P Franceschini

1.2k citations
73 papers · 874 · h-index 17

Impact in

    • Congenital limb and hand anomalies
  • Genetics top 5%
    • Genomic variations and chromosomal abnormalities
    • Connective tissue disorders research
    • Genetic Mapping and Diversity in Plants and Animals
    • Genomics and Rare Diseases

Papers in

    • Genomic variations and chromosomal abnormalities 13
    • Craniofacial Disorders and Treatments 6
    • Connective tissue disorders research 5
    • Dermatological and Skeletal Disorders 4

P Franceschini

68 papers receiving 821 citations

Peers

P Franceschini
Comparison fields: 5 of 78
  • Developmental Biology 53
  • Genetics 435
  • Pharmacy 26
  • Urology 32
  • Microbiology 32
Replace Birgit Meyer with:
Birgit Meyer Germany
Sylvie Manouvrier‐Hanu France
Sara Kaffe United States
Pia Kuss United States
J Civatte France
K. Morgan Canada
Darrell Salk United States
M S Pollack United States
Susan J. Bayliss United States
Sultan Al‐Khenaizan Saudi Arabia
P Franceschini relative to Birgit Meyer Germany Birgit Meyer's profile →
Citations per field
00.5×10×13×
Birgit Meyer · 1×
Citations per year

Countries citing papers authored by P Franceschini

Since Specialization
Citations

This map shows the geographic impact of P Franceschini'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 Franceschini with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites P Franceschini more than expected).

Fields of papers citing papers by P Franceschini

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by P Franceschini. 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 Franceschini. The network helps show where P Franceschini may publish in the future.

Co-authors

The 25 scholars most cited alongside P Franceschini, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with P Franceschini Line = papers co-authored together P Franceschini links everyone, so they are left out of the graph.

All Works

20 of 20 papers shown

Showing the 20 most-cited of 73 papers — load more, or switch the sort, to bring in the rest.

#Work
1 199559
2 198847
3 200045
4 199342
5 197139
6 196638
7 200038
8 198235
9 199932
10 198730
11 197829
12 199528
13 198328
14 199527
15 199225
16 199319
17 198817
18 198316
19 196815
20 198414

About P Franceschini

P Franceschini is a scholar working on Genetics, Molecular Biology, Developmental Biology, Rheumatology and Surgery, having authored 73 papers that have together received 874 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (13 papers), Congenital limb and hand anomalies (10 papers), Craniofacial Disorders and Treatments (6 papers), Connective tissue disorders research (5 papers), Syphilis Diagnosis and Treatment (4 papers), Dermatological and Skeletal Disorders (4 papers), Congenital Anomalies and Fetal Surgery (4 papers) and Prenatal Screening and Diagnostics (4 papers). The work is most often cited by research in Developmental Biology (53 citations), Genetics (435 citations), Pharmacy (26 citations), Urology (32 citations) and Microbiology (32 citations). P Franceschini has collaborated with scholars based in Italy, Germany and Brazil. Frequent co-authors include Margherita Silengo, D. Franceschini, Andrea Guala, Giuseppe Di Cara, M. Biagioli, R. Bianco, Norman P. Salzman, M. A. Pellegrino, P Durel and Andrea Guala. Their work appears in journals such as Clinical Genetics, Human Genetics, Sexually Transmitted Infections, Experimental Cell Research and Acta Paediatrica.

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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