P. Petit

1.1k citations
72 papers · 765 indexed · h-index 16
Topics
Genomic variations and chromosomal abnormalities (28 papers)Chromosomal and Genetic Variations (17 papers)Prenatal Screening and Diagnostics (9 papers)

In The Last Decade

P. Petit

67 papers receiving 727 citations

Peers

P. Petit
Comparison fields: 5 of 67
  • Genetics 465
  • Molecular Biology 261
  • Plant Science 230
  • Pediatrics, Perinatology and Child Health 145
  • Hematology 91
Replace R. A. Pfeiffer with:
R. A. Pfeiffer Germany
Marie‐France Portnoï France
J. O. Van Hemel Netherlands
James Tepperberg United States
Elisena Morizio Italy
Ikuko Teshima Canada
Azzedine Aboura France
Udo Trautmann Germany
R. A. Pfeiffer Germany
F. J. Dill Canada
P. Petit relative to R. A. Pfeiffer Germany R. A. Pfeiffer's profile →
Citations per field
00.5×5.5×
R. A. Pfeiffer · 1×
Citations per year

Countries citing papers authored by P. Petit

Since Specialization
Citations

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

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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-authorship network of co-authors of P. Petit

This figure shows the co-authorship network connecting the top 25 collaborators of P. Petit. A scholar is included among the top collaborators of P. Petit based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with P. Petit. P. Petit is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
#WorkIndexed citations
1 17
2 0
3 21
4
musculoskeletal imaging - Radiography of scoliosis: comparative dosimetry between conventional technique and digital fluorography
1
5
FAIT CLINIQUE SPLÉNOSE PÉRITONÉALE SIMULANT UNE MASSE RÉTROPÉRITONÉALE DROITE
1
6 1
7 10
8 8
9
Médecine esthétique et mésothérapie. Les principales indications
0
10 1
11 9
12 6
13
On two patients with and without the complete Wolf-Hirschorn syndrome sharing the same chromosome 4p16.3-specific probe deletion: evidence of a contiguous gene deletion syndrome
3
14 62
15 3
16 5
17 3
18 6
19 32
20 26

About P. Petit

P. Petit is a scholar working on Genetics, Urology and Anatomy, having authored 72 papers that have together received 765 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (28 papers), Chromosomal and Genetic Variations (17 papers) and Prenatal Screening and Diagnostics (9 papers). The work is most often cited by research in Genetics (465 citations), Hematology (91 citations) and Pediatrics, Perinatology and Child Health (145 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, Joris Vermeesch, Peter Marynen, J P Fryns, W. De Meurichy, Marc Alexander, Pierre Fondu and Jean‐Pierre Fryns. Their work appears in journals such as The Lancet, American Journal of Roentgenology and Journal of Medical Genetics.

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.

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2026