Leda Dalprà
Impact in
- Genetics top 2%
- Genomic variations and chromosomal abnormalities
- Genetics and Neurodevelopmental Disorders
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
- Cancer Research top 5%
- Carcinogens and Genotoxicity Assessment
Papers in
-
- Epigenetics and DNA Methylation 16
- Genetics 51
- Genomic variations and chromosomal abnormalities 31
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 9
- Co-authors
- Angela Bentivegna (26 shared papers)Walter Vegetti (9 shared papers)Serena Redaelli (34 shared papers)Anna Marozzi (9 shared papers)Enrico Ginelli (7 shared papers)Maria Grazia Tibiletti (6 shared papers)Simona Baronchelli (10 shared papers)G Tredici (7 shared papers)
- Journals
- Human Reproduction (9 papers)Prenatal Diagnosis (8 papers)International Journal of Cancer (6 papers)Molecular Cytogenetics (5 papers)International Journal of Molecular Sciences (5 papers)
- Partner nations
- ItalyUnited StatesUnited Kingdom
In The Last Decade
Leda Dalprà
118 papers receiving 3.1k citations
Peers
Comparison fields: 5 of 117
- Genetics 1.2k
- Genetics 384
- Cancer Research 491
- Reproductive Medicine 267
- Chemical Health and Safety 19
Countries citing papers authored by Leda Dalprà
This map shows the geographic impact of Leda Dalprà'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 Leda Dalprà with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Leda Dalprà more than expected).
Fields of papers citing papers by Leda Dalprà
This network shows the impact of papers produced by Leda Dalprà. 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 Leda Dalprà. The network helps show where Leda Dalprà may publish in the future.
Co-authors
The 25 scholars most cited alongside Leda Dalprà, 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 119 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Age-related increase of baseline frequencies of sister chromatid exchanges, chromosome aberrations, and micronuclei in human lymphocytes. | 1997 | 168 |
| 2 | 2009 | 154 | |
| 3 | 2005 | 143 | |
| 4 | 2008 | 120 | |
| 5 | 1998 | 116 | |
| 6 | 2017 | 107 | |
| 7 | 2000 | 105 | |
| 8 | The same molecular mechanism at the maternal meiosis I produces mono- and dicentric 8p duplications. | 1996 | 95 |
| 9 | 2012 | 88 | |
| 10 | Influence of sex on cytogenetic end points: evidence from a large human sample and review of the literature. | 1995 | 86 |
| 11 | 2002 | 79 | |
| 12 | 2000 | 78 | |
| 13 | 2008 | 77 | |
| 14 | 2004 | 77 | |
| 15 | 2005 | 70 | |
| 16 | 2009 | 68 | |
| 17 | 2000 | 65 | |
| 18 | 2009 | 59 | |
| 19 | 1994 | 58 | |
| 20 | 2000 | 58 |
About Leda Dalprà
Leda Dalprà is a scholar working on Molecular Biology, Genetics, Pediatrics, Perinatology and Child Health, Plant Science and Surgery, having authored 119 papers that have together received 3.3k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (31 papers), Prenatal Screening and Diagnostics (23 papers), Epigenetics and DNA Methylation (16 papers), Chromosomal and Genetic Variations (16 papers), Neuroscience and Neuropharmacology Research (11 papers), Sarcoma Diagnosis and Treatment (9 papers), Reproductive Biology and Fertility (9 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (9 papers). The work is most often cited by research in Genetics (1.2k citations), Genetics (384 citations), Cancer Research (491 citations), Reproductive Medicine (267 citations) and Chemical Health and Safety (19 citations). Leda Dalprà has collaborated with scholars based in Italy, United States and United Kingdom. Frequent co-authors include Angela Bentivegna, Walter Vegetti, Serena Redaelli, Anna Marozzi, Enrico Ginelli, Maria Grazia Tibiletti, Simona Baronchelli, G Tredici, Pier Giorgio Crosignani and Gabriele Riva. Their work appears in journals such as Human Reproduction, Prenatal Diagnosis, International Journal of Cancer, Molecular Cytogenetics and International Journal of Molecular Sciences.
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.