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Lista de obras de David Collier

A COMT gene haplotype associated with methamphetamine abuse.

artículo científico publicado en 2011

A common variant in DRD3 receptor is associated with autism spectrum disorder

artículo científico publicado en 2008

A contribution of novel CNVs to schizophrenia from a genome-wide study of 41,321 subjects

A genome-wide association analysis of a broad psychosis phenotype identifies three loci for further investigation

artículo científico publicado en 2013

A genome-wide association study for quantitative traits in schizophrenia in China.

artículo científico publicado en 2011

A genome-wide association study in individuals of African ancestry reveals the importance of the Duffy-null genotype in the assessment of clozapine-related neutropenia

artículo científico publicado en 2019

A large replication study and meta-analysis in European samples provides further support for association of AHI1 markers with schizophrenia

artículo científico publicado en 2010

A new social-family model for eating disorders: A European multicentre project using a case-control design

artículo científico publicado en 2015

A psychosocial risk factor model for female eating disorders: a European multicentre project.

artículo científico publicado en 2014

Aberrant spontaneous neural activity and correlation with evoked-brain potentials in first-episode, treatment-naïve patients with deficit and non-deficit schizophrenia.

artículo científico publicado en 2017

Advanced paternal age increases the risk of schizophrenia and obsessive-compulsive disorder in a Chinese Han population.

artículo científico publicado en 2012

Advances in the genetics of schizophrenia: toward a network and pathway view for drug discovery

artículo científico publicado en 2016

Advances in the genetics of schizophrenia: will high-risk copy number variants be useful in clinical genetics or diagnostics?

artículo científico publicado en 2009

Altered effect of dopamine transporter 3'UTR VNTR genotype on prefrontal and striatal function in schizophrenia.

artículo científico publicado en 2009

Altered social behaviours in neurexin 1α knockout mice resemble core symptoms in neurodevelopmental disorders.

artículo científico publicado en 2013

An integrated genetic-epigenetic analysis of schizophrenia: evidence for co-localization of genetic associations and differential DNA methylation

artículo científico publicado en 2016

Analysis of Intellectual Disability Copy Number Variants for Association With Schizophrenia

artículo científico publicado en 2016

Assessment of white matter abnormalities in paranoid schizophrenia and bipolar mania patients ⬇️

artículo científico publicado el 12 de noviembre de 2011

Association Study of Nonsynonymous Single Nucleotide Polymorphisms in Schizophrenia

article by Noa Carrera et al published January 2012 in Biological Psychiatry

Association analysis of STX1A gene variants in common forms of migraine

artículo científico publicado en 2012

Association between BDNF val66 met genotype and episodic memory

artículo científico publicado en 2005

Association between the COMT gene and neurological abnormalities and poorer executive function in psychosis

artículo científico publicado en 2015

Association of BDNF with anorexia, bulimia and age of onset of weight loss in six European populations

artículo científico publicado en 2004

Association of BDNF with restricting anorexia nervosa and minimum body mass index: a family-based association study of eight European populations

artículo científico publicado en 2005

Association study of dysbindin gene with clinical and outcome measures in a representative cohort of Italian schizophrenic patients

artículo científico publicado en 2007

Associations between childhood maltreatment and inflammatory markers

artículo científico publicado en 2019

Associations of individual and family eating patterns during childhood and early adolescence: a multicentre European study of associated eating disorder factors.

artículo científico publicado en 2008

At-risk variant in TCF7L2 for type II diabetes increases risk of schizophrenia

artículo científico publicado en 2011

Author Correction: Expression-based drug screening of neural progenitor cells from individuals with schizophrenia

artículo científico publicado en 2018

BBGRE: brain and body genetic resource exchange

artículo científico publicado en 2013

Bridging of childhood obsessive‐compulsive personality disorder traits and adult eating disorder symptoms: A network analysis approach

artículo científico publicado en 2022

Candidate gene analysis of the human natural killer-1 carbohydrate pathway and perineuronal nets in schizophrenia: B3GAT2 is associated with disease risk and cortical surface area

artículo científico publicado en 2010

Case???control and combined family trios analysis of three polymorphisms in the ghrelin gene in European patients with anorexia and bulimia nervosa

article

Clinical utility gene card for: 15q13.3 microdeletion syndrome.

artículo científico publicado en 2014

Clinical utility gene card for: 16p13.11 microdeletion syndrome

artículo científico publicado en 2013

Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder

artículo científico publicado en 2008

Common schizophrenia alleles are enriched in mutation-intolerant genes and in regions under strong background selection.

artículo científico publicado en 2018

Common variant at 16p11.2 conferring risk of psychosis.

artículo científico publicado en 2012

Common variants at VRK2 and TCF4 conferring risk of schizophrenia

artículo científico publicado en 2011

Common variants conferring risk of schizophrenia

artículo científico publicado en 2009

Common variants near CAV1 and CAV2 are associated with primary open-angle glaucoma

artículo científico publicado en 2010

Common variants on 8p12 and 1q24.2 confer risk of schizophrenia

artículo científico publicado en 2011

Conference Report: Psychiatric Genomics Consortium Meeting: Pathways to Drugs, London, March 2017.

artículo científico publicado en 2018

Consensus paper of the WFSBP Task Force on Genetics: Genetics, epigenetics and gene expression markers of major depressive disorder and antidepressant response

artículo científico publicado en 2016

Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects

artículo científico publicado en 2016

Correlation and familial aggregation of dimensions of psychosis in affected sibling pairs from China

artículo científico publicado en 2008

Correlation of miRNA expression with intensity of neuropathic pain in man

scientific article published on 01 January 2019

Detection of metabolites in the white matter of frontal lobes and hippocampus with proton in first-episode treatment-naïve schizophrenia patients.

artículo científico publicado en 2011

Differential effects of DAAO on regional activation and functional connectivity in schizophrenia, bipolar disorder and controls.

artículo científico publicado en 2011

Disruption of the neurexin 1 gene is associated with schizophrenia

artículo científico publicado en 2009

Effect of COMT genotype on aggressive behaviour in a community cohort of schizophrenic patients.

artículo científico publicado en 2011

Effect of D-amino acid oxidase activator (DAOA; G72) on brain function during verbal fluency

artículo científico publicado en 2011

Effect of DISC1 on the P300 waveform in psychosis

artículo científico publicado en 2011

Effects of the CACNA1C risk allele for bipolar disorder on cerebral gray matter volume in healthy individuals

artículo científico publicado en 2009

Epilepsy-associated GRIN2A mutations reduce NMDA receptor trafficking and agonist potency - molecular profiling and functional rescue

artículo científico publicado en 2017

Episodic memory performance predicted by the 2bp deletion in exon 6 of the "alpha 7-like" nicotinic receptor subunit gene

artículo científico publicado en 2006

Epistasis between the DAT 3' UTR VNTR and the COMT Val158Met SNP on cortical function in healthy subjects and patients with schizophrenia

scholarly article

Erratum: Evidence for three genetic loci involved in both anorexia nervosa risk and variation of body mass index

article

Erratum: Identification of increased genetic risk scores for schizophrenia in treatment-resistant patients

artículo científico publicado en 2015

Establishing the characteristics of an effective pharmacogenetic test for clozapine-induced agranulocytosis

artículo científico publicado en 2015

Evaluation of a susceptibility gene for schizophrenia: genotype based meta-analysis of RGS4 polymorphisms from thirteen independent samples

artículo científico publicado en 2006

Evidence of association of KIBRA genotype with episodic memory in families of psychotic patients and controls

artículo científico publicado en 2010

Expression analysis in a rat psychosis model identifies novel candidate genes validated in a large case-control sample of schizophrenia.

artículo científico publicado en 2015

Expression-based drug screening of neural progenitor cells from individuals with schizophrenia

artículo científico publicado en 2018

Extensive brain structural network abnormality in first-episode treatment-naive patients with schizophrenia: morphometrical and covariation study

artículo científico publicado en 2014

Factor structures of the neurocognitive assessments and familial analysis in first-episode schizophrenia patients, their relatives and controls.

artículo científico publicado en 2010

Factors of risk and maintenance for eating disorders: psychometric exploration of the cross-cultural questionnaire (CCQ) across five European countries.

artículo científico publicado en 2010

Fronto-parietal white matter microstructural deficits are linked to performance IQ in a first-episode schizophrenia Han Chinese sample ⬇️

artículo científico publicado el 14 de diciembre de 2012

Gender-specific interactions between alcohol metabolism genes and severity of quantitative alcohol-related-traits in a Tibetan population ⬇️

artículo científico publicado el 21 de marzo de 2011

Gene variants associated with schizophrenia in a Norwegian genome-wide study are replicated in a large European cohort

scientific journal article

Gene-set analysis based on the pharmacological profiles of drugs to identify repurposing opportunities in schizophrenia.

artículo científico publicado en 2016

Genetic modulation of neural response during working memory in healthy individuals: interaction of glucocorticoid receptor and dopaminergic genes.

artículo científico publicado en 2011

Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs

artículo científico publicado en 2013

Genetic targeting of NRXN2 in mice unveils role in excitatory cortical synapse function and social behaviors

artículo científico publicado en 2015

Genetics of schizophrenia: A consensus paper of the WFSBP Task Force on Genetics

artículo científico publicado en 2017

Genome-Wide Association of Heroin Dependence in Han Chinese

artículo científico publicado en 2016

Genome-wide RNAseq study of the molecular mechanisms underlying microglia activation in response to pathological tau perturbation in the rTg4510 tau transgenic animal model

article

Genome-wide association analysis identifies 13 new risk loci for schizophrenia

artículo científico publicado en 2013

Genome-wide association study identifies a sequence variant within the DAB2IP gene conferring susceptibility to abdominal aortic aneurysm

scientific journal article

Genome-wide common and rare variant analysis provides novel insights into clozapine-associated neutropenia

artículo científico publicado en 2016

Genome-wide common and rare variant analysis provides novel insights into clozapine-associated neutropenia.

artículo científico publicado en 2016

Genomic dissection of bipolar disorder and schizophrenia including 28 subphenotypes

artículo científico publicado en 2017

High-throughput DNA methylation analysis in anorexia nervosa confirms TNXB hypermethylation

artículo científico publicado en 2016

Hypermethylation in the ZBTB20 gene is associated with major depressive disorder

artículo científico publicado en 2014

Identification and Potential Regulatory Properties of Evolutionary Conserved Regions (ECRs) at the Schizophrenia-Associated MIR137 Locus.

artículo científico publicado en 2016

Identification and validation of biomarkers for autism spectrum disorders

artículo científico publicado en 2015

Independent modulation of engagement and connectivity of the facial network during affect processing by CACNA1C and ANK3 risk genes for bipolar disorder

artículo científico publicado en 2013

Influence of X chromosome and hormones on human brain development: a magnetic resonance imaging and proton magnetic resonance spectroscopy study of Turner syndrome.

artículo científico publicado en 2005

Interaction between effects of genes coding for dopamine and glutamate transmission on striatal and parahippocampal function.

artículo científico publicado en 2012

Is neuregulin 1 involved in determining cerebral volumes in schizophrenia? Preliminary results showing a decrease in superior temporal gyrus volume.

artículo científico publicado en 2012

Large recurrent microdeletions associated with schizophrenia

artículo científico publicado en 2008

Loss of Trem2 in microglia leads to widespread disruption of cell coexpression networks in mouse brain

artículo científico publicado en 2018

Low social interactions in eating disorder patients in childhood and adulthood: a multi-centre European case control study.

artículo científico publicado en 2012

Male-biased autosomal effect of 16p13.11 copy number variation in neurodevelopmental disorders.

artículo científico publicado en 2013

Maternally derived microduplications at 15q11-q13: implication of imprinted genes in psychotic illness

artículo científico publicado en 2011

Meta-analysis of the association of urbanicity with schizophrenia

artículo científico publicado en 2012

Microduplications at the pseudoautosomal SHOX locus in autism spectrum disorders and related neurodevelopmental conditions

artículo científico publicado en 2016

Molecular and genetic evidence for abnormalities in the nodes of Ranvier in schizophrenia.

artículo científico publicado en 2011

NRXN1 deletions identified by array comparative genome hybridisation in a clinical case series - further understanding of the relevance of NRXN1 to neurodevelopmental disorders

artículo científico publicado en 2013

Neuregulin-1 and the P300 waveform--a preliminary association study using a psychosis endophenotype

artículo científico publicado en 2008

No association between a common single nucleotide polymorphism, rs4141463, in the MACROD2 gene and autism spectrum disorder

artículo científico publicado en 2011

Novel brain expressed RNA identified at the MIR137 schizophrenia-associated locus.

artículo científico publicado en 2016

Ohnologs are overrepresented in pathogenic copy number mutations

artículo científico publicado en 2013

Opening Pandora's box in the UK: a hypothetical pharmacogenetic test for clozapine

artículo científico publicado en 2013

Opposite effects of catechol-O-methyltransferase Val158Met on cortical function in healthy subjects and patients with schizophrenia.

artículo científico publicado en 2008

PACAP and PAC1 receptor in brain development and behavior

artículo científico

Penetrance for copy number variants associated with schizophrenia

artículo científico publicado en 2010

Perception of autonomy and connectedness prior to the onset of anorexia nervosa and bulimia nervosa.

artículo científico publicado en 2012

Predicting outcomes following cognitive behaviour therapy in child anxiety disorders: the influence of genetic, demographic and clinical information.

artículo científico publicado en 2013

Prenatal exposure to maternal obesity leads to hyperactivity in offspring

artículo científico publicado en 2011

Present and lifetime comorbidity of tobacco, alcohol and drug use in eating disorders: a European multicenter study.

artículo científico publicado en 2008

Protein kinase B (AKT1) genotype mediates sensitivity to cannabis-induced impairments in psychomotor control.

artículo científico publicado en 2014

Publisher Correction: Common schizophrenia alleles are enriched in mutation-intolerant genes and in regions under strong background selection

artículo científico publicado en 2019

Random or stochastic monoallelic expressed genes are enriched for neurodevelopmental disorder candidate genes.

artículo científico publicado en 2013

Rare loss-of-function variants in SETD1A are associated with schizophrenia and developmental disorders.

artículo científico publicado en 2016

Regulatory characterisation of the schizophrenia-associated CACNA1C proximal promoter and the potential role for the transcription factor EZH2 in schizophrenia aetiology.

artículo científico publicado en 2018

Relevance of social and self-standards in eating disorders.

artículo científico publicado en 2011

Replication of association of 3p21.1 with susceptibility to bipolar disorder but not major depression

artículo científico publicado en 2011

Replication study and meta-analysis in European samples supports association of the 3p21.1 locus with bipolar disorder

artículo científico publicado en 2012

Risk factors, correlates, and markers in early-onset bulimia nervosa and EDNOS.

artículo científico publicado en 2011

SU116. Longitudinal Epigenetic Analysis of Clozapine Use in Treatment-Resistant Schizophrenia.

artículo científico publicado en 2017

Sensorimotor gating and D2 receptor signalling: evidence from a molecular genetic approach

scientific article published on 16 January 2012

Systematic meta-analyses and field synopsis of genetic association studies of violence and aggression

artículo científico publicado en 2014

TCF4 (e2-2; ITF2): a schizophrenia-associated gene with pleiotropic effects on human disease

artículo científico publicado en 2012

The Association between COMT, BDNF, and NRG1 and Premorbid Social Functioning in Patients with Psychosis, Their Relatives, and Controls

artículo científico publicado en 2012

The Schizophrenia Risk Allele C of the TCF4 rs9960767 Polymorphism Disrupts Sensorimotor Gating in Schizophrenia Spectrum and Healthy Volunteers

artículo científico publicado en 2011

The androgen receptor gene polyglycine repeat polymorphism is associated with memory performance in healthy Chinese individuals

artículo científico publicado en 2009

The association of white matter volume in psychotic disorders with genotypic variation in NRG1, MOG and CNP: a voxel-based analysis in affected individuals and their unaffected relatives

artículo científico publicado en 2012

The cognitive impact of the ANK3 risk variant for bipolar disorder: initial evidence of selectivity to signal detection during sustained attention

artículo científico publicado en 2011

The effects of neuregulin1 on brain function in controls and patients with schizophrenia and bipolar disorder.

artículo científico publicado en 2008

The impact of CACNA1C allelic variation on effective connectivity during emotional processing in bipolar disorder

artículo científico publicado en 2013

The impact of the CACNA1C gene polymorphism on frontolimbic function in bipolar disorder.

artículo científico publicado en 2011

The role of single nucleotide polymorphism of D2 dopamine receptor gene on major depressive disorder and response to antidepressant treatment.

artículo científico publicado en 2012

The same sequence variant on 9p21 associates with myocardial infarction, abdominal aortic aneurysm and intracranial aneurysm

article

Therapygenetics: the 5HTTLPR and response to psychological therapy.

artículo científico publicado en 2011

TractaViewer: a genome-wide tool for preliminary assessment of therapeutic target druggability

scientific article published on 01 November 2019

Translating genome-wide association findings into new therapeutics for psychiatry

artículo científico publicado en 2016

Ulk4 Regulates Neural Stem Cell Pool

artículo científico publicado en 2016

Using genetic findings in autism for the development of new pharmaceutical compounds.

artículo científico publicado en 2013

Volume increases in putamen associated with positive symptom reduction in previously drug-naive schizophrenia after 6 weeks antipsychotic treatment.

artículo científico publicado en 2011

White-matter microstructure in previously drug-naive patients with schizophrenia after 6 weeks of treatment ⬇️

artículo científico publicado el 27 de febrero de 2013

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