Roberta Bottega

893 total citations
26 papers, 384 citations indexed

About

Roberta Bottega is a scholar working on Hematology, Molecular Biology and Genetics. According to data from OpenAlex, Roberta Bottega has authored 26 papers receiving a total of 384 indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Hematology, 10 papers in Molecular Biology and 5 papers in Genetics. Recurrent topics in Roberta Bottega's work include Platelet Disorders and Treatments (10 papers), DNA Repair Mechanisms (6 papers) and Blood groups and transfusion (6 papers). Roberta Bottega is often cited by papers focused on Platelet Disorders and Treatments (10 papers), DNA Repair Mechanisms (6 papers) and Blood groups and transfusion (6 papers). Roberta Bottega collaborates with scholars based in Italy, Spain and Argentina. Roberta Bottega's co-authors include Anna Savoia, Patrizia Noris, Alessandro Pecci, Daniela De Rocco, Enrico Cappelli, Silvia Ravera, Michela Faleschini, Carlo L. Balduini, Paolo Degan and Paola Cuccarolo and has published in prestigious journals such as Blood, PLoS ONE and Scientific Reports.

In The Last Decade

Roberta Bottega

25 papers receiving 383 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Roberta Bottega Italy 11 184 145 77 62 57 26 384
Nicholas Bockett New Zealand 10 84 0.5× 302 2.1× 108 1.4× 47 0.8× 38 0.7× 21 497
Pak Leng Cheong Australia 8 84 0.5× 148 1.0× 33 0.4× 32 0.5× 83 1.5× 17 321
Tiphaine Bouriez‐Jones United Kingdom 10 150 0.8× 166 1.1× 54 0.7× 38 0.6× 52 0.9× 14 547
Amal Arachiche United States 8 125 0.7× 131 0.9× 46 0.6× 11 0.2× 53 0.9× 11 299
Delia C. Tang United States 11 162 0.9× 212 1.5× 42 0.5× 30 0.5× 198 3.5× 17 478
Daniel Snell United Kingdom 9 291 1.6× 179 1.2× 58 0.8× 84 1.4× 22 0.4× 14 516
Mohammad Azam India 7 44 0.2× 191 1.3× 40 0.5× 98 1.6× 21 0.4× 20 415
Jinlan Pan China 13 369 2.0× 234 1.6× 62 0.8× 44 0.7× 177 3.1× 104 603
Ashley M. Wellendorf United States 11 122 0.7× 197 1.4× 53 0.7× 18 0.3× 40 0.7× 22 401
Chengyu Prince United States 11 62 0.3× 333 2.3× 43 0.6× 84 1.4× 30 0.5× 20 540

Countries citing papers authored by Roberta Bottega

Since Specialization
Citations

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

Fields of papers citing papers by Roberta Bottega

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Roberta Bottega

This figure shows the co-authorship network connecting the top 25 collaborators of Roberta Bottega. A scholar is included among the top collaborators of Roberta Bottega 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 Roberta Bottega. Roberta Bottega 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.
2.
Barozzi, Serena, Caterina Marconi, Roberta Bottega, et al.. (2024). ACTN1‐related thrombocytopenia: Homozygosity for an ACTN1 variant results in a more severe phenotype. British Journal of Haematology. 204(6). 2453–2457. 2 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.
Faleschini, Michela, et al.. (2023). Phenotype reversion as “natural gene therapy” in Fanconi anemia by a gene conversion event. Frontiers in Genetics. 14. 1240758–1240758.
5.
Marzollo, Antonio, Roberta Bottega, Valeria Capaci, et al.. (2023). A novel mutation in MECOM affects MPL regulation in vitro and results in thrombocytopenia and bone marrow failure. British Journal of Haematology. 203(5). 852–859. 2 indexed citations
6.
Faleschini, Michela, Enrico Cappelli, Fabio Corsolini, et al.. (2023). A self-repair history: compensatory effect of a de novo variant on the FANCA c.2778+83C>G splicing mutation. Frontiers in Genetics. 14. 1209138–1209138. 2 indexed citations
7.
Marconi, Caterina, Alessandro Pecci, Flavia Palombo, et al.. (2022). Exome sequencing in 116 patients with inherited thrombocytopenia that remained of unknown origin after systematic phenotype-driven diagnostic workup. Haematologica. 108(7). 1909–1919. 1 indexed citations
8.
Faleschini, Michela, Caterina Alfano, Roberta Bottega, et al.. (2022). ETV6-related thrombocytopenia: dominant negative effect of mutations as common pathogenic mechanism. Haematologica. 107(9). 2249–2254. 6 indexed citations
9.
Faleschini, Michela, Marie‐Christine Morel‐Kopp, Caterina Marconi, et al.. (2021). Dysregulation of oncogenic factors by GFI1B p32: investigation of a novel <I>GFI1B</I> germline mutation. Haematologica. 107(1). 260–267. 1 indexed citations
10.
Bottega, Roberta, et al.. (2021). Anti-inflammatory properties of a proprietary bromelain extract (Bromeyal™) after in vitro simulated gastrointestinal digestion. International Journal of Immunopathology and Pharmacology. 35. 3938505278–3938505278. 22 indexed citations
11.
Bottega, Roberta, Silvia Ravera, Luisa M. R. Napolitano, et al.. (2021). Genomic integrity and mitochondrial metabolism defects in Warsaw syndrome cells: a comparison with Fanconi anemia. Journal of Cellular Physiology. 236(8). 5664–5675. 3 indexed citations
12.
Bottega, Roberta, Katy Vecchiato, Andrea Taddio, et al.. (2019). Functional analysis of the third identified SLC25A19 mutation causative for the thiamine metabolism dysfunction syndrome 4. Journal of Human Genetics. 64(11). 1075–1081. 18 indexed citations
13.
Faleschini, Michela, Federica Melazzini, Caterina Marconi, et al.. (2018). ACTN1 mutations lead to a benign form of platelet macrocytosis not always associated with thrombocytopenia. British Journal of Haematology. 183(2). 276–288. 16 indexed citations
14.
Cappelli, Enrico, Paola Cuccarolo, Maurizio Miano, et al.. (2017). Defects in mitochondrial energetic function compels Fanconi Anaemia cells to glycolytic metabolism. Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease. 1863(6). 1214–1221. 42 indexed citations
15.
Bottega, Roberta, Elena Nicchia, Enrico Cappelli, et al.. (2017). Hypomorphic FANCA mutations correlate with mild mitochondrial and clinical phenotype in Fanconi anemia. Haematologica. 103(3). 417–426. 27 indexed citations
16.
Ravera, Silvia, Carlo Dufour, Simone Cesaro, et al.. (2016). Evaluation of energy metabolism and calcium homeostasis in cells affected by Shwachman-Diamond syndrome. Scientific Reports. 6(1). 25441–25441. 38 indexed citations
17.
Comar, Manola, Daniela De Rocco, Enrico Cappelli, et al.. (2013). Fanconi Anemia Patients Are More Susceptible to Infection with Tumor Virus SV40. PLoS ONE. 8(11). e79683–e79683. 7 indexed citations
18.
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
19.
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
20.
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

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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