Publications by authors named "Johane Robitaille"

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Sphingosine-1-phosphate receptor 2 inhibition ameliorates familial exudative vitreoretinopathy models.
Hirad A Feridooni, Rachel Fody, Mahtab Tavasoli, Mariam Alkandari, Sarah van der Ende, Johane M Robitaille

J Biol Chem· December 2025

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Gene Variant Spectrum in Probands With Familial Exudative Vitreoretinopathy Using an Expanded Panel.
Sarah van der Ende, Karen Bedard, Karin Wallace, Michael P Mackley, Mathew Nightingale, Johane M Robitaille

Invest Ophthalmol Vis Sci· February 2025

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Multimodal imaging of white preretinal lesions in atypical familial exudative vitreoretinopathy: Case report and literature review.
Liam D Redden, Douglas S M Iaboni, Sarah van der Ende, Mathew Nightingale, Daniel Gaston, Johane M Robitaille

Am J Ophthalmol Case Rep· June 2024

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Long-Term Visual Outcomes in Prematurely Born Children.
Johane M Robitaille

J Binocul Vis Ocul Motil· March 2024

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Recurrence of a BBS1 variant in Bardet-Biedl patients from Prince Edward Island.
Fahad A Alghaith, Sara MacKay, Karin Wallace, Jeff Locke, Johane M Robitaille

Clin Genet· December 2023

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Lack of evidence of association between ZNF408 variant and ROP.
Amit V Mishra, Johane M Robitaille

Ophthalmic Genet· April 2023

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Severe Familial Exudative Vitreoretinopathy, Congenital Hearing Loss, and Developmental Delay in a Child With Biallelic Variants in FZD4.
Sarah R van der Ende, Benjamin S Meyers, Jenina E Capasso, Mario Sasongko, Yoshihiro Yonekawa, Johane M Robitaille

JAMA Ophthalmol· September 2022

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Psychosocial Distress in Parents with Children Awaiting Surgery during the COVID-19 Pandemic.
David Forner, Patricia K Leslie, Abdullah Aldaihani, Michael Bezuhly, Christopher W Noel, Johane Robitaille

Children (Basel)· January 2022

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Binocularity outcomes following treatment for retinopathy of prematurity.
Sonia Manuchian, Kamiar Mireskandari, Nasrin N Tehrani, Maram Isaac, Johane M Robitaille

Can J Ophthalmol· June 2021

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Frizzled 4 regulates ventral blood vessel remodeling in the zebrafish retina.
Lucia Caceres, Sergey V Prykhozhij, Elizabeth Cairns, Harald Gjerde, Nicole M Duff, Johane M Robitaille

Dev Dyn· December 2019

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Optimized knock-in of point mutations in zebrafish using CRISPR/Cas9.
Sergey V Prykhozhij, Charlotte Fuller, Shelby L Steele, Chansey J Veinotte, Babak Razaghi, Johane M Robitaille

Nucleic Acids Res· September 2018

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Optimized knock-in of point mutations in zebrafish using CRISPR/Cas9.
Sergey V Prykhozhij, Charlotte Fuller, Shelby L Steele, Chansey J Veinotte, Babak Razaghi, Johane M Robitaille

Nucleic Acids Res· September 2018

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Fzd4 Haploinsufficiency Delays Retinal Revascularization in the Mouse Model of Oxygen Induced Retinopathy.
Michael H Ngo, Joanna Borowska-Fielding, Godfrey Heathcote, Sara Nejat, Melanie E Kelly, Johane M Robitaille

PLoS One· August 2017

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Stability of Attitudes to the Ethical Issues Raised by the Return of Incidental Genomic Research Findings in Children: A Follow-Up Study.
Conrad V Fernandez, Colleen OʼConnell, Meghan Ferguson, Andrew C Orr, Johane M Robitaille

Public Health Genomics· June 2016

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Congenital Bilateral Retinal Detachment in Two Siblings with Osteoporosis-Pseudoglioma Syndrome.
Lotte G Welinder, Johane M Robitaille, Rosemarie Rupps, Cornelius F Boerkoel, Christopher J Lyons

Ophthalmic Genet· April 2016

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Phenotypic overlap between familial exudative vitreoretinopathy and microcephaly, lymphedema, and chorioretinal dysplasia caused by KIF11 mutations.
Johane M Robitaille, Roxanne M Gillett, Marissa A LeBlanc, Daniel Gaston, Mathew Nightingale

JAMA Ophthalmol· December 2014

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Attitudes of parents toward the return of targeted and incidental genomic research findings in children.
Conrad V Fernandez, Eric Bouffet, David Malkin, Nada Jabado, Colleen O'Connell, Johane M Robitaille

Genet Med· August 2014

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Has rising pediatric obesity increased the incidence of idiopathic intracranial hypertension in children?
Lulu L C D Bursztyn, Sapna Sharan, Leah Walsh, G Robert LaRoche, Johane Robitaille

Can J Ophthalmol· February 2014

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The role of Frizzled-4 mutations in familial exudative vitreoretinopathy and Coats disease.
Johane M Robitaille, Binyou Zheng, Karin Wallace, M Jill Beis, Cuneyt Tatlidil

Br J Ophthalmol· April 2011

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Severe retinopathy of prematurity associated with FZD4 mutations.
Anna Ells, Duane L Guernsey, Karin Wallace, Binyou Zheng, Michael Vincer, Johane M Robitaille

Ophthalmic Genet· March 2010

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Application of homozygosity haplotype analysis to genetic mapping with high-density SNP genotype data.
Haiyan Jiang, Andrew Orr, Duane L Guernsey, Johane Robitaille, Géraldine Asselin

PLoS One· July 2009

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Phenotypic overlap of familial exudative vitreoretinopathy (FEVR) with persistent fetal vasculature (PFV) caused by FZD4 mutations in two distinct pedigrees.
Johane M Robitaille, Karin Wallace, Binyou Zheng, M Jill Beis, Mark Samuels

Ophthalmic Genet· March 2009

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Ocular features of CHARGE syndrome.
Karen McMain, Kim Blake, Isabel Smith, Judy Johnson, Ellen Wood, Johane Robitaille

J AAPOS· October 2008

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Mutant frizzled-4 disrupts retinal angiogenesis in familial exudative vitreoretinopathy.
Johane Robitaille, Marcia L E MacDonald, Ajamete Kaykas, Laird C Sheldahl, Jutta Zeisler

Nat Genet· October 2002

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Pigmented medulloepithelioma of the ciliary body.
Jerry A Shields, Ralph C Eagle, Carol L Shields, Arun D Singh, Johane Robitaille

Arch Ophthalmol· February 2002

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