John D. Rioux

72.6k total citations · 2 hit papers
163 papers, 10.9k citations indexed

About

John D. Rioux is a scholar working on Genetics, Immunology and Molecular Biology. According to data from OpenAlex, John D. Rioux has authored 163 papers receiving a total of 10.9k indexed citations (citations by other indexed papers that have themselves been cited), including 78 papers in Genetics, 75 papers in Immunology and 41 papers in Molecular Biology. Recurrent topics in John D. Rioux's work include Inflammatory Bowel Disease (54 papers), T-cell and B-cell Immunology (27 papers) and Helicobacter pylori-related gastroenterology studies (22 papers). John D. Rioux is often cited by papers focused on Inflammatory Bowel Disease (54 papers), T-cell and B-cell Immunology (27 papers) and Helicobacter pylori-related gastroenterology studies (22 papers). John D. Rioux collaborates with scholars based in Canada, United States and United Kingdom. John D. Rioux's co-authors include Mark J. Daly, Eric S. Lander, Thomas J. Hudson, S. F. Schaffner, Philippe Goyette, Ramnik J. Xavier, Timothy J. Vyse, Guillaume Lettre, Philip L. De Jager and Alan Huett and has published in prestigious journals such as Nature, Science and Cell.

In The Last Decade

John D. Rioux

160 papers receiving 10.6k citations

Hit Papers

High-resolution haplotype structure in the human genome 2001 2026 2009 2017 2001 2015 400 800 1.2k

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
John D. Rioux Canada 52 4.5k 4.0k 3.4k 1.7k 1.5k 163 10.9k
Judy H. Cho United States 47 6.2k 1.4× 4.3k 1.1× 3.4k 1.0× 3.1k 1.9× 574 0.4× 170 12.3k
Flemming Pociot Denmark 61 7.2k 1.6× 4.5k 1.1× 4.6k 1.4× 1.6k 1.0× 840 0.5× 326 16.2k
Heather J. Cordell United Kingdom 49 5.0k 1.1× 1.7k 0.4× 3.1k 0.9× 1.3k 0.8× 785 0.5× 186 10.8k
Daniël W. Hommes Netherlands 58 5.5k 1.2× 2.9k 0.7× 2.8k 0.8× 3.7k 2.3× 579 0.4× 217 12.6k
Raja Atreya Germany 48 3.7k 0.8× 3.3k 0.8× 1.9k 0.6× 2.0k 1.2× 424 0.3× 269 8.8k
Susanna Nikolaus Germany 40 4.0k 0.9× 2.4k 0.6× 2.4k 0.7× 2.0k 1.2× 349 0.2× 96 8.1k
Jochen Hampe Germany 61 4.7k 1.0× 3.2k 0.8× 3.8k 1.1× 3.8k 2.3× 430 0.3× 285 13.3k
F. Susan Wong United Kingdom 55 4.6k 1.0× 4.8k 1.2× 3.0k 0.9× 900 0.5× 287 0.2× 220 11.0k
Patrick Concannon United States 60 6.0k 1.4× 3.9k 1.0× 7.6k 2.3× 954 0.6× 513 0.3× 228 15.8k
Irving H. Fox United States 45 5.9k 1.3× 2.6k 0.6× 3.5k 1.0× 5.9k 3.6× 769 0.5× 194 12.1k

Countries citing papers authored by John D. Rioux

Since Specialization
Citations

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

Fields of papers citing papers by John D. Rioux

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by John D. Rioux. 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 John D. Rioux. The network helps show where John D. Rioux may publish in the future.

Co-authorship network of co-authors of John D. Rioux

This figure shows the co-authorship network connecting the top 25 collaborators of John D. Rioux. A scholar is included among the top collaborators of John D. Rioux 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 John D. Rioux. John D. Rioux 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.
Nayeri, Shadi, Jiayi Ji, Cristian Hernández-Rocha, et al.. (2021). A Role for CXCR3 Ligands as Biomarkers of Post-Operative Crohn’s Disease Recurrence. Journal of Crohn s and Colitis. 16(6). 900–910. 15 indexed citations
2.
Stevens, Christine, Kai Yuan, Aleksejs Sazonovs, et al.. (2021). 778 EXOME SEQUENCING IN 30,000 CASES DEFINES NOVEL RISK FACTORS FOR CROHN'S DISEASE. Gastroenterology. 160(6). S–156. 1 indexed citations
3.
Webster, Gregory, Elhadi H. Aburawi, Marie Chaix, et al.. (2020). Life-threatening arrhythmias with autosomal recessive TECRL variants. EP Europace. 23(5). 781–788. 18 indexed citations
4.
Moayyedi, Paul, Glenda MacQueen, Çharles N. Bernstein, et al.. (2020). IMAGINE Network’s Mind And Gut Interactions Cohort (MAGIC) Study: a protocol for a prospective observational multicentre cohort study in inflammatory bowel disease and irritable bowel syndrome. BMJ Open. 10(10). e041733–e041733. 11 indexed citations
5.
Mitchell, Rebecca, Foram N. Ashar, Marjo‐Riitta Järvelin, et al.. (2019). Effect of Sex and Underlying Disease on the Genetic Association of QT Interval and Sudden Cardiac Death. Journal of the American Heart Association. 8(23). e013751–e013751. 8 indexed citations
6.
MacDonald, Katherine N., Anne M. Pesenacker, S. Juvet, et al.. (2019). Innate Control of Tissue-Reparative Human Regulatory T Cells. The Journal of Immunology. 202(8). 2195–2209. 36 indexed citations
7.
Veilleux, Sophie, et al.. (2019). Inflammatory bowel disease patient perceptions of diagnostic and monitoring tests and procedures. BMC Gastroenterology. 19(1). 30–30. 25 indexed citations
8.
Mohanan, Vishnu, Toru Nakata, A. Nicole Desch, et al.. (2018). C1orf106 is a colitis risk gene that regulates stability of epithelial adherens junctions. Science. 359(6380). 1161–1166. 78 indexed citations
9.
Chaix, Marie, Tamara T. Koopmann, Philippe Goyette, et al.. (2016). Novel CALM3 mutations in pediatric long QT syndrome patients support a CALM3-specific calmodulinopathy. HeartRhythm Case Reports. 2(3). 250–254. 19 indexed citations
10.
Bentham, James, David Morris, Deborah S. Cunninghame Graham, et al.. (2015). Genetic association analyses implicate aberrant regulation of innate and adaptive immunity genes in the pathogenesis of systemic lupus erythematosus. Nature Genetics. 47(12). 1457–1464. 600 indexed citations breakdown →
11.
Lefebvre, Christine, et al.. (2012). Evaluation of Toll‐like receptor and adaptor molecule polymorphisms for susceptibility to tuberculosis in a Colombian population. International Journal of Immunogenetics. 39(3). 216–223. 47 indexed citations
12.
Festen, Eleonora A., Philippe Goyette, Todd J. Green, et al.. (2011). A Meta-Analysis of Genome-Wide Association Scans Identifies IL18RAP, PTPN2, TAGAP, and PUS10 As Shared Risk Loci for Crohn's Disease and Celiac Disease. PLoS Genetics. 7(1). e1001283–e1001283. 162 indexed citations
13.
Jager, Philip L. De, KG Simon, Kassandra L. Munger, et al.. (2008). Integrating risk factors. Neurology. 70(13_part_2). 1113–1118. 134 indexed citations
14.
Kuballa, Petric, Alan Huett, John D. Rioux, Mark J. Daly, & Ramnik J. Xavier. (2008). Impaired Autophagy of an Intracellular Pathogen Induced by a Crohn's Disease Associated ATG16L1 Variant. PLoS ONE. 3(10). e3391–e3391. 249 indexed citations
15.
Rigby, Robert J., et al.. (2006). Interferon-inducibile genes on chromosome 1 contribute to lupus susceptibility. Lara D. Veeken. 45. 1 indexed citations
16.
Giallourakis, Cosmas, Zhifang Cao, Todd J. Green, et al.. (2006). A molecular-properties-based approach to understanding PDZ domain proteins and PDZ ligands. Genome Research. 16(8). 1056–1072. 43 indexed citations
17.
Jager, Philip L. De, Robert Graham, Lisa Farwell, et al.. (2006). The role of inflammatory bowel disease susceptibility loci in multiple sclerosis and systemic lupus erythematosus. Genes and Immunity. 7(4). 327–334. 29 indexed citations
18.
Heel, David A. van, Sheila Fisher, Andrew Kirby, et al.. (2004). Inflammatory bowel disease susceptibility loci defined by genome scan meta-analysis of 1952 affected relative pairs. Human Molecular Genetics. 13(7). 763–770. 184 indexed citations
19.
Mootha, Vamsi K., Patricia Lepage, Kathleen A. Miller, et al.. (2003). Identification of a gene causing human cytochrome c oxidase deficiency by integrative genomics. Proceedings of the National Academy of Sciences. 100(2). 605–610. 452 indexed citations
20.
Richter, Andréa, John D. Rioux, Jean‐Pierre Bouchard, et al.. (1999). Location Score and Haplotype Analyses of the Locus for Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay, in Chromosome Region 13q11. The American Journal of Human Genetics. 64(3). 768–775. 61 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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