Grethe Grenaker Alnæs

researcher

Grethe Grenaker Alnæs is …
instance of (P31):
humanQ5

P108employerOslo University HospitalQ3111191
P735given nameGretheQ1546039
GretheQ1546039
P106occupationresearcherQ1650915
P21sex or genderfemaleQ6581072

Reverse relations

author (P50)
Q3601638611q13 is a susceptibility locus for hormone receptor positive breast cancer
Q3587156719p13.1 is a triple-negative-specific breast cancer susceptibility locus
Q338488952q36.3 is associated with prognosis for oestrogen receptor-negative breast cancer patients treated with chemotherapy
Q37619303A large-scale assessment of two-way SNP interactions in breast cancer susceptibility using 46,450 cases and 42,461 controls from the breast cancer association consortium
Q35870483A polymorphism in the base excision repair gene PARP2 is associated with differential prognosis by chemotherapy among postmenopausal breast cancer patients
Q57121969A quality assessment survey of SNP genotyping laboratories
Q57421083ABCB1 and GST polymorphisms associated with TP53 status in breast cancer
Q35218520Assessment of variation in immunosuppressive pathway genes reveals TGFBR2 to be associated with prognosis of estrogen receptor-negative breast cancer after chemotherapy
Q45979098Association analysis identifies 65 new breast cancer risk loci.
Q37684672Association of breast cancer risk with genetic variants showing differential allelic expression: Identification of a novel breast cancer susceptibility locus at 4q21.
Q36449203CHEK2*1100delC heterozygosity in women with breast cancer associated with early death, breast cancer-specific death, and increased risk of a second breast cancer
Q35587062Canine Mammary Tumours Are Affected by Frequent Copy Number Aberrations, including Amplification of MYC and Loss of PTEN
Q36600605Common breast cancer susceptibility variants in LSP1 and RAD51L1 are associated with mammographic density measures that predict breast cancer risk
Q31082788Comparison of 6q25 breast cancer hits from Asian and European Genome Wide Association Studies in the Breast Cancer Association Consortium (BCAC)
Q34181322Confirmation of 5p12 as a susceptibility locus for progesterone-receptor-positive, lower grade breast cancer
Q57278898Correction: Comparison of 6q25 Breast Cancer Hits from Asian and European Genome Wide Association Studies in the Breast Cancer Association Consortium (BCAC)
Q37702047DNA methylation signature (SAM40) identifies subgroups of the Luminal A breast cancer samples with distinct survival
Q35064451Evidence that breast cancer risk at the 2q35 locus is mediated through IGFBP5 regulation
Q35693944Expression of an estrogen-regulated variant transcript of the peroxisomal branched chain fatty acid oxidase ACOX2 in breast carcinomas
Q83876489Fatigued breast cancer survivors and gene polymorphisms in the inflammatory pathway
Q35524465Fine-mapping identifies two additional breast cancer susceptibility loci at 9q31.2.
Q37367871Fine-scale mapping of the FGFR2 breast cancer risk locus: putative functional variants differentially bind FOXA1 and E2F1.
Q34979715Five polymorphisms and breast cancer risk: results from the Breast Cancer Association Consortium
Q43278804Functional glutathione S-transferase genotypes among testicular germ cell tumor survivors: associations with primary and post-chemotherapy tumor histology
Q42439010GSTP1 promoter haplotypes affect DNA methylation levels and promoter activity in breast carcinomas.
Q36465244Genes harbouring susceptibility SNPs are differentially expressed in the breast cancer subtypes
Q35179897Genetic variation at CYP3A is associated with age at menarche and breast cancer risk: a case-control study
Q53485693Genome-wide analysis identifies 16q deletion associated with survival, molecular subtypes, mRNA expression, and germline haplotypes in breast cancer patients.
Q36842233Genome-wide association analysis identifies three new breast cancer susceptibility loci
Q35996692Genome-wide association analysis of more than 120,000 individuals identifies 15 new susceptibility loci for breast cancer
Q64040390Genome-wide association study of germline variants and breast cancer-specific mortality
Q36276540Height and Breast Cancer Risk: Evidence From Prospective Studies and Mendelian Randomization
Q46103372Identification of ten variants associated with risk of estrogen-receptor-negative breast cancer
Q28302352Individual and combined effects of DNA methylation and copy number alterations on miRNA expression in breast tumors
Q53626868Interaction between p53 mutation and a somatic HDMX biomarker better defines metastatic potential in breast cancer.
Q35119701Low penetrance breast cancer susceptibility loci are associated with specific breast tumor subtypes: findings from the Breast Cancer Association Consortium
Q54774700Multiplex single-tube screening for mutations in the Nijmegen Breakage Syndrome (NBS1) gene in Hodgkin's and non-Hodgkin's lymphoma patients of Slavic origin.
Q35752042Novel Associations between Common Breast Cancer Susceptibility Variants and Risk-Predicting Mammographic Density Measures
Q28584533PALB2, CHEK2 and ATM rare variants and cancer risk: data from COGS
Q27863385Pathway based analysis of SNPs with relevance to 5-FU therapy: relation to intratumoral mRNA expression and survival.
Q62583133Polygenic Risk Scores for Prediction of Breast Cancer and Breast Cancer Subtypes
Q36583004Prediction of breast cancer risk based on profiling with common genetic variants
Q55508030Publisher Correction: Evidence that breast cancer risk at the 2q35 locus is mediated through IGFBP5 regulation.
Q47099651Serum concentrations of active tamoxifen metabolites predict long-term survival in adjuvantly treated breast cancer patients
Q37661498The 5p12 breast cancer susceptibility locus affects MRPS30 expression in estrogen-receptor positive tumors
Q33911898Widespread alternative exon usage in clinically distinct subtypes of Invasive Ductal Carcinoma

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