Common genetic variants modulate pathogen-sensing responses in human dendritic cells. All Authors: Author Profiles: Publish Date: Journal: , Read Publication
Fine mapping seronegative and seropositive rheumatoid arthritis to shared and distinct HLA alleles by adjusting for the effects of heterogeneity. All Authors: Author Profiles: Publish Date: Journal: , Read Publication
An international effort towards developing standards for best practices in analysis, interpretation and reporting of clinical genome sequencing results in the CLARITY Challenge. All Authors: Author Profiles: Publish Date: Journal: , Read Publication
Predicting HLA alleles from high-resolution SNP data in three Southeast Asian populations. All Authors: Author Profiles: Publish Date: Journal: , Read Publication
Polarization of the effects of autoimmune and neurodegenerative risk alleles in leukocytes. All Authors: Author Profiles: Publish Date: Journal: , Read Publication
SNPsea: an algorithm to identify cell types, tissues and pathways affected by risk loci. All Authors: Author Profiles: Publish Date: Journal: , Read Publication
Whole-exome sequencing identifies rare, functional CFH variants in families with macular degeneration. All Authors: Author Profiles: Publish Date: Journal: , Read Publication
Genetic association study of QT interval highlights role for calcium signaling pathways in myocardial repolarization. All Authors: Author Profiles: Publish Date: Journal: , Read Publication
Regulation of gene expression in autoimmune disease loci and the genetic basis of proliferation in CD4+ effector memory T cells. All Authors: Author Profiles: Publish Date: Journal: , Read Publication
Genetic variants in the complement system predisposing to age-related macular degeneration: a review. All Authors: Author Profiles: Publish Date: Journal: , Read Publication
