G. V. Sciarratta

491 citations

27 papers · 387 indexed · h-index 11

Impact in

Genetics top 5%
- Hemoglobinopathies and Related Disorders
Hematology top 5%
- Iron Metabolism and Disorders
- Blood groups and transfusion

Papers in ⓘ

Genetics 22
- Hemoglobinopathies and Related Disorders 22
Hematology 15
- Iron Metabolism and Disorders 11
- Blood groups and transfusion 6

Co-authors: G Sansone (10 shared papers)A Bank (1 shared paper)Catherine Driscoll (1 shared paper)Morgan Baird (1 shared paper)Antonio Cao (6 shared papers)S Murru (6 shared papers)Mario Pirastu (6 shared papers)Gilles Ivaldi (10 shared papers)
Journals: British Journal of Haematology (4 papers)Human Mutation (2 papers)Annals of the New York Academy of Sciences (2 papers)Hemoglobin (11 papers)Acta Haematologica (1 paper)
Partner nations: Italy United States United Kingdom

In The Last Decade

G. V. Sciarratta

26 papers receiving 368 citations

Peers

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-authors

The 25 scholars most cited alongside G. V. Sciarratta, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with G. V. Sciarratta Line = papers co-authored together G. V. Sciarratta links everyone, so they are left out of the graph.

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

Showing the 20 most-cited of 27 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	A nucleotide change at a splice junction in the human beta-globin gene is associated with beta 0-thalassemia. Proceedings of the National Academy of Sciences ·Morgan Baird, Catherine Driscoll, H Schreiner, G. V. Sciarratta, G Sansone, Gulzar Niazi, F Ramirez, A Bank	1981	93
2	The occurrence of different levels of ^Gγ chain and of the ^Aγ^T variant of fetal hemoglobin in newborn babies from several countries American Journal of Hematology ·T. H. J. Huisman, A. L. Reese, Melissa Gardiner, J. B. Wilson, H. Lam, Ana Reynolds, Scott K. Nagle, P. Trowell, Yi‐Tao Zeng, Huang Shu‐zheng, P. K. Sukumaran, Shiro Miwa, Г. Д. Ефремов, G. Petkov, G. V. Sciarratta, G Sansone	1983	52
3	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 ·Maria Serafina Ristaldi, S Murru, Georgios Loudianos, Letizia Casula, Susanna Porcu, D. Pigheddu, B. Fanni, G. V. Sciarratta, Steven J. Agosti, M. I. Parodi, Daniela Leone, Clara Camaschella, Anna Serra, Mario Pirastu, Antonio Cao	1990	31
4	A β‐thalassaemia phenotype not linked to the β‐globin cluster in an Italian family British Journal of Haematology ·S Murru, Georgios Loudianos, Susanna Porcu, G. V. Sciarratta, Steven J. Agosti, MI Parodi, Antonio Cao, Mario Pirastu	1992	31
5	Promoter mutations producing mild β‐thalassaemia in the Italian population British Journal of Haematology ·Alessandra Meloni, Maria Cristina Rosatelli, V. Faà, R Sardu, L. Saba, S Murru, G. V. Sciarratta, Maurizia Baldi, N Tannoia, A. Vitucci, Antonio Cao	1992	27
6	Molecular Analysis of Atypical β‐Thalassemia Heterozygotes^a Annals of the New York Academy of Sciences ·Mario Pirastu, Maria Serafina Ristaldi, Georgios Loudianos, S Murru, G. V. Sciarratta, M. I. Parodi, Daniela Leone, Steven J. Agosti, Antonio Cao	1990	19
7	Identification of Mediterranean β-Thalassemia Mutations by Reverse DOT-Blot in Italians and Egyptians Hemoglobin ·Magdy Rady, Maria Baffico, Amal Khalifa, Nahla Heshmat, S. El-Moselhy, G. V. Sciarratta, Ibtessam R. Hussein, Samia A. Temtamy, Giovanni Romeo	1997	18
8	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 ·Sergio Ottolenghi, Clara Camaschella, Paola Comi, Barbára Giglioni, Maurizio Longinotti, L Oggiano, Sylvain Doré, G. V. Sciarratta, Gilles Ivaldi, Giuseppe Saglio, Anna Serra, Angela Loi, Mario Pirastu	1988	18
9	Mild elliptocytosis associated with the alpha 34 Arg-->Trp mutation in spectrin Genova (alpha I/74) Blood ·Silverio Perrotta, Emanuele Miraglia del Giudice, Nicole Alloisio, G. V. Sciarratta, Luciano Pinto, J. Delaunay, S Cutillo, Achille Iolascon	1994	16
10	Severe poikilocytosis associated with a de novoα28 Arg→Cys mutation in spectrin British Journal of Haematology ·Felipe Lorenzo, Emanuele Miraglia del Giudice, Nicole Alloisio, Laurette Morlé, A. Forissier, Silverio Perrotta, G. V. Sciarratta, Achille Iolascon, J. Delaunay	1993	15
11	The Characterization of Hemoglobin Manitoba or α₂102(G9)Ser→Argβ₂and Hemoglobin Contaldo or α₂103(G10)HIS→ARGβ₂By High Performance Liquid Chromatography Hemoglobin ·G. V. Sciarratta, Gilles Ivaldi, G Molaro, G Sansone, M.L. Salkie, J. B. Wilson, A. L. Reese, T. H. J. Huisman	1984	14
12	Alternate Organization of α G-Philadelphia Globin Genes Among U.S. Black and Italian Caucasian Heterozygotes Hemoglobin ·G. V. Sciarratta, G Sansone, Gilles Ivaldi, Alex E. Felice, T. H. J. Huisman	1984	8
13	A novel β-globin structural mutant, Hb Brescia (β114 Leu-Pro), causing a severe β-thalassemia intermedia phenotype Human Mutation ·S Murru, Daniela Poddie, G. V. Sciarratta, Steven J. Agosti, Maria Baffico, C Melevendi, Mario Pirastu, Antonio Cao	1992	7
14	Hb Hatera [β55(D6)Met↣Lys]: A new Unstable Hemoglobin Variant in an Italian Family Hemoglobin ·G. V. Sciarratta, Gilles Ivaldi	1990	6
15	Hb Volga or α₂β₂27(B9)Ala→Asp in an Italian Family Hemoglobin ·G. V. Sciarratta, Gilles Ivaldi, G Sansone, J. B. Wilson, B. B. Webber, T. H. J. Huisman	1985	5
16	The Silent Carrier of β‐Thalassemia Annals of the New York Academy of Sciences ·G. V. Sciarratta, M. I. Parodi, S. F. AGOSTI VALLERINO, G Sansone	1985	5
17	The silent carrier of beta thalassemia: interaction with the typical beta thalassemic trait Annals of Hematology ·Giorgio Aicardi, Arturo Naselli, G. V. Sciarratta, G Sansone	1979	4
18	Hb J-Guantanamo in a Chilean Baby Hemoglobin ·G. V. Sciarratta, Gilles Ivaldi, F. Moruzzi	1990	4
19	Haemoglobin Shepherds Bush (<i>β</i>74 [E18] Gly→Asp) in an Italian Family Acta Haematologica ·G Sansone, G. V. Sciarratta, R Genova, Philippa D. Darbre, Helmar C. Lehmann	1977	3
20	A New γ Chain Variant: Hb F-Pordenone [γ6(A3) GLU à GLN: 75ILE: 136ALA] Hemoglobin ·T. Nakatsuji, B. B. Webber, H. Lam, J. B. Wilson, T. H. J. Huisman, G. V. Sciarratta, G Sansone, G Molaro	1982	3

About G. V. Sciarratta

G. V. Sciarratta is a scholar working on Genetics, Hematology, Cell Biology, Physiology and Pediatrics, Perinatology and Child Health, having authored 27 papers that have together received 387 indexed citations. Recurring topics across this work include Hemoglobinopathies and Related Disorders (22 papers), Iron Metabolism and Disorders (11 papers), Hemoglobin structure and function (8 papers), Erythrocyte Function and Pathophysiology (8 papers), Blood groups and transfusion (6 papers), Neonatal Health and Biochemistry (4 papers), Prenatal Screening and Diagnostics (3 papers) and DNA and Nucleic Acid Chemistry (3 papers). The work is most often cited by research in Genetics (292 citations), Hematology (193 citations), Pediatrics, Perinatology and Child Health (88 citations), Physiology (68 citations) and Cell Biology (40 citations). G. V. Sciarratta has collaborated with scholars based in Italy, United States and United Kingdom. Frequent co-authors include G Sansone, A Bank, Catherine Driscoll, Morgan Baird, Antonio Cao, S Murru, Mario Pirastu, Gilles Ivaldi, Steven J. Agosti and Georgios Loudianos. Their work appears in journals such as British Journal of Haematology, Human Mutation, Annals of the New York Academy of Sciences, Hemoglobin and Acta Haematologica.

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.

Explore authors with similar magnitude of impact