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Author Details
Full Name
Carrie Sougnez
Affiliation
The Broad Institute of Harvard and MIT
ORCID
Career Start Year
1998
Papers
64
H Index
58
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
30559381
Addendum: The Cancer Cell Line Encyclopedia enables predictive modelling of anticancer drug sensitivity.
Nature
2019
30559381
Addendum: The Cancer Cell Line Encyclopedia enables predictive modelling of anticancer drug sensitivity.
Nature
2019
27199251
Clonal evolution in patients with chronic lymphocytic leukaemia developing resistance to BTK inhibition.
Nat Commun
2016
27199251
Clonal evolution in patients with chronic lymphocytic leukaemia developing resistance to BTK inhibition.
Nat Commun
2016
26536169
Comprehensive Molecular Characterization of Papillary Renal-Cell Carcinoma.
N Engl J Med
2016
26536169
Comprehensive Molecular Characterization of Papillary Renal-Cell Carcinoma.
N Engl J Med
2016
25650244
Whole-genome and multisector exome sequencing of primary and post-treatment glioblastoma reveals patterns of tumor evolution.
Genome Res
2015
28843286
Integrative Clinical Genomics of Advanced Prostate Cancer.
Cell
2015
25650244
Whole-genome and multisector exome sequencing of primary and post-treatment glioblastoma reveals patterns of tumor evolution.
Genome Res
2015
26061751
Comprehensive, Integrative Genomic Analysis of Diffuse Lower-Grade Gliomas.
N Engl J Med
2015
26181029
Genomic Correlate of Exceptional Erlotinib Response in Head and Neck Squamous Cell Carcinoma.
JAMA Oncol
2015
26000489
Integrative clinical genomics of advanced prostate cancer.
Cell
2015
26638776
Whole-genome sequencing reveals activation-induced cytidine deaminase signatures during indolent chronic lymphocytic leukaemia evolution.
Nat Commun
2015
26466571
Mutations driving CLL and their evolution in progression and relapse.
Nature
2015
26253028
A Dominant Mutation in Human RAD51 Reveals Its Function in DNA Interstrand Crosslink Repair Independent of Homologous Recombination.
Mol Cell
2015
26119737
Deficiency of UBE2T, the E2Â Ubiquitin Ligase Necessary for FANCD2 and FANCI Ubiquitination, Causes FA-T Subtype of Fanconi Anemia.
Cell Rep
2015
26372948
Comprehensive analysis of cancer-associated somatic mutations in class I HLA genes.
Nat Biotechnol
2015
26410082
Genomic Characterization of Brain Metastases Reveals Branched Evolution and Potential Therapeutic Targets.
Cancer Discov
2015
28843286
Integrative Clinical Genomics of Advanced Prostate Cancer.
Cell
2015
26466571
Mutations driving CLL and their evolution in progression and relapse.
Nature
2015
26253028
A Dominant Mutation in Human RAD51 Reveals Its Function in DNA Interstrand Crosslink Repair Independent of Homologous Recombination.
Mol Cell
2015
26410082
Genomic Characterization of Brain Metastases Reveals Branched Evolution and Potential Therapeutic Targets.
Cancer Discov
2015
26372948
Comprehensive analysis of cancer-associated somatic mutations in class I HLA genes.
Nat Biotechnol
2015
26638776
Whole-genome sequencing reveals activation-induced cytidine deaminase signatures during indolent chronic lymphocytic leukaemia evolution.
Nat Commun
2015
26181029
Genomic Correlate of Exceptional Erlotinib Response in Head and Neck Squamous Cell Carcinoma.
JAMA Oncol
2015
26119737
Deficiency of UBE2T, the E2Â Ubiquitin Ligase Necessary for FANCD2 and FANCI Ubiquitination, Causes FA-T Subtype of Fanconi Anemia.
Cell Rep
2015
26061751
Comprehensive, Integrative Genomic Analysis of Diffuse Lower-Grade Gliomas.
N Engl J Med
2015
26000489
Integrative clinical genomics of advanced prostate cancer.
Cell
2015
24434212
Widespread genetic heterogeneity in multiple myeloma: implications for targeted therapy.
Cancer Cell
2014
25490447
Locally disordered methylation forms the basis of intratumor methylome variation in chronic lymphocytic leukemia.
Cancer Cell
2014
25512523
Complementary genomic approaches highlight the PI3K/mTOR pathway as a common vulnerability in osteosarcoma.
Proc Natl Acad Sci U S A
2014
24434212
Widespread genetic heterogeneity in multiple myeloma: implications for targeted therapy.
Cancer Cell
2014
24630729
Genetic and clonal dissection of murine small cell lung carcinoma progression by genome sequencing.
Cell
2014
24894453
Colon cancer-derived oncogenic EGFR G724S mutant identified by whole genome sequence analysis is dependent on asymmetric dimerization and sensitive to cetuximab.
Mol Cancer
2014
24752078
Whole-exome sequencing of circulating tumor cells provides a window into metastatic prostate cancer.
Nat Biotechnol
2014
24891321
Systematic identification of personal tumor-specific neoantigens in chronic lymphocytic leukemia.
Blood
2014
24823667
Somatic retrotransposition in human cancer revealed by whole-genome and exome sequencing.
Genome Res
2014
24778153
Somatic mutation as a mechanism of Wnt/β-catenin pathway activation in CLL.
Blood
2014
25490447
Locally disordered methylation forms the basis of intratumor methylome variation in chronic lymphocytic leukemia.
Cancer Cell
2014
25512523
Complementary genomic approaches highlight the PI3K/mTOR pathway as a common vulnerability in osteosarcoma.
Proc Natl Acad Sci U S A
2014
24752078
Whole-exome sequencing of circulating tumor cells provides a window into metastatic prostate cancer.
Nat Biotechnol
2014
24778153
Somatic mutation as a mechanism of Wnt/β-catenin pathway activation in CLL.
Blood
2014
24823667
Somatic retrotransposition in human cancer revealed by whole-genome and exome sequencing.
Genome Res
2014
24894453
Colon cancer-derived oncogenic EGFR G724S mutant identified by whole genome sequence analysis is dependent on asymmetric dimerization and sensitive to cetuximab.
Mol Cancer
2014
24891321
Systematic identification of personal tumor-specific neoantigens in chronic lymphocytic leukemia.
Blood
2014
24630729
Genetic and clonal dissection of murine small cell lung carcinoma progression by genome sequencing.
Cell
2014
23334666
The genetic landscape of high-risk neuroblastoma.
Nat Genet
2013
24120142
The somatic genomic landscape of glioblastoma.
Cell
2013
23770567
Mutational heterogeneity in cancer and the search for new cancer-associated genes.
Nature
2013
24071852
Pan-cancer patterns of somatic copy number alteration.
Nat Genet
2013
1 - 50 of 128
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Petar Stojanov
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Kristin G Ardlie
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Douglas Voet
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Catherine J Wu
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