List of works - Jelena D. Milosevic Feenstra

8p11 myeloproliferative syndrome: diagnostic challenges and pitfalls

scientific article

Antioxidative enzymes in the response of buckwheat (Fagopyrum esculentum moench) to ultraviolet B radiation

scientific article published on 01 December 2006

CALR exon 9 mutations are somatically acquired events in familial cases of essential thrombocythemia or primary myelofibrosis

scientific article published on 19 February 2014

CDK6 coordinates JAK2 V617F mutant MPN via NF-κB and apoptotic networks

scientific article published on 11 January 2019

Clonal Hematopoiesis with Oncogenic Potential (CHOP): Separation from CHIP and Roads to AML

scientific article published on 12 February 2019

Complex patterns of chromosome 11 aberrations in myeloid malignancies target CBL, MLL, DDB1 and LMO2.

scientific article

Cooperation of germ line JAK2 mutations E846D and R1063H in hereditary erythrocytosis with megakaryocytic atypia

scientific article

Efficacy of ruxolitinib in myeloid neoplasms with PCM1-JAK2 fusion gene.

scientific article

Frequent deletions of JARID2 in leukemic transformation of chronic myeloid malignancies.

scientific article

Germline RBBP6 mutations in familial myeloproliferative neoplasms.

scientific article published on 16 November 2015

Inverted duplication with deletion: first interstitial case suggesting a novel undescribed mechanism of formation.

scientific article

JAK2 or CALR mutation status defines subtypes of essential thrombocythemia with substantially different clinical course and outcomes.

scientific article published on 23 December 2013

LNK mutations in familial myeloproliferative neoplasms.

scientific article published on 23 May 2016

Low rate of calreticulin mutations in refractory anaemia with ring sideroblasts and marked thrombocytosis

scientific article published on 30 January 2014

Mutational landscape of the transcriptome offers putative targets for immunotherapy of myeloproliferative neoplasms

scientific article published on 07 May 2019

Somatic mutations of calreticulin in myeloproliferative neoplasms

scientific article

Whole-exome sequencing identifies novel MPL and JAK2 mutations in triple-negative myeloproliferative neoplasms

scientific article published on 30 September 2015

β Thalassemia major due to acquired uniparental disomy in a previously healthy adolescent.

scientific article

List of works by Jelena D. Milosevic Feenstra

8p11 myeloproliferative syndrome: diagnostic challenges and pitfalls

Antioxidative enzymes in the response of buckwheat (Fagopyrum esculentum moench) to ultraviolet B radiation

CALR exon 9 mutations are somatically acquired events in familial cases of essential thrombocythemia or primary myelofibrosis

CDK6 coordinates JAK2 V617F mutant MPN via NF-κB and apoptotic networks

Clonal Hematopoiesis with Oncogenic Potential (CHOP): Separation from CHIP and Roads to AML

Complex patterns of chromosome 11 aberrations in myeloid malignancies target CBL, MLL, DDB1 and LMO2.

Cooperation of germ line JAK2 mutations E846D and R1063H in hereditary erythrocytosis with megakaryocytic atypia

Efficacy of ruxolitinib in myeloid neoplasms with PCM1-JAK2 fusion gene.

Frequent deletions of JARID2 in leukemic transformation of chronic myeloid malignancies.

Germline RBBP6 mutations in familial myeloproliferative neoplasms.

Inverted duplication with deletion: first interstitial case suggesting a novel undescribed mechanism of formation.

JAK2 or CALR mutation status defines subtypes of essential thrombocythemia with substantially different clinical course and outcomes.

LNK mutations in familial myeloproliferative neoplasms.

Low rate of calreticulin mutations in refractory anaemia with ring sideroblasts and marked thrombocytosis

Mutational landscape of the transcriptome offers putative targets for immunotherapy of myeloproliferative neoplasms

Somatic mutations of calreticulin in myeloproliferative neoplasms

Whole-exome sequencing identifies novel MPL and JAK2 mutations in triple-negative myeloproliferative neoplasms

β Thalassemia major due to acquired uniparental disomy in a previously healthy adolescent.