Daniela Marchetti

665 total citations
21 papers, 495 citations indexed

About

Daniela Marchetti is a scholar working on Molecular Biology, Genetics and Oncology. According to data from OpenAlex, Daniela Marchetti has authored 21 papers receiving a total of 495 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Molecular Biology, 11 papers in Genetics and 4 papers in Oncology. Recurrent topics in Daniela Marchetti's work include Genomics and Rare Diseases (5 papers), Genomic variations and chromosomal abnormalities (5 papers) and RNA modifications and cancer (4 papers). Daniela Marchetti is often cited by papers focused on Genomics and Rare Diseases (5 papers), Genomic variations and chromosomal abnormalities (5 papers) and RNA modifications and cancer (4 papers). Daniela Marchetti collaborates with scholars based in Italy, United States and Switzerland. Daniela Marchetti's co-authors include Giulia Taraboletti, Raffaella Giavazzi, Maria Iascone, Antonio Pavan, Danilo Millimaggi, Ilaria Giusti, Patrizia Borsotti, Vincenza Dolo, Laura Pezzoli and Marco Rusnati and has published in prestigious journals such as Circulation, Blood and Bioinformatics.

In The Last Decade

Daniela Marchetti

19 papers receiving 488 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Daniela Marchetti Italy 10 351 145 113 65 64 21 495
Jordy Coffa Netherlands 11 375 1.1× 141 1.0× 145 1.3× 65 1.0× 69 1.1× 14 597
Margaret L. McKinnon Canada 12 332 0.9× 150 1.0× 117 1.0× 44 0.7× 51 0.8× 14 603
Sanna‐Maria Karppinen Finland 14 398 1.1× 124 0.9× 190 1.7× 50 0.8× 26 0.4× 23 606
Alexandra Friemel Germany 15 223 0.6× 79 0.5× 63 0.6× 36 0.6× 67 1.0× 24 519
Vivienne McConnell United Kingdom 12 186 0.5× 59 0.4× 191 1.7× 34 0.5× 37 0.6× 20 502
Roxane M. Pommier France 11 224 0.6× 107 0.7× 50 0.4× 30 0.5× 87 1.4× 19 443
Mari Aikio Finland 10 170 0.5× 63 0.4× 48 0.4× 69 1.1× 28 0.4× 10 360
Claudia Cappuzzello Italy 12 263 0.7× 127 0.9× 69 0.6× 51 0.8× 51 0.8× 19 538
Gunnhildur Ásta Traustadóttir Iceland 13 281 0.8× 66 0.5× 79 0.7× 37 0.6× 32 0.5× 23 446
Rodney Staggs United States 7 385 1.1× 90 0.6× 74 0.7× 26 0.4× 28 0.4× 8 556

Countries citing papers authored by Daniela Marchetti

Since Specialization
Citations

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

Fields of papers citing papers by Daniela Marchetti

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Daniela Marchetti

This figure shows the co-authorship network connecting the top 25 collaborators of Daniela Marchetti. A scholar is included among the top collaborators of Daniela Marchetti 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 Daniela Marchetti. Daniela Marchetti 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.
Pezzani, Lidia, Laura Pezzoli, Daniela Marchetti, et al.. (2023). Comparison of first‐tier whole‐exome sequencing with a multi‐step traditional approach for diagnosing paediatric outpatients: An Italian prospective study. Molecular Genetics & Genomic Medicine. 12(1). e2316–e2316. 4 indexed citations
2.
Pezzani, Lidia, Enrico Alfei, Laura Pezzoli, et al.. (2023). Rock around DYRK1A: Ethnic diversity, clinical challenges. American Journal of Medical Genetics Part A. 191(5). 1459–1464.
3.
Pezzani, Lidia, Laura Pezzoli, Anna Cereda, et al.. (2023). Double somatic mosaicism in Cornelia de Lange syndrome. American Journal of Medical Genetics Part A. 194(5). e63512–e63512. 3 indexed citations
4.
Alfei, Enrico, Maria Iascone, Daniela Marchetti, et al.. (2023). Menkes disease complicated by concurrent ACY1 deficiency: A case report. Frontiers in Genetics. 14. 1077625–1077625. 2 indexed citations
5.
Pezzani, Lidia, Laura Pezzoli, Daniela Marchetti, et al.. (2022). Atypical, Composite, or Blended Phenotypes: How Different Molecular Mechanisms Could Associate in Double-Diagnosed Patients. Genes. 13(7). 1275–1275. 17 indexed citations
6.
Rinaldi, Berardo, Claudia Cesaretti, Simona Boito, et al.. (2022). Family history is key to the interpretation of exome sequencing in the prenatal context: unexpected diagnosis of Basal Cell Nevus Syndrome. Prenatal Diagnosis. 42(7). 927–933.
7.
Franceschi, Roberto, Maria Iascone, Silvia Maitz, et al.. (2022). A missense mutation in DDRGK1 gene associated to Shohat‐type spondyloepimetaphyseal dysplasia: Two case reports and a review of literature. American Journal of Medical Genetics Part A. 188(8). 2434–2437. 2 indexed citations
8.
Saettini, Francesco, Grazia Fazio, Maria Teresa Bonati, et al.. (2022). Identical EP300 variant leading to Rubinstein–Taybi syndrome with different clinical and immunologic phenotype. American Journal of Medical Genetics Part A. 188(7). 2129–2134. 3 indexed citations
9.
Peron, Angela, et al.. (2020). PIGW‐related glycosylphosphatidylinositol deficiency: Description of a new patient and review of the literature. American Journal of Medical Genetics Part A. 182(6). 1477–1482. 8 indexed citations
10.
Pezzani, Lidia, Laura Pezzoli, Daniela Marchetti, et al.. (2020). Double homozygosity in CEP57 and DYNC2H1 genes detected by WES: Composite or expanded phenotype?. Molecular Genetics & Genomic Medicine. 8(3). e1064–e1064. 8 indexed citations
11.
Nicastro, Emanuele, Angelo Di Giorgio, Daniela Marchetti, et al.. (2019). Diagnostic Yield of an Algorithm for Neonatal and Infantile Cholestasis Integrating Next-Generation Sequencing. The Journal of Pediatrics. 211. 54–62.e4. 34 indexed citations
12.
Pezzani, Lidia, Daniela Marchetti, Anna Cereda, et al.. (2018). Atypical presentation of pediatric BRAF RASopathy with acute encephalopathy. American Journal of Medical Genetics Part A. 176(12). 2867–2871. 24 indexed citations
13.
Marchetti, Daniela, et al.. (2018). Expanding the phenotype of MED 17 mutations: Description of two new cases and review of the literature. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 177(8). 687–690. 9 indexed citations
14.
Bossi, Grazia, Giuseppe Giordano, Giuseppe Maggiore, et al.. (2017). Atypical Clinical Presentation and Successful Treatment With Oral Cholic Acid of a Child with Defective Bile Acid Synthesis due to a Novel Mutation in the HSD3B7 Gene. Pediatric Reports. 9(3). 7266–7266. 9 indexed citations
15.
Sana, Maria Elena, Lawrence A. Quilliam, Andrea Spitaleri, et al.. (2016). A Novel HRAS Mutation Independently Contributes to Left Ventricular Hypertrophy in a Family with a Known MYH7 Mutation. PLoS ONE. 11(12). e0168501–e0168501. 8 indexed citations
16.
Iascone, Maria, Roberto Ciccone, Lorenzo Galletti, et al.. (2011). Identification of de novo mutations and rare variants in hypoplastic left heart syndrome. Clinical Genetics. 81(6). 542–554. 81 indexed citations
17.
Sana, Maria Elena, Maria Iascone, Daniela Marchetti, et al.. (2010). GAMES identifies and annotates mutations in next-generation sequencing projects. Bioinformatics. 27(1). 9–13. 25 indexed citations
18.
Iascone, Maria, et al.. (2007). Gene symbol: MYH7.. PubMed. 120(6). 915–915. 4 indexed citations
19.
Taraboletti, Giulia, Ilaria Giusti, Daniela Marchetti, et al.. (2006). Bioavailability of VEGF in Tumor-Shed Vesicles Depends on Vesicle Burst Induced by Acidic pH. Neoplasia. 8(2). 96–103. 165 indexed citations
20.
Marchetti, Daniela, Veronica Vergani, Raffaella Giavazzi, et al.. (2003). Thrombospondin 1 as a scavenger for matrix-associated fibroblast growth factor 2. Blood. 102(13). 4399–4406. 72 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.

Explore authors with similar magnitude of impact

Breakdown of academic impact, for papers by Jordy Coffa Breakdown of academic impact, for papers by Margaret L. McKinnon Breakdown of academic impact, for papers by Sanna‐Maria Karppinen Breakdown of academic impact, for papers by Alexandra Friemel Breakdown of academic impact, for papers by Vivienne McConnell Breakdown of academic impact, for papers by Roxane M. Pommier Breakdown of academic impact, for papers by Mari Aikio Breakdown of academic impact, for papers by Claudia Cappuzzello Breakdown of academic impact, for papers by Gunnhildur Ásta Traustadóttir Breakdown of academic impact, for papers by Rodney Staggs
Rankless by CCL
2026