder

Rogers F. Silva, B. Franke, V. Calhoun, 2020, bioRxiv.

Explaining Missing Heritability Using Gaussian Process Regression

Hilbert J. Kappen, Wim Wiegerinck, Cornelis A. Albers, 2016, bioRxiv.

Structural brain alterations and their association with cognitive function and symptoms in Attention-deficit/Hyperactivity Disorder families

B. Franke, J. Turner, J. Buitelaar, 2019, NeuroImage: Clinical.

Neural correlates of cognitive function and symptoms in attention-deficit/hyperactivity disorder in adults

B. Franke, V. Calhoun, J. Turner, 2018, NeuroImage: Clinical.

G‐protein genomic association with normal variation in gray matter density

B. Franke, V. Calhoun, J. Turner, 2015, Human brain mapping.

Developmentally stable whole-brain volume reductions and developmentally sensitive caudate and putamen volume alterations in those with attention-deficit/hyperactivity disorder and their unaffected siblings.

B. Franke, M. Mennes, J. Buitelaar, 2015, JAMA psychiatry.

Genetic overlap between Attention-Deficit / Hyperactivity Disorder and Bipolar Disorder : Evidence from GWAS meta-analysis

B. Franke, O. Andreassen, J. Kelsoe, 2017 .

A genetic-epidemiologic study of Alzheimer’s disease

A. Arias-Vasquez, A. Arias-Vásquez, 2006 .

Angiotensin converting enzyme gene, smoking and mortality in a population‐based study

A. Hofman, J. Witteman, C. V. van Duijn, 2005, European journal of clinical investigation.

A genome‐wide search for quantitative trait loci affecting the cortical surface area and thickness of Heschl's gyrus

C. Francks, K. Hegenscheid, P. Hagoort, 2014, Genes, brain, and behavior.

Increase in Serum Brain-Derived Neurotrophic Factor in Met Allele Carriers of the BDNF Val66Met Polymorphism Is Specific to Males

B. Franke, A. Arias-Vasquez, R. O. Voshaar, 2012, Neuropsychobiology.

Genetic Architecture of Subcortical Brain Structures in Over 40,000 Individuals Worldwide

Michael W. Weiner, Anders M. Dale, Robert C. Green, 2017, bioRxiv.

Case-control genome-wide association study of persistent attention-deficit hyperactivity disorder identifies FBXO33 as a novel susceptibility gene for the disorder.

L. Kiemeney, B. Franke, K. Lesch, 2015, Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology.

Aetiology for the covariation between combined type ADHD and reading difficulties in a family study: the role of IQ.

B. Franke, J. Buitelaar, S. Faraone, 2012, Journal of child psychology and psychiatry, and allied disciplines.

Quantitative Linkage for Autism Spectrum Disorders Symptoms in Attention-Deficit/Hyperactivity Disorder: Significant Locus on Chromosome 7q11

B. Franke, J. Buitelaar, J. Sergeant, 2014, Journal of autism and developmental disorders.

Polymorphisms of the renin–angiotensin system are associated with blood pressure, atherosclerosis and cerebral white matter pathology

A. Hofman, J. Witteman, C. V. van Duijn, 2007, Journal of Neurology, Neurosurgery, and Psychiatry.

Cyclin-dependent kinase 5 is associated with risk for Alzheimer’s disease in a Dutch population-based study

A. Hofman, C. Broeckhoven, K. Sleegers, 2008, Journal of Neurology.

MIR137HG risk variant rs1625579 genotype is related to corpus callosum volume in schizophrenia

Jessica A. Turner, Vince D. Calhoun, Juan R. Bustillo, 2015, Neuroscience Letters.

High activity of Monoamine oxidase A is associated with externalizing behaviour in maltreated and nonmaltreated adoptees

B. Oostra, H. Tiemeier, F. Verhulst, 2009, Psychiatric genetics.

Meta-analysis of the DRD5 VNTR in persistent ADHD

L. Kiemeney, B. Franke, K. Lesch, 2016, European Neuropsychopharmacology.

Lower white matter microstructure in the superior longitudinal fasciculus is associated with increased response time variability in adults with attention-deficit/ hyperactivity disorder.

B. Franke, J. Buitelaar, M. Zwiers, 2015, Journal of psychiatry & neuroscience : JPN.

Novel genetic loci associated with hippocampal volume

Benjamin S Aribisala, Wiro J Niessen, Peter Kochunov, 2017, Nature Communications.

Genetic architecture of subcortical brain structures in 38,851 individuals

Benjamin S Aribisala, Tien Yin Wong, Wiro J Niessen, 2019, Nature Genetics.

A review and analysis of the relationship between neuropsychological measures and DAT1 in ADHD

Jan K Buitelaar, Barbara Franke, Stephen V Faraone, 2008, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

Transforming-growth factor beta1 Leu10Pro polymorphism and breast cancer morbidity.

A. Hofman, J. Coebergh, C. V. van Duijn, 2007, European journal of cancer.

Neural Correlates of Reactive Aggression in Adult Attention-Deficit/Hyperactivity Disorder

B. Franke, J. Buitelaar, A. Arias-Vasquez, 2022, Frontiers in Psychiatry.

Edinburgh Research Explorer Human subcortical brain asymmetries in 15,847 people worldwide reveal effects of age and sex

Benjamin S. Aribisala, Vatche G. Baboyan, Samantha J. Brooks, 2017 .

Transferrin and HFE genes interact in Alzheimer's disease risk: the Epistasis Project

Yurii S. Aulchenko, M. Arfan Ikram, Mario Cortina-Borja, 2012, Neurobiology of Aging.

Edinburgh Explorer No evidence for association between tau gene haplotypic variants and susceptibility to Creutzfeldt-Jakob disease

C. Duijn, A. Arias-Vasquez, P. Sánchez-Juan, 2018 .

Allelic Mutations of KITLG, Encoding KIT Ligand, Cause Asymmetric and Unilateral Hearing Loss and Waardenburg Syndrome Type 2.

J. Lupski, D. Muzny, S. Jhangiani, 2015, American journal of human genetics.

CR1 genotype is associated with entorhinal cortex volume in young healthy adults

Guillén Fernández, Mark Rijpkema, Han G. Brunner, 2011, Neurobiology of Aging.

Exploration of scanning effects in multi-site structural MRI studies

Jessica A. Turner, Vince D. Calhoun, Jingyu Liu, 2014, Journal of Neuroscience Methods.

No effect of schizophrenia risk genes MIR137, TCF4, and ZNF804A on macroscopic brain structure

Paul J. Harrison, B. Franke, M. Zwiers, 2014, Schizophrenia Research.

Inhibitory control in BALB/c mice sub-strains during extinction learning

J. Glennon, J. Buitelaar, A. Arias-Vasquez, 2019, European Neuropsychopharmacology.

Stress matters: Randomized controlled trial on the effect of probiotics on neurocognition

K. Roelofs, N. Kohn, E. Aarts, 2018, Neurobiology of Stress.

CDH13 is associated with working memory performance in attention deficit/hyperactivity disorder

B. Franke, J. Buitelaar, S. Faraone, 2011, Genes, brain, and behavior.

Quantitative Linkage for Autism Spectrum Disorders Symptoms in Attention-Deficit/Hyperactivity Disorder: Significant Locus on Chromosome 7q11

B. Franke, J. Buitelaar, J. Sergeant, 2014, Journal of Autism and Developmental Disorders.

Quantitative Linkage for ASD symptoms in ADHD : Significant Locus on Chromosome 7 q 11

A. Arias-Vasquez, J. Nijmeijer, N. Nanda, 2011 .

Brain imaging genetics in ADHD and beyond – Mapping pathways from gene to disorder at different levels of complexity

Martine Hoogman, Barbara Franke, Thomas Wolfers, 2017, Neuroscience & Biobehavioral Reviews.

Shared genetic background between children and adults with attention deficit/hyperactivity disorder

M. S. Artigas, B. Franke, K. Lesch, 2019, bioRxiv.

Genetic markers of ADHD-related variations in intracranial volume

B. Franke, P. Thompson, B. Neale, 2017, bioRxiv.

Modulation of cognitive flexibility by reward and punishment in BALB/cJ and BALB/cByJ mice

J. Glennon, J. Buitelaar, A. Arias-Vasquez, 2020, Behavioural Brain Research.

GLRB allelic variation associated with agoraphobic cognitions, increased startle response and fear network activation: a potential neurogenetic pathway to panic disorder

S. Cichon, L. Kiemeney, M. Nöthen, 2017, Molecular Psychiatry.

Differential association between MAOA, ADHD and neuropsychological functioning in boys and girls

B. Franke, J. Buitelaar, S. Faraone, 2008, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

Genome‐wide association uncovers shared genetic effects among personality traits and mood states

I. Deary, D. Rujescu, I. Giegling, 2012, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

Genetic Determinants of Cortical Structure (Thickness, Surface Area and Volumes) among Disease Free Adults in the CHARGE Consortium

Anders M. Dale, Robert C. Green, Shannon L. Risacher, 2018, bioRxiv.

Open Access Journal of Neuroinflammation Replication by the Epistasis Project of the Interaction between the Genes for Il-6 and Il-10 in the Risk of Alzheimer's Disease

Mario Cortina-Borja, Rhian Gwilliam, Naomi Hammond, 2022 .

The impact of apolipoprotein E on dementia in persons with Down's syndrome

C. M. van Duijn, C. Duijn, A. Arias-Vasquez, 2008, Neurobiology of Aging.

Identifying loci for the overlap between attention-deficit/hyperactivity disorder and autism spectrum disorder using a genome-wide QTL linkage approach.

B. Franke, M. Gill, R. Anney, 2010, Journal of the American Academy of Child and Adolescent Psychiatry.

Identifying Loci for the Overlap Between ADHD and ASD Using a Genome-Wide QTL Linkage Approach

A. Arias-Vasquez, J. Nijmeijer, A. Arias-Vásquez, 2010 .

The role of age in association analyses of ADHD and related neurocognitive functioning: A proof of concept for dopaminergic and serotonergic genes

B. Franke, J. Buitelaar, C. Hartman, 2015, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

Candidate genetic pathways for attention-deficit/hyperactivity disorder (ADHD) show association to hyperactive/impulsive symptoms in children with ADHD.

B. Franke, M. Gill, R. Ebstein, 2013, Journal of the American Academy of Child and Adolescent Psychiatry.

Neuropsychological intra‐individual variability explains unique genetic variance of ADHD and shows suggestive linkage to chromosomes 12, 13, and 17

B. Franke, J. Buitelaar, S. Faraone, 2012, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

The ATXN1 and TRIM31 genes are related to intelligence in an ADHD background: Evidence from a large collaborative study totaling 4,963 Subjects

David M. Evans, I. Deary, B. Franke, 2010, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

Effects of maternal and paternal smoking on attentional control in children with and without ADHD

B. Franke, J. Buitelaar, S. Faraone, 2009, European Child & Adolescent Psychiatry.

Conduct disorder and ADHD: Evaluation of conduct problems as a categorical and quantitative trait in the international multicentre ADHD genetics study

Aribert Rothenberger, Herbert Roeyers, Tobias Banaschewski, 2008, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

The dopamine receptor D4 7-repeat allele and prenatal smoking in ADHD-affected children and their unaffected siblings: no gene-environment interaction.

B. Franke, M. Gill, R. Anney, 2008, Journal of child psychology and psychiatry, and allied disciplines.

Neuropsychological endophenotype approach to genome-wide linkage analysis identifies susceptibility loci for ADHD on 2q21.1 and 13q12.11.

B. Franke, J. Buitelaar, S. Faraone, 2008, American journal of human genetics.

Angiogenic, neurotrophic, and inflammatory system SNPs moderate the association between birth weight and ADHD symptom severity

B. Franke, M. Gill, J. Buitelaar, 2014, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

Converging evidence does not support GIT1 as an ADHD risk gene

B. Franke, J. Buitelaar, M. Zwiers, 2015, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

Common variants in DGKK are strongly associated with risk of hypospadias

L. Kiemeney, B. Franke, J. Veltman, 2011, Nature Genetics.

Effects of the Mediterranean Diet or Nut Consumption On Gut Microbiota Composition and Fecal Metabolites and their Relationship With Cardiometabolic Risk Factors.

A. Arias-Vasquez, J. Basora, M. Bulló, 2021, Molecular nutrition & food research.

Gut microbiota signature in treatment-naïve attention-deficit/hyperactivity disorder

C. Sánchez-Mora, J. Ramos-Quiroga, M. Ribasés, 2021, Translational Psychiatry.

Genetic Overlap Between Attention-Deficit/Hyperactivity Disorder and Bipolar Disorder: Evidence From Genome-wide Association Study Meta-analysis

B. Franke, O. Andreassen, J. Kelsoe, 2017, Biological Psychiatry.

No evidence for association between tau gene haplotypic variants and susceptibility to Creutzfeldt-Jakob disease

C. V. van Duijn, A. Arias-Vasquez, P. Sánchez-Juan, 2007, BMC Medical Genetics.

Interaction of the 5-HTTLPR and childhood trauma influences memory bias in healthy individuals.

B. Franke, A. Schene, I. Tendolkar, 2015, Journal of affective disorders.

The relationship between ADHD and key cognitive phenotypes is not mediated by shared familial effects with IQ

M. Gill, J. Buitelaar, S. Faraone, 2010, Psychological Medicine.

Measuring Integrated Novel Dimensions in Neurodevelopmental and Stress-related Mental Disorders (MIND-Set): a cross-sectional comorbidity study from an RDoC perspective

A. Schene, I. Tendolkar, A. Arias-Vasquez, 2021, medRxiv.

Diet, Physical Activity, and Disinhibition in Middle-Aged and Older Adults: A UK Biobank Study

C. Hartman, J. Buitelaar, A. Arias-Vasquez, 2021, Nutrients.

Attention‐deficit/hyperactivity disorder symptoms and dietary habits in adulthood: A large population‐based twin study in Sweden

C. Hartman, A. Arias-Vasquez, R. Kuja‐Halkola, 2020, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

The cholesteryl ester transfer protein (CETP) gene and the risk of Alzheimer’s disease

A. Hofman, A. Isaacs, M. Breteler, 2007, Neurogenetics.

Current Self-Reported Symptoms of Attention Deficit/Hyperactivity Disorder Are Associated with Total Brain Volume in Healthy Adults

B. Franke, J. Buitelaar, G. Fernández, 2012, PloS one.

The Role of the Gut-Brain Axis in Attention-Deficit/Hyperactivity Disorder.

A. Arias-Vasquez, J. Mostert, M. Bloemendaal, 2019, Gastroenterology clinics of North America.

A two arm randomized controlled trial comparing the short and long term effects of an elimination diet and a healthy diet in children with ADHD (TRACE study). Rationale, study design and methods

Annick Bosch, J. Buitelaar, R. Donders, 2020, BMC Psychiatry.

Treating impulsivity with probiotics in adults (PROBIA): study protocol of a multicenter, double-blind, randomized, placebo-controlled trial

I. Bitter, J. Réthelyi, J. Ramos-Quiroga, 2020, Trials.

A comparison of bioinformatics pipelines for compositional analysis of the human gut microbiome

B. Franke, J. Buitelaar, A. Arias-Vasquez, 2023, bioRxiv.