Irene Bottillo
Impact in
- Neurology top 5%
- Neurofibromatosis and Schwannoma Cases
- Developmental Biology top 10%
Papers in
-
- Congenital heart defects research 5
- Protein Tyrosine Phosphatases 4
- Genetics 16
- Genomic variations and chromosomal abnormalities 7
- Co-authors
- Bruno Dallapiccola (17 shared papers)Laura Bernardini (9 shared papers)Antonio Novelli (8 shared papers)Paola Grammatico (33 shared papers)Alessandro De Luca (7 shared papers)Ragnhild A. Lothe (2 shared papers)Terje Ahlquist (2 shared papers)Annalisa Schirinzi (5 shared papers)
In The Last Decade
Irene Bottillo
59 papers receiving 1.1k citations
Peers
Comparison fields: 5 of 76
- Neurology 248
- Developmental Biology 24
- Genetics 224
- Pathology and Forensic Medicine 123
- Rheumatology 94
Countries citing papers authored by Irene Bottillo
This map shows the geographic impact of Irene Bottillo'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 Irene Bottillo with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Irene Bottillo more than expected).
Fields of papers citing papers by Irene Bottillo
This network shows the impact of papers produced by Irene Bottillo. 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 Irene Bottillo. The network helps show where Irene Bottillo may publish in the future.
Co-authors
The 25 scholars most cited alongside Irene Bottillo, 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 67 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2005 | 106 | |
| 2 | 2008 | 98 | |
| 3 | 2010 | 93 | |
| 4 | 2007 | 59 | |
| 5 | 2008 | 48 | |
| 6 | 2009 | 45 | |
| 7 | 2004 | 41 | |
| 8 | 2008 | 34 | |
| 9 | 2016 | 34 | |
| 10 | 2015 | 31 | |
| 11 | 2007 | 29 | |
| 12 | A novel homozygous splice site mutation in the HPGD gene causes mild primary hypertrophic osteoarthropathy. | 2010 | 29 |
| 13 | 2007 | 27 | |
| 14 | 2021 | 21 | |
| 15 | 2015 | 19 | |
| 16 | 2010 | 19 | |
| 17 | 2020 | 19 | |
| 18 | 2009 | 19 | |
| 19 | 2021 | 18 | |
| 20 | 2010 | 17 |
About Irene Bottillo
Irene Bottillo is a scholar working on Molecular Biology, Genetics, Pulmonary and Respiratory Medicine, Pathology and Forensic Medicine and Neurology, having authored 67 papers that have together received 1.1k indexed citations. Recurring topics across this work include Neurofibromatosis and Schwannoma Cases (9 papers), Genomic variations and chromosomal abnormalities (7 papers), Cancer Genomics and Diagnostics (6 papers), Congenital heart defects research (5 papers), Sarcoma Diagnosis and Treatment (5 papers), Genetic factors in colorectal cancer (5 papers), Cardiomyopathy and Myosin Studies (5 papers) and Protein Tyrosine Phosphatases (4 papers). The work is most often cited by research in Neurology (248 citations), Developmental Biology (24 citations), Genetics (224 citations), Pathology and Forensic Medicine (123 citations) and Rheumatology (94 citations). Irene Bottillo has collaborated with scholars based in Italy, Lebanon and China. Frequent co-authors include Bruno Dallapiccola, Laura Bernardini, Antonio Novelli, Paola Grammatico, Alessandro De Luca, Ragnhild A. Lothe, Terje Ahlquist, Annalisa Schirinzi, Stine A. Danielsen and Isabella Torrente. Their work appears in journals such as Human Mutation, European Journal of Human Genetics, Genes, Cardiovascular Pathology and European Journal of Medical 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.