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Author Details

Mathieu Chicard
INSERM U830 Cancer, Institut Curie Research Center, PSL Research University
2015
14
10
Nathan Sheffield (CM4AI)
PMIDPaper TitleJournal TitlePublished Year
37444642Cell-Free DNA Extracted from CSF for the Molecular Diagnosis of Pediatric Embryonal Brain Tumors.Cancers (Basel)2023
34794856The feasibility of using liquid biopsies as a complementary assay for copy number aberration profiling in routinely collected paediatric cancer patient samples.Eur J Cancer2022
36265118Molecular Characterization of Circulating Tumor DNA in Pediatric Rhabdomyosarcoma: A Feasibility Study.JCO Precis Oncol2022
35292802The European MAPPYACTS Trial: Precision Medicine Program in Pediatric and Adolescent Patients with Recurrent Malignancies.Cancer Discov2022
32662719Minimally invasive classification of paediatric solid tumours using reduced representation bisulphite sequencing of cell-free DNA: a proof-of-principle study.Epigenetics2021
34298378Molecular diagnosis of retinoblastoma by circulating tumor DNA analysis.Eur J Cancer2021
34050156Multimodal analysis of cell-free DNA whole-genome sequencing for pediatric cancers with low mutational burden.Nat Commun2021
31018240Study of chromatin remodeling genes implicates SMARCA4 as a putative player in oncogenesis in neuroblastoma.Int J Cancer2019
29923174Circulating tumor DNA analysis enables molecular characterization of pediatric renal tumors at diagnosis.Int J Cancer2019
29191970Whole-Exome Sequencing of Cell-Free DNA Reveals Temporo-spatial Heterogeneity and Identifies Treatment-Resistant Clones in Neuroblastoma.Clin Cancer Res2018
29342233QuantumClone: clonal assessment of functional mutations in cancer based on a genotype-aware method for clonal reconstruction.Bioinformatics2018
27283765Aneuploidy: the impact of chromosome imbalance on nuclear organization and overall genome expression.Clin Genet2016
27440268Genomic Copy Number Profiling Using Circulating Free Tumor DNA Highlights Heterogeneity in Neuroblastoma.Clin Cancer Res2016
26121087Relapsed neuroblastomas show frequent RAS-MAPK pathway mutations.Nat Genet2015
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Collaborators

Institut Curie
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PSL Research University, Institut Curie Research Center, INSERM U, Institut Curie
Co-authored papers 11
Institut Curie
Co-authored papers 8
Institut Curie Hospital
Co-authored papers 8
Institut Curie
Co-authored papers 5
Institut Curie and University Paris Cite
Co-authored papers 3
Children's Hospital of Philadelphia
Co-authored papers 2
SIREDO Oncology Center, Institut Curie Hospital, and Universite de Paris
Co-authored papers 2
Balgrist University Hospital, University of Zurich (UZH)
Co-authored papers 2
University College London, Cancer Institute
Co-authored papers 1
St. Anna Children's Cancer Research Institute
Co-authored papers 1
Co-authored papers 1
University Hospital Erlangen
Co-authored papers 1
Co-authored papers 1
University Hospital Essen, West German Cancer Center
Co-authored papers 1
St. Anna Children's Cancer Research Institute (CCRI)
Co-authored papers 1
INSERM U1245
Co-authored papers 1
CeMM Research Center for Molecular Medicine of the Austrian Academy of Sciences
Co-authored papers 1
Co-authored papers 1
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St. Anna Children's Cancer Research Institute (CCRI)
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University Hospital Erlangen
Co-authored papers 1
Department of Oncology and Children's Research Center, University Children's Hospital
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Baylor College of Medicine
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Children's Hospital of Philadelphia
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CeMM Research Center for Molecular Medicine of the Austrian Academy of Sciences
Co-authored papers 1
National Cancer Institute
Co-authored papers 1
Institut Curie, Universite PSL
Co-authored papers 1
Children's Cancer Research Institute
Co-authored papers 1
Co-authored papers 1