Marco Di Duca

2.9k total citations
49 papers, 1.8k citations indexed

About

Marco Di Duca is a scholar working on Molecular Biology, Surgery and Genetics. According to data from OpenAlex, Marco Di Duca has authored 49 papers receiving a total of 1.8k indexed citations (citations by other indexed papers that have themselves been cited), including 22 papers in Molecular Biology, 12 papers in Surgery and 11 papers in Genetics. Recurrent topics in Marco Di Duca's work include Renal Diseases and Glomerulopathies (7 papers), Digestive system and related health (7 papers) and Neonatal Respiratory Health Research (6 papers). Marco Di Duca is often cited by papers focused on Renal Diseases and Glomerulopathies (7 papers), Digestive system and related health (7 papers) and Neonatal Respiratory Health Research (6 papers). Marco Di Duca collaborates with scholars based in Italy, United States and Türkiye. Marco Di Duca's co-authors include Roberto Ravazzolo, Isabella Ceccherini, Gian Marco Ghiggeri, Tiziana Bachetti, Silvia Borghini, Gianluca Caridi, Giuseppe Santamaria, R Gusmano, Roberta Bertelli and Francesco Perfumo and has published in prestigious journals such as Journal of Biological Chemistry, PLoS ONE and Biochemical Journal.

In The Last Decade

Marco Di Duca

48 papers receiving 1.8k citations

Peers

Marco Di Duca
Claudine H. Kos United States
Mary Ann Mitnick United States
Hosung Min United States
Derek P. DiRocco United States
Tatjana Levi United States
Horia Stanescu United Kingdom
Michito Hamada Japan
Masato Hoshi Japan
H.J.M. Smeets Netherlands
Naoshi Obara Japan
Claudine H. Kos United States
Marco Di Duca
Citations per year, relative to Marco Di Duca Marco Di Duca (= 1×) peers Claudine H. Kos

Countries citing papers authored by Marco Di Duca

Since Specialization
Citations

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

Fields of papers citing papers by Marco Di Duca

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Marco Di Duca. 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 Marco Di Duca. The network helps show where Marco Di Duca may publish in the future.

Co-authorship network of co-authors of Marco Di Duca

This figure shows the co-authorship network connecting the top 25 collaborators of Marco Di Duca. A scholar is included among the top collaborators of Marco Di Duca 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 Marco Di Duca. Marco Di Duca 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.
Musante, Ilaria, Davide Cangelosi, Fanny Jaudon, et al.. (2025). CACNA1A loss-of-function affects neurogenesis in human iPSC-derived neural models. Cellular and Molecular Life Sciences. 82(1). 234–234. 1 indexed citations
2.
Traverso, Monica, Michele Iacomino, Marco Di Duca, et al.. (2024). DAG1 haploinsufficiency is associated with sporadic and familial isolated or pauci-symptomatic hyperCKemia. European Journal of Human Genetics. 32(3). 342–349. 1 indexed citations
3.
Brolatti, Noemi, Patrizia De Marco, Marzia Ognibene, et al.. (2024). Novel causative variants in Legius syndrome: SPRED1 Genotype spectrum expansion. American Journal of Medical Genetics Part A. 194(12). e63824–e63824. 5 indexed citations
4.
Scala, Marcello, Patrizia De Marco, Marzia Ognibene, et al.. (2023). Somatic Double Inactivation of NF1 Associated with NF1-Related Pectus Excavatum Deformity. Human Mutation. 2023. 1–7. 3 indexed citations
5.
Iacomino, Michele, Monica Traverso, Mariasavina Severino, et al.. (2023). Refining the electroclinical spectrum of NPRL3‐related epilepsy: A novel multiplex family and literature review. Epilepsia Open. 8(4). 1314–1330. 6 indexed citations
6.
Bertoni, Arinna, Sonia Carta, Chiara Baldovini, et al.. (2019). A novel knock-in mouse model of cryopyrin-associated periodic syndromes with development of amyloidosis: Therapeutic efficacy of proton pump inhibitors. Journal of Allergy and Clinical Immunology. 145(1). 368–378.e13. 16 indexed citations
7.
Faraci, Maura, Francesca Bagnasco, Stefano Giardino, et al.. (2017). Evaluation of Chimerism Dynamics after Allogeneic Hematopoietic Stem Cell Transplantation in Children with Nonmalignant Diseases. Biology of Blood and Marrow Transplantation. 24(5). 1088–1093. 17 indexed citations
8.
Matera, Ivana, Marco Musso, Paola Griseri, et al.. (2013). Allele-Specific Expression at theRETLocus in Blood and Gut Tissue of Individuals Carrying Risk Alleles for Hirschsprung Disease. Human Mutation. 34(5). 754–762. 3 indexed citations
9.
Borghini, Silvia, Michele Fiore, Marco Di Duca, et al.. (2011). Candidate Genes in Patients with Autoinflammatory Syndrome Resembling Tumor Necrosis Factor Receptor-associated Periodic Syndrome Without Mutations in the TNFRSF1A Gene. The Journal of Rheumatology. 38(7). 1378–1384. 13 indexed citations
10.
Borghini, Silvia, Sara Tassi, Sabrina Chiesa, et al.. (2010). Clinical presentation and pathogenesis of cold-induced autoinflammatory disease in a family with recurrence of an NLRP12 mutation. Arthritis & Rheumatism. 63(3). 830–839. 141 indexed citations
11.
Duca, Marco Di, Roberta Oleggini, Simone Sanna‐Cherchi, et al.. (2006). Cis and trans regulatory elements in NPHS2 promoter: Implications in proteinuria and progression of renal diseases. Kidney International. 70(7). 1332–1341. 17 indexed citations
12.
Bachetti, Tiziana, Ivana Matera, Silvia Borghini, et al.. (2005). Distinct pathogenetic mechanisms for PHOX2B associated polyalanine expansions and frameshift mutations in congenital central hypoventilation syndrome. Human Molecular Genetics. 14(13). 1815–1824. 95 indexed citations
13.
Filocamo, Mirella, Stefano Regis, Fabio Corsolini, et al.. (2003). Expression studies of two novel in CIS‐mutations identified in an intermediate case of Hunter syndrome. American Journal of Medical Genetics Part A. 120A(1). 84–87. 13 indexed citations
14.
Regis, Stefano, et al.. (2003). An unusual arylsulfatase A pseudodeficiency allele carrying a splice site mutation in a metachromatic leukodystrophy patient. European Journal of Human Genetics. 12(2). 150–154. 9 indexed citations
15.
Regis, Stefano, et al.. (2003). An Alu-mediated rearrangement as cause of exon skipping in Hunter disease. Human Genetics. 112(4). 419–425. 28 indexed citations
16.
Bertelli, Roberta, Fabrizio Ginevri, Gianluca Caridi, et al.. (2003). Recurrence of focal segmental glomerulosclerosis after renal transplantation in patients with mutations of podocin. American Journal of Kidney Diseases. 41(6). 1314–1321. 101 indexed citations
17.
Bolino, Alessandra, Valeria Marigo, Julie Loader, et al.. (2002). Molecular characterization and expression analysis of Mtmr2 , mouse homologue of MTMR2 , the Myotubularin-related 2 gene, mutated in CMT4B. Gene. 283(1-2). 17–26. 26 indexed citations
18.
Caridi, Gianluca, Roberta Bertelli, Alba Carrea, et al.. (2001). Prevalence, Genetics, and Clinical Features of Patients Carrying Podocin Mutations in Steroid-Resistant Nonfamilial Focal Segmental Glomerulosclerosis. Journal of the American Society of Nephrology. 12(12). 2742–2746. 140 indexed citations
19.
Botti, Gerardo, Marco Di Duca, Gian Marco Ghiggeri, et al.. (2000). Lysyl Oxidase Activates the Transcription Activity of Human Collagene III Promoter. Journal of Biological Chemistry. 275(46). 36341–36349. 111 indexed citations
20.

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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