Chiara Pescucci

1.9k total citations
37 papers, 1.3k citations indexed

About

Chiara Pescucci is a scholar working on Genetics, Molecular Biology and Cognitive Neuroscience. According to data from OpenAlex, Chiara Pescucci has authored 37 papers receiving a total of 1.3k indexed citations (citations by other indexed papers that have themselves been cited), including 22 papers in Genetics, 20 papers in Molecular Biology and 6 papers in Cognitive Neuroscience. Recurrent topics in Chiara Pescucci's work include Genetics and Neurodevelopmental Disorders (12 papers), Genomic variations and chromosomal abnormalities (10 papers) and Autism Spectrum Disorder Research (6 papers). Chiara Pescucci is often cited by papers focused on Genetics and Neurodevelopmental Disorders (12 papers), Genomic variations and chromosomal abnormalities (10 papers) and Autism Spectrum Disorder Research (6 papers). Chiara Pescucci collaborates with scholars based in Italy, United States and Germany. Chiara Pescucci's co-authors include Alessandra Renieri, Francesca Mari, Ilaria Longo, Francesca Ariani, Rossella Caselli, Francesca Torricelli, Ilaria Meloni, Michele Zappella, Joussef Hayek and Giuseppina Marseglia and has published in prestigious journals such as SHILAP Revista de lepidopterología, Bioinformatics and Scientific Reports.

In The Last Decade

Chiara Pescucci

37 papers receiving 1.2k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Chiara Pescucci Italy 19 745 692 224 119 96 37 1.3k
Mirella Bruttini Italy 22 777 1.0× 1.0k 1.5× 289 1.3× 294 2.5× 70 0.7× 40 1.6k
David Geneviève France 24 1.1k 1.5× 1.3k 1.9× 83 0.4× 45 0.4× 235 2.4× 80 2.3k
Rosangela Artuso Italy 14 606 0.8× 447 0.6× 210 0.9× 85 0.7× 51 0.5× 23 900
Yo Niida Japan 21 334 0.4× 453 0.7× 155 0.7× 35 0.3× 73 0.8× 93 1.6k
Sarah Smithson United Kingdom 16 731 1.0× 767 1.1× 101 0.5× 65 0.5× 57 0.6× 55 1.5k
Lamei Yuan China 19 268 0.4× 551 0.8× 31 0.1× 78 0.7× 37 0.4× 83 1.0k
Rossella Caselli Italy 15 607 0.8× 401 0.6× 139 0.6× 99 0.8× 12 0.1× 20 796
Pauline Terhal Netherlands 18 632 0.8× 574 0.8× 28 0.1× 45 0.4× 59 0.6× 28 1.0k
Dorien Lugtenberg Netherlands 18 920 1.2× 1.0k 1.5× 209 0.9× 15 0.1× 45 0.5× 34 1.6k
Ziva Ben‐Neriah Israel 20 404 0.5× 774 1.1× 48 0.2× 59 0.5× 44 0.5× 40 1.4k

Countries citing papers authored by Chiara Pescucci

Since Specialization
Citations

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

Fields of papers citing papers by Chiara Pescucci

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Chiara Pescucci

This figure shows the co-authorship network connecting the top 25 collaborators of Chiara Pescucci. A scholar is included among the top collaborators of Chiara Pescucci 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 Chiara Pescucci. Chiara Pescucci 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.
Pescucci, Chiara, et al.. (2023). Identification and characterization of novel ETV4 splice variants in prostate cancer. Scientific Reports. 13(1). 5267–5267. 3 indexed citations
2.
Marseglia, Giuseppina, et al.. (2013). An additional case of cerebrofaciothoracic dysplasia associated with Chiari type I malformation. Clinical Dysmorphology. 22(3). 115–117. 7 indexed citations
3.
Marseglia, Giuseppina, Chiara Pescucci, Valeria Scandurra, et al.. (2012). 372 kb microdeletion in 18q12.3 causing SETBP1 haploinsufficiency associated with mild mental retardation and expressive speech impairment. European Journal of Medical Genetics. 55(3). 216–221. 44 indexed citations
4.
5.
Frezzotti, Paolo, Chiara Pescucci, Fabrizio Papa, et al.. (2010). Association between primary open-angle glaucoma (POAG) and WDR36 sequence variance in Italian families affected by POAG. British Journal of Ophthalmology. 95(5). 624–626. 13 indexed citations
6.
Caselli, Rossella, Maria Antonietta Mencarelli, Filomena Tiziana Papa, et al.. (2007). A 2.6 Mb deletion of 6q24.3–25.1 in a patient with growth failure, cardiac septal defect, thin upperlip and asymmetric dysmorphic ears. European Journal of Medical Genetics. 50(4). 315–321. 16 indexed citations
7.
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
8.
Mencarelli, Maria Antonietta, Rossella Caselli, Chiara Pescucci, et al.. (2007). Clinical and molecular characterization of a patient with a 2q31.2‐32.3 deletion identified by array‐CGH. American Journal of Medical Genetics Part A. 143A(8). 858–865. 34 indexed citations
9.
Pescucci, Chiara, Rossella Caselli, Salvatore Grosso, et al.. (2006). 2q24–q31 Deletion: Report of a case and review of the literature. European Journal of Medical Genetics. 50(1). 21–32. 61 indexed citations
10.
Ariani, Francesca, Ilaria Longo, Paolo Frezzotti, et al.. (2006). Optineurin gene is not involved in the common high-tension form of primary open-angle glaucoma. Graefe s Archive for Clinical and Experimental Ophthalmology. 244(9). 1077–1082. 10 indexed citations
11.
Mari, Francesca, Rossella Caselli, Silvia Russo, et al.. (2005). Germline mosaicism in Rett syndrome identified by prenatal diagnosis. Clinical Genetics. 67(3). 258–260. 21 indexed citations
12.
Longo, Ilaria, Francesca Mari, Rossella Caselli, et al.. (2005). Autosomal recessive Alport syndrome: an in-depth clinical and molecular analysis of five families. Nephrology Dialysis Transplantation. 21(3). 665–671. 38 indexed citations
13.
Pescucci, Chiara, Francesca Mari, Ilaria Longo, et al.. (2004). Autosomal-dominant Alport syndrome: Natural history of a disease due to COL4A3 or COL4A4 gene. Kidney International. 65(5). 1598–1603. 101 indexed citations
14.
Floridia, Giovanna, Marco Salvatore, Chiara Pescucci, et al.. (2004). Chromosomal alterations detected by comparative genomic hybridization in nonfunctioning endocrine pancreatic tumors. Cancer Genetics and Cytogenetics. 156(1). 23–30. 17 indexed citations
15.
Longo, Ilaria, Luisa Russo, Ilaria Meloni, et al.. (2004). Three Rett patients with both MECP2 mutation and 15q11–13 rearrangements. European Journal of Human Genetics. 12(8). 682–685. 11 indexed citations
16.
Ariani, Francesca, Francesca Mari, Chiara Pescucci, et al.. (2004). Real-time quantitative PCR as a routine method for screening large rearrangements in Rett syndrome: Report of one case of MECP2 deletion and one case of MECP2 duplication. Human Mutation. 24(2). 172–177. 83 indexed citations
17.
Pescucci, Chiara, Ilaria Longo, Mirella Bruttini, Francesca Mari, & Alessandra Renieri. (2003). Type-IV collagen related diseases. Journal of Nephrology. 16(2). 314–316. 18 indexed citations
18.
Renieri, Alessandra, Ilaria Meloni, Ilaria Longo, et al.. (2003). Rett syndrome: the complex nature of a monogenic disease. Journal of Molecular Medicine. 81(6). 346–354. 64 indexed citations
19.
Pescucci, Chiara, Ilaria Meloni, Mirella Bruttini, et al.. (2003). Chromosome 2 deletion encompassing the MAP2 gene in a patient with autism and Rett‐like features. Clinical Genetics. 64(6). 497–501. 45 indexed citations
20.
Torricelli, Francesca & Chiara Pescucci. (2001). Isolation of Fetal Cells from the Maternal Circu-lation:Prospects for the Non-Invasive Prenatal Diagnosis. Clinical Chemistry and Laboratory Medicine (CCLM). 39(6). 494–500. 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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