Work

High-throughput identification of noncoding functional SNPs via type IIS enzyme restriction

Year: 2018

Type: article

Source: Nature Genetics

DOI: 10.1038/s41588-018-0159-z

Authors: Gang Li, Marta Martínez-Bonet, Di Wu, Yu Yang, Jing Cui, Hung N. Nguyen, Pierre Cunin, Anaïs Levescot, Ming Bai, Harm-Jan Westra, Yukinori Okada, Michael B. Brenner, Soumya Raychaudhuri, Eric A. Hendrickson, Richard L. Maas, Peter A. Nigrovic

Institutions: Brigham and Women's Hospital, Harvard University, University of Pittsburgh, University of North Carolina at Chapel Hill, The University of Osaka, Broad Institute, University of Manchester, University of Minnesota, Boston Children's Hospital

Language: English

Topic: Genetic Associations and Epidemiology

Subfield: Genetics

Field: Biochemistry, Genetics and Molecular Biology

Domain: Life Sciences

SDG: Good health and well-being

Open Access status: green

Funders: National Multiple Sclerosis Society, Arthritis National Research Foundation, Rheumatology Research Foundation, Fundación Bechara, National Institutes of Health, National Cancer Institute, National Institute of General Medical Sciences, National Institute of Neurological Disorders and Stroke, National Institute of Environmental Health Sciences, National Institute of Arthritis and Musculoskeletal and Skin Diseases

Awards: G1012670328, G1017297203, G1457778459, The mechanism of Cas9/CRISPR-initiated genome modification in human somatic cells, Identifying and Characterizing the Functional SNPs on RA-Associated loci involved in CD40/NF-kB Signal, Using High Throughput Approach to Identify/Characterize Functional Variants on MS, UNC Center for Environmental Health and Susceptibility, Joint Biology Consortium Resource-based Center

OpenAlex ID: W2884550124

FWCI: 2.081

Cites: 46

Cited by: 36

Related to: 10