Mads Thomassen


Ontology type: schema:Person     


Person Info

NAME

Mads

SURNAME

Thomassen

Publications in SciGraph latest 50 shown

  • 2019-12 Shared heritability and functional enrichment across six solid cancers in NATURE COMMUNICATIONS
  • 2019-02 Tumor-specific genetic aberrations in cell-free DNA of gastroesophageal cancer patients in JOURNAL OF GASTROENTEROLOGY
  • 2018-12 Differential effect of surgical manipulation on gene expression in normal breast tissue and breast tumor tissue in MOLECULAR MEDICINE
  • 2018-12 Publisher Correction: Epigenetic changes in myelofibrosis: Distinct methylation changes in the myeloid compartments and in cases with ASXL1 mutations in SCIENTIFIC REPORTS
  • 2017-12 Genomic Analyses of Breast Cancer Progression Reveal Distinct Routes of Metastasis Emergence in SCIENTIFIC REPORTS
  • 2017-12 Epigenetic changes in myelofibrosis: Distinct methylation changes in the myeloid compartments and in cases with ASXL1 mutations in SCIENTIFIC REPORTS
  • 2017-12 Identification of ten variants associated with risk of estrogen-receptor-negative breast cancer in NATURE GENETICS
  • 2017-05 Identification of 12 new susceptibility loci for different histotypes of epithelial ovarian cancer in NATURE GENETICS
  • 2017-01 Association of breast cancer risk in BRCA1 and BRCA2 mutation carriers with genetic variants showing differential allelic expression: identification of a modifier of breast cancer risk at locus 11q22.3 in BREAST CANCER RESEARCH AND TREATMENT
  • 2016-12 Inheritance of deleterious mutations at both BRCA1 and BRCA2 in an international sample of 32,295 women in BREAST CANCER RESEARCH
  • 2016-12 Male breast cancer in BRCA1 and BRCA2 mutation carriers: pathology data from the Consortium of Investigators of Modifiers of BRCA1/2 in BREAST CANCER RESEARCH
  • 2016-12 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
  • 2016-10 BRCA1/BRCA2 founder mutations and cancer risks: impact in the western Danish population in FAMILIAL CANCER
  • 2016-10 Migrating glioma cells express stem cell markers and give rise to new tumors upon xenografting in JOURNAL OF NEURO-ONCOLOGY
  • 2016-07 Shift of microRNA profile upon orthotopic xenografting of glioblastoma spheroid cultures in JOURNAL OF NEURO-ONCOLOGY
  • 2016-04-27 Identification of four novel susceptibility loci for oestrogen receptor negative breast cancer in NATURE COMMUNICATIONS
  • 2016-04 Breast cancer risk variants at 6q25 display different phenotype associations and regulate ESR1, RMND1 and CCDC170 in NATURE GENETICS
  • 2015-12 An original phylogenetic approach identified mitochondrial haplogroup T1a1 as inversely associated with breast cancer risk in BRCA2 mutation carriers in BREAST CANCER RESEARCH
  • 2015-12 Long non-coding RNA expression profiles predict metastasis in lymph node-negative breast cancer independently of traditional prognostic markers in BREAST CANCER RESEARCH
  • 2015-09 Clinical utility gene card for: Alport syndrome – update 2014 in EUROPEAN JOURNAL OF HUMAN GENETICS
  • 2015-05 Efficient Sample Tracking With OpenLabFramework in SCIENTIFIC REPORTS
  • 2015-02 Identification of six new susceptibility loci for invasive epithelial ovarian cancer in NATURE GENETICS
  • 2014-12 Refined histopathological predictors of BRCA1 and BRCA2mutation status: a large-scale analysis of breast cancer characteristics from the BCAC, CIMBA, and ENIGMA consortia in BREAST CANCER RESEARCH
  • 2014-12 Associations of common breast cancer susceptibility alleles with risk of breast cancer subtypes in BRCA1 and BRCA2 mutation carriers in BREAST CANCER RESEARCH
  • 2014-12 RNA profiling reveals familial aggregation of molecular subtypes in non-BRCA1/2 breast cancer families in BMC MEDICAL GENOMICS
  • 2014-06 Hierarchical linear modeling of longitudinal pedigree data for genetic association analysis in BMC PROCEEDINGS
  • 2013-12 Long non-coding RNA HOTAIR is an independent prognostic marker of metastasis in estrogen receptor-positive primary breast cancer in BREAST CANCER RESEARCH AND TREATMENT
  • 2013-06 COMPLEXO: identifying the missing heritability of breast cancer via next generation collaboration in BREAST CANCER RESEARCH
  • 2013-04 Multiple independent variants at the TERT locus are associated with telomere length and risks of breast and ovarian cancer in NATURE GENETICS
  • 2012-12 A multi-centre international quality control study comparing mRNA splicing assay protocols and reporting practices from the ENIGMA consortium in HEREDITARY CANCER IN CLINICAL PRACTICE
  • 2012-11 Evaluation of chromosome 6p22 as a breast cancer risk modifier locus in a follow-up study of BRCA2 mutation carriers in BREAST CANCER RESEARCH AND TREATMENT
  • 2012-11 Genome-wide linkage and association scans for pulse pressure in Chinese twins in HYPERTENSION RESEARCH
  • 2012-06 Clinical utility gene card for: Alport syndrome in EUROPEAN JOURNAL OF HUMAN GENETICS
  • 2012-06 Association of PHB 1630 C>T and MTHFR 677 C>T polymorphisms with breast and ovarian cancer risk in BRCA1/2 mutation carriers: results from a multicenter study in BRITISH JOURNAL OF CANCER
  • 2012-04 Characterization of BRCA1 and BRCA2 splicing variants: a collaborative report by ENIGMA consortium members in BREAST CANCER RESEARCH AND TREATMENT
  • 2012-02 Common variants at 12p11, 12q24, 9p21, 9q31.2 and in ZNF365 are associated with breast cancer risk for BRCA1 and/or BRCA2mutation carriers in BREAST CANCER RESEARCH
  • 2011-12 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 in BREAST CANCER RESEARCH
  • 2011-07 A BRCA2 mutation incorrectly mapped in the original BRCA2 reference sequence, is a common West Danish founder mutation disrupting mRNA splicing in BREAST CANCER RESEARCH AND TREATMENT
  • 2011-06 International distribution and age estimation of the Portuguese BRCA2 c.156_157insAlu founder mutation in BREAST CANCER RESEARCH AND TREATMENT
  • 2011-03 On the origin and diffusion of BRCA1 c.5266dupC (5382insC) in European populations in EUROPEAN JOURNAL OF HUMAN GENETICS
  • 2010-10 A locus on 19p13 modifies risk of breast cancer in BRCA1 mutation carriers and is associated with hormone receptor–negative breast cancer in the general population in NATURE GENETICS
  • 2010-09 Genome-Wide Expression Analysis of Human In Vivo Irritated Epidermis: Differential Profiles Induced by Sodium Lauryl Sulfate and Nonanoic Acid in JOURNAL OF INVESTIGATIVE DERMATOLOGY
  • 2009-12 Evaluation of a candidate breast cancer associated SNP in ERCC4 as a risk modifier in BRCA1 and BRCA2 mutation carriers. Results from the Consortium of Investigators of Modifiers of BRCA1/BRCA2 (CIMBA) in BRITISH JOURNAL OF CANCER
  • 2009-01 Gene expression meta-analysis identifies chromosomal regions and candidate genes involved in breast cancer metastasis in BREAST CANCER RESEARCH AND TREATMENT
  • 2009-01 Gene expression meta-analysis identifies chromosomal regions and candidate genes involved in breast cancer metastasis in BREAST CANCER RESEARCH AND TREATMENT
  • 2008-12 Gene expression meta-analysis identifies metastatic pathways and transcription factors in breast cancer in BMC CANCER
  • 2008 Gene Selection for Predicting Survival Outcomes of Cancer Patients in Microarray Studies in ADVANCES IN COMPUTER AND INFORMATION SCIENCES AND ENGINEERING
  • 2008 Evolutionary Algorithm for Feature Subset Selection in Predicting Tumor Outcomes Using Microarray Data in BIOINFORMATICS RESEARCH AND APPLICATIONS
  • 2004-10 Loss of heterozygosity at BRCA2 in a ductal carcinoma in situ and three invasive breast carcinomas in a family with a germline BRCA2 mutation in BREAST CANCER RESEARCH AND TREATMENT
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