Detalhe da pesquisa
1.
Turning the Page on Breast Cancer in Ohio: Lessons learned from implementing a multilevel intervention to reduce breast cancer mortality among Black women.
Cancer
; 129(S19): 3114-3127, 2023 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-37691524
2.
Ovarian cancer pathology characteristics as predictors of variant pathogenicity in BRCA1 and BRCA2.
Br J Cancer
; 128(12): 2283-2294, 2023 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-37076566
3.
Molecular Characteristics of Early-Onset Colorectal Cancer According to Detailed Anatomical Locations: Comparison With Later-Onset Cases.
Am J Gastroenterol
; 118(4): 712-726, 2023 04 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-36707929
4.
Diabetes mellitus in relation to colorectal tumor molecular subtypes: A pooled analysis of more than 9000 cases.
Int J Cancer
; 151(3): 348-360, 2022 08 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-35383926
5.
Risks of breast and ovarian cancer for women harboring pathogenic missense variants in BRCA1 and BRCA2 compared with those harboring protein truncating variants.
Genet Med
; 24(1): 119-129, 2022 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-34906479
6.
Genetic architectures of proximal and distal colorectal cancer are partly distinct.
Gut
; 70(7): 1325-1334, 2021 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-33632709
7.
The p.Ser64Leu and p.Pro104Leu missense variants of PALB2 identified in familial pancreatic cancer patients compromise the DNA damage response.
Hum Mutat
; 42(2): 150-163, 2021 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-33169439
8.
Metastatic breast cancer patient perceptions of somatic tumor genomic testing.
BMC Cancer
; 20(1): 389, 2020 May 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-32375690
9.
Maternal age at delivery and fertility of the next generation.
Paediatr Perinat Epidemiol
; 34(6): 629-636, 2020 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-32150298
10.
BRCA1 and BRCA2 pathogenic sequence variants in women of African origin or ancestry.
Hum Mutat
; 40(10): 1781-1796, 2019 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-31112363
11.
BRCA1/2 Functional Loss Defines a Targetable Subset in Leiomyosarcoma.
Oncologist
; 24(7): 973-979, 2019 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-30541756
12.
Single Nucleotide Polymorphisms in ß-Carotene Oxygenase 1 are Associated with Plasma Lycopene Responses to a Tomato-Soy Juice Intervention in Men with Prostate Cancer.
J Nutr
; 149(3): 381-397, 2019 03 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-30801647
13.
Understanding BRCA Mutation Carriers' Preferences for Communication of Genetic Modifiers of Breast Cancer Risk.
J Health Commun
; 24(4): 377-384, 2019.
Artigo
em Inglês
| MEDLINE | ID: mdl-31060454
14.
Expanding the feasibility of large genomic skin studies using epidermal DNA collected via tape stripping.
Br J Dermatol
; 189(6): 654-655, 2023 11 16.
Artigo
em Inglês
| MEDLINE | ID: mdl-37739394
15.
Operationalizing the Reciprocal Engagement Model of Genetic Counseling Practice: a Framework for the Scalable Delivery of Genomic Counseling and Testing.
J Genet Couns
; 27(5): 1111-1129, 2018 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-29460110
16.
Breast-cancer risk in families with mutations in PALB2.
N Engl J Med
; 371(6): 497-506, 2014 Aug 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-25099575
17.
Risks of breast and ovarian cancer for women harboring pathogenic missense variants in BRCA1 and BRCA2 compared with those harboring protein truncating variants.
Genet Med
; 24(10): 2208, 2022 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-36205748
18.
Counselees' Perspectives of Genomic Counseling Following Online Receipt of Multiple Actionable Complex Disease and Pharmacogenomic Results: a Qualitative Research Study.
J Genet Couns
; 26(4): 738-751, 2017 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-27921197
19.
Functional Analysis of BARD1 Missense Variants in Homology-Directed Repair of DNA Double Strand Breaks.
Hum Mutat
; 36(12): 1205-14, 2015 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-26350354
20.
Lessons learned from two decades of BRCA1 and BRCA2 genetic testing: the evolution of data sharing and variant classification.
Genet Med
; 21(7): 1476-1480, 2019 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-30474649