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Author Details

Laurie Burdett
National Cancer Institute, Frederick National Laboratory for Cancer Research
2005
78
35
PMIDPaper TitleJournal TitlePublished Year
36787739Targeted long-read sequencing of the Ewing sarcoma 6p25.1 susceptibility locus identifies germline-somatic interactions with EWSR1-FLI1 binding.Am J Hum Genet2023
37666943Correction: Distinct germline genetic susceptibility profiles identified for common non-Hodgkin lymphoma subtypes.Leukemia2023
37236969Genome-wide association study of lung adenocarcinoma in East Asia and comparison with a European population.Nat Commun2023
36787739Targeted long-read sequencing of the Ewing sarcoma 6p25.1 susceptibility locus identifies germline-somatic interactions with EWSR1-FLI1 binding.Am J Hum Genet2023
37666943Correction: Distinct germline genetic susceptibility profiles identified for common non-Hodgkin lymphoma subtypes.Leukemia2023
37236969Genome-wide association study of lung adenocarcinoma in East Asia and comparison with a European population.Nat Commun2023
34696378Phylogenomic Analysis of Human Papillomavirus Type 31 and Cervical Carcinogenesis: A Study of 2093 Viral Genomes.Viruses2021
34696378Phylogenomic Analysis of Human Papillomavirus Type 31 and Cervical Carcinogenesis: A Study of 2093 Viral Genomes.Viruses2021
31306748Tuberculosis infection and lung adenocarcinoma: Mendelian randomization and pathway analysis of genome-wide association study data from never-smoking Asian women.Genomics2020
32363580Association of HPV35 with cervical carcinogenesis among women of African ancestry: Evidence of viral-host interaction with implications for disease intervention.Int J Cancer2020
32060290Mutations in the HPV16 genome induced by APOBEC3 are associated with viral clearance.Nat Commun2020
32004448Genome-wide Association Study Identifies HLA-DPB1 as a Significant Risk Factor for Severe Aplastic Anemia.Am J Hum Genet2020
32881892Low-frequency variation near common germline susceptibility loci are associated with risk of Ewing sarcoma.PLoS One2020
31306748Tuberculosis infection and lung adenocarcinoma: Mendelian randomization and pathway analysis of genome-wide association study data from never-smoking Asian women.Genomics2020
32060290Mutations in the HPV16 genome induced by APOBEC3 are associated with viral clearance.Nat Commun2020
32004448Genome-wide Association Study Identifies HLA-DPB1 as a Significant Risk Factor for Severe Aplastic Anemia.Am J Hum Genet2020
32881892Low-frequency variation near common germline susceptibility loci are associated with risk of Ewing sarcoma.PLoS One2020
32363580Association of HPV35 with cervical carcinogenesis among women of African ancestry: Evidence of viral-host interaction with implications for disease intervention.Int J Cancer2020
29687880Combined somatic mutation and copy number analysis in the survival of familial CLL.Br J Haematol2018
30093639Genome-wide association study identifies multiple new loci associated with Ewing sarcoma susceptibility.Nat Commun2018
29687880Combined somatic mutation and copy number analysis in the survival of familial CLL.Br J Haematol2018
30093639Genome-wide association study identifies multiple new loci associated with Ewing sarcoma susceptibility.Nat Commun2018
28025329Association between GWAS-identified lung adenocarcinoma susceptibility loci and EGFR mutations in never-smoking Asian women, and comparison with findings from Western populations.Hum Mol Genet2017
28680059GWAS follow-up study of esophageal squamous cell carcinoma identifies potential genetic loci associated with family history of upper gastrointestinal cancer.Sci Rep2017
28886384HPV16 E7 Genetic Conservation Is Critical to Carcinogenesis.Cell2017
28025329Association between GWAS-identified lung adenocarcinoma susceptibility loci and EGFR mutations in never-smoking Asian women, and comparison with findings from Western populations.Hum Mol Genet2017
28886384HPV16 E7 Genetic Conservation Is Critical to Carcinogenesis.Cell2017
28680059GWAS follow-up study of esophageal squamous cell carcinoma identifies potential genetic loci associated with family history of upper gastrointestinal cancer.Sci Rep2017
26732427Identification 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 Genet2016
27291797Female chromosome X mosaicism is age-related and preferentially affects the inactivated X chromosome.Nat Commun2016
27008888Genetically predicted longer telomere length is associated with increased risk of B-cell lymphoma subtypes.Hum Mol Genet2016
26956414Meta-analysis of genome-wide association studies discovers multiple loci for chronic lymphocytic leukemia.Nat Commun2016
26732429Meta-analysis of genome-wide association studies identifies multiple lung cancer susceptibility loci in never-smoking Asian women.Hum Mol Genet2016
26732427Identification 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 Genet2016
27365461Whole exome sequencing in families at high risk for Hodgkin lymphoma: identification of a predisposing mutation in the KDR gene.Haematologica2016
27130930HPV16 Sublineage Associations With Histology-Specific Cancer Risk Using HPV Whole-Genome Sequences in 3200 Women.J Natl Cancer Inst2016
27449771Multiple 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 Genet2016
26635288Pathway, in silico and tissue-specific expression quantitative analyses of oesophageal squamous cell carcinoma genome-wide association studies data.Int J Epidemiol2016
27917368Sex Steroid Hormone Single-Nucleotide Polymorphisms, Pesticide Use, and the Risk of Prostate Cancer: A Nested Case-Control Study within the Agricultural Health Study.Front Oncol2016
27629550Whole exome sequencing in families with CLL detects a variant in Integrin β 2 associated with disease susceptibility.Blood2016
26635288Pathway, in silico and tissue-specific expression quantitative analyses of oesophageal squamous cell carcinoma genome-wide association studies data.Int J Epidemiol2016
27629550Whole exome sequencing in families with CLL detects a variant in Integrin β 2 associated with disease susceptibility.Blood2016
27917368Sex Steroid Hormone Single-Nucleotide Polymorphisms, Pesticide Use, and the Risk of Prostate Cancer: A Nested Case-Control Study within the Agricultural Health Study.Front Oncol2016
27365461Whole exome sequencing in families at high risk for Hodgkin lymphoma: identification of a predisposing mutation in the KDR gene.Haematologica2016
27449771Multiple 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 Genet2016
27291797Female chromosome X mosaicism is age-related and preferentially affects the inactivated X chromosome.Nat Commun2016
27130930HPV16 Sublineage Associations With Histology-Specific Cancer Risk Using HPV Whole-Genome Sequences in 3200 Women.J Natl Cancer Inst2016
26956414Meta-analysis of genome-wide association studies discovers multiple loci for chronic lymphocytic leukemia.Nat Commun2016
27008888Genetically predicted longer telomere length is associated with increased risk of B-cell lymphoma subtypes.Hum Mol Genet2016
26732429Meta-analysis of genome-wide association studies identifies multiple lung cancer susceptibility loci in never-smoking Asian women.Hum Mol Genet2016
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Collaborators

Frederick National Laboratory for Cancer Research
Co-authored papers 61
National Cancer Institute, National Institutes of Health
Co-authored papers 58
St Jude Children's Research Hospital
Co-authored papers 33
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National Cancer Institute
Co-authored papers 24
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Co-authored papers 24
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Co-authored papers 19
National Cancer Institute
Co-authored papers 17
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National Cancer Institute, National Institutes of Health, Inc.
Co-authored papers 16
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Co-authored papers 16
Co-authored papers 15
Clinical Genetics Branch, National Cancer Institute (NCI)
Co-authored papers 15
Co-authored papers 15
The Kolling Institute, University of Sydney, and Royal North Shore Hospital
Co-authored papers 14
National Cancer Institute
Co-authored papers 14
Co-authored papers 13
Co-authored papers 12
Co-authored papers 12
Co-authored papers 11
Harvard T. H. Chan School of Public Health
Co-authored papers 11
Harvard T.H. Chan School of Public Health
Co-authored papers 11
Co-authored papers 10
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National Cancer Institute
Co-authored papers 10
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Frederick National Laboratory for Cancer Research
Co-authored papers 10