Detalhe da pesquisa
1.
Evolutionary histories of breast cancer and related clones.
Nature
; 620(7974): 607-614, 2023 Aug.
Artigo
Inglês
| MEDLINE | ID: mdl-37495687
2.
DOCK2 is involved in the host genetics and biology of severe COVID-19.
Nature
; 609(7928): 754-760, 2022 09.
Artigo
Inglês
| MEDLINE | ID: mdl-35940203
3.
Landscape of driver mutations and their clinical effects on Down syndrome-related myeloid neoplasms.
Blood
; 2024 Mar 21.
Artigo
Inglês
| MEDLINE | ID: mdl-38513239
4.
Germ line DDX41 mutations define a unique subtype of myeloid neoplasms.
Blood
; 141(5): 534-549, 2023 02 02.
Artigo
Inglês
| MEDLINE | ID: mdl-36322930
5.
Clonal evidence for the development of neuroblastoma with extensive copy-neutral loss of heterozygosity arising in a mature teratoma.
Cancer Sci
; 112(7): 2921-2927, 2021 Jul.
Artigo
Inglês
| MEDLINE | ID: mdl-33934450
6.
Clonal hematopoiesis is associated with improved survival in patients with metastatic colorectal cancer from the FIRE-3 trial.
Blood
; 139(10): 1593-1597, 2022 03 10.
Artigo
Inglês
| MEDLINE | ID: mdl-34932794
7.
Adult Low-Hypodiploid Acute Lymphoblastic Leukemia Evolves from TP53-Mutated Clonal Hematopoiesis.
Blood Cancer Discov
; 4(2): 102-105, 2023 03 01.
Artigo
Inglês
| MEDLINE | ID: mdl-36779909
8.
Amplified EPOR/JAK2 Genes Define a Unique Subtype of Acute Erythroid Leukemia.
Blood Cancer Discov
; 3(5): 410-427, 2022 09 06.
Artigo
Inglês
| MEDLINE | ID: mdl-35839275
9.
The whole blood transcriptional regulation landscape in 465 COVID-19 infected samples from Japan COVID-19 Task Force.
Nat Commun
; 13(1): 4830, 2022 08 22.
Artigo
Inglês
| MEDLINE | ID: mdl-35995775
10.
Combined landscape of single-nucleotide variants and copy number alterations in clonal hematopoiesis.
Nat Med
; 27(7): 1239-1249, 2021 07.
Artigo
Inglês
| MEDLINE | ID: mdl-34239136
11.
Unbiased Detection of Driver Mutations in Extramammary Paget Disease.
Clin Cancer Res
; 27(6): 1756-1765, 2021 03 15.
Artigo
Inglês
| MEDLINE | ID: mdl-33323405
12.
Molecular pathogenesis of progression to myeloid leukemia from TET-insufficient status.
Blood Adv
; 4(5): 845-854, 2020 03 10.
Artigo
Inglês
| MEDLINE | ID: mdl-32126143
13.
Combined Cohesin-RUNX1 Deficiency Synergistically Perturbs Chromatin Looping and Causes Myelodysplastic Syndromes.
Cancer Discov
; 10(6): 836-853, 2020 06.
Artigo
Inglês
| MEDLINE | ID: mdl-32249213
14.
Implications of TP53 allelic state for genome stability, clinical presentation and outcomes in myelodysplastic syndromes.
Nat Med
; 26(10): 1549-1556, 2020 10.
Artigo
Inglês
| MEDLINE | ID: mdl-32747829
15.
Author Correction: Implications of TP53 allelic state for genome stability, clinical presentation and outcomes in myelodysplastic syndromes.
Nat Med
; 27(5): 927, 2021 May.
Artigo
Inglês
| MEDLINE | ID: mdl-33948021
16.
Author Correction: Implications of TP53 allelic state for genome stability, clinical presentation and outcomes in myelodysplastic syndromes.
Nat Med
; 27(3): 562, 2021 Mar.
Artigo
Inglês
| MEDLINE | ID: mdl-33564192