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Author Details
Full Name
Daniel B Mirel
Affiliation
Broad Institute of Harvard and MIT
ORCID
Career Start Year
1989
Papers
67
H Index
43
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
37968452
Author Correction: Genetic variation in the human leukocyte antigen region confers susceptibility to Clostridioides difficile infection.
Sci Rep
2023
37898691
Genetic variation in the human leukocyte antigen region confers susceptibility to Clostridioides difficile infection.
Sci Rep
2023
37968452
Author Correction: Genetic variation in the human leukocyte antigen region confers susceptibility to Clostridioides difficile infection.
Sci Rep
2023
37898691
Genetic variation in the human leukocyte antigen region confers susceptibility to Clostridioides difficile infection.
Sci Rep
2023
25043339
Limited clinical utility of a genetic risk score for the prediction of fracture risk in elderly subjects.
J Bone Miner Res
2015
25748358
Characterization of large structural genetic mosaicism in human autosomes.
Am J Hum Genet
2015
25297839
Genetic variation in the HLA region is associated with susceptibility to herpes zoster.
Genes Immun
2015
25043339
Limited clinical utility of a genetic risk score for the prediction of fracture risk in elderly subjects.
J Bone Miner Res
2015
25748358
Characterization of large structural genetic mosaicism in human autosomes.
Am J Hum Genet
2015
25297839
Genetic variation in the HLA region is associated with susceptibility to herpes zoster.
Genes Immun
2015
23716066
Association between low density lipoprotein and rheumatoid arthritis genetic factors with low density lipoprotein levels in rheumatoid arthritis and non-rheumatoid arthritis controls.
Ann Rheum Dis
2014
24390342
Genetics of rheumatoid arthritis contributes to biology and drug discovery.
Nature
2014
23716066
Association between low density lipoprotein and rheumatoid arthritis genetic factors with low density lipoprotein levels in rheumatoid arthritis and non-rheumatoid arthritis controls.
Ann Rheum Dis
2014
24520335
Integration of sequence data from a Consanguineous family with genetic data from an outbred population identifies PLB1 as a candidate rheumatoid arthritis risk gene.
PLoS One
2014
24520335
Integration of sequence data from a Consanguineous family with genetic data from an outbred population identifies PLB1 as a candidate rheumatoid arthritis risk gene.
PLoS One
2014
24390342
Genetics of rheumatoid arthritis contributes to biology and drug discovery.
Nature
2014
22889921
Genome-wide association study of obsessive-compulsive disorder.
Mol Psychiatry
2013
22889924
Genome-wide association study of Tourette's syndrome.
Mol Psychiatry
2013
22889921
Genome-wide association study of obsessive-compulsive disorder.
Mol Psychiatry
2013
23903356
Identification of HKDC1 and BACE2 as genes influencing glycemic traits during pregnancy through genome-wide association studies.
Diabetes
2013
23762230
Enhancing the power of genetic association studies through the use of silver standard cases derived from electronic medical records.
PLoS One
2013
23363732
Incidental genetic findings in randomized clinical trials: recommendations from the Genomics and Randomized Trials Network (GARNET).
Genome Med
2013
23314186
Genetic variation associated with circulating monocyte count in the eMERGE Network.
Hum Mol Genet
2013
23267103
Linkage analysis identifies a locus for plasma von Willebrand factor undetected by genome-wide association.
Proc Natl Acad Sci U S A
2013
23413431
Genomic, transcriptomic, and lipidomic profiling highlights the role of inflammation in individuals with low high-density lipoprotein cholesterol.
Arterioscler Thromb Vasc Biol
2013
23575227
The chromosome 3q25 genomic region is associated with measures of adiposity in newborns in a multi-ethnic genome-wide association study.
Hum Mol Genet
2013
23903356
Identification of HKDC1 and BACE2 as genes influencing glycemic traits during pregnancy through genome-wide association studies.
Diabetes
2013
23762230
Enhancing the power of genetic association studies through the use of silver standard cases derived from electronic medical records.
PLoS One
2013
23413431
Genomic, transcriptomic, and lipidomic profiling highlights the role of inflammation in individuals with low high-density lipoprotein cholesterol.
Arterioscler Thromb Vasc Biol
2013
23575227
The chromosome 3q25 genomic region is associated with measures of adiposity in newborns in a multi-ethnic genome-wide association study.
Hum Mol Genet
2013
23267103
Linkage analysis identifies a locus for plasma von Willebrand factor undetected by genome-wide association.
Proc Natl Acad Sci U S A
2013
23314186
Genetic variation associated with circulating monocyte count in the eMERGE Network.
Hum Mol Genet
2013
23363732
Incidental genetic findings in randomized clinical trials: recommendations from the Genomics and Randomized Trials Network (GARNET).
Genome Med
2013
22889924
Genome-wide association study of Tourette's syndrome.
Mol Psychiatry
2013
22037903
Genetic variants associated with the white blood cell count in 13,923 subjects in the eMERGE Network.
Hum Genet
2012
22658725
Is 'forward' the same as 'plus'?⿦and other adventures in SNP allele nomenclature.
Trends Genet
2012
22923026
Evaluating genetic risk for prostate cancer among Japanese and Latinos.
Cancer Epidemiol Biomarkers Prev
2012
22829776
A genome-wide association meta-analysis of circulating sex hormone-binding globulin reveals multiple Loci implicated in sex steroid hormone regulation.
PLoS Genet
2012
22570617
Common variants at 9p21 and 8q22 are associated with increased susceptibility to optic nerve degeneration in glaucoma.
PLoS Genet
2012
22561516
Detectable clonal mosaicism from birth to old age and its relationship to cancer.
Nat Genet
2012
22361898
Return of individual research results from genome-wide association studies: experience of the Electronic Medical Records and Genomics (eMERGE) Network.
Genet Med
2012
23028342
New susceptibility loci associated with kidney disease in type 1 diabetes.
PLoS Genet
2012
23284291
Genome-wide joint meta-analysis of SNP and SNP-by-smoking interaction identifies novel loci for pulmonary function.
PLoS Genet
2012
22037903
Genetic variants associated with the white blood cell count in 13,923 subjects in the eMERGE Network.
Hum Genet
2012
23284291
Genome-wide joint meta-analysis of SNP and SNP-by-smoking interaction identifies novel loci for pulmonary function.
PLoS Genet
2012
23028342
New susceptibility loci associated with kidney disease in type 1 diabetes.
PLoS Genet
2012
22829776
A genome-wide association meta-analysis of circulating sex hormone-binding globulin reveals multiple Loci implicated in sex steroid hormone regulation.
PLoS Genet
2012
22923026
Evaluating genetic risk for prostate cancer among Japanese and Latinos.
Cancer Epidemiol Biomarkers Prev
2012
22561516
Detectable clonal mosaicism from birth to old age and its relationship to cancer.
Nat Genet
2012
22658725
Is 'forward' the same as 'plus'?⿦and other adventures in SNP allele nomenclature.
Trends Genet
2012
1 - 50 of 134
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Jonathan L Haines
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Catherine A McCarty
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Stacey Gabriel
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7
Teri A Manolio
National Human Genome Research Institute
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David R Crosslin
University of Washington Medical Center
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Joshua C Denny
Vanderbilt University
Co-authored papers
7
Marilyn C Cornelis
Co-authored papers
6
Frank B Hu
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Philip L De Jager
Columbia University Medical Center
Co-authored papers
6
Dana C Crawford
Cleveland Institute for Computational Biology, Case Western Reserve University
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Christopher S Carlson
University of Washington
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David J Hunter
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