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ERAP1/ERAP2 and RUNX3 polymorphisms are not associated with ankylosing spondylitis susceptibility in Chinese Han.

• Authors : Su W; The First Affiliated Hospital of Chongqing Medical University, Chongqing Key Laboratory of Ophthalmology and Chongqing Eye Institute, Chongqing, China.; Du L

Subjects: Aminopeptidases/Aminopeptidases/Aminopeptidases/*genetics ; Core Binding Factor Alpha 3 Subunit/Core Binding Factor Alpha 3 Subunit/Core Binding Factor Alpha 3 Subunit/*genetics ; Genetic Predisposition to Disease/Genetic Predisposition to Disease/Genetic Predisposition to Disease/*genetics

• Source: Clinical and experimental immunology [Clin Exp Immunol] 2018 Jul; Vol. 193 (1), pp. 95-102. Date of Electronic Publication: 2018 Mar 30.Publisher: Oxford University Press Country of Publication: England NLM ID: 0057202 Publication Model: Print-Electronic Cited

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Activating killer immunoglobulin-like receptors genes are associated with increased susceptibility to ankylosing spondylitis.

• Authors : Díaz-Peña R; Department of Immunology, Hospital Universitario Central de Asturias, Oviedo, Spain; Faculty of Health Sciences, Universidad Autónoma de Chile, Talca, Chile.

Subjects: Gene Frequency* ; Genetic Predisposition to Disease* ; Genotype*

• Source: Clinical and experimental immunology [Clin Exp Immunol] 2015 May; Vol. 180 (2), pp. 201-6.Publisher: Oxford University Press Country of Publication: England NLM ID: 0057202 Publication Model: Print Cited Medium:

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IBD Genetic Risk Profile in Healthy First-Degree Relatives of Crohn's Disease Patients.

• Authors : Kevans D; Silverberg MS ...

Subjects: Family* ; Genetic Predisposition to Disease* ; Polymorphism, Single Nucleotide*

• Source: Journal of Crohn's & colitis [J Crohns Colitis] 2016 Feb; Vol. 10 (2), pp. 209-15. Date of Electronic Publication: 2015 Oct 28.Publisher: Oxford University Press Country of Publication: England NLM ID: 101318676 Publication Model: Print-Electronic

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A genetic link between risk for Alzheimer's disease and severe COVID-19 outcomes via the OAS1 gene

• Authors : Umran Yaman; Jennifer M. Pocock; Tamar Guetta-Baranes

Subjects: Male; Adolescent; Genetic Linkage

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An Intronic HCP5 Variant Is Associated With Age of Onset and Susceptibility to Graves Disease in UK and Polish Cohorts

• Authors : Beata Jurecka-Lubieniecka; Jacek Daroszewski; Tomasz Bednarczuk

Subjects: Oncology; Male; Linkage disequilibrium

• Source: The Journal of Clinical Endocrinology and Metabolism

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Refinement of the associations between risk of colorectal cancer and polymorphisms on chromosomes 1q41 and 12q13.13

• Authors : Spain, S.; Carvajal-Carmona, L.; Howarth, K.

Subjects: Chromosomes; Human; Pair 1

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Leveraging lung tissue transcriptome to uncover candidate causal genes in COPD genetic associations

• Authors : Jean-Christophe Bérubé; Maxime Lamontagne; Ke Hao ...

Subjects: 0301 basic medicine; Candidate gene; Quantitative Trait Loci

• Source: Human Molecular Genetics, 27(10), 1819-1829. Oxford University Press

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Describing the genetic architecture of epilepsy through heritability analysis

• Authors : Speed, D; O'Brien, TJ; Palotie, A

Subjects: Asian Continental Ancestry Group; Genotype; Genotyping Techniques

• Source: Brain

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Application of statistical and functional methodologies for the investigation of genetic determinants of coronary heart disease biomarkers: lipoprotein lipase genotype and plasma triglycerides as an exemplar

• Authors : Wendy Putt; Jutta Palmen; Andrew J. Smith

Subjects: Male; Genotype; Gene Expression

• Source: Human Molecular Genetics

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SNPinfo: integrating GWAS and candidate gene information into functional SNP selection for genetic association studies

• Authors : Jack A. Taylor; Zongli Xu

Subjects: Male; Linkage disequilibrium; Genetic Linkage

• Source: Nucleic Acids Research

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