Mark N Brook

researcher ORCID ID = 0000-0002-8969-2378

Mark N Brook is …
instance of (P31):
humanQ5

External links are
P496ORCID iD0000-0002-8969-2378

P69educated atUniversity of NottinghamQ472316
London School of Hygiene & Tropical MedicineQ1126189
P108employerInstitute of Cancer ResearchQ6039999
P734family nameBrookQ16860536
BrookQ16860536
BrookQ16860536
P735given nameMarkQ13610143
MarkQ13610143
P106occupationresearcherQ1650915
P21sex or gendermaleQ6581097

Reverse relations

author (P50)
Q89506041Adult weight change and premenopausal breast cancer risk: A prospective pooled analysis of data from 628,463 women
Q57305944Association analyses of more than 140,000 men identify 63 new prostate cancer susceptibility loci
Q56089359Association of Body Mass Index and Age With Subsequent Breast Cancer Risk in Premenopausal Women
Q63966080Author Correction: Association analyses of more than 140,000 men identify 63 new prostate cancer susceptibility loci
Q64118820Author Correction: Association analyses of more than 140,000 men identify 63 new prostate cancer susceptibility loci
Q60907509Author Correction: Germline variation at 8q24 and prostate cancer risk in men of European ancestry
Q62583499Breast Cancer Risk After Recent Childbirth
Q92528444Comparative Validation of Breast Cancer Risk Prediction Models and Projections for Future Risk Stratification
Q62583503Comparative validation of breast cancer risk prediction models and projections for future risk stratification
Q92150094Correction: Rare germline variants in DNA repair genes and the angiogenesis pathway predispose prostate cancer patients to develop metastatic disease
Q55311842Fine-mapping of prostate cancer susceptibility loci in a large meta-analysis identifies candidate causal variants.
Q35925620Genetic predisposition to ductal carcinoma in situ of the breast
Q35151684Genetic predisposition to in situ and invasive lobular carcinoma of the breast
Q24622610Genome-wide association studies identify four ER negative-specific breast cancer risk loci
Q91685253Germline DNA Repair Gene Mutations in Young-onset Prostate Cancer Cases in the UK: Evidence for a More Extensive Genetic Panel
Q58611475Germline variation at 8q24 and prostate cancer risk in men of European ancestry
Q64074106Homeobox B13 G84E Mutation and Prostate Cancer Risk
Q47190168Joint associations of a polygenic risk score and environmental risk factors for breast cancer in the Breast Cancer Association Consortium
Q39006395Mitochondrial DNA Copy Number in Peripheral Blood Cells and Risk of Developing Breast Cancer
Q36873786Performance of automated scoring of ER, PR, HER2, CK5/6 and EGFR in breast cancer tissue microarrays in the Breast Cancer Association Consortium
Q36583004Prediction of breast cancer risk based on profiling with common genetic variants
Q62583659Prostate Cancer Risk-Associated Single-Nucleotide Polymorphism Affects Prostate-Specific Antigen Glycosylation and Its Function
Q90242034Publisher Correction: Shared heritability and functional enrichment across six solid cancers
Q99561517Relationship of self-reported body size and shape with risk for prostate cancer: A UK case-control study
Q61118451Shared heritability and functional enrichment across six solid cancers
Q64004349Shared heritability and functional enrichment across six solid cancers
Q44903190Temporal stability and determinants of white blood cell DNA methylation in the breakthrough generations study
Q38370371The Premenopausal Breast Cancer Collaboration: A Pooling Project of Studies Participating in the National Cancer Institute Cohort Consortium
Q89547730iCARE: An R package to build, validate and apply absolute risk models

Search more.