Valentina Guida

3.4k total citations
43 papers, 1.6k citations indexed

About

Valentina Guida is a scholar working on Molecular Biology, Genetics and Genetics. According to data from OpenAlex, Valentina Guida has authored 43 papers receiving a total of 1.6k indexed citations (citations by other indexed papers that have themselves been cited), including 25 papers in Molecular Biology, 19 papers in Genetics and 10 papers in Genetics. Recurrent topics in Valentina Guida's work include Congenital heart defects research (8 papers), Hemoglobinopathies and Related Disorders (6 papers) and Genomic variations and chromosomal abnormalities (5 papers). Valentina Guida is often cited by papers focused on Congenital heart defects research (8 papers), Hemoglobinopathies and Related Disorders (6 papers) and Genomic variations and chromosomal abnormalities (5 papers). Valentina Guida collaborates with scholars based in Italy, Spain and United Kingdom. Valentina Guida's co-authors include Fulvio Cruciani, Rosaria Scozzari, Antonio Torroni, Martin Richards, Vincent Macaulay, Bruno Dallapiccola, Alessandro De Luca, Batsheva Bonné‐Tamir, Eileen Hickey and Bryan Sykes and has published in prestigious journals such as SHILAP Revista de lepidopterología, Diabetes and The American Journal of Human Genetics.

In The Last Decade

Valentina Guida

40 papers receiving 1.6k citations

Peers

Valentina Guida
D.S. Rath United States
Yasemin Alanay Türkiye
Samia A. Temtamy Egypt
Mona Aglan Egypt
Tetsuya Amano Japan
Patrycja A. Krakowiak United States
Marie Legendre France
Ágnes Czibula Hungary
Ana Elisa C. Billerbeck Brazil
Xiu‐Feng Huang China
D.S. Rath United States
Valentina Guida
Citations per year, relative to Valentina Guida Valentina Guida (= 1×) peers D.S. Rath

Countries citing papers authored by Valentina Guida

Since Specialization
Citations

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

Fields of papers citing papers by Valentina Guida

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Valentina Guida

This figure shows the co-authorship network connecting the top 25 collaborators of Valentina Guida. A scholar is included among the top collaborators of Valentina Guida 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 Valentina Guida. Valentina Guida 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.
Frustaci, Andrea, Alessandro De Luca, Romina Verardo, et al.. (2024). Novel ATP2A2 Gene Mutation c.118G>A Causing Keratinocyte and Cardiomyocyte Disconnection in Darier Disease. Biomedicines. 12(5). 1060–1060.
2.
Bernardini, Laura, Marzia Pollazzon, Maria Grazia Giuffrida, et al.. (2023). Split Hand-Foot and Deafness in a Patient with 7q21.13-q21.3 Deletion Not Including the DLX5/6 Genes. Genes. 14(8). 1526–1526. 2 indexed citations
3.
Frustaci, Andrea, Alessandro De Luca, Nicola Galea, et al.. (2021). Novel Dilated Cardiomyopathy Associated to Calreticulin and Myo7A Gene Mutation in Usher Syndrome. ESC Heart Failure. 8(3). 2310–2315. 4 indexed citations
4.
Sirchia, Fabio, Ilaria Fantasia, Elisa Giorgio, et al.. (2021). Prenatal findings of cataract and arthrogryposis: recurrence of cerebro-oculo-facio-skeletal syndrome and review of differential diagnosis. BMC Medical Genomics. 14(1). 89–89.
5.
Ullah, Asmat, Julián Nevado, Ruken Yıldırım, et al.. (2017). GLI1 inactivation is associated with developmental phenotypes overlapping with Ellis–van Creveld syndrome. Human Molecular Genetics. 26(23). 4556–4571. 39 indexed citations
6.
Margiotti, Katia, Giulia Pascolini, Federica Consoli, et al.. (2017). Lack of pathogenic mutations in SOS1 gene in phenytoin-induced gingival overgrowth patients. Archives of Oral Biology. 80. 160–163. 2 indexed citations
7.
Torrente, Isabella, Federica Consoli, Rosangela Ferese, et al.. (2012). Novel and recurrent EVC and EVC2 mutations in Ellis-van Creveld syndrome and Weyers acrofacial dyostosis. European Journal of Medical Genetics. 56(2). 80–87. 49 indexed citations
8.
Guida, Valentina, Rosangela Ferese, Marcella Rocchetti, et al.. (2012). A variant in the carboxyl-terminus of connexin 40 alters GAP junctions and increases risk for tetralogy of Fallot. European Journal of Human Genetics. 21(1). 69–75. 35 indexed citations
9.
Digilio, M. Cristina, Laura Bernardini, Francesca Romana Lepri, et al.. (2011). Ebstein anomaly: Genetic heterogeneity and association with microdeletions 1p36 and 8p23.1. American Journal of Medical Genetics Part A. 155(9). 2196–2202. 25 indexed citations
10.
Salerno, Aurelio, Maria Oliviero, Ernesto Di Maio, et al.. (2010). Design of novel three-phase PCL/TZ–HA biomaterials for use in bone regeneration applications. Journal of Materials Science Materials in Medicine. 21(9). 2569–2581. 31 indexed citations
11.
Luca, Alessandro De, Anna Sárközy, Federica Consoli, et al.. (2009). Familial transposition of the great arteries caused by multiple mutations in laterality genes. Heart. 96(9). 673–677. 85 indexed citations
12.
Tornesello, Maria Lina, Valentina Guida, Simona Losito, et al.. (2008). Analysis of TP53 codon 72 polymorphism in HPV-positive and HPV-negative penile carcinoma. Cancer Letters. 269(1). 159–164. 13 indexed citations
13.
Torrente, Isabella, Salvatore De Cosmo, Valentina Guida, et al.. (2007). Interaction of DIO2 T92A and PPARγ2 P12A Polymorphisms in the Modulation of Metabolic Syndrome. Obesity. 15(12). 2889–2895. 22 indexed citations
14.
Bottillo, Irene, Alessandro De Luca, Annalisa Schirinzi, et al.. (2007). Functional analysis of splicing mutations in exon 7 of NF1gene. BMC Medical Genetics. 8(1). 4–4. 27 indexed citations
15.
Colosimo, Alessia, Valentina Guida, Paola Grisanti, et al.. (2006). Detection of a Rare β-Globin Nonsense Mutation [Codon 59 (AAG→TAG)] in an Italian Family. Hemoglobin. 30(3). 405–407. 3 indexed citations
16.
Cruciani, Fulvio, P. Santolamazza, Daniele Sellitto, et al.. (2004). Phylogeographic Analysis of Haplogroup E3b (E-M215) Y Chromosomes Reveals Multiple Migratory Events Within and Out Of Africa. The American Journal of Human Genetics. 74(5). 1014–1022. 176 indexed citations
17.
Colosimo, Alessia, Valentina Guida, Alessandro De Luca, et al.. (2003). Validation of dHPLC for Molecular Diagnosis of β-Thalassemia in Southern Italy. Genetic Testing. 7(3). 269–275. 8 indexed citations
18.
Colosimo, Alessia, Valentina Guida, Luciana Rigoli, et al.. (2003). Molecular detection of novel WFS1 mutations in patients with Wolfram syndrome by a DHPLC-based assay. Human Mutation. 21(6). 622–629. 38 indexed citations
19.
Colosimo, Alessia, Valentina Guida, Giandomenico Palka, & Bruno Dallapiccola. (2002). Extrachromosomal genes: a powerful tool in gene targeting approaches. Gene Therapy. 9(11). 679–682. 3 indexed citations
20.
Torroni, Antonio, Chiara Rengo, Valentina Guida, et al.. (2001). Do the Four Clades of the mtDNA Haplogroup L2 Evolve at Different Rates?. The American Journal of Human Genetics. 69(6). 1348–1356. 165 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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