1,030 results on '"Syngal, Sapna"'
Search Results
2. PREMM5 distinguishes sporadic from Lynch syndrome-associated MMR-deficient/MSI-high colorectal cancer
3. Literacy-adapted, electronic family history assessment for genetics referral in primary care: patient user insights from qualitative interviews
4. Gastrointestinal Cancer Precursor Conditions and Their Detection
5. Community Collaboration to Advance Racial/Ethnic Equity in Colorectal Cancer Screening: Protocol for a Multilevel Intervention to Improve Screening and Follow-up in Community Health Centers
6. A Randomized Trial of Two Remote Health Care Delivery Models on the Uptake of Genetic Testing and Impact on Patient-Reported Psychological Outcomes in Families With Pancreatic Cancer: The Genetic Education, Risk Assessment, and Testing (GENERATE) Study
7. Young-onset colorectal cancer
8. Feasibility of an electronic patient-facing cancer family history tool in medically underserved populations
9. Novel Models of Genetic Education and Testing for Pancreatic Cancer Interception: Preliminary Results from the GENERATE Study
10. Most people share genetic test results with relatives even if the findings are normal: Family communication in a diverse population
11. Delphi Initiative for Early-Onset Colorectal Cancer (DIRECt) International Management Guidelines
12. Mutational signature profiling classifies subtypes of clinically different mismatch-repair-deficient tumours with a differential immunogenic response potential
13. Adaptation and early implementation of the PREdiction model for gene mutations (PREMM5™) for lynch syndrome risk assessment in a diverse population
14. Timeline of Development of Pancreatic Cancer and Implications for Successful Early Detection in High-Risk Individuals
15. Pancreatic Cancer Surveillance and Survival of High-Risk Individuals.
16. A risk prediction tool for individuals with a family history of breast, ovarian, or pancreatic cancer: BRCAPANCPRO
17. A prospective prostate cancer screening programme for men with pathogenic variants in mismatch repair genes (IMPACT): initial results from an international prospective study
18. Community Collaboration To Advance Racial/Ethnic Equity in Colorectal Cancer Screening: Protocol for a Multilevel Intervention to Improve Screening, Follow-Up, and Biorepository Participation in Community Health Centers
19. Variation in the risk of colorectal cancer in families with Lynch syndrome: a retrospective cohort study
20. Characterizing germline APC and MUTYH variants in Ashkenazi Jews compared to other individuals
21. Clinical Factors Associated With Gastric Cancer in Individuals With Lynch Syndrome
22. Endoscopic Removal of Colorectal Lesions—Recommendations by the US Multi-Society Task Force on Colorectal Cancer
23. Recommendations for Follow-Up After Colonoscopy and Polypectomy: A Consensus Update by the US Multi-Society Task Force on Colorectal Cancer
24. Oncologists' Selection of Genetic and Molecular Testing in the Evolving Landscape of Stage II Colorectal Cancer.
25. Health behaviours and beliefs in individuals with familial pancreatic cancer
26. Mutations in the pancreatic secretory enzymes CPA1 and CPB1 are associated with pancreatic cancer
27. Poor performance of clinical prediction models: the harm of commonly applied methods
28. Community Practice Implementation of a Self-administered Version of PREMM1,2,6 to Assess Risk for Lynch Syndrome
29. Mutations in RABL3 alter KRAS prenylation and are associated with hereditary pancreatic cancer
30. Implementation of a Systematic Tumor Screening Program for Lynch Syndrome in an Integrated Health Care Setting
31. Recent advances in Lynch syndrome
32. Germline cancer susceptibility gene variants, somatic second hits, and survival outcomes in patients with resected pancreatic cancer
33. Impact of genetic testing on endometrial cancer risk-reducing practices in women at risk for Lynch syndrome
34. Systemic Barriers to Risk-Reducing Interventions for Hereditary Cancer Syndromes: Implications for Health Care Inequities
35. Clinical Implications of Pathogenic Germline Variants in Small Intestine Neuroendocrine Tumors (SI-NETs)
36. Letter to the Editor-Recent advances in Lynch syndrome: response to Møller et al.
37. Perspective on This Article from Microsatellite Instability and DNA Mismatch Repair Protein Deficiency in Lynch Syndrome Colorectal Polyps
38. Supplementary Table 2 from A Multi-Institutional Cohort of Therapy-Associated Polyposis in Childhood and Young Adulthood Cancer Survivors
39. Data from Chromoendoscopy Detects More Adenomas than Colonoscopy Using Intensive Inspection without Dye Spraying
40. Data from ATM Mutations in Patients with Hereditary Pancreatic Cancer
41. Data from Microsatellite Instability and DNA Mismatch Repair Protein Deficiency in Lynch Syndrome Colorectal Polyps
42. Data from Whole Genome Sequencing Defines the Genetic Heterogeneity of Familial Pancreatic Cancer
43. Supplementary Tables S1 - S12 from Whole Genome Sequencing Defines the Genetic Heterogeneity of Familial Pancreatic Cancer
44. Supplement 1 from Novel Models of Genetic Education and Testing for Pancreatic Cancer Interception: Preliminary Results from the GENERATE Study
45. Data from A Multi-Institutional Cohort of Therapy-Associated Polyposis in Childhood and Young Adulthood Cancer Survivors
46. Perspective on this Article from Chromoendoscopy Detects More Adenomas than Colonoscopy Using Intensive Inspection without Dye Spraying
47. Supplementary Table 1 from A Multi-Institutional Cohort of Therapy-Associated Polyposis in Childhood and Young Adulthood Cancer Survivors
48. Supplementary Table 3 from A Multi-Institutional Cohort of Therapy-Associated Polyposis in Childhood and Young Adulthood Cancer Survivors
49. Perspective on This Article from Health Benefits and Cost-Effectiveness of Primary Genetic Screening for Lynch Syndrome in the General Population
50. Supplement 4 from Novel Models of Genetic Education and Testing for Pancreatic Cancer Interception: Preliminary Results from the GENERATE Study
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