Statistical and functional convergence of common and rare genetic influences on autism at chromosome 16p. All Authors: Author Profiles: Publish Date: Journal: , Read Publication
Polygenic architecture of rare coding variation across 394,783 exomes. All Authors: Author Profiles: Publish Date: Journal: , Read Publication
Association Between Systemic Vasculitis and Coronary Microvascular Dysfunction in the Absence of Obstructive Coronary Artery Disease. All Authors: Author Profiles: Publish Date: Journal: , Read Publication
Autoantibodies against citrullinated and native proteins and prediction of rheumatoid arthritis-associated interstitial lung disease: A nested case-control study. All Authors: Author Profiles: Publish Date: Journal: , Read Publication
Multimodal representation learning for predicting molecule-disease relations. All Authors: Author Profiles: Publish Date: Journal: , Read Publication
Framework of the Centralized Interactive Phenomics Resource (CIPHER) standard for electronic health data-based phenomics knowledgebase. All Authors: Author Profiles: Publish Date: Journal: , Read Publication
Identifying shared genetic architecture between rheumatoid arthritis and other conditions: a phenome-wide association study with genetic risk scores. All Authors: Author Profiles: Publish Date: Journal: , Read Publication
Potential pitfalls in the use of real-world data for studying long COVID. All Authors: Author Profiles: Publish Date: Journal: , Read Publication
ARCH: Large-scale Knowledge Graph via Aggregated Narrative Codified Health Records Analysis. All Authors: Author Profiles: Publish Date: Journal: Read Publication
Shared inflammatory pathways of rheumatoid arthritis and atherosclerotic cardiovascular disease. All Authors: Author Profiles: Publish Date: Journal: , Read Publication
