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33 results on '"Arndt V"'

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

2. Mendelian randomisation study of smoking exposure in relation to breast cancer risk

3. Common variants in breast cancer risk loci predispose to distinct tumor subtypes

4. Assessment of interactions between 205 breast cancer susceptibility loci and 13 established risk factors in relation to breast cancer risk, in the Breast Cancer Association Consortium

5. Fine-mapping of 150 breast cancer risk regions identifies 191 likely target genes

6. Fine-mapping of 150 breast cancer risk regions identifies 191 likely target genes

7. World Health Organization cardiovascular disease risk charts: revised models to estimate risk in 21 global regions

8. Two truncating variants in FANCC and breast cancer risk

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

10. The BRCA2 c.68-7T > A variant is not pathogenic: A model for clinical calibration of spliceogenicity

11. Increased High-Density Lipoprotein Levels Associated with Age-Related Macular Degeneration: Evidence from the EYE-RISK and European Eye Epidemiology Consortia

12. Gene-environment interactions involving functional variants

13. Body mass index and breast cancer survival: a Mendelian randomization analysis

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

15. Evidence that the 5p12 Variant rs10941679 Confers Susceptibility to Estrogen-Receptor-Positive Breast Cancer through FGF10 and MRPS30 Regulation

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

17. Genetic predisposition to ductal carcinoma in situ of the breast

18. Atlas of prostate cancer heritability in European and African-American men pinpoints tissue-specific regulation

19. Annexin A1 expression in a pooled breast cancer series: association with tumor subtypes and prognosis

20. No evidence that protein truncating variants in BRIP1 are associated with breast cancer risk: implications for gene panel testing

21. Prediction of Breast Cancer Risk Based on Profiling With Common Genetic Variants

22. Identification of novel genetic markers of breast cancer survival

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

24. Identification of Novel Genetic Markers of Breast Cancer Survival

25. Common non-synonymous SNPs associated with breast cancer susceptibility: findings from the Breast Cancer Association Consortium

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

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

28. A large-scale assessment of two-way SNP interactions in breast cancer susceptibility using 46,450 cases and 42,461 controls from the breast cancer association consortium

29. MicroRNA related polymorphisms and breast cancer risk

30. Large-scale genotyping identifies 41 new loci associated with breast cancer risk

31. Functional mechanisms underlying pleiotropic risk alleles at the 19p13.1 breast-ovarian cancer susceptibility locus

32. Age- and Tumor Subtype-Specific Breast Cancer Risk Estimates for CHEK2*1100delC Carriers

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

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