Detalhe da pesquisa
1.
Functional analysis and clinical classification of 462 germline BRCA2 missense variants affecting the DNA binding domain.
Am J Hum Genet
; 111(3): 584-593, 2024 Mar 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-38417439
2.
A Population-Based Study of Genes Previously Implicated in Breast Cancer.
N Engl J Med
; 384(5): 440-451, 2021 02 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-33471974
3.
Progression and survival of MBL: a screening study of 10 139 individuals.
Blood
; 140(15): 1702-1709, 2022 10 13.
Artigo
em Inglês
| MEDLINE | ID: mdl-35969843
4.
Natural history of monoclonal B-cell lymphocytosis among relatives in CLL families.
Blood
; 137(15): 2046-2056, 2021 04 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-33512457
5.
Chronic lymphocytic leukemia (CLL) risk is mediated by multiple enhancer variants within CLL risk loci.
Hum Mol Genet
; 29(16): 2761-2774, 2020 09 29.
Artigo
em Inglês
| MEDLINE | ID: mdl-32744316
6.
Anthracycline treatment, cardiovascular risk factors and the cumulative incidence of cardiovascular disease in a cohort of newly diagnosed lymphoma patients from the modern treatment era.
Am J Hematol
; 96(8): 979-988, 2021 08 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-33971040
7.
Tumor mutational load predicts time to first treatment in chronic lymphocytic leukemia (CLL) and monoclonal B-cell lymphocytosis beyond the CLL international prognostic index.
Am J Hematol
; 95(8): 906-917, 2020 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-32279347
8.
Genomic evaluation of feed efficiency component traits in Duroc pigs using 80K, 650K and whole-genome sequence variants.
Genet Sel Evol
; 50(1): 14, 2018 04 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-29625549
9.
Not All SCID Pigs Are Created Equally: Two Independent Mutations in the Artemis Gene Cause SCID in Pigs.
J Immunol
; 195(7): 3171-9, 2015 Oct 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-26320255
10.
Identification of a putative quantitative trait nucleotide in guanylate binding protein 5 for host response to PRRS virus infection.
BMC Genomics
; 16: 412, 2015 May 28.
Artigo
em Inglês
| MEDLINE | ID: mdl-26016888
11.
Genome-wide association and genomic prediction for host response to porcine reproductive and respiratory syndrome virus infection.
Genet Sel Evol
; 46: 18, 2014 Mar 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-24592976
12.
Tumor mutational load is prognostic for progression to therapy among high-count monoclonal B-cell lymphocytosis.
Blood Adv
; 8(9): 2118-2129, 2024 May 14.
Artigo
em Inglês
| MEDLINE | ID: mdl-38359367
13.
Differences in polygenic score distributions in European ancestry populations: implications for breast cancer risk prediction.
medRxiv
; 2024 Feb 13.
Artigo
em Inglês
| MEDLINE | ID: mdl-38410445
14.
Differential prognosis of single and multiple TP53 abnormalities in high-count MBL and untreated CLL.
Blood Adv
; 7(13): 3169-3179, 2023 07 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-36877634
15.
Saturation genome editing-based functional evaluation and clinical classification of BRCA2 single nucleotide variants.
bioRxiv
; 2023 Dec 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-38168194
16.
Contralateral Breast Cancer Risk Among Carriers of Germline Pathogenic Variants in ATM, BRCA1, BRCA2, CHEK2, and PALB2.
J Clin Oncol
; 41(9): 1703-1713, 2023 03 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-36623243
17.
Functional and Clinical Characterization of Variants of Uncertain Significance Identifies a Hotspot for Inactivating Missense Variants in RAD51C.
Cancer Res
; 83(15): 2557-2571, 2023 08 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-37253112
18.
ENIGMA CHEK2gether Project: A Comprehensive Study Identifies Functionally Impaired CHEK2 Germline Missense Variants Associated with Increased Breast Cancer Risk.
Clin Cancer Res
; 29(16): 3037-3050, 2023 08 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-37449874
19.
Polygenic risk score and risk of monoclonal B-cell lymphocytosis in caucasians and risk of chronic lymphocytic leukemia (CLL) in African Americans.
Leukemia
; 36(1): 119-125, 2022 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-34285341
20.
Risk of Breast Cancer Among Carriers of Pathogenic Variants in Breast Cancer Predisposition Genes Varies by Polygenic Risk Score.
J Clin Oncol
; 39(23): 2564-2573, 2021 08 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-34101481