Karlene Mason

1.7k total citations · 1 hit paper
38 papers, 1.2k citations indexed

About

Karlene Mason is a scholar working on Genetics, Hematology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Karlene Mason has authored 38 papers receiving a total of 1.2k indexed citations (citations by other indexed papers that have themselves been cited), including 36 papers in Genetics, 32 papers in Hematology and 11 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Karlene Mason's work include Hemoglobinopathies and Related Disorders (36 papers), Iron Metabolism and Disorders (31 papers) and Prenatal Screening and Diagnostics (11 papers). Karlene Mason is often cited by papers focused on Hemoglobinopathies and Related Disorders (36 papers), Iron Metabolism and Disorders (31 papers) and Prenatal Screening and Diagnostics (11 papers). Karlene Mason collaborates with scholars based in Jamaica, United Kingdom and Barbados. Karlene Mason's co-authors include G. R. Serjeant, B. E. Serjeant, Beryl E. Serjeant, Yvonne Grandison, Richard Hayes, J M Topley, Rosmawati Mohamed, Shane Jones, J Pattison and Douglas R. Higgs and has published in prestigious journals such as New England Journal of Medicine, The Lancet and SHILAP Revista de lepidopterología.

In The Last Decade

Karlene Mason

36 papers receiving 1.2k citations

Hit Papers

OUTBREAK OF APLASTIC CRISES IN SICKLE CELL ANAEMIA ASSOCI... 1981 2026 1996 2011 1981 100 200 300

Peers

Karlene Mason
Prasad Rao Koduri United States
Ronald S. Oseas United States
Doug Rizzo United States
C. A. Reindorf United States
Prasad Rao Koduri United States
Karlene Mason
Citations per year, relative to Karlene Mason Karlene Mason (= 1×) peers Prasad Rao Koduri

Countries citing papers authored by Karlene Mason

Since Specialization
Citations

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

Fields of papers citing papers by Karlene Mason

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Karlene Mason

This figure shows the co-authorship network connecting the top 25 collaborators of Karlene Mason. A scholar is included among the top collaborators of Karlene Mason 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 Karlene Mason. Karlene Mason 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.
Serjeant, G. R., Karlene Mason, Ian Hambleton, & Beryl E. Serjeant. (2023). Acute splenic sequestration in HbSS: observations from the Jamaican birth cohort. Archives of Disease in Childhood. 109(2). 100–105. 1 indexed citations
2.
Serjeant, G. R., B. E. Serjeant, Karlene Mason, et al.. (2022). The haematology of Jamaicans: red cell indices in HbAA, HbAS, HbAC, and HbA-HPFH genotypes. Journal of Community Genetics. 13(2). 229–234. 2 indexed citations
3.
Walker, Thomas, Ian Hambleton, Karlene Mason, & G. R. Serjeant. (2022). Spleen size in homozygous sickle cell disease: trends in a birth cohort using ultrasound. British Journal of Radiology. 95(1140). 20220634–20220634. 4 indexed citations
4.
Serjeant, G. R., Monika Asnani, Beryl E. Serjeant, et al.. (2018). Causes of death and early life determinants of survival in homozygous sickle cell disease: The Jamaican cohort study from birth. PLoS ONE. 13(3). e0192710–e0192710. 36 indexed citations
5.
Serjeant, G. R., et al.. (2017). Voluntary premarital screening to prevent sickle cell disease in Jamaica: does it work?. Journal of Community Genetics. 8(2). 133–139. 19 indexed citations
6.
Serjeant, G. R., et al.. (2016). Newborn screening for sickle cell disease in Jamaica: logistics and experience with umbilical cord samples. Journal of Community Genetics. 8(1). 17–22. 7 indexed citations
7.
Mason, Karlene, et al.. (2015). Prevention of sickle cell disease: observations on females with the sickle cell trait from the Manchester project, Jamaica. Journal of Community Genetics. 7(2). 127–132. 5 indexed citations
8.
Mason, Karlene, F. D. Gibson, Ian Hambleton, B. E. Serjeant, & G. R. Serjeant. (2015). Iron Deficiency among Jamaican Adolescents. West Indian Medical Journal. 63(6). 561–5. 3 indexed citations
9.
Mason, Karlene, F. D. Gibson, Lorraine Warren, et al.. (2015). Newborn Screening for Sickle Cell Disease: Jamaican Experience. West Indian Medical Journal. 65(1). 18–26. 3 indexed citations
10.
Gibson, F. D., Karlene Mason, Beryl E. Serjeant, et al.. (2011). Screening for the beta-thalassaemia trait: hazards among populations of West African Ancestry. Journal of Community Genetics. 3(1). 13–18. 5 indexed citations
11.
Serjeant, G. R., et al.. (2008). The changing face of homozygous sickle cell disease: 102 patients over 60 years. International Journal of Laboratory Hematology. 31(6). 585–596. 32 indexed citations
12.
Thame, M, Karlene Mason, Douglas R. Higgs, et al.. (2008). The red cell distribution width in sickle cell disease-is it of clinical value?. Clinical & Laboratory Haematology. 13(3). 229–237. 6 indexed citations
13.
Morris, J, David Dunn, Yvonne Grandison, et al.. (1991). The haematology of homozygous sickle cell disease after the age of 40 years. British Journal of Haematology. 77(3). 382–385. 27 indexed citations
14.
Maude, G. H., Douglas R. Higgs, Yvonne Grandison, et al.. (1985). Alpha thalassaemia and the haematology of normal Jamaican children. Clinical & Laboratory Haematology. 7(4). 289–295. 10 indexed citations
15.
Serjeant, B. E., Karlene Mason, P I Condon, et al.. (1984). Blood rheology and proliferative retinopathy in sickle cell-haemoglobin C disease.. British Journal of Ophthalmology. 68(5). 325–328. 13 indexed citations
16.
Stevens, Michaël C.G., Hermann Lehmann, Karlene Mason, Beryl E. Serjeant, & G. R. Serjeant. (1982). Sickle cell-Hb Lepore Boston syndrome. Uncommon differential diagnosis to homozygous sickle cell disease.. PubMed. 136(1). 19–22. 3 indexed citations
17.
Higgs, Douglas R., Janette Lamb, John Clegg, et al.. (1982). The Interaction of Alpha-Thalassemia and Homozygous Sickle-Cell Disease. New England Journal of Medicine. 306(24). 1441–1446. 262 indexed citations
18.
Serjeant, G. R., Karlene Mason, J M Topley, et al.. (1981). OUTBREAK OF APLASTIC CRISES IN SICKLE CELL ANAEMIA ASSOCIATED WITH PARVOVIRUS-LIKE AGENT. The Lancet. 318(8247). 595–597. 307 indexed citations breakdown →
19.
Serjeant, G. R., et al.. (1980). Haematological indices in normal negro children: a Jamaican cohort from birth to five years. Clinical & Laboratory Haematology. 2(3). 169–178. 30 indexed citations
20.
Serjeant, G. R., Karlene Mason, & B. E. Serjeant. (1980). Negro alpha-thalassaemia: genetic studies in homozygous sickle cell disease.. Journal of Medical Genetics. 17(4). 281–284. 7 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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