P. Petit
Impact in
- Genetics top 5%
- Genomic variations and chromosomal abnormalities
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
- Genetics and Neurodevelopmental Disorders
- Hematology top 10%
- Acute Myeloid Leukemia Research
- Chronic Myeloid Leukemia Treatments
Papers in
- Genetics 41
- Genomic variations and chromosomal abnormalities 28
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 8
- Genetics and Neurodevelopmental Disorders 7
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- Chromosomal and Genetic Variations 17
- Co-authors
- Herman Van den Berghe (17 shared papers)J. P. Fryns (12 shared papers)A Kleczkowska (6 shared papers)J P Fryns (5 shared papers)Pierre Fondu (1 shared paper)Marc Alexander (1 shared paper)Joris Vermeesch (5 shared papers)Fryns Jp (6 shared papers)
- Journals
- Clinical Genetics (9 papers)Human Genetics (8 papers)The Lancet (2 papers)European Journal of Pediatrics (1 paper)American Journal of Roentgenology (1 paper)
- Partner nations
- BelgiumFranceUnited States
In The Last Decade
P. Petit
67 papers receiving 686 citations
Peers
Comparison fields: 5 of 65
- Genetics 436
- Hematology 91
- Pediatrics, Perinatology and Child Health 131
- Genetics 65
- Developmental Biology 11
Countries citing papers authored by P. Petit
This map shows the geographic impact of P. Petit'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. Petit with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites P. Petit more than expected).
Fields of papers citing papers by P. Petit
This network shows the impact of papers produced by P. Petit. 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. Petit. The network helps show where P. Petit may publish in the future.
Co-authors
The 25 scholars most cited alongside P. Petit, 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 72 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 1984 | 47 | |
| 2 | 1973 | 40 | |
| 3 | 1982 | 36 | |
| 4 | 1984 | 32 | |
| 5 | 1977 | 31 | |
| 6 | 1997 | 31 | |
| 7 | 1982 | 27 | |
| 8 | 1983 | 26 | |
| 9 | 1986 | 25 | |
| 10 | 1981 | 22 | |
| 11 | 2010 | 21 | |
| 12 | 1979 | 20 | |
| 13 | 8p trisomy in a malformed foetus. | 1982 | 20 |
| 14 | 2008 | 19 | |
| 15 | 2016 | 18 | |
| 16 | Interstitial deletion 2p accompanied by marker chromosome formation of the deleted segment resulting in a stable acentric marker chromosome. | 1997 | 18 |
| 17 | 1988 | 15 | |
| 18 | The chromosomes of the EB virus-positive Burkitt cell line P3J.HR1K studied by the fluorescent staining technique. | 1972 | 15 |
| 19 | 1982 | 14 | |
| 20 | 1983 | 13 |
About P. Petit
P. Petit is a scholar working on Genetics, Plant Science, Molecular Biology, Pediatrics, Perinatology and Child Health and Surgery, having authored 72 papers that have together received 723 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (28 papers), Chromosomal and Genetic Variations (17 papers), Prenatal Screening and Diagnostics (9 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (8 papers), Genetics and Neurodevelopmental Disorders (7 papers), Urological Disorders and Treatments (5 papers), Sexual Differentiation and Disorders (4 papers) and Chronic Myeloid Leukemia Treatments (4 papers). The work is most often cited by research in Genetics (436 citations), Hematology (91 citations), Pediatrics, Perinatology and Child Health (131 citations), Genetics (65 citations) and Developmental Biology (11 citations). P. Petit has collaborated with scholars based in Belgium, France and United States. Frequent co-authors include Herman Van den Berghe, J. P. Fryns, A Kleczkowska, J P Fryns, Pierre Fondu, Marc Alexander, Joris Vermeesch, Fryns Jp, Jean‐Pierre Fryns and Jean‐Pierre Fryns. Their work appears in journals such as Clinical Genetics, Human Genetics, The Lancet, European Journal of Pediatrics and American Journal of Roentgenology.
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.