P Giordano

454 total citations
20 papers, 316 citations indexed

About

P Giordano is a scholar working on Genetics, Hematology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, P Giordano has authored 20 papers receiving a total of 316 indexed citations (citations by other indexed papers that have themselves been cited), including 17 papers in Genetics, 13 papers in Hematology and 9 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in P Giordano's work include Hemoglobinopathies and Related Disorders (17 papers), Iron Metabolism and Disorders (11 papers) and Neonatal Health and Biochemistry (5 papers). P Giordano is often cited by papers focused on Hemoglobinopathies and Related Disorders (17 papers), Iron Metabolism and Disorders (11 papers) and Neonatal Health and Biochemistry (5 papers). P Giordano collaborates with scholars based in Netherlands, Italy and United Kingdom. P Giordano's co-authors include Cornelis L. Harteveld, M. Angastiniotis, Barbara Wild, Suthat Fucharoen, Victor Chan, Andrea Mosca, E. Baysal, Frans J. Smiers, Micah D.J. Peters and Harriët Heijboer and has published in prestigious journals such as Blood, Annals of the New York Academy of Sciences and American Journal of Obstetrics and Gynecology.

In The Last Decade

P Giordano

18 papers receiving 307 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
P Giordano Netherlands 10 271 229 122 37 25 20 316
Pratibha Sawant India 12 466 1.7× 410 1.8× 130 1.1× 39 1.1× 37 1.5× 31 523
Marie Belloy France 8 286 1.1× 238 1.0× 73 0.6× 22 0.6× 23 0.9× 14 321
Michele Rizzo Italy 7 270 1.0× 256 1.1× 63 0.5× 23 0.6× 14 0.6× 14 330
Johara Hassan United States 4 190 0.7× 146 0.6× 76 0.6× 21 0.6× 32 1.3× 10 222
Renée C. Rees United States 7 340 1.3× 295 1.3× 153 1.3× 14 0.4× 13 0.5× 16 356
M. T. Scalas Italy 10 310 1.1× 226 1.0× 151 1.2× 17 0.5× 53 2.1× 20 387
Maria Grazia Neonato France 5 275 1.0× 234 1.0× 79 0.6× 36 1.0× 31 1.2× 6 308
Angela Allen United Kingdom 10 217 0.8× 207 0.9× 40 0.3× 39 1.1× 17 0.7× 28 290
Mariane de Montalembert France 7 227 0.8× 206 0.9× 51 0.4× 74 2.0× 11 0.4× 12 248
Catherine Segbefia Ghana 7 248 0.9× 194 0.8× 139 1.1× 21 0.6× 12 0.5× 28 301

Countries citing papers authored by P Giordano

Since Specialization
Citations

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

Fields of papers citing papers by P Giordano

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of P Giordano

This figure shows the co-authorship network connecting the top 25 collaborators of P Giordano. A scholar is included among the top collaborators of P Giordano 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 Giordano. P Giordano 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.
Giordano, P, et al.. (2025). Identifying novel drug targets with computational precision. Advances in pharmacology. 103. 231–263.
2.
Suijker, Monique H., Lian Roovers, Natasja Dors, et al.. (2014). Hemoglobinopathie in de 21e eeuw : incidentie, diagnose en hielprikscreening (Haemoglobinopathy in the 21st century: incidence, diagnosis and heel prick screening). Nederlandsch tijdschrift voor geneeskunde/Nederlands tijdschrift voor geneeskunde/NTvG-databank. 158(33). 1259. 2 indexed citations
3.
Angastiniotis, Michael, Androulla Eleftheriou, R. Galanello, et al.. (2013). Prevention of Thalassaemias and Other Haemoglobin Disorders: Volume 1: Principles. Europe PMC (PubMed Central). 13 indexed citations
4.
Harteveld, Cornelis L., et al.. (2012). Hb Haaglanden: a new nonsickling β7Glu>Val variant. Consequences for basic diagnostics, screening, and risk assessment when dealing with HbS‐like variants. International Journal of Laboratory Hematology. 34(5). 551–555. 9 indexed citations
5.
Peters, Micah D.J., Harriët Heijboer, Frans J. Smiers, & P Giordano. (2012). Diagnosis and management of thalassaemia. BMJ. 344(jan25 4). e228–e228. 35 indexed citations
6.
Harteveld, Cornelis L., Antonino Giambona, Claudia Ruivenkamp, et al.. (2012). Mosaic segmental uniparental isodisomy and progressive clonal selection: a common mechanism of late onset  -thalassemia major. Haematologica. 98(5). 691–695. 6 indexed citations
7.
Giordano, P. (2012). Newborn Screening for Hemoglobinopathies Using Capillary Electrophoresis. Methods in molecular biology. 919. 131–145. 5 indexed citations
8.
Smit, Johannes W. A., et al.. (2012). Basic haemoglobinopathy diagnostics in Dutch laboratories; providing an informative test result. International Journal of Laboratory Hematology. 35(4). 428–435. 4 indexed citations
9.
Angastiniotis, M., E. Baysal, Victor Chan, et al.. (2011). ICSH recommendations for the measurement of Haemoglobin F. International Journal of Laboratory Hematology. 34(1). 14–20. 50 indexed citations
10.
Stephens, A. D., M. Angastiniotis, E. Baysal, et al.. (2011). ICSH recommendations for the measurement of Haemoglobin A2. International Journal of Laboratory Hematology. 34(1). 1–13. 67 indexed citations
11.
12.
Giordano, P. (2008). Starting neonatal screening for haemoglobinopathies in The Netherlands. Journal of Clinical Pathology. 62(1). 18–21. 19 indexed citations
13.
Giordano, P & Cornelis L. Harteveld. (2006). [Prevention of hereditary haemoglobinopathies in The Netherlands].. PubMed. 150(39). 2137–41. 12 indexed citations
14.
Yavarian, Majid, et al.. (2006). Survival Analysis of Transfusion Dependent β-Thalassemia Major Patients. Journal of Research in Health Sciences. 6(2). 8–13. 4 indexed citations
15.
Giordano, P. (2005). Hemoglobinopathieën. Bijblijven. 21(3). 108–117.
16.
Egberts, J., et al.. (1995). Disappearance rates of fetal and donor red blood cells in alloimmunized fetuses. American Journal of Obstetrics and Gynecology. 172(1). 429–429. 17 indexed citations
17.
Bernini, Luigi F., et al.. (1994). Prenatal Diagnosis of Homozygous αº‐Thalassemia by an Immunological Method. Annals of the New York Academy of Sciences. 731(1). 193–196. 4 indexed citations
18.
Gasperini, D., R. Galanello, Marco Melis, et al.. (1993). Hemoglobin Sabine [beta 91 (F7) Leu-->Pro]: occurrence in a Sardinian individual with hemolytic anemia and inclusion bodies.. PubMed. 77(5). 381–3. 5 indexed citations
19.
20.
Cao, Antonio, Maria Antonietta Melis, R. Galanello, et al.. (1982). Delta beta (F)-thalassaemia in Sardinia.. Journal of Medical Genetics. 19(3). 184–192. 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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