Fátima Lopes
Impact in
- Genetics top 2%
- Genetics and Neurodevelopmental Disorders
- Genomics and Rare Diseases
- Genomic variations and chromosomal abnormalities
- Cognitive Neuroscience top 2%
- Autism Spectrum Disorder Research
Papers in
- Genetics 15
- Genetics and Neurodevelopmental Disorders 11
- Genomic variations and chromosomal abnormalities 6
- Genomics and Rare Diseases 3
-
- Congenital heart defects research 3
- Muscle Physiology and Disorders 2
- Epigenetics and DNA Methylation 2
- RNA modifications and cancer 2
- Co-authors
- Patrı́cia Maciel (9 shared papers)Gabriela Soares (5 shared papers)Marisa Haenni (1 shared paper)Philippe Moreillon (1 shared paper)Benoît Zuber (1 shared paper)Tânia Bragança Ribeiro (1 shared paper)Jacques Dubochet (1 shared paper)Mafalda Barbosa (3 shared papers)
- Journals
- Frontiers in Genetics (2 papers)Orphanet Journal of Rare Diseases (2 papers)Journal of Medical Genetics (2 papers)International Journal of Developmental Neuroscience (2 papers)Neurogenetics (1 paper)
- Partner nations
- PortugalUnited StatesCanada
In The Last Decade
Fátima Lopes
23 papers receiving 2.1k citations
Fátima Lopes's Hit Papers
Peers
Comparison fields: 5 of 114
- Genetics 1.1k
- Cognitive Neuroscience 684
- Developmental Neuroscience 65
- Molecular Biology 1.0k
- Aging 26
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
Showing the 20 most-cited of 23 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Large-Scale Exome Sequencing Study Implicates Both Developmental and Functional Changes in the Neurobiology of Autism Hit paper breakdown → | 2020 | 1519 |
| 2 | 2016 | 157 | |
| 3 | 2006 | 86 | |
| 4 | 2018 | 69 | |
| 5 | 2015 | 60 | |
| 6 | 2018 | 33 | |
| 7 | 2019 | 31 | |
| 8 | 2018 | 31 | |
| 9 | 2015 | 25 | |
| 10 | 2013 | 23 | |
| 11 | 2017 | 15 | |
| 12 | [Psychiatric manifestations of a new variant of Creutzfeldt-Jakob disease. Apropos of a case]. | 2001 | 12 |
| 13 | 2019 | 10 | |
| 14 | 2020 | 9 | |
| 15 | 2021 | 9 | |
| 16 | 2009 | 8 | |
| 17 | 2018 | 7 | |
| 18 | 2012 | 5 | |
| 19 | 2001 | 4 | |
| 20 | 2017 | 3 |
About Fátima Lopes
Fátima Lopes is a scholar working on Genetics, Molecular Biology, Process Chemistry and Technology, Health Information Management and Nephrology, having authored 23 papers that have together received 2.1k indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (11 papers), Genomic variations and chromosomal abnormalities (6 papers), Genomics and Rare Diseases (3 papers), Congenital heart defects research (3 papers), Muscle Physiology and Disorders (2 papers), Epigenetics and DNA Methylation (2 papers), RNA modifications and cancer (2 papers) and Chromosomal and Genetic Variations (2 papers). The work is most often cited by research in Genetics (1.1k citations), Cognitive Neuroscience (684 citations), Developmental Neuroscience (65 citations), Molecular Biology (1.0k citations) and Aging (26 citations). Fátima Lopes has collaborated with scholars based in Portugal, United States and Canada. Frequent co-authors include Patrı́cia Maciel, Gabriela Soares, Marisa Haenni, Philippe Moreillon, Benoît Zuber, Tânia Bragança Ribeiro, Jacques Dubochet, Mafalda Barbosa, Teresa Padrao Temudo and José Pedro Vieira. Their work appears in journals such as Frontiers in Genetics, Orphanet Journal of Rare Diseases, Journal of Medical Genetics, International Journal of Developmental Neuroscience 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.