Marina Goldoni

1.0k total citations
18 papers, 362 citations indexed

About

Marina Goldoni is a scholar working on Molecular Biology, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Marina Goldoni has authored 18 papers receiving a total of 362 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Molecular Biology, 11 papers in Genetics and 3 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Marina Goldoni's work include Genomic variations and chromosomal abnormalities (6 papers), Genetics and Neurodevelopmental Disorders (5 papers) and Genetic Syndromes and Imprinting (3 papers). Marina Goldoni is often cited by papers focused on Genomic variations and chromosomal abnormalities (6 papers), Genetics and Neurodevelopmental Disorders (5 papers) and Genetic Syndromes and Imprinting (3 papers). Marina Goldoni collaborates with scholars based in Italy, Romania and Denmark. Marina Goldoni's co-authors include Giuseppe Macino, Valerio Fulci, Debora Franceschini, Nicoletta Carucci, Franca Citarella, Claudia Carissimi, Francesca Meloni, Vincenzo Barnaba, Graziella Curtale and Carlo Cogoni and has published in prestigious journals such as SHILAP Revista de lepidopterología, Blood and Frontiers in Genetics.

In The Last Decade

Marina Goldoni

16 papers receiving 355 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Marina Goldoni Italy 4 234 178 93 57 23 18 362
Tamer Ali Germany 7 376 1.6× 238 1.3× 21 0.2× 55 1.0× 13 0.6× 9 453
Yaxun Wei China 13 291 1.2× 142 0.8× 58 0.6× 16 0.3× 23 1.0× 22 411
Hyerim Yi South Korea 7 764 3.3× 143 0.8× 112 1.2× 25 0.4× 23 1.0× 8 838
Courtney K. JnBaptiste United States 5 521 2.2× 313 1.8× 29 0.3× 14 0.2× 14 0.6× 5 573
Mrinmoyee Majumder United States 11 370 1.6× 136 0.8× 40 0.4× 11 0.2× 40 1.7× 16 453
Justine Nuytens Belgium 6 489 2.1× 377 2.1× 24 0.3× 18 0.3× 13 0.6× 9 576
Arijita Sarkar United States 10 225 1.0× 99 0.6× 20 0.2× 147 2.6× 19 0.8× 19 378
Jelena Perovanović United States 9 403 1.7× 73 0.4× 32 0.3× 13 0.2× 26 1.1× 13 489

Countries citing papers authored by Marina Goldoni

Since Specialization
Citations

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

Fields of papers citing papers by Marina Goldoni

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Marina Goldoni

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

All Works

18 of 18 papers shown
1.
Siracusano, Martina, Assia Riccioni, Romina Moavero, et al.. (2025). Autism spectrum disorder and 3p24.3p23 triplication: a case report. Journal of Medical Case Reports. 19(1). 106–106.
2.
Petrarca, Laura, Valentina Guida, Raffaella Nenna, et al.. (2025). Genotype‐Phenotype Correlation in a Group of Italian Patients With Primary Ciliary Dyskinesia. Pediatric Pulmonology. 60(4). e71057–e71057. 1 indexed citations
3.
Torres, Bárbara, Marina Goldoni, Laura Bernardini, et al.. (2023). Mosaic genome‐wide paternal uniparental disomy after discordant results from primary fetal samples and cultured cells. American Journal of Medical Genetics Part A. 191(4). 1101–1106. 3 indexed citations
4.
Sciacchitano, Salvatore, Maria Piane, Claudia De Vitis, et al.. (2022). Complete Pseudo-Anodontia in an Adult Woman with Pseudo-Hypoparathyroidism Type 1a: A New Additional Nonclassical Feature?. Diagnostics. 12(12). 2997–2997. 3 indexed citations
5.
Giuffrida, Maria Grazia, Marina Goldoni, Giovanna Carpentieri, et al.. (2022). 3′UTR Deletion of NONO Leads to Corpus Callosum Anomaly, Left Ventricular Non-Compaction and Ebstein’s Anomaly in a Male Fetus. Diagnostics. 12(10). 2354–2354. 3 indexed citations
6.
Torres, Bárbara, et al.. (2022). Case Report: A Novel Homozygous Missense Variant of FBN3 Supporting It Is a New Candidate Gene Causative of a Bardet–Biedl Syndrome–Like Phenotype. Frontiers in Genetics. 13. 924362–924362. 1 indexed citations
7.
Mastrangelo, Mario, et al.. (2020). Neurodevelopmental Impairment As the Main Phenotypic Hallmark Associated with the Translocation t(7;10)(7p22.3;q26.11). Journal of Pediatric Genetics. 11(1). 68–73. 1 indexed citations
8.
Ferrari, Daniela, Laura Bernardini, Marina Goldoni, et al.. (2020). Generation of an induced pluripotent stem cell line, CSSi011-A (6534), from an Amyotrophic lateral sclerosis patient with heterozygous L145F mutation in SOD1 gene. Stem Cell Research. 47. 101924–101924. 3 indexed citations
9.
Bernardini, Laura, Roberta Battini, Marina Goldoni, et al.. (2020). Correlating Neuroimaging and CNVs Data: 7 Years of Cytogenomic Microarray Analysis on Patients Affected by Neurodevelopmental Disorders. Journal of Pediatric Genetics. 10(4). 292–299.
10.
Arghir, Aurora, Sorina Mihaela Papuc, Sara Loddo, et al.. (2020). Autism and severe clinical phenotype in a patient with 8p21.2p11.21 deletion: Case report and literature review. SHILAP Revista de lepidopterología. 9(1). 314–321. 2 indexed citations
11.
Miolo, Gianmaria, Laura Bernardini, Anna Capalbo, et al.. (2020). Identification of a De Novo Xq26.2 Microduplication Encompassing FIRRE Gene in a Child with Intellectual Disability. Diagnostics. 10(12). 1009–1009. 1 indexed citations
12.
Ferrari, Daniela, Marina Goldoni, Laura Bernardini, et al.. (2019). Generation of induced pluripotent stem cell line CSSi008-A (4698) from a patient affected by advanced stage of Dentato-Rubral-Pallidoluysian atrophy (DRPLA). Stem Cell Research. 40. 101551–101551. 8 indexed citations
13.
Ferrari, Daniela, Bárbara Torres, Marina Goldoni, et al.. (2018). Copy number variations in healthy subjects. Case study: iPSC line CSSi005-A (3544) production from an individual with variation in 15q13.3 chromosome duplicating gene CHRNA7. Stem Cell Research. 32. 73–77. 2 indexed citations
14.
Rosati, Jessica, Marina Goldoni, Daniela Ferrari, et al.. (2018). Production and characterization of human induced pluripotent stem cells (iPSCs) from Joubert Syndrome: CSSi001-A (2850). Stem Cell Research. 27. 74–77. 1 indexed citations
15.
Brinciotti, M., et al.. (2018). Epilepsy phenotype in patients with Xp22.31 microduplication. Epilepsy & Behavior Case Reports. 11. 31–34. 4 indexed citations
16.
Curtale, Graziella, Franca Citarella, Claudia Carissimi, et al.. (2009). An emerging player in the adaptive immune response: microRNA-146a is a modulator of IL-2 expression and activation-induced cell death in T lymphocytes. Blood. 115(2). 265–273. 244 indexed citations
17.
18.
Goldoni, Marina, Gianluca Azzalin, Giuseppe Macino, & Carlo Cogoni. (2004). Efficient gene silencing by expression of double stranded RNA in Neurospora crassa. Fungal Genetics and Biology. 41(11). 1016–1024. 83 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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