List of works - Torben A Kruse

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

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

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)

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

scientific article

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

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

scientific article

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

scientific article

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

scientific article published on 15 February 2018

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 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 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

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

scientific article

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

scientific article published on 27 June 2006

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

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

scientific article

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

scientific article

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

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

scientific article published on 22 July 2010

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

scientific article published on 27 August 2008

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

scientific article

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

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

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

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

scientific article

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

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

scientific article

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

scientific article published on 31 January 2014

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

scientific article

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

scientific article

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

scientific article published on 01 April 2002

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

scientific article

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

Dissecting complex phenotypes using the genomics of twins

scientific article published on 10 February 2010

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

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

scientific article

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

scientific article published on 15 August 2012

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

scientific article

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

scientific article

Hierarchical linear modeling of longitudinal pedigree data for genetic association analysis

scientific article

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

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

scientific article published in January 2004

Efficient sample tracking with OpenLabFramework

scientific article

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

article

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

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

scientific article published on 18 April 2005

List of works by Torben A Kruse

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

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

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

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

Long non-coding RNA HOTAIR is an independent prognostic marker of metastasis in estrogen receptor-positive primary breast 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 of 12 new susceptibility loci for different histotypes of epithelial ovarian cancer

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

Dissecting complex phenotypes using the genomics of twins

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

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

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

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

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

Hierarchical linear modeling of longitudinal pedigree data for genetic association analysis

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

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

Efficient sample tracking with OpenLabFramework

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

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

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