P. E. Polani
Impact in
- Genetics top 1%
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
- Genomic variations and chromosomal abnormalities
- Animal Genetics and Reproduction
-
- Prenatal Screening and Diagnostics
Papers in
- Genetics 45
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 25
- Genomic variations and chromosomal abnormalities 12
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- Sexual Differentiation and Disorders 13
- DNA Repair Mechanisms 8
- Co-authors
- F. Giannelli (7 shared papers)C. E. Ford (2 shared papers)Mary J. Seller (9 shared papers)Matteo Adinolfí (9 shared papers)J.L. Hamerton (6 shared papers)N J Wald (2 shared papers)H S Cuckle (1 shared paper)Richárd Pető (1 shared paper)
- Journals
- The Lancet (13 papers)Nature (12 papers)Annals of Human Genetics (9 papers)Journal of Medical Genetics (9 papers)Developmental Medicine & Child Neurology (9 papers)
- Partner nations
- United KingdomUnited StatesSweden
In The Last Decade
P. E. Polani
122 papers receiving 3.4k citations
P. E. Polani's Hit Papers
Peers
Comparison fields: 5 of 145
- Genetics 1.7k
- Pediatrics, Perinatology and Child Health 924
- Developmental Biology 116
- Reproductive Medicine 189
- Molecular Biology 1.5k
Countries citing papers authored by P. E. Polani
This map shows the geographic impact of P. E. Polani'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 P. E. Polani with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites P. E. Polani more than expected).
Fields of papers citing papers by P. E. Polani
This network shows the impact of papers produced by P. E. Polani. 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 P. E. Polani. The network helps show where P. E. Polani may publish in the future.
Co-authors
The 25 scholars most cited alongside P. E. Polani, 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 130 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Maternal serum-alpha-fetoprotein measurement in antenatal screening for anencephaly and spina bifida in early pregnancy. Report of U.K. collaborative study on alpha-fetoprotein in relation to neural-tube defects. Hit paper breakdown → | 1977 | 384 |
| 2 | 1960 | 229 | |
| 3 | 1977 | 202 | |
| 4 | 1959 | 164 | |
| 5 | 1977 | 140 | |
| 6 | 1954 | 115 | |
| 7 | 1960 | 98 | |
| 8 | 1982 | 92 | |
| 9 | 1967 | 85 | |
| 10 | 1961 | 82 | |
| 11 | The neurological examination of the infant | 1960 | 77 |
| 12 | 1965 | 75 | |
| 13 | 1971 | 74 | |
| 14 | 1955 | 74 | |
| 15 | 1972 | 72 | |
| 16 | 1972 | 69 | |
| 17 | 1979 | 65 | |
| 18 | 1979 | 64 | |
| 19 | 1982 | 63 | |
| 20 | 1972 | 62 |
About P. E. Polani
P. E. Polani is a scholar working on Genetics, Molecular Biology, Pediatrics, Perinatology and Child Health, Plant Science and Surgery, having authored 130 papers that have together received 4.0k indexed citations. Recurring topics across this work include Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (25 papers), Prenatal Screening and Diagnostics (16 papers), Sexual Differentiation and Disorders (13 papers), Genomic variations and chromosomal abnormalities (12 papers), Chromosomal and Genetic Variations (12 papers), DNA Repair Mechanisms (8 papers), Congenital Anomalies and Fetal Surgery (7 papers) and Carcinogens and Genotoxicity Assessment (6 papers). The work is most often cited by research in Genetics (1.7k citations), Pediatrics, Perinatology and Child Health (924 citations), Developmental Biology (116 citations), Reproductive Medicine (189 citations) and Molecular Biology (1.5k citations). P. E. Polani has collaborated with scholars based in United Kingdom, United States and Sweden. Frequent co-authors include F. Giannelli, C. E. Ford, Mary J. Seller, Matteo Adinolfí, J.L. Hamerton, N J Wald, H S Cuckle, Richárd Pető, Maurice Campbell and J Brock. Their work appears in journals such as The Lancet, Nature, Annals of Human Genetics, Journal of Medical Genetics and Developmental Medicine & Child Neurology.
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.