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Author Details
Full Name
Carolyn M Hutter
Affiliation
National Human Genome Research Institute, National Institutes of Health
ORCID
Career Start Year
1995
Papers
90
H Index
43
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
36640770
Elucidating the structure and function of the nucleus-The NIH Common Fund 4D Nucleome program.
Mol Cell
2023
36640770
Elucidating the structure and function of the nucleus-The NIH Common Fund 4D Nucleome program.
Mol Cell
2023
33116284
Strategic vision for improving human health at The Forefront of Genomics.
Nature
2020
33116284
Strategic vision for improving human health at The Forefront of Genomics.
Nature
2020
29144510
Characterizing reduced coverage regions through comparison of exome and genome sequencing data across 10 centers.
Genet Med
2018
29898407
Integrated Molecular Characterization of Testicular Germ Cell Tumors.
Cell Rep
2018
29625049
Perspective on Oncogenic Processes at the End of the Beginning of Cancer Genomics.
Cell
2018
29625045
The Cancer Genome Atlas: Creating Lasting Value beyond Its Data.
Cell
2018
29596782
Scalable Open Science Approach for Mutation Calling of Tumor Exomes Using Multiple Genomic Pipelines.
Cell Syst
2018
29151588
Prioritizing diversity in human genomics research.
Nat Rev Genet
2018
29105735
Research Directions in Genetic Predispositions to Stevens-Johnson Syndrome / Toxic Epidermal Necrolysis.
Clin Pharmacol Ther
2018
29144510
Characterizing reduced coverage regions through comparison of exome and genome sequencing data across 10 centers.
Genet Med
2018
29898407
Integrated Molecular Characterization of Testicular Germ Cell Tumors.
Cell Rep
2018
29625049
Perspective on Oncogenic Processes at the End of the Beginning of Cancer Genomics.
Cell
2018
29625045
The Cancer Genome Atlas: Creating Lasting Value beyond Its Data.
Cell
2018
29596782
Scalable Open Science Approach for Mutation Calling of Tumor Exomes Using Multiple Genomic Pipelines.
Cell Syst
2018
29105735
Research Directions in Genetic Predispositions to Stevens-Johnson Syndrome / Toxic Epidermal Necrolysis.
Clin Pharmacol Ther
2018
29151588
Prioritizing diversity in human genomics research.
Nat Rev Genet
2018
28978193
Current Challenges and New Opportunities for Gene-Environment Interaction Studies of Complex Diseases.
Am J Epidemiol
2017
28978193
Current Challenges and New Opportunities for Gene-Environment Interaction Studies of Complex Diseases.
Am J Epidemiol
2017
26766742
CYP24A1 variant modifies the association between use of oestrogen plus progestogen therapy and colorectal cancer risk.
Br J Cancer
2016
27392080
Clinical Sequencing Exploratory Research Consortium: Accelerating Evidence-Based Practice of Genomic Medicine.
Am J Hum Genet
2016
27181682
Clinical Sequencing Exploratory Research Consortium: Accelerating Evidence-Based Practice of Genomic Medicine.
Am J Hum Genet
2016
26766742
CYP24A1 variant modifies the association between use of oestrogen plus progestogen therapy and colorectal cancer risk.
Br J Cancer
2016
26586795
Common genetic variation and survival after colorectal cancer diagnosis: a genome-wide analysis.
Carcinogenesis
2016
26536169
Comprehensive Molecular Characterization of Papillary Renal-Cell Carcinoma.
N Engl J Med
2016
27723779
Genome-Wide Interaction Analyses between Genetic Variants and Alcohol Consumption and Smoking for Risk of Colorectal Cancer.
PLoS Genet
2016
26536169
Comprehensive Molecular Characterization of Papillary Renal-Cell Carcinoma.
N Engl J Med
2016
26586795
Common genetic variation and survival after colorectal cancer diagnosis: a genome-wide analysis.
Carcinogenesis
2016
27723779
Genome-Wide Interaction Analyses between Genetic Variants and Alcohol Consumption and Smoking for Risk of Colorectal Cancer.
PLoS Genet
2016
27392080
Clinical Sequencing Exploratory Research Consortium: Accelerating Evidence-Based Practice of Genomic Medicine.
Am J Hum Genet
2016
27181682
Clinical Sequencing Exploratory Research Consortium: Accelerating Evidence-Based Practice of Genomic Medicine.
Am J Hum Genet
2016
25371374
Genetic simulation tools for post-genome wide association studies of complex diseases.
Genet Epidemiol
2015
25371374
Genetic simulation tools for post-genome wide association studies of complex diseases.
Genet Epidemiol
2015
25789475
Pleiotropic and sex-specific effects of cancer GWAS SNPs on melanoma risk in the population architecture using genomics and epidemiology (PAGE) study.
PLoS One
2015
25781442
Association of aspirin and NSAID use with risk of colorectal cancer according to genetic variants.
JAMA
2015
25683114
A model to determine colorectal cancer risk using common genetic susceptibility loci.
Gastroenterology
2015
26498495
Corrigendum: genome-wide association study of colorectal cancer identifies six new susceptibility loci.
Nat Commun
2015
26071399
Identification of a common variant with potential pleiotropic effect on risk of inflammatory bowel disease and colorectal cancer.
Carcinogenesis
2015
26151821
Genome-wide association study of colorectal cancer identifies six new susceptibility loci.
Nat Commun
2015
26061751
Comprehensive, Integrative Genomic Analysis of Diffuse Lower-Grade Gliomas.
N Engl J Med
2015
26498495
Corrigendum: genome-wide association study of colorectal cancer identifies six new susceptibility loci.
Nat Commun
2015
26071399
Identification of a common variant with potential pleiotropic effect on risk of inflammatory bowel disease and colorectal cancer.
Carcinogenesis
2015
26151821
Genome-wide association study of colorectal cancer identifies six new susceptibility loci.
Nat Commun
2015
26061751
Comprehensive, Integrative Genomic Analysis of Diffuse Lower-Grade Gliomas.
N Engl J Med
2015
25683114
A model to determine colorectal cancer risk using common genetic susceptibility loci.
Gastroenterology
2015
25789475
Pleiotropic and sex-specific effects of cancer GWAS SNPs on melanoma risk in the population architecture using genomics and epidemiology (PAGE) study.
PLoS One
2015
25781442
Association of aspirin and NSAID use with risk of colorectal cancer according to genetic variants.
JAMA
2015
23935004
Pleiotropic effects of genetic risk variants for other cancers on colorectal cancer risk: PAGE, GECCO and CCFR consortia.
Gut
2014
24156912
Association mapping of the PARK10 region for Parkinson's disease susceptibility genes.
Parkinsonism Relat Disord
2014
1 - 50 of 180
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