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Article

IFIH1 loss-of-function variants contribute to very early-onset inflammatory bowel disease

29 Jun 2021

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Share to Cytomegalovirus and herpesvirus research
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Source

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 34185153
DOI: 10.1007/s00439-021-02300-4

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 5 Sept 2026.

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IFIH1 loss-of-function variants contribute to very early-onset inflammatory bowel diseasePMID 34185153Read ↗

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Cell-type-resolved genetic regulatory variation shapes inflammatory bowel disease riskSemantic proximity Read ↗

IFIH1 loss-of-function predisposes to inflammatory and SARS-CoV-2-related infectious diseasesSemantic proximity Read ↗

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Aicardi-Goutières Syndrome Is Caused by IFIH1 MutationsSemantic proximity Read ↗

Exploring the genetic architecture of inflammatory bowel disease by whole genome sequencing identifies association at <i>ADCY7</i>Semantic proximity Read ↗

Intestinal somatic mutations in inflammatory bowel disease patients are enriched in very early onset IBD and primary immunodeficiency genesSemantic proximity Read ↗

Autosomal dominant IFIH1 gain-of-function mutations cause Aicardi-Goutières syndrome.Semantic proximity Read ↗

TTC7A: Steward of Intestinal HealthSemantic proximity Read ↗

Cell-type-resolved genetic variation shapes inflammatory bowel disease risk.Semantic proximity Read ↗

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