Fátima Lopes
Impact in
-
- Genetics and Neurodevelopmental Disorders
- Genomic variations and chromosomal abnormalities
- Genomics and Rare Diseases
- Bacterial Genetics and Biotechnology
Papers in ⓘ
- Genetics 10
- Genetics and Neurodevelopmental Disorders 8
- Genomic variations and chromosomal abnormalities 3
- Genomics and Rare Diseases 2
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- Congenital heart defects research 2
- Bacterial biofilms and quorum sensing 1
- Co-authors
- Patrı́cia Maciel (8 shared papers)Tânia Ribeiro (1 shared paper)Benoît Zuber (1 shared paper)Gabriela Soares (5 shared papers)Philippe Moreillon (1 shared paper)Marisa Haenni (1 shared paper)Jacques Dubochet (1 shared paper)Mafalda Barbosa (3 shared papers)
- Journals
- Frontiers in Genetics (2 papers)International Journal of Developmental Neuroscience (2 papers)Journal of Bacteriology (1 paper)Orphanet Journal of Rare Diseases (1 paper)Neurogenetics (1 paper)
- Partner nations
- PortugalUnited StatesNetherlands
In The Last Decade
Fátima Lopes
13 papers receiving 317 citations
Peers
Comparison fields: 5 of 83
- Structural Biology 11
- Genetics 173
- Molecular Biology 192
- Cellular and Molecular Neuroscience 36
- Cognitive Neuroscience 30
Countries citing papers authored by Fátima Lopes
This map shows the geographic impact of Fátima Lopes'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 Fátima Lopes with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Fátima Lopes more than expected).
Fields of papers citing papers by Fátima Lopes
This network shows the impact of papers produced by Fátima Lopes. 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 Fátima Lopes. The network helps show where Fátima Lopes may publish in the future.
Co-authors
The 25 scholars most cited alongside Fátima Lopes, 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 | 2016 | 126 | |
| 2 | 2006 | 77 | |
| 3 | 2018 | 26 | |
| 4 | 2015 | 24 | |
| 5 | 2013 | 21 | |
| 6 | 2017 | 14 | |
| 7 | [Psychiatric manifestations of a new variant of Creutzfeldt-Jakob disease. Apropos of a case]. | 2001 | 12 |
| 8 | 2019 | 8 | |
| 9 | 2021 | 8 | |
| 10 | 2009 | 8 | |
| 11 | 2020 | 7 | |
| 12 | 2017 | 2 | |
| 13 | 2020 | 1 | |
| 14 | 2015 | 0 |
About Fátima Lopes
Fátima Lopes is a scholar working on Genetics, Molecular Biology, Plant Science, Surgery and Nephrology, having authored 14 papers that have together received 334 indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (8 papers), Chromosomal and Genetic Variations (3 papers), Genomic variations and chromosomal abnormalities (3 papers), Congenital heart defects research (2 papers), Genomics and Rare Diseases (2 papers), Water Treatment and Disinfection (1 paper), Case Reports on Hematomas (1 paper) and Bacterial biofilms and quorum sensing (1 paper). The work is most often cited by research in Structural Biology (11 citations), Genetics (173 citations), Molecular Biology (192 citations), Cellular and Molecular Neuroscience (36 citations) and Cognitive Neuroscience (30 citations). Fátima Lopes has collaborated with scholars based in Portugal, United States and Netherlands. Frequent co-authors include Patrı́cia Maciel, Tânia Ribeiro, Benoît Zuber, Gabriela Soares, Philippe Moreillon, Marisa Haenni, Jacques Dubochet, Mafalda Barbosa, José Pedro Vieira and Teresa Temudo. Their work appears in journals such as Frontiers in Genetics, International Journal of Developmental Neuroscience, Journal of Bacteriology, Orphanet Journal of Rare Diseases and Neurogenetics.
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.