Federica Mottadelli

404 total citations
13 papers, 282 citations indexed

About

Federica Mottadelli is a scholar working on Hematology, Genetics and Developmental Biology. According to data from OpenAlex, Federica Mottadelli has authored 13 papers receiving a total of 282 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Hematology, 5 papers in Genetics and 4 papers in Developmental Biology. Recurrent topics in Federica Mottadelli's work include Acute Myeloid Leukemia Research (4 papers), Congenital limb and hand anomalies (4 papers) and Acute Lymphoblastic Leukemia research (4 papers). Federica Mottadelli is often cited by papers focused on Acute Myeloid Leukemia Research (4 papers), Congenital limb and hand anomalies (4 papers) and Acute Lymphoblastic Leukemia research (4 papers). Federica Mottadelli collaborates with scholars based in Italy, United Kingdom and Spain. Federica Mottadelli's co-authors include Lidia Larizza, Angelo Selicorni, Cristina Gervasini, Giovanni Cazzaniga, Andrea Biondi, Gioacchino Scarano, Monique L. den Boer, Markéta Žaliová, Angela Bentivegna and Jan Trka and has published in prestigious journals such as Blood, Genomics and Journal of Medical Genetics.

In The Last Decade

Federica Mottadelli

11 papers receiving 280 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Federica Mottadelli Italy	7	105	104	92	91	76	13	282
M. Elizabeth McCready Canada	10	15 0.1×	36 0.3×	80 0.9×	16 0.2×	120 1.6×	25	254
Eduardo S. Cantú United States	10	107 1.0×	47 0.5×	288 3.1×	6 0.1×	304 4.0×	18	499
B-W Gu China	6	123 1.2×	29 0.3×	208 2.3×	52 0.6×	62 0.8×	10	262
Jean‐Louis Taillemite France	12	19 0.2×	23 0.2×	193 2.1×	10 0.1×	247 3.3×	15	368
Özge Özalp Yüreğir Türkiye	8	46 0.4×	25 0.2×	137 1.5×	3 0.0×	133 1.8×	20	288
Iskra Petković Croatia	11	53 0.5×	36 0.3×	179 1.9×	3 0.0×	164 2.2×	31	305
Jill K. Northup United States	8	15 0.1×	10 0.1×	115 1.3×	12 0.1×	155 2.0×	13	224
Franca Bernardi Italy	10	37 0.4×	34 0.3×	116 1.3×	3 0.0×	246 3.2×	13	367
Sigrid Sahlén Sweden	11	41 0.4×	52 0.5×	243 2.6×	3 0.0×	327 4.3×	21	466
Isabelle Gicquel France	13	62 0.6×	4 0.0×	312 3.4×	29 0.3×	236 3.1×	21	453

Countries citing papers authored by Federica Mottadelli

Since Specialization

Citations

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

Fields of papers citing papers by Federica Mottadelli

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Federica Mottadelli

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

All Works

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13 of 13 papers shown

Vendemini, Francesca, Vincenzo L’Imperio, Federica Mottadelli, et al.. (2025). Bone Marrow CD8 + Abundance Inversely Correlates with Progressive Marrow Fibrosis and Myelodysplastic Evolution in GATA2 Deficiency: Case Report. Journal of Clinical Immunology. 45(1). 77–77.

Mottadelli, Federica, Fabio Pagni, Giovanni Cazzaniga, et al.. (2025). Next Generation Sequencing Identifies Subgroups of Patients With Triple Negative Primary Thrombocytosis With Different Clinical Thrombotic Outcomes. International Journal of Laboratory Hematology. 47(5). 869–876.

Elli, Elena Maria, Mario Mauri, Diletta Fontana, et al.. (2024). Idiopathic erythrocytosis: a germline disease?. Clinical and Experimental Medicine. 24(1). 11–11. 3 indexed citations

Rambaldi, Benedetta, Samantha Donsante, Federica Mottadelli, et al.. (2020). Heterogeneity of the bone marrow niche in patients with myeloproliferative neoplasms: ActivinA secretion by mesenchymal stromal cells correlates with the degree of marrow fibrosis. Annals of Hematology. 100(1). 105–116. 7 indexed citations

Parma, Matteo, A Colombo, Federica Mottadelli, et al.. (2015). GOOD OUTCOME FOR VERY HIGH RISK ADULT B-CELL ACUTE LYMPHOBLASTIC LEUKAEMIA CARRYING GENETIC ABNORMALITIES t(4;11)(q21;q23) or t(9;22)(q34;q11), IF PROMPTLY SUBMITTED TO ALLOGENEIC TRANSPLANTATION, AFTER OBTAINING A GOOD MOLECULAR REMISSION.. Mediterranean Journal of Hematology and Infectious Diseases. 7(1). e2015041–e2015041. 2 indexed citations

Cazzaniga, Valeria, Paola De Lorenzo, Federica Mottadelli, et al.. (2015). Clonal Evolution and Lack of BCR-ABL1 Mutations in Pediatric Ph+ ALL Patients Resistant/Refractory to Imatinib Treatment. Blood. 126(23). 2622–2622. 2 indexed citations

Veer, Arian van der, Markéta Žaliová, Federica Mottadelli, et al.. (2013). Ikzf1 Deletion Status Discriminates For Outcome In Imatinibtreated Bcr-Abl1-Positive Childhood ALL. Haematologica. 98. 1 indexed citations

Veer, Arian van der, Markéta Žaliová, Federica Mottadelli, et al.. (2013). IKZF1 status as a prognostic feature in BCR-ABL1–positive childhood ALL. Blood. 123(11). 1691–1698. 100 indexed citations

López‐Atalaya, José P., Cristina Gervasini, Federica Mottadelli, et al.. (2011). Histone acetylation deficits in lymphoblastoid cell lines from patients with Rubinstein–Taybi syndrome. Journal of Medical Genetics. 49(1). 66–74. 57 indexed citations

10.

Gervasini, Cristina, Federica Mottadelli, Roberto Ciccone, et al.. (2010). High frequency of copy number imbalances in Rubinstein–Taybi patients negative to CREBBP mutational analysis. European Journal of Human Genetics. 18(7). 768–775. 9 indexed citations

11.

Pedranzini, Laura, Federica Mottadelli, Simona Ronzoni, et al.. (2010). Differential cytogenomics and miRNA signature of the Acute Myeloid Leukaemia Kasumi-1 cell line CD34+38− compartment. Leukemia Research. 34(10). 1287–1295. 17 indexed citations

12.

Gervasini, Cristina, Paola Castronovo, Angela Bentivegna, et al.. (2007). High frequency of mosaic CREBBP deletions in Rubinstein–Taybi syndrome patients and mapping of somatic and germ-line breakpoints. Genomics. 90(5). 567–573. 34 indexed citations

13.

Bentivegna, Angela, Donatella Milani, Cristina Gervasini, et al.. (2006). Rubinstein-Taybi Syndrome: spectrum of CREBBP mutations in Italian patients. BMC Medical Genetics. 7(1). 77–77. 50 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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