Search Results - "DANOY, Patrick"
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Genome-wide association study identifies susceptibility loci for open angle glaucoma at TMCO1 and CDKN2B-AS1
Published in Nature genetics (01-06-2011)“…Jamie Craig and colleagues report a genome-wide association study for advanced open angle glaucoma (OAG). They identify variants near TMCO1 and in CDKN2B-AS1…”
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Association of variants at 1q32 and STAT3 with ankylosing spondylitis suggests genetic overlap with Crohn's disease
Published in PLoS genetics (01-12-2010)“…Ankylosing spondylitis (AS) is a common inflammatory arthritic condition. Overt inflammatory bowel disease (IBD) occurs in about 10% of AS patients, and in…”
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A novel serogenetic approach determines the community prevalence of celiac disease and informs improved diagnostic pathways
Published in BMC medicine (28-08-2013)“…Changing perspectives on the natural history of celiac disease (CD), new serology and genetic tests, and amended histological criteria for diagnosis cast doubt…”
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Association of STAT3 and TNFRSF1A with ankylosing spondylitis in Han Chinese
Published in Annals of the rheumatic diseases (01-02-2011)“…Recent association studies by the Australo-Anglo-American Spondyloarthritis Consortium (TASC) in Caucasian European populations from Australia, North America…”
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Glaucoma Risk Alleles at CDKN2B-AS1 Are Associated with Lower Intraocular Pressure, Normal-Tension Glaucoma, and Advanced Glaucoma
Published in Ophthalmology (Rochester, Minn.) (01-08-2012)“…Purpose Genetic variation at the 9p21 locus encompassing the CDKN2B-AS1 , CDKN2A , and CDKN2B genes has been associated with primary open-angle glaucoma (POAG)…”
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A polymorphism in the HLA-DPB1 gene is associated with susceptibility to multiple sclerosis
Published in PloS one (26-10-2010)“…We conducted an association study across the human leukocyte antigen (HLA) complex to identify loci associated with multiple sclerosis (MS). Comparing 1927…”
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Multiple sclerosis susceptibility-associated SNPs do not influence disease severity measures in a cohort of Australian MS patients
Published in PloS one (02-04-2010)“…Recent association studies in multiple sclerosis (MS) have identified and replicated several single nucleotide polymorphism (SNP) susceptibility loci including…”
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A new regulatory variant in the interleukin-6 receptor gene associates with asthma risk
Published in Genes and immunity (01-10-2013)“…The main genetic determinant of soluble interleukin 6 receptor (sIL-6R) levels is the missense variant rs2228145 that maps to the cleavage site of IL-6R. For…”
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Omission of Author Name in the Article by Davidson et al (Arthritis Rheum, July 2013)
Published in Arthritis & rheumatology (Hoboken, N.J.) (01-09-2013)Get full text
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Brief Report: High‐Throughput Sequencing of IL23R Reveals a Low‐Frequency, Nonsynonymous Single‐Nucleotide Polymorphism That Is Associated With Ankylosing Spondylitis in a Han Chinese Population
Published in Arthritis & rheumatology (Hoboken, N.J.) (01-07-2013)“…Objective Ankylosing spondylitis (AS) is a highly heritable common inflammatory arthritis that targets the spine and sacroiliac joints of the pelvis, causing…”
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A naturally occurring genetic variant of human XRCC2 (R188H) confers increased resistance to cisplatin-induced DNA damage
Published in Biochemical and biophysical research communications (19-01-2007)“…Homologous recombination, a major double strand break repair pathway, plays critical roles in maintaining genome stability. Genetic polymorphisms in HR genes…”
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Genetic influences on the end-stage effector phase of arthritis
Published in The Journal of experimental medicine (06-08-2001)“…K/BxN T cell receptor transgenic mice are a model of inflammatory arthritis, most similar to rheumatoid arthritis, that is critically dependent on both T and B…”
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A High-Resolution Consensus Linkage Map of the Rat, Integrating Radiation Hybrid and Genetic Maps
Published in Genomics (San Diego, Calif.) (01-07-2001)“…We have constructed a high-resolution consensus genetic map of the rat in a single large intercross, which integrates 747 framework markers and 687 positions…”
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Genome-wide association study identifies five new schizophrenia loci
Published in Nature genetics (01-10-2011)“…We examined the role of common genetic variation in schizophrenia in a genome-wide association study of substantial size: a stage 1 discovery sample of 21,856…”
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Association of ERAP1, but not IL23R, with ankylosing spondylitis in a Han Chinese population
Published in Arthritis and rheumatism (01-11-2009)“…Objective The results of a recent genome‐wide association study have shown that ERAP1 and IL23R are associated with ankylosing spondylitis (AS) in Caucasian…”
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Genome-wide association analysis identifies 11 risk variants associated with the asthma with hay fever phenotype
Published in Journal of allergy and clinical immunology (01-06-2014)“…Background To date, no genome-wide association study (GWAS) has considered the combined phenotype of asthma with hay fever. Previous analyses of family data…”
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WNT16 influences bone mineral density, cortical bone thickness, bone strength, and osteoporotic fracture risk
Published in PLoS genetics (01-07-2012)“…We aimed to identify genetic variants associated with cortical bone thickness (CBT) and bone mineral density (BMD) by performing two separate genome-wide…”
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Genome-wide association study identifies new multiple sclerosis susceptibility loci on chromosomes 12 and 20
Published in Nature genetics (01-07-2009)“…To identify multiple sclerosis (MS) susceptibility loci, we conducted a genome-wide association study (GWAS) in 1,618 cases and used shared data for 3,413…”
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Genome-wide association study of ankylosing spondylitis identifies non-MHC susceptibility loci
Published in Nature genetics (01-02-2010)“…To identify susceptibility loci for ankylosing spondylitis, we undertook a genome-wide association study in 2,053 unrelated ankylosing spondylitis cases among…”
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Identification of IL6R and chromosome 11q13.5 as risk loci for asthma
Published in The Lancet (British edition) (10-09-2011)“…Summary Background We aimed to identify novel genetic variants affecting asthma risk, since these might provide novel insights into molecular mechanisms…”
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