Detalhe da pesquisa
1.
TNRC18 engages H3K9me3 to mediate silencing of endogenous retrotransposons.
Nature
; 623(7987): 633-642, 2023 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-37938770
2.
Genomic landscape of non-small cell lung cancer in smokers and never-smokers.
Cell
; 150(6): 1121-34, 2012 Sep 14.
Artigo
em Inglês
| MEDLINE | ID: mdl-22980976
3.
Mapping and characterization of structural variation in 17,795 human genomes.
Nature
; 583(7814): 83-89, 2020 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-32460305
4.
Author Correction: Exome sequencing of Finnish isolates enhances rare-variant association power.
Nature
; 575(7783): E4, 2019 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-31686056
5.
Exome sequencing of Finnish isolates enhances rare-variant association power.
Nature
; 572(7769): 323-328, 2019 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-31367044
6.
Association of structural variation with cardiometabolic traits in Finns.
Am J Hum Genet
; 108(4): 583-596, 2021 04 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-33798444
7.
Characterization of Macrophage-Tropic HIV-1 Infection of Central Nervous System Cells and the Influence of Inflammation.
J Virol
; 96(17): e0095722, 2022 09 14.
Artigo
em Inglês
| MEDLINE | ID: mdl-35975998
8.
Mitochondrial genome copy number measured by DNA sequencing in human blood is strongly associated with metabolic traits via cell-type composition differences.
Hum Genomics
; 15(1): 34, 2021 06 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-34099068
9.
Correction: Tumor Evolution in Two Patients with Basal-like Breast Cancer: A Retrospective Genomics Study of Multiple Metastases.
PLoS Med
; 14(1): e1002222, 2017 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-28068332
10.
Genomic analysis of germ line and somatic variants in familial myelodysplasia/acute myeloid leukemia.
Blood
; 126(22): 2484-90, 2015 Nov 26.
Artigo
em Inglês
| MEDLINE | ID: mdl-26492932
11.
Tumor Evolution in Two Patients with Basal-like Breast Cancer: A Retrospective Genomics Study of Multiple Metastases.
PLoS Med
; 13(12): e1002174, 2016 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-27923045
12.
Genomic and epigenomic landscapes of adult de novo acute myeloid leukemia.
N Engl J Med
; 368(22): 2059-74, 2013 05 30.
Artigo
em Inglês
| MEDLINE | ID: mdl-23634996
13.
A living ex vivo platform for functional, personalized brain cancer diagnosis.
Cell Rep Med
; 4(6): 101042, 2023 06 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-37192626
14.
Rapid idiosyncratic mechanisms of clinical resistance to KRAS G12C inhibition.
J Clin Invest
; 132(4)2022 02 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-34990404
15.
Genomic profiling of murine mammary tumors identifies potential personalized drug targets for p53-deficient mammary cancers.
Dis Model Mech
; 9(7): 749-57, 2016 07 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-27149990
16.
Rare Variation in TET2 Is Associated with Clinically Relevant Prostate Carcinoma in African Americans.
Cancer Epidemiol Biomarkers Prev
; 25(11): 1456-1463, 2016 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-27486019
17.
Inactivation of RASA1 promotes melanoma tumorigenesis via R-Ras activation.
Oncotarget
; 7(17): 23885-96, 2016 Apr 26.
Artigo
em Inglês
| MEDLINE | ID: mdl-26993606
18.
Truncating Prolactin Receptor Mutations Promote Tumor Growth in Murine Estrogen Receptor-Alpha Mammary Carcinomas.
Cell Rep
; 17(1): 249-260, 2016 09 27.
Artigo
em Inglês
| MEDLINE | ID: mdl-27681435
19.
Genomic analysis to define molecular basis of aggressiveness in a mouse model of oral cancer.
Genom Data
; 3: 61-62, 2015 Mar 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-25729643
20.
Patterns and functional implications of rare germline variants across 12 cancer types.
Nat Commun
; 6: 10086, 2015 Dec 22.
Artigo
em Inglês
| MEDLINE | ID: mdl-26689913