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1. A prospective prostate cancer screening programme for men with pathogenic variants in mismatch repair genes (IMPACT): initial results from an international prospective study

2. Assessing associations between the AURKA-HMMR-TPX2-TUBG1 functional module and breast cancer risk in BRCA1/2 mutation carriers.

4. Data from Common Breast Cancer Susceptibility Alleles and the Risk of Breast Cancer for BRCA1 and BRCA2 Mutation Carriers: Implications for Risk Prediction

5. Supplementary Methods, Tables 1-3, Figure 1 from Common Breast Cancer Susceptibility Alleles and the Risk of Breast Cancer for BRCA1 and BRCA2 Mutation Carriers: Implications for Risk Prediction

8. A prospective prostate cancer screening programme for men with pathogenic variants in mismatch repair genes (IMPACT): initial results from an international prospective study

11. Update Swiss guideline for counselling and testing for predisposition to breast, ovarian, pancreatic and prostate cancer

12. Occult ovarian cancers identified at risk-reducing salpingo-oophorectomy in a prospective cohort of BRCA1/2 mutation carriers

13. Association of risk-reducing surgery in BRCA1 or BRCA2 mutation carriers with cancer risk and mortality

15. No evidence that GATA3 rs570613 SNP modifies breast cancer risk

20. Genetic Variation at 9p22.2 and Ovarian Cancer Risk for BRCA1 and BRCA2 Mutation Carriers

22. Psychosocial impact of undergoing prostate cancer screening for men with BRCA1 or BRCA2 mutations

25. Screening for Familial Ovarian Cancer: Failure of Current Protocols to Detect Ovarian Cancer at an Early Stage According to the International Federation of Gynecology and Obstetrics System

27. Psychosocial impact of undergoing prostate cancer screening for men with BRCA1 or BRCA2 mutations

32. Rare Hereditary Cancers : Diagnosis and Management / edited by Gabriella Pichert, Chris Jacobs.

34. Assessing Associations between the AURKA-HMMR-TPX2-TUBG1 Functional Module and Breast Cancer Risk in BRCA1/2 Mutation Carriers

35. Targeted Prostate Cancer Screening in BRCA1 and BRCA2 Mutation Carriers: Results from the Initial Screening Round of the IMPACT Study

36. Breast cancer risk and 6q22.33 : combined results from Breast Cancer Association Consortium and Consortium of Investigators on Modifiers of BRCA1/2

37. Multiple self-healing squamous epithelioma is caused by a disease-specific spectrum of mutations in TGFBR1

38. Common breast cancer susceptibility alleles and the risk of breast cancer for BRCA1 and BRCA2 mutation carriers : implications for risk prediction

39. No evidence that GATA3 rs570613 SNP modifies breast cancer risk

40. Abstract LB-245: Loss of function of the TGFβRI receptor leads to the spontaneously regressing squamous carcinoma condition, multiple self-healing squamous epithelioma (Ferguson-Smith disease)

42. Multiple self-healing squamous epithelioma is caused by a disease-specific spectrum of mutations in TGFBR1

44. Common Breast Cancer Susceptibility Alleles and the Risk of Breast Cancer for BRCA1 and BRCA2 Mutation Carriers: Implications for Risk Prediction

47. Common Breast Cancer-Predisposition Alleles Are Associated with Breast Cancer Risk in BRCA1 and BRCA2 Mutation Carriers

48. Multiple Self-Healing Squamous Epithelioma in Different Ethnic Groups: More than a Founder Mutation Disorder?

50. Loss of Heterozygosity at theBRCA1andBRCA2Loci Detected in Ductal Lavage Fluid fromBRCAGene Mutation Carriers and Controls

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