Judith St‐Onge

5.0k total citations
32 papers, 1.3k citations indexed

About

Judith St‐Onge is a scholar working on Genetics, Molecular Biology and Neurology. According to data from OpenAlex, Judith St‐Onge has authored 32 papers receiving a total of 1.3k indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Genetics, 14 papers in Molecular Biology and 11 papers in Neurology. Recurrent topics in Judith St‐Onge's work include Parkinson's Disease Mechanisms and Treatments (7 papers), Restless Legs Syndrome Research (7 papers) and Genetics and Neurodevelopmental Disorders (7 papers). Judith St‐Onge is often cited by papers focused on Parkinson's Disease Mechanisms and Treatments (7 papers), Restless Legs Syndrome Research (7 papers) and Genetics and Neurodevelopmental Disorders (7 papers). Judith St‐Onge collaborates with scholars based in Canada, France and United States. Judith St‐Onge's co-authors include Guy A. Rouleau, Jean‐Baptiste Rivière, Sandra B. Laurent, Ridha Joober, Julie Gauthier, Laurent Mottron, Éric Fombonne, Lan Xiong, Аnastasia Levchenko and Ronald G. Lafrenière and has published in prestigious journals such as Brain, Neurology and Diabetes Care.

In The Last Decade

Judith St‐Onge

31 papers receiving 1.2k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Judith St‐Onge Canada 17 581 534 379 286 246 32 1.3k
Kiran K. Mantripragada United Kingdom 22 853 1.5× 773 1.4× 274 0.7× 304 1.1× 104 0.4× 41 1.8k
Alessandra Murgia Italy 23 638 1.1× 724 1.4× 254 0.7× 114 0.4× 74 0.3× 76 1.6k
Maria T. Acosta United States 20 253 0.4× 386 0.7× 333 0.9× 403 1.4× 174 0.7× 63 1.3k
Chiara Pantaleoni Italy 24 335 0.6× 496 0.9× 221 0.6× 188 0.7× 82 0.3× 84 1.5k
Atle Melberg Sweden 25 239 0.4× 1.4k 2.6× 323 0.9× 285 1.0× 121 0.5× 44 2.1k
Jeff M. Milunsky United States 22 822 1.4× 704 1.3× 252 0.7× 85 0.3× 50 0.2× 70 1.7k
Dawna D. Armstrong United States 21 754 1.3× 730 1.4× 510 1.3× 87 0.3× 49 0.2× 33 1.6k
Erwin Petek Austria 21 469 0.8× 669 1.3× 229 0.6× 77 0.3× 88 0.4× 60 1.5k
Jean‐Baptiste Rivière Canada 18 575 1.0× 591 1.1× 101 0.3× 98 0.3× 85 0.3× 36 1.2k
Anthony J. Griswold United States 18 350 0.6× 651 1.2× 236 0.6× 63 0.2× 101 0.4× 75 1.4k

Countries citing papers authored by Judith St‐Onge

Since Specialization
Citations

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

Fields of papers citing papers by Judith St‐Onge

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Judith St‐Onge. 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 Judith St‐Onge. The network helps show where Judith St‐Onge may publish in the future.

Co-authorship network of co-authors of Judith St‐Onge

This figure shows the co-authorship network connecting the top 25 collaborators of Judith St‐Onge. A scholar is included among the top collaborators of Judith St‐Onge 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 Judith St‐Onge. Judith St‐Onge 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.
St‐Onge, Judith, Ahmed N. Sahly, Kenneth A. Myers, et al.. (2024). Defining the Genetic Landscape of Congenital Mirror Movements in 80 Affected Individuals. Movement Disorders. 39(2). 400–410. 8 indexed citations
2.
Accogli, Andrea, Laura Russell, Guillaume Sébire, et al.. (2019). Pathogenic variants in AIMP1 cause pontocerebellar hypoplasia. Neurogenetics. 20(2). 103–108. 13 indexed citations
3.
Kuentz, Paul, Yannis Duffourd, Judith St‐Onge, et al.. (2016). 186 Mutational spectrum in PIK3CA -Related Overgrowth Spectrum (PROS) and recommendations for molecular testing. Journal of Investigative Dermatology. 136(9). S192–S192. 1 indexed citations
4.
Thévenon, Julien, Laurence Duplomb, Shubha R. Phadke, et al.. (2016). Autosomal recessive IFT57 hypomorphic mutation cause ciliary transport defect in unclassified oral–facial–digital syndrome with short stature and brachymesophalangia. Clinical Genetics. 90(6). 509–517. 18 indexed citations
5.
Jansen, Laura A., Ghayda Mirzaa, Gisele E. Ishak, et al.. (2015). PI3K/AKT pathway mutations cause a spectrum of brain malformations from megalencephaly to focal cortical dysplasia. Brain. 138(6). 1613–1628. 237 indexed citations
6.
Gueneau, Lucie, Laurence Duplomb, Pierre Sarda, et al.. (2013). Congenital neutropenia with retinopathy, a new phenotype without intellectual deficiency or obesity secondary to VPS13B mutations. American Journal of Medical Genetics Part A. 164(2). 522–527. 11 indexed citations
7.
Belzil, Véronique, Hussein Daoud, Judith St‐Onge, et al.. (2011). Identification of novelFUSmutations in sporadic cases of amyotrophic lateral sclerosis. Amyotrophic Lateral Sclerosis. 12(2). 113–117. 25 indexed citations
8.
Belzil, Véronique, Judith St‐Onge, Hussein Daoud, et al.. (2010). Identification of a FUS splicing mutation in a large family with amyotrophic lateral sclerosis. Journal of Human Genetics. 56(3). 247–249. 17 indexed citations
9.
Rivière, Jean‐Baptiste, Judith St‐Onge, Cláudia Gaspar, et al.. (2010). Genome-Wide TDT Analysis in French-Canadian Families with Tourette Syndrome. Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques. 37(1). 110–112. 3 indexed citations
10.
Valdmanis, Paul N., Véronique Belzil, Patrick A. Dion, et al.. (2009). A Mutation that Creates a Pseudoexon in SOD1 Causes Familial ALS. Annals of Human Genetics. 73(6). 652–657. 31 indexed citations
11.
Gauthier, Julie, Dan Spiegelman, Amélie Piton, et al.. (2008). Novel de novo SHANK3 mutation in autistic patients. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 150B(3). 421–424. 245 indexed citations
12.
Levchenko, Аnastasia, Géraldine Asselin, Sylvie Provost, et al.. (2008). Autosomal‐dominant locus for restless legs syndrome in French‐Canadians on chromosome 16p12.1. Movement Disorders. 24(1). 40–50. 36 indexed citations
13.
Meijer, Inge A., Nicolas Dupré, Bernard Brais, et al.. (2007). SPG4 Founder Effect in French Canadians with Hereditary Spastic Paraplegia. Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques. 34(2). 211–214. 5 indexed citations
14.
Xiong, Lan, Аnastasia Levchenko, Jacques Montplaisir, et al.. (2007). Genetic association studies of neurotensin gene and restless legs syndrome in French Canadians. Sleep Medicine. 9(3). 273–282. 4 indexed citations
15.
Xiong, Lan, Patrick A. Dion, Jacques Montplaisir, et al.. (2007). Molecular genetic studies ofDMT1on 12q in French‐Canadian restless legs syndrome patients and families. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 144B(7). 911–917. 20 indexed citations
16.
Valdmanis, Paul N., et al.. (2006). A founder haplotype for autosomal dominant sensory ataxia in Eastern Canada. Neurology. 67(12). 2239–2242. 7 indexed citations
17.
Gauthier, J, Ridha Joober, Marie‐Pierre Dubé, et al.. (2005). Autism spectrum disorders associated with X chromosome markers in French-Canadian males. Molecular Psychiatry. 11(2). 206–213. 11 indexed citations
18.
Levchenko, Аnastasia, Marie‐Pierre Dubé, Jean‐Baptiste Rivière, et al.. (2004). The 14q restless legs syndrome locus in the French Canadian population. Annals of Neurology. 55(6). 887–891. 56 indexed citations
19.
Xiong, Lan, Guy A. Rouleau, Lynn E. DeLisi, et al.. (2004). CAA insertion polymorphism in the 3′UTR of Nogo gene on 2p14 is not associated with schizophrenia. Molecular Brain Research. 133(1). 153–156. 10 indexed citations
20.
Gauthier, Julie, Anna Bonnel, Judith St‐Onge, et al.. (2004). NLGN3/NLGN4 gene mutations are not responsible for autism in the Quebec population. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 132B(1). 74–75. 90 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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