Jorge Sequeiros
Impact in
- Cellular and Molecular Neuroscience top 0.2%
- Genetic Neurodegenerative Diseases
- Hereditary Neurological Disorders
- Psychiatry and Mental health top 2%
- Migraine and Headache Studies
Papers in
-
- Genetic Neurodegenerative Diseases 141
- Hereditary Neurological Disorders 20
- Genetics 43
- Genomics and Rare Diseases 17
- BRCA gene mutations in cancer 13
- Co-authors
- Paula Coutinho (39 shared papers)Isabel Silveira (36 shared papers)Alda Sousa (35 shared papers)José Barros (32 shared papers)Isabel da Conceição Moreira Pereira Alonso (49 shared papers)Patrı́cia Maciel (30 shared papers)Teresa Coelho (17 shared papers)Laura Bannach Jardim (18 shared papers)
- Journals
- European Journal of Human Genetics (23 papers)Clinical Genetics (12 papers)The American Journal of Human Genetics (7 papers)Neurology (6 papers)Public Health Genomics (6 papers)
- Partner nations
- PortugalUnited KingdomUnited States
In The Last Decade
Jorge Sequeiros
251 papers receiving 8k citations
Peers
Comparison fields: 5 of 126
- Cellular and Molecular Neuroscience 4.1k
- Psychiatry and Mental health 622
- Genetics 980
- Neurology 428
- Molecular Biology 1.7k
Countries citing papers authored by Jorge Sequeiros
This map shows the geographic impact of Jorge Sequeiros'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 Jorge Sequeiros with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Jorge Sequeiros more than expected).
Fields of papers citing papers by Jorge Sequeiros
This network shows the impact of papers produced by Jorge Sequeiros. 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 Jorge Sequeiros. The network helps show where Jorge Sequeiros may publish in the future.
Co-authors
The 25 scholars most cited alongside Jorge Sequeiros, 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 256 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2004 | 431 | |
| 2 | 2001 | 365 | |
| 3 | 2012 | 286 | |
| 4 | 2010 | 285 | |
| 5 | 2009 | 202 | |
| 6 | 1995 | 198 | |
| 7 | Epidemiology and clinical aspects of Machado-Joseph disease. | 1993 | 169 |
| 8 | 2002 | 154 | |
| 9 | 2002 | 146 | |
| 10 | 2001 | 134 | |
| 11 | 2006 | 125 | |
| 12 | 2015 | 115 | |
| 13 | 2013 | 114 | |
| 14 | 2017 | 109 | |
| 15 | 2001 | 105 | |
| 16 | 2011 | 103 | |
| 17 | 1996 | 93 | |
| 18 | 2001 | 82 | |
| 19 | 2008 | 81 | |
| 20 | 2010 | 80 |
About Jorge Sequeiros
Jorge Sequeiros is a scholar working on Cellular and Molecular Neuroscience, Genetics, Psychiatry and Mental health, Molecular Biology and Public Health, Environmental and Occupational Health, having authored 256 papers that have together received 8.2k indexed citations. Recurring topics across this work include Genetic Neurodegenerative Diseases (141 papers), Amyloidosis: Diagnosis, Treatment, Outcomes (33 papers), Migraine and Headache Studies (21 papers), Hereditary Neurological Disorders (20 papers), Medical and Health Sciences Research (19 papers), Genomics and Rare Diseases (17 papers), BRCA gene mutations in cancer (13 papers) and Ethics and bioethics in healthcare (9 papers). The work is most often cited by research in Cellular and Molecular Neuroscience (4.1k citations), Psychiatry and Mental health (622 citations), Genetics (980 citations), Neurology (428 citations) and Molecular Biology (1.7k citations). Jorge Sequeiros has collaborated with scholars based in Portugal, United Kingdom and United States. Frequent co-authors include Paula Coutinho, Isabel Silveira, Alda Sousa, José Barros, Isabel da Conceição Moreira Pereira Alonso, Patrı́cia Maciel, Teresa Coelho, Laura Bannach Jardim, Carolina Lemos and Milena Paneque. Their work appears in journals such as European Journal of Human Genetics, Clinical Genetics, The American Journal of Human Genetics, Neurology and Public Health Genomics.
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.