Cited by 8Genetic Associations and EpidemiologyBioinformatics and Genomic NetworksGenomics and Chromatin Dynamics

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Making the most of new genetic risk factors – genetic and epigenetic fine mapping of causal autoimmune disease variants

Mells, G.F., Hirschfield, G.M.·2015·Clinics and Research in Hepatology and Gastroenterology

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Crossref · 10.1016/j.clinre.2015.05.002

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  • Identified genetic associations mirror the pattern and nature seen in autoimmune diseases with the combination of a significant number of genetic associations with low OR for risk, typically in genes regulating the magnitude and nature of the immune response.

    “Identified genetic associations mirror the pattern and nature seen in autoimmune diseases with the combination of a significant number of genetic associations with low OR for risk, typically in genes regulating the magnitude and nature of the immune response.55”

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Research works printed but not linked: 3

  1. Farh, 2015, Genetic and epigenetic fine mapping of causal autoimmune disease variants, Nature, 518, 337, 10.1038/nature13835 · DOI · Paper page
  2. Liu, 2012, Dense fine-mapping study identifies new susceptibility loci for primary biliary cirrhosis, Nat Genet, 44, 1137, 10.1038/ng.2395 · DOI · Paper page
  3. Roadmap Epigenomics Consortium, 2015, Integrative analysis of 111 reference human epigenomes, Nature, 518, 317, 10.1038/nature14248 · DOI · Paper page

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Metadata

Authors
Mells, G. F., & Hirschfield, G. M.
Affiliations
  • University of Cambridge (GB)
  • University of Birmingham (GB)
Corresponding author
Mells, G.F.
Venue
Clinics and Research in Hepatology and Gastroenterology
Publisher
Elsevier BV
Published
2015-09
Volume
39
Issue
4
Pages
408-411
ISSN
2210-7401 (ISSN-L)
OpenAlex
W2221156492
Cited by
8
References
0
Citations by year
2026: 1 · 2020: 2 · 2019: 1 · 2018: 2 · 2017: 2
FWCI
0.91
Type
journal article
Language
en
Open access
closed
Locations
  • Clinics and Research in Hepatology and Gastroenterology (publishedVersion)
  • PubMed (publishedVersion)
  • University of Birmingham Research Portal (University of Birmingham) (submittedVersion)
Funders
Academy of Medical Sciences (AMS-SGCL9-Mells)
Topics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Genetic Associations and Epidemiology
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Bioinformatics and Genomic Networks
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Genomics and Chromatin Dynamics
Keywords
autoimmune disease, genetic risk factors, non-coding variants, 3D chromatin interactions, trans-regulation, transcriptional dysregulation, multi-omics integration
MeSH terms
Autoimmune Diseases, Gastrointestinal Diseases, Humans, Risk Factors, Polymorphism, Single Nucleotide, Epigenesis, Genetic, Genome-Wide Association Study

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