Detalhe da pesquisa
1.
The repertoire of mutational signatures in human cancer.
Nature
; 578(7793): 94-101, 2020 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-32025018
2.
Author Correction: The repertoire of mutational signatures in human cancer.
Nature
; 614(7948): E41, 2023 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-36697836
3.
Functional genomics identifies specific vulnerabilities in PTEN-deficient breast cancer.
Breast Cancer Res
; 20(1): 22, 2018 03 22.
Artigo
em Inglês
| MEDLINE | ID: mdl-29566768
4.
SETD2 histone modifier loss in aggressive GI stromal tumours.
Gut
; 65(12): 1960-1972, 2016 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-26338826
5.
A formalin-fixed paraffin-embedded (FFPE)-based prognostic signature to predict metastasis in clinically low risk stage I/II microsatellite stable colorectal cancer.
Cancer Lett
; 403: 13-20, 2017 09 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-28624625
6.
Whole-Genome and Epigenomic Landscapes of Etiologically Distinct Subtypes of Cholangiocarcinoma.
Cancer Discov
; 7(10): 1116-1135, 2017 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-28667006
7.
Transcription-associated mutation of lasR in Pseudomonas aeruginosa.
DNA Repair (Amst)
; 46: 9-19, 2016 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-27650847
8.
Exome sequencing reveals recurrent REV3L mutations in cisplatin-resistant squamous cell carcinoma of head and neck.
Sci Rep
; 6: 19552, 2016 Jan 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-26790612
9.
MSIseq: Software for Assessing Microsatellite Instability from Catalogs of Somatic Mutations.
Sci Rep
; 5: 13321, 2015 Aug 26.
Artigo
em Inglês
| MEDLINE | ID: mdl-26306458
10.
Whole-exome sequencing studies of parathyroid carcinomas reveal novel PRUNE2 mutations, distinctive mutational spectra related to APOBEC-catalyzed DNA mutagenesis and mutational enrichment in kinases associated with cell migration and invasion.
J Clin Endocrinol Metab
; 100(2): E360-4, 2015 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-25387265
11.
Mutation signatures implicate aristolochic acid in bladder cancer development.
Genome Med
; 7(1): 38, 2015.
Artigo
em Inglês
| MEDLINE | ID: mdl-26015808
12.
High-depth sequencing of over 750 genes supports linear progression of primary tumors and metastases in most patients with liver-limited metastatic colorectal cancer.
Genome Biol
; 16: 32, 2015 Feb 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-25808843
13.
Mutational landscapes of tongue carcinoma reveal recurrent mutations in genes of therapeutic and prognostic relevance.
Genome Med
; 7: 98, 2015 Sep 23.
Artigo
em Inglês
| MEDLINE | ID: mdl-26395002
14.
Genomic landscapes of breast fibroepithelial tumors.
Nat Genet
; 47(11): 1341-5, 2015 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-26437033
15.
Mutation signatures of carcinogen exposure: genome-wide detection and new opportunities for cancer prevention.
Genome Med
; 6(3): 24, 2014.
Artigo
em Inglês
| MEDLINE | ID: mdl-25031618
16.
The NF1 gene revisited - from bench to bedside.
Oncotarget
; 5(15): 5873-92, 2014 Aug 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-25026295
17.
Exome sequencing identifies highly recurrent MED12 somatic mutations in breast fibroadenoma.
Nat Genet
; 46(8): 877-80, 2014 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-25038752
18.
Exome sequencing identifies distinct mutational patterns in liver fluke-related and non-infection-related bile duct cancers.
Nat Genet
; 45(12): 1474-8, 2013 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-24185513
19.
Genome-wide mutational signatures of aristolochic acid and its application as a screening tool.
Sci Transl Med
; 5(197): 197ra101, 2013 Aug 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-23926199
20.
Exome sequencing of liver fluke-associated cholangiocarcinoma.
Nat Genet
; 44(6): 690-3, 2012 May 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-22561520