Author

Alison M. May

Observed names: A May, A. MAY, A. May, ALISON MAY, Alison May

Observed institutions: University of Leeds, University of Pavia, University Hospital of Wales, Western Infirmary, The Royal Free Hospital, Princess of Wales Hospital, University Hospital Llandough, Policlinico San Matteo Fondazione, Institute of Predictive and Personalized Medicine of Cancer, University College London, Cardiff University, University of Wales, Icahn School of Medicine at Mount Sinai

OpenAlex ID: A5014377696

Mutations in TRNT1 cause congenital sideroblastic anemia with immunodeficiency, fevers, and developmental delay (SIFD)

2014 · Pranesh K. Chakraborty, Klaus Schmitz-Abe, et al. · Blood · 190

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Autosomal dominant reticuloendothelial iron overload associated with a 3–base pair deletion in the ferroportin 1 gene(SLC11A3)

2002 · Vinod Devalia, Kymberley Carter, et al. · Blood · 189

A novel syndrome of congenital sideroblastic anemia, B-cell immunodeficiency, periodic fevers, and developmental delay (SIFD)

2013 · Daniel H. Wiseman, Alison May, et al. · Blood · 124

EMQN Best Practice Guidelines for molecular and haematology methods for carrier identification and prenatal diagnosis of the haemoglobinopathies

2014 · on behalf of contributors to the EMQN haemoglobinopathies best practice meeting, Joanne Traeger-Synodinos, et al. · European Journal of Human Genetics · 122

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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.

1995 · P D Cotter, A May, et al. · Journal of Clinical Investigation · 102

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Familial-skewed X-chromosome inactivation as a predisposing factor for late-onset X-linked sideroblastic anemia in carrier females

2000 · Mario Cazzola, Alison May, et al. · Blood · 95

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

1999 · Philip D. Cotter, Alison May, et al. · Blood · 90

The molecular biology and pyridoxine responsiveness of X-linked sideroblastic anaemia.

1998 · A May, D F Bishop · PubMed · 84

Hereditary haemochromatosis: only 1% of adult HFE C282Y homozygotes in South Wales have a clinical diagnosis of iron overload

2002 · Anne McCune, Layla Al-Jader, et al. · Human Genetics · 76

Congenital sideroblastic anemia due to mutations in the mitochondrial HSP70 homologue HSPA9

2015 · Klaus Schmitz-Abe, Szymon J. Ciesielski, et al. · Blood · 75

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X‐linked cerebellar ataxia and sideroblastic anaemia associated with a missense mutation in the ABC7 gene predicting V411L

2001 · Andrew Maguire, Kate Hellier, et al. · British Journal of Haematology · 73

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Missense SLC25A38 variations play an important role in autosomal recessive inherited sideroblastic anemia

2011 · C. Kannengiesser, M. Sanchez, et al. · Haematologica · 60

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Incidence of haemoglobinopathies in various populations — The impact of immigration

2009 · Shirley Henderson, Adele Timbs, et al. · Clinical Biochemistry · 59

X‐linked sideroblastic anemia due to ALAS2 intron 1 enhancer element GATA‐binding site mutations

2013 · Dean R. Campagna, Charlotte I. de Bie, et al. · American Journal of Hematology · 51

A promoter mutation in the erythroid-specific 5-aminolevulinate synthase (ALAS2) gene causes X-linked sideroblastic anemia

2003 · Soumeya Bekri, Alison May, et al. · Blood · 49

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A recurring mutation in the respiratory complex 1 protein NDUFB11 is responsible for a novel form of X-linked sideroblastic anemia

2016 · Daniel A. Lichtenstein, Andrew W. Crispin, et al. · Blood · 39

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Iron Deficiency Anaemia and Iron Overload

2017 · Mark Worwood, Alison M. May, et al. · Elsevier eBooks · 38

Enrichment of erythroblasts from human bone marrow using complement‐mediated lysis: measurement of ferritin

1983 · Faieza M. K. Ali, Alison May, et al. · British Journal of Haematology · 31

6 Sideroblastic anaemia

1994 · Alison May, Edward Fitzsimons · Baillière s Clinical Haematology · 29

Absent phenotypic expression of X-linked sideroblastic anemia in one of 2 brothers with a novel ALAS2 mutation

2002 · Mario Cazzola, Alison May, et al. · Blood · 28

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Erythroblast iron metabolism in sideroblastic marrows

1982 · A. May, P. de Souza, et al. · British Journal of Haematology · 28

The molecular basis of the sideroblastic anemias

1996 · Edward J. Fitzsimons, Alison May · Current Opinion in Hematology · 26

Uptake and intracellular distribution of iron from transferrin and chelators in erythroid cells

1990 · George J. Kontoghiorghes, Alison May · BioMetals · 26

Erratum: EMQN Best Practice Guidelines for molecular and haematology methods for carrier identification and prenatal diagnosis of the haemoglobinopathies

2015 · on behalf of contributors to the EMQN haemoglobinopathies best practice meeting, Joanne Traeger-Synodinos, et al. · European Journal of Human Genetics · 20

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Iron deficiency anaemia and iron overload

2012 · Mark Worwood, Alison May · Elsevier eBooks · 20

Works count: 53

Citation count: 1,902

H-index: 23

I10-index: 34