S L Thein

1.9k total citations
35 papers, 1.5k citations indexed

About

S L Thein is a scholar working on Genetics, Hematology and Molecular Biology. According to data from OpenAlex, S L Thein has authored 35 papers receiving a total of 1.5k indexed citations (citations by other indexed papers that have themselves been cited), including 25 papers in Genetics, 18 papers in Hematology and 10 papers in Molecular Biology. Recurrent topics in S L Thein's work include Hemoglobinopathies and Related Disorders (25 papers), Iron Metabolism and Disorders (9 papers) and Blood Coagulation and Thrombosis Mechanisms (5 papers). S L Thein is often cited by papers focused on Hemoglobinopathies and Related Disorders (25 papers), Iron Metabolism and Disorders (9 papers) and Blood Coagulation and Thrombosis Mechanisms (5 papers). S L Thein collaborates with scholars based in United Kingdom, India and Italy. S L Thein's co-authors include Douglas R. Higgs, Joyce E. Reittie, C. Garner, Martin Farrall, Thanusak Tatu, Tim D. Spector, J. H. Darley, Timothy J. Littlewood, Adrian V. S. Hill and David A. Lane and has published in prestigious journals such as Cell, Proceedings of the National Academy of Sciences and Nucleic Acids Research.

In The Last Decade

S L Thein

34 papers receiving 1.4k citations

Peers

S L Thein

GENET

HEMAT

PPCH

GENET

SL Thein United Kingdom

Joyce E. Reittie United Kingdom

J. Gregory Mears United States

Shirley Henderson United Kingdom

Gabriele Strauß Germany

L Steinmann United States

Catherine Driscoll United States

Andrew L. Young United States

Kazuko Hamamoto Japan

H. Behrendt Netherlands

SL Thein United Kingdom

S L Thein

1.0k ×1.1

GENET

1.1k ×1.2

HEMAT

387 ×1.1

310 ×1.0

PPCH

156 ×0.6

GENET

Citations per year, relative to S L Thein S L Thein (= 1×) peers SL Thein

Countries citing papers authored by S L Thein

Since Specialization

Citations

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

Fields of papers citing papers by S L Thein

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by S L Thein. 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 S L Thein. The network helps show where S L Thein may publish in the future.

Co-authorship network of co-authors of S L Thein

This figure shows the co-authorship network connecting the top 25 collaborators of S L Thein. A scholar is included among the top collaborators of S L Thein 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 S L Thein. S L Thein 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

Rees, David C., S L Thein, Emma Drašar, et al.. (2015). The clinical significance of K-Cl cotransport activity in red cells of patients with HbSC disease. Haematologica. 100(5). 595–600. 17 indexed citations

Thein, S L. (2013). The Molecular Basis of -Thalassemia. Cold Spring Harbor Perspectives in Medicine. 3(5). a011700–a011700. 268 indexed citations

Day, Thomas G., Emma Drašar, Tony Fulford, Claire C. Sharpe, & S L Thein. (2011). Association between hemolysis and albuminuria in adults with sickle cell anemia. Haematologica. 97(2). 201–205. 83 indexed citations

Deane, Colin, David Goss, Jack Bartram, et al.. (2010). Extracranial internal carotid arterial disease in children with sickle cell anemia. Haematologica. 95(8). 1287–1292. 39 indexed citations

Thein, S L, et al.. (2008). Thalassaemia: Classification, Genetics and Relationship to Other Inherited Disorders of Haemoglobin. 121–132. 6 indexed citations

Thein, S L. (2005). Genetic modifiers of B thalassaemia.. Haematologica. 649–660. 4 indexed citations

Garner, C., Thanusak Tatu, Joyce E. Reittie, et al.. (2000). Genetic influences on F cells and other hematologic variables: a twin heritability study. Blood. 95(1). 342–346. 200 indexed citations

Garner, C., Thanusak Tatu, Laurence Gamé, et al.. (1999). A candidate gene study of F cell levels in sibling pairs using a joint linkage and association analysis.. Blood. 94. 2 indexed citations

Thein, S L & Jamie E. Craig. (1998). Genetics of Hb F/F Cell Variance in Adults and Heterocellular Hereditary Persistence of Fetal Hemoglobin. Hemoglobin. 22(5-6). 401–414. 59 indexed citations

10.

Thein, S L & Joyce E. Reittie. (1998). F Cells by Immunofluorescent Staining of Erythrocyte Smears. Hemoglobin. 22(5-6). 415–417. 7 indexed citations

11.

Paterakis, Georgios, S L Thein, Eitan Fibach, & Maria Domenica Cappellini. (1998). Cross Evaluation of Three Flow Cytometric F Cell Counting Methods Performed by Different Laboratories. Hemoglobin. 22(5-6). 427–444. 6 indexed citations

12.

Hall, Georgina, S L Thein, Adrian C. Newland, et al.. (1993). A base substitution (T→C) in codon 29 of the α2‐globin gene causes α thalassaemia. British Journal of Haematology. 85(3). 546–552. 38 indexed citations

13.

Olds, R.J., David A. Lane, M Boisclair, et al.. (1992). Antithrombin Budapest 3 An antithrombin variant with reduced heparin affinity resulting from the substitution L99F. FEBS Letters. 300(3). 241–246. 47 indexed citations

14.

Lane, David A., et al.. (1992). Antithrombin and its deficiency states. Blood Coagulation & Fibrinolysis. 3(3). 315–342. 44 indexed citations

15.

Jeffreys, A. J., Victoria Wilson, & S L Thein. (1992). Hypervariable 'minisatellite' regions in human DNA. 1985.. PubMed. 24. 467–72. 21 indexed citations

16.

Olds, R.J., et al.. (1989). Antithrombin III Milano 2: a single base substitution in the thrombin binding domain detected with PCR and direct genomic sequencing. Nucleic Acids Research. 17(24). 10511–10511. 17 indexed citations

17.

Higgs, Douglas R., James S. Wainscoat, Jonathan Flint, et al.. (1986). Analysis of the human alpha-globin gene cluster reveals a highly informative genetic locus.. Proceedings of the National Academy of Sciences. 83(14). 5165–5169. 129 indexed citations

18.

Weatherall, D. J., J. S. Wainscoat, S L Thein, et al.. (1985). Genetic and Molecular Analysis of Mild Forms of Homozygous β‐Thalassemia. Annals of the New York Academy of Sciences. 445(1). 68–80. 20 indexed citations

19.

Hill, Adrian V. S., D. K. Bowden, R J Trent, et al.. (1985). Melanesians and Polynesians share a unique alpha-thalassemia mutation.. PubMed. 37(3). 571–80. 70 indexed citations

20.

Wainscoat, J. S., James Bell, S L Thein, et al.. (1983). Multiple origins of the sickle mutation: evidence from beta S globin gene cluster polymorphisms.. Oxford University Research Archive (ORA) (University of Oxford). 50 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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