Chiara Pescucci

1.9k citations

37 papers · 1.3k indexed · h-index 19

Co-authors: Alessandra Renieri Francesca Mari Ilaria Longo Francesca Ariani Rossella Caselli Francesca Torricelli Ilaria Meloni Michele Zappella
Topics: Genetics and Neurodevelopmental Disorders (12 papers)Genomic variations and chromosomal abnormalities (10 papers)Autism Spectrum Disorder Research (6 papers)
Cited by: Genetics Immunology and Allergy Nephrology
Journals: SHILAP Revista de lepidopterologíaBioinformatics Scientific Reports
Partner nations: Italy United States Germany

In The Last Decade

Chiara Pescucci

37 papers receiving 1.2k citations

Peers

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

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

20 of 20 papers shown

#	Work	Indexed citations
1	Identification and characterization of novel ETV4 splice variants in prostate cancer 2023 ·Scientific Reports ·(unknown),(unknown),Chiara Pescucci,(unknown),Salvatore Di Giorgio,(unknown),Silvestro G. Conticello,Rosario Notaro,Maria De Angioletti	3
2	An additional case of cerebrofaciothoracic dysplasia associated with Chiari type I malformation 2013 ·Clinical Dysmorphology ·(unknown),(unknown),(unknown),Giuseppina Marseglia,Chiara Pescucci,(unknown),Francesca Torricelli,Alfredo Orrico	7
3	372 kb microdeletion in 18q12.3 causing SETBP1 haploinsufficiency associated with mild mental retardation and expressive speech impairment 2012 ·European Journal of Medical Genetics ·Giuseppina Marseglia,(unknown),Chiara Pescucci,(unknown),(unknown),Valeria Scandurra,(unknown),Alberto Magi,Matteo Benelli,Francesca Torricelli	44
4	Overexpression of ETV4 is oncogenic in prostate cells through promotion of both cell proliferation and epithelial to mesenchymal transition 2012 ·Oncogenesis ·(unknown),Chiara Pescucci,(unknown),Cristina Luceri,(unknown),Michela Sica,Rosario Notaro,Maria De Angioletti	55
5	Association between primary open-angle glaucoma (POAG) and WDR36 sequence variance in Italian families affected by POAG 2010 ·British Journal of Ophthalmology ·Paolo Frezzotti,Chiara Pescucci,Fabrizio Papa,Michele Iester,(unknown),I. Motolese,(unknown),Rosangela Artuso,Ilaria Longo,Maria Antonietta Mencarelli,(unknown),Eduardo Motolese,Alessandra Renieri	13
6	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 2007 ·European Journal of Medical Genetics ·Rossella Caselli,Maria Antonietta Mencarelli,Filomena Tiziana Papa,Vera Uliana,Stefania Schiavone,Mirella Strambi,Chiara Pescucci,Francesca Ariani,Valentina A. Rossi,Ilaria Longo,Ilaria Meloni,Alessandra Renieri,Francesca Mari	16
7	Retinoblastoma and mental retardation microdeletion syndrome: clinical characterization and molecular dissection using array CGH 2007 ·Journal of Human Genetics ·Rossella Caselli,(unknown),Chiara Pescucci,Vera Uliana,Katia Sampieri,Mirella Bruttini,Ilaria Longo,Sonia De Francesco,Tiziano Pramparo,Orsetta Zuffardi,R. Frezzotti,Antonio Acquaviva,Theodora Hadjistilianou,Alessandra Renieri,Francesca Mari	19
8	Clinical and molecular characterization of a patient with a 2q31.2‐32.3 deletion identified by array‐CGH 2007 ·American Journal of Medical Genetics Part A ·Maria Antonietta Mencarelli,Rossella Caselli,Chiara Pescucci,Joussef Hayek,Michele Zappella,Alessandra Renieri,Francesca Mari	34
9	2q24–q31 Deletion: Report of a case and review of the literature 2006 ·European Journal of Medical Genetics ·Chiara Pescucci,Rossella Caselli,Salvatore Grosso,Maria Antonietta Mencarelli,Francesca Mari,(unknown),Barbara Piccini,Rosangela Artuso,Mirella Bruttini,Manuela Priolo,Orsetta Zuffardi,Stefania Gimelli,Paolo Balestri,Alessandra Renieri	61
10	Optineurin gene is not involved in the common high-tension form of primary open-angle glaucoma 2006 ·Graefe s Archive for Clinical and Experimental Ophthalmology ·Francesca Ariani,Ilaria Longo,Paolo Frezzotti,Chiara Pescucci,Francesca Mari,Aldo Caporossi,R. Frezzotti,Alessandra Renieri	10
11	Germline mosaicism in Rett syndrome identified by prenatal diagnosis 2005 ·Clinical Genetics ·Francesca Mari,Rossella Caselli,Silvia Russo,Francesca Cogliati,Francesca Ariani,Ilaria Longo,Mirella Bruttini,Ilaria Meloni,Chiara Pescucci,(unknown),Paolo Toti,Maria Tassini,Lidia Larizza,Joussef Hayek,Michele Zappella,Alessandra Renieri	21
12	Autosomal recessive Alport syndrome: an in-depth clinical and molecular analysis of five families 2005 ·Nephrology Dialysis Transplantation ·Ilaria Longo,(unknown),Francesca Mari,Rossella Caselli,Chiara Pescucci,Maria Antonietta Mencarelli,(unknown),Marisa Giani,Elena Bresin,(unknown),(unknown),Komudi Siriwardena,Ingrid Winship,Alessandra Renieri,Ilaria Meloni	38
13	Autosomal-dominant Alport syndrome: Natural history of a disease due to COL4A3 or COL4A4 gene 2004 ·Kidney International ·Chiara Pescucci,Francesca Mari,Ilaria Longo,Paraskevi Vogiatzi,Rossella Caselli,(unknown),Cataldo Abaterusso,R Gusmano,Marco Seri,Nunzia Miglietti,Elena Bresin,Alessandra Renieri	101
14	Chromosomal alterations detected by comparative genomic hybridization in nonfunctioning endocrine pancreatic tumors 2004 ·Cancer Genetics and Cytogenetics ·Giovanna Floridia,(unknown),Marco Salvatore,Chiara Pescucci,Patrick S. Moore,Aldo Scarpa,Domenica Taruscio	17
15	Three Rett patients with both MECP2 mutation and 15q11–13 rearrangements 2004 ·European Journal of Human Genetics ·Ilaria Longo,Luisa Russo,Ilaria Meloni,(unknown),Francesca Ariani,Chiara Pescucci,(unknown),Roberto Canitano,Joussef Hayek,Michele Zappella,Giovanni Neri,Alessandra Renieri,Fiorella Gurrieri	11
16	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 2004 ·Human Mutation ·Francesca Ariani,Francesca Mari,Chiara Pescucci,Ilaria Longo,Mirella Bruttini,Ilaria Meloni,Joussef Hayek,Raffaele Rocchi,Michele Zappella,Alessandra Renieri	83
17	Type-IV collagen related diseases 2003 ·Journal of Nephrology ·Chiara Pescucci,Ilaria Longo,Mirella Bruttini,Francesca Mari,Alessandra Renieri	18
18	Rett syndrome: the complex nature of a monogenic disease 2003 ·Journal of Molecular Medicine ·Alessandra Renieri,Ilaria Meloni,Ilaria Longo,Francesca Ariani,Francesca Mari,Chiara Pescucci,Franca Cambi	64
19	Chromosome 2 deletion encompassing the MAP2 gene in a patient with autism and Rett‐like features 2003 ·Clinical Genetics ·Chiara Pescucci,Ilaria Meloni,Mirella Bruttini,Francesca Ariani,Ilaria Longo,Francesca Mari,Roberto Canitano,Joussef Hayek,Michele Zappella,Alessandra Renieri	45
20	Isolation of Fetal Cells from the Maternal Circu-lation:Prospects for the Non-Invasive Prenatal Diagnosis 2001 ·Clinical Chemistry and Laboratory Medicine (CCLM) ·Francesca Torricelli,Chiara Pescucci	8

About Chiara Pescucci

Chiara Pescucci is a scholar working on Genetics, Immunology and Allergy and Transplantation, having authored 37 papers that have together received 1.3k indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (12 papers), Genomic variations and chromosomal abnormalities (10 papers) and Autism Spectrum Disorder Research (6 papers). The work is most often cited by research in Genetics (745 citations), Immunology and Allergy (119 citations) and Nephrology (83 citations). Chiara Pescucci has collaborated with scholars based in Italy, United States and Germany. Frequent co-authors include Alessandra Renieri, Francesca Mari, Ilaria Longo, Francesca Ariani, Rossella Caselli, Francesca Torricelli, Ilaria Meloni, Michele Zappella, Joussef Hayek and Giuseppina Marseglia. Their work appears in journals such as SHILAP Revista de lepidopterología, Bioinformatics and Scientific Reports.

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