Area of research
Pathology and Forensic Medicine · Genetics
Research interest
Research interests include Lymphoma Diagnosis and Treatment, Chronic Lymphocytic Leukemia Research, Acute Lymphoblastic Leukemia research, and Viral-associated cancers and disorders.
A Historical Survey of Key Epidemiological Studies of Ionizing Radiation Exposure
Targeted long-read sequencing of the Ewing sarcoma 6p25.1 susceptibility locus identifies germline-somatic interactions with EWSR1-FLI1 binding
Inflated expectations: Rare-variant association analysis using public controls
Correction: Distinct germline genetic susceptibility profiles identified for common non-Hodgkin lymphoma subtypes
Distinct germline genetic susceptibility profiles identified for common non-Hodgkin lymphoma subtypes
Association of Changes in Cancer Therapy Over 3 Decades With Risk of Subsequent Breast Cancer Among Female Childhood Cancer Survivors
A Novel Locus on 6p21.2 for Cancer Treatment–Induced Cardiac Dysfunction Among Childhood Cancer Survivors
Frequency of Pathogenic Germline Variants in Cancer-Susceptibility Genes in the Childhood Cancer Survivor Study
Contribution of Polygenic Risk to Hypertension Among Long-Term Survivors of Childhood Cancer
Polygenic Risk Score Improves Risk Stratification and Prediction of Subsequent Thyroid Cancer after Childhood Cancer
Cancer therapy shapes the fitness landscape of clonal hematopoiesis
Frequency of Pathogenic Germline Variants in Cancer-Susceptibility Genes in Patients With Osteosarcoma
Genetic variation in POT1 and risk of thyroid subsequent malignant neoplasm: A report from the Childhood Cancer Survivor Study
Subsequent Primary Neoplasms
Subsequent Neoplasm Risk Associated With Rare Variants in DNA Damage Response and Clinical Radiation Sensitivity Syndrome Genes in the Childhood Cancer Survivor Study
Generalizability of “GWAS Hits” in Clinical Populations: Lessons from Childhood Cancer Survivors
Low-frequency variation near common germline susceptibility loci are associated with risk of Ewing sarcoma
Genetically Determined Height and Risk of Non-hodgkin Lymphoma
Association of Breast Cancer Risk After Childhood Cancer With Radiation Dose to the Breast and Anthracycline Use
Genetic overlap between autoimmune diseases and non‐Hodgkin lymphoma subtypes
Genome-Wide Association Study in Irradiated Childhood Cancer Survivors Identifies HTR2A for Subsequent Basal Cell Carcinoma
Genome-wide association study identifies multiple new loci associated with Ewing sarcoma susceptibility
HLA Class I and II Diversity Contributes to the Etiologic Heterogeneity of Non-Hodgkin Lymphoma Subtypes
Association of polygenic risk score with the risk of chronic lymphocytic leukemia and monoclonal B-cell lymphocytosis
Two high-risk susceptibility loci at 6p25.3 and 14q32.13 for Waldenström macroglobulinemia
Successful use of whole genome amplified DNA from multiple source types for high-density Illumina SNP microarrays
Genome-wide association analysis implicates dysregulation of immunity genes in chronic lymphocytic leukaemia
Genome-Wide Association Study to Identify Susceptibility Loci That Modify Radiation-Related Risk for Breast Cancer After Childhood Cancer
Lupus-related single nucleotide polymorphisms and risk of diffuse large B-cell lymphoma
A High-risk Haplotype for Premature Menopause in Childhood Cancer Survivors Exposed to Gonadotoxic Therapy