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        Chronic and Severe Diseases

        The Chronic and Severe Diseases research theme consists of five programs: Diabetes, Metabolism and Clinical Sciences, Cancer, Perioperative Care, Precision Health, and Respiratory Health. ...

        Research

        A genome-wide association study identifies new psoriasis susceptibility loci and an interaction between HLA-C and ERAP1

        To identify new susceptibility loci for psoriasis, we undertook a genome-wide association study of 594,224 SNPs in 2,622 individuals with psoriasis... ...

        Research

        Detecting genotyping error using measures of degree of Hardy-Weinberg disequilibrium - art. no. 5

        Tests for Hardy-Weinberg equilibrium (HWE) have been used to detect genotyping error, but those tests have low power unless the sample size is very large. ...

        Research

        Risk of childhood acute lymphoblastic leukaemia following parental occupational exposure to pesticides

        Risk of childhood acute lymphoblastic leukaemia following parental occupational exposure to pesticides. ...

        Discover Series: Autism

        What would you discover to help a child? At Telethon Kids, our researchers are committed to Autism research that makes a real difference. ...

        About

        Rett syndrome is a rare but serious neurological disorder that affects about 1 in 9,000 girls. Even more rarely, boys may be affected. ...

        Research

        Novel non-TCR chromosome translocations t(3;11)(q25;p13) and t(X;11)(q25;p13) activating LMO2

        In T-cell acute lymphoblastic leukemia (T-ALL) cytogenetic alterations juxtapose the LIM-domain-only-2 gene (LMO2) with T-cell receptor loci. ...

        Research

        Candidate gene association study for diabetic retinopathy in persons with type 2 diabetes: the Candidate gene Association Resource (CARe)

        To investigate whether variants in cardiovascular candidate genes, some of which have been previously associated with type 2 diabetes (T2D), diabetic... ...

        Inching towards answers for children with ultra-rare CDKL5

        Did you know? CDKL5 Development Disorder (CDD) is caused by mutations in the cyclin-dependent kinase-like 5 (CDKL5) gene, which provides instructions ...

        Research

        Common variants at the MHC locus and at chromosome 16q24.1 predispose to Barrett's esophagus

        Barrett's esophagus is an increasingly common disease that is strongly associated with reflux of stomach acid and usually a hiatus hernia,... ...

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