Lista de obras -

ALK germline mutations in patients with neuroblastoma: a rare and weakly penetrant syndrome

artículo científico publicado en 2011

Accumulation of Segmental Alterations Determines Progression in Neuroblastoma

artículo científico publicado en 2010

Accurate outcome prediction in neuroblastoma across independent data sets using a multigene signature

artículo científico publicado en 2010

Activated Alk triggers prolonged neurogenesis and Ret upregulation providing a therapeutic target in ALK-mutated neuroblastoma

artículo científico publicado en 2014

Breakpoint features of genomic rearrangements in neuroblastoma with unbalanced translocations and chromothripsis

artículo científico publicado en 2013

Characterization of amplicons in neuroblastoma: High-resolution mapping using DNA microarrays, relationship with outcome, and identification of overexpressed genes

article

Characterization of rearrangements involving the ALK gene reveals a novel truncated form associated with tumor aggressiveness in neuroblastoma

artículo científico publicado en 2012

Circulating tumor DNA analysis enables molecular characterization of pediatric renal tumors at diagnosis

artículo científico publicado en 2018

Clinical characteristics and outcome of patients with neuroblastoma presenting genomic amplification of loci other than MYCN.

artículo científico publicado en 2014

Combined 24-color karyotyping and comparative genomic hybridization analysis indicates predominant rearrangements of early replicating chromosome regions in neuroblastoma

artículo científico publicado en 2003

Control-FREEC: a tool for assessing copy number and allelic content using next-generation sequencing data

artículo científico publicado en 2011

Deep Sequencing Reveals Occurrence of Subclonal ALK Mutations in Neuroblastoma at Diagnosis.

artículo científico publicado en 2015

Emergence of new ALK mutations at relapse of neuroblastoma

artículo científico publicado en 2014

Feasibility and clinical integration of molecular profiling for target identification in pediatric solid tumors

artículo científico publicado en 2016

From class waivers to precision medicine in paediatric oncology.

artículo científico publicado en 2017

Gene expression profiling of 1p35-36 genes in neuroblastoma

artículo científico publicado en 2004

Genomic Copy Number Profiling Using Circulating Free Tumor DNA Highlights Heterogeneity in Neuroblastoma.

artículo científico publicado en 2016

Germline mutations of the paired-like homeobox 2B (PHOX2B) gene in neuroblastoma

artículo científico publicado en 2004

Heterogeneity of neuroblastoma cell identity defined by transcriptional circuitries.

artículo científico publicado en 2017

Learning smoothing models of copy number profiles using breakpoint annotations

artículo científico publicado en 2013

Meta-mining of copy number profiles of high-risk neuroblastoma tumors

scientific article published on 30 October 2018

Minimally invasive surgery of neuroblastic tumors in children: Indications depend on anatomical location and image-defined risk factors

artículo científico publicado en 2014

Mosaicism for oncogenic G12D KRAS mutation associated with epidermal nevus, polycystic kidneys and rhabdomyosarcoma

artículo científico publicado en 2010

Oncologic Phenotype of Peripheral Neuroblastic Tumors Associated With PHOX2B Non-Polyalanine Repeat Expansion Mutations

artículo científico publicado en 2015

Opsoclonus-myoclonus in children associated or not with neuroblastoma.

artículo científico publicado en 2010

Overall genomic pattern is a predictor of outcome in neuroblastoma

artículo científico publicado en 2009

Parental smoking, maternal alcohol consumption during pregnancy and the risk of neuroblastoma in children. A pooled analysis of the ESCALE and ESTELLE French studies

artículo científico publicado en 2019

Pediatric Patient With Renal Cell Carcinoma Treated by Successive Antiangiogenics Drugs: A Case Report and Review of the Literature

artículo científico publicado en 2017

Predicting outcomes for children with neuroblastoma using a multigene-expression signature: a retrospective SIOPEN/COG/GPOH study

artículo científico publicado en 2009

Preferential occurrence of chromosome breakpoints within early replicating regions in neuroblastoma

artículo científico publicado en 2005

Prognostic impact of gene expression-based classification for neuroblastoma.

artículo científico publicado en 2010

QuantumClone: Clonal assessment of functional mutations in cancer based on a genotype-aware method for clonal reconstruction

artículo científico publicado en 2018

Radiogenomics of neuroblastomas: Relationships between imaging phenotypes, tumor genomic profile and survival.

artículo científico publicado en 2017

Recent insights into the biology of neuroblastoma

artículo científico publicado en 2014

Relapsed neuroblastomas show frequent RAS-MAPK pathway mutations

artículo científico publicado en 2015

Revised risk estimation and treatment stratification of low- and intermediate-risk neuroblastoma patients by integrating clinical and molecular prognostic markers

artículo científico publicado en 2014

SegAnnDB: interactive Web-based genomic segmentation

artículo científico publicado en 2014

Segmental Chromosomal Aberrations in Localized Neuroblastoma Can be Detected in Formalin-Fixed Paraffin-Embedded Tissue Samples and Are Associated With Recurrence

artículo científico publicado en 2016

Somatic and germline activating mutations of the ALK kinase receptor in neuroblastoma

artículo científico publicado en 2008

Stepwise occurrence of a complex unbalanced translocation in neuroblastoma leading to insertion of a telomere sequence and late chromosome 17q gain.

artículo científico publicado en 2005

Study of chromatin remodeling genes implicates SMARCA4 as a putative player in oncogenesis in neuroblastoma

scientific article published on 31 May 2019

TBX2 is a neuroblastoma core regulatory circuitry component enhancing MYCN/FOXM1 reactivation of DREAM targets

artículo científico publicado en 2018

Variety and complexity of chromosome 17 translocations in neuroblastoma

artículo científico

Whole exome sequencing of cell-free DNA reveals temporo-spatial heterogeneity and identifies treatment-resistant clones in neuroblastoma

artículo científico publicado en 2017

[Genetic alterations in neuroblastoma and their usefulness for clinical management]

artículo científico publicado en 2011

Lista de obras de

ALK germline mutations in patients with neuroblastoma: a rare and weakly penetrant syndrome

Accumulation of Segmental Alterations Determines Progression in Neuroblastoma

Accurate outcome prediction in neuroblastoma across independent data sets using a multigene signature

Activated Alk triggers prolonged neurogenesis and Ret upregulation providing a therapeutic target in ALK-mutated neuroblastoma

Breakpoint features of genomic rearrangements in neuroblastoma with unbalanced translocations and chromothripsis

Characterization of amplicons in neuroblastoma: High-resolution mapping using DNA microarrays, relationship with outcome, and identification of overexpressed genes

Characterization of rearrangements involving the ALK gene reveals a novel truncated form associated with tumor aggressiveness in neuroblastoma

Circulating tumor DNA analysis enables molecular characterization of pediatric renal tumors at diagnosis

Clinical characteristics and outcome of patients with neuroblastoma presenting genomic amplification of loci other than MYCN.

Combined 24-color karyotyping and comparative genomic hybridization analysis indicates predominant rearrangements of early replicating chromosome regions in neuroblastoma

Control-FREEC: a tool for assessing copy number and allelic content using next-generation sequencing data

Deep Sequencing Reveals Occurrence of Subclonal ALK Mutations in Neuroblastoma at Diagnosis.

Emergence of new ALK mutations at relapse of neuroblastoma

Feasibility and clinical integration of molecular profiling for target identification in pediatric solid tumors

From class waivers to precision medicine in paediatric oncology.

Gene expression profiling of 1p35-36 genes in neuroblastoma

Genomic Copy Number Profiling Using Circulating Free Tumor DNA Highlights Heterogeneity in Neuroblastoma.

Germline mutations of the paired-like homeobox 2B (PHOX2B) gene in neuroblastoma

Heterogeneity of neuroblastoma cell identity defined by transcriptional circuitries.

Learning smoothing models of copy number profiles using breakpoint annotations

Meta-mining of copy number profiles of high-risk neuroblastoma tumors

Minimally invasive surgery of neuroblastic tumors in children: Indications depend on anatomical location and image-defined risk factors

Mosaicism for oncogenic G12D KRAS mutation associated with epidermal nevus, polycystic kidneys and rhabdomyosarcoma

Oncologic Phenotype of Peripheral Neuroblastic Tumors Associated With PHOX2B Non-Polyalanine Repeat Expansion Mutations

Opsoclonus-myoclonus in children associated or not with neuroblastoma.

Overall genomic pattern is a predictor of outcome in neuroblastoma

Parental smoking, maternal alcohol consumption during pregnancy and the risk of neuroblastoma in children. A pooled analysis of the ESCALE and ESTELLE French studies

Pediatric Patient With Renal Cell Carcinoma Treated by Successive Antiangiogenics Drugs: A Case Report and Review of the Literature

Predicting outcomes for children with neuroblastoma using a multigene-expression signature: a retrospective SIOPEN/COG/GPOH study

Preferential occurrence of chromosome breakpoints within early replicating regions in neuroblastoma

Prognostic impact of gene expression-based classification for neuroblastoma.

QuantumClone: Clonal assessment of functional mutations in cancer based on a genotype-aware method for clonal reconstruction

Radiogenomics of neuroblastomas: Relationships between imaging phenotypes, tumor genomic profile and survival.

Recent insights into the biology of neuroblastoma

Relapsed neuroblastomas show frequent RAS-MAPK pathway mutations

Revised risk estimation and treatment stratification of low- and intermediate-risk neuroblastoma patients by integrating clinical and molecular prognostic markers

SegAnnDB: interactive Web-based genomic segmentation

Segmental Chromosomal Aberrations in Localized Neuroblastoma Can be Detected in Formalin-Fixed Paraffin-Embedded Tissue Samples and Are Associated With Recurrence

Somatic and germline activating mutations of the ALK kinase receptor in neuroblastoma

Stepwise occurrence of a complex unbalanced translocation in neuroblastoma leading to insertion of a telomere sequence and late chromosome 17q gain.

Study of chromatin remodeling genes implicates SMARCA4 as a putative player in oncogenesis in neuroblastoma

TBX2 is a neuroblastoma core regulatory circuitry component enhancing MYCN/FOXM1 reactivation of DREAM targets

Variety and complexity of chromosome 17 translocations in neuroblastoma

Whole exome sequencing of cell-free DNA reveals temporo-spatial heterogeneity and identifies treatment-resistant clones in neuroblastoma

[Genetic alterations in neuroblastoma and their usefulness for clinical management]