Detalhe da pesquisa
1.
Loss of ribonuclease DIS3 hampers genome integrity in myeloma by disrupting DNA:RNA hybrid metabolism.
EMBO J
; 41(22): e108040, 2022 11 17.
Artigo
em Inglês
| MEDLINE | ID: mdl-36215697
2.
Meta-analysis of breast cancer risk for individuals with PALB2 pathogenic variants.
Genet Epidemiol
; 2024 Apr 23.
Artigo
em Inglês
| MEDLINE | ID: mdl-38654400
3.
High-dose melphalan treatment significantly increases mutational burden at relapse in multiple myeloma.
Blood
; 141(14): 1724-1736, 2023 04 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-36603186
4.
The Pancreatic Cancer Early Detection (PRECEDE) Study is a Global Effort to Drive Early Detection: Baseline Imaging Findings in High-Risk Individuals.
J Natl Compr Canc Netw
; 22(3): 158-166, 2024 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-38626807
5.
Bayesian meta-analysis of penetrance for cancer risk.
Biometrics
; 80(2)2024 Mar 27.
Artigo
em Inglês
| MEDLINE | ID: mdl-38819308
6.
Rejoinder to the discussion on "Bayesian meta-analysis of penetrance for cancer risk".
Biometrics
; 80(2)2024 Mar 27.
Artigo
em Inglês
| MEDLINE | ID: mdl-38819314
7.
Optimal ensemble construction for multistudy prediction with applications to mortality estimation.
Stat Med
; 43(9): 1774-1789, 2024 Apr 30.
Artigo
em Inglês
| MEDLINE | ID: mdl-38396313
8.
Statistical methods for Mendelian models with multiple genes and cancers.
Genet Epidemiol
; 46(7): 395-414, 2022 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-35583099
9.
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
10.
IgM-MM is predominantly a pre-germinal center disorder and has a distinct genomic and transcriptomic signature from WM.
Blood
; 138(20): 1980-1985, 2021 11 18.
Artigo
em Inglês
| MEDLINE | ID: mdl-34792571
11.
BRCA1 recruitment to transcriptional pause sites is required for R-loop-driven DNA damage repair.
Mol Cell
; 57(4): 636-647, 2015 Feb 19.
Artigo
em Inglês
| MEDLINE | ID: mdl-25699710
12.
Statistical approaches for meta-analysis of genetic mutation prevalence.
Genet Epidemiol
; 45(2): 154-170, 2021 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-33000511
13.
Variation in cancer risk among families with genetic susceptibility.
Genet Epidemiol
; 45(2): 209-221, 2021 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-33030277
14.
Validity and Relative Validity of Alternative Methods of Assessing Physical Activity in Epidemiologic Studies: Findings From the Men's Lifestyle Validation Study.
Am J Epidemiol
; 191(7): 1307-1322, 2022 06 27.
Artigo
em Inglês
| MEDLINE | ID: mdl-35292800
15.
Robustifying genomic classifiers to batch effects via ensemble learning.
Bioinformatics
; 37(11): 1521-1527, 2021 07 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-33245114
16.
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
17.
Practical implementation of frailty models in Mendelian risk prediction.
Genet Epidemiol
; 44(6): 564-578, 2020 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-32506746
18.
A risk prediction tool for individuals with a family history of breast, ovarian, or pancreatic cancer: BRCAPANCPRO.
Br J Cancer
; 125(12): 1712-1717, 2021 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-34703010
19.
The impact of different sources of heterogeneity on loss of accuracy from genomic prediction models.
Biostatistics
; 21(2): 253-268, 2020 04 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-30202918
20.
A likelihood-based approach to assessing frequency of pathogenicity among variants of unknown significance in susceptibility genes.
Stat Med
; 40(3): 593-606, 2021 02 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-33120437