GeneticsNature GeneticsPeer-reviewed
Fine-mapping identifies causal variants for RA and T1D in DNASE1L3, SIRPG, MEG3, TNFAIP3 and CD28/CTLA4 loci
Harm-Jan Westra, Marta Martínez‐Bonet, Suna Önengüt-Gümüşcü…·Soumya Raychaudhuri
This study fine-maps RA and T1D loci outside the MHC, identifying causal variants and confirming their functional impact through allele-specific binding and enhancer activity.
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