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
- Reproductive Medicine top 2%
Papers in
- Genetics 51
- Genomic variations and chromosomal abnormalities 30
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 9
- Genetics and Neurodevelopmental Disorders 8
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- Epigenetics and DNA Methylation 12
- Co-authors
- Angela Bentivegna (27 shared papers)Walter Vegetti (10 shared papers)Serena Redaelli (35 shared papers)Anna Marozzi (9 shared papers)Pier Giorgio Crosignani (8 shared papers)Enrico Ginelli (7 shared papers)Maria Grazia Tibiletti (6 shared papers)Romina Combi (10 shared papers)
- Journals
- Human Reproduction (10 papers)Prenatal Diagnosis (8 papers)International Journal of Cancer (6 papers)International Journal of Molecular Sciences (5 papers)Molecular Cytogenetics (5 papers)
- Partner nations
- ItalyUnited StatesUnited Kingdom
In The Last Decade
Leda Dalprà
121 papers receiving 3.4k citations
Peers
Comparison fields: 5 of 119
- Genetics 1.1k
- Genetics 360
- Reproductive Medicine 270
- Cancer Research 469
- Pediatrics, Perinatology and Child Health 503
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 124 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 | 171 |
| 2 | 2009 | 157 | |
| 3 | 2005 | 150 | |
| 4 | 2008 | 138 | |
| 5 | 1998 | 130 | |
| 6 | 2000 | 114 | |
| 7 | 2017 | 112 | |
| 8 | The same molecular mechanism at the maternal meiosis I produces mono- and dicentric 8p duplications. | 1996 | 98 |
| 9 | 2012 | 96 | |
| 10 | 2002 | 89 | |
| 11 | Influence of sex on cytogenetic end points: evidence from a large human sample and review of the literature. | 1995 | 87 |
| 12 | 2000 | 81 | |
| 13 | 2004 | 80 | |
| 14 | 2008 | 79 | |
| 15 | 2000 | 78 | |
| 16 | 2009 | 71 | |
| 17 | 2005 | 69 | |
| 18 | 1994 | 61 | |
| 19 | 2001 | 61 | |
| 20 | 1999 | 61 |
About Leda Dalprà
Leda Dalprà is a scholar working on Genetics, Molecular Biology, Pediatrics, Perinatology and Child Health, Surgery and Plant Science, having authored 124 papers that have together received 3.7k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (30 papers), Prenatal Screening and Diagnostics (22 papers), Chromosomal and Genetic Variations (13 papers), Neuroscience and Neuropharmacology Research (12 papers), Epigenetics and DNA Methylation (12 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (9 papers), Sarcoma Diagnosis and Treatment (9 papers) and Genetics and Neurodevelopmental Disorders (8 papers). The work is most often cited by research in Genetics (1.1k citations), Genetics (360 citations), Reproductive Medicine (270 citations), Cancer Research (469 citations) and Pediatrics, Perinatology and Child Health (503 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, Pier Giorgio Crosignani, Enrico Ginelli, Maria Grazia Tibiletti, Romina Combi, Simona Baronchelli and G Tredici. Their work appears in journals such as Human Reproduction, Prenatal Diagnosis, International Journal of Cancer, International Journal of Molecular Sciences and Molecular Cytogenetics.
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.