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424 results on '"Arif, B."'

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1. Lifetime ovulatory years and risk of epithelial ovarian cancer: a multinational pooled analysis

2. Aggregation tests identify new gene associations with breast cancer in populations with diverse ancestry

3. A saturated map of common genetic variants associated with human height

4. Association 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

5. Functional annotation of the 2q35 breast cancer risk locus implicates a structural variant in influencing activity of a long-range enhancer element

6. Combined Associations of a Polygenic Risk Score and Classical Risk Factors With Breast Cancer Risk.

7. Breast Cancer Risk Genes — Association Analysis in More than 113,000 Women

8. Cross-Cancer Genome-Wide Association Study of Endometrial Cancer and Epithelial Ovarian Cancer Identifies Genetic Risk Regions Associated with Risk of Both Cancers

9. Germline variants and breast cancer survival in patients with distant metastases at primary breast cancer diagnosis

10. Variants in SCAF4 Cause a Neurodevelopmental Disorder and Are Associated with Impaired mRNA Processing

11. Genome-wide association study identifies 32 novel breast cancer susceptibility loci from overall and subtype-specific analyses.

12. Two truncating variants in FANCC and breast cancer risk.

13. Genome-wide association study of germline variants and breast cancer-specific mortality.

14. Polygenic Risk Scores for Prediction of Breast Cancer and Breast Cancer Subtypes.

15. rs495139 in the TYMS-ENOSF1 Region and Risk of Ovarian Carcinoma of Mucinous Histology.

16. Variants in genes encoding small GTPases and association with epithelial ovarian cancer susceptibility

17. Association analysis identifies 65 new breast cancer risk loci

18. PALB2, CHEK2 and ATM rare variants and cancer risk: data from COGS

19. Assessment of variation in immunosuppressive pathway genes reveals TGFBR2 to be associated with risk of clear cell ovarian cancer

20. Genome-Wide Meta-Analyses of Breast, Ovarian, and Prostate Cancer Association Studies Identify Multiple New Susceptibility Loci Shared by at Least Two Cancer Types

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

22. Identification of four novel susceptibility loci for oestrogen receptor negative breast cancer.

23. Germline polymorphisms in an enhancer of PSIP1 are associated with progression-free survival in epithelial ovarian cancer

24. CYP19A1 fine-mapping and Mendelian randomization: estradiol is causal for endometrial cancer

25. Evidence of a genetic link between endometriosis and ovarian cancer

26. Genome-wide Analysis Identifies Novel Loci Associated with Ovarian Cancer Outcomes: Findings from the Ovarian Cancer Association Consortium

27. Epithelial-Mesenchymal Transition (EMT) Gene Variants and Epithelial Ovarian Cancer (EOC) Risk.

28. Height and Breast Cancer Risk: Evidence From Prospective Studies and Mendelian Randomization

29. Common variants at the CHEK2 gene locus and risk of epithelial ovarian cancer

30. Network-Based Integration of GWAS and Gene Expression Identifies a HOX-Centric Network Associated with Serous Ovarian Cancer Risk.

31. Cis-eQTL analysis and functional validation of candidate susceptibility genes for high-grade serous ovarian cancer.

32. Genome-wide significant risk associations for mucinous ovarian carcinoma

33. Polymorphisms in a Putative Enhancer at the 10q21.2 Breast Cancer Risk Locus Regulate NRBF2 Expression

34. Cell-type-specific enrichment of risk-associated regulatory elements at ovarian cancer susceptibility loci

35. Fine-mapping identifies two additional breast cancer susceptibility loci at 9q31.2.

36. Investigation of gene‐environment interactions between 47 newly identified breast cancer susceptibility loci and environmental risk factors

37. Fine-mapping of the HNF1B multicancer locus identifies candidate variants that mediate endometrial cancer risk

38. Evaluating the ovarian cancer gonadotropin hypothesis: a candidate gene study.

39. Candidate locus analysis of the TERT–CLPTM1L cancer risk region on chromosome 5p15 identifies multiple independent variants associated with endometrial cancer risk

40. Inherited variants in the inner centromere protein (INCENP) gene of the chromosomal passenger complex contribute to the susceptibility of ER-negative breast cancer

41. Fine-Scale Mapping of the 5q11.2 Breast Cancer Locus Reveals at Least Three Independent Risk Variants Regulating MAP3K1

42. Common Genetic Variation In Cellular Transport Genes and Epithelial Ovarian Cancer (EOC) Risk

43. Identification and characterization of novel associations in the CASP8/ALS2CR12 region on chromosome 2 with breast cancer risk.

44. Refined histopathological predictors of BRCA1 and BRCA2 mutation status: a large-scale analysis of breast cancer characteristics from the BCAC, CIMBA, and ENIGMA consortia.

45. Refined histopathological predictors of BRCA1 and BRCA2mutation status: a large-scale analysis of breast cancer characteristics from the BCAC, CIMBA, and ENIGMA consortia

46. Genetic variation in mitotic regulatory pathway genes is associated with breast tumor grade.

47. Consortium analysis of gene and gene-folate interactions in purine and pyrimidine metabolism pathways with ovarian carcinoma risk.

48. ABCA transporter gene expression and poor outcome in epithelial ovarian cancer.

49. Variation in NF-κB Signaling Pathways and Survival in Invasive Epithelial Ovarian Cancer

50. Genetic variation at CYP3A is associated with age at menarche and breast cancer risk: a case-control study.

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