Azim M. Mohamedali

London, ENG, United Kingdom

Last Updated: 09/26/2026

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Found 19 publications

Uniparental disomy (UPD) of a novel bisphosphoglycerate mutase (BPGM) mutation leading to erythrocytosis.

Uniparental disomy (UPD) of a novel bisphosphoglycerate mutase (BPGM) mutation leading to erythrocytosis.

Journal: British journal of haematology
Published: November 20, 2020

Non-del(5q) myelodysplastic syndromes-associated loci detected by SNP-array genome-wide association meta-analysis.

Non-del(5q) myelodysplastic syndromes-associated loci detected by SNP-array genome-wide association meta-analysis.

Journal: Blood advances
Published: August 30, 2019

Clonal hematopoiesis in patients with multiple myeloma undergoing autologous stem cell transplantation.

Clonal hematopoiesis in patients with multiple myeloma undergoing autologous stem cell transplantation.

Journal: Leukemia
Published: January 29, 2018

Preclinical modeling of myelodysplastic syndromes.

Preclinical modeling of myelodysplastic syndromes.

Journal: Leukemia
Published: February 24, 2017

FLT3 and JAK2 Mutations in Acute Myeloid Leukemia Promote Interchromosomal Homologous Recombination and the Potential for Copy Neutral Loss of Heterozygosity.

FLT3 and JAK2 Mutations in Acute Myeloid Leukemia Promote Interchromosomal Homologous Recombination and the Potential for Copy Neutral Loss of Heterozygosity.

Journal: Cancer research
Published: June 23, 2016

CSNK1A1 mutations and isolated del(5q) abnormality in myelodysplastic syndrome: a retrospective mutational analysis.

CSNK1A1 mutations and isolated del(5q) abnormality in myelodysplastic syndrome: a retrospective mutational analysis.

Journal: The Lancet. Haematology
Published: January 13, 2015

High concordance of genomic and cytogenetic aberrations between peripheral blood and bone marrow in myelodysplastic syndrome (MDS).

High concordance of genomic and cytogenetic aberrations between peripheral blood and bone marrow in myelodysplastic syndrome (MDS).

Journal: Leukemia
Published: December 18, 2014

Somatic mutations identify a subgroup of aplastic anemia patients who progress to myelodysplastic syndrome.

Somatic mutations identify a subgroup of aplastic anemia patients who progress to myelodysplastic syndrome.

Journal: Blood
Published: August 21, 2014

Recent advances in understanding the molecular pathogenesis of myelodysplastic syndromes.

Recent advances in understanding the molecular pathogenesis of myelodysplastic syndromes.

Journal: British journal of haematology
Published: July 23, 2013

Utility of peripheral blood for cytogenetic and mutation analysis in myelodysplastic syndrome.

Utility of peripheral blood for cytogenetic and mutation analysis in myelodysplastic syndrome.

Journal: Blood
Published: June 14, 2013

Microsatellite instability induced mutations in DNA repair genes CtIP and MRE11 confer hypersensitivity to poly (ADP-ribose) polymerase inhibitors in myeloid malignancies.

Microsatellite instability induced mutations in DNA repair genes CtIP and MRE11 confer hypersensitivity to poly (ADP-ribose) polymerase inhibitors in myeloid malignancies.

Journal: Haematologica
Published: January 26, 2013

Spliceosome mutations exhibit specific associations with epigenetic modifiers and proto-oncogenes mutated in myelodysplastic syndrome.

Spliceosome mutations exhibit specific associations with epigenetic modifiers and proto-oncogenes mutated in myelodysplastic syndrome.

Journal: Haematologica
Published: January 10, 2013
Showing 1-12 of 19

Last Updated: 09/26/2026