Roger J. Amos

403 total citations
10 papers, 213 citations indexed

About

Roger J. Amos is a scholar working on Genetics, Hematology and Infectious Diseases. According to data from OpenAlex, Roger J. Amos has authored 10 papers receiving a total of 213 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Genetics, 5 papers in Hematology and 2 papers in Infectious Diseases. Recurrent topics in Roger J. Amos's work include Hemoglobinopathies and Related Disorders (8 papers), Blood groups and transfusion (4 papers) and Bone and Joint Diseases (2 papers). Roger J. Amos is often cited by papers focused on Hemoglobinopathies and Related Disorders (8 papers), Blood groups and transfusion (4 papers) and Bone and Joint Diseases (2 papers). Roger J. Amos collaborates with scholars based in United Kingdom. Roger J. Amos's co-authors include Dimitris A. Tsitsikas, Paul Greaves, Giorgio Gallinella, Henry Seligman, James Elander, John Old, A. D. Stephens, Chris Fisher, Ruben Nzouakou and Vivek Mathew and has published in prestigious journals such as Journal of Behavioral Medicine, Disability and Rehabilitation and Journal of Clinical Medicine.

In The Last Decade

Roger J. Amos

10 papers receiving 209 citations

Peers

Roger J. Amos

GENET

HEMAT

ID

PPCH

OSM

Marie Belloy France

Angela Rankine‐Mullings Jamaica

B. Wibaut France

Gianluca Vergine Italy

Michael P. Meyer South Africa

Maria Mylona Greece

V. Chamouard France

James Castleman United Kingdom

Jantien Visser Netherlands

Michelle Kush United States

Marie Belloy France

Roger J. Amos

286 ×1.7

GENET

238 ×2.3

HEMAT

16 ×0.3

ID

73 ×1.7

PPCH

20 ×0.5

OSM

Citations per year, relative to Roger J. Amos Roger J. Amos (= 1×) peers Marie Belloy

Countries citing papers authored by Roger J. Amos

Since Specialization

Citations

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

Fields of papers citing papers by Roger J. Amos

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Roger J. Amos. 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 Roger J. Amos. The network helps show where Roger J. Amos may publish in the future.

Co-authorship network of co-authors of Roger J. Amos

This figure shows the co-authorship network connecting the top 25 collaborators of Roger J. Amos. A scholar is included among the top collaborators of Roger J. Amos 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 Roger J. Amos. Roger J. Amos is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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10 of 10 papers shown

1.

Tsitsikas, Dimitris A., et al.. (2021). Automated Red Cell Exchange in the Management of Sickle Cell Disease. Journal of Clinical Medicine. 10(4). 767–767. 16 indexed citations

2.

Tsitsikas, Dimitris A., et al.. (2017). Distinct patterns of response to transfusion therapy for different chronic complications of sickle cell disease: A useful insight. Transfusion and Apheresis Science. 56(5). 713–716. 7 indexed citations

3.

Greaves, Paul, Vivek Mathew, Catherine Peters, et al.. (2016). Successful outcome of three patients with sickle‐cell disease and fat embolism syndrome treated with intensive exchange transfusion. Clinical Case Reports. 5(1). 39–43. 13 indexed citations

4.

Tsitsikas, Dimitris A., et al.. (2016). Safety, tolerability, and outcomes of regular automated red cell exchange transfusion in the management of sickle cell disease. Journal of Clinical Apheresis. 31(6). 545–550. 17 indexed citations

5.

Tsitsikas, Dimitris A., et al.. (2014). Bone marrow necrosis and fat embolism syndrome in sickle cell disease: Increased susceptibility of patients with non-SS genotypes and a possible association with human parvovirus B19 infection. Blood Reviews. 28(1). 23–30. 83 indexed citations

6.

Tsitsikas, Dimitris A., et al.. (2013). Comparison of serial serum ferritin measurements and liver iron concentration assessed by MRI in adult transfused patients with sickle cell disease. European Journal Of Haematology. 92(2). 164–167. 12 indexed citations

7.

Elander, James, et al.. (2006). Factors Affecting Hospital Staff Judgments About Sickle Cell Disease Pain. Journal of Behavioral Medicine. 29(2). 203–214. 26 indexed citations

8.

Fisher, Chris, et al.. (2006). Hb Bart's in Cord Blood: An Accurate Indicator of α-Thalassemia. Hemoglobin. 30(1). 57–62. 31 indexed citations

9.

Elliott, Brent, Priyanka Patel, Manjit Matharu, et al.. (2006). Prophylaxis of venous thromboembolism during early inpatient rehabilitation after acquired brain injury: How guidelines change management. Disability and Rehabilitation. 28(5). 333–337. 2 indexed citations

10.

Horton, Michael A., Roger J. Amos, & Richard J. Jones. (1983). The Effect of Histamine H2 Receptor Antagonists on Platelet Aggregation in Man. Scandinavian Journal of Haematology. 31(1). 15–19. 6 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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