T Tuveri

794 total citations
30 papers, 649 citations indexed

About

T Tuveri is a scholar working on Genetics, Hematology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, T Tuveri has authored 30 papers receiving a total of 649 indexed citations (citations by other indexed papers that have themselves been cited), including 29 papers in Genetics, 26 papers in Hematology and 18 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in T Tuveri's work include Hemoglobinopathies and Related Disorders (29 papers), Iron Metabolism and Disorders (20 papers) and Prenatal Screening and Diagnostics (11 papers). T Tuveri is often cited by papers focused on Hemoglobinopathies and Related Disorders (29 papers), Iron Metabolism and Disorders (20 papers) and Prenatal Screening and Diagnostics (11 papers). T Tuveri collaborates with scholars based in Italy, Netherlands and Greece. T Tuveri's co-authors include Antonio Cao, Maria Cristina Rosatelli, M. T. Scalas, M. Furbetta, R. Galanello, Mario Pirastu, Angela Maria Falchi, Giovanni Monni, MA Melis and A. Tucci and has published in prestigious journals such as Proceedings of the National Academy of Sciences, The Lancet and Blood.

In The Last Decade

T Tuveri

29 papers receiving 611 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
T Tuveri Italy	14	537	406	238	89	85	30	649
D.J. Weatherall United Kingdom	4	698 1.3×	571 1.4×	199 0.8×	64 0.7×	94 1.1×	8	783
Danielle Lena‐Russo France	10	285 0.5×	225 0.6×	148 0.6×	37 0.4×	28 0.3×	28	373
JULIAN R. DAVIS United States	5	385 0.7×	305 0.8×	89 0.4×	30 0.3×	57 0.7×	7	458
R. P. Perrine United Kingdom	7	528 1.0×	406 1.0×	152 0.6×	24 0.3×	83 1.0×	8	573
Carlo Dessì Italy	12	549 1.0×	499 1.2×	190 0.8×	17 0.2×	27 0.3×	19	675
Suhaib Ahmed Pakistan	11	345 0.6×	287 0.7×	115 0.5×	62 0.7×	39 0.5×	35	474
Can Liao China	14	470 0.9×	401 1.0×	189 0.8×	45 0.5×	38 0.4×	54	528
Manna Sun China	8	265 0.5×	223 0.5×	180 0.8×	55 0.6×	55 0.6×	22	416
Hildegard Braun Germany	4	325 0.6×	371 0.9×	307 1.3×	41 0.5×	35 0.4×	7	644
Deogratius Soka Tanzania	7	473 0.9×	420 1.0×	179 0.8×	28 0.3×	52 0.6×	15	520

Countries citing papers authored by T Tuveri

Since Specialization

Citations

This map shows the geographic impact of T Tuveri'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 T Tuveri with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites T Tuveri more than expected).

Fields of papers citing papers by T Tuveri

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of T Tuveri

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

Phylipsen, Marion, A. Amato, Joanne Traeger‐Synodinos, et al.. (2009). Two new -thalassemia deletions compromising prenatal diagnosis in an Italian and a Turkish couple seeking prevention. Haematologica. 94(9). 1289–1292. 9 indexed citations

Orofino, Maria Grazia, Francesca Argiolu, Maria Cristina Rosatelli, et al.. (2003). Fetal HLA typing in β thalassaemia: implications for haemopoietic stem-cell transplantation. The Lancet. 362(9377). 41–42. 16 indexed citations

Rosatelli, Maria Cristina, T Tuveri, V. Faà, et al.. (1992). Molecular screening and fetal diagnosis of ?-thalassemia in the Italian population. Human Genetics. 89(6). 585–9. 58 indexed citations

Rosatelli, Maria Cristina, T Tuveri, M. T. Scalas, et al.. (1992). Heterozygous β‐thalassemia: Relationship between the hematological phenotype and the type of β‐thalassemia mutation. American Journal of Hematology. 39(1). 1–4. 34 indexed citations

Cao, Antonio, et al.. (1990). Antenatal Diagnosis of β‐Thalassemia in Sardinia^a. Annals of the New York Academy of Sciences. 612(1). 215–225. 27 indexed citations

Rosatelli, Maria Cristina, T Tuveri, M. T. Scalas, et al.. (1990). Reliability of prenatal diagnosis of genetic diseases by analysis of amplified trophoblast DNA.. Journal of Medical Genetics. 27(4). 249–251. 6 indexed citations

Tuveri, T, A. Tucci, M. T. Scalas, et al.. (1989). Thalassemia intermedia resulting from a mild beta-thalassemia mutation. Blood. 73(2). 601–605.

Galanello, R., Maria Addis, Maria Antonietta Melis, et al.. (1988). Pitfalls in genetic counselling for β‐thalassemia: an individual with 4 different thalassemia mutations. Clinical Genetics. 33(3). 151–155. 7 indexed citations

Pirastu, Mario, R. Galanello, Marie Doherty, et al.. (1987). The same beta-globin gene mutation is present on nine different beta-thalassemia chromosomes in a Sardinian population.. Proceedings of the National Academy of Sciences. 84(9). 2882–2885. 52 indexed citations

10.

Cao, Antonio, et al.. (1986). Prenatal diagnosis of thalassemia major by fetal blood analysis: Experience with 1000 cases. Prenatal Diagnosis. 6(3). 159–167. 10 indexed citations

11.

Monni, Giovanni, Maria Cristina Rosatelli, Angela Maria Falchi, et al.. (1986). First trimester diagnosis of β‐thalassaemia in a twin pregnancy. Prenatal Diagnosis. 6(1). 63–68. 6 indexed citations

12.

Cao, Antonio, P Cossu, Angela Maria Falchi, et al.. (1985). Antenatal Diagnosis of Thalassemia Major in Sardinia^a. Annals of the New York Academy of Sciences. 445(1). 380–392. 12 indexed citations

13.

Melis, MA, Mario Pirastu, R. Galanello, et al.. (1983). Phenotypic effect of heterozygous alpha and beta 0-thalassemia interaction. Blood. 62(1). 226–229. 60 indexed citations

14.

Melis, MA, et al.. (1983). Phenotypic effect of heterozygous alpha and beta 0-thalassemia interaction. Blood. 62(1). 226–229. 53 indexed citations

15.

Furbetta, M., R. Galanello, Andrea Angius, et al.. (1982). Control of homozygous beta-thalassemia by carrier screening and antenatal diagnosis in Sardinia.. PubMed. 18(7). 303–11. 3 indexed citations

16.

Cao, Antonio, M. Furbetta, Andrea Angius, et al.. (1982). Haematological and obstetric aspects of antenatal diagnosis of beta-thalassaemia: experience with 200 cases.. Journal of Medical Genetics. 19(2). 81–87. 7 indexed citations

17.

Cao, Antonio, M. Furbetta, R. Galanello, et al.. (1981). Prevention of homozygous beta-thalassemia by carrier screening and prenatal diagnosis in Sardinia.. PubMed. 33(4). 592–605. 47 indexed citations

18.

Furbetta, M., R. Galanello, Andrea Angius, et al.. (1981). Prevention of homozyous /-thalassemia by carrier screening and prenatal diagnosis in Sardinia. 1 indexed citations

19.

Furbetta, M., Andrea Angius, T Tuveri, et al.. (1981). Diagnosis of the β⁰Thalassemia Trait at Birth. Hemoglobin. 5(3). 217–229. 5 indexed citations

20.

Furbetta, M., Andrea Angius, T Tuveri, et al.. (1980). Prenatal Diagnosis of β Thalassaemia by Fetal Red Cell Enrichment with NH₄Cl‐NH₄HCO₃ Differential Lysis of Maternal Cells. British Journal of Haematology. 44(3). 441–450. 15 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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