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List of works by Niroshan Nadarajah

AML with gain of chromosome 8 as the sole chromosomal abnormality (+8sole) is associated with a specific molecular mutation pattern including ASXL1 mutations in 46.8% of the patients.

scientific article published on 16 December 2014

Application of an NGS-based 28-gene panel in myeloproliferative neoplasms reveals distinct mutation patterns in essential thrombocythaemia, primary myelofibrosis and polycythaemia vera.

scientific article

BRCC3 mutations in myeloid neoplasms

scientific article published on 22 May 2015

Dark-matter matters: Discriminating subtle blood cancers using the darkest DNA

scientific article published on 30 August 2019

Detection of recurrent and of novel fusion transcripts in myeloid malignancies by targeted RNA sequencing

scientific article published on 26 February 2018

Karyotype evolution and acquisition of FLT3 or RAS pathway alterations drive progression of myelodysplastic syndrome to acute myeloid leukemia

scientific article published on 20 August 2015

Multilineage dysplasia does not influence prognosis in CEBPA-mutated AML, supporting the WHO proposal to classify these patients as a unique entity ⬇️

scientific article published on March 22, 2012

Refractory anemia with ring sideroblasts and marked thrombocytosis cases harbor mutations in SF3B1 or other spliceosome genes accompanied by JAK2V617F and ASXL1 mutations

scientific article published on 19 December 2014

Ultra-deep sequencing leads to earlier and more sensitive detection of the tyrosine kinase inhibitor resistance mutation T315I in chronic myeloid leukemia

scientific article published on 21 April 2016

mutated AML can relapse with wild-type : persistent clonal hematopoiesis can drive relapse

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