Charles Morin

1.4k total citations
21 papers, 844 citations indexed

About

Charles Morin is a scholar working on Molecular Biology, Clinical Biochemistry and Rheumatology. According to data from OpenAlex, Charles Morin has authored 21 papers receiving a total of 844 indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Molecular Biology, 5 papers in Clinical Biochemistry and 2 papers in Rheumatology. Recurrent topics in Charles Morin's work include Mitochondrial Function and Pathology (12 papers), ATP Synthase and ATPases Research (5 papers) and Metabolism and Genetic Disorders (5 papers). Charles Morin is often cited by papers focused on Mitochondrial Function and Pathology (12 papers), ATP Synthase and ATPases Research (5 papers) and Metabolism and Genetic Disorders (5 papers). Charles Morin collaborates with scholars based in Canada, United States and Germany. Charles Morin's co-authors include Grant A. Mitchell, Fenghao Xu, Brian H. Robinson, Eric S. Lander, Thomas J. Hudson, Terrye Delmonte, John D. Rioux, Cameron Ackerley, Jakob Bunkenborg and Brian Robinson and has published in prestigious journals such as Proceedings of the National Academy of Sciences, PLoS ONE and Annals of Neurology.

In The Last Decade

Charles Morin

21 papers receiving 828 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Charles Morin Canada 11 684 240 73 72 49 21 844
Carin A. F. Buskens Netherlands 8 525 0.8× 228 0.9× 58 0.8× 37 0.5× 128 2.6× 10 675
Merel S. Ebberink Netherlands 14 786 1.1× 227 0.9× 55 0.8× 142 2.0× 26 0.5× 22 872
Lisa M. Crowther Switzerland 14 323 0.5× 107 0.4× 128 1.8× 56 0.8× 33 0.7× 17 491
Takashi Sakai Japan 9 581 0.8× 43 0.2× 59 0.8× 39 0.5× 54 1.1× 13 772
Hayase Shisa Japan 14 454 0.7× 53 0.2× 108 1.5× 39 0.5× 29 0.6× 52 678
Elliot Surgenor Australia 7 497 0.7× 106 0.4× 43 0.6× 51 0.7× 28 0.6× 9 668
Mathew Nightingale Canada 10 387 0.6× 58 0.2× 120 1.6× 35 0.5× 44 0.9× 14 625
Miriam Di Re United Kingdom 9 641 0.9× 251 1.0× 26 0.4× 40 0.6× 51 1.0× 9 706
Ponugoti Vasantha Rao United States 14 472 0.7× 27 0.1× 42 0.6× 61 0.8× 163 3.3× 43 607
Marco Schiavone Italy 18 632 0.9× 36 0.1× 46 0.6× 87 1.2× 140 2.9× 32 797

Countries citing papers authored by Charles Morin

Since Specialization
Citations

This map shows the geographic impact of Charles Morin'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 Charles Morin with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Charles Morin more than expected).

Fields of papers citing papers by Charles Morin

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Charles Morin. 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 Charles Morin. The network helps show where Charles Morin may publish in the future.

Co-authorship network of co-authors of Charles Morin

This figure shows the co-authorship network connecting the top 25 collaborators of Charles Morin. A scholar is included among the top collaborators of Charles Morin 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 Charles Morin. Charles Morin 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.
Bchetnia, Mbarka, et al.. (2024). Pathological Mechanisms Involved in Epidermolysis Bullosa Simplex: Current Knowledge and Therapeutic Perspectives. International Journal of Molecular Sciences. 25(17). 9495–9495. 4 indexed citations
2.
3.
Bchetnia, Mbarka, Julie Powell, Charles Morin, et al.. (2022). Allele-Specific Inactivation of an Autosomal Dominant Epidermolysis Bullosa Simplex Mutation Using CRISPR-Cas9. The CRISPR Journal. 5(4). 586–597. 8 indexed citations
4.
Bchetnia, Mbarka, Jessica Tardif, Charles Morin, & Catherine Laprise. (2022). Expression signature of the Leigh syndrome French-Canadian type. Molecular Genetics and Metabolism Reports. 30. 100847–100847. 6 indexed citations
5.
Mariño, Tania Cruz, Philippe Caron, Charles Morin, et al.. (2021). French-Canadian families from Saguenay-Lac-Saint-Jean: a new founder population for APECED. Endocrine. 75(1). 48–58. 1 indexed citations
6.
Bchetnia, Mbarka, Luigi Bouchard, Jean Mathieu, et al.. (2021). Genetic burden linked to founder effects in Saguenay–Lac-Saint-Jean illustrates the importance of genetic screening test availability. Journal of Medical Genetics. 58(10). 653–665. 17 indexed citations
7.
Langlois, Alexandra, Charles Morin, Jonathan Lacombe‐Barrios, et al.. (2020). Determinants of omalizumab dose–related efficacy in oral immunotherapy: Evidence from a cohort of 181 patients. Journal of Allergy and Clinical Immunology. 147(1). 233–243. 36 indexed citations
8.
Legault, Julie, Christian Renaud, Charles Morin, et al.. (2020). Humoral responses to the measles, mumps and rubella vaccine are impaired in Leigh Syndrome French Canadian patients. PLoS ONE. 15(10). e0239860–e0239860. 5 indexed citations
9.
Meloche, Jolyane, et al.. (2019). Exome sequencing study of partial agenesis of the corpus callosum in men with developmental delay, epilepsy, and microcephaly. Molecular Genetics & Genomic Medicine. 8(1). e992–e992. 9 indexed citations
10.
Morin, Charles, et al.. (2017). Premature Ovarian Failure in French Canadian Leigh Syndrome. The Journal of Pediatrics. 184. 227–229.e1. 13 indexed citations
11.
Burelle, Yan, Chantal Bémeur, Marie-Ève Rivard, et al.. (2015). Mitochondrial Vulnerability and Increased Susceptibility to Nutrient-Induced Cytotoxicity in Fibroblasts from Leigh Syndrome French Canadian Patients. PLoS ONE. 10(4). e0120767–e0120767. 19 indexed citations
12.
Lévesque, Sébastien, Charles Morin, Simon‐Pierre Guay, et al.. (2012). A founder mutation in the PEX6 gene is responsible for increased incidence of Zellweger syndrome in a French Canadian population. BMC Medical Genetics. 13(1). 72–72. 31 indexed citations
13.
Bchetnia, Mbarka, Julie Powell, Catherine McCuaïg, et al.. (2011). Expression signature of epidermolysis bullosa simplex. Human Genetics. 131(3). 393–406. 14 indexed citations
14.
Legault, Jean, Isabelle Côté, Line Bouchard, et al.. (2011). Low-Concentration Methylene Blue Maintains Energy Production and Strongly Improves Survival of Leigh Syndrome French Canadian Skin Fibroblasts. Journal of Pharmacy & Pharmaceutical Sciences. 14(3). 438–438. 7 indexed citations
15.
Mootha, Vamsi K., Patricia Lepage, Kathleen A. Miller, et al.. (2003). Identification of a gene causing human cytochrome c oxidase deficiency by integrative genomics. Proceedings of the National Academy of Sciences. 100(2). 605–610. 452 indexed citations
16.
Liet, Jean‐Michel, Véronique Pelletier, Brian H. Robinson, et al.. (2003). The effect of short-term dimethylglycine treatment on oxygen consumption in cytochrome oxidase deficiency: A double-blind randomized crossover clinical trial. The Journal of Pediatrics. 142(1). 62–66. 25 indexed citations
17.
Lee, Nana, Mark J. Daly, Terrye Delmonte, et al.. (2001). A Genomewide Linkage-Disequilibrium Scan Localizes the Saguenay–Lac-Saint-Jean Cytochrome Oxidase Deficiency to 2p16. The American Journal of Human Genetics. 68(2). 397–409. 31 indexed citations
18.
Morin, Charles, Brian H. Robinson, Jacques Lacroix, et al.. (1999). Stroke‐like episodes in autosomal recessive cytochrome oxidase deficiency. Annals of Neurology. 45(3). 389–392. 1 indexed citations
19.
Morin, Charles, Brian H. Robinson, Jacques Lacroix, et al.. (1999). Stroke-like episodes in autosomal recessive cytochrome oxidase deficiency. Annals of Neurology. 45(3). 389–392. 21 indexed citations
20.
Lee, Nana, et al.. (1998). Saguenay Lac Saint Jean cytochrome oxidase deficiency: sequence analysis of nuclear encoded COX subunits, chromosomal localization and a sequence anomaly in subunit VIc. Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease. 1406(1). 1–4. 8 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.

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