Mathieu Lemire
Impact in
- Cancer Research top 2%
- Cancer Genomics and Diagnostics
-
- Genetic factors in colorectal cancer
Papers in
- Genetics 43
- Genetic Associations and Epidemiology 33
- Genetic and phenotypic traits in livestock 6
- Genetic Syndromes and Imprinting 6
-
- Genetic factors in colorectal cancer 16
- Co-authors
- Thomas Jay Hudson (24 shared papers)Brent W. Zanke (5 shared papers)Steven N. Gallinger (3 shared papers)Darci T. Butcher (2 shared papers)Rosanna Weksberg (2 shared papers)Sanaa Choufani (1 shared paper)Daria Grafodatskaya (1 shared paper)Y. Ann Chen (1 shared paper)
- Journals
- PLoS ONE (7 papers)Gastroenterology (6 papers)Cancer Epidemiology Biomarkers & Prevention (4 papers)Nature Genetics (4 papers)Nature Communications (4 papers)
- Partner nations
- CanadaUnited StatesGermany
In The Last Decade
Mathieu Lemire
96 papers receiving 8.2k citations
Mathieu Lemire's Hit Papers
Peers
Comparison fields: 5 of 140
- Cancer Research 1.2k
- Pathology and Forensic Medicine 1.1k
- Genetics 1.8k
- Oncology 1.6k
- Molecular Biology 3.3k
Countries citing papers authored by Mathieu Lemire
This map shows the geographic impact of Mathieu Lemire'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 Mathieu Lemire with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Mathieu Lemire more than expected).
Fields of papers citing papers by Mathieu Lemire
This network shows the impact of papers produced by Mathieu Lemire. 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 Mathieu Lemire. The network helps show where Mathieu Lemire may publish in the future.
Co-authors
The 25 scholars most cited alongside Mathieu Lemire, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
Showing the 20 most-cited of 96 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Discovery of cross-reactive probes and polymorphic CpGs in the Illumina Infinium HumanMethylation450 microarray Hit paper breakdown → | 2013 | 1164 |
| 2 | Functional normalization of 450k methylation array data improves replication in large cancer studies Hit paper breakdown → | 2014 | 614 |
| 3 | 2008 | 465 | |
| 4 | 2017 | 456 | |
| 5 | A renewed model of pancreatic cancer evolution based on genomic rearrangement patterns Hit paper breakdown → | 2016 | 432 |
| 6 | Discovery of common and rare genetic risk variants for colorectal cancer Hit paper breakdown → | 2018 | 388 |
| 7 | 2016 | 342 | |
| 8 | 2012 | 278 | |
| 9 | 2016 | 229 | |
| 10 | 2004 | 220 | |
| 11 | 2010 | 196 | |
| 12 | 2011 | 179 | |
| 13 | 2019 | 178 | |
| 14 | 2015 | 169 | |
| 15 | 2002 | 145 | |
| 16 | 2020 | 145 | |
| 17 | 2012 | 144 | |
| 18 | 2015 | 138 | |
| 19 | 2018 | 124 | |
| 20 | 2009 | 119 |
About Mathieu Lemire
Mathieu Lemire is a scholar working on Genetics, Pathology and Forensic Medicine, Oncology, Cancer Research and Molecular Biology, having authored 96 papers that have together received 8.3k indexed citations. Recurring topics across this work include Genetic Associations and Epidemiology (33 papers), Genetic factors in colorectal cancer (16 papers), Epigenetics and DNA Methylation (12 papers), Cancer Genomics and Diagnostics (7 papers), Asthma and respiratory diseases (7 papers), Genetic and phenotypic traits in livestock (6 papers), Genetic Syndromes and Imprinting (6 papers) and Obsessive-Compulsive Spectrum Disorders (5 papers). The work is most often cited by research in Cancer Research (1.2k citations), Pathology and Forensic Medicine (1.1k citations), Genetics (1.8k citations), Oncology (1.6k citations) and Molecular Biology (3.3k citations). Mathieu Lemire has collaborated with scholars based in Canada, United States and Germany. Frequent co-authors include Thomas Jay Hudson, Brent W. Zanke, Steven N. Gallinger, Darci T. Butcher, Rosanna Weksberg, Sanaa Choufani, Daria Grafodatskaya, Y. Ann Chen, Celia M.T. Greenwood and Aurélie M. T. Labbé. Their work appears in journals such as PLoS ONE, Gastroenterology, Cancer Epidemiology Biomarkers & Prevention, Nature Genetics and Nature Communications.
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.