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Author Details
Full Name
Laurie Burdett
Affiliation
National Cancer Institute, Frederick National Laboratory for Cancer Research
ORCID
Career Start Year
2005
Papers
78
H Index
35
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
36787739
Targeted long-read sequencing of the Ewing sarcoma 6p25.1 susceptibility locus identifies germline-somatic interactions with EWSR1-FLI1 binding.
Am J Hum Genet
2023
37666943
Correction: Distinct germline genetic susceptibility profiles identified for common non-Hodgkin lymphoma subtypes.
Leukemia
2023
37236969
Genome-wide association study of lung adenocarcinoma in East Asia and comparison with a European population.
Nat Commun
2023
36787739
Targeted long-read sequencing of the Ewing sarcoma 6p25.1 susceptibility locus identifies germline-somatic interactions with EWSR1-FLI1 binding.
Am J Hum Genet
2023
37666943
Correction: Distinct germline genetic susceptibility profiles identified for common non-Hodgkin lymphoma subtypes.
Leukemia
2023
37236969
Genome-wide association study of lung adenocarcinoma in East Asia and comparison with a European population.
Nat Commun
2023
34696378
Phylogenomic Analysis of Human Papillomavirus Type 31 and Cervical Carcinogenesis: A Study of 2093 Viral Genomes.
Viruses
2021
34696378
Phylogenomic Analysis of Human Papillomavirus Type 31 and Cervical Carcinogenesis: A Study of 2093 Viral Genomes.
Viruses
2021
31306748
Tuberculosis infection and lung adenocarcinoma: Mendelian randomization and pathway analysis of genome-wide association study data from never-smoking Asian women.
Genomics
2020
32363580
Association of HPV35 with cervical carcinogenesis among women of African ancestry: Evidence of viral-host interaction with implications for disease intervention.
Int J Cancer
2020
32060290
Mutations in the HPV16 genome induced by APOBEC3 are associated with viral clearance.
Nat Commun
2020
32004448
Genome-wide Association Study Identifies HLA-DPB1 as a Significant Risk Factor for Severe Aplastic Anemia.
Am J Hum Genet
2020
32881892
Low-frequency variation near common germline susceptibility loci are associated with risk of Ewing sarcoma.
PLoS One
2020
31306748
Tuberculosis infection and lung adenocarcinoma: Mendelian randomization and pathway analysis of genome-wide association study data from never-smoking Asian women.
Genomics
2020
32060290
Mutations in the HPV16 genome induced by APOBEC3 are associated with viral clearance.
Nat Commun
2020
32004448
Genome-wide Association Study Identifies HLA-DPB1 as a Significant Risk Factor for Severe Aplastic Anemia.
Am J Hum Genet
2020
32881892
Low-frequency variation near common germline susceptibility loci are associated with risk of Ewing sarcoma.
PLoS One
2020
32363580
Association of HPV35 with cervical carcinogenesis among women of African ancestry: Evidence of viral-host interaction with implications for disease intervention.
Int J Cancer
2020
29687880
Combined somatic mutation and copy number analysis in the survival of familial CLL.
Br J Haematol
2018
30093639
Genome-wide association study identifies multiple new loci associated with Ewing sarcoma susceptibility.
Nat Commun
2018
29687880
Combined somatic mutation and copy number analysis in the survival of familial CLL.
Br J Haematol
2018
30093639
Genome-wide association study identifies multiple new loci associated with Ewing sarcoma susceptibility.
Nat Commun
2018
28025329
Association between GWAS-identified lung adenocarcinoma susceptibility loci and EGFR mutations in never-smoking Asian women, and comparison with findings from Western populations.
Hum Mol Genet
2017
28680059
GWAS follow-up study of esophageal squamous cell carcinoma identifies potential genetic loci associated with family history of upper gastrointestinal cancer.
Sci Rep
2017
28886384
HPV16 E7 Genetic Conservation Is Critical to Carcinogenesis.
Cell
2017
28025329
Association between GWAS-identified lung adenocarcinoma susceptibility loci and EGFR mutations in never-smoking Asian women, and comparison with findings from Western populations.
Hum Mol Genet
2017
28886384
HPV16 E7 Genetic Conservation Is Critical to Carcinogenesis.
Cell
2017
28680059
GWAS follow-up study of esophageal squamous cell carcinoma identifies potential genetic loci associated with family history of upper gastrointestinal cancer.
Sci Rep
2017
26732427
Identification of a novel susceptibility locus at 13q34 and refinement of the 20p12.2 region as a multi-signal locus associated with bladder cancer risk in individuals of European ancestry.
Hum Mol Genet
2016
27291797
Female chromosome X mosaicism is age-related and preferentially affects the inactivated X chromosome.
Nat Commun
2016
27008888
Genetically predicted longer telomere length is associated with increased risk of B-cell lymphoma subtypes.
Hum Mol Genet
2016
26956414
Meta-analysis of genome-wide association studies discovers multiple loci for chronic lymphocytic leukemia.
Nat Commun
2016
26732429
Meta-analysis of genome-wide association studies identifies multiple lung cancer susceptibility loci in never-smoking Asian women.
Hum Mol Genet
2016
26732427
Identification of a novel susceptibility locus at 13q34 and refinement of the 20p12.2 region as a multi-signal locus associated with bladder cancer risk in individuals of European ancestry.
Hum Mol Genet
2016
27365461
Whole exome sequencing in families at high risk for Hodgkin lymphoma: identification of a predisposing mutation in the KDR gene.
Haematologica
2016
27130930
HPV16 Sublineage Associations With Histology-Specific Cancer Risk Using HPV Whole-Genome Sequences in 3200 Women.
J Natl Cancer Inst
2016
27449771
Multiple rare variants in high-risk pancreatic cancer-related genes may increase risk for pancreatic cancer in a subset of patients with and without germline CDKN2A mutations.
Hum Genet
2016
26635288
Pathway, in silico and tissue-specific expression quantitative analyses of oesophageal squamous cell carcinoma genome-wide association studies data.
Int J Epidemiol
2016
27917368
Sex Steroid Hormone Single-Nucleotide Polymorphisms, Pesticide Use, and the Risk of Prostate Cancer: A Nested Case-Control Study within the Agricultural Health Study.
Front Oncol
2016
27629550
Whole exome sequencing in families with CLL detects a variant in Integrin β 2 associated with disease susceptibility.
Blood
2016
26635288
Pathway, in silico and tissue-specific expression quantitative analyses of oesophageal squamous cell carcinoma genome-wide association studies data.
Int J Epidemiol
2016
27629550
Whole exome sequencing in families with CLL detects a variant in Integrin β 2 associated with disease susceptibility.
Blood
2016
27917368
Sex Steroid Hormone Single-Nucleotide Polymorphisms, Pesticide Use, and the Risk of Prostate Cancer: A Nested Case-Control Study within the Agricultural Health Study.
Front Oncol
2016
27365461
Whole exome sequencing in families at high risk for Hodgkin lymphoma: identification of a predisposing mutation in the KDR gene.
Haematologica
2016
27449771
Multiple rare variants in high-risk pancreatic cancer-related genes may increase risk for pancreatic cancer in a subset of patients with and without germline CDKN2A mutations.
Hum Genet
2016
27291797
Female chromosome X mosaicism is age-related and preferentially affects the inactivated X chromosome.
Nat Commun
2016
27130930
HPV16 Sublineage Associations With Histology-Specific Cancer Risk Using HPV Whole-Genome Sequences in 3200 Women.
J Natl Cancer Inst
2016
26956414
Meta-analysis of genome-wide association studies discovers multiple loci for chronic lymphocytic leukemia.
Nat Commun
2016
27008888
Genetically predicted longer telomere length is associated with increased risk of B-cell lymphoma subtypes.
Hum Mol Genet
2016
26732429
Meta-analysis of genome-wide association studies identifies multiple lung cancer susceptibility loci in never-smoking Asian women.
Hum Mol Genet
2016
1 - 50 of 156
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