215 results on '"Goldin, Lynn"'
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2. 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
3. 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
4. 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
5. 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
6. 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
7. 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
8. Discovery of novel predisposing coding and noncoding variants in familial Hodgkin lymphoma
9. Genome-wide DNA methylation profiling in chronic lymphocytic leukaemia
10. Genome-Wide DNA Methylation Profiling in Chronic Lymphocytic Leukaemia
11. Genetics in Lymphomagenesis
12. Association of elevated serumfree light chains with chronic lymphocytic leukemia and monoclonal B-cell lymphocytosis
13. Parental longevity and survival among patients with multiple myeloma and monoclonal gammopathy of undetermined significance: a population‐based study
14. Sex-related DNA methylation differences in B cell chronic lymphocytic leukemia
15. Prevalence of pathogenic/likely pathogenic variants in the 24 cancer genes of the ACMG Secondary Findings v2.0 list in a large cancer cohort and ethnicity-matched controls
16. Two high-risk susceptibility loci at 6p25.3 and 14q32.13 for Waldenström macroglobulinemia
17. Association of polygenic risk score with the risk of chronic lymphocytic leukemia and monoclonal B-cell lymphocytosis
18. Germline mutations in Protection of Telomeres 1 in two families with Hodgkin lymphoma
19. Combined somatic mutation and copy number analysis in the survival of familial CLL
20. Abstract 1318: A genome-wide association study of Waldenström macroglobulinemia/lymphoplasmacytic lymphoma demonstrates association with chromosome 6
21. Mosaic chromosome 20q deletions are more frequent in the aging population
22. Genome-wide association analysis implicates dysregulation of immunity genes in chronic lymphocytic leukaemia
23. Whole exome sequencing in families with CLL detects a variant in Integrin β 2 associated with disease susceptibility
24. History of autoimmune disease is associated with impaired survival in multiple myeloma and monoclonal gammopathy of undetermined significance: a population-based study
25. Female chromosome X mosaicism is age-related and preferentially affects the inactivated X chromosome
26. Meta-analysis of genome-wide association studies discovers multiple loci for chronic lymphocytic leukemia
27. Hoyeraal-Hreidarsson Syndrome due to PARN Mutations: Fourteen Years of Follow-Up
28. Mosaic 13q14 deletions in peripheral leukocytes of non-hematologic cancer cases and healthy controls
29. Abstract 3709: Second cancers following Waldenström macroglobulinemia/lymphoplasmacytic lymphoma in the United States: analysis of Surveillance, Epidemiology and End Results (SEER) registry data, 1992 - 2011
30. Abstract 2756: Whole-exome sequencing reveals a novel germline variant in CEBPA-associated familial acute myeloid leukemia: 45-year follow-up of a large family
31. Survival in patients with familial and sporadic myeloproliferative neoplasms
32. Population-based study on the impact of the familial form of Waldenström macroglobulinemia on overall survival
33. Lung Cancer Prognosis Before and After Recurrence in a Population-Based Setting
34. Hodgkin lymphoma risk following infectious and chronic inflammatory diseases: a large population-based case–control study from Sweden
35. Characterization of Large Structural Genetic Mosaicism in Human Autosomes
36. Patterns of Infectious Morbidity in Patients with Waldenström’s Macroglobulinaemia/Lymphoplasmacytic Lymphoma: A Population-Based Study
37. Elevated Phenylethylamine Excretion in Women
38. Power of Genetic Linkage Studies for Heterogeneous Disorders
39. Genetic Studies of Affective Illness
40. Abstract 1300: Exploration of rare variants from exome sequencing in families with Waldenstrom macroglobulinemia (WM)
41. Monoclonal gammopathy of undetermined significance and risk of lymphoid and myeloid malignancies: 728 cases followed up to 30 years in Sweden
42. Monoclonal Gammopathy Of Undetermined Significance and Risk Of Lymphoid and Myeloid Malignancies: 743 Cases Followed For Up To 30 Years In Sweden
43. Impact Of History Of Autoimmune Disease On Survival In Multiple Myeloma and Monoclonal Gammopathy Of Undetermined Significance: A Population-Based Study
44. Genetic Susceptibility to Chronic Lymphocytic Leukemia
45. No familial aggregation in chronic myeloid leukemia
46. Genome-wide association study identifies multiple risk loci for chronic lymphocytic leukemia
47. Precursors to Lymphoproliferative Malignancies
48. 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
49. Genetic evidence of PTPN22 effects on chronic lymphocytic leukemia
50. Elevated Risk of Venous but Not Arterial Thrombosis in Waldenström's Macroglobulinemia and Lymphoplasmacytic Lymphoma
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