D. Franceschini

608 total citations
25 papers, 402 citations indexed

About

D. Franceschini is a scholar working on Genetics, Molecular Biology and Surgery. According to data from OpenAlex, D. Franceschini has authored 25 papers receiving a total of 402 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Genetics, 8 papers in Molecular Biology and 6 papers in Surgery. Recurrent topics in D. Franceschini's work include Congenital limb and hand anomalies (6 papers), Connective tissue disorders research (4 papers) and Protein Tyrosine Phosphatases (3 papers). D. Franceschini is often cited by papers focused on Congenital limb and hand anomalies (6 papers), Connective tissue disorders research (4 papers) and Protein Tyrosine Phosphatases (3 papers). D. Franceschini collaborates with scholars based in Italy and Switzerland. D. Franceschini's co-authors include Andrea Guala, P Franceschini, Giuseppe Di Cara, Piergiorgio Franceschini, Andrea Saporito, Luciano Anselmi, José Aguirre, P. Chiabotto, Andrea Corrias and Alain Borgeat and has published in prestigious journals such as British Journal of Anaesthesia, American Journal of Medical Genetics and European Journal of Pediatrics.

In The Last Decade

D. Franceschini

23 papers receiving 391 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
D. Franceschini Italy 11 203 133 117 65 47 25 402
Licia Turolla Italy 11 175 0.9× 95 0.7× 83 0.7× 67 1.0× 10 0.2× 23 345
Jürgen Herrmann United States 8 283 1.4× 184 1.4× 124 1.1× 75 1.2× 19 0.4× 10 470
Ying Yu China 10 83 0.4× 51 0.4× 60 0.5× 8 0.1× 45 1.0× 45 367
Hala Mégarbané Lebanon 12 161 0.8× 325 2.4× 39 0.3× 20 0.3× 6 0.1× 24 495
Jae Ho Lee United States 10 73 0.4× 197 1.5× 145 1.2× 35 0.5× 54 1.1× 14 433
Taihei Tanaka Japan 13 32 0.2× 203 1.5× 71 0.6× 71 1.1× 39 0.8× 33 462
Thomas Faciszewski United States 12 127 0.6× 98 0.7× 350 3.0× 22 0.3× 14 0.3× 15 471
Torsten Lönnerholm Sweden 11 46 0.2× 61 0.5× 147 1.3× 20 0.3× 16 0.3× 29 307
Necat İmirzalıoğlu Türkiye 11 128 0.6× 159 1.2× 56 0.5× 146 2.2× 14 0.3× 31 429
Mariangela Palladino Italy 10 30 0.1× 175 1.3× 39 0.3× 38 0.6× 10 0.2× 18 363

Countries citing papers authored by D. Franceschini

Since Specialization
Citations

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

Fields of papers citing papers by D. Franceschini

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of D. Franceschini

This figure shows the co-authorship network connecting the top 25 collaborators of D. Franceschini. A scholar is included among the top collaborators of D. 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 D. Franceschini. D. 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.
Passanisi, Maurizio, Gianluca Scalia, Paolo Palmisciano, et al.. (2021). Difficulty differentiating between a posterior extradural lumbar tumor versus sequestered disc even with gadolinum-enhanced MRI. Surgical Neurology International. 12. 267–267. 10 indexed citations
2.
Ceruti, Samuele, Luciano Anselmi, D. Franceschini, et al.. (2017). Prevention of arterial hypotension after spinal anaesthesia using vena cava ultrasound to guide fluid management. British Journal of Anaesthesia. 120(1). 101–108. 45 indexed citations
3.
Saporito, Andrea, et al.. (2013). Thoracic ultrasound confirmation of correct lung exclusion before one-lung ventilation during thoracic surgery. Journal of Ultrasound. 16(4). 195–199. 16 indexed citations
4.
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
5.
Franceschini, Piergiorgio, et al.. (2003). Patterson–Lowry rhizomelic dysplasia: Report of two new patients. American Journal of Medical Genetics Part A. 127A(1). 86–92. 2 indexed citations
6.
Franceschini, P, et al.. (2001). Peculiar facial appearance and generalized brachydactyly in a patient with congenital onychodysplasia of the index fingers (Iso-Kikuchi syndrome). American Journal of Medical Genetics. 98(4). 330–335. 10 indexed citations
7.
Franceschini, P, et al.. (2000). Macrocephaly-cutis marmorata telangiectatica congenita without cutis marmorata?. American Journal of Medical Genetics. 90(4). 265–269. 38 indexed citations
8.
Franceschini, P, et al.. (2000). Arterial tortuosity syndrome. American Journal of Medical Genetics. 91(2). 141–141. 3 indexed citations
9.
Franceschini, P, et al.. (1999). Bladder carcinoma in Costello syndrome: Report on a patient born to consanguineous parents and review. American Journal of Medical Genetics. 86(2). 174–179. 32 indexed citations
10.
Franceschini, Piergiorgio, et al.. (1998). Long first metacarpal in monozygotic twins with probable Baller-Gerold syndrome. American Journal of Medical Genetics. 80(4). 303–308. 5 indexed citations
11.
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
12.
Franceschini, Piergiorgio, et al.. (1996). Ullrich-Turner phenotype with unusual manifestation in a patient with mosaicism 45,X/47,XX,+18. American Journal of Medical Genetics. 62(1). 26–28. 11 indexed citations
13.
Franceschini, P, Andrea Guala, D. Franceschini, et al.. (1996). The Williams syndrome: an Italian collaborative study.. PubMed. 48(10). 421–8. 7 indexed citations
14.
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
15.
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
16.
Franceschini, P, et al.. (1994). Rigid mask-like face, ear anomalies, deafness, preaxial polydactyly and toe malformations in a patient with normal intelligence. Clinical Dysmorphology. 3(3). 234???237–234???237.
17.
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
18.
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
19.
Franceschini, Piergiorgio, et al.. (1993). Monozygotic twinning and Wiedemann‐Beckwith syndrome. American Journal of Medical Genetics. 46(3). 353–354. 41 indexed citations
20.
Franceschini, P, et al.. (1992). Possible relationship between ulnar‐mammary syndrome and split hand with aplasia of the ulna syndrome. American Journal of Medical Genetics. 44(6). 807–812. 13 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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