Ariele Spanhol-Rosseto

964 total citations
6 papers, 437 citations indexed

About

Ariele Spanhol-Rosseto is a scholar working on Molecular Biology, Clinical Psychology and Cognitive Neuroscience. According to data from OpenAlex, Ariele Spanhol-Rosseto has authored 6 papers receiving a total of 437 indexed citations (citations by other indexed papers that have themselves been cited), including 3 papers in Molecular Biology, 2 papers in Clinical Psychology and 2 papers in Cognitive Neuroscience. Recurrent topics in Ariele Spanhol-Rosseto's work include Acute Myeloid Leukemia Research (2 papers), Cancer Genomics and Diagnostics (2 papers) and Genetics and Neurodevelopmental Disorders (2 papers). Ariele Spanhol-Rosseto is often cited by papers focused on Acute Myeloid Leukemia Research (2 papers), Cancer Genomics and Diagnostics (2 papers) and Genetics and Neurodevelopmental Disorders (2 papers). Ariele Spanhol-Rosseto collaborates with scholars based in Italy, Germany and United States. Ariele Spanhol-Rosseto's co-authors include Francesca Mari, Francesca Ariani, Alessandra Renieri, Rosangela Artuso, Maria Antonietta Mencarelli, Ottavia Spiga, Michele Zappella, Sabrina Buoni, Sara Ricciardi and Marzia Pollazzon and has published in prestigious journals such as Blood, The American Journal of Human Genetics and Leukemia.

In The Last Decade

Ariele Spanhol-Rosseto

6 papers receiving 433 citations

Peers

Ariele Spanhol-Rosseto

GENET

MB

CN

GENET

CP

Zhou Xp China

Sureni V. Mullegama United States

Matthew Pastore United States

Marina Grasso Italy

R. Curtis Rogers United States

Vera Beyer Germany

Amanda K. Tilot United States

Stavroula Psoni Greece

Kristen M. West United States

Lars Riff Jensen Germany

Zhou Xp China

Ariele Spanhol-Rosseto

306 ×1.0

GENET

416 ×1.9

MB

227 ×1.6

CN

39 ×0.7

GENET

15 ×0.4

CP

Citations per year, relative to Ariele Spanhol-Rosseto Ariele Spanhol-Rosseto (= 1×) peers Zhou Xp

Countries citing papers authored by Ariele Spanhol-Rosseto

Since Specialization

Citations

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

Fields of papers citing papers by Ariele Spanhol-Rosseto

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Ariele Spanhol-Rosseto. 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 Ariele Spanhol-Rosseto. The network helps show where Ariele Spanhol-Rosseto may publish in the future.

Co-authorship network of co-authors of Ariele Spanhol-Rosseto

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

All Works

Sort: Min cites: Since: Top N: Style:

6 of 6 papers shown

1.

Pettirossi, Valentina, Alessandra Venanzi, Ariele Spanhol-Rosseto, et al.. (2023). The gene mutation landscape of acute myeloid leukemia cell lines and its exemplar use to study the BCOR tumor suppressor. Leukemia. 37(2). 473–477. 3 indexed citations

2.

Tiacci, Enrico, Gianluca Schiavoni, Erik Ladewig, et al.. (2016). New Recurrently Mutated Genes in Classical Hodgkin Lymphoma Revealed By Whole-Exome Sequencing of Microdissected Tumor Cells. Blood. 128(22). 1088–1088. 4 indexed citations

3.

Pettirossi, Valentina, Alessia Santi, Alessandra Pucciarini, et al.. (2014). BRAF inhibitors reverse the unique molecular signature and phenotype of hairy cell leukemia and exert potent antileukemic activity. Blood. 125(8). 1207–1216. 58 indexed citations

4.

Falini, Brunangelo, Vera Großmann, Enrico Tiacci, et al.. (2011). Whole-Exome Sequencing Identifies Recurrent Mutations of BCOR in Acute Myeloid Leukemia with Normal Karyotype. Blood. 118(21). 71–71. 1 indexed citations

5.

Mencarelli, Maria Antonietta, Ariele Spanhol-Rosseto, Rosangela Artuso, et al.. (2009). Novel FOXG1 mutations associated with the congenital variant of Rett syndrome. Journal of Medical Genetics. 47(1). 49–53. 74 indexed citations

6.

Ariani, Francesca, Joussef Hayek, Rosangela Artuso, et al.. (2008). FOXG1 Is Responsible for the Congenital Variant of Rett Syndrome. The American Journal of Human Genetics. 83(1). 89–93. 297 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