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Article

Controversies in RELN/reelin expression in otosclerosis.

European archives of oto-rhino-laryngology : official journal of the European Federation of Oto-Rhino-Laryngological Societies (EUFOS) : affiliated with the German Society for Oto-Rhino-Laryngology - Head and Neck Surgery - 1 Feb 2012

Csomor Péter, Sziklai István, Karosi Tamás

Abstract excerpt

Several studies have reported a potential genetic association between disease-specific single nucleotide polymorphism (SNPs) of RELN and otosclerosis and confirmed RELN expression in human stapes footplates. These are conflicting results, since RELN expression has been attributed exclusively to neural tissues and to odontoblasts. Otosclerosis is a disease of complex bone remodeling disorder, which is limited to...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Share to Vestibule, Labyrinth

Source

Identifiers

PMID: 21630058
DOI: 10.1007/s00405-011-1653-4

Genes

RELN

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Controversies in RELN/reelin expression in otosclerosis.PMID 21630058Read ↗

A genome-wide analysis identifies genetic variants in the RELN gene associated with otosclerosis.Semantic proximity Read ↗

The risks of RELN polymorphisms and its expression in the development of otosclerosis.Semantic proximity Read ↗

The rs39335 polymorphism of the RELN gene is not associated with otosclerosis in a southern Italian population.Semantic proximity Read ↗

Genome-wide screen of otosclerosis in population biobanks: 27 loci and shared associations with skeletal structure.Semantic proximity Read ↗

Genetic variants in RELN are associated with otosclerosis in a non-European population from Tunisia.Semantic proximity Read ↗

Genetic association analysis in a clinically and histologically confirmed otosclerosis population confirms association with the TGFB1 gene but suggests an association of the RELN gene with a clinically indistinguishable otosclerosis-like phenotype.Semantic proximity Read ↗

Lack of association between SNP rs3914132 of the RELN gene and otosclerosis in India.Semantic proximity Read ↗

Genetics of OtosclerosisSemantic proximity Read ↗

Genetic variants in the RELN gene are associated with otosclerosis in multiple European populations.Semantic proximity Read ↗

Evidence of distinct RELN and TGFB1 genetic associations in familial and non-familial otosclerosis in a British population.Semantic proximity Read ↗

No evidence for disturbed COL1A1 and A2 expression in otosclerosis.Semantic proximity Read ↗

Current research in otosclerosis.Semantic proximity Read ↗

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