Detalhe da pesquisa
1.
Systematic evidence review and meta-analysis of outcomes associated with cancer genetic counseling.
Genet Med
; 26(1): 100980, 2024 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-37688462
2.
Clinical implications of conflicting variant interpretations in the cancer genetics clinic.
Genet Med
; 25(7): 100837, 2023 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-37057674
3.
Integration of Universal Germline Genetic Testing for All New Breast Cancer Patients.
Ann Surg Oncol
; 30(2): 1017-1025, 2023 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-36161375
4.
Clinical and laboratory genetic counselor attitudes on the reporting of variants of uncertain significance for multigene cancer panels.
J Genet Couns
; 32(3): 706-716, 2023 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-36747331
5.
Transcriptome analysis provides critical answers to the "variants of uncertain significance" conundrum.
Hum Mutat
; 43(11): 1590-1608, 2022 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-35510381
6.
Psychosocial outcomes following germline multigene panel testing in an ethnically and economically diverse cohort of patients.
Cancer
; 127(8): 1275-1285, 2021 04 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-33320347
7.
Inhibition of poly(ADP-ribose) polymerase induces synthetic lethality in BRIP1 deficient ovarian epithelial cells.
Gynecol Oncol
; 159(3): 869-876, 2020 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-33032822
8.
ASO Author Reflections: A Green Light for Genetic Testing in All Patients with Breast Cancer.
Ann Surg Oncol
; 30(2): 1026-1027, 2023 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-36241948
9.
ASO Visual Abstract: Integration of Universal Germline Genetic Testing for All New Breast Cancer Patients.
Ann Surg Oncol
; 30(2): 1028, 2023 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-36319870
10.
Genetics, genomics, and cancer risk assessment: State of the Art and Future Directions in the Era of Personalized Medicine.
CA Cancer J Clin
; 61(5): 327-59, 2011.
Artigo
em Inglês
| MEDLINE | ID: mdl-21858794
11.
Essential elements of genetic cancer risk assessment, counseling, and testing: updated recommendations of the National Society of Genetic Counselors.
J Genet Couns
; 21(2): 151-61, 2012 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-22134580
12.
Closing the loop: action research in a multimodal hereditary cancer patient conference is an effective tool to assess and address patient needs.
J Cancer Educ
; 27(3): 467-77, 2012 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-22610836
13.
Risk of colorectal and endometrial cancers in EPCAM deletion-positive Lynch syndrome: a cohort study.
Lancet Oncol
; 12(1): 49-55, 2011 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-21145788
14.
Risk-reducing mastectomy decisions among women with mutations in high- and moderate- penetrance breast cancer susceptibility genes.
Mol Genet Genomic Med
; 10(10): e2031, 2022 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-36054727
15.
Recurrence and variability of germline EPCAM deletions in Lynch syndrome.
Hum Mutat
; 32(4): 407-14, 2011 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-21309036
16.
Personalized cancer genetics training for personalized medicine: improving community-based healthcare through a genetically literate workforce.
Genet Med
; 13(9): 832-40, 2011 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-21629123
17.
Development and evaluation of a decision aid for BRCA carriers with breast cancer.
J Genet Couns
; 20(3): 294-307, 2011 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-21369831
18.
Cancer Risks Associated With Germline PALB2 Pathogenic Variants: An International Study of 524 Families.
J Clin Oncol
; 38(7): 674-685, 2020 03 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-31841383
19.
Breast cancer risk communication: assessment of primary care physicians by standardized patients.
Genet Med
; 11(10): 735-41, 2009 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-19661809
20.
Multicenter Prospective Cohort Study of the Diagnostic Yield and Patient Experience of Multiplex Gene Panel Testing For Hereditary Cancer Risk.
JCO Precis Oncol
; 32019 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-34322651