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Article

Genetic variants in the FOXO1 and ZNF469 genes are associated with keratoconus in Sweden: a case-control study.

BMC ophthalmology - 24 Jan 2024

Wonneberger Wolf, Sterner Bertil, MacLean Ulrika, Claesson Margareta, Johansson Lena Havstam, Skoog Ingmar, Zetterberg Madeleine, Zettergren Anna

Abstract excerpt

BACKGROUND: Keratoconus (KC) is characterized by pathological thinning and bulging of the cornea that may lead to visual impairment. The etiology of sporadic KC remains enigmatic despite intensive research in recent decades. The purpose of this study was to examine the relationship between previously highlighted genetic variants associated with KC and sporadic KC in a Swedish cohort. METHODS: A total of 176...

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Identifiers

PMID: 38267912
DOI: 10.1186/s12886-024-03299-8
PMCID: PMC10809587

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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.

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