Publication: Genome-wide enhancer maps link risk variants to disease genes

PubMed ID: 33828297

Citation: Nasser J, Bergman DT, Fulco CP, et al. Genome-wide enhancer maps link risk variants to disease genes. Nature. 2021;593(7858):238-243. doi:10.1038/s41586-021-03446-x

Funding: This work was supported by the Broad Institute (E.S.L.); an NIH Pathway to Independence Award (K99HG009917 and R00HG009917 to J.M.E.); an NHGRI Genomic Innovator Award (R35HG011324 to J.M.E.); the Harvard Society of Fellows (J.M.E.); Gordon and Betty Moore and the BASE Research Initiative at the Lucile Packard Children’s Hospital at Stanford University (J.M.E.); NHGRI P50HG006193 (N.H.); NIDDK P30DK043351 (R.J.X.); NIH U01 CA200059 (F.L. and H.P.); U01 HG009379, R01 MH101244, and R37 MH107649 (A.K.P.); NIDDK K01DK114379 (H.H.); the Zhengxu and Ying He Foundation (H.H.); the Stanley Center for Psychiatric Research (H.H.); NIAID K22AI153648 (J.P.R.); and a Siebel Scholarship (F.L.).