Giorgio Sirugo
- Infectious Diseases top 2%
- Tuberculosis Research and Epidemiology 21
- Genetics top 2%
- Genetic Associations and Epidemiology 8
- Genomics and Rare Diseases 6
- Hemoglobinopathies and Related Disorders 6
- Immunology top 5%
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- Genetic Neurodegenerative Diseases 18
- Molecular Biology top 5%
- Mitochondrial Function and Pathology 12
- DNA Repair Mechanisms 6
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- Mycobacterium research and diagnosis 9
- Co-authors
- Scott M. WilliamsSarah A. TishkoffColette AdidaGrazia AmbrosiniDario C. AltieriJean‐Louis MandelChristian WejseAdrian V. S. Hill
- Journals
- Cell (1 paper)Proceedings of the National Academy of Sciences (3 papers)Nucleic Acids Research (1 paper)
- Partner nations
- United StatesItalyGambia
In The Last Decade
Giorgio Sirugo
81 papers receiving 3.9k citations
Hit Papers
Peers
Comparison fields: 5 of 158
- Infectious Diseases 726
- Genetics 1.1k
- Immunology 727
- Cellular and Molecular Neuroscience 423
- Molecular Biology 1.5k
Countries citing papers authored by Giorgio Sirugo
This map shows the geographic impact of Giorgio Sirugo'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 Giorgio Sirugo with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Giorgio Sirugo more than expected).
Fields of papers citing papers by Giorgio Sirugo
This network shows the impact of papers produced by Giorgio Sirugo. 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 Giorgio Sirugo. The network helps show where Giorgio Sirugo may publish in the future.
Co-authorship network
The 25 scholars most cited alongside Giorgio Sirugo, 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 | 2024 | 10 | |
| 2 | 2024 | 0 | |
| 3 | 2021 | 1 | |
| 4 | 2020 | 40 | |
| 5 | The Missing Diversity in Human Genetic Studiesbreakdown → | 2019 | 743 |
| 6 | 2017 | 25 | |
| 7 | 2016 | 71 | |
| 8 | 2014 | 19 | |
| 9 | 2012 | 10 | |
| 10 | 2012 | 78 | |
| 11 | 2010 | 16 | |
| 12 | 2010 | 7 | |
| 13 | 2009 | 134 | |
| 14 | 2008 | 61 | |
| 15 | 2008 | 64 | |
| 16 | 2007 | 138 | |
| 17 | 2003 | 13 | |
| 18 | 2000 | 74 | |
| 19 | 1997 | 21 | |
| 20 | Study of large inbred Friedreich ataxia families reveals a recombination between D9S15 and the disease locus. | 1992 | 11 |
About Giorgio Sirugo
Giorgio Sirugo is a scholar working on Infectious Diseases, Cellular and Molecular Neuroscience and Immunology, having authored 83 papers that have together received 4.0k indexed citations. Recurring topics across this work include Tuberculosis Research and Epidemiology (21 papers), Genetic Neurodegenerative Diseases (18 papers), Mitochondrial Function and Pathology (12 papers), Mycobacterium research and diagnosis (9 papers), Genetic Associations and Epidemiology (8 papers), Genomics and Rare Diseases (6 papers), DNA Repair Mechanisms (6 papers) and Hemoglobinopathies and Related Disorders (6 papers). The work is most often cited by research in Infectious Diseases (726 citations), Genetics (1.1k citations) and Immunology (727 citations). Giorgio Sirugo has collaborated with scholars based in United States, Italy and Gambia. Frequent co-authors include Scott M. Williams, Sarah A. Tishkoff, Colette Adida, Grazia Ambrosini, Dario C. Altieri, Jean‐Louis Mandel, Christian Wejse, Adrian V. S. Hill, Branwen J. Hennig and Nicola M. Zetola. Their work appears in journals such as Cell, Proceedings of the National Academy of Sciences and Nucleic Acids 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.