May‐Jean King

Medicine · Health Sciences

11h-index1.0kcitations22works0.02yr avg
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Research Topics

Erythrocyte Function and Pathophysiology(18), Blood properties and coagulation(10), Blood groups and transfusion(7), Neonatal Health and Biochemistry(7), Hemoglobinopathies and Related Disorders(5)

Publications22 total

Hereditary spherocytosis
Paediatrics and Child Health·2019· 3 cited
Targeted next generation sequencing identifies a novel β‐spectrin gene mutation A2059P in two Omani children with hereditary pyropoikilocytosis
American Journal of Hematology·2017· 8 citedOpen Access
Hereditary spherocytosis
Paediatrics and Child Health·2015· 4 cited
Toward the harmonization of result presentation for the eosin-5′-maleimide binding test in the diagnosis of hereditary spherocytosis
Cytometry Part B Clinical Cytometry·2014· 32 cited
Towards the harmonization of result presentation for the eosin-5’- maleimide (EMA) binding test in the diagnosis of hereditary spherocytosis
Cytometry Part B Clinical Cytometry·2014· 9 cited
The diagnostic challenge of congenital dyserythropoietic anaemia: two cases of ‘CDA type II’
Journal of Clinical Pathology·2014· 5 cited
Hereditary red cell membrane disorders and laboratory diagnostic
2013· 1 cited
2.19 Laboratory diagnosis of hereditary spherocytosis
2012
Hemolytic Anemias Associated with Disorders of Erythrocyte Membrane and Cytoskeleton Proteins
2012· 4 cited
Guidelines for the diagnosis and management of hereditary spherocytosis – 2011 update
British Journal of Haematology·2011· 383 citedOpen Access
Phenotype and mRNA Expression of Syncytiotrophoblast Microparticles Isolated from Human Placenta
Annals of the New York Academy of Sciences·2008· 22 cited
Using the eosin‐5‐maleimide binding test in the differential diagnosis of hereditary spherocytosis and hereditary pyropoikilocytosis
Cytometry Part B Clinical Cytometry·2008· 73 citedOpen Access
Eosin‐5‐maleimide binding to band 3 and Rh‐related proteins forms the basis of a screening test for hereditary spherocytosis
British Journal of Haematology·2003· 107 cited
Rapid flow cytometric test for the diagnosis of membrane cytoskeleton‐associated haemolytic anaemia
British Journal of Haematology·2000· 186 citedOpen Access
Rapid flow cytometric test for the diagnosis of membrane cytoskeleton-associated haemolytic anaemia
British Journal of Haematology·2000· 61 cited
STRUCTURE, POLYMORPHISMS AND BIOLOGICAL ROLE OF GLYCOPHORINS A, B, C AND D
PUBLISHED BY IMPERIAL COLLEGE PRESS AND DISTRIBUTED BY WORLD SCIENTIFIC PUBLISHING CO. eBooks·2000· 2 cited
Human Blood Cells
PUBLISHED BY IMPERIAL COLLEGE PRESS AND DISTRIBUTED BY WORLD SCIENTIFIC PUBLISHING CO. eBooks·2000· 5 cited
Coinheritance of α- and β-Spectrin Gene Mutations in a Case of Hereditary Elliptocytosis
Blood·1998· 13 cited
Two different glycosyltransferase defects that result in GalNAcα-O-peptide (Tn) expression
Glycobiology·1994· 31 cited
Blood group antigens on human erythrocytes-distribution, structure and possible functions
Biochimica et Biophysica Acta (BBA) - Reviews on Biomembranes·1994· 41 cited
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Frequent Co-authors

David Greenwood(4), D Dhermy(3), Achille Iolascon(2), Judith Behrens(2), Chris Rogers(2), Clare Flynn(2), Keith Chambers(2), Linda Hunt(2), H. Heimpel(2), Nigel Noel(2), Alastair Whiteway(2), Sara Trompeter(2), Paula Bolton‐Maggs(1), Jacob C. Langer(1), Paul Tittensor(1), Jonathan S. Smythe(1), Rosey Mushens(1), Paul Telfer(1), Heather MacKinnon(1), Lisa Langabeer(1)