G. V. Sciarratta

491 total citations
27 papers, 387 citations indexed

About

G. V. Sciarratta is a scholar working on Genetics, Hematology and Cell Biology. According to data from OpenAlex, G. V. Sciarratta has authored 27 papers receiving a total of 387 indexed citations (citations by other indexed papers that have themselves been cited), including 22 papers in Genetics, 15 papers in Hematology and 8 papers in Cell Biology. Recurrent topics in G. V. Sciarratta's work include Hemoglobinopathies and Related Disorders (22 papers), Iron Metabolism and Disorders (11 papers) and Erythrocyte Function and Pathophysiology (8 papers). G. V. Sciarratta is often cited by papers focused on Hemoglobinopathies and Related Disorders (22 papers), Iron Metabolism and Disorders (11 papers) and Erythrocyte Function and Pathophysiology (8 papers). G. V. Sciarratta collaborates with scholars based in Italy, United States and Egypt. G. V. Sciarratta's co-authors include G Sansone, Morgan Baird, Catherine Driscoll, A Bank, S Murru, Antonio Cao, Mario Pirastu, Gilles Ivaldi, Steven J. Agosti and Georgios Loudianos and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Blood and Annals of the New York Academy of Sciences.

In The Last Decade

G. V. Sciarratta

26 papers receiving 368 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
G. V. Sciarratta Italy 11 292 193 108 88 68 27 387
C Altay United States 12 476 1.6× 375 1.9× 121 1.1× 113 1.3× 87 1.3× 29 561
G. P. Tamagnini Portugal 11 235 0.8× 232 1.2× 133 1.2× 83 0.9× 151 2.2× 20 457
G. Mérault France 12 226 0.8× 152 0.8× 123 1.1× 48 0.5× 43 0.6× 22 366
DL Rucknagel United States 11 214 0.7× 124 0.6× 109 1.0× 85 1.0× 169 2.5× 16 376
M Patterson Canada 12 359 1.2× 262 1.4× 148 1.4× 90 1.0× 163 2.4× 27 505
K. Sofroniadou Greece 9 265 0.9× 167 0.9× 64 0.6× 54 0.6× 46 0.7× 12 314
C Hesketh United Kingdom 7 309 1.1× 236 1.2× 121 1.1× 58 0.7× 49 0.7× 7 432
Jean Atwater United States 12 336 1.2× 249 1.3× 37 0.3× 88 1.0× 93 1.4× 20 393
PE Nute United States 6 309 1.1× 254 1.3× 77 0.7× 119 1.4× 146 2.1× 8 393
K. G. Yang United States 10 224 0.8× 158 0.8× 69 0.6× 41 0.5× 37 0.5× 15 278

Countries citing papers authored by G. V. Sciarratta

Since Specialization
Citations

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

Fields of papers citing papers by G. V. Sciarratta

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by G. V. Sciarratta. 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 G. V. Sciarratta. The network helps show where G. V. Sciarratta may publish in the future.

Co-authorship network of co-authors of G. V. Sciarratta

This figure shows the co-authorship network connecting the top 25 collaborators of G. V. Sciarratta. A scholar is included among the top collaborators of G. V. Sciarratta 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 G. V. Sciarratta. G. V. Sciarratta 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.
Khalifa, Amal, et al.. (1997). Identification of Mediterranean β-Thalassemia Mutations by Reverse DOT-Blot in Italians and Egyptians. Hemoglobin. 21(1). 59–69. 18 indexed citations
2.
Lorenzo, Felipe, Emanuele Miraglia del Giudice, Nicole Alloisio, et al.. (1993). Severe poikilocytosis associated with a de novoα28 Arg→Cys mutation in spectrin. British Journal of Haematology. 83(1). 152–157. 15 indexed citations
3.
Lendaro, Eugenio, Rodolfo Ippoliti, Andrea Brancaccio, et al.. (1992). Hemoglobin Dallas (α97(G4)Asn→Lys):functional characterization of a high oxygen affinity natural mutant. Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease. 1180(1). 15–20. 2 indexed citations
4.
Murru, S, Georgios Loudianos, Susanna Porcu, et al.. (1992). A β‐thalassaemia phenotype not linked to the β‐globin cluster in an Italian family. British Journal of Haematology. 81(2). 283–287. 31 indexed citations
5.
Loudianos, Georgios, S Murru, Maria Serafina Ristaldi, et al.. (1992). A novel δ-thalassemia mutation A G→C substitution at codon 30 of the δ-globin gene in a person of Southern Italian origin. Human Mutation. 1(2). 169–171. 1 indexed citations
6.
Murru, S, G. V. Sciarratta, Steven J. Agosti, et al.. (1992). A novel β-globin structural mutant, Hb Brescia (β114 Leu-Pro), causing a severe β-thalassemia intermedia phenotype. Human Mutation. 1(2). 124–128. 7 indexed citations
7.
Meloni, Alessandra, Maria Cristina Rosatelli, V. Faà, et al.. (1992). Promoter mutations producing mild β‐thalassaemia in the Italian population. British Journal of Haematology. 80(2). 222–226. 27 indexed citations
8.
Ristaldi, Maria Serafina, S Murru, Georgios Loudianos, et al.. (1990). The C–T substitution in the distal CACCC box of the β‐globin gene promoter is a common cause of silent β thalassaemia in the Italian population. British Journal of Haematology. 74(4). 480–486. 31 indexed citations
9.
Pirastu, Mario, Maria Serafina Ristaldi, Georgios Loudianos, et al.. (1990). Molecular Analysis of Atypical β‐Thalassemia Heterozygotesa. Annals of the New York Academy of Sciences. 612(1). 90–97. 19 indexed citations
10.
Sciarratta, G. V. & Gilles Ivaldi. (1990). Hb Hatera [β55(D6)Met↣Lys]: A new Unstable Hemoglobin Variant in an Italian Family. Hemoglobin. 14(1). 79–85. 6 indexed citations
11.
Sciarratta, G. V., et al.. (1990). Hb J-Guantanamo in a Chilean Baby. Hemoglobin. 14(1). 115–117. 4 indexed citations
12.
Zhao, Weixing, J. B. Wilson, B. B. Webber, et al.. (1990). A Second Observation of HB Abruzzo [α2β2143(H21)HIS→ARG] in an Italian Family. Hemoglobin. 14(4). 463–466. 2 indexed citations
13.
Zhao, Weixing, et al.. (1990). HB Camperdown or α2β2104(G6)Arg→ser in Two Italian Males. Hemoglobin. 14(4). 459–461.
14.
Ottolenghi, Sergio, Clara Camaschella, Paola Comi, et al.. (1988). A frequent A?-persistence of fetal hemoglobin in northern Sardinia: its molecular basis and hematologic phenotype in heterozygotes and compound heterozygotes with ?-thalassemia. Human Genetics. 79(1). 13–17. 18 indexed citations
15.
Sciarratta, G. V., et al.. (1985). Hb 0-Arab [β121 (Gh4) Glu→Lys] in Italy. Hemoglobin. 9(5). 513–515. 1 indexed citations
16.
Sciarratta, G. V., G Sansone, Gilles Ivaldi, Alex E. Felice, & T. H. J. Huisman. (1984). Alternate Organization of α G-Philadelphia Globin Genes Among U.S. Black and Italian Caucasian Heterozygotes. Hemoglobin. 8(6). 537–547. 8 indexed citations
17.
Huisman, T. H. J., A. L. Reese, Melissa Gardiner, et al.. (1983). The occurrence of different levels of Gγ chain and of the AγT variant of fetal hemoglobin in newborn babies from several countries. American Journal of Hematology. 14(2). 133–148. 52 indexed citations
18.
Sansone, G, et al.. (1982). Hb Belfast (β15 Trp à Arg) in an Italian Family. Hemoglobin. 6(4). 391–396. 1 indexed citations
19.
Aicardi, Giorgio, Arturo Naselli, G. V. Sciarratta, & G Sansone. (1979). The silent carrier of beta thalassemia: interaction with the typical beta thalassemic trait. Annals of Hematology. 38(6). 473–478. 4 indexed citations
20.
Sansone, G, et al.. (1977). Haemoglobin Shepherds Bush (<i>β</i>74 [E18] Gly→Asp) in an Italian Family. Acta Haematologica. 57(2). 102–108. 3 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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