641 results on '"Houlston, R"'
Search Results
2. Meeting report from the joint IARC–NCI international cancer seminar series: a focus on colorectal cancer
3. Genome-wide association study of immunoglobulin light chain amyloidosis in three patient cohorts: comparison with myeloma
4. Prediction of outcome in newly diagnosed myeloma: a meta-analysis of the molecular profiles of 1905 trial patients
5. Mendelian randomisation analysis provides no evidence for a relationship between adult height and testicular cancer risk
6. A genome-wide association study identifies risk loci for childhood acute lymphoblastic leukemia at 10q26.13 and 12q23.1
7. Correction: Whole-genome sequencing of chronic lymphocytic leukaemia reveals distinct differences in the mutational landscape between IgHVmut and IgHVunmut subgroups
8. Inherited genetic susceptibility to multiple myeloma
9. Genetic factors influencing the risk of multiple myeloma bone disease
10. Implications of polygenic risk for personalised colorectal cancer screening
11. Erratum: Whole-genome sequencing of chronic lymphocytic leukaemia reveals distinct differences in the mutational landscape between IgHVmut and IgHVunmut subgroups
12. Common variation at 12q24.13 (OAS3) influences chronic lymphocytic leukemia risk
13. Risk of developing chronic lymphocytic leukemia is influenced by HLA-A class I variation
14. Common genetic variation contributes significantly to the risk of childhood B-cell precursor acute lymphoblastic leukemia
15. The 14q22.2 colorectal cancer variant rs4444235 shows cis-acting regulation of BMP4
16. Variant IRF4/MUM1 associates with CD38 status and treatment-free survival in chronic lymphocytic leukaemia
17. Association between chromosomal instability and prognosis in colorectal cancer: a meta-analysis
18. Germline mutations in SPI1 and MADD do not contribute to familial chronic lymphocytic leukaemia
19. Localisation of merosin-positive congenital muscular dystrophy to chromosome 4p16.3
20. CLL family ‘Pedigree 14’ revisited: 1947–2004
21. Association between hormonal genetic polymorphisms and early-onset prostate cancer
22. The C/C_ 13910 mismatch repairgenotype of adult-type hypolactasia is associated with an increased risk of colorectal cancer in the Finnish population
23. Exon 3 betacatenin mutations are specifically associated with colorectal carcinomas in hereditary non-polyposis colorectal cancer syndrome
24. Association between the GCG polymorphism of the selenium dependent GPX1 gene and the risk of young onset prostate cancer
25. Apparent Mendelian inheritance of breast and colorectal cancer: chance, genetic heterogeneity or a new gene?
26. Genotyping methodologies
27. Linkage of recessive Robinow syndrome to a 4 cM interval on chromosome 9q22
28. The carrier clinic: an evaluation of a novel clinic dedicated to the follow-up of BRCA1 and BRCA2 carriers—implications for oncogenetics practice
29. Association between polymorphisms of the GPX1 gene and second primary tumours after index squamous cell cancer of the head and neck
30. 123 (PB-036) Poster - Analysis of rare disruptive germline mutations in 2135 enriched BRCA-negative breast cancer cases excludes additional high-impact susceptibility genes
31. Interobserver agreement in grading of colorectal cancers – findings from a nationwide web-based survey of histopathologists
32. Inherited predisposition to colorectal adenomas caused by multiple rare alleles of MUTYH but not OGG1, NUDT1, NTH1 or NEIL 1, 2 or 3
33. Lack of a relationship between the common 8q24 variant rs6983267 and risk of chronic lymphocytic leukemia
34. Further evidence that germline CEBPA mutations cause dominant inheritance of acute myeloid leukaemia
35. A prospective, blinded analysis of thymidylate synthase and p53 expression as prognostic markers in the adjuvant treatment of colorectal cancer
36. A Prospective Study Confirms Mismatch Repair Status Predicts Outcome in Colorectal Cancer
37. STK11 status and intussusception risk in Peutz-Jeghers syndrome
38. Is the E133K allele of VG5Q associated with Klippel-Trenaunay and other overgrowth syndromes?
39. Exonic STK11 deletions are not a rare cause of Peutz-Jeghers syndrome
40. Monoclonal B-cell lymphocytosis (MBL) in CLL families: substantial increase in relative risk for young adults
41. Germline mutations in fumarate hydratase (FH) do not predispose to prostate cancer
42. The C/C−13910 genotype of adult-type hypolactasia is associated with an increased risk of colorectal cancer in the Finnish population
43. Loci other than 21q22.12 (RUNX1) and 16q21-23.2 cause familial AML
44. Exon 3 β-catenin mutations are specifically associated with colorectal carcinomas in hereditary non-polyposis colorectal cancer syndrome
45. Systematic Review of Microsatellite Instability and Colorectal Cancer Prognosis
46. Increased sex concordance of sibling pairs with chronic lymphocytic leukemia
47. Pulmonary Masses Presenting 11 Years after Abdominal Surgery
48. Distinct Genetic and Epigenetic Changes in Medullary Breast Cancer
49. Association between leptin receptor gene polymorphisms and early-onset prostate cancer
50. A systematic review and meta-analysis of familial prostate cancer risk
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