P Franceschini

1.2k citations

73 papers · 873 indexed · h-index 17

Impact in

Developmental Biology top 5%
- 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
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities

Papers in ⓘ

Genetics 33
- Genomic variations and chromosomal abnormalities 13
- Craniofacial Disorders and Treatments 6
- Connective tissue disorders research 5
- Dermatological and Skeletal Disorders 4
Molecular Biology 22

Co-authors: Margherita Silengo (21 shared papers)D. Franceschini (18 shared papers)Andrea Guala (18 shared papers)Giuseppe Di Cara (12 shared papers)M. Biagioli (10 shared papers)R. Bianco (7 shared papers)P Durel (1 shared paper)M. A. Pellegrino (1 shared paper)
Journals: Clinical Genetics (8 papers)Human Genetics (4 papers)Sexually Transmitted Infections (3 papers)Acta Paediatrica (2 papers)Experimental Cell Research (2 papers)
Partner nations: Italy Peru Germany

In The Last Decade

P Franceschini

68 papers receiving 818 citations

Peers

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

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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	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 ·P. Ajnone-Marsan, G. Monfredini, Werner F. Ludwig, Albrecht E. Melchinger, P Franceschini, G. Pagnotto, M. Motto	1995	59
2	X/Y translocation in a family with X‐linked ichthyosis, chondrodysplasia punctata, and mental retardation: DNA analysis reveals deletion of the steroid sulphatase gene and translocation of its Y pseudogene Clinical Genetics ·Andrea Ballabio, Giancarlo Parenti, Rosalba Carrozzo, Giovanni V. Coppa, L. Felici, Valeria Migliori, Margherita Silengo, P Franceschini, Generoso Andria	1988	47
3	Arterial tortuosity syndrome American Journal of Medical Genetics ·P Franceschini, Andrea Guala, D Licata, Giuseppe Di Cara, D. Franceschini	2000	43
4	Lower lip pits and complete idiopathic precocious puberty in a patient with Kabuki make‐up (Niikawa‐Kuroki) syndrome American Journal of Medical Genetics ·P Franceschini, M. P. Vardeu, Andrea Guala, D. Franceschini, A. Testa, Andrea Corrias, P. Chiabotto	1993	42
5	Experimental rabbit syphilis. Sexually Transmitted Infections ·P Collart, P Franceschini, P Durel	1971	40
6	Biochemical changes in phytohemagglutinin stimulated human lymphocytes Experimental Cell Research ·Norman P. Salzman, M. A. Pellegrino, P Franceschini	1966	39
7	Macrocephaly-cutis marmorata telangiectatica congenita without cutis marmorata? American Journal of Medical Genetics ·P Franceschini, D Licata, Giuseppe Di Cara, Andrea Guala, D. Franceschini, Lorenzo Genitori	2000	38
8	Distinctive hair changes (pili torti) in Rapp‐Hodgkin ectodermal dysplasia syndrome Clinical Genetics ·Margherita Silengo, G. Davì, R. Bianco, Marcello Costa, A. DeMarco, Redkar Ve, P Franceschini	1982	35
9	Bladder carcinoma in Costello syndrome: Report on a patient born to consanguineous parents and review American Journal of Medical Genetics ·P Franceschini, D Licata, Giuseppe Di Cara, Andrea Guala, Marco E. Bianchi, G. Ingrosso, D. Franceschini	1999	32
10	Oro‐facial‐digital syndrome II. Transitional type between the Mohr and the Majewski syndromes: report of two new cases Clinical Genetics ·Margherita Silengo, G. Lopez Bell, M. Biagiou, P Franceschini	1987	30
11	Interstitial deletion of the long arm of chromosome 7 46,XX,del(7)(pter?q2200::q3200?qter) Human Genetics ·P Franceschini, Margherita Silengo, G. Davì, Matteo Santoro, G. Prandi, C Fabris	1978	29
12	Short rib‐dysplasia group (with/without polydactyly): Report of a patient suggesting the existence of a continuous spectrum American Journal of Medical Genetics ·P Franceschini, Andrea Guala, M. P. Vardeu, F. Signorile, D. Franceschini, M. P. Bolgiani	1995	28
13	Interstitial deletion of the long arm of chromosome 2 (q31q33) in a girl with multiple anomalies and mental retardation Human Genetics ·P Franceschini, Margherita Silengo, G. Davì, R. Bianco, M. Biagioli	1983	28
14	Variability of clinical and immunological phenotype in immunodeficiency-centromeric instability-facial anomalies syndrome European Journal of Pediatrics ·P Franceschini, Silvana Martino, M. Ciocchini, E Ciuti, M. P. Vardeu, Andrea Guala, F. Signorile, Patrizia Camerano, D. Franceschini, Pier‐Angelo Tovo	1995	27
15	Kenny–Caffey syndrome in two sibs born to consanguineous parents: Evidence for an autosomal recessive variant American Journal of Medical Genetics ·P Franceschini, A. Testa, G Bogetti, E Girardo, Andrea Guala, Graciela Lopez‐Bell, G. Buzio, E. Ferrario, E Piccato	1992	25
16	Variability of the Brachmann‐de Lange Syndrome American Journal of Medical Genetics ·Angelo Selicorni, Faustina Lalatta, E. Livini, Vincenza Briscioli, T. Piguzzi, D. Clerici Bagozzi, P Mastroiacovo, Giuseppe Zampino, G Gaeta, Aniello Pugliese, P. Cerutti‐Mainaroli, Andrea Guala, Leopoldo Zelante, M Stabile, S. Belli, P Franceschini, Ambra Gianotti, Gioacchino Scarano	1993	19
17	Partial deletion of the short arm of chromosome 20: 46,XX,del(20)(p11)/46,XX mosaicism Clinical Genetics ·Margherita Silengo, G. Lopez Bell, M. Biagioli, P Franceschini	1988	17
18	Interstitial deletion of the long arm of chromosome 3 in a patient with mental retardation and congenital anomalies Human Genetics ·P Franceschini, Margherita Silengo, G. Davì, R. Bianco, M. Biagioli	1983	16
19	FEEBLEMINDEDNESS AND XXXX KARYOTYPE† Journal of Intellectual Disability Research* ·L Di Cagno, P Franceschini	1968	15
20	Interstitial deletion of chromosome 1 (q23–25). Report of a case Clinical Genetics ·Margherita Silengo, G. Davì, R. Bianco, M. Biagioli, Andrea Guala, P Franceschini, Giuseppe Novelli	1984	14

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 873 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), Eosinophilic Disorders and Syndromes (4 papers), Dermatological and Skeletal Disorders (4 papers), Syphilis Diagnosis and Treatment (4 papers) and Prenatal Screening and Diagnostics (4 papers). The work is most often cited by research in Developmental Biology (54 citations), Genetics (454 citations), Pharmacy (27 citations), Microbiology (33 citations) and Molecular Biology (357 citations). P Franceschini has collaborated with scholars based in Italy, Peru and Germany. Frequent 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. Their work appears in journals such as Clinical Genetics, Human Genetics, Sexually Transmitted Infections, Acta Paediatrica and Experimental Cell Research.

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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