This map shows the geographic impact of P Balestrazzi'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 P Balestrazzi with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites P Balestrazzi more than expected).
This network shows the impact of papers produced by P Balestrazzi. 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 P Balestrazzi. The network helps show where P Balestrazzi may publish in the future.
Co-authorship network of co-authors of P Balestrazzi
This figure shows the co-authorship network connecting the top 25 collaborators of P Balestrazzi.
A scholar is included among the top collaborators of P Balestrazzi 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 P Balestrazzi. P Balestrazzi is excluded from
the visualization to improve readability, since they are connected to all nodes in the network.
Sorcini, M, Cristina Fazzini, Antonella Olivieri, et al.. (1994). [Neonatal screening in congenital hypothyroidism in Italy. The National Registry].. PubMed. 30(3). 275–87.8 indexed citations
6.
Virdis, R, et al.. (1994). Hypertension in children with neurofibromatosis.. PubMed. 8(5). 395–7.16 indexed citations
Balestrazzi, P, et al.. (1989). Periaqueductal gliosis causing hydrocephalus in a patient with neurofibromatosis type 1.. PubMed. 2(5-6). 322–5.9 indexed citations
10.
Balestrazzi, P, et al.. (1986). Juvenile rheumatoid arthritis in Turner's syndrome.. PubMed. 4(1). 61–2.18 indexed citations
11.
Balestrazzi, P. (1985). [Sex-linked inheritance in fronto-metaphyseal dysplasia].. PubMed. 33(5). 419–25.2 indexed citations
Mattéi, Marie‐Geneviève, et al.. (1983). Familial pericentric inversion of chromosome 9, INV(9)(p22q32) with recurrent duplication-deletion.. PubMed. 24(3). 220–2.6 indexed citations
14.
Banchini, G, et al.. (1981). [Double cysts of the thyroglossal duct. Description of a case].. PubMed. 52(1). 71–4.1 indexed citations
15.
Virdis, R, S Bernasconi, Maria Cossu Rocca, et al.. (1981). Blood pressure levels related to age and puberal development at adolescence.. PubMed. 22(4). 223–7.3 indexed citations
Dallapiccola, Bruno, Paolo Curatolo, & P Balestrazzi. (1979). ‘De novo’ trisomy 16q11→pter. Human Genetics. 49(1). 1–6.20 indexed citations
19.
Balestrazzi, P, et al.. (1979). [Phenotype variability of the Holt-Oram/syndrome. Identification of unusual skeletal and cardiac malformations].. PubMed. 31(4). 275–82.1 indexed citations
20.
Vanelli, M, S Bernasconi, P Balestrazzi, & G Giovannelli. (1978). Absence congenitale et isolee du clitoris.. 35(2).2 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.