Mark Worwood - Concepedia

Author

Mark Worwood

University of Wales

Also Known As

M E Pembrey, M WORWOOD, M Worwood, M. WORWOOD, M. Worwood, MARK WORWOOD, Mark W. Worwood, Mark Worwood, Worwood, Mark

231

Publications

9.3K

Citations

H-Index

144

Concepts

All Affiliations

University of Wales Welsh Government Cardiff University University Hospital of Wales

About

Mark Worwood is an author at University of Wales specializing in medicine, hematology, and pathology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	37	77	5.2K
2	Health Sciences	18	20	1.9K
3	Public Health	8	8	490
4	Natural Sciences	5	5	531
5	Engineering	3	3	182

Mark Worwood

108

Publications

6.9K

Citations

H-Index

Page 1

	Year	Citations
Serum ferritin concentration and iron stores in normal subjects G.O Walters, Frederick W. Miller, Mark Worwood Journal of Clinical Pathology Iron DeficiencyNutritionNutrient BioavailabilityStorage IronPhysiology	1973	620
Ferritin in the Serum of Normal Subjects and Patients with Iron Deficiency and Iron Overload Alice K. Jacobs, Frederick W. Miller, Mark Worwood, BMJ AnemiaNutrient BioavailabilityStorage IronIron MetabolismChronic Kidney Disease	1972	513
Increased frequency of the haemochromatosis Cys282Tyr mutation in sporadic porphyria cutanea tarda Andrew G. Roberts, Sharon D. Whatley, Rhian Morgan, The Lancet BiologyNatural SciencesGeneticsMolecular GeneticsMicrobiology	1997	321
<i>HFE</i> mutations, iron deficiency and overload in 10 500 blood donors H Jackson, Kymberley Carter, C. Darke, British Journal of Haematology	2001	223
FMS mutations in myelodysplastic, leukemic, and normal subjects. S. Ridge, Mark Worwood, David Oscier, Proceedings of the National Academy of Sciences GeneticsImmunologyPathologyTumor BiologyClinical Genetics	1990	222
A simple genetic test identifies 90% of UK patients with haemochromatosis Robson Kjh., Mark Worwood, JD Shearman, UCL Discovery (University College London) Genetic TestingGeneticsGenetic EpidemiologyPathologyUnited Kingdom	1997	201
Autosomal dominant reticuloendothelial iron overload associated with a 3–base pair deletion in the ferroportin 1 gene(SLC11A3) Vinod Devalia, Kymberley Carter, Ann P. Walker, Blood	2002	189
The origin and spread of the HFE-C282Y haemochromatosis mutation S Distante, Kathryn Robson, James Graham‐Campbell, Human Genetics Hfe-c282y Haemochromatosis MutationGeneticsHematologyHeme HomeostasisMolecular Diagnostics	2004	161
Ferritinaemia in Leukaemia and Hodgkin's Disease Patricia A. Jones, Frederick W. Miller, Mark Worwood, British Journal of Cancer Malignant Blood DisorderHematologyHistopathologyImmunologyPathology	1973	144
Ferritin in Human Tissues and Serum Mark Worwood Clinics in Haematology FibrosisBioanalysisHematologyPathologyHeme Signaling	1982	143

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