Detalhe da pesquisa
1.
Complex balanced intrachromosomal rearrangement involving PITX2 identified as a cause of Axenfeld-Rieger Syndrome.
Am J Med Genet A
; 194(5): e63542, 2024 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-38234180
2.
Theragnostic chromosomal rearrangements in treatment-naive pancreatic ductal adenocarcinomas obtained via endoscopic ultrasound.
J Cell Mol Med
; 25(8): 4110-4123, 2021 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-33704908
3.
Optimizing clinical cytology touch preparations for next generation sequencing.
Genomics
; 112(6): 5313-5323, 2020 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-33144219
4.
UCH-L1 bypasses mTOR to promote protein biosynthesis and is required for MYC-driven lymphomagenesis in mice.
Blood
; 132(24): 2564-2574, 2018 12 13.
Artigo
em Inglês
| MEDLINE | ID: mdl-30257881
5.
Detection of cryptic CCND1 rearrangements in mantle cell lymphoma by next generation sequencing.
Ann Diagn Pathol
; 46: 151533, 2020 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-32408254
6.
Genome U-Plot: a whole genome visualization.
Bioinformatics
; 34(10): 1629-1634, 2018 05 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-29281001
7.
Mate pair sequencing improves detection of genomic abnormalities in acute myeloid leukemia.
Eur J Haematol
; 102(1): 87-96, 2019 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-30270457
8.
Copy number variant analysis using genome-wide mate-pair sequencing.
Genes Chromosomes Cancer
; 57(9): 459-470, 2018 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-29726617
9.
Integrated mate-pair and RNA sequencing identifies novel, targetable gene fusions in peripheral T-cell lymphoma.
Blood
; 128(9): 1234-45, 2016 09 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-27297792
10.
Chromoanasynthesis is a common mechanism that leads to ERBB2 amplifications in a cohort of early stage HER2+ breast cancer samples.
BMC Cancer
; 18(1): 738, 2018 Jul 13.
Artigo
em Inglês
| MEDLINE | ID: mdl-30005627
11.
Common fragile sites (CFS) and extremely large CFS genes are targets for human papillomavirus integrations and chromosome rearrangements in oropharyngeal squamous cell carcinoma.
Genes Chromosomes Cancer
; 56(1): 59-74, 2017 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-27636103
12.
Genomic rearrangements in sporadic lymphangioleiomyomatosis: an evolving genetic story.
Mod Pathol
; 30(9): 1223-1233, 2017 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-28643793
13.
TFEB-VEGFA (6p21.1) co-amplified renal cell carcinoma: a distinct entity with potential implications for clinical management.
Mod Pathol
; 30(7): 998-1012, 2017 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-28338654
14.
Integrated analysis of the genomic instability of PTEN in clinically insignificant and significant prostate cancer.
Mod Pathol
; 29(2): 143-56, 2016 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-26612463
15.
Chromosomal rearrangements and copy number abnormalities of TP63 correlate with p63 protein expression in lung adenocarcinoma.
Mod Pathol
; 28(3): 359-66, 2015 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-25189640
16.
BIMA V3: an aligner customized for mate pair library sequencing.
Bioinformatics
; 30(11): 1627-9, 2014 Jun 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-24526710
17.
Genome-wide analysis reveals recurrent structural abnormalities of TP63 and other p53-related genes in peripheral T-cell lymphomas.
Blood
; 120(11): 2280-9, 2012 Sep 13.
Artigo
em Inglês
| MEDLINE | ID: mdl-22855598
18.
Novel TRAF1-ALK fusion identified by deep RNA sequencing of anaplastic large cell lymphoma.
Genes Chromosomes Cancer
; 52(11): 1097-102, 2013 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-23999969
19.
Discovery of recurrent t(6;7)(p25.3;q32.3) translocations in ALK-negative anaplastic large cell lymphomas by massively parallel genomic sequencing.
Blood
; 117(3): 915-9, 2011 Jan 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-21030553
20.
Identification of submicroscopic genetic changes and precise breakpoint mapping in myelofibrosis using high resolution mate-pair sequencing.
Am J Hematol
; 88(9): 741-6, 2013 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-23733509