List of works - Torben A Kruse

A BRCA2 mutation incorrectly mapped in the original BRCA2 reference sequence, is a common West Danish founder mutation disrupting mRNA splicing

scientific article published on 24 December 2010

A combinatory approach for selecting prognostic genes in microarray studies of tumour survivals

scientific article published on 30 July 2009

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

scientific article

A growth curve model with fractional polynomials for analysing incomplete time-course data in microarray gene expression studies.

scientific article

A novel permutation test for case-only analysis identifies epistatic effects on human longevity in the FOXO gene family

scientific article published on 15 May 2013

An original phylogenetic approach identified mitochondrial haplogroup T1a1 as inversely associated with breast cancer risk in BRCA2 mutation carriers

scientific article published on 25 April 2015

Analyzing age-specific genetic effects on human extreme age survival in cohort-based longitudinal studies

scientific article published on 15 August 2012

Apolipoprotein E genotype frequency patterns in aged Danes as revealed by logistic regression models

scientific article published in January 2004

Assessing associations between the AURKA-HMMR-TPX2-TUBG1 functional module and breast cancer risk in BRCA1/2 mutation carriers

scientific article

Association of Genomic Domains in BRCA1 and BRCA2 with Prostate Cancer Risk and Aggressiveness

scientific article published on 13 November 2019

Association of miR-548c-5p, miR-7-5p, miR-210-3p, miR-128-3p with recurrence in systemically untreated breast cancer.

scientific article

Association of type and location of BRCA1 and BRCA2 mutations with risk of breast and ovarian cancer

scientific article

Breast and Prostate Cancer Risks for Male BRCA1 and BRCA2 Pathogenic Variant Carriers Using Polygenic Risk Scores

scientific article published on 11 January 2022

Candidate gene polymorphisms in the serotonergic pathway: influence on depression symptomatology in an elderly population

scientific article published on 27 June 2006

Classification of breast cancer subtypes by combining gene expression and DNA methylation data.

scientific article

Common alleles at 6q25.1 and 1p11.2 are associated with breast cancer risk for BRCA1 and BRCA2 mutation carriers

scientific article published on 18 May 2011

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.

scientific article published on 2 November 2011

Common variants at 12p11, 12q24, 9p21, 9q31.2 and in ZNF365 are associated with breast cancer risk for BRCA1 and/or BRCA2 mutation carriers

scientific article

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

scientific article published on 20 February 2012

Comparison of mRNA splicing assay protocols across multiple laboratories: recommendations for best practice in standardized clinical testing

scientific article

DNA glycosylases involved in base excision repair may be associated with cancer risk in BRCA1 and BRCA2 mutation carriers

scientific article

Design and analysis in genetic studies of human ageing and longevity.

scientific article

Differential and correlation analyses of microarray gene expression data in the CEPH Utah families

scientific article

Dissecting complex phenotypes using the genomics of twins

scientific article published on 10 February 2010

Efficient sample tracking with OpenLabFramework

scientific article

Estimating haplotype relative risks on human survival in population-based association studies

scientific article published on 18 April 2005

European combined analysis of the CTG18.1 and the ERDA1 CAG/CTG repeats in bipolar disorder

scientific article published on 01 April 2002

Evaluation of Polygenic Risk Scores for Breast and Ovarian Cancer Risk Prediction in BRCA1 and BRCA2 Mutation Carriers

scientific article

Exploratory analysis of age and sex dependent DNA methylation patterns on the X-chromosome in whole blood samples

scientific article published on 28 April 2020

Gender-specific patterns in age-related decline in general health among Danish and Chinese: a cross-national comparative study

scientific article published on 23 December 2011

Genetic and environmental dissections of sub-phenotypes of metabolic syndrome in the Chinese population: a twin-based heritability study.

scientific article published on 7 April 2011

Genetic association analysis of human longevity in cohort studies of elderly subjects: an example of the PON1 gene in the Danish 1905 birth cohort.

scientific article

Genetic variation at 9p22.2 and ovarian cancer risk for BRCA1 and BRCA2 mutation carriers

scientific article

Genome scan meta-analysis of schizophrenia and bipolar disorder, part III: Bipolar disorder

scientific article

Genome-wide association study in BRCA1 mutation carriers identifies novel loci associated with breast and ovarian cancer risk

scientific article (publication date: 2013)

Genome-wide linkage and association scans for pulse pressure in Chinese twins

article

Hierarchical linear modeling of longitudinal pedigree data for genetic association analysis

scientific article

High-Resolution Genome-Wide Linkage Mapping Identifies Susceptibility Loci for BMI in the Chinese Population

article

Human longevity and variation in DNA damage response and repair: study of the contribution of sub-processes using competitive gene-set analysis

scientific article

Identification of 12 new susceptibility loci for different histotypes of epithelial ovarian cancer

scientific article

Identification of six new susceptibility loci for invasive epithelial ovarian cancer

scientific article published on 12 January 2015

Identification of ten variants associated with risk of estrogen-receptor-negative breast cancer

scientific article published on 23 October 2017

Identification, replication and characterization of epigenetic remodelling in the aging genome: a cross population analysis

scientific article

International distribution and age estimation of the Portuguese BRCA2 c.156_157insAlu founder mutation.

scientific article published on 22 July 2010

Large scale multifactorial likelihood quantitative analysis of BRCA1 and BRCA2 variants: An ENIGMA resource to support clinical variant classification

scientific article published on 01 September 2019

Long non-coding RNA HOTAIR is an independent prognostic marker of metastasis in estrogen receptor-positive primary breast cancer

scientific article published on 21 November 2013

Long non-coding RNA expression profiles predict metastasis in lymph node-negative breast cancer independently of traditional prognostic markers

scientific article published on 11 April 2015

Microarray-based RNA profiling of breast cancer: batch effect removal improves cross-platform consistency.

scientific article

Multiple independent variants at the TERT locus are associated with telomere length and risks of breast and ovarian cancer

scientific article published on April 2013

Mutational Spectrum in a Worldwide Study of 29,700 Families with BRCA1 or BRCA2 Mutations

scientific article published on 15 February 2018

Ovarian cancer susceptibility alleles and risk of ovarian cancer in BRCA1 and BRCA2 mutation carriers

scientific article

Pathology of breast and ovarian cancers among BRCA1 and BRCA2 mutation carriers: results from the Consortium of Investigators of Modifiers of BRCA1/2 (CIMBA)

scientific article published on 5 December 2011

Polygenic risk scores and breast and epithelial ovarian cancer risks for carriers of BRCA1 and BRCA2 pathogenic variants

scientific article published on 15 July 2020

Power assessment for genetic association study of human longevity using offspring of long-lived subjects

scientific article

Power estimation for gene-longevity association analysis using concordant twins

scientific article published on 16 September 2014

Power for genetic association study of human longevity using the case-control design

scientific article published on 27 August 2008

Prediction of Breast and Prostate Cancer Risks in Male BRCA1 and BRCA2 Mutation Carriers Using Polygenic Risk Scores

scientific article

RNA profiling reveals familial aggregation of molecular subtypes in non-BRCA1/2 breast cancer families

scientific article published on 31 January 2014

Retrospective analysis of main and interaction effects in genetic association studies of human complex traits

scientific article

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

scientific article published on 10 May 2017

Twins for epigenetic studies of human aging and development

scientific article

List of works by Torben A Kruse

A BRCA2 mutation incorrectly mapped in the original BRCA2 reference sequence, is a common West Danish founder mutation disrupting mRNA splicing

A combinatory approach for selecting prognostic genes in microarray studies of tumour survivals

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

A growth curve model with fractional polynomials for analysing incomplete time-course data in microarray gene expression studies.

A novel permutation test for case-only analysis identifies epistatic effects on human longevity in the FOXO gene family

An original phylogenetic approach identified mitochondrial haplogroup T1a1 as inversely associated with breast cancer risk in BRCA2 mutation carriers

Analyzing age-specific genetic effects on human extreme age survival in cohort-based longitudinal studies

Apolipoprotein E genotype frequency patterns in aged Danes as revealed by logistic regression models

Assessing associations between the AURKA-HMMR-TPX2-TUBG1 functional module and breast cancer risk in BRCA1/2 mutation carriers

Association of Genomic Domains in BRCA1 and BRCA2 with Prostate Cancer Risk and Aggressiveness

Association of miR-548c-5p, miR-7-5p, miR-210-3p, miR-128-3p with recurrence in systemically untreated breast cancer.

Association of type and location of BRCA1 and BRCA2 mutations with risk of breast and ovarian cancer

Breast and Prostate Cancer Risks for Male BRCA1 and BRCA2 Pathogenic Variant Carriers Using Polygenic Risk Scores

Candidate gene polymorphisms in the serotonergic pathway: influence on depression symptomatology in an elderly population

Classification of breast cancer subtypes by combining gene expression and DNA methylation data.

Common alleles at 6q25.1 and 1p11.2 are associated with breast cancer risk for BRCA1 and BRCA2 mutation carriers

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.

Common variants at 12p11, 12q24, 9p21, 9q31.2 and in ZNF365 are associated with breast cancer risk for BRCA1 and/or BRCA2 mutation carriers

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

Comparison of mRNA splicing assay protocols across multiple laboratories: recommendations for best practice in standardized clinical testing

DNA glycosylases involved in base excision repair may be associated with cancer risk in BRCA1 and BRCA2 mutation carriers

Design and analysis in genetic studies of human ageing and longevity.

Differential and correlation analyses of microarray gene expression data in the CEPH Utah families

Dissecting complex phenotypes using the genomics of twins

Efficient sample tracking with OpenLabFramework

Estimating haplotype relative risks on human survival in population-based association studies

European combined analysis of the CTG18.1 and the ERDA1 CAG/CTG repeats in bipolar disorder

Evaluation of Polygenic Risk Scores for Breast and Ovarian Cancer Risk Prediction in BRCA1 and BRCA2 Mutation Carriers

Exploratory analysis of age and sex dependent DNA methylation patterns on the X-chromosome in whole blood samples

Gender-specific patterns in age-related decline in general health among Danish and Chinese: a cross-national comparative study

Genetic and environmental dissections of sub-phenotypes of metabolic syndrome in the Chinese population: a twin-based heritability study.

Genetic association analysis of human longevity in cohort studies of elderly subjects: an example of the PON1 gene in the Danish 1905 birth cohort.

Genetic variation at 9p22.2 and ovarian cancer risk for BRCA1 and BRCA2 mutation carriers

Genome scan meta-analysis of schizophrenia and bipolar disorder, part III: Bipolar disorder

Genome-wide association study in BRCA1 mutation carriers identifies novel loci associated with breast and ovarian cancer risk

Genome-wide linkage and association scans for pulse pressure in Chinese twins

Hierarchical linear modeling of longitudinal pedigree data for genetic association analysis

High-Resolution Genome-Wide Linkage Mapping Identifies Susceptibility Loci for BMI in the Chinese Population

Human longevity and variation in DNA damage response and repair: study of the contribution of sub-processes using competitive gene-set analysis

Identification of 12 new susceptibility loci for different histotypes of epithelial ovarian cancer

Identification of six new susceptibility loci for invasive epithelial ovarian cancer

Identification of ten variants associated with risk of estrogen-receptor-negative breast cancer

Identification, replication and characterization of epigenetic remodelling in the aging genome: a cross population analysis

International distribution and age estimation of the Portuguese BRCA2 c.156_157insAlu founder mutation.

Large scale multifactorial likelihood quantitative analysis of BRCA1 and BRCA2 variants: An ENIGMA resource to support clinical variant classification

Long non-coding RNA HOTAIR is an independent prognostic marker of metastasis in estrogen receptor-positive primary breast cancer

Long non-coding RNA expression profiles predict metastasis in lymph node-negative breast cancer independently of traditional prognostic markers

Microarray-based RNA profiling of breast cancer: batch effect removal improves cross-platform consistency.

Multiple independent variants at the TERT locus are associated with telomere length and risks of breast and ovarian cancer

Mutational Spectrum in a Worldwide Study of 29,700 Families with BRCA1 or BRCA2 Mutations

Ovarian cancer susceptibility alleles and risk of ovarian cancer in BRCA1 and BRCA2 mutation carriers

Pathology of breast and ovarian cancers among BRCA1 and BRCA2 mutation carriers: results from the Consortium of Investigators of Modifiers of BRCA1/2 (CIMBA)

Polygenic risk scores and breast and epithelial ovarian cancer risks for carriers of BRCA1 and BRCA2 pathogenic variants

Power assessment for genetic association study of human longevity using offspring of long-lived subjects

Power estimation for gene-longevity association analysis using concordant twins

Power for genetic association study of human longevity using the case-control design

Prediction of Breast and Prostate Cancer Risks in Male BRCA1 and BRCA2 Mutation Carriers Using Polygenic Risk Scores

RNA profiling reveals familial aggregation of molecular subtypes in non-BRCA1/2 breast cancer families

Retrospective analysis of main and interaction effects in genetic association studies of human complex traits

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

Twins for epigenetic studies of human aging and development