Miriam V Dwek

researcher (ORCID 0000-0001-7184-2932)

Miriam V Dwek is …
instance of (P31):
humanQ5

External links are
P496ORCID iD0000-0001-7184-2932

P735given nameMiriamQ1938195
MiriamQ1938195
P106occupationresearcherQ1650915

Reverse relations

author (P50)
Q3587156719p13.1 is a triple-negative-specific breast cancer susceptibility locus
Q92711687A network analysis to identify mediators of germline-driven differences in breast cancer prognosis
Q57305942A transcriptome-wide association study of 229,000 women identifies new candidate susceptibility genes for breast cancer
Q71656073Altered expression of N-acetyl galactosamine glycoproteins by breast cancers
Q45979098Association analysis identifies 65 new breast cancer risk loci.
Q114182713Association of germline genetic variants with breast cancer-specific survival in patient subgroups defined by clinic-pathological variables related to tumor biology and type of systemic treatment
Q57056093Associations of obesity and circulating insulin and glucose with breast cancer risk: a Mendelian randomization analysis
Q61230414Fine-mapping of 150 breast cancer risk regions identifies 178 high confidence target genes
Q92480972Fine-mapping of 150 breast cancer risk regions identifies 191 likely target genes
Q114182808Functional annotation of the 2q35 breast cancer risk locus implicates a structural variant in influencing activity of a long-range enhancer element
Q35151684Genetic predisposition to in situ and invasive lobular carcinoma of the breast
Q63681757Genome-wide association and transcriptome studies identify target genes and risk loci for breast cancer
Q95329367Genome-wide association study identifies 32 novel breast cancer susceptibility loci from overall and subtype-specific analyses
Q64040390Genome-wide association study of germline variants and breast cancer-specific mortality
Q36086247Identification of independent association signals and putative functional variants for breast cancer risk through fine-scale mapping of the 12p11 locus
Q46103372Identification of ten variants associated with risk of estrogen-receptor-negative breast cancer
Q114184688Incorporating progesterone receptor expression into the PREDICT breast prognostic model
Q114182490Mendelian randomisation study of smoking exposure in relation to breast cancer risk
Q62583133Polygenic Risk Scores for Prediction of Breast Cancer and Breast Cancer Subtypes
Q36583004Prediction of breast cancer risk based on profiling with common genetic variants
Q90242034Publisher Correction: Shared heritability and functional enrichment across six solid cancers
Q35155449Refined histopathological predictors of BRCA1 and BRCA2 mutation status: a large-scale analysis of breast cancer characteristics from the BCAC, CIMBA, and ENIGMA consortia
Q92181268Serum IgA1 shows increased levels of α2,6-linked sialic acid in breast cancer
Q61118451Shared heritability and functional enrichment across six solid cancers
Q64004349Shared heritability and functional enrichment across six solid cancers
Q91178389The FANCM:p.Arg658* truncating variant is associated with risk of triple-negative breast cancer
Q89961489Transcriptome-wide association study of breast cancer risk by estrogen-receptor status
Q92994868Two truncating variants in FANCC and breast cancer risk

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