Detalhe da pesquisa
1.
Single-cell mutation analysis of clonal evolution in myeloid malignancies.
Nature;
587(7834): 477-482, 2020 11.
Artigo
em Inglês
| MEDLINE
| ID: mdl-33116311
2.
Author Correction: Tumour lineage shapes BRCA-mediated phenotypes.
Nature;
577(7789): E1, 2020 01.
Artigo
em Inglês
| MEDLINE
| ID: mdl-31822847
3.
Tumour lineage shapes BRCA-mediated phenotypes.
Nature;
571(7766): 576-579, 2019 07.
Artigo
em Inglês
| MEDLINE
| ID: mdl-31292550
4.
Universal germline genetic testing in patients with hematologic malignancies using DNA isolated from nail clippings.
Haematologica;
2024 Apr 04.
Artigo
em Inglês
| MEDLINE
| ID: mdl-38572560
5.
Cell-free DNA from nail clippings as source of normal control for genomic studies in hematologic malignancies.
Haematologica;
2024 Mar 07.
Artigo
em Inglês
| MEDLINE
| ID: mdl-38450530
6.
Genomic profiling identifies somatic mutations predicting thromboembolic risk in patients with solid tumors.
Blood;
137(15): 2103-2113, 2021 04 15.
Artigo
em Inglês
| MEDLINE
| ID: mdl-33270827
7.
Disparities in cancer genetics care by race/ethnicity among pan-cancer patients with pathogenic germline variants.
Cancer;
128(21): 3870-3879, 2022 11 01.
Artigo
em Inglês
| MEDLINE
| ID: mdl-36041233
8.
Evaluation of a Combined Multilocus Sequence Typing and Whole-Genome Sequencing Two-Step Algorithm for Routine Typing of Clostridioides difficile.
J Clin Microbiol;
59(2)2021 01 21.
Artigo
em Inglês
| MEDLINE
| ID: mdl-33177119
9.
Mesonephric and mesonephric-like carcinomas of the female genital tract: molecular characterization including cases with mixed histology and matched metastases.
Mod Pathol;
34(8): 1570-1587, 2021 08.
Artigo
em Inglês
| MEDLINE
| ID: mdl-33772212
10.
Next-generation assessment of human epidermal growth factor receptor 2 gene (ERBB2) amplification status in invasive breast carcinoma: a focus on Group 4 by use of the 2018 American Society of Clinical Oncology/College of American Pathologists HER2 testing guideline.
Histopathology;
78(4): 498-507, 2021 Mar.
Artigo
em Inglês
| MEDLINE
| ID: mdl-32841416
11.
Genetic and molecular subtype heterogeneity in newly diagnosed early- and advanced-stage endometrial cancer.
Gynecol Oncol;
161(2): 535-544, 2021 05.
Artigo
em Inglês
| MEDLINE
| ID: mdl-33622519
12.
Fumarate hydratase FH c.1431_1433dupAAA (p.Lys477dup) variant is not associated with cancer including renal cell carcinoma.
Hum Mutat;
41(1): 103-109, 2020 01.
Artigo
em Inglês
| MEDLINE
| ID: mdl-31444830
13.
Molecular profiling and analysis of genetic aberrations aimed at identifying potential therapeutic targets in fibrolamellar carcinoma of the liver.
Cancer;
126(18): 4126-4135, 2020 09 15.
Artigo
em Inglês
| MEDLINE
| ID: mdl-32663328
14.
Retained mismatch repair protein expression occurs in approximately 6% of microsatellite instability-high cancers and is associated with missense mutations in mismatch repair genes.
Mod Pathol;
33(5): 871-879, 2020 05.
Artigo
em Inglês
| MEDLINE
| ID: mdl-31857677
15.
NTRK fusion detection across multiple assays and 33,997 cases: diagnostic implications and pitfalls.
Mod Pathol;
33(1): 38-46, 2020 01.
Artigo
em Inglês
| MEDLINE
| ID: mdl-31375766
16.
Ampullary cancer: Evaluation of somatic and germline genetic alterations and association with clinical outcomes.
Cancer;
125(9): 1441-1448, 2019 05 01.
Artigo
em Inglês
| MEDLINE
| ID: mdl-30620386
17.
Inherited DNA-Repair Gene Mutations in Men with Metastatic Prostate Cancer.
N Engl J Med;
375(5): 443-53, 2016 Aug 04.
Artigo
em Inglês
| MEDLINE
| ID: mdl-27433846
18.
Immunohistochemical analysis of estrogen receptor in breast cancer with ESR1 mutations detected by hybrid capture-based next-generation sequencing.
Mod Pathol;
32(1): 81-87, 2019 01.
Artigo
em Inglês
| MEDLINE
| ID: mdl-30158597
19.
The value of cell-free DNA for molecular pathology.
J Pathol;
244(5): 616-627, 2018 04.
Artigo
em Inglês
| MEDLINE
| ID: mdl-29380875
20.
A FISH assay efficiently screens for BRAF gene rearrangements in pancreatic acinar-type neoplasms.
Mod Pathol;
31(1): 132-140, 2018 01.
Artigo
em Inglês
| MEDLINE
| ID: mdl-28884748