List of works - Jérôme Couturier

A SUMOylation-defective MITF germline mutation predisposes to melanoma and renal carcinoma

scientific article

A deep intronic mutation in the RB1 gene leads to intronic sequence exonisation

scientific article published on 14 February 2007

A high-risk retinoblastoma subtype with stemness features, dedifferentiated cone states and neuronal/ganglion cell gene expression

scientific article published on 22 September 2021

Accumulation of Segmental Alterations Determines Progression in Neuroblastoma

scientific article published on 01 June 2010

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

scientific article

Cytopathologie des tumeurs malignes du blastème

scientific article published on 01 December 2004

Erratum: Corrigendum: A SUMOylation-defective MITF germline mutation predisposes to melanoma and renal carcinoma

scientific article published in Nature

Fine mapping of whole RB1 gene deletions in retinoblastoma patients confirms PCDH8 as a candidate gene for psychomotor delay

scientific article published on 22 August 2012

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

scientific article published on 9 November 2010

Genotype-phenotype correlations in hereditary familial retinoblastoma

scientific article published on 01 March 2007

Isolated generalized dystonia in biallelic missense mutations of the ATM gene

scientific article published on 2 May 2013

MDM2 as a modifier gene in retinoblastoma

scientific article published on 4 November 2010

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

scientific article

Morbidity and mortality from ataxia-telangiectasia are associated with ATM genotype ⬇️

scientific article published on June 12, 2011

Overall genomic pattern is a predictor of outcome in neuroblastoma

scientific article

Phenotypic cellular characterization of an ataxia telangiectasia patient carrying a causal homozygous missense mutation

scientific article published on February 2003

Three new BLM gene mutations associated with Bloom syndrome

scientific article

Visualizing Chromosomes as Transcriptome Correlation Maps: Evidence of Chromosomal Domains Containing Co-expressed Genes—A Study of 130 Invasive Ductal Breast Carcinomas

article

List of works by Jérôme Couturier

A SUMOylation-defective MITF germline mutation predisposes to melanoma and renal carcinoma

A deep intronic mutation in the RB1 gene leads to intronic sequence exonisation

A high-risk retinoblastoma subtype with stemness features, dedifferentiated cone states and neuronal/ganglion cell gene expression

Accumulation of Segmental Alterations Determines Progression in Neuroblastoma

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

Cytopathologie des tumeurs malignes du blastème

Erratum: Corrigendum: A SUMOylation-defective MITF germline mutation predisposes to melanoma and renal carcinoma

Fine mapping of whole RB1 gene deletions in retinoblastoma patients confirms PCDH8 as a candidate gene for psychomotor delay

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

Genotype-phenotype correlations in hereditary familial retinoblastoma

Isolated generalized dystonia in biallelic missense mutations of the ATM gene

MDM2 as a modifier gene in retinoblastoma

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

Morbidity and mortality from ataxia-telangiectasia are associated with ATM genotype ⬇️

Overall genomic pattern is a predictor of outcome in neuroblastoma

Phenotypic cellular characterization of an ataxia telangiectasia patient carrying a causal homozygous missense mutation

Three new BLM gene mutations associated with Bloom syndrome

Visualizing Chromosomes as Transcriptome Correlation Maps: Evidence of Chromosomal Domains Containing Co-expressed Genes—A Study of 130 Invasive Ductal Breast Carcinomas