List of works - Matthew A. Brown

Interleukin-23 mediates the intestinal response to microbial β-1,3-glucan and the development of spondyloarthritis pathology in SKG mice

article

Genetics and genomics of ankylosing spondylitis

scientific article published on January 1, 2010

The multiple sclerosis whole blood mRNA transcriptome and genetic associations indicate dysregulation of specific T cell pathways in pathogenesis

article

Genetic analyses in a sample of individuals with high or low BMD shows association with multiple Wnt pathway genes

scientific article

Dense genotyping of immune-related susceptibility loci reveals new insights into the genetics of psoriatic arthritis

scientific article

Influence of LRP5 Polymorphisms on Normal Variation in BMD

article

Short-rib polydactyly and Jeune syndromes are caused by mutations in WDR60

scientific journal article

Genetics of ankylosing spondylitis

scientific article published on 31 July 2013

Suggestive Linkage of the Parathyroid Receptor Type 1 to Osteoporosis

article

Mutations in the gene encoding IFT dynein complex component WDR34 cause Jeune asphyxiating thoracic dystrophy

scientific journal article

Pathogenesis of ankylosing spondylitis - recent advances and future directions.

scientific article

Genome-wide association studies of asthma in population-based cohorts confirm known and suggested loci and identify an additional association near HLA.

scientific article

Integrated genome-wide chromatin occupancy and expression analyses identify key myeloid pro-differentiation transcription factors repressed by Myb

scientific article

Ankylosing spondylitis in West Africans--evidence for a non-HLA-B27 protective effect

scientific article published on January 1997

Autosomal dominant familial calcium pyrophosphate dihydrate deposition disease is caused by mutation in the transmembrane protein ANKH

scientific article

Novel risk loci for rheumatoid arthritis in Han Chinese and congruence with risk variants in Europeans

scientific article

Whole-exome re-sequencing in a family quartet identifies POP1 mutations as the cause of a novel skeletal dysplasia

scientific article

Site and Gender Specificity of Inheritance of Bone Mineral Density

article

Discovery of candidate serum proteomic and metabolomic biomarkers in ankylosing spondylitis

scientific article

Common variants in the HLA-DRB1-HLA-DQA1 HLA class II region are associated with susceptibility to visceral leishmaniasis

scientific article published on 6 January 2013

Is disease severity in ankylosing spondylitis genetically determined?

scientific article published on 01 June 2001

Association between the interleukin 23 receptor and ankylosing spondylitis is confirmed by a new UK case-control study and meta-analysis of published series

scientific article published on 2 February 2009

Excessive bone formation in a mouse model of ankylosing spondylitis is associated with decreases in Wnt pathway inhibitors

scientific article published on 22 November 2012

A genome-wide screen for susceptibility loci in ankylosing spondylitis

scientific article published on 01 April 1998

Finnish HLA studies confirm the increased risk conferred by HLA-B27 homozygosity in ankylosing spondylitis

scientific article published on 25 October 2005

Genetic determinants of heel bone properties: genome-wide association meta-analysis and replication in the GEFOS/GENOMOS consortium

scientific article

Role ofNOD2 variants in spondylarthritis

scientific article published on 01 June 2002

The interleukin 1 gene cluster contains a major susceptibility locus for ankylosing spondylitis

scientific article

Novel mutations in ACVR1 result in atypical features in two fibrodysplasia ossificans progressiva patients

scientific article

Multicentric carpotarsal osteolysis is caused by mutations clustering in the amino-terminal transcriptional activation domain of MAFB.

scientific article published in March 2012

Prospective meta-analysis of interleukin 1 gene complex polymorphisms confirms associations with ankylosing spondylitis

article

Genetic dissection of acute anterior uveitis reveals similarities and differences in associations observed with ankylosing spondylitis

scientific article

Elucidating the chromosome 9 association with AS; CARD9 is a candidate gene

scientific article

Whole blood transcriptional profiling in ankylosing spondylitis identifies novel candidate genes that might contribute to the inflammatory and tissue-destructive disease aspects

scientific article

ERAP2 is associated with ankylosing spondylitis in HLA-B27-positive and HLA-B27-negative patients

scientific article published on 27 April 2015

Autosomal dominant spondylocostal dysostosis is caused by mutation in TBX6.

scientific article

NAD Deficiency, Congenital Malformations, and Niacin Supplementation.

scientific article published in August 2017

Comparing genotyping algorithms for Illumina's Infinium whole-genome SNP BeadChips

scientific article published on 8 March 2011

Association study of genes related to bone formation and resorption and the extent of radiographic change in ankylosing spondylitis

scientific article published on 20 March 2014

Effects of PTPN22 C1858T polymorphism on susceptibility and clinical characteristics of British Caucasian rheumatoid arthritis patients.

scientific article published on 20 February 2006

Polymorphisms of the CYP2D6 gene increase susceptibility to ankylosing spondylitis

article

Genetic disorders of the LRP5-Wnt signalling pathway affecting the skeleton

scientific article

Saliva-Derived DNA Performs Well in Large-Scale, High-Density Single-Nucleotide Polymorphism Microarray Studies

scientific article published on 03 March 2010

Genetic and genomic studies of PADI4 in rheumatoid arthritis

scientific article published on 06 April 2005

Genetic studies of disorders of calcium crystal deposition.

scientific article

The effect of HLA-DR genes on susceptibility to and severity of ankylosing spondylitis

scientific article published on 01 March 1998

Genetics of ankylosing spondylitis

article

A novel serogenetic approach determines the community prevalence of celiac disease and informs improved diagnostic pathways.

scientific article

Microbes, the gut and ankylosing spondylitis

scientific article

Genetic control of bone density and turnover: role of the collagen 1alpha1, estrogen receptor, and vitamin D receptor genes

scientific article published in April 2001

List of works by Matthew A. Brown

Interleukin-23 mediates the intestinal response to microbial β-1,3-glucan and the development of spondyloarthritis pathology in SKG mice

Genetics and genomics of ankylosing spondylitis

The multiple sclerosis whole blood mRNA transcriptome and genetic associations indicate dysregulation of specific T cell pathways in pathogenesis

Genetic analyses in a sample of individuals with high or low BMD shows association with multiple Wnt pathway genes

Dense genotyping of immune-related susceptibility loci reveals new insights into the genetics of psoriatic arthritis

Influence of LRP5 Polymorphisms on Normal Variation in BMD

Short-rib polydactyly and Jeune syndromes are caused by mutations in WDR60

Genetics of ankylosing spondylitis

Suggestive Linkage of the Parathyroid Receptor Type 1 to Osteoporosis

Mutations in the gene encoding IFT dynein complex component WDR34 cause Jeune asphyxiating thoracic dystrophy

Pathogenesis of ankylosing spondylitis - recent advances and future directions.

Genome-wide association studies of asthma in population-based cohorts confirm known and suggested loci and identify an additional association near HLA.

Integrated genome-wide chromatin occupancy and expression analyses identify key myeloid pro-differentiation transcription factors repressed by Myb

Ankylosing spondylitis in West Africans--evidence for a non-HLA-B27 protective effect

Autosomal dominant familial calcium pyrophosphate dihydrate deposition disease is caused by mutation in the transmembrane protein ANKH

Novel risk loci for rheumatoid arthritis in Han Chinese and congruence with risk variants in Europeans

Whole-exome re-sequencing in a family quartet identifies POP1 mutations as the cause of a novel skeletal dysplasia

Site and Gender Specificity of Inheritance of Bone Mineral Density

Discovery of candidate serum proteomic and metabolomic biomarkers in ankylosing spondylitis

Common variants in the HLA-DRB1-HLA-DQA1 HLA class II region are associated with susceptibility to visceral leishmaniasis

Is disease severity in ankylosing spondylitis genetically determined?

Association between the interleukin 23 receptor and ankylosing spondylitis is confirmed by a new UK case-control study and meta-analysis of published series

Excessive bone formation in a mouse model of ankylosing spondylitis is associated with decreases in Wnt pathway inhibitors

A genome-wide screen for susceptibility loci in ankylosing spondylitis

Finnish HLA studies confirm the increased risk conferred by HLA-B27 homozygosity in ankylosing spondylitis

Genetic determinants of heel bone properties: genome-wide association meta-analysis and replication in the GEFOS/GENOMOS consortium

Role ofNOD2 variants in spondylarthritis

The interleukin 1 gene cluster contains a major susceptibility locus for ankylosing spondylitis

Novel mutations in ACVR1 result in atypical features in two fibrodysplasia ossificans progressiva patients

Multicentric carpotarsal osteolysis is caused by mutations clustering in the amino-terminal transcriptional activation domain of MAFB.

Prospective meta-analysis of interleukin 1 gene complex polymorphisms confirms associations with ankylosing spondylitis

Genetic dissection of acute anterior uveitis reveals similarities and differences in associations observed with ankylosing spondylitis

Elucidating the chromosome 9 association with AS; CARD9 is a candidate gene

Whole blood transcriptional profiling in ankylosing spondylitis identifies novel candidate genes that might contribute to the inflammatory and tissue-destructive disease aspects

ERAP2 is associated with ankylosing spondylitis in HLA-B27-positive and HLA-B27-negative patients

Autosomal dominant spondylocostal dysostosis is caused by mutation in TBX6.

NAD Deficiency, Congenital Malformations, and Niacin Supplementation.

Comparing genotyping algorithms for Illumina's Infinium whole-genome SNP BeadChips

Association study of genes related to bone formation and resorption and the extent of radiographic change in ankylosing spondylitis

Effects of PTPN22 C1858T polymorphism on susceptibility and clinical characteristics of British Caucasian rheumatoid arthritis patients.

Polymorphisms of the CYP2D6 gene increase susceptibility to ankylosing spondylitis

Genetic disorders of the LRP5-Wnt signalling pathway affecting the skeleton

Saliva-Derived DNA Performs Well in Large-Scale, High-Density Single-Nucleotide Polymorphism Microarray Studies

Genetic and genomic studies of PADI4 in rheumatoid arthritis

Genetic studies of disorders of calcium crystal deposition.

The effect of HLA-DR genes on susceptibility to and severity of ankylosing spondylitis

Genetics of ankylosing spondylitis

A novel serogenetic approach determines the community prevalence of celiac disease and informs improved diagnostic pathways.

Microbes, the gut and ankylosing spondylitis

Genetic control of bone density and turnover: role of the collagen 1alpha1, estrogen receptor, and vitamin D receptor genes