Daniela De Rocco

2.6k total citations
30 papers, 571 citations indexed

About

Daniela De Rocco is a scholar working on Hematology, Molecular Biology and Immunology and Allergy. According to data from OpenAlex, Daniela De Rocco has authored 30 papers receiving a total of 571 indexed citations (citations by other indexed papers that have themselves been cited), including 17 papers in Hematology, 8 papers in Molecular Biology and 8 papers in Immunology and Allergy. Recurrent topics in Daniela De Rocco's work include Platelet Disorders and Treatments (15 papers), Cell Adhesion Molecules Research (8 papers) and Blood groups and transfusion (6 papers). Daniela De Rocco is often cited by papers focused on Platelet Disorders and Treatments (15 papers), Cell Adhesion Molecules Research (8 papers) and Blood groups and transfusion (6 papers). Daniela De Rocco collaborates with scholars based in Italy, Argentina and Spain. Daniela De Rocco's co-authors include Anna Savoia, Alessandro Pecci, Valeria Bozzi, Patrizia Noris, Carlo L. Balduini, Annalisa Pastore, Roberta Bottega, Núria Pujol‐Moix, Paula G. Heller and Elena Nicchia and has published in prestigious journals such as PLoS ONE, International Journal of Molecular Sciences and Human Reproduction.

In The Last Decade

Daniela De Rocco

29 papers receiving 567 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 De Rocco Italy 14 339 154 108 93 83 30 571
Yuji Miyajima Japan 14 181 0.5× 132 0.9× 93 0.9× 77 0.8× 76 0.9× 29 592
Rens de Groot United Kingdom 15 422 1.2× 124 0.8× 51 0.5× 186 2.0× 62 0.7× 33 850
Sonia Águila Spain 16 450 1.3× 207 1.3× 81 0.8× 80 0.9× 36 0.4× 40 760
Vincent Jallu France 15 452 1.3× 97 0.6× 189 1.8× 38 0.4× 101 1.2× 32 597
Stephanie K. Watson United Kingdom 7 251 0.7× 190 1.2× 164 1.5× 19 0.2× 103 1.2× 8 587
Zeping Zhou China 15 356 1.1× 55 0.4× 21 0.2× 113 1.2× 47 0.6× 59 499
J. Disse Germany 9 241 0.7× 179 1.2× 17 0.2× 80 0.9× 38 0.5× 10 477
С. В. Лапин Russia 13 108 0.3× 130 0.8× 29 0.3× 48 0.5× 73 0.9× 139 678
Nobukuni Sawai Japan 15 227 0.7× 363 2.4× 197 1.8× 102 1.1× 38 0.5× 28 713
Simona Casarini Italy 13 124 0.4× 609 4.0× 73 0.7× 157 1.7× 26 0.3× 15 679

Countries citing papers authored by Daniela De Rocco

Since Specialization
Citations

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

Fields of papers citing papers by Daniela De Rocco

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Daniela De Rocco

This figure shows the co-authorship network connecting the top 25 collaborators of Daniela De Rocco. A scholar is included among the top collaborators of Daniela De Rocco 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 De Rocco. Daniela De Rocco 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.
Gianoncelli, Alessandra, Simone Sala, Maik Kahnt, et al.. (2025). Impact of Fixation Protocols on Elemental Content in Human Sperm. X-Ray Spectrometry. 55(1). 66–75.
2.
Marzollo, Antonio, Stefania Zampieri, Serena Barozzi, et al.. (2024). Thrombocytopenia 4 (THC4): Six novel families with mutations of the cytochrome c gene. British Journal of Haematology. 205(1). 306–315. 6 indexed citations
3.
Andreuzzi, Eva, Marco Toffoli, Gabriella Zito, et al.. (2024). P-424 Placental extracellular matrix remodelling in pregnancies by oocyte donation shows similarities with preeclamptic placenta: a pilot study. Human Reproduction. 39(Supplement_1). 1 indexed citations
4.
Barozzi, Serena, Valeria Bozzi, Daniela De Rocco, et al.. (2021). A Novel Mutation in GP1BB Reveals the Role of the Cytoplasmic Domain of GPIbβ in the Pathophysiology of Bernard-Soulier Syndrome and GPIb-IX Complex Assembly. International Journal of Molecular Sciences. 22(19). 10190–10190. 6 indexed citations
5.
Zaninetti, Carlo, Daniela De Rocco, Tania Giangregorio, et al.. (2018). MYH9-Related Thrombocytopenia: Four Novel Variants Affecting the Tail Domain of the Non-Muscle Myosin Heavy Chain IIA Associated with a Mild Clinical Evolution of the Disorder. Hämostaseologie. 39(1). 87–94. 1 indexed citations
6.
Pecci, Alessandro, Iman Ragab, Valeria Bozzi, et al.. (2017). Thrombopoietin mutation in congenital amegakaryocytic thrombocytopenia treatable with romiplostim. EMBO Molecular Medicine. 10(1). 63–75. 41 indexed citations
7.
Nicchia, Elena, Paola Giordano, Chiara Greco, Daniela De Rocco, & Anna Savoia. (2016). Molecular diagnosis of thrombocytopenia‐absent radius syndrome using next‐generation sequencing. International Journal of Laboratory Hematology. 38(4). 412–418. 7 indexed citations
8.
Parodi, Alessia, Francesca Kalli, Johanna Svahn, et al.. (2015). Impaired immune response to Candida albicans in cells from Fanconi anemia patients. Cytokine. 73(1). 203–207. 5 indexed citations
9.
Pianigiani, Giulia, et al.. (2014). Unusual splice site mutations disrupt FANCA exon 8 definition. Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease. 1842(7). 1052–1058. 15 indexed citations
10.
Rocco, Daniela De, Cristina Cerqua, P Goffrini, et al.. (2013). Mutations of cytochrome c identified in patients with thrombocytopenia THC4 affect both apoptosis and cellular bioenergetics. Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease. 1842(2). 269–274. 65 indexed citations
11.
Glembotsky, Ana C., Rosana F. Marta, Alessandro Pecci, et al.. (2012). International collaboration as a tool for diagnosis of patients with inherited thrombocytopenia in the setting of a developing country. Journal of Thrombosis and Haemostasis. 10(8). 1653–1661. 22 indexed citations
12.
Bottega, Roberta, Alessandro Pecci, Erica De Candia, et al.. (2012). Correlation between platelet phenotype and NBEAL2 genotype in patients with congenital thrombocytopenia and  -granule deficiency. Haematologica. 98(6). 868–874. 41 indexed citations
13.
Rocco, Daniela De, Barbara Zieger, Helen Platokouki, et al.. (2012). MYH9-related disease: Five novel mutations expanding the spectrum of causative mutations and confirming genotype/phenotype correlations. European Journal of Medical Genetics. 56(1). 7–12. 22 indexed citations
14.
Rocco, Daniela De, Emanuele Panza, Valeria Bozzi, et al.. (2010). Heavy chain myosin 9-related disease (MYH9-RD): Neutrophil inclusions of myosin-9 as a pathognomonic sign of the disorder. Thrombosis and Haemostasis. 103(4). 826–832. 66 indexed citations
15.
Savoia, Anna, Alessandro Pastore, Daniela De Rocco, et al.. (2010). Clinical and genetic aspects of Bernard-Soulier syndrome: searching for genotype/phenotype correlations. Haematologica. 96(3). 417–423. 70 indexed citations
16.
Vettore, Silvia, Daniela De Rocco, B. Gerber, et al.. (2010). A G to C transversion at the last nucleotide of exon 25 of the MYH9 gene results in a missense mutation rather than in a splicing defect. European Journal of Medical Genetics. 53(5). 256–260. 8 indexed citations
17.
Savoia, Anna, Fred G. Pluthero, Hilary Christensen, et al.. (2009). Megakaryocyte and platelet abnormalities in a patient with a W33C mutation in the conserved SH3-like domain of myosin heavy chain IIA. Thrombosis and Haemostasis. 102(12). 1241–1250. 12 indexed citations
18.
Rocco, Daniela De, Núria Pujol‐Moix, Alessandro Pecci, et al.. (2009). Identification of the first duplication in MYH9-related disease: A hot spot for unequal crossing-over within exon 24 of the MYH9 gene. European Journal of Medical Genetics. 52(4). 191–194. 14 indexed citations
19.
Rocco, Daniela De, Paula G. Heller, Giorgia Girotto, et al.. (2009). MYH9related disease: A novel missense Ala95Asp mutation of theMYH9gene. Platelets. 20(8). 598–602. 7 indexed citations
20.
Rocco, Daniela De, et al.. (2001). Type III Ehlers–Danlos syndrome: correlations among clinical signs, ultrasound, and histologic findings in a study of 35 cases. International Journal of Dermatology. 40(3). 175–178. 7 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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