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List of works by Lance Doucette

A novel deletion in SMPX causes a rare form of X-linked progressive hearing loss in two families due to a founder effect

scientific article published on 11 October 2012

A novel, non-stop mutation in FOXE3 causes an autosomal dominant form of variable anterior segment dysgenesis including Peters anomaly

scientific article

FOXC1 Regulates Expression of Prostaglandin Receptors Leading to an Attenuated Response to Latanoprost

scientific article published on 01 May 2018

FOXC1 modulates MYOC secretion through regulation of the exocytic proteins RAB3GAP1, RAB3GAP2 and SNAP25.

scientific article

Identification of a novel in-frame deletion in KCNQ4 (DFNA2A) and evidence of multiple phenocopies of unknown origin in a family with ADSNHL.

scientific article

Molecular genetics of achromatopsia in Newfoundland reveal genetic heterogeneity, founder effects and the first cases of Jalili syndrome in North America.

scientific article published on 30 January 2013

Profound, prelingual nonsyndromic deafness maps to chromosome 10q21 and is caused by a novel missense mutation in the Usher syndrome type IF gene PCDH15.

scientific article

Prostaglandins in the eye: Function, expression, and roles in glaucoma.

scientific article

The interactions of genes, age, and environment in glaucoma pathogenesis.

scientific article published on 04 February 2015

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