Irene Rainville
-
- Cancer, Hypoxia, and Metabolism 2
-
- Lung Cancer Treatments and Mutations 3
-
- BRCA gene mutations in cancer 6
- Genomics and Rare Diseases 3
-
- Genetic factors in colorectal cancer 3
-
- Biochemical and Molecular Research 3
- DNA Repair Mechanisms 2
-
- Immunodeficiency and Autoimmune Disorders 2
- Co-authors
- Huma Q. RanaJudy E. GarberJanice A. NicklasAngel M. CroninZoltán SzállásiSándor SpisákElisa M. LedetJia Li
- Partner nations
- United StatesGermanyArgentina
In The Last Decade
Irene Rainville
22 papers receiving 415 citations
Peers
Comparison fields: 5 of 51
- Cancer Research 146
- Pulmonary and Respiratory Medicine 198
- Oncology 138
- Genetics 121
- Pathology and Forensic Medicine 66
Countries citing papers authored by Irene Rainville
This map shows the geographic impact of Irene Rainville'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 Irene Rainville with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Irene Rainville more than expected).
Fields of papers citing papers by Irene Rainville
This network shows the impact of papers produced by Irene Rainville. 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 Irene Rainville. The network helps show where Irene Rainville may publish in the future.
Co-authorship network
The 25 scholars most cited alongside Irene Rainville, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
| # | Work | ||
|---|---|---|---|
| 1 | 2023 | 12 | |
| 2 | 2020 | 31 | |
| 3 | 2017 | 193 | |
| 4 | 2017 | 21 | |
| 5 | 2014 | 15 | |
| 6 | 2014 | 42 | |
| 7 | Dysphagia, melanosis, gastrointestinal stromal tumors and a germinal mutation of the KIT gene in an Argentine family. | 2014 | 11 |
| 8 | 2013 | 2 | |
| 9 | 2013 | 1 | |
| 10 | 2012 | 4 | |
| 11 | 2008 | 2 | |
| 12 | 2008 | 8 | |
| 13 | 2007 | 1 | |
| 14 | 2002 | 13 | |
| 15 | 2002 | 15 | |
| 16 | 1998 | 16 | |
| 17 | 1997 | 6 | |
| 18 | 1995 | 18 | |
| 19 | PCR amplification and DNA sequence analysis of in vivo and in vitro derived hprt deletion mutations in human T-lymphocytes | 1994 | 2 |
| 20 | 1994 | 7 |
About Irene Rainville
Irene Rainville is a scholar working on Gastroenterology, Genetics and Pathology and Forensic Medicine, having authored 22 papers that have together received 423 indexed citations. Recurring topics across this work include BRCA gene mutations in cancer (6 papers), Genomics and Rare Diseases (3 papers), Biochemical and Molecular Research (3 papers), Genetic factors in colorectal cancer (3 papers), Lung Cancer Treatments and Mutations (3 papers), DNA Repair Mechanisms (2 papers), Cancer, Hypoxia, and Metabolism (2 papers) and Immunodeficiency and Autoimmune Disorders (2 papers). The work is most often cited by research in Cancer Research (146 citations), Pulmonary and Respiratory Medicine (198 citations) and Oncology (138 citations). Irene Rainville has collaborated with scholars based in United States, Germany and Argentina. Frequent co-authors include Huma Q. Rana, Judy E. Garber, Janice A. Nicklas, Angel M. Cronin, Zoltán Szállási, Sándor Spisák, Elisa M. Ledet, Jia Li, Adam S. Kibel and Mark M. Pomerantz. Their work appears in journals such as Journal of Clinical Oncology, Cancer and Cancer Research.
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.