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Author Details

Carolyn M Hutter
National Human Genome Research Institute, National Institutes of Health
1995
90
43
PMIDPaper TitleJournal TitlePublished Year
36640770Elucidating the structure and function of the nucleus-The NIH Common Fund 4D Nucleome program.Mol Cell2023
36640770Elucidating the structure and function of the nucleus-The NIH Common Fund 4D Nucleome program.Mol Cell2023
33116284Strategic vision for improving human health at The Forefront of Genomics.Nature2020
33116284Strategic vision for improving human health at The Forefront of Genomics.Nature2020
29144510Characterizing reduced coverage regions through comparison of exome and genome sequencing data across 10 centers.Genet Med2018
29898407Integrated Molecular Characterization of Testicular Germ Cell Tumors.Cell Rep2018
29625049Perspective on Oncogenic Processes at the End of the Beginning of Cancer Genomics.Cell2018
29625045The Cancer Genome Atlas: Creating Lasting Value beyond Its Data.Cell2018
29596782Scalable Open Science Approach for Mutation Calling of Tumor Exomes Using Multiple Genomic Pipelines.Cell Syst2018
29151588Prioritizing diversity in human genomics research.Nat Rev Genet2018
29105735Research Directions in Genetic Predispositions to Stevens-Johnson Syndrome / Toxic Epidermal Necrolysis.Clin Pharmacol Ther2018
29144510Characterizing reduced coverage regions through comparison of exome and genome sequencing data across 10 centers.Genet Med2018
29898407Integrated Molecular Characterization of Testicular Germ Cell Tumors.Cell Rep2018
29625049Perspective on Oncogenic Processes at the End of the Beginning of Cancer Genomics.Cell2018
29625045The Cancer Genome Atlas: Creating Lasting Value beyond Its Data.Cell2018
29596782Scalable Open Science Approach for Mutation Calling of Tumor Exomes Using Multiple Genomic Pipelines.Cell Syst2018
29105735Research Directions in Genetic Predispositions to Stevens-Johnson Syndrome / Toxic Epidermal Necrolysis.Clin Pharmacol Ther2018
29151588Prioritizing diversity in human genomics research.Nat Rev Genet2018
28978193Current Challenges and New Opportunities for Gene-Environment Interaction Studies of Complex Diseases.Am J Epidemiol2017
28978193Current Challenges and New Opportunities for Gene-Environment Interaction Studies of Complex Diseases.Am J Epidemiol2017
26766742CYP24A1 variant modifies the association between use of oestrogen plus progestogen therapy and colorectal cancer risk.Br J Cancer2016
27392080Clinical Sequencing Exploratory Research Consortium: Accelerating Evidence-Based Practice of Genomic Medicine.Am J Hum Genet2016
27181682Clinical Sequencing Exploratory Research Consortium: Accelerating Evidence-Based Practice of Genomic Medicine.Am J Hum Genet2016
26766742CYP24A1 variant modifies the association between use of oestrogen plus progestogen therapy and colorectal cancer risk.Br J Cancer2016
26586795Common genetic variation and survival after colorectal cancer diagnosis: a genome-wide analysis.Carcinogenesis2016
26536169Comprehensive Molecular Characterization of Papillary Renal-Cell Carcinoma.N Engl J Med2016
27723779Genome-Wide Interaction Analyses between Genetic Variants and Alcohol Consumption and Smoking for Risk of Colorectal Cancer.PLoS Genet2016
26536169Comprehensive Molecular Characterization of Papillary Renal-Cell Carcinoma.N Engl J Med2016
26586795Common genetic variation and survival after colorectal cancer diagnosis: a genome-wide analysis.Carcinogenesis2016
27723779Genome-Wide Interaction Analyses between Genetic Variants and Alcohol Consumption and Smoking for Risk of Colorectal Cancer.PLoS Genet2016
27392080Clinical Sequencing Exploratory Research Consortium: Accelerating Evidence-Based Practice of Genomic Medicine.Am J Hum Genet2016
27181682Clinical Sequencing Exploratory Research Consortium: Accelerating Evidence-Based Practice of Genomic Medicine.Am J Hum Genet2016
25371374Genetic simulation tools for post-genome wide association studies of complex diseases.Genet Epidemiol2015
25371374Genetic simulation tools for post-genome wide association studies of complex diseases.Genet Epidemiol2015
25789475Pleiotropic and sex-specific effects of cancer GWAS SNPs on melanoma risk in the population architecture using genomics and epidemiology (PAGE) study.PLoS One2015
25781442Association of aspirin and NSAID use with risk of colorectal cancer according to genetic variants.JAMA2015
25683114A model to determine colorectal cancer risk using common genetic susceptibility loci.Gastroenterology2015
26498495Corrigendum: genome-wide association study of colorectal cancer identifies six new susceptibility loci.Nat Commun2015
26071399Identification of a common variant with potential pleiotropic effect on risk of inflammatory bowel disease and colorectal cancer.Carcinogenesis2015
26151821Genome-wide association study of colorectal cancer identifies six new susceptibility loci.Nat Commun2015
26061751Comprehensive, Integrative Genomic Analysis of Diffuse Lower-Grade Gliomas.N Engl J Med2015
26498495Corrigendum: genome-wide association study of colorectal cancer identifies six new susceptibility loci.Nat Commun2015
26071399Identification of a common variant with potential pleiotropic effect on risk of inflammatory bowel disease and colorectal cancer.Carcinogenesis2015
26151821Genome-wide association study of colorectal cancer identifies six new susceptibility loci.Nat Commun2015
26061751Comprehensive, Integrative Genomic Analysis of Diffuse Lower-Grade Gliomas.N Engl J Med2015
25683114A model to determine colorectal cancer risk using common genetic susceptibility loci.Gastroenterology2015
25789475Pleiotropic and sex-specific effects of cancer GWAS SNPs on melanoma risk in the population architecture using genomics and epidemiology (PAGE) study.PLoS One2015
25781442Association of aspirin and NSAID use with risk of colorectal cancer according to genetic variants.JAMA2015
23935004Pleiotropic effects of genetic risk variants for other cancers on colorectal cancer risk: PAGE, GECCO and CCFR consortia.Gut2014
24156912Association mapping of the PARK10 region for Parkinson's disease susceptibility genes.Parkinsonism Relat Disord2014
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