Patrizia Colapietro

1.2k total citations
35 papers, 865 citations indexed

About

Patrizia Colapietro is a scholar working on Molecular Biology, Genetics and Hematology. According to data from OpenAlex, Patrizia Colapietro has authored 35 papers receiving a total of 865 indexed citations (citations by other indexed papers that have themselves been cited), including 22 papers in Molecular Biology, 14 papers in Genetics and 6 papers in Hematology. Recurrent topics in Patrizia Colapietro's work include Epigenetics and DNA Methylation (9 papers), Genetic Syndromes and Imprinting (8 papers) and Acute Myeloid Leukemia Research (5 papers). Patrizia Colapietro is often cited by papers focused on Epigenetics and DNA Methylation (9 papers), Genetic Syndromes and Imprinting (8 papers) and Acute Myeloid Leukemia Research (5 papers). Patrizia Colapietro collaborates with scholars based in Italy, United Kingdom and Belarus. Patrizia Colapietro's co-authors include Lidia Larizza, Monica Miozzo, Silvia Tabano, Silvia Maria Sirchia, Cristina Gervasini, Roberto Cairoli, Alessandro Beghini, Francesca Romana Grati, Enrica Morra and Irene Cetin and has published in prestigious journals such as Blood, International Journal of Molecular Sciences and European Journal of Cancer.

In The Last Decade

Patrizia Colapietro

34 papers receiving 860 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Patrizia Colapietro Italy 17 469 221 164 150 132 35 865
Christina Evers Germany 16 293 0.6× 274 1.2× 62 0.4× 53 0.4× 71 0.5× 33 743
Ayelet Avraham Israel 14 368 0.8× 107 0.5× 241 1.5× 49 0.3× 98 0.7× 21 774
M.J.E. Walenkamp Netherlands 18 427 0.9× 515 2.3× 74 0.5× 287 1.9× 37 0.3× 26 1.2k
Amy P. Webster United Kingdom 7 609 1.3× 130 0.6× 162 1.0× 90 0.6× 41 0.3× 11 879
Nicole L. Hoppman United States 14 279 0.6× 279 1.3× 92 0.6× 115 0.8× 173 1.3× 62 704
Solaf M. Elsayed Egypt 15 548 1.2× 471 2.1× 57 0.3× 109 0.7× 100 0.8× 63 1.1k
Nisha Padmanabhan United Kingdom 14 457 1.0× 119 0.5× 188 1.1× 171 1.1× 22 0.2× 19 832
Koray Boduroğlu Türkiye 20 457 1.0× 421 1.9× 28 0.2× 176 1.2× 48 0.4× 109 1.0k
Charlotte Asker Sweden 14 467 1.0× 67 0.3× 123 0.8× 143 1.0× 33 0.3× 22 894
Tracy Dudding Australia 16 239 0.5× 276 1.2× 30 0.2× 148 1.0× 115 0.9× 24 752

Countries citing papers authored by Patrizia Colapietro

Since Specialization
Citations

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

Fields of papers citing papers by Patrizia Colapietro

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Patrizia Colapietro

This figure shows the co-authorship network connecting the top 25 collaborators of Patrizia Colapietro. A scholar is included among the top collaborators of Patrizia Colapietro 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 Patrizia Colapietro. Patrizia Colapietro 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.
Pileggi, Silvana, Elisa Adele Colombo, Roberto Quadri, et al.. (2024). Dysfunction in IGF2R Pathway and Associated Perturbations in Autophagy and WNT Processes in Beckwith–Wiedemann Syndrome Cell Lines. International Journal of Molecular Sciences. 25(7). 3586–3586.
2.
Piccinini, A., Paolo Bailo, Giussy Barbàra, et al.. (2023). Violence against Women and Stress-Related Disorders: Seeking for Associated Epigenetic Signatures, a Pilot Study. Healthcare. 11(2). 173–173. 10 indexed citations
3.
Bianchi, Nicoletta, Luisa Doneda, Luca Elli, et al.. (2022). Circulating microRNAs Suggest Networks Associated with Biological Functions in Aggressive Refractory Type 2 Celiac Disease. Biomedicines. 10(6). 1408–1408. 3 indexed citations
4.
Tabano, Silvia, Lorenzo Tassi, Gabriella Gaudioso, et al.. (2022). Mental health and the effects on methylation of stress-related genes in front-line versus other health care professionals during the second wave of COVID-19 pandemic: an Italian pilot study. European Archives of Psychiatry and Clinical Neuroscience. 273(2). 347–356. 12 indexed citations
5.
Pileggi, Silvana, Elisa Adele Colombo, Laura Fontana, et al.. (2021). Cohesin Mutations Induce Chromatin Conformation Perturbation of the H19/IGF2 Imprinted Region and Gene Expression Dysregulation in Cornelia de Lange Syndrome Cell Lines. Biomolecules. 11(11). 1622–1622. 4 indexed citations
6.
Costanza, Jole, Silvia Tabano, Laura Fontana, et al.. (2021). Extensive Placental Methylation Profiling in Normal Pregnancies. International Journal of Molecular Sciences. 22(4). 2136–2136. 6 indexed citations
7.
Tabano, Silvia, Alice Caldiroli, Andrea Terrasi, et al.. (2019). A miRNome analysis of drug-free manic psychotic bipolar patients versus healthy controls. European Archives of Psychiatry and Clinical Neuroscience. 270(7). 893–900. 16 indexed citations
8.
Paganini, Leda, Loubna Abdel Hadi, Massimiliano Chetta, et al.. (2018). A HS6ST2 gene variant associated with X‐linked intellectual disability and severe myopia in two male twins. Clinical Genetics. 95(3). 368–374. 17 indexed citations
9.
Mandò, Chiara, Silvia Tabano, P. Pileri, et al.. (2013). SNAT2 expression and regulation in human growth-restricted placentas. Pediatric Research. 74(2). 104–110. 36 indexed citations
10.
Salsano, Ettore, Silvia Tabano, Silvia Maria Sirchia, et al.. (2012). Preferential expression of mutant ABCD1 allele is common in adrenoleukodystrophy female carriers but unrelated to clinical symptoms. Orphanet Journal of Rare Diseases. 7(1). 10–10. 27 indexed citations
11.
Manoukian, Siranoush, Paolo Verderio, Silvia Tabano, et al.. (2012). X chromosome inactivation pattern in BRCA gene mutation carriers. European Journal of Cancer. 49(5). 1136–1141. 12 indexed citations
12.
Gervasini, Cristina, Francesca Romana Grati, Faustina Lalatta, et al.. (2010). SHOX duplications found in some cases with type I Mayer-Rokitansky-Kuster-Hauser syndrome. Genetics in Medicine. 12(10). 634–640. 55 indexed citations
13.
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
14.
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
15.
Beghini, Alessandro, Melissa Bellini, Ivana Magnani, et al.. (2005). STI 571 inhibition effect on KITAsn822Lys-mediated signal transduction cascade. Experimental Hematology. 33(6). 682–688. 18 indexed citations
16.
Gervasini, Cristina, Francesca Orzan, Angela Bentivegna, et al.. (2004). Evidence for non-homologous end joining and non-allelic homologous recombination in atypical NF1 microdeletions. Human Genetics. 115(1). 69–80. 31 indexed citations
17.
Colapietro, Patrizia, Mauro Bozzola, Gian Luigi Marseglia, et al.. (2004). Smith-Magenis syndrome and growth hormone deficiency. European Journal of Pediatrics. 163(7). 353–8. 6 indexed citations
18.
Beghini, Alessandro, Carla B. Ripamonti, Roberto Cairoli, et al.. (2004). KIT activating mutations: incidence in adult and pediatric acute myeloid leukemia, and identification of an internal tandem duplication.. PubMed. 89(8). 920–5. 125 indexed citations
19.
Colapietro, Patrizia, Cristina Gervasini, Federica Natacci, et al.. (2003). NF1 exon�7 skipping and sequence alterations in exonic splice enhancers (ESEs) in a neurofibromatosis�1 patient. Human Genetics. 113(6). 551–554. 28 indexed citations
20.
Riva, Paola, Lucia Corrado, Patrizia Colapietro, & Lidia Larizza. (1999). A rapid and simple method for the generation of locus-specific probes for fish analysis. 4(1). 16–20. 8 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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