Anne Noreau

3.4k total citations
22 papers, 814 citations indexed

About

Anne Noreau is a scholar working on Cellular and Molecular Neuroscience, Molecular Biology and Neurology. According to data from OpenAlex, Anne Noreau has authored 22 papers receiving a total of 814 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Cellular and Molecular Neuroscience, 9 papers in Molecular Biology and 9 papers in Neurology. Recurrent topics in Anne Noreau's work include Mitochondrial Function and Pathology (6 papers), Genetic Neurodegenerative Diseases (6 papers) and Neurogenetic and Muscular Disorders Research (5 papers). Anne Noreau is often cited by papers focused on Mitochondrial Function and Pathology (6 papers), Genetic Neurodegenerative Diseases (6 papers) and Neurogenetic and Muscular Disorders Research (5 papers). Anne Noreau collaborates with scholars based in Canada, France and Austria. Anne Noreau's co-authors include Guy A. Rouleau, Patrick A. Dion, Hussein Daoud, Véronique Belzil, Nicolas Dupré, Simon Girard, Pascale Hince, Julie Gauthier, Sylvia Dobrzeniecka and Alexandre Dionne‐Laporte and has published in prestigious journals such as PLoS ONE, Brain and Neurology.

In The Last Decade

Anne Noreau

22 papers receiving 808 citations

Peers

Anne Noreau
Noam D. Rudnick United States
Ione Woollacott United Kingdom
Michael P. Hart United States
Weirui Guo United States
Mark R. Pitzer United States
Anne Noreau
Citations per year, relative to Anne Noreau Anne Noreau (= 1×) peers Kathrin Müller

Countries citing papers authored by Anne Noreau

Since Specialization
Citations

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

Fields of papers citing papers by Anne Noreau

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Anne Noreau

This figure shows the co-authorship network connecting the top 25 collaborators of Anne Noreau. A scholar is included among the top collaborators of Anne Noreau 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 Anne Noreau. Anne Noreau 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
2.
Girard, Simon, Cynthia V. Bourassa, Louis‐Philippe Lemieux Perreault, et al.. (2016). Paternal Age Explains a Major Portion of De Novo Germline Mutation Rate Variability in Healthy Individuals. PLoS ONE. 11(10). e0164212–e0164212. 32 indexed citations
3.
Gan‐Or, Ziv, Anne Noreau, Claire S. Leblond, et al.. (2015). Parkinson’s Disease Genetic Loci in Rapid Eye Movement Sleep Behavior Disorder. Journal of Molecular Neuroscience. 56(3). 617–622. 40 indexed citations
4.
Noreau, Anne, Roberta La Piana, Patrick A. Dion, et al.. (2015). Novel SIL1 mutations cause cerebellar ataxia and atrophy in a French-Canadian family. Neurogenetics. 16(4). 315–318. 6 indexed citations
5.
Kaneb, Hannah, Andrew W. Folkmann, Véronique Belzil, et al.. (2014). Deleterious mutations in the essential mRNA metabolism factor, hGle1, in amyotrophic lateral sclerosis. Human Molecular Genetics. 24(5). 1363–1373. 101 indexed citations
7.
Habak, Claudine, Anne Noreau, Atsuko Nagano‐Saito, et al.. (2014). Dopamine transporter SLC6A3 genotype affects cortico-striatal activity of set-shifts in Parkinson’s disease. Brain. 137(11). 3025–3035. 27 indexed citations
8.
Noreau, Anne, Patrick A. Dion, & Guy A. Rouleau. (2014). Molecular aspects of hereditary spastic paraplegia. Experimental Cell Research. 325(1). 18–26. 41 indexed citations
9.
Noreau, Anne, et al.. (2014). Therapies for Ataxias. Current Treatment Options in Neurology. 16(7). 300–300. 4 indexed citations
10.
Noreau, Anne, Cynthia V. Bourassa, Anna Szuto, et al.. (2013). SYNE1Mutations in Autosomal Recessive Cerebellar Ataxia. JAMA Neurology. 70(10). 1296–31. 45 indexed citations
11.
Daoud, Hussein, Anne Noreau, Daniel Rochefort, et al.. (2012). Investigation of C9orf72 repeat expansions in Parkinson's disease. Neurobiology of Aging. 34(6). 1710.e7–1710.e9. 18 indexed citations
12.
Noreau, Anne, Patrick A. Dion, Anna Szuto, et al.. (2012). CYP7B1 Mutations in French-Canadian Hereditary Spastic Paraplegia Subjects. Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques. 39(1). 91–94. 1 indexed citations
13.
Noreau, Anne, Nicolas Dupré, Jean‐Pierre Bouchard, Patrick A. Dion, & Guy A. Rouleau. (2012). Autosomal Recessive Cerebellar Ataxias. 2177–2191. 2 indexed citations
14.
Daoud, Hussein, Sirui Zhou, Anne Noreau, et al.. (2011). Exome sequencing reveals SPG11 mutations causing juvenile ALS. Neurobiology of Aging. 33(4). 839.e5–839.e9. 74 indexed citations
15.
Noreau, Anne, Franco Leporé, Michel Boivin, et al.. (2011). Early influence of the rs4675690 on the neural substrates of sadness. Journal of Affective Disorders. 135(1-3). 336–340. 8 indexed citations
16.
Catoire, Hélène, Patrick A. Dion, Lan Xiong, et al.. (2011). Restless legs syndrome‐associated MEIS1 risk variant influences iron homeostasis. Annals of Neurology. 70(1). 170–175. 64 indexed citations
17.
Noreau, Anne, Jean‐Baptiste Rivière, Sabrina Diab, et al.. (2011). Glucocerebrosidase Mutations in a French-Canadian Parkinson's Disease Cohort. Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques. 38(5). 772–773. 14 indexed citations
18.
Noreau, Anne, Franco Leporé, Michel Boivin, et al.. (2010). Early impact of 5-HTTLPR polymorphism on the neural correlates of sadness. Neuroscience Letters. 485(3). 261–265. 23 indexed citations
19.
Hamdan, Fadi F., Amélie Piton, Julie Gauthier, et al.. (2009). De novo STXBP1 mutations in mental retardation and nonsyndromic epilepsy. Annals of Neurology. 65(6). 748–753. 108 indexed citations
20.
Belzil, Véronique, Paul N. Valdmanis, Patrick A. Dion, et al.. (2009). Mutations in FUS cause FALS and SALS in French and French Canadian populations. Neurology. 73(15). 1176–1179. 114 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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