Dr. Lance Doucette, PhD

Pronouns: he/him

Contact Publications Research Students

Contact

Adjunct Assistant Professor, Faculty of Medicine & Dentistry - Department of Ophthalmology & Visual Science

Email: lancedoucette@ualberta.ca
Phone: (780) 492-2875
Address: 7-030 Katz Group Centre For Research
11315 - 87 Ave NW

Edmonton AB

T6G 2H5

Featured Publications

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

INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES. 2023 January; 10.3390/IJMS241914423

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

NATURE COMMUNICATIONS. 2022 January; 10.1038/S41467-022-33820-W

PEX6 Mutations in Peroxisomal Biogenesis Disorders <i>An Usher Syndrome Mimic</i>

OPHTHALMOLOGY SCIENCE. 2021 January; 10.1016/J.XOPS.2021.100028

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

EUROPEAN JOURNAL OF HUMAN GENETICS. 2021 January; 10.1038/S41431-021-00872-3

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

INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE. 2018 January; 10.1167/IOVS.17-23223

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

PLOS ONE. 2017 January; 10.1371/JOURNAL.PONE.0178518

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

SURVEY OF OPHTHALMOLOGY. 2015 January; 10.1016/J.SURVOPHTHAL.2015.01.004

Molecular Genetics of Achromatopsia in Newfoundland Reveal Genetic Heterogeneity, Founder Effects and the First Cases of Jalili Syndrome in North America

OPHTHALMIC GENETICS. 2013 January; 10.3109/13816810.2013.763993

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

EUROPEAN JOURNAL OF HUMAN GENETICS. 2011 January; 10.1038/EJHG.2010.210

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

EUROPEAN JOURNAL OF HUMAN GENETICS. 2009 January; 10.1038/EJHG.2008.231

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Research Students

Currently accepting undergraduate students for research project supervision.