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1.
Population-specific validation and comparison of the performance of 77- and 313-variant polygenic risk scores for breast cancer risk prediction.
Cancer
; 2024 May 08.
Artículo
en Inglés
| MEDLINE | ID: mdl-38718029
2.
Implementing mainstream genetic counseling within the area-wide network of the German Consortium Hereditary Breast and Ovarian Cancer (GC-HBOC): Satisfaction of primary care providers with the provided state-of-the-art training by the Cologne Center.
J Genet Couns
; 33(1): 206-215, 2024 02.
Artículo
en Inglés
| MEDLINE | ID: mdl-38351721
3.
Impact of nirsevimab prophylaxis on paediatric respiratory syncytial virus (RSV)-related hospitalisations during the initial 2023/24 season in Luxembourg.
Euro Surveill
; 29(4)2024 Jan.
Artículo
en Inglés
| MEDLINE | ID: mdl-38275017
4.
Sensitivity and specificity of loss of heterozygosity analysis for the classification of rare germline variants in BRCA1/2: results of the observational AGO-TR1 study (NCT02222883).
J Med Genet
; 59(3): 248-252, 2022 03.
Artículo
en Inglés
| MEDLINE | ID: mdl-33273034
5.
Polygenic risk scores indicate extreme ages at onset of breast cancer in female BRCA1/2 pathogenic variant carriers.
BMC Cancer
; 22(1): 706, 2022 Jun 27.
Artículo
en Inglés
| MEDLINE | ID: mdl-35761208
6.
Increasing risk of breakthrough COVID-19 in outbreaks with high attack rates in European long-term care facilities, July to October 2021.
Euro Surveill
; 26(49)2021 12.
Artículo
en Inglés
| MEDLINE | ID: mdl-34886946
7.
[HerediCaRe: Documentation and IT Solution of a Specialized Registry for Hereditary Breast and Ovarian Cancer]. / HerediCaRe: Dokumentations- und IT-Lösung eines spezialisierten Registers für erblichen Brust- und Eierstockkrebs.
Gesundheitswesen
; 83(S 01): S12-S17, 2021 Nov.
Artículo
en Alemán
| MEDLINE | ID: mdl-34731888
8.
Deleterious somatic variants in 473 consecutive individuals with ovarian cancer: results of the observational AGO-TR1 study (NCT02222883).
J Med Genet
; 56(9): 574-580, 2019 09.
Artículo
en Inglés
| MEDLINE | ID: mdl-30979843
9.
Germline loss-of-function variants in the BARD1 gene are associated with early-onset familial breast cancer but not ovarian cancer.
Breast Cancer Res
; 21(1): 55, 2019 04 29.
Artículo
en Inglés
| MEDLINE | ID: mdl-31036035
10.
Diagnosis of Li-Fraumeni Syndrome: Differentiating TP53 germline mutations from clonal hematopoiesis: Results of the observational AGO-TR1 trial.
Hum Mutat
; 39(12): 2040-2046, 2018 12.
Artículo
en Inglés
| MEDLINE | ID: mdl-30216591
11.
BRIP1 loss-of-function mutations confer high risk for familial ovarian cancer, but not familial breast cancer.
Breast Cancer Res
; 20(1): 7, 2018 01 24.
Artículo
en Inglés
| MEDLINE | ID: mdl-29368626
12.
How to make a tumour: cell type specific dissection of Ustilago maydis-induced tumour development in maize leaves.
New Phytol
; 217(4): 1681-1695, 2018 03.
Artículo
en Inglés
| MEDLINE | ID: mdl-29314018
13.
EDGAR 2.0: an enhanced software platform for comparative gene content analyses.
Nucleic Acids Res
; 44(W1): W22-8, 2016 Jul 08.
Artículo
en Inglés
| MEDLINE | ID: mdl-27098043
14.
The GPRC5A frameshift variant c.183del is not associated with increased breast cancer risk in BRCA1 mutation carriers.
Int J Cancer
; 144(7): 1761-1763, 2019 04 01.
Artículo
en Inglés
| MEDLINE | ID: mdl-30474284
15.
Olaparib Addition to Maintenance Bevacizumab Therapy in Ovarian Carcinoma With BRCA-Like Genomic Aberrations.
JAMA Netw Open
; 7(4): e245552, 2024 Apr 01.
Artículo
en Inglés
| MEDLINE | ID: mdl-38592722
16.
Clinical implications of incorporating genetic and non-genetic risk factors in CanRisk-based breast cancer risk prediction.
Breast
; 73: 103615, 2024 Feb.
Artículo
en Inglés
| MEDLINE | ID: mdl-38061307
17.
A deep intronic recurrent CHEK2 variant c.1009-118_1009-87delinsC affects pre-mRNA splicing and contributes to hereditary breast cancer predisposition.
Breast
; 75: 103721, 2024 Jun.
Artículo
en Inglés
| MEDLINE | ID: mdl-38554551
18.
A Molecular and Epidemiological Investigation of a Large SARS-CoV-2 Outbreak in a Long-Term Care Facility in Luxembourg, 2021.
Geriatrics (Basel)
; 8(1)2023 Jan 26.
Artículo
en Inglés
| MEDLINE | ID: mdl-36826361
19.
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.
Artículo
en Inglés
| MEDLINE | ID: mdl-37449874
20.
Clonal Hematopoiesis-Associated Gene Mutations in a Clinical Cohort of 448 Patients With Ovarian Cancer.
J Natl Cancer Inst
; 114(4): 565-570, 2022 04 11.
Artículo
en Inglés
| MEDLINE | ID: mdl-34963005