Katia Sampieri

1.7k total citations
14 papers, 1.0k citations indexed

About

Katia Sampieri is a scholar working on Molecular Biology, Genetics and Oncology. According to data from OpenAlex, Katia Sampieri has authored 14 papers receiving a total of 1.0k indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Molecular Biology, 7 papers in Genetics and 5 papers in Oncology. Recurrent topics in Katia Sampieri's work include Genetics and Neurodevelopmental Disorders (5 papers), Genomic variations and chromosomal abnormalities (5 papers) and Hedgehog Signaling Pathway Studies (3 papers). Katia Sampieri is often cited by papers focused on Genetics and Neurodevelopmental Disorders (5 papers), Genomic variations and chromosomal abnormalities (5 papers) and Hedgehog Signaling Pathway Studies (3 papers). Katia Sampieri collaborates with scholars based in Italy, Netherlands and Denmark. Katia Sampieri's co-authors include Riccardo Fodde, Ainara Egia, Leonardo Salmena, Jiangwen Zhang, Edi Brogi, John G. Clohessy, Pier Paolo Pandolfi, Andrea L. Richardson, Caterina Nardella and Arkaitz Carracedo and has published in prestigious journals such as Nature Genetics, British Journal of Cancer and Seminars in Cancer Biology.

In The Last Decade

Katia Sampieri

14 papers receiving 1.0k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Katia Sampieri Italy 11 619 325 248 221 102 14 1.0k
Michael F. Buckley Australia 12 841 1.4× 692 2.1× 189 0.8× 275 1.2× 142 1.4× 21 1.4k
Donatella Malanga Italy 20 731 1.2× 433 1.3× 290 1.2× 71 0.3× 234 2.3× 45 1.3k
Takeshi Namiki Japan 13 460 0.7× 194 0.6× 134 0.5× 99 0.4× 129 1.3× 58 1.0k
Angela Di Vinci Italy 19 452 0.7× 255 0.8× 311 1.3× 105 0.5× 72 0.7× 42 922
E. Antecka Canada 18 319 0.5× 165 0.5× 73 0.3× 40 0.2× 84 0.8× 59 843
Jie Ran China 19 752 1.2× 202 0.6× 66 0.3× 273 1.2× 44 0.4× 48 991
Anna M. Eiring United States 19 657 1.1× 192 0.6× 134 0.5× 43 0.2× 45 0.4× 65 1.5k
Indira V. Subramanian United States 12 699 1.1× 101 0.3× 483 1.9× 93 0.4× 61 0.6× 15 1.0k
Tina L. Yuan United States 13 468 0.8× 176 0.5× 120 0.5× 32 0.1× 38 0.4× 16 636

Countries citing papers authored by Katia Sampieri

Since Specialization
Citations

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

Fields of papers citing papers by Katia Sampieri

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Katia Sampieri

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

All Works

14 of 14 papers shown
1.
Calvaresi, Valeria, Werner Pansegrau, Erika Bartolini, et al.. (2024). Neisserial adhesin A (NadA) binds human Siglec-5 and Siglec-14 with high affinity and promotes bacterial adhesion/invasion. mBio. 15(8). e0110724–e0110724. 2 indexed citations
2.
Bastiaannet, Esther, Katia Sampieri, Olaf M. Dekkers, et al.. (2012). Use of Aspirin postdiagnosis improves survival for colon cancer patients. British Journal of Cancer. 106(9). 1564–1570. 132 indexed citations
3.
Sampieri, Katia & Riccardo Fodde. (2012). Cancer stem cells and metastasis. Seminars in Cancer Biology. 22(3). 187–193. 173 indexed citations
4.
Alimonti, Andrea, Arkaitz Carracedo, John G. Clohessy, et al.. (2010). Subtle variations in Pten dose determine cancer susceptibility. Nature Genetics. 42(5). 454–458. 441 indexed citations
5.
Sampieri, Katia, Mariangela Amenduni, Filomena Tiziana Papa, et al.. (2009). Array comparative genomic hybridization in retinoma and retinoblastoma tissues. Cancer Science. 100(3). 465–471. 29 indexed citations
6.
Sampieri, Katia, Maria Antonietta Mencarelli, Maria Carmela Epistolato, et al.. (2008). Genomic differences between retinoma and retinoblastoma. Acta Oncologica. 47(8). 1483–1492. 36 indexed citations
7.
Mencarelli, Maria Antonietta, Eleni Katzaki, Filomena Tiziana Papa, et al.. (2008). Private inherited microdeletion/microduplications: Implications in clinical practice. European Journal of Medical Genetics. 51(5). 409–416. 53 indexed citations
8.
Papa, Filomena Tiziana, Maria Antonietta Mencarelli, Rossella Caselli, et al.. (2008). A 3 Mb deletion in 14q12 causes severe mental retardation, mild facial dysmorphisms and Rett‐like features. American Journal of Medical Genetics Part A. 146A(15). 1994–1998. 47 indexed citations
9.
Caselli, Rossella, Chiara Pescucci, Vera Uliana, et al.. (2007). Retinoblastoma and mental retardation microdeletion syndrome: clinical characterization and molecular dissection using array CGH. Journal of Human Genetics. 52(6). 535–542. 19 indexed citations
10.
Longo, Ilaria, Katia Sampieri, Eleni Katzaki, et al.. (2007). MECP2 deletions and genotype–phenotype correlation in Rett syndrome. American Journal of Medical Genetics Part A. 143A(23). 2775–2784. 41 indexed citations
11.
Pescucci, Chiara, Rossella Caselli, Francesca Mari, et al.. (2006). The Italian XLMR bank: a clinical and molecular database. Human Mutation. 28(1). 13–18. 1 indexed citations
12.
Mari, Francesca, Daniela Giachino, Lucia Russo, et al.. (2006). Blepharophimosis, Ptosis, and Epicanthus Inversus Syndrome: Clinical and Molecular Analysis of a Case. Journal of American Association for Pediatric Ophthalmology and Strabismus. 10(3). 279–280. 5 indexed citations
13.
Sampieri, Katia, Theodora Hadjistilianou, Francesca Mari, et al.. (2006). Mutational screening of the RB1 gene in Italian patients with retinoblastoma reveals 11 novel mutations. Journal of Human Genetics. 51(3). 209–216. 24 indexed citations
14.
Sampieri, Katia, Ilaria Meloni, Francesca Ariani, et al.. (2006). Italian Rett database and biobank. Human Mutation. 28(4). 329–335. 25 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

Breakdown of academic impact, for papers by Michael F. Buckley Breakdown of academic impact, for papers by Donatella Malanga Breakdown of academic impact, for papers by Takeshi Namiki Breakdown of academic impact, for papers by Angela Di Vinci Breakdown of academic impact, for papers by E. Antecka Breakdown of academic impact, for papers by Jie Ran Breakdown of academic impact, for papers by Anna M. Eiring Breakdown of academic impact, for papers by Indira V. Subramanian Breakdown of academic impact, for papers by Tina L. Yuan
Rankless by CCL
2026