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401. Mortality by age, gene and gender in carriers of pathogenic mismatch repair gene variants receiving surveillance for early cancer diagnosis and treatment:a report from the prospective Lynch syndrome database

402. Author Correction : Deciphering colorectal cancer genetics through multi-omic analysis of 100,204 cases and 154,587 controls of European and east Asian ancestries

403. Towards a process-based understanding of rifted continental margins

404. A new record of the Cenomanian–Turonian transgression preserved in the Ikorfat Fault zone, Nuussuaq Basin, West Greenland

405. RADIFUSION: A multi-radiomics deep learning based breast cancer risk prediction model using sequential mammographic images with image attention and bilateral asymmetry refinement

406. Associations of a Breast Cancer Polygenic Risk Score With Tumor Characteristics and Survival

408. No clinical utility of KRAS variant rs61764370 for ovarian or breast cancer

409. International Consortium on Mammographic Density: Methodology and population diversity captured across 22 countries

410. Polymorphisms affecting vitamin D–binding protein modify the relationship between serum vitamin D (25[OH]D3) and food allergy

412. Association of genetic susceptibility variants for type 2 diabetes with breast cancer risk in women of European ancestry

414. Understanding the genetic complexity of puberty timing across the allele frequency spectrum

417. Alcohol consumption, cigarette smoking, and familial breast cancer risk: findings from the Prospective Family Study Cohort (ProF-SC)

419. List of Contributors

422. Publisher Correction: Shared heritability and functional enrichment across six solid cancers

423. Two truncating variants in FANCC and breast cancer risk

424. Joint association of mammographic density adjusted for age and body mass index and polygenic risk score with breast cancer risk

425. Association analyses identify 31 new risk loci for colorectal cancer susceptibility

426. Regular use of aspirin and other non-steroidal anti-inflammatory drugs and breast cancer risk for women at familial or genetic risk: a cohort study

427. Genome-wide association and transcriptome studies identify target genes and risk loci for breast cancer

428. Shared heritability and functional enrichment across six solid cancers

429. Sex differences in lifetime prevalence of low back pain: A multinational study of opposite‐sex twin pairs.

430. Causal relationships between breast cancer risk factors based on mammographic features.

431. Variance of age-specific log incidence decomposition (VALID): a unifying model of measured and unmeasured genetic and non-genetic risks.

432. Educational attainment, health outcomes and mortality: a within-sibship Mendelian randomization study.

434. Using DEPendency of Association on the Number of Top Hits (DEPTH) as a Complementary Tool to Identify Novel Colorectal Cancer Susceptibility Loci.

438. Author Correction: Deciphering colorectal cancer genetics through multi-omic analysis of 100,204 cases and 154,587 controls of European and east Asian ancestries

439. Association of the CHEK2 c.1100delC variant, radiotherapy, and systemic treatment with contralateral breast cancer risk and breast cancer-specific survival

440. Causal relationships between breast cancer mammogram risk scores based on textural features and density

443. Evaluating Multiple Next-Generation Sequencing–Derived Tumor Features to Accurately Predict DNA Mismatch Repair Status

444. Combining Asian-European Genome-Wide Association Studies of Colorectal Cancer Improves Risk Prediction Across Race and Ethnicity

450. Deciphering colorectal cancer genetics through multi-omic analysis of 100,204 cases and 154,587 controls of European and east Asian ancestries

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