Alexandre Montpetit
Impact in
- Genetics top 0.2%
- Genetic Associations and Epidemiology
- Glioma Diagnosis and Treatment
- Genomic variations and chromosomal abnormalities
- Genomics and Rare Diseases
- Genetic Mapping and Diversity in Plants and Animals
- Cancer Research top 1%
Papers in
- Genetics 32
- Genetic Associations and Epidemiology 18
- Genomics and Rare Diseases 8
- Glioma Diagnosis and Treatment 8
- Genomic variations and chromosomal abnormalities 7
-
- RNA modifications and cancer 11
- Epigenetics and DNA Methylation 9
- Chromatin Remodeling and Cancer 7
- Co-authors
- Thomas Jay Hudson (19 shared papers)Nada Jabado (3 shared papers)Adele Dessa Sadovnick (7 shared papers)George C. Ebers (7 shared papers)David Alexandre Dyment (5 shared papers)Emilie Lalonde (1 shared paper)Jacek Majewski (1 shared paper)Jeremy Schwartzentruber (1 shared paper)
- Journals
- Nature Genetics (9 papers)PLoS Genetics (5 papers)Nature (5 papers)The American Journal of Human Genetics (4 papers)Human Genetics (4 papers)
- Partner nations
- CanadaUnited StatesUnited Kingdom
In The Last Decade
Alexandre Montpetit
98 papers receiving 19.3k citations
Alexandre Montpetit's Hit Papers
Peers
Comparison fields: 5 of 178
- Genetics 2.8k
- Genetics 6.1k
- Cancer Research 1.8k
- Molecular Biology 8.0k
- Pathology and Forensic Medicine 1.7k
Countries citing papers authored by Alexandre Montpetit
This map shows the geographic impact of Alexandre Montpetit'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 Alexandre Montpetit with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Alexandre Montpetit more than expected).
Fields of papers citing papers by Alexandre Montpetit
This network shows the impact of papers produced by Alexandre Montpetit. 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 Alexandre Montpetit. The network helps show where Alexandre Montpetit may publish in the future.
Co-authors
The 25 scholars most cited alongside Alexandre Montpetit, 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 99 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | The International HapMap Project Hit paper breakdown → | 2003 | 4921 |
| 2 | A genome-wide association study identifies novel risk loci for type 2 diabetes Hit paper breakdown → | 2007 | 2434 |
| 3 | Driver mutations in histone H3.3 and chromatin remodelling genes in paediatric glioblastoma Hit paper breakdown → | 2012 | 2075 |
| 4 | K27M mutation in histone H3.3 defines clinically and biologically distinct subgroups of pediatric diffuse intrinsic pontine gliomas Hit paper breakdown → | 2012 | 810 |
| 5 | 2007 | 626 | |
| 6 | 2009 | 540 | |
| 7 | Genomic analysis of diffuse intrinsic pontine gliomas identifies three molecular subgroups and recurrent activating ACVR1 mutations Hit paper breakdown → | 2014 | 512 |
| 8 | Genome-wide association scan identifies a colorectal cancer susceptibility locus on 11q23 and replicates risk loci at 8q24 and 18q21 Hit paper breakdown → | 2008 | 499 |
| 9 | 2008 | 481 | |
| 10 | 2009 | 392 | |
| 11 | 2004 | 380 | |
| 12 | 2008 | 331 | |
| 13 | 2011 | 275 | |
| 14 | 2005 | 266 | |
| 15 | 2013 | 245 | |
| 16 | 2019 | 235 | |
| 17 | 2004 | 220 | |
| 18 | 2016 | 203 | |
| 19 | 2008 | 198 | |
| 20 | 2009 | 194 |
About Alexandre Montpetit
Alexandre Montpetit is a scholar working on Genetics, Molecular Biology, Immunology, Pathology and Forensic Medicine and Genetics, having authored 99 papers that have together received 19.8k indexed citations. Recurring topics across this work include Genetic Associations and Epidemiology (18 papers), RNA modifications and cancer (11 papers), Epigenetics and DNA Methylation (9 papers), Genomics and Rare Diseases (8 papers), Glioma Diagnosis and Treatment (8 papers), Genomic variations and chromosomal abnormalities (7 papers), Chromatin Remodeling and Cancer (7 papers) and Genetic factors in colorectal cancer (6 papers). The work is most often cited by research in Genetics (2.8k citations), Genetics (6.1k citations), Cancer Research (1.8k citations), Molecular Biology (8.0k citations) and Pathology and Forensic Medicine (1.7k citations). Alexandre Montpetit has collaborated with scholars based in Canada, United States and United Kingdom. Frequent co-authors include Thomas Jay Hudson, Nada Jabado, Adele Dessa Sadovnick, George C. Ebers, David Alexandre Dyment, Emilie Lalonde, Jacek Majewski, Jeremy Schwartzentruber, James C. Engert and Matthew R. Lincoln. Their work appears in journals such as Nature Genetics, PLoS Genetics, Nature, The American Journal of Human Genetics and Human Genetics.
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.