374 results on '"Winship, Ingrid M."'
Search Results
2. Inherited BRCA1 and RNF43 pathogenic variants in a familial colorectal cancer type X family
3. A mosaic pathogenic variant in MSH6 causes MSH6-deficient colorectal and endometrial cancer in a patient classified as suspected Lynch syndrome: a case report
4. The clinical utility and costs of whole-genome sequencing to detect cancer susceptibility variants—a multi-site prospective cohort study
5. A tumor focused approach to resolving the etiology of DNA mismatch repair deficient tumors classified as suspected Lynch syndrome
6. Elucidating the Risk of Colorectal Cancer for Variants in Hereditary Colorectal Cancer Genes
7. Dermatologic manifestations and diagnostic assessments of the Ehlers-Danlos syndromes: A clinical review
8. Rare germline variants in the AXIN2 gene in families with colonic polyposis and colorectal cancer
9. Informed choice and attitudes regarding a genomic test to predict risk of colorectal cancer in general practice
10. Identifying colorectal cancer caused by biallelic MUTYH pathogenic variants using tumor mutational signatures
11. Body Mass Index, sex, non-steroidal anti-inflammatory drug medications, smoking and alcohol are differentially associated with World Health Organisation criteria and colorectal cancer risk in people with Serrated Polyposis Syndrome: an Australian case-control study
12. Population-based estimates of age-specific cumulative risk of breast cancer for pathogenic variants in ATM
13. Heterogeneity in the psychosocial and behavioral responses associated with a diagnosis of suspected Lynch syndrome in women with endometrial cancer
14. Evaluating Multiple Next-Generation Sequencing–Derived Tumor Features to Accurately Predict DNA Mismatch Repair Status
15. Intratumoral presence of the genotoxic gut bacteria pks+ E. coli, Enterotoxigenic Bacteroides fragilis, and Fusobacterium nucleatum and their association with clinicopathological and molecular features of colorectal cancer
16. A Genomic Test for Colorectal Cancer Risk : Is This Acceptable and Feasible in Primary Care?
17. Inherited BRCA1 and RNF43 pathogenic variants in a familial colorectal cancer type X family
18. DNA Mismatch Repair Gene Variant Classification: Evaluating the Utility of Somatic Mutations and Mismatch Repair Deficient Colonic Crypts and Endometrial Glands
19. Cancer risks by gene, age, and gender in 6350 carriers of pathogenic mismatch repair variants: findings from the Prospective Lynch Syndrome Database
20. Type 2 diabetes mellitus, blood cholesterol, triglyceride and colorectal cancer risk in Lynch syndrome
21. Ability of known susceptibility SNPs to predict colorectal cancer risk for persons with and without a family history
22. Identifying primary and secondary MLH1 epimutation carriers displaying low-level constitutional MLH1 methylation using droplet digital PCR and genome-wide DNA methylation profiling of colorectal cancers
23. Elucidating the Risk of Colorectal Cancer for Variants in Hereditary Colorectal Cancer Genes
24. Phenotypic confirmation of oligodontia, colorectal polyposis and cancer in a family carrying an exon 7 nonsense variant in the AXIN2 gene
25. Hemangioblastoma in Hereditary Leiomyomatosis and Renal Cell Cancer Syndrome: a phenotypic overlap between VHL and HLRCC Syndromes
26. A mosaic pathogenic variant in MSH6 causes MSH6-deficient colorectal and endometrial cancer in a patient classified as suspected Lynch syndrome: a case report
27. Data from Weight is More Informative than Body Mass Index for Predicting Postmenopausal Breast Cancer Risk: Prospective Family Study Cohort (ProF-SC)
28. Supplementary Data from Weight is More Informative than Body Mass Index for Predicting Postmenopausal Breast Cancer Risk: Prospective Family Study Cohort (ProF-SC)
29. Supplementary Figure from Aspirin and the Risk of Colorectal Cancer According to Genetic Susceptibility among Older Individuals
30. Data from Aspirin and the Risk of Colorectal Cancer According to Genetic Susceptibility among Older Individuals
31. Risk of colorectal cancer for carriers of a germ-line mutation in POLE or POLD1
32. Supplementary Tables from SNP rs16906252C>T Is an Expression and Methylation Quantitative Trait Locus Associated with an Increased Risk of Developing MGMT-Methylated Colorectal Cancer
33. Supplementary Figures from SNP rs16906252C>T Is an Expression and Methylation Quantitative Trait Locus Associated with an Increased Risk of Developing MGMT-Methylated Colorectal Cancer
34. Supplementary Methods from SNP rs16906252C>T Is an Expression and Methylation Quantitative Trait Locus Associated with an Increased Risk of Developing MGMT-Methylated Colorectal Cancer
35. Genotoxic colibactin mutational signature in colorectal cancer is associated with clinicopathological features, specific genomic alterations and better survival
36. Evaluating Multiple Next-Generation Sequencing–Derived Tumor Features to Accurately Predict DNA Mismatch Repair Status
37. Extracutaneous features and complications of the Ehlers-Danlos syndromes: A systematic review
38. Additional file 1 of A tumor focused approach to resolving the etiology of DNA mismatch repair deficient tumors classified as suspected Lynch syndrome
39. Extracutaneous features and complications of the Ehlers-Danlos syndromes: A systematic review
40. The role of cutaneous manifestations in the diagnosis of the Ehlers-Danlos syndromes
41. Public willingness to participate in population DNA screening in Australia.
42. Public willingness to participate in population DNA screening in Australia
43. Using a Modified Delphi Approach and Nominal Group Technique for Organisational Priority Setting of Evidence-Based Interventions That Advance Women in Healthcare Leadership
44. Germline mutations inWNK2could be associated with serrated polyposis syndrome
45. Somatic mutations of the coding microsatellites within the beta-2-microglobulin gene in mismatch repair-deficient colorectal cancers and adenomas
46. Should the grading of colorectal adenocarcinoma include microsatellite instability status?
47. Correction: Cancer risks by gene, age, and gender in 6350 carriers of pathogenic mismatch repair variants: findings from the Prospective Lynch Syndrome Database
48. The role of cutaneous manifestations in the diagnosis of the Ehlers‐Danlos syndromes
49. Real world outcomes and implementation pathways of exome sequencing in an adult genetic department
50. Trends in the surgical management of stage 1 renal cell carcinoma: findings from a population‐based study
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