Mario Falchi
Impact in
Papers in
- Genetics 35
- Genetic Associations and Epidemiology 28
- Genetic Mapping and Diversity in Plants and Animals 10
- Nephrology 11
- Renal Diseases and Glomerulopathies 8
- Co-authors
- Tim D. Spector (37 shared papers)Alessia Visconti (28 shared papers)Ana Maria Valdes (7 shared papers)Cristina Menni (13 shared papers)Claire J. Steves (10 shared papers)Ruth C. E. Bowyer (8 shared papers)Massimo Mangino (8 shared papers)Julia Sarah El-Sayed Moustafa (8 shared papers)
- Journals
- Nature Communications (8 papers)Human Molecular Genetics (6 papers)The American Journal of Human Genetics (6 papers)Nature Genetics (5 papers)Bioinformatics (4 papers)
- Partner nations
- United KingdomUnited StatesItaly
In The Last Decade
Mario Falchi
124 papers receiving 10.6k citations
Mario Falchi's Hit Papers
Peers
Comparison fields: 5 of 184
- Neurology 1.4k
- Genetics 2.2k
- Physiology 1.4k
- Nephrology 395
- Molecular Biology 3.6k
Countries citing papers authored by Mario Falchi
This map shows the geographic impact of Mario Falchi'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 Mario Falchi with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Mario Falchi more than expected).
Fields of papers citing papers by Mario Falchi
This network shows the impact of papers produced by Mario Falchi. 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 Mario Falchi. The network helps show where Mario Falchi may publish in the future.
Co-authors
The 25 scholars most cited alongside Mario Falchi, 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 127 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Phenotype, genotype, and worldwide genetic penetrance of LRRK2-associated Parkinson's disease: a case-control study Hit paper breakdown → | 2008 | 1251 |
| 2 | Real-time tracking of self-reported symptoms to predict potential COVID-19 Hit paper breakdown → | 2020 | 988 |
| 3 | Bone mineral density, osteoporosis, and osteoporotic fractures: a genome-wide association study Hit paper breakdown → | 2008 | 576 |
| 4 | Interplay between the human gut microbiome and host metabolism Hit paper breakdown → | 2019 | 570 |
| 5 | 2010 | 420 | |
| 6 | 2009 | 416 | |
| 7 | 2008 | 371 | |
| 8 | 2011 | 340 | |
| 9 | A reference map of potential determinants for the human serum metabolome Hit paper breakdown → | 2020 | 331 |
| 10 | The person-to-person transmission landscape of the gut and oral microbiomes Hit paper breakdown → | 2023 | 304 |
| 11 | 2016 | 229 | |
| 12 | 2006 | 227 | |
| 13 | 2010 | 212 | |
| 14 | 2014 | 201 | |
| 15 | 2009 | 183 | |
| 16 | 2007 | 168 | |
| 17 | 2020 | 162 | |
| 18 | 2021 | 139 | |
| 19 | 2017 | 132 | |
| 20 | 2019 | 130 |
About Mario Falchi
Mario Falchi is a scholar working on Genetics, Nephrology, Dermatology, Molecular Biology and Physiology, having authored 127 papers that have together received 10.9k indexed citations. Recurring topics across this work include Genetic Associations and Epidemiology (28 papers), Genetic Mapping and Diversity in Plants and Animals (10 papers), Gut microbiota and health (9 papers), Renal Diseases and Glomerulopathies (8 papers), Skin Protection and Aging (8 papers), melanin and skin pigmentation (7 papers), Metabolomics and Mass Spectrometry Studies (7 papers) and Cutaneous Melanoma Detection and Management (7 papers). The work is most often cited by research in Neurology (1.4k citations), Genetics (2.2k citations), Physiology (1.4k citations), Nephrology (395 citations) and Molecular Biology (3.6k citations). Mario Falchi has collaborated with scholars based in United Kingdom, United States and Italy. Frequent co-authors include Tim D. Spector, Alessia Visconti, Ana Maria Valdes, Cristina Menni, Claire J. Steves, Ruth C. E. Bowyer, Massimo Mangino, Julia Sarah El-Sayed Moustafa, Niccolò Rossi and Jordana T. Bell. Their work appears in journals such as Nature Communications, Human Molecular Genetics, The American Journal of Human Genetics, Nature Genetics and Bioinformatics.
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.