Detalles de la búsqueda
1.
Universal germline genetic testing in patients with hematologic malignancies using DNA isolated from nail clippings.
Haematologica
; 2024 Apr 04.
Artículo
en Inglés
| MEDLINE | ID: mdl-38572560
2.
Cell-free DNA from nail clippings as source of normal control for genomic studies in hematologic malignancies.
Haematologica
; 2024 Mar 07.
Artículo
en Inglés
| MEDLINE | ID: mdl-38450530
3.
A validation of models for prediction of pathogenic variants in mismatch repair genes.
Genet Med
; 24(10): 2155-2166, 2022 10.
Artículo
en Inglés
| MEDLINE | ID: mdl-35997715
4.
Induction of sarcomas by mutant IDH2.
Genes Dev
; 27(18): 1986-98, 2013 Sep 15.
Artículo
en Inglés
| MEDLINE | ID: mdl-24065766
5.
Diagnosis of known sarcoma fusions and novel fusion partners by targeted RNA sequencing with identification of a recurrent ACTB-FOSB fusion in pseudomyogenic hemangioendothelioma.
Mod Pathol
; 32(5): 609-620, 2019 05.
Artículo
en Inglés
| MEDLINE | ID: mdl-30459475
6.
Frequent IDH2 R172 mutations in undifferentiated and poorly-differentiated sinonasal carcinomas.
J Pathol
; 242(4): 400-408, 2017 08.
Artículo
en Inglés
| MEDLINE | ID: mdl-28493366
7.
Mutation Detection in Patients With Advanced Cancer by Universal Sequencing of Cancer-Related Genes in Tumor and Normal DNA vs Guideline-Based Germline Testing.
JAMA
; 318(9): 825-835, 2017 09 05.
Artículo
en Inglés
| MEDLINE | ID: mdl-28873162
8.
Genomic aberrations frequently alter chromatin regulatory genes in chordoma.
Genes Chromosomes Cancer
; 55(7): 591-600, 2016 07.
Artículo
en Inglés
| MEDLINE | ID: mdl-27072194
9.
Novel oncogene and tumor suppressor mutations in KIT and PDGFRA wild type gastrointestinal stromal tumors revealed by next generation sequencing.
Genes Chromosomes Cancer
; 54(3): 177-84, 2015 Mar.
Artículo
en Inglés
| MEDLINE | ID: mdl-25427437
10.
Consistent copy number changes and recurrent PRKAR1A mutations distinguish Melanotic Schwannomas from Melanomas: SNP-array and next generation sequencing analysis.
Genes Chromosomes Cancer
; 54(8): 463-471, 2015 Aug.
Artículo
en Inglés
| MEDLINE | ID: mdl-26031761
11.
Additional Primary Malignancies in Patients with Gastrointestinal Stromal Tumor (GIST): A Clinicopathologic Study of 260 Patients with Molecular Analysis and Review of the Literature.
Ann Surg Oncol
; 22(8): 2633-9, 2015 Aug.
Artículo
en Inglés
| MEDLINE | ID: mdl-25564173
12.
The t(11;14)(q13;q32)/CCND1-IGH translocation in chronic lymphocytic leukaemia/small lymphocytic lymphoma: an unusual genetic aberration during the natural clinical course.
Histopathology
; 75(2): 291-294, 2019 08.
Artículo
en Inglés
| MEDLINE | ID: mdl-31021442
13.
Microsatellite Instability and Mismatch Repair Deficiency Define a Distinct Subset of Lung Cancers Characterized by Smoking Exposure, High Tumor Mutational Burden, and Recurrent Somatic MLH1 Inactivation.
J Thorac Oncol
; 19(3): 409-424, 2024 Mar.
Artículo
en Inglés
| MEDLINE | ID: mdl-37838086
14.
Quantification of Measurable Residual Disease Detection by Next-Generation Sequencing-Based Clonality Testing in B-Cell and Plasma Cell Neoplasms.
J Mol Diagn
; 26(3): 168-178, 2024 Mar.
Artículo
en Inglés
| MEDLINE | ID: mdl-38103591
15.
Validation of a High-Sensitivity Assay for Detection of Chimeric Antigen Receptor T-Cell Vectors Using Low-Partition Digital PCR Technology.
J Mol Diagn
; 25(9): 634-645, 2023 09.
Artículo
en Inglés
| MEDLINE | ID: mdl-37330049
16.
Clonal Characterization and Somatic Hypermutation Assessment by Next-Generation Sequencing in Chronic Lymphocytic Leukemia/Small Lymphocytic Lymphoma: A Detailed Description of the Technical Performance, Clinical Utility, and Platform Comparison.
J Mol Diagn
; 25(6): 352-366, 2023 06.
Artículo
en Inglés
| MEDLINE | ID: mdl-36963483
17.
Enhanced clinical assessment of hematologic malignancies through routine paired tumor and normal sequencing.
Nat Commun
; 14(1): 6895, 2023 10 28.
Artículo
en Inglés
| MEDLINE | ID: mdl-37898613
18.
Clinical Utility and Performance of an Ultrarapid Multiplex RNA-Based Assay for Detection of ALK, ROS1, RET, and NTRK1/2/3 Rearrangements and MET Exon 14 Skipping Alterations.
J Mol Diagn
; 24(6): 642-654, 2022 06.
Artículo
en Inglés
| MEDLINE | ID: mdl-35430374
19.
BRAF mutation analysis of fine-needle aspiration biopsies of papillary thyroid carcinoma: impact on diagnosis and prognosis.
Acta Cytol
; 55(6): 563-9, 2011.
Artículo
en Inglés
| MEDLINE | ID: mdl-22156467
20.
Rapid EGFR Mutation Detection Using the Idylla Platform: Single-Institution Experience of 1200 Cases Analyzed by an In-House Developed Pipeline and Comparison with Concurrent Next-Generation Sequencing Results.
J Mol Diagn
; 23(3): 310-322, 2021 03.
Artículo
en Inglés
| MEDLINE | ID: mdl-33346146