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• W2168806301 abstract "Aim To identify risk alleles contributing towards type 1 diabetes in Pakistani patients. Introduction Type 1 diabetes (T1D) is an autoimmune disease which is caused by destruction of insulin producing β cells by immune system. Genetic predisposition as well as environmental factors contribute to its etiology. To date more than 40 risk loci have been identified for T1D. Methodology A total of 191 family-based and unrelated T1D cases and controls were recruited. DNA was extracted and 32 genome-wide significant single nucleotide polymorphisms (SNPs) previously reported in Europeans were genotyped. Genotyping was performed using TaqMan SNP genotyping assays and the data was analyzed using FamCC software. Results Our results showed significant association of 10 single nucleotide polymorphisms (SNPs) with T1D at p < 0.01, including HLA-DQA1/rs9272346, ERBB3/rs2292239, SIRPG/rs2281808, IL2-KIAA1109/rs4505848, GLIS3/rs7020673, CD226/rs763361, PTPN2/rs478582, IKZF1/rs10272724, BACH2/rs11755527, C6orf173/rs9388489, whereas 5 more SNPs showed their association at 0.01 < p < 0.05 in Pakistani population. Conclusion We have replicated many of the T1D loci established among Europeans in a Pakistani population." @default.
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• W2168806301 date "2015-04-01" @default.
• W2168806301 modified "2023-10-04" @default.
• W2168806301 title "Association of 32 type 1 diabetes risk loci in Pakistani patients" @default.
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• W2168806301 doi "https://doi.org/10.1016/j.diabres.2015.01.022" @default.
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