Detalhe da pesquisa
1.
ERα-associated translocations underlie oncogene amplifications in breast cancer.
Nature
; 618(7967): 1024-1032, 2023 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-37198482
2.
Computational analysis of cancer genome sequencing data.
Nat Rev Genet
; 23(5): 298-314, 2022 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-34880424
3.
Accurate and sensitive mutational signature analysis with MuSiCal.
Nat Genet
; 56(3): 541-552, 2024 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-38361034
4.
Chromosome evolution screens recapitulate tissue-specific tumor aneuploidy patterns.
Nat Genet
; 56(5): 900-912, 2024 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-38388848
5.
A Panel-Based Mutational Signature of Mismatch Repair Deficiency is Associated With Durable Response to Pembrolizumab in Metastatic Castration-Resistant Prostate Cancer.
Clin Genitourin Cancer
; 22(2): 558-568.e3, 2024 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-38342659
6.
Predicting response to immune checkpoint blockade therapy among mismatch repair-deficient patients using mutational signatures.
medRxiv
; 2024 Jan 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-38293061
7.
De novo identification of expressed cancer somatic mutations from single-cell RNA sequencing data.
Genome Med
; 15(1): 115, 2023 Dec 18.
Artigo
em Inglês
| MEDLINE | ID: mdl-38111063
8.
Hyper-Dependence on NHEJ Enables Synergy between DNA-PK Inhibitors and Low-Dose Doxorubicin in Leiomyosarcoma.
Clin Cancer Res
; 29(24): 5128-5139, 2023 12 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-37773632
9.
Optimized detection of homologous recombination deficiency improves the prediction of clinical outcomes in cancer.
NPJ Precis Oncol
; 6(1): 96, 2022 Dec 29.
Artigo
em Inglês
| MEDLINE | ID: mdl-36581696
10.
Mutational Signature 3 Detected from Clinical Panel Sequencing is Associated with Responses to Olaparib in Breast and Ovarian Cancers.
Clin Cancer Res
; 28(21): 4714-4723, 2022 11 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-36048535
11.
The origins and genetic interactions of KRAS mutations are allele- and tissue-specific.
Nat Commun
; 12(1): 1808, 2021 03 22.
Artigo
em Inglês
| MEDLINE | ID: mdl-33753749
12.
The landscape of somatic mutation in cerebral cortex of autistic and neurotypical individuals revealed by ultra-deep whole-genome sequencing.
Nat Neurosci
; 24(2): 176-185, 2021 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-33432195
13.
Heterogeneity and Clonal Evolution of Acquired PARP Inhibitor Resistance in TP53- and BRCA1-Deficient Cells.
Cancer Res
; 81(10): 2774-2787, 2021 05 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-33514515
14.
Author Correction: Immunogenomic profiling determines responses to combined PARP and PD-1 inhibition in ovarian cancer.
Nat Commun
; 11(1): 2543, 2020 05 18.
Artigo
em Inglês
| MEDLINE | ID: mdl-32424117
15.
Immunogenomic profiling determines responses to combined PARP and PD-1 inhibition in ovarian cancer.
Nat Commun
; 11(1): 1459, 2020 03 19.
Artigo
em Inglês
| MEDLINE | ID: mdl-32193378
16.
Detecting the mutational signature of homologous recombination deficiency in clinical samples.
Nat Genet
; 51(5): 912-919, 2019 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-30988514
17.
Linked-read analysis identifies mutations in single-cell DNA-sequencing data.
Nat Genet
; 51(4): 749-754, 2019 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-30886424
18.
Phase II Study of Avelumab in Patients With Mismatch Repair Deficient and Mismatch Repair Proficient Recurrent/Persistent Endometrial Cancer.
J Clin Oncol
; 37(30): 2786-2794, 2019 10 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-31461377
19.
Author Correction: The landscape of somatic mutation in cerebral cortex of autistic and neurotypical individuals revealed by ultra-deep whole-genome sequencing.
Nat Neurosci
; 26(10): 1833, 2023 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-37644260
20.
Author Correction: The landscape of somatic mutation in cerebral cortex of autistic and neurotypical individuals revealed by ultra-deep whole-genome sequencing.
Nat Neurosci
; 24(4): 611, 2021 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-33753946