The following pages link to Torben A Kruse (Q87518225):
Displaying 50 items.
- DNA glycosylases involved in base excision repair may be associated with cancer risk in BRCA1 and BRCA2 mutation carriers (Q21144874) (← links)
- Genome scan meta-analysis of schizophrenia and bipolar disorder, part III: Bipolar disorder (Q22242975) (← links)
- Genome-wide association study in BRCA1 mutation carriers identifies novel loci associated with breast and ovarian cancer risk (Q27008356) (← links)
- Comparison of mRNA splicing assay protocols across multiple laboratories: recommendations for best practice in standardized clinical testing (Q28652730) (← links)
- Identification of 12 new susceptibility loci for different histotypes of epithelial ovarian cancer (Q30252854) (← links)
- Classification of breast cancer subtypes by combining gene expression and DNA methylation data. (Q30832675) (← links)
- Hierarchical linear modeling of longitudinal pedigree data for genetic association analysis (Q30879790) (← links)
- Differential and correlation analyses of microarray gene expression data in the CEPH Utah families (Q31157322) (← links)
- Retrospective analysis of main and interaction effects in genetic association studies of human complex traits (Q33302714) (← links)
- Evaluation of Polygenic Risk Scores for Breast and Ovarian Cancer Risk Prediction in BRCA1 and BRCA2 Mutation Carriers (Q33614244) (← links)
- Microarray-based RNA profiling of breast cancer: batch effect removal improves cross-platform consistency. (Q33914600) (← links)
- A growth curve model with fractional polynomials for analysing incomplete time-course data in microarray gene expression studies. (Q34037725) (← links)
- Human longevity and variation in DNA damage response and repair: study of the contribution of sub-processes using competitive gene-set analysis (Q34055752) (← links)
- Power assessment for genetic association study of human longevity using offspring of long-lived subjects (Q34332815) (← links)
- Genetic association analysis of human longevity in cohort studies of elderly subjects: an example of the PON1 gene in the Danish 1905 birth cohort. (Q34588117) (← links)
- Genetic variation at 9p22.2 and ovarian cancer risk for BRCA1 and BRCA2 mutation carriers (Q35022825) (← links)
- Efficient sample tracking with OpenLabFramework (Q35109661) (← links)
- Assessing associations between the AURKA-HMMR-TPX2-TUBG1 functional module and breast cancer risk in BRCA1/2 mutation carriers (Q35242849) (← links)
- Identification of six new susceptibility loci for invasive epithelial ovarian cancer (Q35541663) (← links)
- Long non-coding RNA expression profiles predict metastasis in lymph node-negative breast cancer independently of traditional prognostic markers (Q35559368) (← links)
- An original phylogenetic approach identified mitochondrial haplogroup T1a1 as inversely associated with breast cancer risk in BRCA2 mutation carriers (Q35618307) (← links)
- Pathology of breast and ovarian cancers among BRCA1 and BRCA2 mutation carriers: results from the Consortium of Investigators of Modifiers of BRCA1/2 (CIMBA) (Q35737888) (← links)
- Common variants at the 19p13.1 and ZNF365 loci are associated with ER subtypes of breast cancer and ovarian cancer risk in BRCA1 and BRCA2 mutation carriers (Q35870067) (← links)
- Common breast cancer susceptibility alleles are associated with tumour subtypes in BRCA1 and BRCA2 mutation carriers: results from the Consortium of Investigators of Modifiers of BRCA1/2. (Q35889575) (← links)
- Association of type and location of BRCA1 and BRCA2 mutations with risk of breast and ovarian cancer (Q35957703) (← links)
- Ovarian cancer susceptibility alleles and risk of ovarian cancer in BRCA1 and BRCA2 mutation carriers (Q36280191) (← links)
- Design and analysis in genetic studies of human ageing and longevity. (Q36335899) (← links)
- Prediction of Breast and Prostate Cancer Risks in Male BRCA1 and BRCA2 Mutation Carriers Using Polygenic Risk Scores (Q36356727) (← links)
- Common variants at 12p11, 12q24, 9p21, 9q31.2 and in ZNF365 are associated with breast cancer risk for BRCA1 and/or BRCA2 mutation carriers (Q36393232) (← links)
- Twins for epigenetic studies of human aging and development (Q36431275) (← links)
- Analyzing age-specific genetic effects on human extreme age survival in cohort-based longitudinal studies (Q36686690) (← links)
- Dissecting complex phenotypes using the genomics of twins (Q36775188) (← links)
- Common alleles at 6q25.1 and 1p11.2 are associated with breast cancer risk for BRCA1 and BRCA2 mutation carriers (Q36839777) (← links)
- Multiple independent variants at the TERT locus are associated with telomere length and risks of breast and ovarian cancer (Q36897003) (← links)
- A novel permutation test for case-only analysis identifies epistatic effects on human longevity in the FOXO gene family (Q37022042) (← links)
- Power for genetic association study of human longevity using the case-control design (Q37321462) (← links)
- A combinatory approach for selecting prognostic genes in microarray studies of tumour survivals (Q37420280) (← links)
- RNA profiling reveals familial aggregation of molecular subtypes in non-BRCA1/2 breast cancer families (Q37539804) (← links)
- Identification, replication and characterization of epigenetic remodelling in the aging genome: a cross population analysis (Q38622986) (← links)
- The BRCA1 c. 5096G>A p.Arg1699Gln (R1699Q) intermediate risk variant: breast and ovarian cancer risk estimation and recommendations for clinical management from the ENIGMA consortium (Q38793676) (← links)
- Power estimation for gene-longevity association analysis using concordant twins (Q42924255) (← links)
- Long non-coding RNA HOTAIR is an independent prognostic marker of metastasis in estrogen receptor-positive primary breast cancer (Q44222446) (← links)
- A cross-sectional analysis of age and sex patterns in grip strength, tooth loss, near vision and hearing levels in Chinese aged 50-74 years (Q44308161) (← links)
- Gender-specific patterns in age-related decline in general health among Danish and Chinese: a cross-national comparative study (Q44455756) (← links)
- Candidate gene polymorphisms in the serotonergic pathway: influence on depression symptomatology in an elderly population (Q45238027) (← links)
- Identification of ten variants associated with risk of estrogen-receptor-negative breast cancer (Q46103372) (← links)
- Mutational Spectrum in a Worldwide Study of 29,700 Families with BRCA1 or BRCA2 Mutations (Q49024646) (← links)
- A BRCA2 mutation incorrectly mapped in the original BRCA2 reference sequence, is a common West Danish founder mutation disrupting mRNA splicing (Q50552807) (← links)
- Genetic and environmental dissections of sub-phenotypes of metabolic syndrome in the Chinese population: a twin-based heritability study. (Q51568184) (← links)
- Apolipoprotein E genotype frequency patterns in aged Danes as revealed by logistic regression models. (Q51987602) (← links)