L Giuffrè

457 total citations
21 papers, 271 citations indexed

About

L Giuffrè is a scholar working on Genetics, Pediatrics, Perinatology and Child Health and Developmental Biology. According to data from OpenAlex, L Giuffrè has authored 21 papers receiving a total of 271 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Genetics, 7 papers in Pediatrics, Perinatology and Child Health and 5 papers in Developmental Biology. Recurrent topics in L Giuffrè's work include Congenital limb and hand anomalies (5 papers), Prenatal Screening and Diagnostics (5 papers) and Genomic variations and chromosomal abnormalities (3 papers). L Giuffrè is often cited by papers focused on Congenital limb and hand anomalies (5 papers), Prenatal Screening and Diagnostics (5 papers) and Genomic variations and chromosomal abnormalities (3 papers). L Giuffrè collaborates with scholars based in Italy and United States. L Giuffrè's co-authors include Giovanni Corsello, Antonio Marini, Marcello Lanari, Marcello Giovannini, Giovanni A. Rossi, G Rondini, Gianvincenzo Zuccotti, G Salvioli, Rocco Merolla and Maria Piccione and has published in prestigious journals such as American Journal of Medical Genetics, Pediatric Pulmonology and Pediatric Radiology.

In The Last Decade

L Giuffrè

18 papers receiving 258 citations

Peers

L Giuffrè

EPIDE

PRM

GENET

SURGE

Neil MacLachlan United Kingdom

P Corone France

H Tanda Japan

M. C. Addor Denmark

Maria Sellitto Italy

Abram Kanof United States

Moises Simpser United States

Richard E. Garcia United States

Neil Mulrooney United States

Francisco J.C. Reis Brazil

Neil MacLachlan United Kingdom

L Giuffrè

30 ×0.3

EPIDE

46 ×0.5

PRM

43 ×0.5

GENET

65 ×0.9

SURGE

24 ×0.5

Citations per year, relative to L Giuffrè L Giuffrè (= 1×) peers Neil MacLachlan

Countries citing papers authored by L Giuffrè

Since Specialization

Citations

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

Fields of papers citing papers by L Giuffrè

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of L Giuffrè

This figure shows the co-authorship network connecting the top 25 collaborators of L Giuffrè. A scholar is included among the top collaborators of L Giuffrè 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 L Giuffrè. L Giuffrè is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

Piro, Ettore, et al.. (2005). Growth charts of Down syndrome in sicily: Evaluation of 382 children 0-14 years of age. American Journal of Medical Genetics. 37(S7). 66–70. 25 indexed citations

Lanari, Marcello, Marcello Giovannini, L Giuffrè, et al.. (2002). Prevalence of respiratory syncytial virus infection in Italian infants hospitalized for acute lower respiratory tract infections, and association between respiratory syncytial virus infection risk factors and disease severity. Pediatric Pulmonology. 33(6). 458–465. 115 indexed citations

Bosco, Paolo, Raffaele Ferri, Francesco Calı̀, et al.. (1995). Analysis of the FMR-1 gene and correlation with phenotype in Sicilian families with the fragile X syndrome. 20. 149–151. 1 indexed citations

Gurrieri, Fiorella, et al.. (1995). Ulnar ray defect in an infant with a 6q21;7q31.2 translocation: Further evidence for the existence of a limb defect gene in 6q21. American Journal of Medical Genetics. 55(3). 315–318. 20 indexed citations

Giuffrè, L, et al.. (1994). New syndrome: Autosomal dominant microcephaly and radio‐ulnar synostosis. American Journal of Medical Genetics. 51(3). 266–269. 10 indexed citations

Corsello, Giovanni, A. Aloisio, Geoffrey M. Attardo, et al.. (1994). Indagine Clinico Epidemiologica su 132 Nati da Gravidanze Multiple. Acta geneticae medicae et gemellologiae twin research. 43(1-2). 110–111.

Corsello, Giovanni, et al.. (1992). VATER/VACTERL association: Clinical variability and expanding phenotype including laryngeal stenosis. American Journal of Medical Genetics. 44(6). 813–815. 19 indexed citations

Piro, Ettore, et al.. (1991). Kabuki make-up (Niikawa-Kuroki) syndrome: Clinical and radiological observations in two sicilian children. Pediatric Radiology. 21(6). 428–431. 25 indexed citations

Cammarata, Matteo, et al.. (1991). Genetic factors of recurrent abortions.. PubMed. 20(6). 367–70. 4 indexed citations

10.

Giuffrè, L, et al.. (1991). [Role of diagnostic imaging in Rubinstein-Taybi syndrome. Personal experience with 8 cases].. PubMed. 81(3). 253–61. 2 indexed citations

11.

Corsello, Giovanni, et al.. (1990). Cervico-Oculo-Acusticus (Wildervanck's) syndrome: a clinical variant of Klippel-Feil sequence?. Klinische Pädiatrie. 202(3). 176–179. 9 indexed citations

12.

Corsello, Giovanni, et al.. (1990). Holoprosencephaly: Examples of clinical variability and etiologic heterogeneity. American Journal of Medical Genetics. 37(2). 244–249. 17 indexed citations

13.

Giuffrè, L, et al.. (1988). Two new cases of Thrombocytopenia Absent Radius (TAR) syndrome: Clinical, Genetic and Nosologic Features. Klinische Pädiatrie. 200(1). 10–14. 1 indexed citations

14.

Neri, Giovanni, Piero Pavone, F. Mollica, et al.. (1988). The fragile X in sicily: An epidemiological survey. American Journal of Medical Genetics. 30(1-2). 665–672. 12 indexed citations

15.

Pavone, Piero, Bruno Dallapiccola, Renata Rizzo, et al.. (1988). Phenotypic variability in the Nager syndrome. Report of 4 unrelated patients: A collaborative study. 1. 294–302. 3 indexed citations

16.

Giuffrè, L, et al.. (1987). [Ring chromosome 4 in twins].. PubMed. 9(3). 349–50. 3 indexed citations

17.

Giuffrè, L, et al.. (1986). [Silver-Russell syndrome. A possible example of genetic heterogenicity].. PubMed. 38(19). 849–53. 2 indexed citations

18.

Cammarata, Matteo, et al.. (1985). [Cri-du-chat syndrome: palmar dermatoglyphics of diagnostic significance].. PubMed. 37(5-6). 251–3. 1 indexed citations

19.

Giuffrè, L, et al.. (1967). [Trisomy 13-15 (description of 4 cases)].. PubMed. 80(6). 481–98.

20.

Giuffrè, L, et al.. (1967). Immunoelectrophoretic Analysis of Serum Proteins of Patients Affected by Kala-Azar. Pathobiology. 30(2). 215–221. 1 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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