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Corinna Ernst

Explore the profile of Corinna Ernst including associated specialties, affiliations and a list of published articles. Areas
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Articles 34
Citations 816
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Recent Articles
1.
Richters L, Gluz O, Weber-Lassalle N, Christgen M, Haverkamp H, Kuemmel S, et al.
JAMA Netw Open . 2025 Feb; 8(2):e2461639. PMID: 40009381
Importance: Subgroup definitions for possible deescalation of neoadjuvant cancer treatment are urgently needed in clinical practice. Objective: To investigate the effect of BRCA1 and/or BRCA2 tumor pathogenic variants (tPVs) by...
2.
Baumann A, Ruckert C, Meier C, Hutschenreiter T, Remy R, Schnur B, et al.
Eur J Hum Genet . 2024 Jun; 32(8):987-997. PMID: 38907004
Considering polygenic risk scores (PRSs) in individual risk prediction is increasingly implemented in genetic testing for hereditary breast cancer (BC) based on next-generation sequencing (NGS). To calculate individual BC risks,...
3.
Bejko D, Ernst C, Vergison A, Stranges S, Zeegers M, Mossong J
Vaccine . 2024 Jun; 42(22):126011. PMID: 38825555
Background: Luxembourg experienced major consecutive SARS-CoV-2 infection waves due to Omicron variants during 2022 while having achieved a high vaccination coverage in 2021. We investigated the risk factors associated to...
4.
Hovhannisyan M, Zemankova P, Nehasil P, Matejkova K, Borecka M, cerna M, et al.
Cancer . 2024 May; 130(17):2978-2987. PMID: 38718029
Background: The polygenic risk score (PRS) allows the quantification of the polygenic effect of many low-penetrance alleles on the risk of breast cancer (BC). This study aimed to evaluate the...
5.
Schouten P, Schmidt S, Becker K, Thiele H, Nurnberg P, Richters L, et al.
JAMA Netw Open . 2024 Apr; 7(4):e245552. PMID: 38592722
Importance: Testing for homologous recombination deficiency is required for the optimal treatment of high-grade epithelial ovarian cancer. The search for accurate biomarkers is ongoing. Objective: To investigate whether progression-free survival...
6.
Zemankova P, cerna M, Horackova K, Ernst C, Soukupova J, Borecka M, et al.
Breast . 2024 Mar; 75:103721. PMID: 38554551
Germline CHEK2 pathogenic variants confer an increased risk of female breast cancer (FBC). Here we describe a recurrent germline intronic variant c.1009-118_1009-87delinsC, which showed a splice acceptor shift in RNA...
7.
Herold N, Bredow K, Ernst C, Tuchler A, Blumcke B, Waha A, et al.
J Genet Couns . 2024 Feb; 33(1):206-215. PMID: 38351721
The German Cancer Society (Deutsche Krebsgesellschaft DKG) has published a position paper to address the challenges of cancer patient care in the era of genomic medicine. The German Consortium Hereditary...
8.
Ernst C, Bejko D, Gaasch L, Hannelas E, Kahn I, Pierron C, et al.
Euro Surveill . 2024 Jan; 29(4). PMID: 38275017
After Luxembourg introduced nirsevimab immunisation against respiratory syncytial virus (RSV), estimated neonatal coverage was 84% (1,277 doses/1,524 births) in 2023. That year, paediatric RSV-related hospitalisations, especially concerning infants < 6 ...
9.
Tuchler A, de Pauw A, Ernst C, Anota A, Lakeman I, Dick J, et al.
Breast . 2023 Dec; 73:103615. PMID: 38061307
Background: Breast cancer (BC) risk prediction models consider cancer family history (FH) and germline pathogenic variants (PVs) in risk genes. It remains elusive to what extent complementation with polygenic risk...
10.
Stolarova L, Kleiblova P, Zemankova P, Stastna B, Janatova M, Soukupova J, et al.
Clin Cancer Res . 2023 Jul; 29(16):3037-3050. PMID: 37449874
Purpose: Germline pathogenic variants in CHEK2 confer moderately elevated breast cancer risk (odds ratio, OR ∼ 2.5), qualifying carriers for enhanced breast cancer screening. Besides pathogenic variants, dozens of missense...