Hélène Catoire

1.2k total citations
15 papers, 737 citations indexed

About

Hélène Catoire is a scholar working on Molecular Biology, Neurology and Cellular and Molecular Neuroscience. According to data from OpenAlex, Hélène Catoire has authored 15 papers receiving a total of 737 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Molecular Biology, 7 papers in Neurology and 5 papers in Cellular and Molecular Neuroscience. Recurrent topics in Hélène Catoire's work include Parkinson's Disease Mechanisms and Treatments (5 papers), Restless Legs Syndrome Research (5 papers) and Genetic Neurodegenerative Diseases (4 papers). Hélène Catoire is often cited by papers focused on Parkinson's Disease Mechanisms and Treatments (5 papers), Restless Legs Syndrome Research (5 papers) and Genetic Neurodegenerative Diseases (4 papers). Hélène Catoire collaborates with scholars based in Canada, France and United States. Hélène Catoire's co-authors include J. Alex Parker, Christian Néri, Cendrine Tourette, Emmanuel Lambert, Guy A. Rouleau, Patrick A. Dion, Gustavo Turecki, Jacques Montplaisir, Lan Xiong and Cláudia Gaspar and has published in prestigious journals such as Nature Genetics, Journal of Neuroscience and PLoS ONE.

In The Last Decade

Hélène Catoire

15 papers receiving 725 citations

Peers

Countries citing papers authored by Hélène Catoire

Since Specialization

Citations

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

Fields of papers citing papers by Hélène Catoire

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Hélène Catoire

This figure shows the co-authorship network connecting the top 25 collaborators of Hélène Catoire. A scholar is included among the top collaborators of Hélène Catoire 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 Hélène Catoire. Hélène Catoire is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

Sort: Min cites: Since: Top N: Style:

15 of 15 papers shown

#	Work	Indexed citations
1	Selective Enhancement of REM Sleep in Male Rats through Activation of Melatonin MT₁Receptors Located in the Locus Ceruleus Norepinephrine Neurons 2024 ·Journal of Neuroscience ·Martha López-Canul, (unknown), (unknown), (unknown), Danilo De Gregorio, Rafael Ochoa‐Sanchez, Hélène Catoire, Luca Posa, Guy A. Rouleau, Jean‐Martin Beaulieu, Stefano Comai, Gabriella Gobbi	5
2	Spinal cord extracts of amyotrophic lateral sclerosis spread TDP-43 pathology in cerebral organoids 2023 ·PLoS Genetics ·(unknown), Jay P. Ross, (unknown), (unknown), (unknown), Hélène Catoire, Daniel Rochefort, Makoto Urushitani, Ryōsuke Takahashi, Joshua A. Sonnen, Stefano Stifani, Patrick A. Dion, Guy A. Rouleau	33
3	Transcriptome-wide association study reveals increased neuronal FLT3 expression is associated with Tourette’s syndrome 2022 ·Communications Biology ·Calwing Liao, (unknown), Hélène Catoire, Fulya Akçimen, Jay P. Ross, Cynthia V. Bourassa, Patrick A. Dion, Inge A. Meijer, Guy A. Rouleau	10
4	Transcriptomic Changes Resulting From STK32B Overexpression Identify Pathways Potentially Relevant to Essential Tremor 2020 ·Frontiers in Genetics ·Calwing Liao, (unknown), (unknown), Daniel Rochefort, Fulya Akçimen, (unknown), (unknown), Alexandre D. Laporte, Dan Spiegelman, Qin He, Hélène Catoire, Patrick A. Dion, Guy A. Rouleau	9
5	Genome-wide association study identifies genetic factors that modify age at onset in Machado-Joseph disease 2020 ·Aging ·Fulya Akçimen, Sandra Martins, Calwing Liao, Cynthia V. Bourassa, Hélène Catoire, Garth A. Nicholson, Olaf Rieß, Mafalda Raposo, Marcondes C. França, João Vasconcelos, Manuela Lima, Íscia Lopes‐Cendes, Maria Luiza Saraiva Pereira, Laura Bannach Jardim, Jorge Sequeiros, Patrick A. Dion, Guy A. Rouleau	12
6	Mineral absorption is an enriched pathway in a brain region of restless legs syndrome patients with reduced MEIS1 expression 2019 ·PLoS ONE ·(unknown), Alexandre Dionne‐Laporte, Hélène Catoire, Daniel Rochefort, (unknown), Jay P. Ross, Fulya Akçimen, (unknown), Gustavo Turecki, Patrick A. Dion, Guy A. Rouleau	9
7	Somatic expansion of the C9orf72 hexanucleotide repeat does not occur in ALS spinal cord tissues 2019 ·Neurology Genetics ·Jay P. Ross, Claire S. Leblond, Hélène Catoire, Kathryn Volkening, Michael J. Strong, Lorne Zinman, Janice Robertson, Patrick A. Dion, Guy A. Rouleau	7
8	A direct interaction between two Restless Legs Syndrome predisposing genes: MEIS1 and SKOR1 2018 ·Scientific Reports ·Hélène Catoire, (unknown), (unknown), (unknown), Alanna Grant, Daniel Rochefort, Lan Xiong, Jacques Montplaisir, Christopher J. Earley, Gustavo Turecki, Patrick A. Dion, Guy A. Rouleau	20
9	Reassessing GWAS findings for the shared genetic basis of insomnia and restless legs syndrome 2018 ·SLEEP ·(unknown), (unknown), Lan Xiong, (unknown), Hélène Catoire, Guy A. Rouleau, Jacques Montplaisir, Alex Désautels, Simon C. Warby	11
10	Restless legs syndrome‐associated MEIS1 risk variant influences iron homeostasis 2011 ·Annals of Neurology ·Hélène Catoire, Patrick A. Dion, Lan Xiong, (unknown), Rébecca Gaudet, Simon Girard, Anne Noreau, Cláudia Gaspar, Gustavo Turecki, Jacques Montplaisir, J. Alex Parker, Guy A. Rouleau	64
11	Cross-talk between canonical Wnt signaling and the sirtuin-FoxO longevity pathway to protect against muscular pathology induced by mutant PABPN1 expression in C. elegans 2010 ·Neurobiology of Disease ·Matthieu Y. Pasco, Hélène Catoire, J. Alex Parker, Bernard Brais, Guy A. Rouleau, Christian Néri	14
12	MEIS1 intronic risk haplotype associated with restless legs syndrome affects its mRNA and protein expression levels 2009 ·Human Molecular Genetics ·Lan Xiong, Hélène Catoire, Patrick A. Dion, Cláudia Gaspar, Ronald G. Lafrenière, Simon Girard, Аnastasia Levchenko, Jean‐Baptiste Rivière, Laura M. Fiori, Judith St‐Onge, (unknown), Pascale Thibodeau, Richard P. Allen, Christopher J. Earley, Gustavo Turecki, Jacques Montplaisir, Guy A. Rouleau	67
13	Sirtuin inhibition protects from the polyalanine muscular dystrophy protein PABPN1 2008 ·Human Molecular Genetics ·Hélène Catoire, Matthieu Y. Pasco, (unknown), Sébastien Holbert, Cendrine Tourette, Bernard Brais, Guy A. Rouleau, J. Alex Parker, Christian Néri	52
14	Resveratrol rescues mutant polyglutamine cytotoxicity in nematode and mammalian neurons 2005 ·Nature Genetics ·J. Alex Parker, (unknown), (unknown), Emmanuel Lambert, Cendrine Tourette, Hélène Catoire, Christian Néri	411
15	Neuroprotection par l’activation des sirtuines dans des modèles simplifiés de chorée de Huntington 2005 ·médecine/sciences ·J. Alex Parker, (unknown), (unknown), Emmanuel Lambert, Cendrine Tourette, Hélène Catoire, Christian Néri	13

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