Bruno Dallapiccola
- Genetics top 0.05%
- Genomic variations and chromosomal abnormalities 140
- Genomics and Rare Diseases 49
- Genetics and Neurodevelopmental Disorders 41
- Molecular Biology top 0.2%
- Congenital heart defects research 117
- RNA modifications and cancer 50
- Neurology top 0.5%
- Genetics top 0.5%
- Genomic variations and chromosomal abnormalities 140
- Genomics and Rare Diseases 49
- Genetics and Neurodevelopmental Disorders 41
- Geriatrics and Gerontology top 0.5%
-
- Congenital Heart Disease Studies 63
-
- Prenatal Screening and Diagnostics 60
-
- Chromosomal and Genetic Variations 45
- Co-authors
- Giuseppe NovelliM. Cristina DigilioEnza Maria ValenteRita MingarelliAldo GiannottiBruno MarinoFrancesco BrancatiAnna Sárközy
- Cited by
- GeneticsMolecular BiologyNeurology
- Journals
- Human Genetics (38 papers)Journal of Medical Genetics (27 papers)Clinical Genetics (27 papers)
- Partner nations
- ItalyUnited StatesFrance
In The Last Decade
Bruno Dallapiccola
754 papers receiving 22.3k citations
Hit Papers
Peers
Comparison fields: 5 of 183
- Genetics 6.9k
- Molecular Biology 12.3k
- Neurology 2.1k
- Genetics 1.4k
- Geriatrics and Gerontology 495
Countries citing papers authored by Bruno Dallapiccola
This map shows the geographic impact of Bruno Dallapiccola'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 Bruno Dallapiccola with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Bruno Dallapiccola more than expected).
Fields of papers citing papers by Bruno Dallapiccola
This network shows the impact of papers produced by Bruno Dallapiccola. 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 Bruno Dallapiccola. The network helps show where Bruno Dallapiccola may publish in the future.
Co-authorship network
The 25 scholars most cited alongside Bruno Dallapiccola, 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 | 2023 | 3 | |
| 2 | 2022 | 1 | |
| 3 | 2022 | 2 | |
| 4 | 2021 | 5 | |
| 5 | 2021 | 1 | |
| 6 | 2019 | 17 | |
| 7 | 2019 | 10 | |
| 8 | 2017 | 26 | |
| 9 | 2017 | 17 | |
| 10 | 2008 | 40 | |
| 11 | 2007 | 0 | |
| 12 | 2006 | 22 | |
| 13 | 2006 | 5 | |
| 14 | Noonan's syndrome and related disorders: Clinical-molecular update and guidelines | 2006 | 3 |
| 15 | 2006 | 172 | |
| 16 | 2003 | 8 | |
| 17 | 2001 | 11 | |
| 18 | 1991 | 72 | |
| 19 | 1984 | 5 | |
| 20 | Ovarian dys function in balanced x autosome translocations 2 cases involving band xq 21 | 1979 | 3 |
About Bruno Dallapiccola
Bruno Dallapiccola is a scholar working on Genetics, Developmental Biology and Genetics, having authored 766 papers that have together received 22.9k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (140 papers), Congenital heart defects research (117 papers), Congenital Heart Disease Studies (63 papers), Prenatal Screening and Diagnostics (60 papers), RNA modifications and cancer (50 papers), Genomics and Rare Diseases (49 papers), Chromosomal and Genetic Variations (45 papers) and Genetics and Neurodevelopmental Disorders (41 papers). The work is most often cited by research in Genetics (6.9k citations), Molecular Biology (12.3k citations) and Neurology (2.1k citations). Bruno Dallapiccola has collaborated with scholars based in Italy, United States and France. Frequent co-authors include Giuseppe Novelli, M. Cristina Digilio, Enza Maria Valente, Rita Mingarelli, Aldo Giannotti, Bruno Marino, Francesco Brancati, Anna Sárközy, Antonio Pizzuti and Lorenza Putignani. Their work appears in journals such as Human Genetics, Journal of Medical Genetics, Clinical Genetics, Human Mutation and European 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.