P Franceschini

1.2k total citations
73 papers, 873 citations indexed

About

P Franceschini is a scholar working on Genetics, Molecular Biology and Developmental Biology. According to data from OpenAlex, P Franceschini has authored 73 papers receiving a total of 873 indexed citations (citations by other indexed papers that have themselves been cited), including 33 papers in Genetics, 22 papers in Molecular Biology and 10 papers in Developmental Biology. Recurrent topics in P Franceschini's work include Genomic variations and chromosomal abnormalities (13 papers), Congenital limb and hand anomalies (10 papers) and Craniofacial Disorders and Treatments (6 papers). P Franceschini is often cited by papers focused on Genomic variations and chromosomal abnormalities (13 papers), Congenital limb and hand anomalies (10 papers) and Craniofacial Disorders and Treatments (6 papers). P Franceschini collaborates with scholars based in Italy, Chile and Germany. P Franceschini's co-authors include Margherita Silengo, D. Franceschini, Andrea Guala, Giuseppe Di Cara, M. Biagioli, R. Bianco, P Durel, M. A. Pellegrino, Norman P. Salzman and Andrea Guala and has published in prestigious journals such as Experimental Cell Research, Theoretical and Applied Genetics and Human Genetics.

In The Last Decade

P Franceschini

68 papers receiving 818 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
P Franceschini Italy 17 454 357 107 102 97 73 873
A. J. Therkelsen Denmark 15 292 0.6× 267 0.7× 151 1.4× 80 0.8× 203 2.1× 42 720
J. L. Huret France 18 384 0.8× 405 1.1× 90 0.8× 48 0.5× 121 1.2× 39 1.0k
Sara Kaffe United States 16 546 1.2× 235 0.7× 111 1.0× 89 0.9× 399 4.1× 30 768
D E Rooney United Kingdom 10 291 0.6× 245 0.7× 86 0.8× 84 0.8× 243 2.5× 14 631
K. Morgan Canada 14 541 1.2× 665 1.9× 27 0.3× 106 1.0× 106 1.1× 28 1.2k
Avirachan T. Tharapel United States 19 976 2.1× 443 1.2× 274 2.6× 162 1.6× 881 9.1× 61 1.5k
Susanne Ledig Germany 18 546 1.2× 567 1.6× 38 0.4× 71 0.7× 151 1.6× 33 1.0k
Iris Bartels Germany 20 643 1.4× 305 0.9× 206 1.9× 130 1.3× 738 7.6× 69 1.3k
M S Pollack United States 16 410 0.9× 477 1.3× 25 0.2× 76 0.7× 289 3.0× 36 1.2k
Sylvie Manouvrier‐Hanu France 9 280 0.6× 460 1.3× 17 0.2× 119 1.2× 30 0.3× 20 1.1k

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-authorship network of co-authors of P Franceschini

This figure shows the co-authorship network connecting the top 25 collaborators of P Franceschini. A scholar is included among the top collaborators of P Franceschini 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 Franceschini. P Franceschini 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
1.
Franceschini, P. (2012). Heidegger e Hölderlin: pensamento, errância e o habitar poético. 21–33. 1 indexed citations
2.
Franceschini, P, Andrea Guala, Giovanni Botta, et al.. (2003). Gershoni–Baruch syndrome: Report of a new family confirming autosomal recessive inheritance. American Journal of Medical Genetics Part A. 122A(2). 174–179. 10 indexed citations
3.
Franceschini, P, et al.. (1997). Esophageal atresia with distal tracheoesophageal fistula in a patient with fronto-metaphyseal dysplasia. American Journal of Medical Genetics. 73(1). 10–14. 5 indexed citations
4.
Melchinger, Albrecht E., et al.. (1995). In an elite cross of maize a major quantitative trait locus controls one-fourth of the genetic variation for grain yield. Theoretical and Applied Genetics. 90(3-4). 415–424. 59 indexed citations
5.
Franceschini, P, et al.. (1995). Variability of clinical and immunological phenotype in immunodeficiency-centromeric instability-facial anomalies syndrome. European Journal of Pediatrics. 154(10). 840–846. 27 indexed citations
6.
Franceschini, P, et al.. (1995). Short rib‐dysplasia group (with/without polydactyly): Report of a patient suggesting the existence of a continuous spectrum. American Journal of Medical Genetics. 59(3). 359–364. 28 indexed citations
7.
Franceschini, P, et al.. (1994). Low-risk endometrial hyperplasia: hysteroscopy and histologic evaluation after treatment with LH-RH analogue.. PubMed. 21(2). 79–86. 5 indexed citations
8.
Franceschini, P, et al.. (1993). Inguinal hernia and atrial septal defect in tel Hashomer camptodactyly syndrome: Report of a new case expanding the phenotypic spectrum of the disease. American Journal of Medical Genetics. 46(3). 341–344. 4 indexed citations
9.
Franceschini, P, Andrea Guala, D. Franceschini, et al.. (1993). Lower lip pits and complete idiopathic precocious puberty in a patient with Kabuki make‐up (Niikawa‐Kuroki) syndrome. American Journal of Medical Genetics. 47(3). 423–425. 42 indexed citations
10.
Selicorni, Angelo, Faustina Lalatta, P Mastroiacovo, et al.. (1993). Variability of the Brachmann‐de Lange Syndrome. American Journal of Medical Genetics. 47(7). 977–982. 19 indexed citations
11.
Franceschini, P, et al.. (1992). Kenny–Caffey syndrome in two sibs born to consanguineous parents: Evidence for an autosomal recessive variant. American Journal of Medical Genetics. 42(1). 112–116. 25 indexed citations
12.
13.
Silengo, Margherita, et al.. (1988). Partial deletion of the short arm of chromosome 20: 46,XX,del(20)(p11)/46,XX mosaicism. Clinical Genetics. 33(2). 108–110. 17 indexed citations
14.
Silengo, Margherita, et al.. (1986). Asymmetric crying facies with microcephaly and mental retardation. An autosomal dominant syndrome with variable expressivity. Clinical Genetics. 30(6). 481–484. 10 indexed citations
15.
Silengo, Margherita, R. Bianco, M. Biagioli, et al.. (1984). Interstitial deletion of chromosome 1 (q23–25). Report of a case. Clinical Genetics. 25(6). 549–552. 14 indexed citations
16.
Silengo, Margherita, et al.. (1983). Kniest disease with Pierre Robin syndrome and hydrocephalus. Pediatric Radiology. 13(2). 106–109. 8 indexed citations
17.
Nuzzo, Fiorella, et al.. (1975). A family with three sibs carrying trisomy 21.. PubMed. 18(2). 111–6. 7 indexed citations
18.
Franceschini, P. (1974). Semiconservative DNA duplication in human chromosomes treated with BUdR and stained with acridine orange. Experimental Cell Research. 89(2). 420–421. 12 indexed citations
19.
Franceschini, P. (1973). La pénicilline dans le traitement de la syphilis.. ˜La œNouvelle presse médicale. 2(20).
20.
Ceppellini, R, P Franceschini, V. Miggiano, & Giuseppe Tridente. (1965). DIRECTIONAL ACTIVATION OF MIXED LYMPHOCYTE CULTURES (A PRELIMINARY REPORT).. OSTI OAI (U.S. Department of Energy Office of Scientific and Technical Information). 30(18). 33182–33194. 2 indexed citations

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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