Genetic effects on liver chromatin accessibility identify disease regulatory variants.

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Bibliographic Details
Title: Genetic effects on liver chromatin accessibility identify disease regulatory variants.
Authors: Currin KW; Department of Genetics, University of North Carolina, Chapel Hill, NC 27599, USA., Erdos MR; National Human Genome Research Institute, National Institutes of Health, Bethesda, MD 20892, USA., Narisu N; National Human Genome Research Institute, National Institutes of Health, Bethesda, MD 20892, USA., Rai V; Department of Computational Medicine & Bioinformatics, University of Michigan, Ann Arbor, MI 48109, USA., Vadlamudi S; Department of Genetics, University of North Carolina, Chapel Hill, NC 27599, USA., Perrin HJ; Department of Genetics, University of North Carolina, Chapel Hill, NC 27599, USA., Idol JR; National Human Genome Research Institute, National Institutes of Health, Bethesda, MD 20892, USA., Yan T; National Human Genome Research Institute, National Institutes of Health, Bethesda, MD 20892, USA., Albanus RD; Department of Computational Medicine & Bioinformatics, University of Michigan, Ann Arbor, MI 48109, USA., Broadaway KA; Department of Genetics, University of North Carolina, Chapel Hill, NC 27599, USA., Etheridge AS; Eshelman School of Pharmacy and Center for Pharmacogenomics and Individualized Therapy, University of North Carolina, Chapel Hill, NC 27599, USA., Bonnycastle LL; National Human Genome Research Institute, National Institutes of Health, Bethesda, MD 20892, USA., Orchard P; Department of Computational Medicine & Bioinformatics, University of Michigan, Ann Arbor, MI 48109, USA., Didion JP; National Human Genome Research Institute, National Institutes of Health, Bethesda, MD 20892, USA., Chaudhry AS; Department of Pharmaceutical Sciences, St. Jude Children's Research Hospital, Memphis, TN 38105, USA., Innocenti F; Eshelman School of Pharmacy and Center for Pharmacogenomics and Individualized Therapy, University of North Carolina, Chapel Hill, NC 27599, USA; Lineberger Comprehensive Cancer Center, University of North Carolina, Chapel Hill, NC 27599, USA., Schuetz EG; Department of Pharmaceutical Sciences, St. Jude Children's Research Hospital, Memphis, TN 38105, USA., Scott LJ; Department of Biostatistics and Center for Statistical Genetics, School of Public Health, University of Michigan, Ann Arbor, MI 48109, USA., Parker SCJ; Department of Computational Medicine & Bioinformatics, University of Michigan, Ann Arbor, MI 48109, USA; Department of Human Genetics, University of Michigan, Ann Arbor, MI 48109, USA., Collins FS; National Human Genome Research Institute, National Institutes of Health, Bethesda, MD 20892, USA., Mohlke KL; Department of Genetics, University of North Carolina, Chapel Hill, NC 27599, USA. Electronic address: mohlke@med.unc.edu.
Corporate Authors: NISC Comparative Sequencing Program; National Human Genome Research Institute, National Institutes of Health, Bethesda, MD 20892, USA.
Source: American journal of human genetics [Am J Hum Genet] 2021 Jul 01; Vol. 108 (7), pp. 1169-1189. Date of Electronic Publication: 2021 May 25.
Publication Type: Journal Article; Research Support, N.I.H., Extramural; Research Support, N.I.H., Intramural
Journal Info: Publisher: Cell Press Country of Publication: United States NLM ID: 0370475 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1537-6605 (Electronic) Linking ISSN: 00029297 NLM ISO Abbreviation: Am J Hum Genet Subsets: MEDLINE
Database: MEDLINE Ultimate
Description
ISSN:1537-6605
DOI:10.1016/j.ajhg.2021.05.001