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Step-wise conditional analysis of imputed classical HLA alleles to detect independent associations with Behçet’s disease.

Figshare2016-08-23 更新2026-04-29 收录

HLA遗传关联分析

自身免疫疾病遗传学

数据链接：

https://figshare.com/articles/dataset/Step-wise_conditional_analysis_of_imputed_classical_HLA_alleles_to_detect_independent_associations_with_Beh_et_s_disease_/3751239 数据链接链接失效反馈

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OR, odds ratio; CI, confidence interval.

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创建时间：

2016-08-23

自身免疫疾病遗传学

VDR基因多态性分析

In a previous study, we have reported an increased plasma midkine (MK) and pleiotrophin (PTN) concentrations in patients with systemic lupus erythematosus (SLE) and the increase in MK and PTN associat

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Table_2_Integrative Analysis Identifies Genetic Variants Associated With Autoimmune Diseases Affecting Putative MicroRNA Binding Sites.XLSX

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MicroRNA调控

Genome-wide and fine mapping studies have shown that more than 90% of genetic variants associated with autoimmune diseases (AID) are located in non-coding regions of the human genome and especially in

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Leveraging genetic effects in Graves' disease via cell type-specific network diffusion - Secondary analysis data

自身免疫疾病遗传学

细胞特异性网络分析

Integrated scRNA-seq datasets and TWAS results used in the publication entitled 'Leveraging genetic effects in Graves' disease via cell type-specific network diffusion'

Zenodo2025-10-30 更新00

Link to dataset related to article "X Chromosome Contribution to the Genetic Architecture of Primary Biliary Cholangitis"

自身免疫疾病遗传学

X染色体

Link to dataset related to article "X Chromosome Contribution to the Genetic Architecture of Primary Biliary Cholangitis" Abstract Background & aims: Genome-wide association stud

Zenodo2022-01-21 更新20

Supplementary file 1_Familial and genetic overlap between Sjögren’s disease and other autoimmune diseases.docx

自身免疫疾病遗传学

家族性风险分析

PurposeTo evaluate familial clustering of Sjögren’s disease (SjD) with other autoimmune diseases and to characterize shared genetic architecture using an integrative genomic approach. MethodsMeta-anal

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Step-wise conditional analysis of imputed classical HLA alleles to detect independent associations with Behçet’s disease.

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