Alison May

2.0k citations

51 papers · 1.2k · h-index 19

Impact in

Hematology top 2%
- Iron Metabolism and Disorders
Genetics top 2%
- Hemoglobinopathies and Related Disorders

Papers in

Molecular Biology 24
- Porphyrin Metabolism and Disorders 21
Rheumatology 17
- Folate and B Vitamins Research 17

Co-authors: David F. Bishop (8 shared papers)Edward J. Fitzsimons (7 shared papers)Mark Worwood (5 shared papers)Mario Cazzola (5 shared papers)Philip D. Cotter (4 shared papers)Vinod Devalia (1 shared paper)James Dooley (1 shared paper)Ayesha Al‐Sabah (3 shared papers)
Journals: Blood (11 papers)British Journal of Haematology (9 papers)Journal of Medical Genetics (2 papers)BioMetals (1 paper)European Journal Of Haematology (1 paper)
Partner nations: United Kingdom United States Italy

In The Last Decade

Alison May

48 papers receiving 1.2k citations

Peers

Countries citing papers authored by Alison May

Since Specialization

Citations

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

Fields of papers citing papers by Alison May

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 25 scholars most cited alongside Alison May, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Alison May Line = papers co-authored together Alison May links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

Showing the 20 most-cited of 51 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	Autosomal dominant reticuloendothelial iron overload associated with a 3–base pair deletion in the ferroportin 1 gene(SLC11A3) Blood ·Vinod Devalia, Kymberley Carter, Ann P. Walker, Stephen J. Perkins, Mark Worwood, Alison May, James Dooley	2002	150
2	A novel syndrome of congenital sideroblastic anemia, B-cell immunodeficiency, periodic fevers, and developmental delay (SIFD) Blood ·Daniel H. Wiseman, Alison May, Stephen Jolles, Philip Connor, Colin Powell, Matthew M. Heeney, Patricia J. Giardina, Robert J. Klaassen, Pranesh Chakraborty, Michael T. Geraghty, Nathalie Major-Cook, Caroline Kannengiesser, Isabelle Thuret, Alexis A. Thompson, Lino Marques, Stephen Hughes, Denise Bonney, Sylvia S. Bottomley, Mark D. Fleming, Robert Wynn	2013	81
3	EMQN Best Practice Guidelines for molecular and haematology methods for carrier identification and prenatal diagnosis of the haemoglobinopathies European Journal of Human Genetics ·(unknown), Joanne Traeger‐Synodinos, Cornelis L. Harteveld, John Old, Mary Petrou, Renzo Galanello, Piero C. Giordano, Michael Angastioniotis, Barbara De la Salle, Shirley Henderson, Alison May	2014	81
4	Late-onset X-linked sideroblastic anemia. Missense mutations in the erythroid delta-aminolevulinate synthase (ALAS2) gene in two pyridoxine-responsive patients initially diagnosed with acquired refractory anemia and ringed sideroblasts. Journal of Clinical Investigation ·Philip D. Cotter, Alison May, Edward J. Fitzsimons, T.E. Houston, Barrie Woodcock, Ayesha Al‐Sabah, Leonie C.H. Wong, David F. Bishop	1995	75
5	Familial-skewed X-chromosome inactivation as a predisposing factor for late-onset X-linked sideroblastic anemia in carrier females Blood ·Mario Cazzola, Alison May, Gaetano Bergamaschi, Paola Cerani, Vittorio Rosti, David F. Bishop	2000	73
6	Four New Mutations in the Erythroid-Specific 5-Aminolevulinate Synthase (ALAS2) Gene Causing X-Linked Sideroblastic Anemia: Increased Pyridoxine Responsiveness After Removal of Iron Overload by Phlebotomy and Coinheritance of Hereditary Hemochromatosis Blood ·Philip D. Cotter, Alison May, Liping Li, Ayesha Al‐Sabah, Edward J. Fitzsimons, Mario Cazzola, David F. Bishop	1999	69
7	Hereditary haemochromatosis: only 1% of adult HFE C282Y homozygotes in South Wales have a clinical diagnosis of iron overload Human Genetics ·Anne McCune, Layla N. Al-Jader, Alison May, Sara Hayes, H Jackson, Mark Worwood	2002	64
8	X‐linked cerebellar ataxia and sideroblastic anaemia associated with a missense mutation in the ABC7 gene predicting V411L British Journal of Haematology ·Andrew Maguire, K D Hellier, Simon Hammans, Alison May	2001	59
9	The molecular biology and pyridoxine responsiveness of X-linked sideroblastic anaemia. PubMed ·Alison May, David F. Bishop	1998	58
10	The Routledge Handbook of Forensic Linguistics Portuguese National Funding Agency for Science, Research and Technology (RCAAP Project by FCT) ·Malcolm Coulthard, Alison May, Rui Sousa‐Silva	2020	50
11	Incidence of haemoglobinopathies in various populations — The impact of immigration Clinical Biochemistry ·Shirley Henderson, Adele Timbs, Janice McCarthy, Alice E. Gallienne, Margaretha Van Mourik, Gillian S. Masters, Alison May, Mohamed S.M. Khalil, Anna Schuh, John Old	2009	49
12	A promoter mutation in the erythroid-specific 5-aminolevulinate synthase (ALAS2) gene causes X-linked sideroblastic anemia Blood ·Soumeya Bekri, Alison May, Philip D. Cotter, Ala Al-Sabah, Xiaojun Guo, Gillian S. Masters, David F. Bishop	2003	41
13	Missense SLC25A38 variations play an important role in autosomal recessive inherited sideroblastic anemia Haematologica ·Caroline Kannengiesser, Mayka Sánchez, Marion Sweeney, Gilles Hetet, Briedgeen Kerr, Erica L. Moran, J. L. Fuster Soler, Karim Maloum, Thomas Matthes, Caroline Oudot, Anne‐Sophie Lascaux, Corinne Pondarré, (unknown), Sudharma Vidyatilake, C. Beaumont, Bernard Grandchamp, Alison May	2011	39
14	A recurring mutation in the respiratory complex 1 protein NDUFB11 is responsible for a novel form of X-linked sideroblastic anemia Blood ·Daniel A. Lichtenstein, Andrew Crispin, Anoop K. Sendamarai, Dean R. Campagna, Klaus Schmitz‐Abe, Cristovão M. Sousa, Martin D. Kafina, Paul J. Schmidt, Charlotte M. Niemeyer, John B. Porter, Alison May, Mrinal M. Patnaik, Matthew M. Heeney, Alec C. Kimmelman, Sylvia S. Bottomley, Barry H. Paw, Kyriacos Markianos, Mark D. Fleming	2016	29
15	6 Sideroblastic anaemia Baillière s Clinical Haematology ·Alison May, Edward J. Fitzsimons	1994	29
16	Enrichment of erythroblasts from human bone marrow using complement‐mediated lysis: measurement of ferritin British Journal of Haematology ·Faieza M. K. Ali, Alison May, Brian M. Jones, (unknown)	1983	25
17	Erythroblast iron metabolism in sideroblastic marrows British Journal of Haematology ·Alison May, Philippe de Souza, Katie R. Barnes, S.A. Kaaba, Alice K. Jacobs	1982	21
18	Uptake and intracellular distribution of iron from transferrin and chelators in erythroid cells BioMetals ·George J. Kontoghiorghes, Alison May	1990	21
19	The molecular basis of the sideroblastic anemias Current Opinion in Hematology ·Edward J. Fitzsimons, Alison May	1996	19
20	Absent phenotypic expression of X-linked sideroblastic anemia in one of 2 brothers with a novel ALAS2 mutation Blood ·Mario Cazzola, Alison May, Gaetano Bergamaschi, Paola Cerani, S. Ferrillo, David F. Bishop	2002	18

About Alison May

Alison May is a scholar working on Molecular Biology, Rheumatology, Hematology, Pediatrics, Perinatology and Child Health and Genetics, having authored 51 papers that have together received 1.2k indexed citations. Recurring topics across this work include Porphyrin Metabolism and Disorders (21 papers), Folate and B Vitamins Research (17 papers), Hemoglobinopathies and Related Disorders (13 papers), Neonatal Health and Biochemistry (12 papers), Iron Metabolism and Disorders (9 papers), Metabolism and Genetic Disorders (4 papers), Trace Elements in Health (4 papers) and Erythrocyte Function and Pathophysiology (4 papers). The work is most often cited by research in Hematology (529 citations), Genetics (456 citations), Rheumatology (289 citations), Nutrition and Dietetics (210 citations) and Clinical Biochemistry (84 citations). Alison May has collaborated with scholars based in United Kingdom, United States and Italy. Frequent co-authors include David F. Bishop, Edward J. Fitzsimons, Mark Worwood, Mario Cazzola, Philip D. Cotter, Vinod Devalia, James Dooley, Ayesha Al‐Sabah, Stephen J. Perkins and Ann P. Walker. Their work appears in journals such as Blood, British Journal of Haematology, Journal of Medical Genetics, BioMetals and European Journal Of Haematology.

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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