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Lista de obras de Andrew McQuillin

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

A gene expression and systems pathway analysis of the effects of clozapine compared to haloperidol in the mouse brain implicates susceptibility genes for schizophrenia.

artículo científico

A genetic association study of chromosome 11q22-24 in two different samples implicates the FXYD6 gene, encoding phosphohippolin, in susceptibility to schizophrenia

artículo científico publicado en 2007

A genome-wide association study confirms PNPLA3 and identifies TM6SF2 and MBOAT7 as risk loci for alcohol-related cirrhosis

artículo científico publicado en 2015

A genomewide association study of response to lithium for prevention of recurrence in bipolar disorder.

artículo científico publicado en 2009

A microarray gene expression study of the molecular pharmacology of lithium carbonate on mouse brain mRNA to understand the neurobiology of mood stabilization and treatment of bipolar affective disorder.

artículo científico publicado en 2007

A nonconservative amino acid change in the UPF3B gene in a patient with schizophrenia

article

A novel polymorphism in exon 11 of the WKL1 gene, shows no association with schizophrenia

artículo científico publicado en 2002

A rare functional noncoding variant at the GWAS-implicated MIR137/MIR2682 locus might confer risk to schizophrenia and bipolar disorder

artículo científico publicado en 2014

A threonine to isoleucine missense mutation in the pericentriolar material 1 gene is strongly associated with schizophrenia

artículo científico publicado en 2010

Allelic association, DNA resequencing and copy number variation at the metabotropic glutamate receptor GRM7 gene locus in bipolar disorder

artículo científico publicado en 2014

An inherited duplication at the gene p21 Protein-Activated Kinase 7 (PAK7) is a risk factor for psychosis

artículo científico publicado en 2014

Analysis of ANK3 and CACNA1C variants identified in bipolar disorder whole genome sequence data.

artículo científico publicado en 2014

Analysis of genetic deletions and duplications in the University College London bipolar disorder case control sample

artículo científico publicado en 2011

Analysis of shared heritability in common disorders of the brain

artículo científico publicado en 2018

Analysis of t(9;17)(q33.2;q25.3) chromosomal breakpoint regions and genetic association reveals novel candidate genes for bipolar disorder

artículo científico publicado en 2014

Association of rare variation in the glutamate receptor gene SLC1A2 with susceptibility to bipolar disorder and schizophrenia.

artículo científico publicado en 2014

Author Correction: Genetic meta-analysis of diagnosed Alzheimer's disease identifies new risk loci and implicates Aβ, tau, immunity and lipid processing

scientific article published on 01 September 2019

Case-case genome-wide association analysis shows markers differentially associated with schizophrenia and bipolar disorder and implicates calcium channel genes

artículo científico publicado en 2011

Case-control studies show that a non-conservative amino-acid change from a glutamine to arginine in the P2RX7 purinergic receptor protein is associated with both bipolar- and unipolar-affective disorders

artículo científico publicado en 2008

Cationic liposome-mediated DNA transfection in organotypic explant cultures of the ventral mesencephalon

artículo científico publicado en 1999

Chromosomal microarray testing in adults with intellectual disability presenting with comorbid psychiatric disorders.

artículo científico publicado en 2016

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

artículo científico publicado en 2008

Common variants at ABCA7, MS4A6A/MS4A4E, EPHA1, CD33 and CD2AP are associated with Alzheimer's disease

artículo científico publicado en 2011

Confirmation of prior evidence of genetic susceptibility to alcoholism in a genome-wide association study of comorbid alcoholism and bipolar disorder

artículo científico publicado en 2011

Confirmation of the genetic association between the U2AF homology motif (UHM) kinase 1 (UHMK1) gene and schizophrenia on chromosome 1q23.3.

artículo científico publicado en 2008

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

artículo científico publicado en 2016

Correction: Genetic Evidence Implicates the Immune System and Cholesterol Metabolism in the Aetiology of Alzheimer's Disease.

artículo científico publicado en 2011

DISC1 association, heterogeneity and interplay in schizophrenia and bipolar disorder

artículo científico publicado en 2008

Direct genomic PCR sequencing of the high affinity thiamine transporter (SLC19A2) gene identifies three genetic variants in Wernicke Korsakoff syndrome (WKS)

artículo científico publicado en 2005

Dissecting the Shared Genetic Architecture of Suicide Attempt, Psychiatric Disorders, and Known Risk Factors

artículo científico publicado en 2022

Does rare matter? Copy number variants at 16p11.2 and the risk of psychosis: a systematic review of literature and meta-analysis

artículo científico publicado en 2014

Elevated common variant genetic risk for tourette syndrome in a densely-affected pedigree

artículo científico publicado en 2021

Erratum: Genome-wide association study identifies variants at CLU and PICALM associated with Alzheimer's disease

scholarly article published in Nature Genetics

Erratum: Genome-wide association study identifies variants at CLU and PICALM associated with Alzheimer's disease

article

Evidence for Genetic Overlap Between Schizophrenia and Age at First Birth in Women

artículo científico publicado en 2016

Evidence for genetic susceptibility to the alcohol dependence syndrome from the thiamine transporter 2 gene solute carrier SLC19A3.

scientific article published on June 2014

Evidence for the association of the DAOA (G72) gene with schizophrenia and bipolar disorder but not for the association of the DAO gene with schizophrenia

scientific article published on 08 July 2009

Exome sequence analysis and follow up genotyping implicates rare ULK1 variants to be involved in susceptibility to schizophrenia.

artículo científico publicado en 2017

Failure to confirm allelic and haplotypic association between markers at the chromosome 6p22.3 dystrobrevin-binding protein 1 (DTNBP1) locus and schizophrenia

artículo científico publicado en 2007

Failure to confirm allelic association between markers at the CAPON gene locus and schizophrenia in a British sample

artículo científico publicado en 2005

Failure to confirm genetic association between schizophrenia and markers on chromosome 1q23.3 in the region of the gene encoding the regulator of G-protein signaling 4 protein (RGS4).

artículo científico publicado en 2006

Fine mapping by genetic association implicates the chromosome 1q23.3 gene UHMK1, encoding a serine/threonine protein kinase, as a novel schizophrenia susceptibility gene

artículo científico publicado en 2006

Fine mapping of a susceptibility locus for bipolar and genetically related unipolar affective disorders, to a region containing the C21ORF29 and TRPM2 genes on chromosome 21q22.3.

artículo científico publicado en 2006

GWA study data mining and independent replication identify cardiomyopathy-associated 5 (CMYA5) as a risk gene for schizophrenia

artículo científico publicado en 2010

GWAS of Suicide Attempt in Psychiatric Disorders and Association With Major Depression Polygenic Risk Scores.

artículo científico publicado en 2019

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

artículo científico publicado en 2016

Genetic association and brain morphology studies and the chromosome 8p22 pericentriolar material 1 (PCM1) gene in susceptibility to schizophrenia

artículo científico publicado en 2006

Genetic association and functional characterization of MCPH1 gene variation in bipolar disorder and schizophrenia

artículo científico publicado en 2019

Genetic association and sequencing of the insulin-like growth factor 1 gene in bipolar affective disorder

artículo científico publicado en 2011

Genetic association of the tachykinin receptor 1 TACR1 gene in bipolar disorder, attention deficit hyperactivity disorder, and the alcohol dependence syndrome

artículo científico publicado en 2014

Genetic association studies of schizophrenia using the 8p21-22 genes: prepronociceptin (PNOC), neuronal nicotinic cholinergic receptor alpha polypeptide 2 (CHRNA2) and arylamine N-acetyltransferase 1 (NAT1).

artículo científico publicado en 2001

Genetic association study of GABRA2 single nucleotide polymorphisms and electroencephalography in alcohol dependence

artículo científico publicado en 2011

Genetic association, mutation screening, and functional analysis of a Kozak sequence variant in the metabotropic glutamate receptor 3 gene in bipolar disorder.

artículo científico publicado en 2013

Genetic copy number variants, cognition and psychosis: a meta-analysis and a family study

artículo científico publicado en 2020

Genetic evidence implicates the immune system and cholesterol metabolism in the aetiology of Alzheimer's disease

artículo científico publicado en 2010

Genetic linkage analysis supports the presence of two susceptibility loci for alcoholism and heavy drinking on chromosome 1p22.1-11.2 and 1q21.3-24.2

artículo científico publicado en 2005

Genetic meta-analysis of diagnosed Alzheimer’s disease identifies new risk loci and implicates Aβ, tau, immunity and lipid processing

artículo científico publicado en 2019

Genetic power of a Brazilian three-generation family with generalized aggressive periodontitis

artículo científico publicado en 2010

Genetic power of a Brazilian three-generation family with generalized aggressive periodontitis. II.

artículo científico publicado en 2011

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

artículo científico publicado en 2013

Genetic variants in or near ADH1B and ADH1C affect susceptibility to alcohol dependence in a British and Irish population

artículo científico publicado en 2014

Genetic variation in the miR-708 gene and its binding targets in bipolar disorder.

artículo científico publicado en 2016

Genetics of attention-deficit hyperactivity disorder (ADHD).

artículo científico publicado en 2009

Gene–Brain Structure Relationships: Arbitrary Assumptions of Heterogeneity Generate Unfalsifiable Claims—Reply

article

Genome scan meta-analysis of schizophrenia and bipolar disorder, part II: Schizophrenia

artículo científico publicado en 2003

Genome scan meta-analysis of schizophrenia and bipolar disorder, part III: Bipolar disorder

artículo científico publicado en 2003

Genome scan of Tourette syndrome in a single large pedigree shows some support for linkage to regions of chromosomes 5, 10 and 13.

artículo científico publicado en 2004

Genome scan of pedigrees multiply affected with bipolar disorder provides further support for the presence of a susceptibility locus on chromosome 12q23-q24, and suggests the presence of additional loci on 1p and 1q

Genome-wide association study identifies 30 loci associated with bipolar disorder.

artículo científico publicado en 2019

Genome-wide association study identifies variants at CLU and PICALM associated with Alzheimer's disease

artículo científico publicado en 2009

Genome-wide association study of Alzheimer's disease with psychotic symptoms

artículo científico publicado en 2011

Genome-wide association study of bipolar disorder in Canadian and UK populations corroborates disease loci including SYNE1 and CSMD1

artículo científico publicado en 2014

Genome-wide association study of more than 40,000 bipolar disorder cases provides new insights into the underlying biology

artículo científico publicado en 2021

Genome-wide association study of suicide attempts in mood disorder patients

artículo científico publicado en 2010

Genome-wide association study reveals greater polygenic loading for schizophrenia in cases with a family history of illness

artículo científico publicado en 2015

Genome-wide meta-analysis of problematic alcohol use in 435,563 individuals yields insights into biology and relationships with other traits

artículo científico publicado en 2020

Genomewide association study identifies 30 loci associated with bipolar disorder

Genomewide genetic linkage analysis confirms the presence of susceptibility loci for schizophrenia, on chromosomes 1q32.2, 5q33.2, and 8p21-22 and provides support for linkage to schizophrenia, on chromosomes 11q23.3-24 and 20q12.1-11.23

artículo científico publicado en 2001

Genomic Dissection of Bipolar Disorder and Schizophrenia, Including 28 Subphenotypes

article

Genomic dissection of bipolar disorder and schizophrenia including 28 subphenotypes

artículo científico publicado en 2017

Identification of the Slynar gene (AY070435) and related brain expressed sequences as a candidate gene for susceptibility to affective disorders through allelic and haplotypic association with bipolar disorder on chromosome 12q24.

artículo científico publicado en 2006

Interaction Testing and Polygenic Risk Scoring to Estimate the Association of Common Genetic Variants With Treatment Resistance in Schizophrenia

artículo científico publicado en 2022

Lack of allelic association between markers at the DRD2 and ANKK1 gene loci with the alcohol-dependence syndrome and criminal activity.

artículo científico publicado en 2011

Linkage disequilibrium and demographic history of the isolated population of the Faroe Islands

scientific article published on 01 June 2002

Localization of functional regions of the cucumber mosaic virus RNA replicase using monoclonal and polyclonal antibodies

artículo científico publicado en 1994

Mapping genomic loci implicates genes and synaptic biology in schizophrenia

artículo científico publicado en 2022

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

artículo científico publicado en 2011

Memory decline in Down syndrome and its relationship to iPF2alpha, a urinary marker of oxidative stress

artículo científico publicado en 2014

Meta-analysis of 32 genome-wide linkage studies of schizophrenia.

artículo científico publicado en 2008

Mutations in the Gabrb1 gene promote alcohol consumption through increased tonic inhibition

artículo científico publicado en 2013

NK1 (TACR1) receptor gene 'knockout' mouse phenotype predicts genetic association with ADHD.

scientific article published on 09 February 2009

New data and an old puzzle: the negative association between schizophrenia and rheumatoid arthritis

artículo científico publicado en 2015

No allelic association between bipolar affective disorder and the tryptophan hydroxylase gene

artículo científico publicado en 1999

No association between a neuronal nitric oxide synthase (NOS1) gene polymorphism on chromosome 12q24 and bipolar disorder.

artículo científico publicado en 2004

No evidence for excess runs of homozygosity in bipolar disorder.

artículo científico publicado en 2009

No evidence that extended tracts of homozygosity are associated with Alzheimer's disease.

artículo científico publicado en 2011

Optimization of liposome mediated transfection of a neuronal cell line

artículo científico publicado en 1997

Phenotypic heterogeneity in study populations may significantly confound the results of genetic association studies on alcohol dependence.

artículo científico publicado en 2015

Polygenic dissection of diagnosis and clinical dimensions of bipolar disorder and schizophrenia

artículo científico publicado en 2013

Polygenic dissection of the bipolar phenotype

artículo científico publicado en 2011

Rare chromosomal deletions and duplications increase risk of schizophrenia

artículo científico publicado en 2008

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

artículo científico publicado en 2016

Reply to: "The PNPLA3 SNP rs738409:G allele is associated with increased liver disease-associated mortality but reduced overall mortality in a population-based cohort".

artículo científico publicado en 2017

Sequencing of the ANKYRIN 3 gene (ANK3) encoding ankyrin G in bipolar disorder reveals a non-conservative amino acid change in a short isoform of ankyrin G.

artículo científico publicado en 2012

Sex-Dependent Shared and Nonshared Genetic Architecture Across Mood and Psychotic Disorders

artículo científico publicado en 2022

Support of association between BRD1 and both schizophrenia and bipolar affective disorder.

artículo científico publicado en 2010

Tests of linkage and allelic association between markers in the 1p36 PRKCZ (protein kinase C zeta) gene region and bipolar affective disorder

artículo científico publicado en 2012

The Epsin 4 gene on chromosome 5q, which encodes the clathrin-associated protein enthoprotin, is involved in the genetic susceptibility to schizophrenia

artículo científico publicado en 2005

The effect of clozapine on mRNA expression for genes encoding G protein-coupled receptors and the protein components of clathrin-mediated endocytosis

artículo científico publicado en 2013

The functional GRM3 Kozak sequence variant rs148754219 affects the risk of schizophrenia and alcohol dependence as well as bipolar disorder

artículo científico publicado en 2014

The role of variation at AβPP, PSEN1, PSEN2, and MAPT in late onset Alzheimer's disease

artículo científico publicado en 2012

Variation in the DCP1 gene, encoding the angiotensin converting enzyme ACE, is not associated with increased susceptibility to Alzheimer's disease.

artículo científico publicado en 2003

Whole-exome sequencing of individuals from an isolated population implicates rare risk variants in bipolar disorder

artículo científico publicado en 2017

Whole-genome association study of bipolar disorder

artículo científico publicado en 2008