Antoinette Hollestelle

Ontology type: schema:Person     

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Publications in SciGraph latest 50 shown

  • 2022-01-18 Rare germline copy number variants (CNVs) and breast cancer risk in COMMUNICATIONS BIOLOGY
  • 2022-01-04 Common variants in breast cancer risk loci predispose to distinct tumor subtypes in BREAST CANCER RESEARCH
  • 2021-10-05 Germline variants and breast cancer survival in patients with distant metastases at primary breast cancer diagnosis in SCIENTIFIC REPORTS
  • 2021-05-14 Author Correction: A case-only study to identify genetic modifiers of breast cancer risk for BRCA1/BRCA2 mutation carriers in NATURE COMMUNICATIONS
  • 2021-02-17 A case-only study to identify genetic modifiers of breast cancer risk for BRCA1/BRCA2 mutation carriers in NATURE COMMUNICATIONS
  • 2020-05-18 Genome-wide association study identifies 32 novel breast cancer susceptibility loci from overall and subtype-specific analyses in NATURE GENETICS
  • 2020-01-07 Fine-mapping of 150 breast cancer risk regions identifies 191 likely target genes in NATURE GENETICS
  • 2019-11-23 Characterizing the invasion of different breast cancer cell lines with distinct E-cadherin status in 3D using a microfluidic system in BIOMEDICAL MICRODEVICES
  • 2019-11-01 The FANCM:p.Arg658* truncating variant is associated with risk of triple-negative breast cancer in NPJ BREAST CANCER
  • 2019-04-15 Genome-wide association and transcriptome studies identify target genes and risk loci for breast cancer in NATURE COMMUNICATIONS
  • 2019-02-21 Genome-wide association study of germline variants and breast cancer-specific mortality in BRITISH JOURNAL OF CANCER
  • 2018-06-18 A transcriptome-wide association study of 229,000 women identifies new candidate susceptibility genes for breast cancer in NATURE GENETICS
  • 2017-11-07 Reproductive profiles and risk of breast cancer subtypes: a multi-center case-only study in BREAST CANCER RESEARCH
  • 2017-10-23 Identification of ten variants associated with risk of estrogen-receptor-negative breast cancer in NATURE GENETICS
  • 2017-10-23 Association analysis identifies 65 new breast cancer risk loci in NATURE
  • 2016-11-15 rs2735383, located at a microRNA binding site in the 3’UTR of NBS1, is not associated with breast cancer risk in SCIENTIFIC REPORTS
  • 2016-10-18 Prognostic value of automated KI67 scoring in breast cancer: a centralised evaluation of 8088 patients from 10 study groups in BREAST CANCER RESEARCH
  • 2016-10-06 Genetic modifiers of CHEK2*1100delC-associated breast cancer risk in GENETICS IN MEDICINE
  • 2016-09-07 Functional mechanisms underlying pleiotropic risk alleles at the 19p13.1 breast–ovarian cancer susceptibility locus in NATURE COMMUNICATIONS
  • 2016-09-07 Fine scale mapping of the 17q22 breast cancer locus using dense SNPs, genotyped within the Collaborative Oncological Gene-Environment Study (COGs) in SCIENTIFIC REPORTS
  • 2016-07-18 Recurrent HOXB13 mutations in the Dutch population do not associate with increased breast cancer risk in SCIENTIFIC REPORTS
  • 2016-06-21 Identification of independent association signals and putative functional variants for breast cancer risk through fine-scale mapping of the 12p11 locus in BREAST CANCER RESEARCH
  • 2016-04-27 Identification of four novel susceptibility loci for oestrogen receptor negative breast cancer in NATURE COMMUNICATIONS
  • 2016-02-29 Breast cancer risk variants at 6q25 display different phenotype associations and regulate ESR1, RMND1 and CCDC170 in NATURE GENETICS
  • 2016-02-17 Genetic predisposition to ductal carcinoma in situ of the breast in BREAST CANCER RESEARCH
  • 2015-12-16 A polymorphism in the base excision repair gene PARP2 is associated with differential prognosis by chemotherapy among postmenopausal breast cancer patients in BMC CANCER
  • 2015-07-02 Annexin A1 expression in a pooled breast cancer series: association with tumor subtypes and prognosis in BMC MEDICINE
  • 2015-05-10 Sensitivity to systemic therapy for metastatic breast cancer in CHEK2 1100delC mutation carriers in JOURNAL OF CANCER RESEARCH AND CLINICAL ONCOLOGY
  • 2015-04-22 Common germline polymorphisms associated with breast cancer-specific survival in BREAST CANCER RESEARCH
  • 2015-03-09 Genome-wide association analysis of more than 120,000 individuals identifies 15 new susceptibility loci for breast cancer in NATURE GENETICS
  • 2014-09-30 Growth and metastatic behavior of molecularly well-characterized human breast cancer cell lines in mice in BREAST CANCER RESEARCH AND TREATMENT
  • 2014-06-17 2q36.3 is associated with prognosis for oestrogen receptor-negative breast cancer patients treated with chemotherapy in NATURE COMMUNICATIONS
  • 2014-06-10 Survival and contralateral breast cancer in CHEK2 1100delC breast cancer patients: impact of adjuvant chemotherapy in BRITISH JOURNAL OF CANCER
  • 2014-05-26 Genetic variation at CYP3A is associated with age at menarche and breast cancer risk: a case-control study in BREAST CANCER RESEARCH
  • 2013-05-08 CHEK2*1100delC homozygosity in the Netherlands—prevalence and risk of breast and lung cancer in EUROPEAN JOURNAL OF HUMAN GENETICS
  • 2013-04-19 miRNA expression profiling of 51 human breast cancer cell lines reveals subtype and driver mutation-specific miRNAs in BREAST CANCER RESEARCH
  • 2013-03-27 Large-scale genotyping identifies 41 new loci associated with breast cancer risk in NATURE GENETICS
  • 2013-03-27 Genome-wide association studies identify four ER negative–specific breast cancer risk loci in NATURE GENETICS
  • 2013-03-27 Multiple independent variants at the TERT locus are associated with telomere length and risks of breast and ovarian cancer in NATURE GENETICS
  • 2013-01-22 Loss of E-cadherin is not a necessity for epithelial to mesenchymal transition in human breast cancer in BREAST CANCER RESEARCH AND TREATMENT
  • 2012-09-29 E-cadherin promotor methylation and mutation are inversely related to motility capacity of breast cancer cells in BREAST CANCER RESEARCH AND TREATMENT
  • 2012-09-23 Genome-wide association study identifies a common variant in RAD51B associated with male breast cancer risk in NATURE GENETICS
  • 2012-01-22 Genome-wide association analysis identifies three new breast cancer susceptibility loci in NATURE GENETICS
  • 2010-11-09 A genome-wide association scan on estrogen receptor-negative breast cancer in BREAST CANCER RESEARCH
  • 2010-07-30 Prevalence of the variant allele rs61764370 T>G in the 3′UTR of KRAS among Dutch BRCA1, BRCA2 and non-BRCA1/BRCA2 breast cancer families in BREAST CANCER RESEARCH AND TREATMENT
  • 2009-09-18 Four human breast cancer cell lines with biallelic inactivating α-catenin gene mutations in BREAST CANCER RESEARCH AND TREATMENT
  • 2009-07-16 Low-risk susceptibility alleles in 40 human breast cancer cell lines in BMC CANCER
  • 2009-07-11 Distinct gene mutation profiles among luminal-type and basal-type breast cancer cell lines in BREAST CANCER RESEARCH AND TREATMENT
  • 2008-02-24 Deleterious CHEK2 1100delC and L303X mutants identified among 38 human breast cancer cell lines in BREAST CANCER RESEARCH AND TREATMENT
  • 2004-11-05 Representational Difference Analysis as a Tool in the Search for New Tumor Suppressor Genes in PANCREATIC CANCER
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