Ph. 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
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- Prenatal Screening and Diagnostics
Papers in
- Genetics 42
- Genomic variations and chromosomal abnormalities 28
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 8
- Genetics and Neurodevelopmental Disorders 8
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- Prenatal Screening and Diagnostics 9
- Co-authors
- Herman Van den Berghe (17 shared papers)J. P. Fryns (13 shared papers)Alice Kleczkowska (6 shared papers)J P Fryns (5 shared papers)J. P. Fryns (5 shared papers)Joris Robert Vermeesch (5 shared papers)Marc Alexander (1 shared paper)Pierre Fondu (1 shared paper)
In The Last Decade
Ph. Petit
69 papers receiving 766 citations
Peers
Comparison fields: 5 of 68
- Genetics 510
- Pediatrics, Perinatology and Child Health 164
- Hematology 94
- Developmental Biology 16
- Genetics 67
Countries citing papers authored by Ph. Petit
This map shows the geographic impact of Ph. 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 Ph. Petit with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Ph. Petit more than expected).
Fields of papers citing papers by Ph. Petit
This network shows the impact of papers produced by Ph. 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 Ph. Petit. The network helps show where Ph. Petit may publish in the future.
Co-authors
The 25 scholars most cited alongside Ph. 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 73 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 1984 | 56 | |
| 2 | 1973 | 41 | |
| 3 | 1982 | 38 | |
| 4 | 1977 | 36 | |
| 5 | 1997 | 34 | |
| 6 | 1984 | 32 | |
| 7 | 1983 | 30 | |
| 8 | 1982 | 29 | |
| 9 | 1981 | 26 | |
| 10 | 1987 | 24 | |
| 11 | 1986 | 24 | |
| 12 | 1996 | 24 | |
| 13 | 2016 | 22 | |
| 14 | 2010 | 22 | |
| 15 | 1979 | 21 | |
| 16 | 2008 | 20 | |
| 17 | 1999 | 20 | |
| 18 | 8p trisomy in a malformed foetus. | 1982 | 20 |
| 19 | Interstitial deletion 2p accompanied by marker chromosome formation of the deleted segment resulting in a stable acentric marker chromosome. | 1997 | 19 |
| 20 | The chromosomes of the EB virus-positive Burkitt cell line P3J.HR1K studied by the fluorescent staining technique. | 1972 | 18 |
About Ph. Petit
Ph. Petit is a scholar working on Genetics, Pediatrics, Perinatology and Child Health, Urology, Plant Science and Hematology, having authored 73 papers that have together received 846 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 (8 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 (510 citations), Pediatrics, Perinatology and Child Health (164 citations), Hematology (94 citations), Developmental Biology (16 citations) and Genetics (67 citations). Ph. Petit has collaborated with scholars based in Belgium, France and India. Frequent co-authors include Herman Van den Berghe, J. P. Fryns, Alice Kleczkowska, J P Fryns, J. P. Fryns, Joris Robert Vermeesch, Marc Alexander, Pierre Fondu, Jean‐Pierre Fryns and Fryns Jp. Their work appears in journals such as Clinical Genetics, Human Genetics, The Lancet, Diagnostic and Interventional Imaging 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.