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Article

Proteome-wide analysis of disease-associated SNPs that show allele-specific transcription factor binding.

PLoS genetics - 1 Sept 2012

Butter Falk, Davison Lucy, Viturawong Tar, Scheibe Marion, Vermeulen Michiel, Todd John A, Mann Matthias

Abstract excerpt

A causative role for single nucleotide polymorphisms (SNPs) in many genetic disorders has become evident through numerous genome-wide association studies. However, identification of these common causal variants and the molecular mechanisms underlying these associations remains a major challenge....

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Source

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Identifiers

PMID: 23028375
DOI: 10.1371/journal.pgen.1002982
PMCID: PMC3459973

Genes

RUNX1
TFAP4

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026. Prepared record publication-23028375-2026-09-04.2. Manifest publication-graph-cohort-2026-09-04.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 4 Sept 2026.

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