Pinella Failla

2.6k total citations
30 papers, 396 citations indexed

About

Pinella Failla is a scholar working on Genetics, Molecular Biology and Gastroenterology. According to data from OpenAlex, Pinella Failla has authored 30 papers receiving a total of 396 indexed citations (citations by other indexed papers that have themselves been cited), including 19 papers in Genetics, 11 papers in Molecular Biology and 10 papers in Gastroenterology. Recurrent topics in Pinella Failla's work include Celiac Disease Research and Management (10 papers), Genetics and Neurodevelopmental Disorders (7 papers) and Genomic variations and chromosomal abnormalities (6 papers). Pinella Failla is often cited by papers focused on Celiac Disease Research and Management (10 papers), Genetics and Neurodevelopmental Disorders (7 papers) and Genomic variations and chromosomal abnormalities (6 papers). Pinella Failla collaborates with scholars based in Italy, United Kingdom and United States. Pinella Failla's co-authors include Corrado Romano, Rosa Pettinato, Concetta Barone, G Bottaro, Franco Culasso, P. Mariani, Aldo Giannotti, Generoso Andria, Marco Fichera and Fiorella Balli and has published in prestigious journals such as International Journal of Molecular Sciences, Clinical Chemistry and Human Genetics.

In The Last Decade

Pinella Failla

28 papers receiving 378 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Pinella Failla Italy 11 223 150 149 133 68 30 396
Ramzi El Asmar Italy 3 250 1.1× 140 0.9× 156 1.0× 83 0.6× 72 1.1× 6 385
Mirko Di Ruscio Italy 8 69 0.3× 88 0.6× 118 0.8× 148 1.1× 25 0.4× 19 277
Daniela Follo Italy 6 255 1.1× 123 0.8× 167 1.1× 106 0.8× 9 0.1× 7 362
Arik Alper United States 11 74 0.3× 110 0.7× 74 0.5× 90 0.7× 35 0.5× 22 279
Chen Sarbagili‐Shabat Israel 9 54 0.2× 150 1.0× 163 1.1× 288 2.2× 68 1.0× 24 371
Yasin Şahin Türkiye 9 173 0.8× 105 0.7× 89 0.6× 62 0.5× 12 0.2× 23 230
O’Sullivan United Kingdom 4 324 1.5× 173 1.2× 45 0.3× 20 0.2× 34 0.5× 8 405
Clayton United Kingdom 2 335 1.5× 172 1.1× 40 0.3× 19 0.1× 35 0.5× 2 408
Fabio Chicco Italy 6 39 0.2× 77 0.5× 117 0.8× 163 1.2× 68 1.0× 8 290
M. K. Karlsson Sweden 7 134 0.6× 78 0.5× 70 0.5× 79 0.6× 234 3.4× 13 418

Countries citing papers authored by Pinella Failla

Since Specialization
Citations

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

Fields of papers citing papers by Pinella Failla

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Pinella Failla

This figure shows the co-authorship network connecting the top 25 collaborators of Pinella Failla. A scholar is included among the top collaborators of Pinella Failla 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 Pinella Failla. Pinella Failla 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.
Greco, Donatella, Simone Treccarichi, Maria Bottitta, et al.. (2025). Clinical Application of a Customized Gene Panel for Identifying Autism Spectrum Disorder-Associated Variants. Medicina. 61(7). 1273–1273.
2.
Treccarichi, Simone, Mirella Vinci, Antonino Musumeci, et al.. (2025). Investigating the Role of the Zinc Finger Protein ZC2HC1C on Autism Spectrum Disorder Susceptibility. Medicina. 61(4). 574–574. 3 indexed citations
3.
Calı̀, Francesco, Simone Treccarichi, Antonino Musumeci, et al.. (2025). ZNF496 as Candidate Gene for Neurodevelopmental Disorders: Identification of a Pathogenic De Novo Frameshift Variant. International Journal of Molecular Sciences. 26(15). 7586–7586. 1 indexed citations
4.
Treccarichi, Simone, Pinella Failla, Mirella Vinci, et al.. (2024). UNC5C: Novel Gene Associated with Psychiatric Disorders Impacts Dysregulation of Axon Guidance Pathways. Genes. 15(3). 306–306. 6 indexed citations
5.
Failla, Pinella, Ornella Galesi, Donatella Greco, et al.. (2024). Unveiling Secondary Mutations in Blended Phenotypes: Dual ERCC4 and OTOA Pathogenic Variants Through WES Analysis. International Journal of Molecular Sciences. 25(24). 13471–13471.
6.
Failla, Pinella, et al.. (2023). Trait − driven analysis of the 2p15p16.1 microdeletion syndrome suggests a complex pattern of interactions between candidate genes. Genes & Genomics. 45(4). 491–505. 4 indexed citations
7.
8.
Bianciardi, Laura, Marco Fichera, Pinella Failla, et al.. (2015). MECP2 missense mutations outside the canonical MBD and TRD domains in males with intellectual disability. Journal of Human Genetics. 61(2). 95–101. 20 indexed citations
9.
Calı̀, Francesco, et al.. (2013). Multiplex ligation-dependent probe amplification detection of an unknown large deletion of the CREB-binding protein gene in a patient with Rubinstein-Taybi Syndrome. Genetics and Molecular Research. 12(AOP). 2809–15. 4 indexed citations
10.
Failla, Pinella, Corrado Romano, S Reitano, et al.. (2008). 12q12 deletion: A new patient contributing to genotype–phenotype correlation. American Journal of Medical Genetics Part A. 146A(10). 1354–1357. 10 indexed citations
11.
Romano, Corrado, A Alberti, Donatella Greco, et al.. (2005). Identification of Novel Mutations in Patients with Coffin–Lowry Syndrome by a Denaturing HPLC-Based Assay. Clinical Chemistry. 51(12). 2356–2358. 5 indexed citations
12.
Romano, Corrado, Rosa Pettinato, Letizia Ragusa, et al.. (2002). Is there a relationship between zinc and the peculiar comorbidities of Down syndrome?. Down Syndrome Research and Practice. 8(1). 25–28. 10 indexed citations
13.
Bonamico, Margherita, P. Mariani, Pinella Failla, et al.. (2001). Prevalence and Clinical Picture of Celiac Disease in Italian Down Syndrome Patients: A Multicenter Study. Journal of Pediatric Gastroenterology and Nutrition. 33(2). 139–143. 108 indexed citations
14.
Bonamico, Margherita, P. Mariani, Pinella Failla, et al.. (2001). Prevalence and Clinical Picture of Celiac Disease in Italian Down Syndrome Patients: A Multicenter Study. Journal of Pediatric Gastroenterology and Nutrition. 33(2). 139–143. 7 indexed citations
15.
Romano, Corrado, et al.. (1999). A prevalence study of celiac disease in persons with Down syndrome residing in the United States of America. Acta Paediatrica. 88(9). 953–956. 42 indexed citations
16.
Failla, Pinella, Corrado Romano, & Carmelo Schepis. (1997). Hypomelanosis of Ito: A syndrome requiring a multisystem approach. Australasian Journal of Dermatology. 38(2). 65–70. 6 indexed citations
17.
Failla, Pinella, Maria Pagano, G Bottaro, et al.. (1996). Celiac Disease in Down's Syndrome with HLA Serological and Molecular Studies. Journal of Pediatric Gastroenterology and Nutrition. 23(3). 303–306. 31 indexed citations
18.
Failla, Pinella, Maria Pagano, G Bottaro, et al.. (1996). Celiac Disease in Down's Syndrome with HLA Serological and Molecular Studies. Journal of Pediatric Gastroenterology and Nutrition. 23(3). 303–306. 1 indexed citations
19.
Schepis, Carmelo, Pinella Failla, Maddalena Siragusa, & Corrado Romano. (1994). SKIN‐PICKING: THE BEST CUTANEOUS FEATURE IN THE RECOGNIZATION OF PRADER‐WILLI SYNDROME. International Journal of Dermatology. 33(12). 866–867. 12 indexed citations
20.
Bottaro, G, et al.. (1993). Changes in coeliac disease behaviour over the years. Acta Paediatrica. 82(6-7). 566–568. 21 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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