Vanna Pecile

2.1k total citations
54 papers, 825 citations indexed

About

Vanna Pecile is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Vanna Pecile has authored 54 papers receiving a total of 825 indexed citations (citations by other indexed papers that have themselves been cited), including 35 papers in Genetics, 26 papers in Molecular Biology and 14 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Vanna Pecile's work include Genomic variations and chromosomal abnormalities (22 papers), Genetics and Neurodevelopmental Disorders (14 papers) and Prenatal Screening and Diagnostics (12 papers). Vanna Pecile is often cited by papers focused on Genomic variations and chromosomal abnormalities (22 papers), Genetics and Neurodevelopmental Disorders (14 papers) and Prenatal Screening and Diagnostics (12 papers). Vanna Pecile collaborates with scholars based in Italy, United States and Spain. Vanna Pecile's co-authors include Marcella Zollino, Giuseppe Marangi, Giovanni Neri, Flavio Faletra, Paolo Gasparini, Marina Murdolo, Laura Mazzanti, Cinzia Galasso, G Filippi and Daniela Orteschi and has published in prestigious journals such as SHILAP Revista de lepidopterología, International Journal of Molecular Sciences and Gene.

In The Last Decade

Vanna Pecile

53 papers receiving 787 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Vanna Pecile Italy 17 499 443 175 112 70 54 825
Frédérique Béna Switzerland 15 366 0.7× 440 1.0× 131 0.7× 94 0.8× 55 0.8× 34 819
Courtney Sebold United States 16 437 0.9× 216 0.5× 141 0.8× 97 0.9× 52 0.7× 27 616
Karen Buysse Belgium 15 633 1.3× 456 1.0× 169 1.0× 75 0.7× 45 0.6× 19 959
Monika Cohen Germany 11 488 1.0× 551 1.2× 98 0.6× 84 0.8× 49 0.7× 13 859
Carolina Sismani Cyprus 19 735 1.5× 515 1.2× 266 1.5× 184 1.6× 38 0.5× 75 984
Merete Bugge Denmark 10 584 1.2× 935 2.1× 146 0.8× 107 1.0× 32 0.5× 15 1.2k
Brigitte Benzacken France 20 737 1.5× 462 1.0× 426 2.4× 156 1.4× 57 0.8× 61 1.3k
Leslie Domenici Kulikowski Brazil 15 487 1.0× 337 0.8× 174 1.0× 188 1.7× 69 1.0× 87 799
M. Lance Cooper United States 14 681 1.4× 367 0.8× 229 1.3× 213 1.9× 59 0.8× 19 838
Benno Röthlisberger Switzerland 17 462 0.9× 313 0.7× 163 0.9× 92 0.8× 31 0.4× 34 729

Countries citing papers authored by Vanna Pecile

Since Specialization
Citations

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

Fields of papers citing papers by Vanna Pecile

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Vanna Pecile

This figure shows the co-authorship network connecting the top 25 collaborators of Vanna Pecile. A scholar is included among the top collaborators of Vanna Pecile 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 Vanna Pecile. Vanna Pecile 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.
Bottega, Roberta, Katy Vecchiato, Andrea Taddio, et al.. (2019). Functional analysis of the third identified SLC25A19 mutation causative for the thiamine metabolism dysfunction syndrome 4. Journal of Human Genetics. 64(11). 1075–1081. 18 indexed citations
2.
Recalcati, Maria Paola, Ornella Rodeschini, Chiara Barone, et al.. (2019). Ten new cases of Balanced Reciprocal Translocation Mosaicism (BRTM): Reproductive implications, frequency and mechanism. European Journal of Medical Genetics. 63(2). 103639–103639. 5 indexed citations
3.
Villa, Nicoletta, Donatella Conconi, Gianluca Tornese, et al.. (2017). A complete duplication of X chromosome resulting in a tricentric isochromosome originated by centromere repositioning. Molecular Cytogenetics. 10(1). 22–22. 2 indexed citations
4.
Faletra, Flavio, Rossana Bussani, Vanna Pecile, et al.. (2016). A Case of Prenatal Neurocytoma Associated With ATR‐16 Syndrome. Journal of Ultrasound in Medicine. 35(6). 1359–1361. 2 indexed citations
5.
Pecile, Vanna, et al.. (2015). CTNND2 deletion and intellectual disability. Gene. 565(1). 146–149. 20 indexed citations
6.
Morgan, Anna, et al.. (2014). A novel deletion mutation involving TMEM38B in a patient with autosomal recessive osteogenesis imperfecta. Gene. 545(2). 290–292. 36 indexed citations
7.
Athanasakis, Emmanouil, Danilo Licastro, Flavio Faletra, et al.. (2013). Next generation sequencing in nonsyndromic intellectual disability: From a negative molecular karyotype to a possible causative mutation detection. American Journal of Medical Genetics Part A. 164(1). 170–176. 31 indexed citations
8.
Marangi, Giuseppe, Vincenzo Leuzzi, Filippo Manti, et al.. (2012). TRAPPC9-related autosomal recessive intellectual disability: report of a new mutation and clinical phenotype. European Journal of Human Genetics. 21(2). 229–232. 54 indexed citations
9.
Faletra, Flavio, et al.. (2012). Phylloid Pattern of Hypomelanosis Closely Related to Chromosomal Abnormalities in the 13q Detected by SNP Array Analysis. Dermatology. 225(4). 294–297. 11 indexed citations
10.
Rocca, Maria Santa, Antonella Fabretto, Flavio Faletra, et al.. (2011). Contribution of SNP arrays in diagnosis of deletion 2p11.2–p12. Gene. 492(1). 315–318. 5 indexed citations
11.
Rocca, Maria Santa, et al.. (2011). De novo 911 Kb interstitial deletion on chromosome 1q43 in a boy with mental retardation and short stature. European Journal of Medical Genetics. 55(2). 117–119. 15 indexed citations
12.
Faletra, Flavio, et al.. (2010). A new case of duplication of the MDS region identified by high-density SNP arrays and a review of the literature. Journal of Applied Genetics. 52(1). 77–80. 3 indexed citations
13.
Parentin, Fulvio, Antonella Fabretto, Federico Marchetti, et al.. (2009). Ophthalmic Features in a Dysmorphic Boy with Chromosome 4q Deletion and Duplication. Ophthalmic Genetics. 30(2). 103–105. 2 indexed citations
14.
Costa, Paola, et al.. (2009). Trisomy 12p and Monosomy 4p: Phenotype–Genotype Correlation. Genetic Testing and Molecular Biomarkers. 13(2). 199–204. 3 indexed citations
15.
Lenzini, Elisabetta, Lucia Ballarati, Paola Drigo, et al.. (2009). 1q44-qter Trisomy:Clinical Report and Review of the Literature. Genetic Testing and Molecular Biomarkers. 13(1). 79–86. 3 indexed citations
16.
Zollino, Marcella, Daniela Orteschi, Giuseppe Marangi, et al.. (2009). A case of Beckwith–Wiedemann syndrome caused by a cryptic 11p15 deletion encompassing the centromeric imprinted domain of the BWS locus. Journal of Medical Genetics. 47(6). 429–432. 39 indexed citations
17.
Zollino, Marcella, Marina Murdolo, Giuseppe Marangi, et al.. (2008). On the nosology and pathogenesis of Wolf–Hirschhorn syndrome: Genotype–phenotype correlation analysis of 80 patients and literature review. American Journal of Medical Genetics Part C Seminars in Medical Genetics. 148C(4). 257–269. 112 indexed citations
18.
Crovella, Sérgio, Nicola Marziliano, Silvia Garagna, et al.. (1999). MFASAT: A new alphoid DNA sequence isolated from Macaca fascicularis (Cercopithecidae, Primates). Genome. 42(6). 1066–1070. 4 indexed citations
19.
Marziliano, Nicola, Sérgio Crovella, Enrica Audero, et al.. (1999). Genetic mapping<footref rid="foot01"><sup>1</sup></footref> of the mouse homologue of the human angiopoietin-1 gene <i>(Agpt)</i> to mouse chromosome 9E2 by in situ hybridization. Cytogenetic and Genome Research. 87(3-4). 199–200.
20.
Pecile, Vanna & Giorgio Filippi. (1991). Screening for fra(x) mutation and Klinefelter syndrome in mental institutions. Clinical Genetics. 39(3). 189–193. 1 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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