Detalhe da pesquisa
1.
Pathogenic germline variants in patients with endometrial cancer of diverse ancestry.
Cancer
; 130(4): 576-587, 2024 02 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-37886874
2.
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
3.
Nitrogen limitation and high density responses in rice suggest a role for ethylene under high density stress.
BMC Genomics
; 15: 681, 2014 Aug 13.
Artigo
em Inglês
| MEDLINE | ID: mdl-25128291
4.
Physiological and genetic analysis of Arabidopsis thaliana anthocyanin biosynthesis mutants under chronic adverse environmental conditions.
J Exp Bot
; 64(1): 229-40, 2013 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-23162120
5.
Characterization of a germline variant MSH6 c.4001G > C in a Lynch syndrome family.
Mol Genet Genomic Med
; 11(2): e2104, 2023 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-36691871
6.
Expanded genetic testing of GIST patients identifies high proportion of non-syndromic patients with germline alterations.
NPJ Precis Oncol
; 7(1): 1, 2023 Jan 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-36593350
7.
Genomic Profiling Reveals Germline Predisposition and Homologous Recombination Deficiency in Pancreatic Acinar Cell Carcinoma.
J Clin Oncol
; 41(33): 5151-5162, 2023 Nov 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-37607324
8.
Comprehensive analysis of germline drivers in endometrial cancer.
J Natl Cancer Inst
; 115(5): 560-569, 2023 05 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-36744932
9.
Diagnostic yield and clinical relevance of expanded genetic testing for cancer patients.
Genome Med
; 14(1): 92, 2022 08 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-35971132
10.
Morphologic and Genomic Characteristics of Breast Cancers Occurring in Individuals with Lynch Syndrome.
Clin Cancer Res
; 28(2): 404-413, 2022 01 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-34667028
11.
ATM Germline-Mutated Gastroesophageal Junction Adenocarcinomas: Clinical Descriptors, Molecular Characteristics, and Potential Therapeutic Implications.
J Natl Cancer Inst
; 114(5): 761-770, 2022 05 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-35078243
12.
Paired Tumor-Normal Sequencing Provides Insights Into the TP53-Related Cancer Spectrum in Patients With Li-Fraumeni Syndrome.
J Natl Cancer Inst
; 113(12): 1751-1760, 2021 11 29.
Artigo
em Inglês
| MEDLINE | ID: mdl-34240179
13.
Prevalence and Characterization of Biallelic and Monoallelic NTHL1 and MSH3 Variant Carriers From a Pan-Cancer Patient Population.
JCO Precis Oncol
; 52021.
Artigo
em Inglês
| MEDLINE | ID: mdl-34250384
14.
Assessing the Diagnostic Yield of Targeted Next-Generation Sequencing for Melanoma and Gastrointestinal Tumors.
J Mol Diagn
; 22(4): 467-475, 2020 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-32036084
15.
Somatic Tumor Variant Filtration Strategies to Optimize Tumor-Only Molecular Profiling Using Targeted Next-Generation Sequencing Panels.
J Mol Diagn
; 21(2): 261-273, 2019 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-30576869
16.
Improving validation methods for molecular diagnostics: application of Bland-Altman, Deming and simple linear regression analyses in assay comparison and evaluation for next-generation sequencing.
J Clin Pathol
; 71(2): 117-124, 2018 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-28747393
17.
Integration of Technical, Bioinformatic, and Variant Assessment Approaches in the Validation of a Targeted Next-Generation Sequencing Panel for Myeloid Malignancies.
Arch Pathol Lab Med
; 141(6): 759-775, 2017 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-28557600
18.
Comparison of Next-Generation Sequencing Panels and Platforms for Detection and Verification of Somatic Tumor Variants for Clinical Diagnostics.
J Mol Diagn
; 18(6): 842-850, 2016 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-27770852
19.
A Clinical Approach to Detecting Germline Pathogenic Variants From Tumor-Only Sequencing.
JNCI Cancer Spectr
; 4(3): pkaa019, 2020 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-32596634