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Author Details

Nathalie Conte
The Wellcome Trust Sanger Institute
1983
28
21
PMIDPaper TitleJournal TitlePublished Year
36950387<i>In vivo</i> interrogation of regulatory genomes reveals extensive quasi-insufficiency in cancer evolution.Cell Genom2023
36950387<i>In vivo</i> interrogation of regulatory genomes reveals extensive quasi-insufficiency in cancer evolution.Cell Genom2023
30535239PDX Finder: A portal for patient-derived tumor xenograft model discovery.Nucleic Acids Res2019
30535239PDX Finder: A portal for patient-derived tumor xenograft model discovery.Nucleic Acids Res2019
28662064Identifiers for the 21st century: How to design, provision, and reuse persistent identifiers to maximize utility and impact of life science data.PLoS Biol2017
28662064Identifiers for the 21st century: How to design, provision, and reuse persistent identifiers to maximize utility and impact of life science data.PLoS Biol2017
28835438Molecular synergy underlies the co-occurrence patterns and phenotype of <i>NPM1</i>-mutant acute myeloid leukemia.Blood2017
28650483Disease model discovery from 3,328 gene knockouts by The International Mouse Phenotyping Consortium.Nat Genet2017
29092942PDX-MI: Minimal Information for Patient-Derived Tumor Xenograft Models.Cancer Res2017
29092942PDX-MI: Minimal Information for Patient-Derived Tumor Xenograft Models.Cancer Res2017
28650483Disease model discovery from 3,328 gene knockouts by The International Mouse Phenotyping Consortium.Nat Genet2017
28835438Molecular synergy underlies the co-occurrence patterns and phenotype of <i>NPM1</i>-mutant acute myeloid leukemia.Blood2017
27054363Mutational History of a Human Cell Lineage from Somatic to Induced Pluripotent Stem Cells.PLoS Genet2016
27054363Mutational History of a Human Cell Lineage from Somatic to Induced Pluripotent Stem Cells.PLoS Genet2016
25381129Characterization of gene mutations and copy number changes in acute myeloid leukemia using a rapid target enrichment protocol.Haematologica2015
25381129Characterization of gene mutations and copy number changes in acute myeloid leukemia using a rapid target enrichment protocol.Haematologica2015
26314589A mouse informatics platform for phenotypic and translational discovery.Mamm Genome2015
26314589A mouse informatics platform for phenotypic and translational discovery.Mamm Genome2015
25197064Chromosome instability induced by Mps1 and p53 mutation generates aggressive lymphomas exhibiting aneuploidy-induced stress.Proc Natl Acad Sci U S A2014
25197064Chromosome instability induced by Mps1 and p53 mutation generates aggressive lymphomas exhibiting aneuploidy-induced stress.Proc Natl Acad Sci U S A2014
23358416The piggyBac transposon displays local and distant reintegration preferences and can cause mutations at noncanonical integration sites.Mol Cell Biol2013
23358416The piggyBac transposon displays local and distant reintegration preferences and can cause mutations at noncanonical integration sites.Mol Cell Biol2013
23287868Histone deacetylase 1 and 2 are essential for normal T-cell development and genomic stability in mice.Blood2013
23702683Detailed molecular characterisation of acute myeloid leukaemia with a normal karyotype using targeted DNA capture.Leukemia2013
23702683Detailed molecular characterisation of acute myeloid leukaemia with a normal karyotype using targeted DNA capture.Leukemia2013
23287868Histone deacetylase 1 and 2 are essential for normal T-cell development and genomic stability in mice.Blood2013
20947725PiggyBac transposon mutagenesis: a tool for cancer gene discovery in mice.Science2010
20947725PiggyBac transposon mutagenesis: a tool for cancer gene discovery in mice.Science2010
19474196Analysis of Pax6 contiguous gene deletions in the mouse, Mus musculus, identifies regions distinct from Pax6 responsible for extreme small-eye and belly-spotting phenotypes.Genetics2009
19474196Analysis of Pax6 contiguous gene deletions in the mouse, Mus musculus, identifies regions distinct from Pax6 responsible for extreme small-eye and belly-spotting phenotypes.Genetics2009
18391979Loss of Rassf1a cooperates with Apc(Min) to accelerate intestinal tumourigenesis.Oncogene2008
18988746Extensive genomic copy number variation in embryonic stem cells.Proc Natl Acad Sci U S A2008
18391979Loss of Rassf1a cooperates with Apc(Min) to accelerate intestinal tumourigenesis.Oncogene2008
18988746Extensive genomic copy number variation in embryonic stem cells.Proc Natl Acad Sci U S A2008
15755806Segmental trisomy of chromosome 17: a mouse model of human aneuploidy syndromes.Proc Natl Acad Sci U S A2005
15755806Segmental trisomy of chromosome 17: a mouse model of human aneuploidy syndromes.Proc Natl Acad Sci U S A2005
15064709Aurora B -TACC1 protein complex in cytokinesis.Oncogene2004
15064709Aurora B -TACC1 protein complex in cytokinesis.Oncogene2004
14603251TACC1-chTOG-Aurora A protein complex in breast cancer.Oncogene2003
14603251TACC1-chTOG-Aurora A protein complex in breast cancer.Oncogene2003
12165861Carcinogenesis and translational controls: TACC1 is down-regulated in human cancers and associates with mRNA regulators.Oncogene2002
12165861Carcinogenesis and translational controls: TACC1 is down-regulated in human cancers and associates with mRNA regulators.Oncogene2002
12370745Loss of heterozygosity at microsatellite markers from region p11-21 of chromosome 8 in microdissected breast tumor but not in peritumoral cells.Int J Oncol2002
12368196Distinct and complementary information provided by use of tissue and DNA microarrays in the study of breast tumor markers.Am J Pathol2002
12353263Reciprocal translocations in breast tumor cell lines: cloning of a t(3;20) that targets the FHIT gene.Genes Chromosomes Cancer2002
12370745Loss of heterozygosity at microsatellite markers from region p11-21 of chromosome 8 in microdissected breast tumor but not in peritumoral cells.Int J Oncol2002
12368196Distinct and complementary information provided by use of tissue and DNA microarrays in the study of breast tumor markers.Am J Pathol2002
12353263Reciprocal translocations in breast tumor cell lines: cloning of a t(3;20) that targets the FHIT gene.Genes Chromosomes Cancer2002
10717235Translocation and coamplification of loci from chromosome arms 8p and 11q in the MDA-MB-175 mammary carcinoma cell line.Int J Oncol2000
10717235Translocation and coamplification of loci from chromosome arms 8p and 11q in the MDA-MB-175 mammary carcinoma cell line.Int J Oncol2000
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Collaborators

The Wellcome Trust Sanger Institute
Co-authored papers 13
Co-authored papers 8
European Bioinformatics Institute
Co-authored papers 5
Wellcome Sanger Institute
Co-authored papers 5
European Bioinformatics Institute
Co-authored papers 4
European Molecular Biology Laboratory - European Bioinformatics Institute
Co-authored papers 4
American Medical Informatics Association, Oregon Health and Science University, Oregon State University, University of Colorado Anschutz Medical Campus, University of North Carolina at Chapel Hill, University of Wisconsin-Madison
Co-authored papers 3
Co-authored papers 3
Co-authored papers 3
Oncode Institute, Netherlands Cancer Institute
Co-authored papers 2
International Society for Biocuration, Lawrence Berkeley National Laboratory, University of Edinburgh, University of Edinburgh School of Biological Sciences
Co-authored papers 2
European Bioinformatics Institute
Co-authored papers 2
European Bioinformatics Institute (EMBL-EBI)
Co-authored papers 2
MRC Harwell Institute
Co-authored papers 2
Co-authored papers 2
St. Ambrose University
Co-authored papers 2
College of Science, University of Lincoln
Co-authored papers 2
Medical Research Council Harwell
Co-authored papers 2
Wellcome Sanger Institute
Co-authored papers 2
The Jackson Laboratory Cancer Center
Co-authored papers 2
Seoul National University
Co-authored papers 2
William Harvey Research Institute, Queen Mary University of London
Co-authored papers 2
Cambridge Institute for Medical Research, University of Cambridge
Co-authored papers 2
Co-authored papers 2
European Bioinformatics Institute
Co-authored papers 2
Wellcome Trust Sanger Institute
Co-authored papers 2
The Turing Institute
Co-authored papers 2
William Harvey Research Institute, Queen Mary University of London
Co-authored papers 2
University of California davis
Co-authored papers 2
MRC Harwell Institute
Co-authored papers 2