Detalhe da pesquisa
1.
Diverse mutational landscapes in human lymphocytes.
Nature
; 608(7924): 724-732, 2022 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-35948631
2.
Convergent somatic mutations in metabolism genes in chronic liver disease.
Nature
; 598(7881): 473-478, 2021 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-34646017
3.
The mutational landscape of human somatic and germline cells.
Nature
; 597(7876): 381-386, 2021 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-34433962
4.
The mutational landscape of normal human endometrial epithelium.
Nature
; 580(7805): 640-646, 2020 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-32350471
5.
Genetic and genomic analysis of acute lymphoblastic leukemia in older adults reveals a distinct profile of abnormalities: analysis of 210 patients from the UKALL14 and UKALL60+ clinical trials.
Haematologica
; 107(9): 2051-2063, 2022 09 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-34788984
6.
CDKN2A deletion is a frequent event associated with poor outcome in patients with peripheral T-cell lymphoma not otherwise specified (PTCL-NOS).
Haematologica
; 106(11): 2918-2926, 2021 Nov 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-33054126
7.
Type 1 Interferon Responses Underlie Tumor-Selective Replication of Oncolytic Measles Virus.
Mol Ther
; 28(4): 1043-1055, 2020 04 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-32087150
8.
Correction: Rare germline variants in DNA repair genes and the angiogenesis pathway predispose prostate cancer patients to develop metastatic disease.
Br J Cancer
; 120(8): 867, 2019 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-30837682
9.
Integration of transcriptional and mutational data simplifies the stratification of peripheral T-cell lymphoma.
Am J Hematol
; 94(6): 628-634, 2019 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-30829413
10.
Rare germline variants in DNA repair genes and the angiogenesis pathway predispose prostate cancer patients to develop metastatic disease.
Br J Cancer
; 119(1): 96-104, 2018 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-29915322
11.
Gene and pathway level analyses of germline DNA-repair gene variants and prostate cancer susceptibility using the iCOGS-genotyping array.
Br J Cancer
; 118(6): e9, 2018 03 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-29438362
12.
Multiple novel prostate cancer susceptibility signals identified by fine-mapping of known risk loci among Europeans.
Hum Mol Genet
; 24(19): 5589-602, 2015 Oct 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-26025378
13.
LocusExplorer: a user-friendly tool for integrated visualization of human genetic association data and biological annotations.
Bioinformatics
; 32(6): 949-51, 2016 03 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-26589274
14.
Fine-mapping the HOXB region detects common variants tagging a rare coding allele: evidence for synthetic association in prostate cancer.
PLoS Genet
; 10(2): e1004129, 2014 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-24550738
15.
Gene and pathway level analyses of germline DNA-repair gene variants and prostate cancer susceptibility using the iCOGS-genotyping array.
Br J Cancer
; 114(8): 945-52, 2016 04 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-26964030
16.
Genome-wide association of familial prostate cancer cases identifies evidence for a rare segregating haplotype at 8q24.21.
Hum Genet
; 135(8): 923-38, 2016 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-27262462
17.
Fine-mapping identifies multiple prostate cancer risk loci at 5p15, one of which associates with TERT expression.
Hum Mol Genet
; 22(12): 2520-8, 2013 Jun 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-23535824
18.
Translating genetic risk factors for prostate cancer to the clinic: 2013 and beyond.
Future Oncol
; 10(9): 1679-94, 2014.
Artigo
em Inglês
| MEDLINE | ID: mdl-25145435
19.
Haplotype-specific assembly of shattered chromosomes in esophageal adenocarcinomas.
Cell Genom
; 4(2): 100484, 2024 Feb 14.
Artigo
em Inglês
| MEDLINE | ID: mdl-38232733
20.
Clinical implications of family history of prostate cancer and genetic risk single nucleotide polymorphism (SNP) profiles in an active surveillance cohort.
BJU Int
; 112(5): 666-73, 2013 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-23320731