823 results on '"Goldin, Lynn"'
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2. Whole exome sequencing reveals a C-terminal germline variant in CEBPA-associated acute myeloid leukemia: 45-year follow up of a large family
3. Female chromosome X mosaicism is age-related and preferentially affects the inactivated X chromosome
4. Association of polygenic risk score with the risk of chronic lymphocytic leukemia and monoclonal B-cell lymphocytosis
5. Genome-wide association study identifies multiple risk loci for chronic lymphocytic leukemia
6. Genome-wide association study of follicular lymphoma identifies a risk locus at 6p21.32
7. Sex-related DNA methylation differences in B cell chronic lymphocytic leukemia
8. A High-Density Genome Scan Detects Evidence for a Bipolar-Disorder Susceptibility Locus on 13q32 and Other Potential Loci on 1q32 and 18p11.2
9. Data from Mapping of the IRF8 Gene Identifies a 3′UTR Variant Associated with Risk of Chronic Lymphocytic Leukemia but not Other Common Non-Hodgkin Lymphoma Subtypes
10. Supplementary Table 5 from Mapping of the IRF8 Gene Identifies a 3′UTR Variant Associated with Risk of Chronic Lymphocytic Leukemia but not Other Common Non-Hodgkin Lymphoma Subtypes
11. Supplementary Table 3 from Mapping of the IRF8 Gene Identifies a 3′UTR Variant Associated with Risk of Chronic Lymphocytic Leukemia but not Other Common Non-Hodgkin Lymphoma Subtypes
12. Supplementary Figure 1 from Mapping of the IRF8 Gene Identifies a 3′UTR Variant Associated with Risk of Chronic Lymphocytic Leukemia but not Other Common Non-Hodgkin Lymphoma Subtypes
13. Supplementary Table 1 from Mapping of the IRF8 Gene Identifies a 3′UTR Variant Associated with Risk of Chronic Lymphocytic Leukemia but not Other Common Non-Hodgkin Lymphoma Subtypes
14. Supplementary Table 4 from Mapping of the IRF8 Gene Identifies a 3′UTR Variant Associated with Risk of Chronic Lymphocytic Leukemia but not Other Common Non-Hodgkin Lymphoma Subtypes
15. Supplementary Table 2 from Mapping of the IRF8 Gene Identifies a 3′UTR Variant Associated with Risk of Chronic Lymphocytic Leukemia but not Other Common Non-Hodgkin Lymphoma Subtypes
16. Association of elevated serumfree light chains with chronic lymphocytic leukemia and monoclonal B-cell lymphocytosis
17. Genome-wide DNA methylation profiling in chronic lymphocytic leukaemia
18. History of autoimmune disease is associated with impaired survival in multiple myeloma and monoclonal gammopathy of undetermined significance: a population-based study
19. Genetics in Lymphomagenesis
20. Monoclonal gammopathy of undetermined significance and risk of lymphoid and myeloid malignancies: 728 cases followed up to 30 years in Sweden
21. Two high-risk susceptibility loci at 6p25.3 and 14q32.13 for Waldenström macroglobulinemia
22. Mosaic 13q14 deletions in peripheral leukocytes of non-hematologic cancer cases and healthy controls
23. Juvenile myelomonocytic leukemia due to a germline CBL Y371C mutation: 35-year follow-up of a large family
24. Hodgkin lymphoma risk following infectious and chronic inflammatory diseases: a large population-based case–control study from Sweden
25. Mutations in a Gene Encoding a Midbody Kelch Protein in Familial and Sporadic Classical Hodgkin Lymphoma Lead to Binucleated Cells
26. Lung Cancer Prognosis Before and After Recurrence in a Population-Based Setting
27. Genome-wide association study identifies a novel susceptibility locus at 6p21.3 among familial CLL
28. Genome-wide DNA methylation profiling in chronic lymphocytic leukaemia.
29. Arterial and venous thrombosis in monoclonal gammopathy of undetermined significance and multiple myeloma: a population-based study
30. Risk of plasma cell and lymphoproliferative disorders among 14621 first-degree relatives of 4458 patients with monoclonal gammopathy of undetermined significance in Sweden
31. Chromosome 18 DNA Markers and Manic-Depressive Illness: Evidence for a Susceptibility Gene
32. Familial Cutaneous Malignant Melanoma: Autosomal Dominant Trait Possibly Linked to the Rh Locus
33. Risk of lymphoproliferative disorders among first-degree relatives of lymphoplasmacytic lymphoma/Waldenström macroglobulinemia patients: a population-based study in Sweden
34. Increased risks of polycythemia vera, essential thrombocythemia, and myelofibrosis among 24 577 first-degree relatives of 11 039 patients with myeloproliferative neoplasms in Sweden
35. A genome-wide association study of lung cancer identifies a region of chromosome 5p15 associated with risk for adenocarcinoma
36. Prevalence of monoclonal gammopathy of undetermined significance among men in Ghana
37. Identification of a novel chromosome region, 13q21.33-q22.2, for susceptibility genes in familial chronic lymphocytic leukemia
38. Genomewide linkage screen for Waldenstrom macroglobulinemia susceptibility loci in high-risk families
39. Genome-Wide DNA Methylation Profiling in Chronic Lymphocytic Leukaemia
40. Genetics in Lymphomagenesis
41. Genome scan meta-analysis of schizophrenia and bipolar disorder, Part III: bipolar disorder
42. Familial Aggregation of Lymphoplasmacytic Lymphoma/Waldenström Macroglobulinemia with Solid Tumors and Myeloid Malignancies
43. Common occurrence of monoclonal B-cell lymphocytosis among members of high-risk CLL families
44. Immune-Related and Inflammatory Conditions and Risk of Lymphoplasmacytic Lymphoma or Waldenström Macroglobulinemia
45. Patterns of hematologic malignancies and solid tumors among 37,838 first-degree relatives of 13,896 patients with multiple myeloma in Sweden
46. Common genetic variants in candidate genes and risk of familial lymphoid malignancies
47. Family history of cancer and nonmalignant lung diseases as risk factors for lung cancer
48. Highly increased familial risks for specific lymphoma subtypes
49. Autoimmunity and lymphomagenesis
50. Genetic Predisposition for Monoclonal Gammopathy of Undetermined Significance
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