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3. Assessing the Incremental Contribution of Common Genomic Variants to Melanoma Risk Prediction in Two Population-Based Studies

4. Data from Accuracy of Self-Reported Nevus and Pigmentation Phenotype Compared with Clinical Assessment in a Population-Based Study of Young Australian Adults

5. Supplementary Figure S1 from Accuracy of Self-Reported Nevus and Pigmentation Phenotype Compared with Clinical Assessment in a Population-Based Study of Young Australian Adults

6. Supplementary Table S1 from Accuracy of Self-Reported Nevus and Pigmentation Phenotype Compared with Clinical Assessment in a Population-Based Study of Young Australian Adults

7. Evaluation of the contribution of germline variants in BRCA1 and BRCA2 to uveal and cutaneous melanoma

8. Association of Germline Variants in Telomere Maintenance Genes (POT1, TERF2IP, ACD, TERT) with Spitzoid Morphology in Familial Melanoma: A Multi-Center Case Series

9. Protocol for the implementation of a stepped-care model to address fear of cancer recurrence in patients previously diagnosed with early-stage (0–II) melanoma

11. Nonsense Mutations in the Shelterin Complex Genes ACD and TERF2IP in Familial Melanoma

12. Efficiency of Detecting New Primary Melanoma Among Individuals Treated in a High-risk Clinic for Skin Surveillance

13. Additional file 1 of Birth cohort-specific trends of sun-related behaviors among individuals from an international consortium of melanoma-prone families

14. Additional file 2 of Birth cohort-specific trends of sun-related behaviors among individuals from an international consortium of melanoma-prone families

15. Risk factors for melanoma by anatomical site: an evaluation of aetiological heterogeneity

16. Efficiency of Detecting New Primary Melanoma among Individuals Treated in a High-risk Clinic for Skin Surveillance

17. Birth cohort-specific trends of sun-related behaviors among individuals from an international consortium of melanoma-prone families

18. A novel recurrent mutation in MITF predisposes to familial and sporadic melanoma

22. Melanoma risk for CDKN2A mutation carriers who are relatives of population-based case carriers in Australia and the UK

25. Prevalence and predictors of germline CDKN2A mutations for melanoma cases from Australia, Spain and the United Kingdom

26. Knowledge and attitudes of Australian dermatologists towards sentinel lymph node biopsy for melanoma: a mixed methods study.

27. Estimating CDKN2A mutation carrier probability among global familial melanoma cases using GenoMELPREDICT

28. Assessing the Incremental Contribution of Common Genomic Variants to Melanoma Risk Prediction in Two Population-Based Studies

29. FC1-3: Does Phototherapy Induce Melanoma Simulators? Role of Confocal Microscopy in the Evaluation of Nevi Undergoing nbUVB Irradiation

30. Genetic and developmental analysis of the sex-determining gene ‘double sex' (dsx) of Drosophila melanogaster

31. GPs' involvement in diagnosing, treating, and referring patients with suspected or confirmed primary cutaneous melanoma: a qualitative study.

32. Sunscreen Use and Melanoma Risk Among Young Australian Adults

33. Phenotypic and Histopathological Tumor Characteristics According to CDKN2A Mutation Status among Affected Members of Melanoma Families

34. Phenotypic and Histopathological Tumor Characteristics According to CDKN2A Mutation Status among Affected Members of Melanoma Families

37. Evaluation of the contribution of germline variants in BRCA1and BRCA2to uveal and cutaneous melanoma

38. Accuracy of Self-Reported Nevus and Pigmentation Phenotype Compared with Clinical Assessment in a Population-Based Study of Young Australian Adults

39. Nonsense Mutations in the Shelterin Complex Genes ACD and TERF2IP in Familial Melanoma

40. Genome-wide association study identifies a new melanoma susceptibility locus at 1q21.3

41. Common sequence variants on 20q11.22 confer melanoma susceptibility

42. MC1Rgenotype as a predictor of early-onset melanoma, compared with self-reported and physician-measured traditional risk factors: an Australian case-control-family study

43. Genome-wide association study identifies a new melanoma susceptibility locus at 1q21.3

45. Common sequence variants on 20q11.22 confer melanoma susceptibility

46. Functional characterization of a multi-cancer risk locus on chr5p15.33 reveals regulation of TERT by ZNF148

47. Phenotypic and Histopathological Tumor Characteristics According to CDKN2AMutation Status among Affected Members of Melanoma Families

49. MC1R genotype as a predictor of early-onset melanoma, compared with self-reported and physician-measured traditional risk factors: an Australian case-control-family study.

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