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Barnaby Clark

University of Cambridge
King's College London

32

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343

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A Sri Lankan girl with a new genetic variant in the PKLR gene causing pyruvate kinase deficiency: a case report.

2021 Journal of Medical Case Reports
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TLR9 expression in Chronic Lymphocytic Leukemia identifies a pro-migratory subpopulation and novel therapeutic target.

2021 Blood
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Improving the laboratory diagnosis of pyruvate kinase deficiency.

2021 British Journal of Haematology
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A method for non-invasive prenatal diagnosis of monogenic autosomal recessive disorders.

2019 Blood
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Novel ADA 2 mutation presenting with neutropenia, lymphopenia and bone marrow failure in patients with deficiency in adenosine deaminase 2 ( DADA 2)

2019 British Journal of Haematology
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Pyridoxine-sensitive X-linked ‘sideroblastic’ anaemia in the absence of ring sideroblasts – molecular diagnosis

2018 British Journal of Haematology
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Congenital sideroblastic anemia in a female: MORPHOLOGY UPDATE

2018 American Journal of Hematology
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Sideroblastic anemia with myopathy secondary to novel, pathogenic missense variants in the YARS2 gene

2018 Haematologica
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A Plea for the Newborn Diagnosis of Hb S-Hereditary Persistence of Fetal Hemoglobin

2017 Hemoglobin
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Haemoglobin Variant Screening in Jamaica: Meeting Student's Request

2016 British Journal of Haematology
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