Ursula Giussani

944 total citations
16 papers, 226 citations indexed

About

Ursula Giussani is a scholar working on Molecular Biology, Hematology and Genetics. According to data from OpenAlex, Ursula Giussani has authored 16 papers receiving a total of 226 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Molecular Biology, 7 papers in Hematology and 6 papers in Genetics. Recurrent topics in Ursula Giussani's work include Acute Myeloid Leukemia Research (5 papers), Genomic variations and chromosomal abnormalities (3 papers) and Chronic Myeloid Leukemia Treatments (3 papers). Ursula Giussani is often cited by papers focused on Acute Myeloid Leukemia Research (5 papers), Genomic variations and chromosomal abnormalities (3 papers) and Chronic Myeloid Leukemia Treatments (3 papers). Ursula Giussani collaborates with scholars based in Italy, Netherlands and Germany. Ursula Giussani's co-authors include Orsetta Zuffardi, Johnny Loke, Giovanna Camerino, Alexander Pearlman, R Pallotta, Harry Ostrer, Alessandro Rambaldi, Orietta Radi, Orietta Spinelli and Daniel Adlerstein and has published in prestigious journals such as Blood, PLoS ONE and Neurology.

In The Last Decade

Ursula Giussani

16 papers receiving 223 citations

Peers

Ursula Giussani
Mervyn Humphreys United Kingdom
R.L. Stallings Ireland
Elodie Sanchez France
Pavel Šimara Czechia
G Venti Italy
Jennifer Pham United States
Özge Özalp Yüreğir Türkiye
Ping Hong United States
Karl Vandepoele Belgium
J.G. Dauwerse Netherlands
Mervyn Humphreys United Kingdom
Ursula Giussani
Citations per year, relative to Ursula Giussani Ursula Giussani (= 1×) peers Mervyn Humphreys

Countries citing papers authored by Ursula Giussani

Since Specialization
Citations

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

Fields of papers citing papers by Ursula Giussani

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Ursula Giussani

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

All Works

16 of 16 papers shown
1.
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
2.
Salmoiraghi, Silvia, Roberta Cavagna, Manuela Tosi, et al.. (2020). Immature Immunoglobulin Gene Rearrangements Are Recurrent in B Precursor Adult Acute Lymphoblastic Leukemia Carrying TP53 Molecular Alterations. Genes. 11(9). 960–960. 1 indexed citations
3.
Xumerle, Luciano, Ursula Giussani, Veronica Bertini, et al.. (2018). Insertional translocation involving an additional nonchromothriptic chromosome in constitutional chromothripsis: Rule or exception?. Molecular Genetics & Genomic Medicine. 7(2). e00496–e00496. 8 indexed citations
4.
Vetro, Annalisa, Maria Iascone, Ivan Limongelli, et al.. (2015). Loss-of-FunctionFANCLMutations Associate with Severe Fanconi Anemia Overlapping the VACTERL Association. Human Mutation. 36(5). 562–568. 22 indexed citations
5.
Mecucci, Cristina, Caterina Matteucci, Ursula Giussani, et al.. (2014). Highly aggressive T-cell acute lymphoblastic leukemia with t(8;14)(q24;q11): extensive genetic characterization and achievement of early molecular remission and long-term survival in an adult patient. Blood Cancer Journal. 4(1). e176–e176. 7 indexed citations
6.
Pagani, Ilaria S., Orietta Spinelli, Elia Mattarucchi, et al.. (2014). Genomic quantitative real-time PCR proves residual disease positivity in more than 30% samples with negative mRNA-based qRT-PCR in Chronic Myeloid Leukemia. Oncoscience. 1(7). 510–521. 22 indexed citations
7.
Loke, Johnny, Alexander Pearlman, Orietta Radi, et al.. (2013). Mutations in MAP3K1 tilt the balance from SOX9/FGF9 to WNT/β-catenin signaling. Human Molecular Genetics. 23(4). 1073–1083. 64 indexed citations
8.
Golay, Josée, Clara Albanese, Roberta Ceruti, et al.. (2013). The Polo-Like Kinase 1 (PLK1) Inhibitor NMS-P937 Is Effective in a New Model of Disseminated Primary CD56+ Acute Monoblastic Leukaemia. PLoS ONE. 8(3). e58424–e58424. 30 indexed citations
9.
10.
Mei, Davide, Elena Parrini, Massimo Pasqualetti, et al.. (2007). Multiplex ligation-dependent probe amplification detects DCX gene deletions in band heterotopia. Neurology. 68(6). 446–450. 14 indexed citations
11.
Intermesoli, Tamara, Elena Oldani, Caterina Micò, et al.. (2005). Risk-Adapted Therapy of Adult Acute Myeloid Leukemia (AML): Safety and Efficacy of Repetitive HD-ARA-C Courses with Low-Dose Autologous Blood Stem Cell Support.. Blood. 106(11). 2934–2934. 1 indexed citations
12.
Galli, Mónica, Antonio Nicolucci, Umberto Valentini, et al.. (2005). Feasibility and outcome of tandem stem cell autotransplants in multiple myeloma.. PubMed. 90(12). 1643–9. 10 indexed citations
13.
14.
Grasso, Marina, L Perroni, Stefano Colella, et al.. (1996). Prenatal diagnosis of 30 fetuses at risk for fragile X syndrome. American Journal of Medical Genetics. 64(1). 187–190. 3 indexed citations
15.
Giussani, Ursula, et al.. (1996). Mitotic recombination among acrocentric chromosomes' short arms. Annals of Human Genetics. 60(2). 91–97. 3 indexed citations
16.
Pezzolo, Annalisa, Giorgio Gimelli, M Sposito, et al.. (1994). Definitive assignment of the growth hormone-releasing factor gene to 20q11.2. Human Genetics. 93(2). 213–4. 3 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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