Lance P. Doucette

300 Prince Phillip Drive
St. John's, NL, Canada

Last Updated: 09/26/2026

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Found 13 publications

Disrupting the Repeat Domain of Premelanosome Protein (PMEL) Produces Dysamyloidosis and Dystrophic Ocular Pigment Reflective of Pigmentary Glaucoma.

Disrupting the Repeat Domain of Premelanosome Protein (PMEL) Produces Dysamyloidosis and Dystrophic Ocular Pigment Reflective of Pigmentary Glaucoma.

Journal: International journal of molecular sciences

Published: August 07, 2023

The inner junction protein CFAP20 functions in motile and non-motile cilia and is critical for vision.

The inner junction protein CFAP20 functions in motile and non-motile cilia and is critical for vision.

Journal: Nature communications

Published: August 06, 2021

Autosomal dominant non-syndromic hearing loss maps to DFNA33 (13q34) and co-segregates with splice and frameshift variants in ATP11A, a phospholipid flippase gene.

Autosomal dominant non-syndromic hearing loss maps to DFNA33 (13q34) and co-segregates with splice and frameshift variants in ATP11A, a phospholipid flippase gene.

Journal: Human genetics

Published: May 24, 2021

A pathogenic deletion in Forkhead Box L1 (FOXL1) identifies the first otosclerosis (OTSC) gene.

A pathogenic deletion in Forkhead Box L1 (FOXL1) identifies the first otosclerosis (OTSC) gene.

Journal: Human genetics

Published: May 15, 2021

PEX6 Mutations in Peroxisomal Biogenesis Disorders: An Usher Syndrome Mimic.

PEX6 Mutations in Peroxisomal Biogenesis Disorders: An Usher Syndrome Mimic.

Journal: Ophthalmology science

Published: January 18, 2021

Whole exome sequencing reveals putatively novel associations in retinopathies and drusen formation.

Whole exome sequencing reveals putatively novel associations in retinopathies and drusen formation.

Journal: European journal of human genetics : EJHG

Published: August 18, 2020

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

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

Journal: Investigative ophthalmology & visual science

Published: May 31, 2018

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

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

Journal: PloS one

Published: September 12, 2016

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

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

Journal: Ophthalmic genetics

Published: April 13, 2016

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

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

Journal: Survey of ophthalmology

Published: September 04, 2014

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

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

Journal: Ophthalmic genetics

Published: February 01, 2013

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

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

Journal: Human mutation

Published: April 27, 2012

Showing 1-12 of 13

Last Updated: 09/26/2026