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1. Genome-wide association meta-analyses combining multiple risk phenotypes provide insights into the genetic architecture of cutaneous melanoma susceptibility

2. Gene-Level Associations in Patients With and Without Pathogenic Germline Variants in CDKN2A and Pancreatic Cancer

4. Germline Variation at CDKN2A and Associations with Nevus Phenotypes among Members of Melanoma Families

7. Supplementary Methods, Tables 1-5, Figures 1-4 from Development and Validation of a Melanoma Risk Score Based on Pooled Data from 16 Case–Control Studies

8. Data from Development and Validation of a Melanoma Risk Score Based on Pooled Data from 16 Case–Control Studies

11. Multiple rare variants in high-risk pancreatic cancer-related genes may increase risk for pancreatic cancer in a subset of patients with and without germline CDKN2A mutations

12. Germline TERT promoter mutations are rare in familial melanoma

13. Germline CDKN2A/P16INK4A mutations contribute to genetic determinism of sarcoma

15. Genome-wide meta-analysis identifies five new susceptibility loci for cutaneous malignant melanoma

16. Melanoma risk factors, perceived threat and intentional tanning : an international online survey

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

18. The Emergence of Networks in Human Genome Epidemiology: "Challenges and Opportunities"

21. The Effect on Melanoma Risk of Genes Previously Associated With Telomere Length

22. Fine mapping of genetic susceptibility loci for melanoma reveals a mixture of single variant and multiple variant regions

23. MC1R variants increased the risk of sporadic cutaneous melanoma in darker-pigmented Caucasians: A pooled-analysis from the M-SKIP project

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

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

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

30. An inherited variant in the gene coding for vitamin D-binding protein and survival from cutaneous melanoma: a BioGenoMEL study

33. Genome-wide analysis of constitutional DNA methylation in familial melanoma

34. Additional file 3 of Genome-wide analysis of constitutional DNA methylation in familial melanoma

36. A mutation hotspot at the p14ARF splice site

40. Localization of a novel melanoma susceptibility locus to 1p22

41. The emergence of networks in human genome epidemiology: challenges and opportunities

42. Skin Examination Behavior: The Role of Melanoma History, Skin Type, Psychosocial Factors, and Region of Residence in Determining Clinical and Self-conducted Skin Examination

43. Inherited variants in the MC1R gene and survival from cutaneous melanoma: a BioGenoMEL study

46. Association of HERV-K and LINE-1 hypomethylation with reduced disease-free survival in melanoma patients

47. Association between a 46-SNP Polygenic Risk Score and melanoma risk in Dutch patients with familial melanoma

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