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Functional variants in the LRRK2 gene confer shared effects on risk for Crohn's disease and Parkinson's disease
Prioritizing Crohn's disease genes by integrating association signals with gene expression implicates monocyte subsets.
A myeloid-stromal niche and gp130 rescue in NOD2-driven Crohn's disease
Inflamed Ulcerative Colitis Regions Associated With MRGPRX2-Mediated Mast Cell Degranulation and Cell Activation Modules, Defining a New Therapeutic Target
