Mapping eQTLs with RNA-seq reveals novel susceptibility genes, non-coding RNAs and alternative-splicing events in systemic lupus erythematosus (Q33614670)

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English	Mapping eQTLs with RNA-seq reveals novel susceptibility genes, non-coding RNAs and alternative-splicing events in systemic lupus erythematosus	scientific article

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scholarly article

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5 April 2020

Mapping eQTLs with RNA-seq reveals novel susceptibility genes, non-coding RNAs and alternative-splicing events in systemic lupus erythematosus (English)

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5 April 2020

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alternative mRNA splicing, via spliceosome

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based on heuristic

inferred from title

systemic lupus erythematosus

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based on heuristic

inferred from title

Christopher A Odhams

1

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Kerrin S. Small

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Andrea Cortini

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Alfonso Buil

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Emmanouil T Dermitzakis

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Deborah S Cunninghame Graham

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Timothy J Vyse

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1 March 2017

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Human Molecular Genetics

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1003-1017

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describes a project that uses

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based on heuristic

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Integrative Multi-omic Analysis of Human Platelet eQTLs Reveals Alternative Start Site in Mitofusin 2.

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Union Exon Based Approach for RNA-Seq Gene Quantification: To Be or Not to Be?

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eQTL networks unveil enriched mRNA master integrators downstream of complex disease-associated SNPs.

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Genetic association analyses implicate aberrant regulation of innate and adaptive immunity genes in the pathogenesis of systemic lupus erythematosus.

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Alternative Splicing QTLs in European and African Populations

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A functional variant in microRNA-146a promoter modulates its expression and confers disease risk for systemic lupus erythematosus.

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Genetics of gene expression and its effect on disease

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Genetic variants regulating ORMDL3 expression contribute to the risk of childhood asthma

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Common genetic variants account for differences in gene expression among ethnic groups

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Circular chromosome conformation capture (4C) uncovers extensive networks of epigenetically regulated intra- and interchromosomal interactions.

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Identification of common genetic variants controlling transcript isoform variation in human whole blood

1 reference

https://api.crossref.org/works/10.1093/HMG/DDW417

21 January 2018

Emerging therapies in antineutrophil cytoplasm antibody-associated vasculitis

1 reference

https://api.crossref.org/works/10.1093/HMG/DDW417

21 January 2018

Functional variants in the B-cell gene BANK1 are associated with systemic lupus erythematosus

1 reference

https://api.crossref.org/works/10.1093/HMG/DDW417

21 January 2018

Helios induces epigenetic silencing of IL2 gene expression in regulatory T cells

1 reference

https://api.crossref.org/works/10.1093/HMG/DDW417

21 January 2018

A survey of genetic human cortical gene expression

1 reference

https://api.crossref.org/works/10.1093/HMG/DDW417

21 January 2018

Putative cis-regulatory drivers in colorectal cancer.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5409091

30 October 2018

Identifiers

10.1093/HMG/DDW417

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:28062664 AND SRC:MED&resulttype=core&format=json

5 April 2020

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:28062664 AND SRC:MED&resulttype=core&format=json

5 April 2020

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:28062664 AND SRC:MED&resulttype=core&format=json

5 April 2020

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