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The Balancing Act of Neutrophils

Cell host & microbe, 2014-05, Vol.15 (5), p.526-536

2014

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Development of strategies for SNP detection in RNA-seq data: application to lymphoblastoid cell lines and evaluation using 1000 Genomes data

PloS one, 2013-03, Vol.8 (3), p.e58815-e58815

2013

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Signalling adaptors used by Toll-like receptors: An update

Cytokine (Philadelphia, Pa.), 2008-09, Vol.43 (3), p.342-349

2008

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Bruton's tyrosine kinase mediates the synergistic signalling between TLR9 and the B cell receptor by regulating calcium and calmodulin

PloS one, 2013-08, Vol.8 (8), p.e74103-e74103

2013

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Identification of mechanosensitive genes during skeletal development: alteration of genes associated with cytoskeletal rearrangement and cell signalling pathways

BMC genomics, 2014-01, Vol.15 (1), p.48-48, Article 48

2014

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Structure, function and regulation of the Toll IL-1 receptor adaptor proteins

Immunology and cell biology, 2007-08, Vol.85 (6), p.411-419

2007

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Mycobacterial PIMs inhibit host inflammatory responses through CD14-dependent and CD14-independent mechanisms

PloS one, 2011-09, Vol.6 (9), p.e24631

2011

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Artificial neural network corrosion modeling for metals in an equatorial climate

Corrosion science, 2009-10, Vol.51 (10), p.2266-2278

2009

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Avian resistance to Campylobacter jejuni colonization is associated with an intestinal immunogene expression signature identified by mRNA sequencing

PloS one, 2012-08, Vol.7 (8), p.e40409-e40409

2012

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Next-generation sequencing of the mitochondrial genome and association with IgA nephropathy in a renal transplant population

Scientific reports, 2014-12, Vol.4 (1), p.7379-7379, Article 7379

2014

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Transcriptome analysis of the mouse E14.5 (TS23) developing humerus and differential expression in muscle-less mutant embryos lacking mechanical stimulation

Genomics data, 2014-12, Vol.2 (C), p.32-36

2014

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Assessment of inactivating stop codon mutations in forty Saccharomyces cerevisiae strains: implications for [PSI] prion- mediated phenotypes

PloS one, 2011-12, Vol.6 (12), p.e28684-e28684

2011

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Reducing human DNA bias in cystic fibrosis airway specimens for microbiome analysis

Journal of microbiological methods, 2022-09, Vol.200, p.106540-106540, Article 106540

2022

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The Development of Hot Melt Extruded Biocompatible Controlled Release Drug Delivery Devices

International journal of polymeric materials, 2014-02, Vol.63 (9), p.476-485

2014

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Chitinase-3-Like 1 (CHI3L1) Gene and Schizophrenia: Genetic Association and a Potential Functional Mechanism

Biological psychiatry (1969), 2008-07, Vol.64 (2), p.98-103

2008

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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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SU19A SEARCH FOR RARE GENETIC VARIANTS IN A FAMILY-BASED STUDY OF AUTISM

European neuropsychopharmacology, 2019, Vol.29, p.S1278-S1278

2019

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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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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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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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The SNP ratio test: pathway analysis of genome-wide association datasets

Bioinformatics, 2009-10, Vol.25 (20), p.2762-2763

2009

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Identifying relationships among genomic disease regions: predicting genes at pathogenic SNP associations and rare deletions

PLoS genetics, 2009-06, Vol.5 (6), p.e1000534

2009

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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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Targeted Sequencing of 10,198 Samples Confirms Abnormalities in Neuronal Activity and Implicates Voltage-Gated Sodium Channels in Schizophrenia Pathogenesis

Biological psychiatry (1969), 2019-04, Vol.85 (7), p.554-562

2019

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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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The Balancing Act of Neutrophils

Development of strategies for SNP detection in RNA-seq data: application to lymphoblastoid cell lines and evaluation using 1000 Genomes data

Signalling adaptors used by Toll-like receptors: An update

Bruton's tyrosine kinase mediates the synergistic signalling between TLR9 and the B cell receptor by regulating calcium and calmodulin

Identification of mechanosensitive genes during skeletal development: alteration of genes associated with cytoskeletal rearrangement and cell signalling pathways

Structure, function and regulation of the Toll IL-1 receptor adaptor proteins

Mycobacterial PIMs inhibit host inflammatory responses through CD14-dependent and CD14-independent mechanisms

Artificial neural network corrosion modeling for metals in an equatorial climate

Avian resistance to Campylobacter jejuni colonization is associated with an intestinal immunogene expression signature identified by mRNA sequencing

Next-generation sequencing of the mitochondrial genome and association with IgA nephropathy in a renal transplant population

Transcriptome analysis of the mouse E14.5 (TS23) developing humerus and differential expression in muscle-less mutant embryos lacking mechanical stimulation

Assessment of inactivating stop codon mutations in forty Saccharomyces cerevisiae strains: implications for [PSI] prion- mediated phenotypes

Reducing human DNA bias in cystic fibrosis airway specimens for microbiome analysis

The Development of Hot Melt Extruded Biocompatible Controlled Release Drug Delivery Devices

Chitinase-3-Like 1 (CHI3L1) Gene and Schizophrenia: Genetic Association and a Potential Functional Mechanism

Rare chromosomal deletions and duplications increase risk of schizophrenia

SU19A SEARCH FOR RARE GENETIC VARIANTS IN A FAMILY-BASED STUDY OF AUTISM

Common polygenic variation contributes to risk of schizophrenia and bipolar disorder

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

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

The SNP ratio test: pathway analysis of genome-wide association datasets

Identifying relationships among genomic disease regions: predicting genes at pathogenic SNP associations and rare deletions

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

Targeted Sequencing of 10,198 Samples Confirms Abnormalities in Neuronal Activity and Implicates Voltage-Gated Sodium Channels in Schizophrenia Pathogenesis

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

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