Physician
Pediatric Hematology & Oncology
Dr. Stephen J. Chanock, MD
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Stephen Chanock works in the field of Pediatric Hematology & Oncology. He went to medical school at Harvard Medical School. Harvard Medical School is a one of the best medicals schools. Harvard Medical School is ranked 1/12 in Research/PrimaryCare. Dr. Stephen J. Chanock is a published MD. He published 100 publications, including: 'Interactions between breast cancer susceptibility loci and menopausal hormone therapy in relationship to breast cancer in the Breast and Prostate Cancer Cohort Consort...'
Publications
- LDlink: a web-based application for exploring population-specific haplotype structure and linking correlated alleles of possible functional variants.
- Large-scale genomic analyses link reproductive aging to hypothalamic signaling, breast cancer susceptibility and BRCA1-mediated DNA repair.
- Genome-Wide Association Study of Prostate Cancer-Specific Survival.
- Cross Cancer Genomic Investigation of Inflammation Pathway for Five Common Cancers: Lung, Ovary, Prostate, Breast, and Colorectal Cancer.
- Modification of Occupational Exposures on Bladder Cancer Risk by Common Genetic Polymorphisms.
- Common Genetic Variation and Survival after Colorectal Cancer Diagnosis: A Genome-Wide Analysis.
- Associations of prostate cancer risk variants with disease aggressiveness: results of the NCI-SPORE Genetics Working Group analysis of 18,343 cases.
- Interactions between household air pollution and GWAS-identified lung cancer susceptibility markers in the Female Lung Cancer Consortium in Asia (FLCCA).
- Characterization of large structural genetic mosaicism in human autosomes.
- Association of aspirin and NSAID use with risk of colorectal cancer according to genetic variants.
- Multilevel-analysis identify a cis-expression quantitative trait locus associated with risk of renal cell carcinoma.
- Genetic studies of body mass index yield new insights for obesity biology.
- Genetic susceptibility to diffuse large B-cell lymphoma in a pooled study of three Eastern Asian populations.
- Leveraging population admixture to characterize the heritability of complex traits.
- Genome-wide Association Study Identifies Five Susceptibility Loci for Follicular Lymphoma outside the HLA Region.
- The 19q12 Bladder Cancer GWAS Signal: Association with Cyclin E Function and Aggressive Disease.
- Genome-wide association study identifies multiple susceptibility loci for diffuse large B cell lymphoma.
- A meta-analysis of 87,040 individuals identifies 23 new susceptibility loci for prostate cancer.
- Genome-wide Scan of 29,141 African Americans Finds No Evidence of Directional Selection since Admixture.
- Genome-wide association study identifies multiple susceptibility loci for pancreatic cancer.
- Genetic polymorphisms in the 9p21 region associated with risk of multiple cancers.
- Joint analysis of three genome-wide association studies of esophageal squamous cell carcinoma in Chinese populations.
- Characterization of T gene sequence variants and germline duplications in familial and sporadic chordoma.
- Imputation and subset based association analysis across different cancer types identifies multiple independent risk loci in the TERT-CLPTM1L region on chromosome 5p15.33.
- Generalizability of established prostate cancer risk variants in men of African ancestry.
- Analysis of chemotherapeutic response in ovarian cancers using publicly available high-throughput data.
- Rare variants of large effect in BRCA2 and CHEK2 affect risk of lung cancer.
- Pathway-based analysis of GWAs data identifies association of sex determination genes with susceptibility to testicular germ cell tumors.
- Insulin-like Growth Factor Pathway Genetic Polymorphisms, Circulating IGF1 and IGFBP3, and Prostate Cancer Survival.
- Cross-cancer pleiotropic analysis of endometrial cancer: PAGE and E2C2 consortia.
- Genome-wide diet-gene interaction analyses for risk of colorectal cancer.
- Rare missense variants in POT1 predispose to familial cutaneous malignant melanoma.
- A Genome-wide Association Study of Early-Onset Breast Cancer Identifies PFKM as a Novel Breast Cancer Gene and Supports a Common Genetic Spectrum for Breast Cancer at ...
- Genome-wide interaction study of smoking and bladder cancer risk.
- Estimating the Heritability of Colorectal Cancer.
- Prostate Cancer (PCa) Risk Variants and Risk of Fatal PCa in the National Cancer Institute Breast and Prostate Cancer Cohort Consortium.
- A Genome-Wide Association Study of Renal Cell Carcinoma among African Americans.
- Personal History of Diabetes, Genetic Susceptibility to Diabetes, and Risk of Brain Glioma: A Pooled Analysis of Observational Studies.
- Erratum to: A genome-wide association study of prostate cancer in West African men.
- Genome-wide association study identifies multiple loci associated with bladder cancer risk.
- Breast cancer susceptibility risk associations and heterogeneity by E-cadherin tumor tissue expression.
- Genetic predictors of circulating 25-hydroxyvitamin d and risk of colorectal cancer.
- A genome-wide association study of prostate cancer in West African men.
- Genome-wide association study of endometrial cancer in E2C2.
- A genome-wide association study identifies new susceptibility loci for esophageal adenocarcinoma and Barrett's esophagus.
- The new sequencer on the block: comparison of Life Technology's Proton sequencer to an Illumina HiSeq for whole-exome sequencing.
- The Cancer Genome Atlas Pan-Cancer analysis project.
- Role of one-carbon metabolizing pathway genes and gene-nutrient interaction in the risk of non-Hodgkin lymphoma.
- Pleiotropic effects of genetic risk variants for other cancers on colorectal cancer risk: PAGE, GECCO and CCFR consortia.
- Genetic variants in fas signaling pathway genes and risk of gastric cancer.
- Genome-wide association study identifies multiple risk loci for chronic lymphocytic leukemia.
- Joint effects between five identified risk variants, allergy, and autoimmune conditions on glioma risk.
- Innate immunity gene polymorphisms and the risk of colorectal neoplasia.
- Association of Genetic Variants in CDK6 and XRCC1 with The Risk of Dysplastic Nevi in Melanoma-Prone Families.
- Genome-wide association study identifies two susceptibility loci for osteosarcoma.
- Single-Nucleotide Polymorphisms in Genes Encoding for CC Chemokines were Not Associated with the Risk of Non-Hodgkin Lymphoma.
- Scanning for clues to better use selective estrogen receptor modulators.
- IL10 and TNF variants and risk of non-Hodgkin lymphoma among three Asian populations.
- One thousand genomes imputation in the National Cancer Institute Breast and Prostate Cancer Cohort Consortium aggressive prostate cancer genome-wide association study.
- Genome-wide Analysis of BMI in Adolescents and Young Adults Reveals Additional Insight into the Effects of Genetic Loci over the Life Course.
- Meta-analysis identifies four new loci associated with testicular germ cell tumor.
- Plasma Carotenoid- and Retinol-Weighted Multi-SNP Scores and Risk of Breast Cancer in the National Cancer Institute Breast and Prostate Cancer Cohort Consortium.
- Genome-wide association study of age at menarche in African-American women.
- Common Genetic Polymorphisms Modify the Effect of Smoking on Absolute Risk of Bladder Cancer.
- Genetic variation in the vitamin d pathway in relation to risk of prostate cancer--results from the breast and prostate cancer cohort consortium.
- Transforming epidemiology for 21st century medicine and public health.
- Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture.
- A meta-analysis identifies new loci associated with body mass index in individuals of African ancestry.
- Polymorphisms in DNA repair pathway genes, body mass index, and risk of non-hodgkin lymphoma.
- Common single nucleotide polymorphisms in genes related to immune function and risk of papillary thyroid cancer.
- A Genome-Wide Scan for Breast Cancer Risk Haplotypes among African American Women.
- The Long and Short of Telomeres and Cancer Association Studies.
- Genetic variants in DNA repair pathway genes and risk of esophageal squamous cell carcinoma and gastric adenocarcinoma in a Chinese population.
- Projecting the performance of risk prediction based on polygenic analyses of genome-wide association studies.
- Testicular germ cell tumor susceptibility associated with the UCK2 locus on chromosome 1q23.
- Genome-wide search for gene-gene interactions in colorectal cancer.
- A genome-wide association study of breast cancer in women of African ancestry.
- Diabetes and risk of pancreatic cancer: a pooled analysis from the pancreatic cancer cohort consortium.
- Common genetic variants in the 9p21 region and their associations with multiple tumours.
- Nonsteroidal anti-inflammatory drugs and other analgesic use and bladder cancer in northern New England.
- HGV2012: Leveraging Next-Generation Technology and Large Datasets to Advance Disease Research.
- Identification of Genetic Susceptibility Loci for Colorectal Tumors in a Genome-wide Meta-analysis.
- Common Obesity-Related Genetic Variants and Papillary Thyroid Cancer Risk.
- Genetic variation in innate immunity and inflammation pathways associated with lung cancer risk.
- Genome-wide association analysis identifies new lung cancer susceptibility loci in never-smoking women in Asia.
- Genome-wide association study of survival in patients with pancreatic adenocarcinoma.
- Polymorphisms in pattern-recognition genes in the innate immunity system and risk of non-Hodgkin lymphoma.
- Toward mapping the biology of the genome.
- Inherited genetic variation and overall survival following follicular lymphoma.
- Genetic variant in TP63 on locus 3q28 is associated with risk of lung adenocarcinoma among never-smoking females in Asia.
- Assessing Disease Risk in Genome-wide Association Studies Using Family History.
- Common genetic variants in metabolism and detoxification pathways and the risk of papillary thyroid cancer.
- A two-platform design for next generation genome-wide association studies.
- Single Nucleotide Polymorphisms in the PRDX3 and RPS19 and Risk of HPV Persistence and Cervical Precancer/Cancer.
- Common genetic variants in prostate cancer risk prediction - Results from the NCI Breast and Prostate Cancer Cohort Consortium (BPC3).
- Mapping of the UGT1A locus identifies an uncommon coding variant that affects mRNA expression and protects from bladder cancer.
- 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...
- Interactions between breast cancer susceptibility loci and menopausal hormone therapy in relationship to breast cancer in the Breast and Prostate Cancer Cohort Consort...
- Meta-analysis of genome-wide association studies identifies multiple lung cancer susceptibility loci in never-smoking Asian women.
Schools
Harvard Medical School
Children39s Hospital Boston
Doctors Specialties
- Pediatric Infectious Disease Medicine
- Pediatric Hematology
- Oncology
Accepted Insurances
Education
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Boston Children's Hospital -
Harvard Medical School
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