M.‐J. King

840 total citations
16 papers, 535 citations indexed

About

M.‐J. King is a scholar working on Physiology, Molecular Biology and Hematology. According to data from OpenAlex, M.‐J. King has authored 16 papers receiving a total of 535 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Physiology, 7 papers in Molecular Biology and 7 papers in Hematology. Recurrent topics in M.‐J. King's work include Erythrocyte Function and Pathophysiology (10 papers), Blood groups and transfusion (7 papers) and Glycosylation and Glycoproteins Research (6 papers). M.‐J. King is often cited by papers focused on Erythrocyte Function and Pathophysiology (10 papers), Blood groups and transfusion (7 papers) and Glycosylation and Glycoproteins Research (6 papers). M.‐J. King collaborates with scholars based in United Kingdom, United States and Italy. M.‐J. King's co-authors include Alberto Zanella, G Lamont, Paula Bolton‐Maggs, Richard Stevens, N J Dodd, Achille Iolascon, J. D. Hoyer, Paola Bianchi, V. Picard and Gordon W. Stewart and has published in prestigious journals such as British Journal of Haematology, Transfusion and American Journal of Hematology.

In The Last Decade

M.‐J. King

16 papers receiving 513 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
M.‐J. King United Kingdom 9 383 187 186 165 147 16 535
Lee Ls Taiwan 12 96 0.3× 123 0.7× 91 0.5× 129 0.8× 90 0.6× 39 428
May‐Jean King United Kingdom 10 557 1.5× 215 1.1× 308 1.7× 209 1.3× 260 1.8× 17 702
Manuela Zappa Italy 11 197 0.5× 111 0.6× 43 0.2× 107 0.6× 88 0.6× 21 318
Leonie Frauenfeld Germany 10 220 0.6× 43 0.2× 165 0.9× 38 0.2× 91 0.6× 26 517
Graziana Battini Italy 12 196 0.5× 48 0.3× 49 0.3× 20 0.1× 24 0.2× 34 604
A. Covelli Italy 11 60 0.2× 134 0.7× 24 0.1× 95 0.6× 67 0.5× 23 447
E.H. Hemsted United Kingdom 7 81 0.2× 59 0.3× 39 0.2× 123 0.7× 60 0.4× 9 382
C. F. Lucas United Kingdom 5 90 0.2× 178 1.0× 22 0.1× 50 0.3× 31 0.2× 7 321
F Braconnier France 12 69 0.2× 116 0.6× 17 0.1× 154 0.9× 69 0.5× 27 394
Małgorzata Uhrynowska Poland 14 63 0.2× 319 1.7× 31 0.2× 59 0.4× 46 0.3× 38 542

Countries citing papers authored by M.‐J. King

Since Specialization
Citations

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

Fields of papers citing papers by M.‐J. King

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by M.‐J. King. 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 M.‐J. King. The network helps show where M.‐J. King may publish in the future.

Co-authorship network of co-authors of M.‐J. King

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

All Works

16 of 16 papers shown
1.
Singleton, Belinda K., Momin Ahmed, H. Heimpel, et al.. (2016). CD44 as a Potential Screening Marker for Preliminary Differentiation Between Congenital Dyserythropoietic Anemia Type II and Hereditary Spherocytosis. Cytometry Part B Clinical Cytometry. 94(2). 312–326. 5 indexed citations
2.
King, M.‐J., Loïc Garçon, J. D. Hoyer, et al.. (2015). ICSH guidelines for the laboratory diagnosis of nonimmune hereditary red cell membrane disorders. International Journal of Laboratory Hematology. 37(3). 304–325. 104 indexed citations
3.
King, M.‐J. & Alberto Zanella. (2013). Hereditary red cell membrane disorders and laboratory diagnostic testing. International Journal of Laboratory Hematology. 35(3). 237–243. 90 indexed citations
4.
Chakravorty, Subarna, M.‐J. King, & Barbara J. Bain. (2012). An unexpectedly bizarre blood film in hemoglobin H disease. American Journal of Hematology. 87(12). 1104–1104. 1 indexed citations
5.
Iolascon, Achille, et al.. (2011). A genomic deletion causes truncation of α-spectrin and ellipto-poikilocytosis. Blood Cells Molecules and Diseases. 46(3). 195–200. 8 indexed citations
6.
King, M.‐J., et al.. (2010). Detection of hereditary pyropoikilocytosis by the eosin-5-maleimide (EMA)-binding test is attributable to a marked reduction in EMA-reactive transmembrane proteins. International Journal of Laboratory Hematology. 33(2). 205–211. 22 indexed citations
7.
Bolton‐Maggs, Paula, et al.. (2004). Guidelines for the diagnosis and management of hereditary spherocytosis. British Journal of Haematology. 126(4). 455–474. 175 indexed citations
8.
King, M.‐J., Marion E. Reid, Joyce Poole, et al.. (1997). Co‐presence of a point mutation and a deletion of exon 3 in the glycophorin C gene and concomitant production of a Gerbich‐related antibody. Transfusion. 37(10). 1027–1034. 3 indexed citations
9.
10.
Reid, Marion E., William J. Mawby, M.‐J. King, & P. Sistonen. (1994). Duplication of exon 3 in the glycophorin C gene gives rise to the Lsa blood group antigen. Transfusion. 34(11). 966–969. 6 indexed citations
11.
King, M.‐J., et al.. (1992). Point Mutation in the Glycophorin C Gene Results in the Expression of the Blood Group Antigen Dha. Vox Sanguinis. 63(1). 56–58. 9 indexed citations
12.
King, M.‐J., Stephen F. Parsons, Albert M. Wu, & Nicola Jones. (1991). Immunochemical studies on the differential binding properties of two monoclonal antibodies reacting with Tn red cells. Transfusion. 31(2). 142–149. 20 indexed citations
13.
Poole, Joyce, et al.. (1991). The MiIII phenotype among Chinese donors in Hong Kong: immunochemical and serological studies. Transfusion Medicine. 1(3). 169–175. 40 indexed citations
14.
Sullivan, Susan, M.‐J. King, F. Cockburn, et al.. (1989). Haplotype distribution of the human phenylalanine hydroxylase locus in Scotland and Switzerland.. PubMed. 44(5). 652–9. 32 indexed citations
15.
16.
King, M.‐J. & A. M. Holburn. (1979). Radioassays of blood group M, N and T (Thomsen-Friedenreich) antigens.. PubMed. 38(1). 129–36. 5 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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