Author details

Full Name

Lynn R Goldin

Affiliation

ORCID

Career Start Year

1978

Papers

229

H Index

Expertise

CM4AI Collaborator

PMID	Paper Title	Journal Title	Published Year
36712882	Genome-wide DNA methylation profiling in chronic lymphocytic leukaemia.	Front Genet	2023
31383849	Association of elevated serumfree light chains with chronic lymphocytic leukemia and monoclonal B-cell lymphocytosis.	Blood Cancer J	2019
30616686	Sex-related DNA methylation differences in B cell chronic lymphocytic leukemia.	Biol Sex Differ	2019
30906990	Parental longevity and survival among patients with multiple myeloma and monoclonal gammopathy of undetermined significance: a population-based study.	British Journal of Haematology	2019
29687880	Combined somatic mutation and copy number analysis in the survival of familial CLL.	Br J Haematol	2018
30305637	Two high-risk susceptibility loci at 6p25.3 and 14q32.13 for WaldenstrÃ¶m macroglobulinemia.	Nat Commun	2018
30583724	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.	Genome Med	2018
29674426	Association of polygenic risk score with the risk of chronic lymphocytic leukemia and monoclonal B-cell lymphocytosis.	Blood	2018
29693246	Germline mutations in Protection of Telomeres 1 in two families with Hodgkin lymphoma.	Br J Haematol	2018
28165464	Genome-wide association analysis implicates dysregulation of immunity genes in chronic lymphocytic leukaemia.	Nat Commun	2017
29296952	Mosaic chromosome 20q deletions are more frequent in the aging population.	Blood Adv	2017
27807648	History of autoimmune disease is associated with impaired survival in multiple myeloma and monoclonal gammopathy of undetermined significance: a population-based study.	Annals of Hematology	2017
27629550	Whole exome sequencing in families with CLL detects a variant in Integrin Î² 2 associated with disease susceptibility.	Blood	2016
27291797	Female chromosome X mosaicism is age-related and preferentially affects the inactivated X chromosome.	Nat Commun	2016
26956414	Meta-analysis of genome-wide association studies discovers multiple loci for chronic lymphocytic leukemia.	Nat Commun	2016
27365461	Whole exome sequencing in families at high risk for Hodgkin lymphoma: identification of a predisposing mutation in the KDR gene.	Haematologica	2016
26721895	Whole exome sequencing reveals a C-terminal germline variant in CEBPA-associated acute myeloid leukemia: 45-year follow up of a large family.	Haematologica	2016
26763882	Mosaic 13q14 deletions in peripheral leukocytes of non-hematologic cancer cases and healthy controls.	J Hum Genet	2016
27982015	Evolution of multiple cell clones over a 29-year period of a CLL patient.	Nat Commun	2016
26045595	Survival in patients with familial and sporadic myeloproliferative neoplasms.	Blood	2015
25758095	Hodgkin lymphoma risk following infectious and chronic inflammatory diseases: a large population-based case-control study from Sweden.	Int J Hematol	2015
25802059	Lung cancer prognosis before and after recurrence in a population-based setting.	J Natl Cancer Inst	2015
25748358	Characterization of large structural genetic mosaicism in human autosomes.	Am J Hum Genet	2015
25814489	Population-based study on the impact of the familial form of WaldenstrÃ¶m macroglobulinemia on overall survival.	Blood	2015
25939664	Juvenile myelomonocytic leukemia due to a germline CBL Y371C mutation: 35-year follow-up of a large family.	Hum Genet	2015
24686846	Rare missense variants in POT1 predispose to familial cutaneous malignant melanoma.	Nat Genet	2014
24222331	Monoclonal gammopathy of undetermined significance and risk of lymphoid and myeloid malignancies: 728 cases followed up to 30 years in Sweden.	Blood	2014
25196979	Elevated risk of venous but not arterial thrombosis in WaldenstrÃ¶m macroglobulinemia/lymphoplasmacytic lymphoma.	J Thromb Haemost	2014
23287625	Genetic evidence of PTPN22 effects on chronic lymphocytic leukemia.	Blood	2013
23869079	No familial aggregation in chronic myeloid leukemia.	Blood	2013
23770605	Genome-wide association study identifies multiple risk loci for chronic lymphocytic leukemia.	Nat Genet	2013
24246697	Genetic susceptibility to chronic lymphocytic leukemia.	Semin Hematol	2013
23307532	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.	Cancer Epidemiol Biomarkers Prev	2013
23549397	Precursors to lymphoproliferative malignancies.	Cancer Epidemiol Biomarkers Prev	2013
22162584	Familial aggregation of acute myeloid leukemia and myelodysplastic syndromes.	Journal of Clinical Oncology	2012
22310551	Familial aggregation of lymphoplasmacytic lymphoma/WaldenstrÃ¶m macroglobulinemia with solid tumors and myeloid malignancies.	Acta Haematologica	2012
22700719	Common variation at 6p21.31 (BAK1) influences the risk of chronic lymphocytic leukemia.	Blood	2012
22880133	Mood disorders and risk of lung cancer in the EAGLE case-control study and in the U.S. Veterans Affairs inpatient cohort.	PLoS One	2012
22372994	Family history of venous thromboembolism is associated with increased risk for thrombosis in multiple myeloma: a population-based study.	Journal of Thrombosis and Haemostasis	2012
22561519	Detectable clonal mosaicism and its relationship to aging and cancer.	Nat Genet	2012
22561516	Detectable clonal mosaicism from birth to old age and its relationship to cancer.	Nat Genet	2012
22180421	Monoclonal gammopathy of undetermined significance and risk of infections: a population-based study.	Haematologica	2012
21690473	Chronic immune stimulation might act as a trigger for the development of acute myeloid leukemia or myelodysplastic syndromes.	Journal of Clinical Oncology	2011
28472664	A Genome-wide Association Study of Lung Cancer Identifies a Region of Chromosome 5p15 Associated with Risk for Adenocarcinoma.	Am J Hum Genet	2011
21131588	Genome-wide association study identifies a novel susceptibility locus at 6p21.3 among familial CLL.	Blood	2011
21127175	Infection in infancy and subsequent risk of developing lymphoma in children and young adults.	Blood	2011
21537037	Treatment-related risk factors for transformation to acute myeloid leukemia and myelodysplastic syndromes in myeloproliferative neoplasms.	Journal of Clinical Oncology	2011
21617698	Immunophenotypic and gene expression analysis of monoclonal B-cell lymphocytosis shows biologic characteristics associated with good prognosis CLL.	Leukemia	2011
21998210	Personal and family history of immune-related conditions increase the risk of plasma cell disorders: a population-based study.	Blood	2011
21795746	Risk of acute myeloid leukemia and myelodysplastic syndromes after multiple myeloma and its precursor disease (MGUS).	Blood	2011