Detalhe da pesquisa
1.
Metabolic liver cancer: associations of rare and common germline variants in one-carbon metabolism and DNA methylation genes.
Hum Mol Genet
; 32(16): 2646-2655, 2023 08 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-37369012
2.
ACE2 and TMPRSS2 SARS-CoV-2 infectivity genes: deep mutational scanning and characterization of missense variants.
Hum Mol Genet
; 31(24): 4183-4192, 2022 12 16.
Artigo
em Inglês
| MEDLINE | ID: mdl-35861636
3.
Molecular classification and identification of an aggressive signature in low-grade B-cell lymphomas.
Hematol Oncol
; 41(4): 644-654, 2023 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-37254453
4.
Correction: All2: A tool for selecting mosaic mutations from comprehensive multi-cell comparisons.
PLoS Comput Biol
; 18(11): e1010703, 2022 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-36378632
5.
All2: A tool for selecting mosaic mutations from comprehensive multi-cell comparisons.
PLoS Comput Biol
; 18(4): e1009487, 2022 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-35442945
6.
Inherited variants at 3q13.33 and 3p24.1 are associated with risk of diffuse large B-cell lymphoma and implicate immune pathways.
Hum Mol Genet
; 29(1): 70-79, 2020 01 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-31600786
7.
SLCO1B1: Application and Limitations of Deep Mutational Scanning for Genomic Missense Variant Function.
Drug Metab Dispos
; 49(5): 395-404, 2021 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-33658230
8.
SCELLECTOR: ranking amplification bias in single cells using shallow sequencing.
BMC Bioinformatics
; 21(1): 521, 2020 Nov 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-33183232
9.
Identification of missing variants by combining multiple analytic pipelines.
BMC Bioinformatics
; 19(1): 139, 2018 04 16.
Artigo
em Inglês
| MEDLINE | ID: mdl-29661148
10.
Proteomic detection of immunoglobulin light chain variable region peptides from amyloidosis patient biopsies.
J Proteome Res
; 14(4): 1957-67, 2015 Apr 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-25734799
11.
PatternCNV: a versatile tool for detecting copy number changes from exome sequencing data.
Bioinformatics
; 30(18): 2678-80, 2014 Sep 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-24876377
12.
Host genetic variation in tumor necrosis factor and nuclear factor-κB pathways and overall survival in mantle cell lymphoma: A discovery and replication study.
Am J Hematol
; 94(6): E153-E155, 2019 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-30815899
13.
Follicular lymphoma B cells exhibit heterogeneous transcriptional states with associated somatic alterations and tumor microenvironments.
Cell Rep Med
; 5(3): 101443, 2024 Mar 19.
Artigo
em Inglês
| MEDLINE | ID: mdl-38428430
14.
Molecular Clusters and Tumor-Immune Drivers of IgM Monoclonal Gammopathies.
Clin Cancer Res
; 29(5): 957-970, 2023 03 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-36534518
15.
Multiomic Analysis Identifies a High-Risk Metabolic and TME Depleted Signature that Predicts Early Clinical Failure in DLBCL.
medRxiv
; 2023 Jun 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-37333387
16.
Frequent POLE-driven hypermutation in ovarian endometrioid cancer revealed by mutational signatures in RNA sequencing.
BMC Med Genomics
; 14(1): 165, 2021 06 22.
Artigo
em Inglês
| MEDLINE | ID: mdl-34158040
17.
Early developmental asymmetries in cell lineage trees in living individuals.
Science
; 371(6535): 1245-1248, 2021 03 19.
Artigo
em Inglês
| MEDLINE | ID: mdl-33737484
18.
Impact of variant-level batch effects on identification of genetic risk factors in large sequencing studies.
PLoS One
; 16(4): e0249305, 2021.
Artigo
em Inglês
| MEDLINE | ID: mdl-33861770
19.
Fine-mapping of the non-coding variation driving the Caucasian LRRK2 GWAS signal in Parkinson's disease.
Parkinsonism Relat Disord
; 83: 22-30, 2021 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-33454605
20.
Targeting of inflammatory pathways with R2CHOP in high-risk DLBCL.
Leukemia
; 35(2): 522-533, 2021 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-32139889