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Pathway analyses implicate glial cells in schizophrenia

PloS one, 2014-02, Vol.9 (2), p.e89441

2014

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Genetic modifiers and subtypes in schizophrenia: Investigations of age at onset, severity, sex and family history

Schizophrenia research, 2014-04, Vol.154 (1), p.48-53

2014

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Marked variation in predicted and observed variability of tandem repeat loci across the human genome

BMC genomics, 2008-04, Vol.9 (1), p.175-175

2008

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Tools for the identification of variable and potentially variable tandem repeats

BMC genomics, 2006-11, Vol.7 (1), p.290-290, Article 290

2006

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Population structure and genome-wide patterns of variation in Ireland and Britain

European journal of human genetics : EJHG, 2010-11, Vol.18 (11), p.1248-1254

2010

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Multiplex Target Enrichment Using DNA Indexing for Ultra-High Throughput SNP Detection

DNA research, 2011-02, Vol.18 (1), p.31-38

2011

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Common polygenic variation contributes to risk of schizophrenia and bipolar disorder

Nature (London), 2009-08, Vol.460 (7256), p.748-752

2009

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Tandem repeat copy-number variation in protein-coding regions of human genes

Genome biology, 2005-01, Vol.6 (8), p.R69-R69

2005

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Genome-wide association and Mendelian randomisation analysis provide insights into the pathogenesis of heart failure

Nature communications, 2020, Vol.11 (1), p.163-12, Article 163

2020

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Molecular pathways involved in neuronal cell adhesion and membrane scaffolding contribute to schizophrenia and bipolar disorder susceptibility

Molecular psychiatry, 2011-03, Vol.16 (3), p.286-292

2011

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Genome-Wide Association Study Implicates HLA-C01:02 as a Risk Factor at the Major Histocompatibility Complex Locus in Schizophrenia

Biological psychiatry (1969), 2012-10, Vol.72 (8), p.620-628

2012

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Evaluating the role of common risk variation in the recurrence risk of schizophrenia in multiplex schizophrenia families

Translational psychiatry, 2022-07, Vol.12 (1), p.291-7, Article 291

2022

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Genome-wide association study identifies five new schizophrenia loci

Nature genetics, 2011-10, Vol.43 (10), p.969-976

2011

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Large-scale genome-wide association analysis of bipolar disorder identifies a new susceptibility locus near ODZ4

Nature genetics, 2011-10, Vol.43 (10), p.977-983

2011

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Non-random error in genotype calling procedures: Implications for family-based and case-control genome-wide association studies

American journal of medical genetics. Part B, Neuropsychiatric genetics, 2008-12, Vol.147B (8), p.1379-1386

2008

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Ligand Switching in Cell-Permeable Peptides: Manipulation of the α-Integrin Signature Motif

ACS chemical biology, 2009-06, Vol.4 (6), p.457-471

2009

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Improved Detection of Common Variants Associated with Schizophrenia by Leveraging Pleiotropy with Cardiovascular-Disease Risk Factors

American journal of human genetics, 2013-02, Vol.92 (2), p.197-209

2013

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Identification of pathways for bipolar disorder: a meta-analysis

JAMA psychiatry (Chicago, Ill.), 2014-06, Vol.71 (6), p.657

2014

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Rare chromosomal deletions and duplications increase risk of schizophrenia

Nature, 2008-09, Vol.455 (7210), p.237-241

2008

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Absolute Net Charge and the Biological Activity of Oligopeptides

Journal of chemical information and modeling, 2006-09, Vol.46 (5), p.2183-2190

2006

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An assessment of the Irish population for large-scale genetic mapping studies involving epilepsy and other complex diseases

European journal of human genetics : EJHG, 2008-02, Vol.16 (2), p.176-183

2008

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A bias-reducing pathway enrichment analysis of genome-wide association data confirmed association of the MHC region with schizophrenia

Journal of medical genetics, 2012-02, Vol.49 (2), p.96-103

2012

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Additive Genetic Variation in Schizophrenia Risk Is Shared by Populations of African and European Descent

American journal of human genetics, 2013-09, Vol.93 (3), p.463-470

2013

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Runs of homozygosity implicate autozygosity as a schizophrenia risk factor

PLoS genetics, 2012-04, Vol.8 (4), p.e1002656-e1002656

2012

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Pathway analyses implicate glial cells in schizophrenia

Reciprocal Duplication of the Williams-Beuren Syndrome Deletion on Chromosome 7q11.23 Is Associated with Schizophrenia

Genetic modifiers and subtypes in schizophrenia: Investigations of age at onset, severity, sex and family history

Marked variation in predicted and observed variability of tandem repeat loci across the human genome

Tools for the identification of variable and potentially variable tandem repeats

Population structure and genome-wide patterns of variation in Ireland and Britain

Multiplex Target Enrichment Using DNA Indexing for Ultra-High Throughput SNP Detection

Common polygenic variation contributes to risk of schizophrenia and bipolar disorder

Tandem repeat copy-number variation in protein-coding regions of human genes

Genome-wide association and Mendelian randomisation analysis provide insights into the pathogenesis of heart failure

Molecular pathways involved in neuronal cell adhesion and membrane scaffolding contribute to schizophrenia and bipolar disorder susceptibility

Genome-Wide Association Study Implicates HLA-C01:02 as a Risk Factor at the Major Histocompatibility Complex Locus in Schizophrenia

Evaluating the role of common risk variation in the recurrence risk of schizophrenia in multiplex schizophrenia families

Genome-wide association study identifies five new schizophrenia loci

Large-scale genome-wide association analysis of bipolar disorder identifies a new susceptibility locus near ODZ4

Non-random error in genotype calling procedures: Implications for family-based and case-control genome-wide association studies

Ligand Switching in Cell-Permeable Peptides: Manipulation of the α-Integrin Signature Motif

Improved Detection of Common Variants Associated with Schizophrenia by Leveraging Pleiotropy with Cardiovascular-Disease Risk Factors

Identification of pathways for bipolar disorder: a meta-analysis

Rare chromosomal deletions and duplications increase risk of schizophrenia

Absolute Net Charge and the Biological Activity of Oligopeptides

An assessment of the Irish population for large-scale genetic mapping studies involving epilepsy and other complex diseases

A bias-reducing pathway enrichment analysis of genome-wide association data confirmed association of the MHC region with schizophrenia

Additive Genetic Variation in Schizophrenia Risk Is Shared by Populations of African and European Descent

Runs of homozygosity implicate autozygosity as a schizophrenia risk factor

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