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https://doi.org/10.1007/978-3-...
Part of book or chapter of book . 2019 . Peer-reviewed
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Primary Biliary Cirrhosis, Primary Sclerosing Cholangitis, and Autoimmune Hepatitis

Authors: González-Serna, David; Kerick, Martin; Martín, J.;

Primary Biliary Cirrhosis, Primary Sclerosing Cholangitis, and Autoimmune Hepatitis

Abstract

Autoimmune liver diseases (AILDs), comprising primary biliary cirrhosis (PBC; also referred to as primary biliary cholangitis), primary sclerosing cholangitis (PSC), and autoimmune hepatitis (AIH), are complex conditions in which both genetic and environmental factors may affect the hepatobiliary system. Until recently, risk HLA haplotypes were the only genetic factor identified in these diseases, which were insufficient to explain most of the disease heritability. Nevertheless, thanks to the development of large-scale AILDs patient cohorts and the implementation of high-throughput methods such as genome-wide association studies (GWAS), a large number of genetic associations have emerged. In this chapter, we will provide an overview of the recent insights into genetic background of AILDs.

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selected citations
These citations are derived from selected sources.
This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Citations provided by BIP!
popularity
This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.
BIP!Popularity provided by BIP!
influence
This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Influence provided by BIP!
impulse
This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network.
BIP!Impulse provided by BIP!
views
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