Lista de obras -

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

artículo científico publicado en 2011

ATRT-10. SPATIO-TEMPORAL DELETION OF SMARCB1 DETERMINES MOUSE AT/RT SUBTYPES.

artículo científico publicado en 2018

Accumulation of Segmental Alterations Determines Progression in Neuroblastoma

artículo científico publicado en 2010

Balanced Translocations Disrupting SMARCB1 Are Hallmark Recurrent Genetic Alterations in Renal Medullary Carcinomas.

artículo científico publicado en 2015

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

Cholinergic switch associated with morphological differentiation in neuroblastoma

artículo científico publicado en 2009

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

Constitutive activation of RAS/MAPK pathway cooperates with trisomy 21 and is therapeutically exploitable in Down syndrome B-cell leukemia

scientific article published on 27 March 2020

Conventional chondrosarcoma in a survivor of rhabdoid tumor: enlarging the spectrum of tumors associated with SMARCB1 germline mutations

artículo científico publicado en 2012

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

artículo científico publicado en 2015

Deep intronic hotspot variant explaining rhabdoid tumor predisposition syndrome in two patients with atypical teratoid and rhabdoid tumor

artículo científico publicado en 2017

Does ATRX germline variation predispose to osteosarcoma? Three additional cases of osteosarcoma in two ATR-X syndrome patients

Emergence of new ALK mutations at relapse of neuroblastoma

artículo científico publicado en 2014

Evolutionary Routes in Metastatic Uveal Melanomas Depend on MBD4 Alterations

scientific article published on 21 June 2019

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

artículo científico publicado en 2016

Fine-needle aspiration as a diagnostic technique in 50 cases of primary Ewing sarcoma/peripheral neuroectodermal tumor. Institut Curie's experience

artículo científico publicado en 2010

Genome-wide association study identifies multiple new loci associated with Ewing sarcoma susceptibility

scientific article published in Nature Communications

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

artículo científico publicado en 2016

Germline mutations in FGF receptors and medulloblastomas.

artículo científico publicado en 2013

Heterogeneity of neuroblastoma cell identity defined by transcriptional circuitries.

artículo científico publicado en 2017

High-resolution mapping of amplicons of the short arm of chromosome 1 in two neuroblastoma tumors by microarray-based comparative genomic hybridization

artículo científico publicado en 2004

MYC and MYCN amplification can be reliably assessed by aCGH in medulloblastoma

artículo científico publicado en 2013

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

PHOX2B immunolabeling: a novel tool for the diagnosis of undifferentiated neuroblastomas among childhood small round blue-cell tumors

artículo científico publicado en 2012

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

artículo científico publicado en 2017

Preferential occurrence of chromosome breakpoints within early replicating regions in neuroblastoma

artículo científico publicado en 2005

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

artículo científico publicado en 2017

Rubinstein-Taybi syndrome predisposing to non-WNT, non-SHH, group 3 medulloblastoma.

artículo científico publicado en 2013

SMARCA4 inactivation defines a group of undifferentiated thoracic malignancies transcriptionally related to BAF-deficient sarcomas

artículo científico publicado en 2015

SMARCB1 Deficiency in Tumors From the Peripheral Nervous System

artículo científico publicado en 2012

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

artículo científico publicado en 2008

The occurrence of intracranial rhabdoid tumours in mice depends on temporal control of Smarcb1 inactivation

artículo científico publicado en 2016

VAMP: visualization and analysis of array-CGH, transcriptome and other molecular profiles

artículo científico publicado en 2006

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

artículo científico publicado en 2017

Lista de obras de

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

ATRT-10. SPATIO-TEMPORAL DELETION OF SMARCB1 DETERMINES MOUSE AT/RT SUBTYPES.

Accumulation of Segmental Alterations Determines Progression in Neuroblastoma

Balanced Translocations Disrupting SMARCB1 Are Hallmark Recurrent Genetic Alterations in Renal Medullary Carcinomas.

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

Cholinergic switch associated with morphological differentiation 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.

Constitutive activation of RAS/MAPK pathway cooperates with trisomy 21 and is therapeutically exploitable in Down syndrome B-cell leukemia

Conventional chondrosarcoma in a survivor of rhabdoid tumor: enlarging the spectrum of tumors associated with SMARCB1 germline mutations

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

Deep intronic hotspot variant explaining rhabdoid tumor predisposition syndrome in two patients with atypical teratoid and rhabdoid tumor

Does ATRX germline variation predispose to osteosarcoma? Three additional cases of osteosarcoma in two ATR-X syndrome patients

Emergence of new ALK mutations at relapse of neuroblastoma

Evolutionary Routes in Metastatic Uveal Melanomas Depend on MBD4 Alterations

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

Fine-needle aspiration as a diagnostic technique in 50 cases of primary Ewing sarcoma/peripheral neuroectodermal tumor. Institut Curie's experience

Genome-wide association study identifies multiple new loci associated with Ewing sarcoma susceptibility

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

Germline mutations in FGF receptors and medulloblastomas.

Heterogeneity of neuroblastoma cell identity defined by transcriptional circuitries.

High-resolution mapping of amplicons of the short arm of chromosome 1 in two neuroblastoma tumors by microarray-based comparative genomic hybridization

MYC and MYCN amplification can be reliably assessed by aCGH in medulloblastoma

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

PHOX2B immunolabeling: a novel tool for the diagnosis of undifferentiated neuroblastomas among childhood small round blue-cell tumors

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

Preferential occurrence of chromosome breakpoints within early replicating regions in neuroblastoma

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

Rubinstein-Taybi syndrome predisposing to non-WNT, non-SHH, group 3 medulloblastoma.

SMARCA4 inactivation defines a group of undifferentiated thoracic malignancies transcriptionally related to BAF-deficient sarcomas

SMARCB1 Deficiency in Tumors From the Peripheral Nervous System

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

The occurrence of intracranial rhabdoid tumours in mice depends on temporal control of Smarcb1 inactivation

VAMP: visualization and analysis of array-CGH, transcriptome and other molecular profiles

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