Silvana Beri

2.0k total citations
34 papers, 1.0k citations indexed

About

Silvana Beri is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Silvana Beri has authored 34 papers receiving a total of 1.0k indexed citations (citations by other indexed papers that have themselves been cited), including 25 papers in Genetics, 13 papers in Molecular Biology and 5 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Silvana Beri's work include Genomic variations and chromosomal abnormalities (14 papers), Genetics and Neurodevelopmental Disorders (10 papers) and Congenital heart defects research (5 papers). Silvana Beri is often cited by papers focused on Genomic variations and chromosomal abnormalities (14 papers), Genetics and Neurodevelopmental Disorders (10 papers) and Congenital heart defects research (5 papers). Silvana Beri collaborates with scholars based in Italy, United States and Canada. Silvana Beri's co-authors include Roberto Giorda, Orsetta Zuffardi, Rosario Montirosso, Livio Provenzi, María Clara Bonaglia, Giorgio Gimelli, Giorgia Menozzi, Cecilia Marino, Stefania Gimelli and Francesca Novara and has published in prestigious journals such as PLoS ONE, Child Development and Neuroscience & Biobehavioral Reviews.

In The Last Decade

Silvana Beri

34 papers receiving 997 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Silvana Beri Italy	19	473	397	232	161	130	34	1.0k
Petter Strømme Norway	28	1.1k 2.4×	1.2k 3.0×	296 1.3×	60 0.4×	311 2.4×	76	2.7k
Myriam Srour Canada	20	653 1.4×	703 1.8×	466 2.0×	48 0.3×	197 1.5×	88	1.9k
Kate Day United Kingdom	8	176 0.4×	507 1.3×	248 1.1×	81 0.5×	252 1.9×	9	1.6k
Chahnez Triki Tunisia	17	341 0.7×	409 1.0×	464 2.0×	74 0.5×	175 1.3×	80	1.4k
Manuela Volta Italy	13	523 1.1×	1.5k 3.7×	256 1.1×	41 0.3×	59 0.5×	16	1.9k
Sun-Chong Wang Taiwan	9	652 1.4×	1.0k 2.6×	248 1.1×	42 0.3×	115 0.9×	12	1.4k
R S James United Kingdom	13	951 2.0×	505 1.3×	238 1.0×	32 0.2×	183 1.4×	16	1.3k
Michael Rongione United States	9	567 1.2×	1.8k 4.6×	250 1.1×	55 0.3×	38 0.3×	12	2.3k
Daria Grafodatskaya Canada	16	717 1.5×	1.5k 3.7×	371 1.6×	24 0.1×	192 1.5×	24	1.9k
Thomas Tang Canada	6	578 1.2×	897 2.3×	183 0.8×	39 0.2×	101 0.8×	6	1.2k

Countries citing papers authored by Silvana Beri

Since Specialization

Citations

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

Fields of papers citing papers by Silvana Beri

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Silvana Beri

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

All Works

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20 of 20 papers shown

Provenzi, Livio, Roberto Giorda, Silvana Beri, & Rosario Montirosso. (2016). SLC6A4 methylation as an epigenetic marker of life adversity exposures in humans: A systematic review of literature. Neuroscience & Biobehavioral Reviews. 71. 7–20. 96 indexed citations

Nobile, Maria, Valentina Bianchi, Dario Monzani, et al.. (2015). Effect of family structure and TPH2 G-703T on the stability of dysregulation profile throughout adolescence. Journal of Affective Disorders. 190. 576–584. 5 indexed citations

Provenzi, Livio, Monica Fumagalli, Ida Sirgiovanni, et al.. (2015). Pain-related stress during the Neonatal Intensive Care Unit stay and SLC6A4 methylation in very preterm infants. Frontiers in Behavioral Neuroscience. 9. 99–99. 58 indexed citations

Beri, Silvana, et al.. (2014). Genotype–phenotype relationship in a child with 2.3 Mb de novo interstitial 12p13.33-p13.32 deletion. European Journal of Medical Genetics. 57(7). 334–338. 14 indexed citations

Mascheretti, Sara, et al.. (2014). KIAA0319 and ROBO1: evidence on association with reading and pleiotropic effects on language and mathematics abilities in developmental dyslexia. Journal of Human Genetics. 59(4). 189–197. 47 indexed citations

Novara, Francesca, Enrico Alfei, Stefano D’Arrigo, et al.. (2012). 5p13 microduplication syndrome: A new case and better clinical definition of the syndrome. European Journal of Medical Genetics. 56(1). 54–58. 24 indexed citations

Beri, Silvana, María Clara Bonaglia, & Roberto Giorda. (2012). Low-copy repeats at the human VIPR2 gene predispose to recurrent and nonrecurrent rearrangements. European Journal of Human Genetics. 21(7). 757–761. 14 indexed citations

Rossi, Elena, Roberto Giorda, María Clara Bonaglia, et al.. (2012). De Novo Unbalanced Translocations in Prader-Willi and Angelman Syndrome Might Be the Reciprocal Product of inv dup(15)s. PLoS ONE. 7(6). e39180–e39180. 3 indexed citations

Marco, Patrizia De, Alessandro Raso, Silvana Beri, et al.. (2011). A de novo balanced translocation t(7;12)(p21.2;p12.3) in a patient with Saethre–Chotzen-like phenotype downregulates TWIST and an osteoclastic protein-tyrosine phosphatase, PTP-oc. European Journal of Medical Genetics. 54(5). e478–e483. 6 indexed citations

10.

Giorda, Roberto, Silvana Beri, María Clara Bonaglia, et al.. (2011). Common structural features characterize interstitial intrachromosomal Xp and 18q triplications. American Journal of Medical Genetics Part A. 155(11). 2681–2687. 6 indexed citations

11.

Esch, Hilde Van, Francesca Novara, Silvana Beri, et al.. (2010). Refining the phenotype associated with MEF2C haploinsufficiency. European Journal of Human Genetics. 18. 85–85. 4 indexed citations

12.

Novara, Francesca, Silvana Beri, Roberto Giorda, et al.. (2010). Refining the phenotype associated with MEF2C haploinsufficiency. Clinical Genetics. 78(5). 471–477. 65 indexed citations

13.

Gimelli, Stefania, Gianluca Caridi, Silvana Beri, et al.. (2010). Mutations in SOX17 are associated with congenital anomalies of the kidney and the urinary tract. Human Mutation. 31(12). 1352–1359. 42 indexed citations

14.

Resta, Nicoletta, Roberto Giorda, Rosanna Bagnulo, et al.. (2010). Breakpoint determination of 15 large deletions in Peutz–Jeghers subjects. Human Genetics. 128(4). 373–382. 21 indexed citations

15.

Gimelli, Stefania, Silvana Beri, Harry A. Drabkin, et al.. (2009). The tumor suppressor gene TRC8/RNF139 is disrupted by a constitutional balanced translocation t(8;22)(q24.13;q11.21) in a young girl with dysgerminoma. Molecular Cancer. 8(1). 52–52. 18 indexed citations

16.

Beri, Silvana, Noemi Tonna, Giorgia Menozzi, et al.. (2007). DNA methylation regulates tissue‐specific expression of Shank3. Journal of Neurochemistry. 101(5). 1380–1391. 55 indexed citations

17.

Bocciardi, Renata, Roberto Giorda, Jens Buttgereit, et al.. (2007). Overexpression of the C-type natriuretic peptide (CNP) is associated with overgrowth and bone anomalies in an individual with balanced t(2;7) translocation. Human Mutation. 28(7). 724–731. 100 indexed citations

18.

Giorda, Roberto, Roberto Ciccone, Giorgio Gimelli, et al.. (2007). Two classes of low-copy repeats comediate a new recurrent rearrangement consisting of duplication at 8p23.1 and triplication at 8p23.2. Human Mutation. 28(5). 459–468. 37 indexed citations

19.

Battaglia, Marco, Annalisa Zanoni, Roberto Giorda, et al.. (2006). Effect of the catechol‐O‐methyltransferase val¹⁵⁸met genotype on children’s early phases of facial stimuli processing. Genes Brain & Behavior. 6(4). 364–374. 14 indexed citations

20.

Gimelli, Giorgio, Roberto Giorda, Silvana Beri, Stefania Gimelli, & Orsetta Zuffardi. (2005). A 46,X,inv(Y) young woman with gonadal dysgenesis and gonadoblastoma: Cytogenetics, molecular, and methylation studies. American Journal of Medical Genetics Part A. 140A(1). 40–45. 14 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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