ArticleNature genetics2011
Fine points in mapping autoimmunity.
Article in Nature genetics, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.
What it found
Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.
The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
12 citing papers in PubMed.
- Genetic and Genomic Analysis of Systemic Sclerosis: A Narrative Review of the Recent Advancement.JMA journal · 2026Review
- Functional link between sarcoidosis-associated gene variants and quantitative levels of bronchoalveolar lavage fluid cell types.Frontiers in medicine · 2023Article
- Genetic associations at regulatory phenotypes improve fine-mapping of causal variants for 12 immune-mediated diseases.Nature genetics · 2022Article
- Approaching Shared Pathophysiology in Immune-Mediated Diseases through Functional Genomics.Genes · 2020Review
- Genetics of systemic sclerosis.Journal of scleroderma and related disorders · 2020Review
- Regulatory annotation of genomic intervals based on tissue-specific expression QTLs.Bioinformatics (Oxford, England) · 2020Article
- Regulation of Fn14 Receptor and NF-κB Underlies Inflammation in Meniere's Disease.Frontiers in immunology · 2017Article
- Pathogenesis of Systemic Sclerosis.Frontiers in immunology · 2015Review
- Immunochip analysis identifies multiple susceptibility loci for systemic sclerosis.American journal of human genetics · 2014Article
- A practical and novel method to extract genomic DNA from blood collection kits for plasma protein preservation.Journal of visualized experiments : JoVE · 2013Article
- Admixture mapping in lupus identifies multiple functional variants within IFIH1 associated with apoptosis, inflammation, and autoantibody production.PLoS genetics · 2013Article
- Host genetics and immune control of HIV-1 infection: fine mapping for the extended human MHC region in an African cohort.Genes and immunityArticle
Corrections and comments
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Authors and funding
1 author.
Funding
No grant is acknowledged in the PubMed record.
Abstract
An efficient way to design genotyping arrays for fine mapping is to group phenotypes with common biology. The first application of the Immunochip to celiac disease provides an insightful view of what this strategy can achieve.
Indexed as
Identifiers
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Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.