Marcella Devoto
- Genetics top 1%
- Inflammatory Bowel Disease 14
- Genetic Associations and Epidemiology 11
- Neurology top 1%
- Neuroblastoma Research and Treatments 16
- Molecular Biology top 2%
- RNA regulation and disease 8
- Cancer Research top 5%
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- Cystic Fibrosis Research Advances 20
- Neonatal Respiratory Health Research 8
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- Congenital gastrointestinal and neural anomalies 13
- Pediatric Hepatobiliary Diseases and Treatments 11
- Co-authors
- Håkon HåkonarsonAlessandra BolinoSharon J. DiskinJohn M. MarisMario CapassoAchille IolasconGiovanni RomeoG. Cara Romeo
- Cited by
- GeneticsNeurologyMolecular Biology
- Journals
- European Journal of Human Genetics (11 papers)Human Genetics (10 papers)Human Heredity (6 papers)
- Partner nations
- ItalyUnited StatesUnited Kingdom
In The Last Decade
Marcella Devoto
156 papers receiving 6.4k citations
Hit Papers
Peers
Comparison fields: 5 of 129
- Genetics 1.8k
- Neurology 896
- Molecular Biology 2.7k
- Endocrinology, Diabetes and Metabolism 563
- Cancer Research 492
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-authorship network
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
| # | Work | ||
|---|---|---|---|
| 1 | 2025 | 0 | |
| 2 | 2017 | 63 | |
| 3 | 2014 | 79 | |
| 4 | 2013 | 99 | |
| 5 | 2013 | 96 | |
| 6 | 2012 | 61 | |
| 7 | 2011 | 36 | |
| 8 | 2010 | 30 | |
| 9 | 2009 | 5 | |
| 10 | Novel Locus for High–Grade Myopia in a Hutterite Population on Chromosome 10q | 2006 | 1 |
| 11 | 2000 | 37 | |
| 12 | 2000 | 14 | |
| 13 | Decreased frequency of a neutral sequence variant of the RET proto-oncogene in sporadic Hirschsprung disease. | 1999 | 1 |
| 14 | [Antiochian genealogies in which idiopathic epilepsy presents familial conglomeration. Simulations of power for the detection of genetic linkage]. | 1998 | 1 |
| 15 | 1998 | 1 | |
| 16 | 1997 | 81 | |
| 17 | Genetic linkage studies for the identification of cancer-related genes. | 1996 | 3 |
| 18 | 1993 | 142 | |
| 19 | Polycystic kidney disease | 1992 | 1 |
| 20 | 1990 | 9 |
About Marcella Devoto
Marcella Devoto is a scholar working on Genetics, Genetics and Neurology, having authored 161 papers that have together received 6.6k indexed citations. Recurring topics across this work include Cystic Fibrosis Research Advances (20 papers), Neuroblastoma Research and Treatments (16 papers), Inflammatory Bowel Disease (14 papers), Congenital gastrointestinal and neural anomalies (13 papers), Pediatric Hepatobiliary Diseases and Treatments (11 papers), Genetic Associations and Epidemiology (11 papers), RNA regulation and disease (8 papers) and Neonatal Respiratory Health Research (8 papers). The work is most often cited by research in Genetics (1.8k citations), Neurology (896 citations) and Molecular Biology (2.7k citations). Marcella Devoto has collaborated with scholars based in Italy, United States and United Kingdom. Frequent co-authors include Håkon Håkonarson, Alessandra Bolino, Sharon J. Diskin, John M. Maris, Mario Capasso, Achille Iolascon, Giovanni Romeo, G. Cara Romeo, Maura Diamond and Prasuna Paluru. Their work appears in journals such as European Journal of Human Genetics, Human Genetics, Human Heredity, Human Mutation and The American Journal of Human Genetics.
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.