Bárbara Rivera
Impact in
- Reproductive Medicine top 5%
- Ovarian cancer diagnosis and treatment
- Genetics top 5%
- BRCA gene mutations in cancer
- Glioma Diagnosis and Treatment
Papers in
- Genetics 21
- BRCA gene mutations in cancer 14
- Genomics and Rare Diseases 7
- Glioma Diagnosis and Treatment 5
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- Genetic factors in colorectal cancer 10
- Co-authors
- William David Foulkes (25 shared papers)Anne‐Sophie Chong (12 shared papers)Javier J. Benitez (4 shared papers)Miguel Urioste (4 shared papers)Ester Castellsagué (2 shared papers)Léon C.L.T. van Kempen (1 shared paper)Yuri E. Nikiforov (2 shared papers)José Perea (3 shared papers)
- Journals
- Acta Neuropathologica (6 papers)Journal of Medical Genetics (4 papers)New England Journal of Medicine (2 papers)Human Mutation (2 papers)Nature Genetics (2 papers)
- Partner nations
- CanadaSpainUnited States
In The Last Decade
Bárbara Rivera
51 papers receiving 2.2k citations
Peers
Comparison fields: 5 of 56
- Reproductive Medicine 226
- Genetics 185
- Pathology and Forensic Medicine 356
- Genetics 495
- Cancer Research 194
Countries citing papers authored by Bárbara Rivera
This map shows the geographic impact of Bárbara Rivera'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 Bárbara Rivera with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Bárbara Rivera more than expected).
Fields of papers citing papers by Bárbara Rivera
This network shows the impact of papers produced by Bárbara Rivera. 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 Bárbara Rivera. The network helps show where Bárbara Rivera may publish in the future.
Co-authors
The 25 scholars most cited alongside Bárbara Rivera, 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 55 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2014 | 392 | |
| 2 | 2015 | 156 | |
| 3 | 2016 | 147 | |
| 4 | 2015 | 131 | |
| 5 | 2020 | 131 | |
| 6 | 2019 | 129 | |
| 7 | 2020 | 123 | |
| 8 | 2015 | 75 | |
| 9 | 2013 | 73 | |
| 10 | 2015 | 71 | |
| 11 | 2018 | 64 | |
| 12 | 2019 | 49 | |
| 13 | 2019 | 46 | |
| 14 | 2013 | 44 | |
| 15 | 2023 | 44 | |
| 16 | 2018 | 40 | |
| 17 | 2021 | 40 | |
| 18 | 2017 | 34 | |
| 19 | 2017 | 32 | |
| 20 | 2020 | 32 |
About Bárbara Rivera
Bárbara Rivera is a scholar working on Genetics, Pathology and Forensic Medicine, Cancer Research, Genetics and Neurology, having authored 55 papers that have together received 2.2k indexed citations. Recurring topics across this work include BRCA gene mutations in cancer (14 papers), Genetic factors in colorectal cancer (10 papers), Genomics and Rare Diseases (7 papers), Neurofibromatosis and Schwannoma Cases (5 papers), Glioma Diagnosis and Treatment (5 papers), MicroRNA in disease regulation (5 papers), Congenital Diaphragmatic Hernia Studies (5 papers) and Ovarian cancer diagnosis and treatment (4 papers). The work is most often cited by research in Reproductive Medicine (226 citations), Genetics (185 citations), Pathology and Forensic Medicine (356 citations), Genetics (495 citations) and Cancer Research (194 citations). Bárbara Rivera has collaborated with scholars based in Canada, Spain and United States. Frequent co-authors include William David Foulkes, Anne‐Sophie Chong, Javier J. Benitez, Miguel Urioste, Ester Castellsagué, Léon C.L.T. van Kempen, Yuri E. Nikiforov, José Perea, Leanne de Kock and Marc Robert Fabian. Their work appears in journals such as Acta Neuropathologica, Journal of Medical Genetics, New England Journal of Medicine, Human Mutation and Nature 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.