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Article

Association of LOXL1 polymorphisms with pseudoexfoliation, glaucoma, intraocular pressure, and systemic diseases in a Greek population. The Thessaloniki eye study.

Investigative ophthalmology & visual science - 10 Jun 2014

Anastasopoulos Eleftherios, Coleman Anne L, Wilson M Roy, Sinsheimer Janet S, Yu Fei, Katafigiotis Sokratis, Founti Panayiota, Salonikiou Angeliki, Pappas Theofanis, Koskosas Archimidis, Katopodi Theodora, Lambropoulos Alexandros, Topouzis Fotis

Abstract excerpt

PURPOSE: To investigate the association of the two single-nucleotide polymorphisms (SNPs) in the lysyl oxidase-like 1 (LOXL1) gene with pseudoexfoliation syndrome (PEX), pseudoexfoliative glaucoma (PEXG), and primary open-angle glaucoma (POAG) in a Greek population-based setting, from the Thessal...

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Source

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Identifiers

PMID: 24917141
DOI: 10.1167/iovs.14-13991
PMCID: PMC4095722

Genes

LOXL1

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026. Prepared record publication-24917141-2026-09-04.2. Manifest publication-graph-cohort-2026-09-04.2.

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

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Association of LOXL1 polymorphisms with pseudoexfoliation, glaucoma, intraocular pressure, and systemic diseases in a Greek population. The Thessaloniki eye study.PMID 24917141Read ↗

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