41 results on '"Evans, Gareth D."'
Search Results
2. Body mass index and breast cancer survival: a Mendelian randomization analysis
3. Urgent improvements needed to diagnose and manage Lynch syndrome
4. The Contribution of Whole Gene Deletions and Large Rearrangements to the Mutation Spectrum in Inherited Tumor Predisposing Syndromes
5. Recent developments in neurofibromatoses and RASopathies: Management, diagnosis and current and future therapeutic avenues
6. Germline SMARCE1 mutations predispose to both spinal and cranial clear cell meningiomas
7. Update from the 2013 International Neurofibromatosis Conference
8. Management of women at high risk of breast cancer
9. Threshold for genetic testing in women with breast cancer needs to be determined
10. CTF meeting 2012: Translation of the basic understanding of the biology and genetics of NF1, NF2, and schwannomatosis toward the development of effective therapies
11. A pooled analysis of the outcome of prospective colonoscopic surveillance for familial colorectal cancer
12. The Fragile X Protein binds mRNAs involved in cancer progression and modulates metastasis formation
13. Optimal age to start preventive measures in women with BRCA1/2 mutations or high familial breast cancer risk
14. Familial breast cancer: summary of updated NICE guidance
15. Autism and other psychiatric comorbidity in neurofibromatosis type 1: evidence from a population-based study
16. Key genetic considerations in the management of suspected hereditary colorectal cancer
17. Mosaic PPM1D mutations are associated with predisposition to breast and ovarian cancer
18. Clinical presentation, immunohistochemistry and electron microscopy indicate neurofibromatosis type 2-associated gliomas to be spinal ependymomas
19. Are we ready for targeted early breast cancer detection strategies in women with NF1 aged 30–49 years?
20. Exposure to diagnostic radiation and risk of breast cancer among carriers of BRCA1/2 mutations: retrospective cohort study (GENE-RAD-RISK)
21. An improved coverage and spatial resolution—using dual injection dynamic contrast-enhanced (ICE-DICE) MRI: A novel dynamic contrast-enhanced technique for cerebral tumors
22. Surveillance of women at increased risk of breast cancer using mammography and clinical breast examination: Further evidence of benefit
23. Polymorphisms of CYP19A1 and response to aromatase inhibitors in metastatic breast cancer patients
24. Lack of caveolin-1 (P132L) somatic mutations in breast cancer
25. Vestibular Schwannomas Occur in Schwannomatosis and Should Not Be Considered An Exclusion Criterion for Clinical Diagnosis
26. Consensus Recommendations for Current Treatments and Accelerating Clinical Trials for Patients With Neurofibromatosis Type 2
27. Back to the future: Proceedings from the 2010 NF Conference
28. Comprehensive CYP2D6 genotype and adherence affect outcome in breast cancer patients treated with tamoxifen monotherapy
29. Mutation and association analysis of GEN1 in breast cancer susceptibility
30. Occult ovarian cancers identified at risk-reducing salpingo-oophorectomy in a prospective cohort of BRCA1/2 mutation carriers
31. Guidelines for colorectal cancer screening and surveillance in moderate and high risk groups (update from 2002)
32. Update on genetic predisposition to breast cancer
33. Effect of Aspirin or Resistant Starch on Colorectal Neoplasia in the Lynch Syndrome
34. Bilateral Prophylactic Oophorectomy and Bilateral Prophylactic Mastectomy in a Prospective Cohort of Unaffected BRCA1 and BRCA2 Mutation Carriers
35. Surveillance for familial breast cancer: Differences in outcome according to BRCA mutation status
36. Delivering cancer genetics services-new ways of working
37. The Heterogeneous Nature of Germline Mutations in NF1 Patients With Malignant Peripheral Serve Sheath Tumours (MPNSTs)
38. Evaluation of RAD50 in familial breast cancer predisposition
39. Is It Time to Abandon Microsatellite Instability As a Pre-Screen for Selecting Families for Mutation Testing for Mismatch Repair Genes?
40. Identification of Genetic Aberrations on Chromosome 22 Outside the NF2 Locus in Schwannomatosis and Neurofibromatosis Type 2
41. Physical localisation of the breakpoints of a constitutional translocation t(5;6)(q21;q21) in a child with bilateral Wilms' tumour
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