Ian M MacDonald

Scopus Author ID ORCID

Publication Activity (10 Years)

Years Active: 2018-2023
Publications (10 Years): 11

Top Venues

Ophthalmic genetics

Ocular immunology and inflammation

European journal of human genetics : EJHG

Nature communications

University of Alberta

McGill University (MSC)

This page only lists publications with an associated author ORCID identifier.

Affiliation History

University of Alberta Jul 01 2016

Canada

Emeritus Professor :: Ophthalmology and Visual Sciences

Education History

McGill University Jul 01 1972 - Jun 30 1974

Canada

MSC :: Biology

McGill University Sep 02 1968 - Apr 30 1972

Canada

BSC :: Biology

Publications

Amit V Mishra, Rosanna Martens, Ian M MacDonald
Pseudoxanthoma elasticum and retinitis pigmentosa in a patient with a novel mutation in the ABCC6 gene. Ophthalmic genetics (2023)
Ian M MacDonald
Lessons learned from research on choroideremia. Ophthalmic genetics (2022)
Paul W Chrystal, Nils J Lambacher, Lance P Doucette, James Bellingham, Elena R Schiff, Nicole C L Noel, Chunmei Li, Sofia Tsiropoulou, Geoffrey A Casey, Yi Zhai, Nathan J Nadolski, Mohammed H Majumder, Julia Tagoe, Fabiana D'Esposito, Maria Francesca Cordeiro, Susan Downes, Jill Clayton-Smith, Jamie M Ellingford, null null, Omar A Mahroo, Jennifer C Hocking, Michael E Cheetham, Andrew R Webster, Gert Jansen, Oliver E Blacque, W Ted Allison, Ping Yee Billie Au, Ian M MacDonald, Gavin Arno, Michel R Leroux
The inner junction protein CFAP20 functions in motile and non-motile cilia and is critical for vision. Nature communications 13 (1) (2022)
Nicole C L Noel, Ian M MacDonald, W Ted Allison
Zebrafish Models of Photoreceptor Dysfunction and Degeneration. Biomolecules 11 (1) (2021)
Ann-Marie C Peturson, Nicole C L Noel, Ian M MacDonald
A homozygous POC1B variant causes recessive cone-rod dystrophy. Ophthalmic genetics 42 (3) (2021)
Yi Zhai, Matthew D Benson, Ian M MacDonald
Corneal involvement in a case of autosomal dominant Stargardt-like macular dystrophy (STGD3) with ELOVL4 mutation. Ophthalmic genetics (2021)
Lance P Doucette, Nicole C L Noel, Yi Zhai, Manlong Xu, Oana Caluseriu, Stephanie C Hoang, Alina J Radziwon, Ian M MacDonald
Whole exome sequencing reveals putatively novel associations in retinopathies and drusen formation. European journal of human genetics : EJHG 29 (8) (2021)
Matthew D Benson, David J A Plemel, Paul R Freund, James R Lewis, Jörn Oliver Sass, Luzy Bähr, Corinne Gemperle-Britschgi, Patrick Ferreira, Ian M MacDonald
Severe retinal degeneration in a patient with Canavan disease. Ophthalmic genetics 42 (1) (2020)
Kaylie D Jones, Alina Radziwon, David G Birch, Ian M MacDonald
A novel SVA retrotransposon insertion in the CHM gene results in loss of REP-1 causing choroideremia. Ophthalmic genetics 41 (4) (2020)
Matthew D Benson, David J A Plemel, Elaine Yacyshyn, Irwindeep Sandhu, Ian M MacDonald, Chad F Baker
Combination Treatment with Rituximab and Bortezomib in a Patient with Non-Paraneoplastic Autoimmune Retinopathy. Ocular immunology and inflammation 28 (6) (2019)
Ian M MacDonald, Paul A Sieving
Investigation of the effect of dietary docosahexaenoic acid (DHA) supplementation on macular function in subjects with autosomal recessive Stargardt macular dystrophy. Ophthalmic genetics 39 (4) (2018)

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Publication Activity (10 Years)

Top Topics

Top Venues

Ian M MacDonald