Johane M. Robitaille

1.5k total citations
25 papers, 915 citations indexed

About

Johane M. Robitaille is a scholar working on Molecular Biology, Radiology, Nuclear Medicine and Imaging and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Johane M. Robitaille has authored 25 papers receiving a total of 915 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Molecular Biology, 9 papers in Radiology, Nuclear Medicine and Imaging and 5 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Johane M. Robitaille's work include Retinal Development and Disorders (6 papers), Retinopathy of Prematurity Studies (6 papers) and Wnt/β-catenin signaling in development and cancer (4 papers). Johane M. Robitaille is often cited by papers focused on Retinal Development and Disorders (6 papers), Retinopathy of Prematurity Studies (6 papers) and Wnt/β-catenin signaling in development and cancer (4 papers). Johane M. Robitaille collaborates with scholars based in Canada, United States and United Kingdom. Johane M. Robitaille's co-authors include Duane L. Guernsey, Ann Hoskin-Mott, Mark Samuels, Marie‐Pierre Dubé, Simon N. Pimstone, Y. Paul Goldberg, Laird C. Sheldahl, Jutta Zeisler, Barkur S. Shastry and Roshni R. Singaraja and has published in prestigious journals such as Nucleic Acids Research, Nature Genetics and PLoS ONE.

In The Last Decade

Johane M. Robitaille

25 papers receiving 880 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Johane M. Robitaille Canada 13 617 196 157 140 118 25 915
I Russell‐Eggitt United Kingdom 21 531 0.9× 194 1.0× 228 1.5× 563 4.0× 78 0.7× 38 1.2k
Florence Niel France 17 879 1.4× 241 1.2× 86 0.5× 54 0.4× 125 1.1× 24 1.3k
Lauren Massingham United States 8 365 0.6× 295 1.5× 44 0.3× 64 0.5× 54 0.5× 19 845
Maarten Arends Netherlands 13 783 1.3× 306 1.6× 114 0.7× 231 1.6× 70 0.6× 18 1.5k
Arif O. Khan Saudi Arabia 19 721 1.2× 299 1.5× 146 0.9× 343 2.5× 94 0.8× 74 960
Pilar Villacampa Spain 13 344 0.6× 200 1.0× 84 0.5× 141 1.0× 37 0.3× 21 762
Sı̇bel Aylı̇n Uğur İşerı̇ Türkiye 13 283 0.5× 218 1.1× 39 0.2× 52 0.4× 103 0.9× 39 690
Tadashi Yokoi Japan 16 374 0.6× 90 0.5× 313 2.0× 280 2.0× 71 0.6× 69 720
John R.W. Yates United Kingdom 19 802 1.3× 490 2.5× 233 1.5× 322 2.3× 29 0.2× 30 1.7k
Cheryl Y. Gregory United Kingdom 15 474 0.8× 153 0.8× 153 1.0× 242 1.7× 79 0.7× 25 935

Countries citing papers authored by Johane M. Robitaille

Since Specialization
Citations

This map shows the geographic impact of Johane M. Robitaille's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Johane M. Robitaille with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Johane M. Robitaille more than expected).

Fields of papers citing papers by Johane M. Robitaille

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Johane M. Robitaille. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Johane M. Robitaille. The network helps show where Johane M. Robitaille may publish in the future.

Co-authorship network of co-authors of Johane M. Robitaille

This figure shows the co-authorship network connecting the top 25 collaborators of Johane M. Robitaille. A scholar is included among the top collaborators of Johane M. Robitaille based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Johane M. Robitaille. Johane M. Robitaille is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Bedard, Karen, Karin Wallace, Michael P. Mackley, et al.. (2025). Gene Variant Spectrum in Probands With Familial Exudative Vitreoretinopathy Using an Expanded Panel. Investigative Ophthalmology & Visual Science. 66(2). 23–23. 2 indexed citations
2.
Robitaille, Johane M.. (2023). Long-Term Visual Outcomes in Prematurely Born Children. PubMed. 74(1). 1–8. 4 indexed citations
3.
Forner, David, Michael Bezuhly, Christopher W. Noel, et al.. (2022). Psychosocial Distress in Parents with Children Awaiting Surgery during the COVID-19 Pandemic. Children. 9(1). 87–87. 8 indexed citations
4.
Mireskandari, Kamiar, et al.. (2020). Binocularity outcomes following treatment for retinopathy of prematurity. Canadian Journal of Ophthalmology. 56(3). 179–183. 4 indexed citations
5.
Prykhozhij, Sergey V., Elizabeth A. Cairns, Mike Ngo, et al.. (2019). Frizzled 4 regulates ventral blood vessel remodeling in the zebrafish retina. Developmental Dynamics. 248(12). 1243–1256. 8 indexed citations
6.
Mireskandari, Kamiar, et al.. (2019). Binocularity outcomes following treatment for retinopathy of prematurity. Journal of American Association for Pediatric Ophthalmology and Strabismus. 23(4). e43–e43. 1 indexed citations
7.
Nejat, Sara, et al.. (2016). Fzd4 Haploinsufficiency Delays Retinal Revascularization in the Mouse Model of Oxygen Induced Retinopathy. PLoS ONE. 11(8). e0158320–e0158320. 8 indexed citations
8.
Fernandez, Conrad V., Colleen O’Connell, Meghan Ferguson, et al.. (2015). Stability of Attitudes to the Ethical Issues Raised by the Return of Incidental Genomic Research Findings in Children: A Follow-Up Study. Public Health Genomics. 18(5). 299–308. 9 indexed citations
9.
Robitaille, Johane M., et al.. (2015). Congenital Bilateral Retinal Detachment in Two Siblings with Osteoporosis-Pseudoglioma Syndrome. Ophthalmic Genetics. 36(3). 276–280. 9 indexed citations
10.
Fernandez, Conrad V., Éric Bouffet, David Malkin, et al.. (2014). Attitudes of parents toward the return of targeted and incidental genomic research findings in children. Genetics in Medicine. 16(8). 633–640. 79 indexed citations
11.
Robitaille, Johane M., Karin Wallace, M Beis, et al.. (2010). The role of Frizzled-4 mutations in familial exudative vitreoretinopathy and Coats disease. British Journal of Ophthalmology. 95(4). 574–579. 53 indexed citations
12.
Robitaille, Johane M., et al.. (2009). Phenotypic Variability in Genetically Defined X-linked Congenital Stationary Night Blindness. Investigative Ophthalmology & Visual Science. 50(13). 3721–3721. 2 indexed citations
13.
Robitaille, Johane M., Karin Wallace, M Beis, et al.. (2009). Phenotypic Overlap of Familial Exudative Vitreoretinopathy (FEVR) with Persistent Fetal Vasculature (PFV) Caused byFZD4Mutations in two Distinct Pedigrees. Ophthalmic Genetics. 30(1). 23–30. 48 indexed citations
14.
Jiang, Haiyan, Andrew Orr, Duane L. Guernsey, et al.. (2009). Application of Homozygosity Haplotype Analysis to Genetic Mapping with High-Density SNP Genotype Data. PLoS ONE. 4(4). e5280–e5280. 20 indexed citations
15.
Robitaille, Johane M., Isabel M. Smith, Judy A. Johnson, et al.. (2008). Ocular features of CHARGE syndrome. Journal of American Association for Pediatric Ophthalmology and Strabismus. 12(5). 460–465. 23 indexed citations
16.
Shields, Jerry A., Ralph C. Eagle, Carol L. Shields, Arun D. Singh, & Johane M. Robitaille. (2002). Pigmented Medulloepithelioma of the Ciliary Body. Archives of Ophthalmology. 120(2). 207–207. 15 indexed citations
17.
Orr, Andrew, Johane M. Robitaille, Paul A. Price, et al.. (2001). Exfoliation syndrome: Clinical and genetic features. Ophthalmic Genetics. 22(3). 171–185. 38 indexed citations
18.
Boycott, Kym M., Richard G. Weleber, Johane M. Robitaille, et al.. (2001). A summary of 20 CACNA1F mutations identified in 36 families with incomplete X-linked congenital stationary night blindness, and characterization of splice variants. Human Genetics. 108(2). 91–97. 76 indexed citations
19.
Ells, Anna L., Gaétan Laroche, J. M. Little, et al.. (2000). Guidelines for screening examinations for retinopathy of prematurity. Canadian Journal of Ophthalmology. 35(5). 251–252. 22 indexed citations
20.
Robitaille, Johane M., Lee H. Monsein, & Elias I. Traboulsi. (1996). Coats' disease and central nervous system venous malformation. Ophthalmic Genetics. 17(4). 215–218. 3 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

Explore authors with similar magnitude of impact

Breakdown of academic impact, for papers by I Russell‐Eggitt Breakdown of academic impact, for papers by Florence Niel Breakdown of academic impact, for papers by Lauren Massingham Breakdown of academic impact, for papers by Maarten Arends Breakdown of academic impact, for papers by Arif O. Khan Breakdown of academic impact, for papers by Pilar Villacampa Breakdown of academic impact, for papers by Sı̇bel Aylı̇n Uğur İşerı̇ Breakdown of academic impact, for papers by Tadashi Yokoi Breakdown of academic impact, for papers by John R.W. Yates Breakdown of academic impact, for papers by Cheryl Y. Gregory
Rankless by CCL
2026