Marcella Devoto
Impact in
Papers in
- Co-authors
- Hakon Hakonarson (21 shared papers)Alessandra Bolino (8 shared papers)John M. Maris (9 shared papers)Sharon J. Diskin (9 shared papers)Mario Capasso (9 shared papers)Giovanni Romeo (15 shared papers)Achille Iolascon (8 shared papers)Giovanni Cara Romeo (9 shared papers)
- Journals
- Human Genetics (12 papers)Nature Genetics (11 papers)European Journal of Human Genetics (11 papers)The American Journal of Human Genetics (8 papers)Human Mutation (6 papers)
- Partner nations
- United StatesItalyUnited Kingdom
In The Last Decade
Marcella Devoto
205 papers receiving 14.7k citations
Marcella Devoto's Hit Papers
Peers
Comparison fields: 5 of 153
- Neurology 2.5k
- Genetics 3.7k
- Nutrition and Dietetics 1.6k
- Cancer Research 1.3k
- Molecular Biology 5.3k
Countries citing papers authored by Marcella Devoto
This map shows the geographic impact of Marcella Devoto'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 Marcella Devoto with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Marcella Devoto more than expected).
Fields of papers citing papers by Marcella Devoto
This network shows the impact of papers produced by Marcella Devoto. 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 Marcella Devoto. The network helps show where Marcella Devoto may publish in the future.
Co-authors
The 25 scholars most cited alongside Marcella Devoto, 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 210 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | The Wilson disease gene is a copper transporting ATPase with homology to the Menkes disease gene Hit paper breakdown → | 1993 | 1180 |
| 2 | Identification of ALK as a major familial neuroblastoma predisposition gene Hit paper breakdown → | 2008 | 1096 |
| 3 | Complex genetic signatures in immune cells underlie autoimmunity and inform therapy Hit paper breakdown → | 2020 | 691 |
| 4 | A common molecular basis for three inherited kidney stone diseases Hit paper breakdown → | 1996 | 636 |
| 5 | 2004 | 576 | |
| 6 | 2007 | 448 | |
| 7 | 1997 | 447 | |
| 8 | 2009 | 436 | |
| 9 | 1993 | 408 | |
| 10 | 2000 | 395 | |
| 11 | 2011 | 314 | |
| 12 | 2009 | 299 | |
| 13 | 2009 | 281 | |
| 14 | 2009 | 261 | |
| 15 | 2010 | 258 | |
| 16 | 2008 | 250 | |
| 17 | 2004 | 249 | |
| 18 | 2012 | 223 | |
| 19 | 1998 | 210 | |
| 20 | 1998 | 202 |
About Marcella Devoto
Marcella Devoto is a scholar working on Genetics, Neurology, Molecular Biology, Genetics and Surgery, having authored 210 papers that have together received 15.3k indexed citations. Recurring topics across this work include Cystic Fibrosis Research Advances (22 papers), Neuroblastoma Research and Treatments (22 papers), Inflammatory Bowel Disease (15 papers), Genomic variations and chromosomal abnormalities (14 papers), Congenital gastrointestinal and neural anomalies (12 papers), Congenital heart defects research (11 papers), Neonatal Respiratory Health Research (10 papers) and Pediatric Hepatobiliary Diseases and Treatments (10 papers). The work is most often cited by research in Neurology (2.5k citations), Genetics (3.7k citations), Nutrition and Dietetics (1.6k citations), Cancer Research (1.3k citations) and Molecular Biology (5.3k citations). Marcella Devoto has collaborated with scholars based in United States, Italy and United Kingdom. Frequent co-authors include Hakon Hakonarson, Alessandra Bolino, John M. Maris, Sharon J. Diskin, Mario Capasso, Giovanni Romeo, Achille Iolascon, Giovanni Cara Romeo, Maura A. Diamond and Prasuna C. Paluru. Their work appears in journals such as Human Genetics, Nature Genetics, European Journal of Human Genetics, The American Journal of Human Genetics and Human Mutation.
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.