Detalhe da pesquisa
1.
Author Correction: Tumour lineage shapes BRCA-mediated phenotypes.
Nature
; 577(7789): E1, 2020 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-31822847
2.
Tumour lineage shapes BRCA-mediated phenotypes.
Nature
; 571(7766): 576-579, 2019 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-31292550
3.
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
4.
Pathogenic germline variants in non-BRCA1/2 homologous recombination genes in ovarian cancer: Analysis of tumor phenotype and survival.
Gynecol Oncol
; 180: 35-43, 2024 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-38041901
5.
Unique Genomic Alterations and Microbial Profiles Identified in Patients With Gastric Cancer of African, European, and Asian Ancestry: A Novel Path for Precision Oncology.
Ann Surg
; 278(4): 506-518, 2023 10 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-37436885
6.
Clinical Impact of a Rapid Genetic Testing Model for Advanced Prostate Cancer Patients.
J Urol
; 209(5): 918-927, 2023 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-36974724
7.
Factors associated with detection of hereditary diffuse gastric cancer on endoscopy in individuals with germline CDH1 mutations.
Gastrointest Endosc
; 98(3): 326-336.e3, 2023 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-37094689
8.
Characteristics of Mismatch Repair-Deficient Colon Cancer in Relation to Mismatch Repair Protein Loss, Hypermethylation Silencing, and Constitutional and Biallelic Somatic Mismatch Repair Gene Pathogenic Variants.
Dis Colon Rectum
; 66(4): 549-558, 2023 04 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-35724254
9.
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
10.
Survival After Induction Chemotherapy and Chemoradiation Versus Chemoradiation and Adjuvant Chemotherapy for Locally Advanced Rectal Cancer.
Oncologist
; 27(5): 380-388, 2022 05 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-35278070
11.
Perceptions of patients and medical oncologists toward biospecimen donation in the setting of abnormal breast imaging findings.
Breast Cancer Res Treat
; 192(1): 201-210, 2022 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-35066788
12.
An updated counseling framework for moderate-penetrance colorectal cancer susceptibility genes.
Genet Med
; 24(12): 2587-2590, 2022 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-36222830
13.
Early age of onset and broad cancer spectrum persist in MSH6- and PMS2-associated Lynch syndrome.
Genet Med
; 24(6): 1187-1195, 2022 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-35346574
14.
A validation of models for prediction of pathogenic variants in mismatch repair genes.
Genet Med
; 24(10): 2155-2166, 2022 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-35997715
15.
Effectiveness of a surveillance program of upper endoscopy for upper gastrointestinal cancers in Lynch syndrome patients.
Int J Colorectal Dis
; 37(1): 231-238, 2022 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-34698909
16.
Attitudes toward preimplantation genetic testing and quality of life among individuals with hereditary diffuse gastric cancer syndrome.
Hered Cancer Clin Pract
; 20(1): 31, 2022 Sep 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-36056367
17.
Insertion of an SVA element in MSH2 as a novel cause of Lynch syndrome.
Genes Chromosomes Cancer
; 60(8): 571-576, 2021 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-33822432
18.
Perceptions of patients with early stage breast cancer toward research biopsies.
Cancer
; 127(8): 1208-1219, 2021 04 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-33320362
19.
Pancreas cancer and BRCA: A critical subset of patients with improving therapeutic outcomes.
Cancer
; 127(23): 4393-4402, 2021 12 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-34351646
20.
The RAD51D c.82G>A (p.Val28Met) variant disrupts normal splicing and is associated with hereditary ovarian cancer.
Breast Cancer Res Treat
; 185(3): 869-877, 2021 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-33452952