Jay P. Ross

1.9k total citations
39 papers, 653 citations indexed

About

Jay P. Ross is a scholar working on Neurology, Genetics and Molecular Biology. According to data from OpenAlex, Jay P. Ross has authored 39 papers receiving a total of 653 indexed citations (citations by other indexed papers that have themselves been cited), including 20 papers in Neurology, 9 papers in Genetics and 8 papers in Molecular Biology. Recurrent topics in Jay P. Ross's work include Parkinson's Disease Mechanisms and Treatments (11 papers), Neurogenetic and Muscular Disorders Research (9 papers) and Amyotrophic Lateral Sclerosis Research (9 papers). Jay P. Ross is often cited by papers focused on Parkinson's Disease Mechanisms and Treatments (11 papers), Neurogenetic and Muscular Disorders Research (9 papers) and Amyotrophic Lateral Sclerosis Research (9 papers). Jay P. Ross collaborates with scholars based in Canada, United States and France. Jay P. Ross's co-authors include Patrick A. Dion, Guy A. Rouleau, Carles Vilariño‐Güell, Cecily Q. Bernales, W. D. Kitts, A. Dessa Sadovnick, Anthony Traboulsee, Ziv Gan‐Or, Mary Joy Encarnacion and Calwing Liao and has published in prestigious journals such as Neuron, PLoS ONE and Annals of Neurology.

In The Last Decade

Jay P. Ross

38 papers receiving 631 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Jay P. Ross Canada 15 241 226 111 105 97 39 653
Rebecca Bounds United States 13 197 0.8× 260 1.2× 129 1.2× 94 0.9× 81 0.8× 18 665
Hanna Mierzewska Poland 15 98 0.4× 444 2.0× 105 0.9× 127 1.2× 82 0.8× 57 728
Daniela Sinske Germany 12 115 0.5× 310 1.4× 155 1.4× 34 0.3× 53 0.5× 17 550
Ekaterina Zakharova Russia 16 217 0.9× 311 1.4× 93 0.8× 111 1.1× 439 4.5× 128 962
Jonathan A. Fidler United States 14 202 0.8× 230 1.0× 91 0.8× 108 1.0× 230 2.4× 15 651
Serena Rosner Israel 12 331 1.4× 194 0.9× 107 1.0× 88 0.8× 257 2.6× 12 677
Sarah Camargos Brazil 14 452 1.9× 167 0.7× 269 2.4× 75 0.7× 72 0.7× 51 712
Lemuel Racacho Canada 14 192 0.8× 262 1.2× 164 1.5× 116 1.1× 66 0.7× 18 547
Anita Y. Bahar Australia 11 162 0.7× 160 0.7× 211 1.9× 63 0.6× 74 0.8× 13 763
Phyllis Bieri United States 9 155 0.6× 305 1.3× 243 2.2× 38 0.4× 84 0.9× 13 780

Countries citing papers authored by Jay P. Ross

Since Specialization
Citations

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

Fields of papers citing papers by Jay P. Ross

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Jay P. Ross. 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 Jay P. Ross. The network helps show where Jay P. Ross may publish in the future.

Co-authorship network of co-authors of Jay P. Ross

This figure shows the co-authorship network connecting the top 25 collaborators of Jay P. Ross. A scholar is included among the top collaborators of Jay P. Ross 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 Jay P. Ross. Jay P. Ross 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.
Akçimen, Fulya, Ruth Chia, Sara Sáez-Atiénzar, et al.. (2024). Genomic Analysis Identifies Risk Factors in Restless Legs Syndrome. Annals of Neurology. 96(5). 994–1005. 2 indexed citations
2.
Ross, Jay P., Fulya Akçimen, Calwing Liao, et al.. (2023). Rare-variant and polygenic analyses of amyotrophic lateral sclerosis in the French-Canadian genome. Genetics in Medicine. 26(1). 100967–100967. 1 indexed citations
3.
Ross, Jay P., Fulya Akçimen, Calwing Liao, et al.. (2022). Questioning the Association of the STMN2 Dinucleotide Repeat With Amyotrophic Lateral Sclerosis. Neurology Genetics. 8(4). e678–e678. 1 indexed citations
4.
Liao, Calwing, Anouar Khayachi, Yumin Liu, et al.. (2022). Transcriptomic effects of propranolol and primidone converge on molecular pathways relevant to essential tremor. npj Genomic Medicine. 7(1). 46–46. 9 indexed citations
5.
Liao, Calwing, Hélène Catoire, Fulya Akçimen, et al.. (2022). Transcriptome-wide association study reveals increased neuronal FLT3 expression is associated with Tourette’s syndrome. Communications Biology. 5(1). 289–289. 10 indexed citations
6.
Senkevich, Konstantin, et al.. (2022). Investigation of the causal relationship between ALS and autoimmune disorders: a Mendelian randomization study. BMC Medicine. 20(1). 382–382. 12 indexed citations
7.
Estiar, Mehrdad A., Eric Yu, Jay P. Ross, et al.. (2021). Evidence for Non‐Mendelian Inheritance in Spastic Paraplegia 7. Movement Disorders. 36(7). 1664–1675. 14 indexed citations
8.
Knox, R. E., Yuefeng Ruan, María Antonia Henríquez, et al.. (2020). Historic recombination in a durum wheat breeding panel enables high-resolution mapping of Fusarium head blight resistance quantitative trait loci. Scientific Reports. 10(1). 7567–7567. 12 indexed citations
9.
Akçimen, Fulya, Jay P. Ross, Calwing Liao, et al.. (2019). Genetic and epidemiological characterization of restless legs syndrome in Québec. SLEEP. 43(4). 8 indexed citations
10.
Spataro, Rossella, Maria Kousi, Sali M.K. Farhan, et al.. (2019). Mutations in ATP13A2 (PARK9) are associated with an amyotrophic lateral sclerosis-like phenotype, implicating this locus in further phenotypic expansion. Human Genomics. 13(1). 19–19. 34 indexed citations
11.
Dionne‐Laporte, Alexandre, Hélène Catoire, Daniel Rochefort, et al.. (2019). Mineral absorption is an enriched pathway in a brain region of restless legs syndrome patients with reduced MEIS1 expression. PLoS ONE. 14(11). e0225186–e0225186. 9 indexed citations
12.
Akçimen, Fulya, Jay P. Ross, Cynthia V. Bourassa, et al.. (2019). Investigation of the RFC1 Repeat Expansion in a Canadian and a Brazilian Ataxia Cohort: Identification of Novel Conformations. Frontiers in Genetics. 10. 1219–1219. 45 indexed citations
13.
Ross, Jay P., Etienne Léveillé, Lan Xiong, et al.. (2018). Association study of essential tremor genetic loci in Parkinson's disease. Neurobiology of Aging. 66. 178.e13–178.e15. 7 indexed citations
14.
Zhou, Sirui, Ziv Gan‐Or, Amirthagowri Ambalavanan, et al.. (2018). Genome-wide association analysis identifies new candidate risk loci for familial intracranial aneurysm in the French-Canadian population. Scientific Reports. 8(1). 4356–4356. 10 indexed citations
15.
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
16.
Ross, Jay P., Nicolas Dupré, Yves Dauvilliers, et al.. (2016). Analysis of DNAJC13 mutations in French-Canadian/French cohort of Parkinson's disease. Neurobiology of Aging. 45. 212.e13–212.e17. 28 indexed citations
17.
Wang, Zhe, A. Dessa Sadovnick, Anthony Traboulsee, et al.. (2016). Case-Control Studies Are Not Familial Studies. Neuron. 92(2). 339–341. 6 indexed citations
18.
Wang, Zhe, A. Dessa Sadovnick, Anthony Traboulsee, et al.. (2016). Nuclear Receptor NR1H3 in Familial Multiple Sclerosis. Neuron. 90(5). 948–954. 65 indexed citations
19.
Rajput, Alex, Jay P. Ross, Cecily Q. Bernales, et al.. (2014). VPS35 and DNAJC13 disease-causing variants in essential tremor. European Journal of Human Genetics. 23(6). 887–888. 23 indexed citations
20.
Ross, Jay P., Sruti Rayaprolu, Cecily Q. Bernales, et al.. (2013). SLC1A2 rs3794087 does not associate with essential tremor. Neurobiology of Aging. 35(4). 935.e9–935.e10. 17 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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