List of works - Nicoletta Coccaro

5'RUNX1-3'USP42 chimeric gene in acute myeloid leukemia can occur through an insertion mechanism rather than translocation and may be mediated by genomic segmental duplications

scientific article published on October 2014

A new recurrent chromosomal translocation t(3;11)(q13;q14) in myelodysplastic syndromes associated with overexpression of the ILDR1 gene

article

A novel t(3;9)(q21.2; p24.3) associated with SMARCA2 and ZNF148 genes rearrangement in myelodysplastic syndrome.

scientific article

A novel t(4;16)(q25;q23.1) associated with EGF and ELOVL6 deregulation in acute myeloid leukemia

scientific article published on 9 August 2013

ADAMTS2 gene dysregulation in T/myeloid mixed phenotype acute leukemia

scientific article published on 16 December 2014

Absolute quantification of the pretreatment PML-RARA transcript defines the relapse risk in acute promyelocytic leukemia

scientific article

Acute myeloid leukemia with t(16;16) (p13;q22) showing a new CBFB-MYH11 fusion transcript associated with an atypical leukemic blasts morphology

scientific article published on 3 October 2013

BCL6 corepressor gene dysregulation due to chromosomal translocation in acute myeloid leukemia: a new mechanism based on long non-coding RNA dislocation?

article

BCR-ABL1 e6a2 transcript in chronic myeloid leukemia: biological features and molecular monitoring by droplet digital PCR.

scientific article published on 7 July 2015

Centromeric fragment of chromosome 7 in atypical chronic myeloid leukemia with the SET binding protein 1 gene mutation

article

Cytogenetic and Array-CGH Characterization of a Simple Case of Reciprocal t(3;10) Translocation Reveals a Hidden Deletion at 5q12

scientific article published on 07 June 2021

Decreased TET2 gene expression during chronic myeloid leukemia progression.

scientific article

Droplet Digital PCR Is a Reliable Tool for Monitoring Minimal Residual Disease in Acute Promyelocytic Leukemia.

scientific article published on 4 March 2017

Droplet digital PCR analysis of NOTCH1 gene mutations in chronic lymphocytic leukemia

scientific article

Droplet digital PCR assay for quantifying of CALR mutant allelic burden in myeloproliferative neoplasms

scientific article published in July 2016

Gene expression profiling of chronic myeloid leukemia with variant t(9;22) reveals a different signature from cases with classic translocation

scientific article published on 4 May 2013

Genomic BCR-ABL1 breakpoint characterization by a multi-strategy approach for "personalized monitoring" of residual disease in chronic myeloid leukemia patients

scientific article published on 5 January 2018

Genomic segmental duplications on the basis of the t(9;22) rearrangement in chronic myeloid leukemia

IgG-lymphoplasmacytic lymphoma following polycythemia vera: JAK2 V617F and MYD88 L265P mutations separated in the same house.

scientific article

Lymphoid enhancer binding factor-1 (LEF1) expression as a prognostic factor in adult acute promyelocytic leukemia

scientific article published on February 2014

MYEOV gene overexpression in primary plasma cell leukemia with t(11;14)(q13;q32).

scientific article

Mutational analysis in BCR-ABL1 positive leukemia by deep sequencing based on nanopore MinION technology.

scientific article

Myelodysplastic syndrome with 5q deletion following IgM monoclonal gammopathy, showing gene mutation MYD88 L265P

article

Non random distribution of genomic features in breakpoint regions involved in chronic myeloid leukemia cases with variant t(9;22) or additional chromosomal rearrangements

scientific article

Overexpression of the LSAMP and TUSC7 genes in acute myeloid leukemia following microdeletion/duplication of chromosome 3.

scientific article published on 4 August 2015

SETBP1 and miR_4319 dysregulation in primary myelofibrosis progression to acute myeloid leukemia

scientific article published on 8 August 2012

SETBP1 dysregulation in congenital disorders and myeloid neoplasms.

scientific article published on 19 April 2017

Stat3-positive tumor cells contribute to vessels neoformation in primary central nervous system lymphoma

scientific article

Systemic Mastocytosis with Associated Chronic Lymphocytic Leukemia: A Matter of Diseases or Prognostic Factors?

scientific article

TP53 gene mutation analysis in chronic lymphocytic leukemia by nanopore MinION sequencing

scientific article published on 10 October 2016

List of works by Nicoletta Coccaro

5'RUNX1-3'USP42 chimeric gene in acute myeloid leukemia can occur through an insertion mechanism rather than translocation and may be mediated by genomic segmental duplications

A new recurrent chromosomal translocation t(3;11)(q13;q14) in myelodysplastic syndromes associated with overexpression of the ILDR1 gene

A novel t(3;9)(q21.2; p24.3) associated with SMARCA2 and ZNF148 genes rearrangement in myelodysplastic syndrome.

A novel t(4;16)(q25;q23.1) associated with EGF and ELOVL6 deregulation in acute myeloid leukemia

ADAMTS2 gene dysregulation in T/myeloid mixed phenotype acute leukemia

Absolute quantification of the pretreatment PML-RARA transcript defines the relapse risk in acute promyelocytic leukemia

Acute myeloid leukemia with t(16;16) (p13;q22) showing a new CBFB-MYH11 fusion transcript associated with an atypical leukemic blasts morphology

BCL6 corepressor gene dysregulation due to chromosomal translocation in acute myeloid leukemia: a new mechanism based on long non-coding RNA dislocation?

BCR-ABL1 e6a2 transcript in chronic myeloid leukemia: biological features and molecular monitoring by droplet digital PCR.

Centromeric fragment of chromosome 7 in atypical chronic myeloid leukemia with the SET binding protein 1 gene mutation

Cytogenetic and Array-CGH Characterization of a Simple Case of Reciprocal t(3;10) Translocation Reveals a Hidden Deletion at 5q12

Decreased TET2 gene expression during chronic myeloid leukemia progression.

Droplet Digital PCR Is a Reliable Tool for Monitoring Minimal Residual Disease in Acute Promyelocytic Leukemia.

Droplet digital PCR analysis of NOTCH1 gene mutations in chronic lymphocytic leukemia

Droplet digital PCR assay for quantifying of CALR mutant allelic burden in myeloproliferative neoplasms

Gene expression profiling of chronic myeloid leukemia with variant t(9;22) reveals a different signature from cases with classic translocation

Genomic BCR-ABL1 breakpoint characterization by a multi-strategy approach for "personalized monitoring" of residual disease in chronic myeloid leukemia patients

Genomic segmental duplications on the basis of the t(9;22) rearrangement in chronic myeloid leukemia

IgG-lymphoplasmacytic lymphoma following polycythemia vera: JAK2 V617F and MYD88 L265P mutations separated in the same house.

Lymphoid enhancer binding factor-1 (LEF1) expression as a prognostic factor in adult acute promyelocytic leukemia

MYEOV gene overexpression in primary plasma cell leukemia with t(11;14)(q13;q32).

Mutational analysis in BCR-ABL1 positive leukemia by deep sequencing based on nanopore MinION technology.

Myelodysplastic syndrome with 5q deletion following IgM monoclonal gammopathy, showing gene mutation MYD88 L265P

Non random distribution of genomic features in breakpoint regions involved in chronic myeloid leukemia cases with variant t(9;22) or additional chromosomal rearrangements

Overexpression of the LSAMP and TUSC7 genes in acute myeloid leukemia following microdeletion/duplication of chromosome 3.

SETBP1 and miR_4319 dysregulation in primary myelofibrosis progression to acute myeloid leukemia

SETBP1 dysregulation in congenital disorders and myeloid neoplasms.

Stat3-positive tumor cells contribute to vessels neoformation in primary central nervous system lymphoma

Systemic Mastocytosis with Associated Chronic Lymphocytic Leukemia: A Matter of Diseases or Prognostic Factors?

TP53 gene mutation analysis in chronic lymphocytic leukemia by nanopore MinION sequencing

The double deceit generated by an insertion mechanism in chronic myeloid leukemia with t(9;9;22)