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Author Details
Full Name
Florentine S Hilbers
Affiliation
Netherlands Cancer Institute
ORCID
Career Start Year
2012
Papers
34
H Index
17
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
38059899
Pregnancy After Breast Cancer in Young BRCA Carriers: An International Hospital-Based Cohort Study.
JAMA
2024
37689749
High-dose alkylating chemotherapy in BRCA-altered triple-negative breast cancer: the randomized phase III NeoTN trial.
NPJ Breast Cancer
2023
34625860
Correction to: Tolerability and toxicity of trastuzumab or trastuzumabâ¿¿+â¿¿lapatinib in older patients: a subâ¿¿analysis of the ALTTO trial (BIG 2â¿¿06; NCCTG (Alliance) N063D).
Breast Cancer Res Treat
2022
35587322
Limiting systemic endocrine overtreatment in postmenopausal breast cancer patients with an ultralow classification of the 70-gene signature.
Breast Cancer Res Treat
2022
35610260
Adaptive immune signature in HER2-positive breast cancer in NCCTG (Alliance) N9831 and NeoALTTO trials.
NPJ Breast Cancer
2022
36126477
Ten-year follow-up of the observational RASTER study, prospective evaluation of the 70-gene signature in ER-positive, HER2-negative, node-negative, early breast cancer.
Eur J Cancer
2022
33787900
Tumor Cellularity and Infiltrating Lymphocytes as a Survival Surrogate in HER2-Positive Breast Cancer.
J Natl Cancer Inst
2022
35172272
Serum thymidine kinase activity in patients with hormone receptor-positive and HER2-negative metastatic breast cancer treated with palbociclib and fulvestrant.
Eur J Cancer
2022
32951084
Tolerability and toxicity of trastuzumab or trastuzumabâ¿¿+â¿¿lapatinib in older patients: a sub-analysis of the ALTTO trial (BIG 2-06; NCCTG (Alliance) N063D).
Breast Cancer Res Treat
2021
33721561
70-gene signature as an aid for treatment decisions in early breast cancer: updated results of the phase 3 randomised MINDACT trial with an exploratory analysis by age.
Lancet Oncol
2021
34183353
Genomic and Transcriptomic Analyses of Breast Cancer Primaries and Matched Metastases in AURORA, the Breast International Group (BIG) Molecular Screening Initiative.
Cancer Discov
2021
34312396
Evaluation of multiple transcriptomic gene risk signatures in male breast cancer.
NPJ Breast Cancer
2021
33401235
Body Mass Index and Weight Change in Patients With HER2-Positive Early Breast Cancer: Exploratory Analysis of the ALTTO BIG 2-06 Trial.
J Natl Compr Canc Netw
2021
32203207
Long-term cardiac outcomes of patients with HER2-positive breast cancer treated in the adjuvant lapatinib and/or trastuzumab Treatment Optimization Trial.
Br J Cancer
2020
32085669
Early Modulation of Circulating MicroRNAs Levels in HER2-Positive Breast Cancer Patients Treated with Trastuzumab-Based Neoadjuvant Therapy.
Int J Mol Sci
2020
32083990
Standard Anthracycline Based Versus Docetaxel-Capecitabine in Early High Clinical and/or Genomic Risk Breast Cancer in the EORTC 10041/BIG 3-04 MINDACT Phase III Trial.
J Clin Oncol
2020
33052755
Road Map to Safe and Well-Designed De-escalation Trials of Systemic Adjuvant Therapy for Solid Tumors.
J Clin Oncol
2020
33154022
Prognostic role of distant disease-free interval from completion of adjuvant trastuzumab in HER2-positive early breast cancer: analysis from the ALTTO (BIG 2-06) trial.
ESMO Open
2020
32422170
Expanding the landscape of actionable genomic alterations in metastatic breast cancer: comprehensive genomic profiling for all?
Ann Oncol
2020
32383162
Clustering of known low and moderate risk alleles rather than a novel recessive high-risk gene in non-BRCA1/2 sib trios affected with breast cancer.
Int J Cancer
2020
30335191
Pregnancies during and after trastuzumab and/or lapatinib in patients with human epidermal growth factor receptor 2-positive early breast cancer: Analysis from the NeoALTTO (BIG 1-06) and ALTTO (BIG 2-06) trials.
Cancer
2019
31853266
An RB-1 loss of function gene signature as a tool to predict response to neoadjuvant chemotherapy plus anti-HER2 agents: a substudy of the NeoALTTO trial (BIG 1-06).
Ther Adv Med Oncol
2019
31186341
Addition of a 161-SNP polygenic risk score to family history-based risk prediction: impact on clinical management in non-<i>BRCA1/2</i> breast cancer families.
J Med Genet
2019
30814109
Plasma miRNA Levels for Predicting Therapeutic Response to Neoadjuvant Treatment in HER2-positive Breast Cancer: Results from the NeoALTTO Trial.
Clin Cancer Res
2019
31134488
Dissecting the effect of hormone receptor status in patients with HER2-positive early breast cancer: exploratory analysis from the ALTTO (BIG 2-06) randomized clinical trial.
Breast Cancer Res Treat
2019
27233470
Functional Analysis of Missense Variants in the Putative Breast Cancer Susceptibility Gene XRCC2.
Hum Mutat
2016
26130695
FANCM c.5791C>T nonsense mutation (rs144567652) induces exon skipping, affects DNA repair activity and is a familial breast cancer risk factor.
Hum Mol Genet
2015
23383274
Exome sequencing of germline DNA from non-BRCA1/2 familial breast cancer cases selected on the basis of aCGH tumor profiling.
PLoS One
2013
24025038
The impact of next generation sequencing on the analysis of breast cancer susceptibility: a role for extremely rare genetic variation?
Clin Genet
2013
23809231
COMPLEXO: identifying the missing heritability of breast cancer via next generation collaboration.
Breast Cancer Res
2013
23409019
Whole exome sequencing suggests much of non-BRCA1/BRCA2 familial breast cancer is due to moderate and low penetrance susceptibility alleles.
PLoS One
2013
22100658
Genetic variants in TGFβ-1 and PAI-1 as possible risk factors for cardiovascular disease after radiotherapy for breast cancer.
Radiother Oncol
2012
22464251
Rare mutations in XRCC2 increase the risk of breast cancer.
Am J Hum Genet
2012
23054243
Rare variants in XRCC2 as breast cancer susceptibility alleles.
J Med Genet
2012
1 - 34 of 34
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University of Utah
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