Detalhe da pesquisa
1.
Adherence to Vitamin D Supplementation Recommendations for Breastfed Infants and Young Children: An Analysis of Canadian Community Health Survey Data Cycles From 2015 to 2018.
J Nutr
; 154(5): 1665-1675, 2024 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-38527736
2.
Racial differences in knowledge, attitudes, and sources of information about germline cancer genetic testing in the U.S.A.: An analysis of the health information National Trends Survey System.
Prev Med
; 178: 107779, 2024 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-37967620
3.
Pathogenic variants among females with breast cancer and a non-breast cancer reveal opportunities for cancer interception.
Breast Cancer Res Treat
; 200(1): 63-72, 2023 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-36856935
4.
The clinical and functional effects of TERT variants in myelodysplastic syndrome.
Blood
; 138(10): 898-911, 2021 09 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-34019641
5.
Prevalence and spectrum of pathogenic variants among patients with multiple primary cancers evaluated by clinical characteristics.
Cancer
; 128(6): 1275-1283, 2022 03 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-34875721
6.
CDH1 germline variants are enriched in patients with colorectal cancer, gastric cancer, and breast cancer.
Br J Cancer
; 126(5): 797-803, 2022 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-34949788
7.
Impact of Genetic Counseling on Patient-Reported Electronic Cancer Family History Collection.
J Natl Compr Canc Netw
; 20(8): 898-905.e2, 2022 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-35948032
8.
A polymorphism in the promoter of FRAS1 is a candidate SNP associated with metastatic prostate cancer.
Prostate
; 81(10): 683-693, 2021 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-33956343
9.
Embedding a genetic counselor into oncology clinics improves testing rates and timeliness for women with ovarian cancer.
Gynecol Oncol
; 160(2): 457-463, 2021 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-33229043
10.
Prevalence of pathogenic germline cancer risk variants in high-risk urothelial carcinoma.
Genet Med
; 22(4): 709-718, 2020 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-31844177
11.
Prevalence of germline variants in inflammatory breast cancer.
Cancer
; 125(13): 2194-2202, 2019 07 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-30933323
12.
Genotype-phenotype associations among panel-based TP53+ subjects.
Genet Med
; 21(11): 2478-2484, 2019 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-31105275
13.
Are rare cancer survivors at elevated risk of subsequent new cancers?
BMC Cancer
; 19(1): 166, 2019 Feb 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-30791872
14.
Trans-counseling: A case series of transgender individuals at high risk for BRCA1 pathogenic variants.
J Genet Couns
; 28(3): 708-716, 2019 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-30680866
15.
Correction to: Pathogenic variants among females with breast cancer and a nonbreast cancer reveal opportunities for cancer interception.
Breast Cancer Res Treat
; 200(1): 73, 2023 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-37178433
16.
Call for action: expanding global access to hereditary cancer genetic testing.
Lancet Oncol
; 23(9): 1124-1126, 2022 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-36055301
17.
Assigning clinical meaning to somatic and germ-line whole-exome sequencing data in a prospective cancer precision medicine study.
Genet Med
; 19(7): 787-795, 2017 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-28125075
18.
EPAS1 Mutations and Paragangliomas in Cyanotic Congenital Heart Disease.
N Engl J Med
; 378(13): 1259-1261, 2018 03 29.
Artigo
em Inglês
| MEDLINE | ID: mdl-29601261
19.
Genetic/Familial High-Risk Assessment: Breast and Ovarian, Version 2.2015.
J Natl Compr Canc Netw
; 14(2): 153-62, 2016 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-26850485
20.
Germline TP53 mutations and the changing landscape of Li-Fraumeni syndrome.
Hum Mutat
; 35(6): 654-62, 2014 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-24706533