Detalhe da pesquisa
1.
Genetic insights into biological mechanisms governing human ovarian ageing.
Nature
; 596(7872): 393-397, 2021 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-34349265
2.
The impact of coding germline variants on contralateral breast cancer risk and survival.
Am J Hum Genet
; 110(3): 475-486, 2023 03 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-36827971
3.
Functional annotation of the 2q35 breast cancer risk locus implicates a structural variant in influencing activity of a long-range enhancer element.
Am J Hum Genet
; 108(7): 1190-1203, 2021 07 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-34146516
4.
Disentangling the relationships of body mass index and circulating sex hormone concentrations in mammographic density using Mendelian randomization.
Breast Cancer Res Treat
; 2024 Apr 24.
Artigo
em Inglês
| MEDLINE | ID: mdl-38653906
5.
Evaluation of European-based polygenic risk score for breast cancer in Ashkenazi Jewish women in Israel.
J Med Genet
; 60(12): 1186-1197, 2023 Nov 27.
Artigo
em Inglês
| MEDLINE | ID: mdl-37451831
6.
A likelihood ratio approach for utilizing case-control data in the clinical classification of rare sequence variants: application to BRCA1 and BRCA2.
Hum Mutat
; 20232023.
Artigo
em Inglês
| MEDLINE | ID: mdl-38725546
7.
Associations of height, body mass index, and weight gain with breast cancer risk in carriers of a pathogenic variant in BRCA1 or BRCA2: the BRCA1 and BRCA2 Cohort Consortium.
Breast Cancer Res
; 25(1): 72, 2023 06 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-37340476
8.
A genome-wide gene-environment interaction study of breast cancer risk for women of European ancestry.
Breast Cancer Res
; 25(1): 93, 2023 08 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-37559094
9.
Functional genomics of human clear cell sarcoma: genomic, transcriptomic and chemical biology landscape for clear cell sarcoma.
Br J Cancer
; 128(10): 1941-1954, 2023 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-36959380
10.
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
11.
Breast Cancer Polygenic Risk Score and Contralateral Breast Cancer Risk.
Am J Hum Genet
; 107(5): 837-848, 2020 11 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-33022221
12.
Polymorphisms in genes of melatonin biosynthesis and signaling support the light-at-night hypothesis for breast cancer.
Eur J Epidemiol
; 38(10): 1053-1068, 2023 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-37789226
13.
Common variants in breast cancer risk loci predispose to distinct tumor subtypes.
Breast Cancer Res
; 24(1): 2, 2022 01 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-34983606
14.
Polygenic Risk Scores for Prediction of Breast Cancer and Breast Cancer Subtypes.
Am J Hum Genet
; 104(1): 21-34, 2019 01 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-30554720
15.
Adherence to the 2020 American Cancer Society Guideline for Cancer Prevention and risk of breast cancer for women at increased familial and genetic risk in the Breast Cancer Family Registry: an evaluation of the weight, physical activity, and alcohol consumption recommendations.
Breast Cancer Res Treat
; 194(3): 673-682, 2022 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-35780210
16.
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
17.
Mother and Daughter Perspectives on Genetic Counseling and Testing of Adolescents for Hereditary Breast Cancer Risk.
J Pediatr
; 251: 113-119.e7, 2022 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-35777474
18.
Women's thoughts on receiving and sharing genetic information: Considerations for genetic counseling.
J Genet Couns
; 31(6): 1249-1260, 2022 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-35794807
19.
Physical activity, sedentary time and breast cancer risk: a Mendelian randomisation study.
Br J Sports Med
; 56(20): 1157-1170, 2022 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-36328784
20.
Gene-based and pathway-based testing for rare-variant association in affected sib pairs.
Genet Epidemiol
; 44(4): 368-381, 2020 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-32237178