Genome-wide association study identifies five new breast cancer susceptibility loci

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1. Fine-mapping identifies two additional breast cancer susceptibility loci at 9q31.2
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2. The rs11515 Polymorphism Is More Frequent and Associated With Aggressive Breast Tumors with Increased ANRIL and Decreased p16INK4a Expression
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3. A Review of Whole-Exome Sequencing Efforts Toward Hereditary Breast Cancer Susceptibility Gene Discovery
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4. The Genetics of Pigment Dispersion Syndrome and Pigmentary Glaucoma
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5. Effects of lifestyle and single nucleotide polymorphisms on breast cancer risk: a case–control study in Japanese women
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6. Identification and characterization of novel associations in the CASP8/ALS2CR12 region on chromosome 2 with breast cancer risk
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7. Genetic variations in colorectal cancer risk and clinical outcome
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8. Identification of novel common breast cancer risk variants at the 6q25 locus among Latinas
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9. The SLC4A7 variant rs4973768 is associated with breast cancer risk: evidence from a case–control study and a meta-analysis
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10. Telomere Length and Genetic Variation in Telomere Maintenance Genes in Relation to Ovarian Cancer Risk
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11. Genome-wide association study of endometrial cancer in E2C2
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12. Cell-type-specific enrichment of risk-associated regulatory elements at ovarian cancer susceptibility loci
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13. The Pro Allele of the p53 Codon 72 Polymorphism Is Associated with Decreased Intratumoral Expression of BAX and p21, and Increased Breast Cancer Risk
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14. ANRIL Genetic Variants in Iranian Breast Cancer Patients.
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15. Genome-wide association analysis of chronic lymphocytic leukaemia, Hodgkin lymphoma and multiple myeloma identifies pleiotropic risk loci
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16. Exploring the Link between Germline and Somatic Genetic Alterations in Breast Carcinogenesis
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17. Identification of Inherited Genetic Variations Influencing Prognosis in Early-Onset Breast Cancer
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18. Meta-analysis of 8q24 for seven cancers reveals a locus between NOV and ENPP2 associated with cancer development
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19. FADS2 function at the major cancer hotspot 11q13 locus alters fatty acid metabolism in cancer
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20. Comprehensive Functional Annotation of Seventy-One Breast Cancer Risk Loci
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21. Long noncoding RNA variations in cardiometabolic diseases
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22. Genetic variants in long noncoding RNA H19 contribute to the risk of breast cancer in a southeast China Han population
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23. FGFR2 gene polymorphisms are associated with breast cancer risk in the Han Chinese population.
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24. Gender-Specific Genetic Predisposition to Breast Cancer: BRCA Genes and Beyond
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25. Lack of referral for genetic counseling and testing in BRCA1/2 and Lynch syndromes: a nationwide study based on 240,134 consultations and 134,652 genetic tests
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26. Additive Interactions Between Susceptibility Single-Nucleotide Polymorphisms Identified in Genome-Wide Association Studies and Breast Cancer Risk Factors in the Breast and Prostate Cancer Cohort Consortium
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27. MiR‐142‐3p functions as a tumor suppressor by targeting RAC1/PAK1 pathway in breast cancer
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28. A case-only study to identify genetic modifiers of breast cancer risk for BRCA1/BRCA2 mutation carriers
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29. Genetic variant in 8q24 is associated with prognosis for gastric cancer in a C hinese population
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30. CCDC26,CDKN2BAS,RTEL1andTERTPolymorphisms in pediatric brain tumor susceptibility
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31. Post-GWAS gene–environment interplay in breast cancer: results from the Breast and Prostate Cancer Cohort Consortium and a meta-analysis on 79 000 women
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32. Association of Genetic Polymorphisms in the LncRNAs with Gastric Cancer Risk in a Chinese Population
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33. Genome-Wide Association Study Identifies Four Loci Associated with Eruption of Permanent Teeth
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34. Variants at the 9p21 locus and melanoma risk
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35. Replication and Meta‐analysis of Genome‐Wide Association Studies
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36. Common Genetic Variants in miR-1206 (8q24.2) and miR-612 (11q13.3) Affect Biogenesis of Mature miRNA Forms
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37. Association of breast cancer risk with genetic variants showing differential allelic expression: Identification of a novel breast cancer susceptibility locus at 4q21
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38. Unravelling similarities and differences in the role of circular and linear PVT1 in cancer and human disease
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39. Polymorphisms in a Putative Enhancer at the 10q21.2 Breast Cancer Risk Locus Regulate NRBF2 Expression
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40. A concordance index for matched case-control studies with applications in cancer risk
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41. Combined effect of low-penetrant SNPs on breast cancer risk
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42. Rare Copy Number Variants Observed in Hereditary Breast Cancer Cases Disrupt Genes in Estrogen Signaling and TP53 Tumor Suppression Network
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43. A Study on Genetic Variants of Fibroblast Growth Factor Receptor 2 (FGFR2) and the Risk of Breast Cancer from North India
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44. Progress in defining the biological causes of schizophrenia
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45. Novel and known genetic variants for male breast cancer risk at 8q24.21, 9p21.3, 11q13.3 and 14q24.1: Results from a multicenter study in Italy
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46. The Protein Encoded by the CCDC170 Breast Cancer Gene Functions to Organize the Golgi-Microtubule Network
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47. Rat models of 17β-estradiol-induced mammary cancer reveal novel insights into breast cancer etiology and prevention
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48. The lncRNA ANRIL regulates endothelial dysfunction by targeting the let‐7b/TGF‐βR1 signalling pathway
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49. Association of low-penetrance alleles with male breast cancer risk and clinicopathological characteristics: results from a multicenter study in Italy
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50. 11q13 is a susceptibility locus for hormone receptor positive breast cancer
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51. Polymorphism in ANRIL is associated with relapse in patients with multiple myeloma after autologous stem cell transplant
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53. Applications of Next Generation Sequencing to the Analysis of Familial Breast/Ovarian Cancer
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54. Transcriptome‐wide association study of breast cancer risk by estrogen‐receptor status
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59. Germline DNA Variations in Breast Cancer Predisposition and Prognosis: A Systematic Review of the Literature
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60. Targeted mutation detection in breast cancer using MammaSeq™
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62. Genome-Wide Association Study of Breast Cancer in the Japanese Population
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64. Therapeutic Approaches for Women Predisposed to Breast Cancer
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95. Risk of genome-wide association study newly identified genetic variants for breast cancer in Chinese women of Heilongjiang Province
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96. Tumor suppressor microRNAs: Targeted molecules and signaling pathways in breast cancer
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