Guido Morcaldi

480 total citations
13 papers, 276 citations indexed

About

Guido Morcaldi is a scholar working on Neurology, Molecular Biology and Rheumatology. According to data from OpenAlex, Guido Morcaldi has authored 13 papers receiving a total of 276 indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Neurology, 4 papers in Molecular Biology and 3 papers in Rheumatology. Recurrent topics in Guido Morcaldi's work include Neurofibromatosis and Schwannoma Cases (3 papers), Soft tissue tumor case studies (2 papers) and Lymphatic Disorders and Treatments (2 papers). Guido Morcaldi is often cited by papers focused on Neurofibromatosis and Schwannoma Cases (3 papers), Soft tissue tumor case studies (2 papers) and Lymphatic Disorders and Treatments (2 papers). Guido Morcaldi collaborates with scholars based in Italy, Netherlands and United Kingdom. Guido Morcaldi's co-authors include E Bonioli, Francesco Boccardo, Carlo Bellini, Mariangela Rutigliani, Ezio Fulcheri, Raoul C. M. Hennekam, Roberto Bertorelli, Roberto Gastaldi, Domenico Coviello and Carmen La Rosa and has published in prestigious journals such as Biochemical and Biophysical Research Communications, Human Mutation and Cancers.

In The Last Decade

Guido Morcaldi

12 papers receiving 273 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Guido Morcaldi Italy 8 97 68 62 54 47 13 276
Bernhard Fahrner Austria 5 70 0.7× 29 0.4× 50 0.8× 69 1.3× 136 2.9× 7 236
Sylvie Tenoutasse Belgium 13 25 0.3× 79 1.2× 61 1.0× 108 2.0× 19 0.4× 27 362
Andrea Luczay Hungary 9 13 0.1× 33 0.5× 86 1.4× 38 0.7× 17 0.4× 32 321
B. Nagy Hungary 11 27 0.3× 207 3.0× 82 1.3× 17 0.3× 15 0.3× 17 457
Ahmed Khattab United States 11 57 0.6× 138 2.0× 247 4.0× 41 0.8× 13 0.3× 36 450
John Tziotis Greece 11 16 0.2× 90 1.3× 88 1.4× 35 0.6× 17 0.4× 17 329
Julia Martínez-Sánchez Spain 9 36 0.4× 18 0.3× 69 1.1× 19 0.4× 10 0.2× 20 233
Keiji Fujimoto Japan 9 37 0.4× 11 0.2× 30 0.5× 30 0.6× 24 0.5× 33 284
Yongrong Lai China 8 14 0.1× 29 0.4× 55 0.9× 16 0.3× 13 0.3× 25 269
David Schult Germany 9 54 0.6× 8 0.1× 102 1.6× 16 0.3× 9 0.2× 11 221

Countries citing papers authored by Guido Morcaldi

Since Specialization
Citations

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

Fields of papers citing papers by Guido Morcaldi

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Guido Morcaldi

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

All Works

13 of 13 papers shown
1.
Melloni, Giulia, Marica Eoli, Claudia Cesaretti, et al.. (2019). Risk of Optic Pathway Glioma in Neurofibromatosis Type 1: No Evidence of Genotype–Phenotype Correlations in a Large Independent Cohort. Cancers. 11(12). 1838–1838. 17 indexed citations
2.
Fiorillo, Chiara, Maria Rosaria D’Apice, Federica Trucco, et al.. (2018). Characterization of MDPL Fibroblasts Carrying the Recurrent p.Ser605del Mutation in POLD1 Gene. DNA and Cell Biology. 37(12). 1061–1067. 19 indexed citations
3.
Bellini, Carlo, et al.. (2016). Congenital Chylothorax of the Newborn: Diagnosis and Treatment in Three Pictures.. PubMed. 49(3). 150–6. 6 indexed citations
4.
Brisca, Giacomo, Chiara Fiorillo, Claudia Nesti, et al.. (2015). Early onset cardiomyopathy associated with the mitochondrial tRNALeu(UUR) 3271T>C MELAS mutation. Biochemical and Biophysical Research Communications. 458(3). 601–604. 15 indexed citations
5.
Morcaldi, Guido, Tommaso Bellini, Cesare Rossi, et al.. (2015). LYMPHODYSPLASIA AND KRAS MUTATION: A CASE REPORT AND LITERATURE REVIEW.. PubMed. 48(3). 121–7. 12 indexed citations
6.
Villa, Giuseppe, Gianmario Sambuceti, Cristina Traggiai, et al.. (2014). Lymphoscintigraphy patterns in newborns and children with congenital lymphatic dysplasia.. PubMed. 47(1). 28–39. 15 indexed citations
7.
Morcaldi, Guido, Maurizio Clementi, Giuliana Lama, et al.. (2013). Evaluation of Tibial Osteopathy Occurrence in Neurofibromatosis Type 1 Italian Patients. American Journal of Medical Genetics Part A. 161(5). 927–934. 1 indexed citations
8.
Grandis, Elisa De, Marisol Mirabelli-Badenier, Luca Boeri, et al.. (2011). Response to rituximab in 3 children with opsoclonus-myoclonus syndrome resistant to conventional treatments. European Journal of Paediatric Neurology. 16(2). 192–195. 14 indexed citations
9.
Morcaldi, Guido, et al.. (2010). Congenital lymphatic dysplasia in Kabuki syndrome: first report of an unusual association.. PubMed. 43(4). 188–91.
10.
Bellini, Carlo, Raoul C. M. Hennekam, Ezio Fulcheri, et al.. (2009). Etiology of nonimmune hydrops fetalis: A systematic review. American Journal of Medical Genetics Part A. 149A(5). 844–851. 130 indexed citations
11.
Bonioli, E, Carmen La Rosa, Roberto Bertorelli, et al.. (2005). Heterozygous mutations of growth hormone receptor gene in children with idiopathic short stature. Growth Hormone & IGF Research. 15(6). 405–410. 36 indexed citations
12.
Bonioli, E, Raoul C. M. Hennekam, Guido Morcaldi, et al.. (2004). Aplasia cutis congenita, skull defect, brain heterotopia, and intestinal lymphangiectasia. American Journal of Medical Genetics Part A. 132A(2). 202–205. 6 indexed citations
13.
Origone, Paola, Carlo Bellini, Barbara Banelli, et al.. (2003). Neurofibromatosis eurofibromatosis type 1 (NF1): Identification of eight unreported mutations in NF1 gene in Italian patients. Human Mutation. 22(2). 179–180. 5 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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