Melissa C Southey


Ontology type: schema:Person     


Person Info

NAME

Melissa C

SURNAME

Southey

Publications in SciGraph latest 50 shown

  • 2019-12 Shared heritability and functional enrichment across six solid cancers in NATURE COMMUNICATIONS
  • 2019-02 Author Correction: Association analyses of more than 140,000 men identify 63 new prostate cancer susceptibility loci in NATURE GENETICS
  • 2019-01 Discovery of common and rare genetic risk variants for colorectal cancer in NATURE GENETICS
  • 2018-12 Identification of nine new susceptibility loci for endometrial cancer in NATURE COMMUNICATIONS
  • 2018-12 Causal effect of smoking on DNA methylation in peripheral blood: a twin and family study in CLINICAL EPIGENETICS
  • 2018-12 The utility of DNA extracted from saliva for genome-wide molecular research platforms in BMC RESEARCH NOTES
  • 2018-12 Fine-mapping of prostate cancer susceptibility loci in a large meta-analysis identifies candidate causal variants in NATURE COMMUNICATIONS
  • 2018-12 Predicting interval and screen-detected breast cancers from mammographic density defined by different brightness thresholds in BREAST CANCER RESEARCH
  • 2018-12 Age-specific breast cancer risk by body mass index and familial risk: prospective family study cohort (ProF-SC) in BREAST CANCER RESEARCH
  • 2018-12 Is RNASEL:p.Glu265* a modifier of early-onset breast cancer risk for carriers of high-risk mutations? in BMC CANCER
  • 2018-12 FANCM and RECQL genetic variants and breast cancer susceptibility: relevance to South Poland and West Ukraine in BMC MEDICAL GENETICS
  • 2018-12 Heritable DNA methylation marks associated with susceptibility to breast cancer in NATURE COMMUNICATIONS
  • 2018-12 Epigenetic supersimilarity of monozygotic twin pairs in GENOME BIOLOGY
  • 2018-10 Correction: Risk of colorectal cancer for carriers of a germ-line mutation in POLE or POLD1 in GENETICS IN MEDICINE
  • 2018-08 Risk of colorectal cancer for carriers of a germ-line mutation in POLE or POLD1 in GENETICS IN MEDICINE
  • 2018-07 A transcriptome-wide association study of 229,000 women identifies new candidate susceptibility genes for breast cancer in NATURE GENETICS
  • 2018-07 Targeted massively parallel sequencing characterises the mutation spectrum of PALB2 in breast and ovarian cancer cases from Poland and Ukraine in FAMILIAL CANCER
  • 2018-07 Association analyses of more than 140,000 men identify 63 new prostate cancer susceptibility loci in NATURE GENETICS
  • 2018-06 Germline variants in IL4, MGMT and AKT1 are associated with prostate cancer-specific mortality: An analysis of 12,082 prostate cancer cases in PROSTATE CANCER AND PROSTATIC DISEASES
  • 2018-05-17 Inference about causation between body mass index and DNA methylation in blood from a twin family study in INTERNATIONAL JOURNAL OF OBESITY
  • 2018-04 Novel associations between blood DNA methylation and body mass index in middle-aged and older adults in INTERNATIONAL JOURNAL OF OBESITY
  • 2018-04 Adult height is associated with increased risk of ovarian cancer: a Mendelian randomisation study in BRITISH JOURNAL OF CANCER
  • 2018-04 Obtaining high quality transcriptome data from formalin-fixed, paraffin-embedded diagnostic prostate tumor specimens in LABORATORY INVESTIGATION
  • 2018-01 Somatic mutations of the coding microsatellites within the beta-2-microglobulin gene in mismatch repair-deficient colorectal cancers and adenomas in FAMILIAL CANCER
  • 2017-12 Reproductive profiles and risk of breast cancer subtypes: a multi-center case-only study in BREAST CANCER RESEARCH
  • 2017-12 Characterisation of microbial communities within aggressive prostate cancer tissues in INFECTIOUS AGENTS AND CANCER
  • 2017-12 Increased genomic burden of germline copy number variants is associated with early onset breast cancer: Australian breast cancer family registry in BREAST CANCER RESEARCH
  • 2017-12 Twin birth changes DNA methylation of subsequent siblings in SCIENTIFIC REPORTS
  • 2017-12 Mammographic density and risk of breast cancer by tumor characteristics: a case-control study in BMC CANCER
  • 2017-12 Identification of ten variants associated with risk of estrogen-receptor-negative breast cancer in NATURE GENETICS
  • 2017-11 Association analysis identifies 65 new breast cancer risk loci in NATURE
  • 2017-09 Total and beverage-specific alcohol intake and the risk of aggressive prostate cancer: a case–control study in PROSTATE CANCER AND PROSTATIC DISEASES
  • 2017-08-22 Height, selected genetic markers and prostate cancer risk: results from the PRACTICAL consortium in BRITISH JOURNAL OF CANCER
  • 2017-07 Mutation screening of ACKR3 and COPS8 in kidney cancer cases from the CONFIRM study in FAMILIAL CANCER
  • 2017-06 Association between DNA methylation at SOCS3 gene and body mass index might be due to familial confounding in INTERNATIONAL JOURNAL OF OBESITY
  • 2017-06 Genomic analyses identify hundreds of variants associated with age at menarche and support a role for puberty timing in cancer risk in NATURE GENETICS
  • 2017-05 Identification of 12 new susceptibility loci for different histotypes of epithelial ovarian cancer in NATURE GENETICS
  • 2017-05 Genetic modifiers of CHEK2*1100delC-associated breast cancer risk in GENETICS IN MEDICINE
  • 2017-02-06 Genome-wide association analysis implicates dysregulation of immunity genes in chronic lymphocytic leukaemia in NATURE COMMUNICATIONS
  • 2017-02 Enrichment of putative PAX8 target genes at serous epithelial ovarian cancer susceptibility loci in BRITISH JOURNAL OF CANCER
  • 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
  • 2017-01 A prospective study of peripheral blood DNA methylation at RPTOR, MGRN1 and RAPSN and risk of breast cancer in BREAST CANCER RESEARCH AND TREATMENT
  • 2017-01 Breast cancer risk prediction using a polygenic risk score in the familial setting: a prospective study from the Breast Cancer Family Registry and kConFab in GENETICS IN MEDICINE
  • 2016-12 PALB2: research reaching to clinical outcomes for women with breast cancer in HEREDITARY CANCER IN CLINICAL PRACTICE
  • 2016-12 Mammographic density and risk of breast cancer by mode of detection and tumor size: a case-control study in BREAST CANCER RESEARCH
  • 2016-12 The PALB2 p.Leu939Trp mutation is not associated with breast cancer risk in BREAST CANCER RESEARCH
  • 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 Genetic predisposition to ductal carcinoma in situ of the breast 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 rs2735383, located at a microRNA binding site in the 3’UTR of NBS1, is not associated with breast cancer risk in SCIENTIFIC REPORTS
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