Angelo Valetto

5.6k total citations · 2 hit papers
78 papers, 3.8k citations indexed

About

Angelo Valetto is a scholar working on Genetics, Molecular Biology and Genetics. According to data from OpenAlex, Angelo Valetto has authored 78 papers receiving a total of 3.8k indexed citations (citations by other indexed papers that have themselves been cited), including 42 papers in Genetics, 31 papers in Molecular Biology and 20 papers in Genetics. Recurrent topics in Angelo Valetto's work include Genomic variations and chromosomal abnormalities (27 papers), Genetics and Neurodevelopmental Disorders (16 papers) and Chronic Lymphocytic Leukemia Research (12 papers). Angelo Valetto is often cited by papers focused on Genomic variations and chromosomal abnormalities (27 papers), Genetics and Neurodevelopmental Disorders (16 papers) and Chronic Lymphocytic Leukemia Research (12 papers). Angelo Valetto collaborates with scholars based in Italy, United States and United Kingdom. Angelo Valetto's co-authors include Nicholas Chiorazzi, Manlio Ferrarini, Steven L. Allen, Fabio Ghiotto, R. Kanti, Franco Fais, Philip Schulman, Jonathan E. Kolitz, Rajendra N. Damle and Vincent Vinciguerra and has published in prestigious journals such as Journal of Clinical Investigation, SHILAP Revista de lepidopterología and Blood.

In The Last Decade

Angelo Valetto

73 papers receiving 3.7k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Ig V Gene Mutation Status and CD38 Expression As Novel Prognostic Indicators in Chronic Lymphocytic Leukemia

1999 1.9k citations Franco Fais, Fabio Ghiotto et al. profile →
Chronic lymphocytic leukemia B cells express restricted sets of mutated and unmutated antigen receptors.

1998 690 citations Franco Fais, Fabio Ghiotto et al. Journal of Clinical Investigation profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Angelo Valetto Italy	17	2.9k	2.2k	1.8k	837	405	78	3.8k
Massimo Degan Italy	24	764 0.3×	900 0.4×	826 0.4×	467 0.6×	55 0.1×	67	1.9k
Holger Nückel Germany	27	810 0.3×	625 0.3×	749 0.4×	535 0.6×	72 0.2×	59	1.9k
Roland Schroers Germany	28	718 0.2×	807 0.4×	622 0.3×	807 1.0×	216 0.5×	97	2.4k
Elliot Epner United States	29	886 0.3×	879 0.4×	310 0.2×	2.5k 3.0×	627 1.5×	68	3.8k
Mats Ehinger Sweden	30	761 0.3×	558 0.3×	426 0.2×	1.5k 1.8×	194 0.5×	86	3.2k
Reuben Tooze United Kingdom	26	271 0.1×	555 0.3×	1.0k 0.6×	1.0k 1.2×	130 0.3×	64	2.5k
Daniel L. Van Dyke United States	41	1.4k 0.5×	853 0.4×	504 0.3×	1.8k 2.1×	1.9k 4.8×	183	4.7k
James D. Phelan United States	19	423 0.1×	866 0.4×	490 0.3×	519 0.6×	92 0.2×	51	1.7k
Ivana Pierri Italy	22	447 0.2×	670 0.3×	762 0.4×	268 0.3×	45 0.1×	72	2.0k
Rossano Cesari United States	20	438 0.2×	250 0.1×	443 0.2×	1.1k 1.4×	356 0.9×	34	2.1k

Countries citing papers authored by Angelo Valetto

Since Specialization

Citations

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

Fields of papers citing papers by Angelo Valetto

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Angelo Valetto

This figure shows the co-authorship network connecting the top 25 collaborators of Angelo Valetto. A scholar is included among the top collaborators of Angelo Valetto 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 Angelo Valetto. Angelo Valetto 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:

20 of 20 papers shown

Bertini, Veronica, et al.. (2025). 22q11.21 Deletions: A Review on the Interval Mediated by Low-Copy Repeats C and D. Genes. 16(1). 72–72.

Costagliola, Giorgio, et al.. (2023). Distinct Immunophenotypic Features in Patients Affected by 22q11.2 Deletion Syndrome with Immune Dysregulation and Infectious Phenotype. Journal of Clinical Medicine. 12(24). 7579–7579. 3 indexed citations

Bertini, Veronica, Fulvia Baldinotti, P. Parma, et al.. (2023). In Tandem Intragenic Duplication of Doublesex and Mab-3-Related Transcription Factor 1 (DMRT1) in an SRY-Negative Boy with a 46,XX Disorder of Sex Development. Genes. 14(11). 2067–2067. 1 indexed citations

Ricci, Federica, Francesca Guerrini, Susanna Grassi, et al.. (2020). Sorafenib Induced Complete Cytogenetic and Molecular Response in a Chronic Eosinophilic Leukemia Case with t(12;13) Translocation. SHILAP Revista de lepidopterología. 2(3). 129–129. 2 indexed citations

Rocca, Maria Santa, G. Piatti, Angela Michelucci, et al.. (2020). A novel genetic variant in DNAI2 detected by custom gene panel in a newborn with Primary Ciliary Dyskinesia: case report. BMC Medical Genetics. 21(1). 220–220. 10 indexed citations

Orsini, Alessandro, Angelo Valetto, Veronica Bertini, et al.. (2019). The best evidence for progressive myoclonic epilepsy: A pathway to precision therapy. Seizure. 71. 247–257. 43 indexed citations

Aretini, Paolo, Chiara Maria Mazzanti, Sara Franceschi, et al.. (2018). Next generation sequencing technologies for a successful diagnosis in a cold case of Leigh syndrome. BMC Neurology. 18(1). 99–99. 13 indexed citations

Bertini, Veronica, Alessia Azzarà, Annalisa Legitimo, et al.. (2017). Deletion Extents Are Not the Cause of Clinical Variability in 22q11.2 Deletion Syndrome: Does the Interaction between DGCR8 and miRNA-CNVs Play a Major Role?. Frontiers in Genetics. 8. 47–47. 17 indexed citations

Bertini, Veronica, Rossella Bruno, Alessia Azzarà, et al.. (2017). Maternal Uniparental Disomy 14 (Temple Syndrome) as a Result of a Robertsonian Translocation. Molecular Syndromology. 8(3). 131–138. 13 indexed citations

10.

Bertini, Veronica, Rossella Bruno, Benedetta Toschi, et al.. (2015). 625 kb microduplication at Xp22.12 including RPS6KA3 in a child with mild intellectual disability. Journal of Human Genetics. 60(12). 777–780. 7 indexed citations

11.

Alì, Greta, Agnese Proietti, Cristina Niccoli, et al.. (2013). EML4-ALK translocation in both metachronous second primary lung sarcomatoid carcinoma and lung adenocarcinoma: A case report. Lung Cancer. 81(2). 297–301. 10 indexed citations

12.

Toschi, Benedetta, Angelo Valetto, Veronica Bertini, et al.. (2012). Acro‐cardio‐facial syndrome: A microdeletion syndrome?. American Journal of Medical Genetics Part A. 158A(8). 1994–1999. 10 indexed citations

13.

Bertini, Veronica, Angelo Valetto, Giampiero I. Baroncelli, & Paolo Simi. (2011). Characterization of a complex rearrangement of a chromosome 20 by FISH and array CGH. European Journal of Medical Genetics. 54(4). e419–e424. 1 indexed citations

14.

Bertini, Veronica, Paolo Ghirri, Maria Patrizia Bicocchi, Paolo Simi, & Angelo Valetto. (2010). Molecular cytogenetic definition of a translocation t(X;15) associated with premature ovarian failure. Fertility and Sterility. 94(3). 1097.e5–1097.e8. 19 indexed citations

15.

Valetto, Angelo, et al.. (2009). Molecular cytogenetic characterization of a translocation t(13;22)(q22.3;q11.23) in a patient with idiopathic partial epilepsy. Epilepsy Research. 86(1). 89–93. 1 indexed citations

16.

Martino, Daniela Di, Paola Terranova, Angelo Valetto, et al.. (2008). An unusual pattern of B‐cell immunological reconstitution after allogeneic stem cell transplantation: A possible correlation with CMV reactivation?. Pediatric Transplantation. 13(8). 1050–1052. 2 indexed citations

17.

Bertini, Veronica, Domenico Canale, Maria Patrizia Bicocchi, Paolo Simi, & Angelo Valetto. (2005). Mosaic ring Y chromosome in two normal healthy men with azoospermia. Fertility and Sterility. 84(6). 1744.e1–1744.e4. 13 indexed citations

18.

Martino, Daniela Di, Paola Terranova, Francesca Scuderi, et al.. (2004). VH3 and VH6 Immunoglobulin M Repertoire Reconstitution after Hematopoietic Stem-Cell Transplantation in Children. Transplantation. 79(1). 98–107. 4 indexed citations

19.

Ghiotto, Fabio, Franco Fais, Angelo Valetto, et al.. (2004). Remarkably similar antigen receptors among a subset of patients with chronic lymphocytic leukemia. Journal of Clinical Investigation. 113(7). 1008–1016. 175 indexed citations

20.

Colombo, Monica, Mariella Dono, Paola Gazzola, et al.. (2000). Accumulation of Clonally Related B Lymphocytes in the Cerebrospinal Fluid of Multiple Sclerosis Patients. The Journal of Immunology. 164(5). 2782–2789. 203 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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