Andrew McQuillin

发表

A genetic association study implicates the chromosome 11q23.3 gene FXYD6 in susceptibility to schizophrenia

Datta, David Curtis, Khalid Choudhury, 2006 .

A search for the risk allele for bipolar affective disorder on chromosome 12q24.2.

Torben A. Kruse, David Curtis, Andrew McQuillin, 2000 .

An allelic association study in a UK case-control sample testing the schizophrenia susceptibility locus on chromosome 1q21-22

David Curtis, Andrew McQuillin, N Bass, 2002 .

No linkage found between chromosome 11p15.5 markers and manic-depressive illness.

David Curtis, Andrew McQuillin, Jacob Lawrence, 1998 .

A microarray gene expression and genetic association study of the RGS4 gene in schizophrenia

Datta, David Curtis, Andrew McQuillin, 2004 .

Evidence of allelic association of bipolar disorder with two genes P2RX7 and AY070435 6 MB apart on 12q24

David Curtis, Andrew McQuillin, Puri, 2005 .

Linkage and allelic association studies of the 8p schizophrenia locus.

David Curtis, Andrew McQuillin, Hmd Gurling, 1999 .

Fine mapping of a new bipolar and unipolar affective disorder locus on chromosome 1p36

David Curtis, Khalid Choudhury, Andrew McQuillin, 2006 .

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

Eden R Martin, Seth Love, Brian Lawlor, 2019, Nature Genetics.

Genetics of attention-deficit hyperactivity disorder (ADHD)

Andrew McQuillin, H. Gurling, A. McQuillin, 2009, Neuropharmacology.

Joint Analysis of Psychiatric Disorders Increases Accuracy of Risk Prediction for Schizophrenia, Bipolar Disorder, and Major Depressive Disorder

Laura J. Scott, Naomi R. Wray, Margaret A. Pericak-Vance, 2015, American journal of human genetics.

A rare variant in APOC3 is associated with plasma triglyceride and VLDL levels in Europeans

Gail Clement, Jie Huang, Antonio Ciampi, 2014, Nature Communications.

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

David Curtis, Khalid Choudhury, Andrew McQuillin, 2011, Psychiatric genetics.

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)

David Curtis, Andrew McQuillin, Jacob Lawrence, 2001, European Journal of Human Genetics.

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

Wei Cheng, Jianxin Shi, Elvira Bramon, 2016, Nature Genetics.

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

Seth Love, Brian Lawlor, Martin Rossor, 2010, PloS one.

Genome-wide Association Study of Alzheimer’s disease with Psychotic Symptoms

Brian Lawlor, Oscar L. Lopez, David Craig, 2011, Molecular Psychiatry.

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

Jianxin Shi, Pablo V Gejman, Jubao Duan, 2014, American journal of human genetics.

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

Jianxin Shi, Susmita Datta, Aribert Rothenberger, 2013, Nature Genetics.

Genome-wide association study identifies 30 Loci Associated with Bipolar Disorder

Jakob Grove, Esben Agerbo, Andres Metspalu, 2017, bioRxiv.

Corrigendum: TCTEX1D2 mutations underlie Jeune asphyxiating thoracic dystrophy with impaired retrograde intraflagellar transport

Gail Clement, Jie Huang, Inês Barroso, 2016, Nature Communications.

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

David Curtis, Andrew McQuillin, Srinivasa Thirumalai, 2005, American journal of human genetics.

Genome-wide association study identifies five new schizophrenia loci

Anders D. Børglum, Peter Donnelly, Jianxin Shi, 2011, Nature Genetics.

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

David Curtis, Khalid Choudhury, Andrew McQuillin, 2006, Archives of general psychiatry.

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

Stephan Ripke, Andrew McQuillin, Hugh Gurling, 2016, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

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

Robin M. Murray, Hilleke E. Hulshoff Pol, Marc M. Bohlken, 2016, Genome Biology.

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

Minna Männikkö, David Curtis, Peter Holmans, 2016, Nature Neuroscience.

Psychiatric genome-wide association study analyses implicate neuronal, immune and histone pathways

Laura J. Scott, Naomi R. Wray, Margaret A. Pericak-Vance, 2015, Nature Neuroscience.

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

Leena Peltonen, Andrew McQuillin, Jouko Lönnqvist, 2003, American journal of human genetics.