Alba Pilotta

1.5k total citations
26 papers, 586 citations indexed

About

Alba Pilotta is a scholar working on Molecular Biology, Genetics and Endocrinology, Diabetes and Metabolism. According to data from OpenAlex, Alba Pilotta has authored 26 papers receiving a total of 586 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Molecular Biology, 12 papers in Genetics and 7 papers in Endocrinology, Diabetes and Metabolism. Recurrent topics in Alba Pilotta's work include Genetics and Neurodevelopmental Disorders (7 papers), Genomic variations and chromosomal abnormalities (5 papers) and Growth Hormone and Insulin-like Growth Factors (5 papers). Alba Pilotta is often cited by papers focused on Genetics and Neurodevelopmental Disorders (7 papers), Genomic variations and chromosomal abnormalities (5 papers) and Growth Hormone and Insulin-like Growth Factors (5 papers). Alba Pilotta collaborates with scholars based in Italy, United Kingdom and United States. Alba Pilotta's co-authors include Fabio Buzi, Patrizia Mella, Barbara Felappi, P Adlard, D. Dordoni, L Gargantini, Gaspare Parrinello, L. D. Notarangelo, Andrea Corrias and Giovanni Battista Pozzan and has published in prestigious journals such as The Journal of Clinical Endocrinology & Metabolism, European Journal of Endocrinology and Pediatric Research.

In The Last Decade

Alba Pilotta

26 papers receiving 575 citations

Peers

Alba Pilotta

GENET

EDM

PPCH

Sofia Helena Valente de Lemos‐Marini Brazil

Jiřina Zapletalová Czechia

H F Stirling United Kingdom

H L Lenko Finland

Ronald W. Gotlin United States

Rogelio H.A. Ruvalcaba United States

A.-M. Bertrand France

Line Cleemann Denmark

C. M. Hall United Kingdom

N Stahnke Germany

Sofia Helena Valente de Lemos‐Marini Brazil

Alba Pilotta

440 ×1.6

GENET

526 ×2.3

357 ×2.1

EDM

79 ×0.7

66 ×0.8

PPCH

Citations per year, relative to Alba Pilotta Alba Pilotta (= 1×) peers Sofia Helena Valente de Lemos‐Marini

Countries citing papers authored by Alba Pilotta

Since Specialization

Citations

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

Fields of papers citing papers by Alba Pilotta

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Alba Pilotta

This figure shows the co-authorship network connecting the top 25 collaborators of Alba Pilotta. A scholar is included among the top collaborators of Alba Pilotta 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 Alba Pilotta. Alba Pilotta 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

Pilotta, Alba, Raffaele Badolato, Luca La Via, et al.. (2023). Generation of human induced pluripotent stem cell lines derived from three Noonan syndrome patients from a single family carrying the heterozygous PTPN11 c.188 A > G (p.Y63C) mutation. Stem Cell Research. 74. 103293–103293. 1 indexed citations

Pezzani, Lidia, Laura Pezzoli, Daniela Marchetti, et al.. (2022). Atypical, Composite, or Blended Phenotypes: How Different Molecular Mechanisms Could Associate in Double-Diagnosed Patients. Genes. 13(7). 1275–1275. 17 indexed citations

Magri, Chiara, et al.. (2015). SNP array and FISH analysis of a proband with a 22q13.2- 22qter duplication shed light on the molecular origin of the rearrangement. BMC Medical Genetics. 16(1). 47–47. 5 indexed citations

Meazza, Cristina, et al.. (2015). Five-year response to growth hormone in children with Noonan syndrome and growth hormone deficiency. The Italian Journal of Pediatrics/Italian journal of pediatrics. 41(1). 71–71. 13 indexed citations

Piovani, Giovanna, Michele Traversa, Alba Pilotta, et al.. (2014). De novo 1Mb interstitial deletion of 8p22 in a patient with slight mental retardation and speech delay. Molecular Cytogenetics. 7(1). 25–25. 10 indexed citations

Spena, Silvia, Donatella Milani, Gloria Negri, et al.. (2014). Insights into genotype–phenotype correlations from CREBBP point mutation screening in a cohort of 46 Rubinstein–Taybi syndrome patients. Clinical Genetics. 88(5). 431–440. 43 indexed citations

Notarangelo, Lucia Dora, et al.. (2014). Severe congenital neutropenia due to G6PC3 deficiency: early and delayed phenotype in two patients with two novel mutations. The Italian Journal of Pediatrics/Italian journal of pediatrics. 40(1). 80–80. 6 indexed citations

Savoldi, Gianfranco, Claudia Izzi, Maria Pia Bondioni, et al.. (2013). Prenatal presentation and postnatal evolution of a patient with Jansen metaphyseal dysplasia with a novel missense mutation in PTH1R. American Journal of Medical Genetics Part A. 161(10). 2614–2619. 17 indexed citations

Castelnuovo, Paolo, Stefania Di Candia, L Gargantini, et al.. (2013). Growth Hormone Therapy and Respiratory Disorders: Long-Term Follow-up in PWS Children. The Journal of Clinical Endocrinology & Metabolism. 98(9). E1516–E1523. 45 indexed citations

10.

D’Orazio, Ciro, Rita Padoan, Hannah Blau, et al.. (2012). Growth retardation and reduced growth hormone secretion in cystic fibrosis. Clinical observations from three CF centers. Journal of Cystic Fibrosis. 12(2). 165–169. 20 indexed citations

11.

Magri, Chiara, Giovanna Piovani, Alba Pilotta, et al.. (2011). De novo deletion of chromosome 2q24.2 region in a mentally retarded boy with muscular hypotonia. European Journal of Medical Genetics. 54(3). 361–364. 15 indexed citations

12.

Grugni, Graziano, Antonino Crinò, Sara Pagani, et al.. (2011). Growth hormone secretory pattern in non-obese children and adolescents with Prader-Willi syndrome. Journal of Pediatric Endocrinology and Metabolism. 24(7-8). 477–81. 23 indexed citations

13.

Gervasini, Cristina, Federica Mottadelli, Roberto Ciccone, et al.. (2010). High frequency of copy number imbalances in Rubinstein–Taybi patients negative to CREBBP mutational analysis. European Journal of Human Genetics. 18(7). 768–775. 9 indexed citations

14.

Buzi, Fabio, et al.. (2007). Growth Hormone Receptor Polymorphisms. Endocrine development. 11. 28–35. 22 indexed citations

15.

Pilotta, Alba, Patrizia Mella, Barbara Felappi, et al.. (2006). Common Polymorphisms of the Growth Hormone (GH) Receptor Do Not Correlate with the Growth Response to Exogenous Recombinant Human GH in GH-Deficient Children. The Journal of Clinical Endocrinology & Metabolism. 91(3). 1178–1180. 64 indexed citations

16.

Radetti, Giorgio, Fabio Buzi, Chiara Paganini, Alba Pilotta, & Barbara Felappi. (2003). Treatment of GH-deficient children with two different GH doses: effect on final height and cost-benefit implications. European Journal of Endocrinology. 148(5). 515–518. 16 indexed citations

17.

Buzi, Fabio, Patrizia Mella, Alba Pilotta, et al.. (2001). Frasier Syndrome with Childhood-Onset Renal Failure. Hormone Research in Paediatrics. 55(2). 77–80. 14 indexed citations

18.

Sanctis, Vincenzo De, Andrea Corrias, Silvano Bertelloni, et al.. (2000). Etiology of Central Precocious Puberty in Males: The Results of the Italian Study Group for Physiopathology of Puberty. Journal of Pediatric Endocrinology and Metabolism. 13(Supplement). 687–93. 70 indexed citations

19.

Buzi, Fabio, Daniele Alberti, Jenny Jones, et al.. (1998). Growth, Insulin-Like Growth Factor I (IGF-I), and IGF-Binding Proteins 1 and 3 in Children with Severe Liver Disease before and after Liver Transplantation: A Longitudinal and Cross-Sectional Study. Pediatric Research. 43(4). 478–483. 15 indexed citations

20.

Buzi, Fabio, et al.. (1997). Loperamide test: a simple and highly specific screening test for hypercortisolism in children and adolescents. Acta Paediatrica. 86(11). 1177–1180. 4 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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