Guy A. Rouleau

1.4k total citations
36 papers, 835 citations indexed

About

Guy A. Rouleau is a scholar working on Molecular Biology, Neurology and Genetics. According to data from OpenAlex, Guy A. Rouleau has authored 36 papers receiving a total of 835 indexed citations (citations by other indexed papers that have themselves been cited), including 19 papers in Molecular Biology, 9 papers in Neurology and 9 papers in Genetics. Recurrent topics in Guy A. Rouleau's work include Neurogenetic and Muscular Disorders Research (6 papers), Genetics and Neurodevelopmental Disorders (6 papers) and Genetic Neurodegenerative Diseases (5 papers). Guy A. Rouleau is often cited by papers focused on Neurogenetic and Muscular Disorders Research (6 papers), Genetics and Neurodevelopmental Disorders (6 papers) and Genetic Neurodegenerative Diseases (5 papers). Guy A. Rouleau collaborates with scholars based in Canada, United States and France. Guy A. Rouleau's co-authors include Denise A. Figlewicz, Zoha Kibar, Fei‐Yu Han, Karen Rooke, Jaime O. Claudio, Stylianos E. Antonarakis, Uppala Radhakrishna, C Blanchet‐Bardon, David P. Kelsell and Jonathan Zonana and has published in prestigious journals such as Nucleic Acids Research, Nature Genetics and Neurology.

In The Last Decade

Guy A. Rouleau

35 papers receiving 809 citations

Peers

Guy A. Rouleau

NEURO

CMN

GENET

EPIDE

A.C. Bird United Kingdom

John Wolff United States

Toshika Ohkawa Japan

Félix Prieto Spain

Seher Başaran Türkiye

Jessica A. Panzer United States

Robert B. Hufnagel United States

Cassandre Labelle‐Dumais United States

Jacob Husseman United States

Tuomas Klockars Finland

A.C. Bird United Kingdom

Guy A. Rouleau

557 ×1.3

113 ×0.4

NEURO

106 ×0.7

CMN

114 ×0.8

GENET

89 ×0.9

EPIDE

Citations per year, relative to Guy A. Rouleau Guy A. Rouleau (= 1×) peers A.C. Bird

Countries citing papers authored by Guy A. Rouleau

Since Specialization

Citations

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

Fields of papers citing papers by Guy A. Rouleau

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Guy A. Rouleau. 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 Guy A. Rouleau. The network helps show where Guy A. Rouleau may publish in the future.

Co-authorship network of co-authors of Guy A. Rouleau

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

All Works

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20 of 20 papers shown

Liu, Yumin, Calwing Liao, Daniel Rochefort, et al.. (2025). Lithium partially rescues gene expression and enhancer activity from heterozygous knockout of AKAP11 while inducing novel differential changes. Scientific Reports. 15(1). 37844–37844.

Zhang, Issan, Dušica Maysinger, Martina Perić Bakulić, et al.. (2024). Gold nanoclusters Au ₂₅ AcCys ₁₈ normalize intracellular ROS without increasing cytoplasmic alarmin acHMGB1 abundance in human microglia and neurons. Nanoscale. 17(2). 1092–1104. 1 indexed citations

Ross, Jay P., Nicolas Dupré, Yves Dauvilliers, et al.. (2017). RIC3 variants are not associated with Parkinson's disease in French-Canadians and French. Neurobiology of Aging. 53. 194.e9–194.e11. 8 indexed citations

Rouleau, Guy A., et al.. (2001). Comparative Genomic Analysis of Genes Encoding Translation Elongation Factor 1Bα in Human and Mouse Shows EEF1B1 to Be a Recent Retrotransposition Event. Genomics. 77(3). 145–148. 11 indexed citations

Legoix, Patricia, Sophie Giraud, Frédéric Sor, et al.. (2000). Molecular Characterization of Germline NF2 Gene Rearrangements. Genomics. 65(1). 62–66. 14 indexed citations

Joober, Ridha, Mehrdad Jannatipour, Gustavo Turecki, et al.. (1999). Polyglutamine-containing proteins in schizophrenia. Molecular Psychiatry. 4(1). 53–57. 19 indexed citations

Kibar, Zoha, Ronald G. Lafrenière, Jia‐Chi Wang, et al.. (1999). A Radiation Hybrid Map of 48 Loci Including the Clouston Hidrotic Ectodermal Dysplasia Locus in the Pericentromeric Region of Chromosome 13q. Genomics. 56(1). 127–130. 21 indexed citations

Nechiporuk, Alex, Íscia Lopes‐Cendes, Tamilla Nechiporuk, et al.. (1996). Genetic mapping of the spinocerebellar ataxia type 2 gene on human chromosome 12. Neurology. 46(6). 1731–1735. 20 indexed citations

Melanson, Michel, Colin Chalk, Yves Lapierre, et al.. (1996). Varicella-zoster virus DNA in CSF and arteries in delayed contralateral hemiplegia. Neurology. 47(2). 569–570. 61 indexed citations

10.

Lopes‐Cendes, Íscia, Isabel Silveira, Patrı́cia Maciel, et al.. (1996). Limits of Clinical Assessment in the Accurate Diagnosis of Machado-Joseph Disease. Archives of Neurology. 53(11). 1168–1174. 20 indexed citations

11.

Garofalo, O., Denise A. Figlewicz, S.M. Thomas, et al.. (1995). Superoxide dismutase activity in lymphoblastoid cells from motor neurone disease/amyotrophic lateral sclerosis (MND/ALS) patients. Journal of the Neurological Sciences. 129. 90–92. 10 indexed citations

12.

Claudio, Jaime O., Mohini Lutchman, & Guy A. Rouleau. (1995). Widespread but cell type-specific expression of the mouse neurofibromatosis type 2 gene. Neuroreport. 6(14). 1942–1946. 31 indexed citations

13.

Giannoukakis, Nick, Guy A. Rouleau, & Constantin Polychronakos. (1994). Tissue specificity and variability of imprinted IGF2 expression in humans. The American Journal of Human Genetics. 55. 1 indexed citations

14.

Figlewicz, Denise A., Marie‐Pierre Dubé, & Guy A. Rouleau. (1994). Autosomal dominant familial spastic paraplegia; Linkage analysis and evidence for linkage to chromosome 2p. The American Journal of Human Genetics. 55. 4 indexed citations

15.

Lopes‐Cendes, Íscia, Eva Andermann, & Guy A. Rouleau. (1994). Evidence for the Existence of a Fourth Dominantly Inherited Spinocerebellar Ataxia Locus. Genomics. 21(1). 270–274. 11 indexed citations

16.

Figlewicz, Denise A., Ralph M. Garruto, Aldis Krizus, Richard Yanagihara, & Guy A. Rouleau. (1994). The Cu/Zn superoxide dismutase gene in ALS and Parkinsonism-dementia of Guam. Neuroreport. 5(5). 557–560. 25 indexed citations

17.

Cochius, Jeffrey I., Denise A. Figlewicz, Reetta Kälviäinen, et al.. (1993). Unverricht‐Lundborg disease: Absence of nonallelic genetic heterogeneity. Annals of Neurology. 34(5). 739–741. 5 indexed citations

18.

Nishisho, Isamu, Masayuki Yamamoto, Akihiro Miya, et al.. (1992). Loss of heterozygosity on the long arm of chromosome 22 in pheochromocytoma. Genes Chromosomes and Cancer. 5(4). 399–403. 34 indexed citations

19.

Goto, Jun, et al.. (1992). Dinucleotide repeat polymorphism at the D21S219 locus which flanks the GARS-AIRS-GART gene. Human Molecular Genetics. 1(9). 782–782. 2 indexed citations

20.

Goto, Jun, et al.. (1991). A Pvull RFLP at the HOX 1.4 homeobox locus (HOX1D). Nucleic Acids Research. 19(13). 3755–3755. 1 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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