List of works - Daniel B Mirel

A 100K genome-wide association scan for diabetes and related traits in the Framingham Heart Study: replication and integration with other genome-wide datasets

scientific article published on 11 September 2007

A High Density Association Study of the Extended Major Histocompatibility Locus in Ulcerative Colitis

article published in 2007

A genome-wide association meta-analysis of circulating sex hormone-binding globulin reveals multiple Loci implicated in sex steroid hormone regulation

scientific article

A major histocompatibility Class I locus contributes to multiple sclerosis susceptibility independently from HLA-DRB1*15:01.

scientific article

A polymorphism in the TCF7 gene, C883A, is associated with type 1 diabetes

scientific article

Association and interaction of the IL4R, IL4, and IL13 loci with type 1 diabetes among Filipinos

scientific article

Association of IL4R haplotypes with type 1 diabetes

scientific article

Characterization of large structural genetic mosaicism in human autosome

journal article published in 2015

Common genetic variation in multiple metabolic pathways influences susceptibility to low HDL-cholesterol and coronary heart disease

scientific article

Common variants at 9p21 and 8q22 are associated with increased susceptibility to optic nerve degeneration in glaucoma

scientific article

Common variants near CAV1 and CAV2 are associated with primary open-angle glaucoma in Caucasians from the USA ⬇️

scientific article published on August 26, 2011

Detectable clonal mosaicism from birth to old age and its relationship to cancer

scientific article

Enhancing the power of genetic association studies through the use of silver standard cases derived from electronic medical records

scientific article

Evaluating genetic risk for prostate cancer among Japanese and Latinos

scientific article

Feasibility of High-Throughput Genome-Wide Genotyping using DNA from Stored Buccal Cell Samples

scientific article

Gene-environment interaction effects on the development of immune responses in the 1st year of life

scientific article

Genetic variants associated with the white blood cell count in 13,923 subjects in the eMERGE Network

scientific article published on 30 October 2011

Genetic variants at 2q24 are associated with susceptibility to type 2 diabetes

scientific article

Genetic variants in ABO blood group region, plasma soluble E-selectin levels and risk of type 2 diabetes

scientific article

Genetic variation associated with circulating monocyte count in the eMERGE Network

scientific article published on 12 January 2013

Genetic variation in immunoregulatory pathways and atopic phenotypes in infancy

scientific article published in March 2004

Genetics of rheumatoid arthritis contributes to biology and drug discovery

scientific article

Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants

scientific article

Genome-wide association scan in women with systemic lupus erythematosus identifies susceptibility variants in ITGAM, PXK, KIAA1542 and other loci

scientific article

Genome-wide association study identifies polymorphisms in LEPR as determinants of plasma soluble leptin receptor levels

scientific article

Genome-wide association study identifies polymorphisms in LEPR as determinants of plasma soluble leptin receptor levels

Genome-wide association study identifies variants at the IL18-BCO2 locus associated with interleukin-18 levels

scientific article

Genome-wide association study in a high-risk isolate for multiple sclerosis reveals associated variants in STAT3 gene

scientific article

Genome-wide joint meta-analysis of SNP and SNP-by-smoking interaction identifies novel loci for pulmonary function

scientific article

Genomic, Transcriptomic, and Lipidomic Profiling Highlights the Role of Inflammation in Individuals With Low High-density Lipoprotein Cholesterol

Identification of HKDC1 and BACE2 as genes influencing glycemic traits during pregnancy through genome-wide association studies

scientific article

Incidental genetic findings in randomized clinical trials: recommendations from the Genomics and Randomized Trials Network (GARNET).

scientific article

Integration of sequence data from a Consanguineous family with genetic data from an outbred population identifies PLB1 as a candidate rheumatoid arthritis risk gene

scientific article

Is 'forward' the same as 'plus'?…and other adventures in SNP allele nomenclature

scientific article published on 2 June 2012

Lack of association between the Trp719Arg polymorphism in kinesin-like protein-6 and coronary artery disease in 19 case-control studies

scientific article

Limited clinical utility of a genetic risk score for the prediction of fracture risk in elderly subjects

scientific article

Linkage analysis identifies a locus for plasma von Willebrand factor undetected by genome-wide association

scientific article

Mapping of multiple susceptibility variants within the MHC region for 7 immune-mediated diseases

scientific article published on 21 October 2009

New susceptibility loci associated with kidney disease in type 1 diabetes

scientific article

Pitfalls of merging GWAS data: lessons learned in the eMERGE network and quality control procedures to maintain high data quality

scientific article

Quality control and quality assurance in genotypic data for genome-wide association studies

scientific article

Quality control procedures for genome-wide association studies

scientific article published in 2011

Return of individual research results from genome-wide association studies: experience of the Electronic Medical Records and Genomics (eMERGE) Network

scientific article (publication date: April 2012)

The Gene, Environment Association Studies consortium (GENEVA): maximizing the knowledge obtained from GWAS by collaboration across studies of multiple conditions

scientific article (publication date: May 2010)

The chromosome 3q25 genomic region is associated with measures of adiposity in newborns in a multi-ethnic genome-wide association study

scientific article published on 10 April 2013

List of works by Daniel B Mirel

A 100K genome-wide association scan for diabetes and related traits in the Framingham Heart Study: replication and integration with other genome-wide datasets

A High Density Association Study of the Extended Major Histocompatibility Locus in Ulcerative Colitis

A genome-wide association meta-analysis of circulating sex hormone-binding globulin reveals multiple Loci implicated in sex steroid hormone regulation

A major histocompatibility Class I locus contributes to multiple sclerosis susceptibility independently from HLA-DRB1*15:01.

A polymorphism in the TCF7 gene, C883A, is associated with type 1 diabetes

Association and interaction of the IL4R, IL4, and IL13 loci with type 1 diabetes among Filipinos

Association of IL4R haplotypes with type 1 diabetes

Characterization of large structural genetic mosaicism in human autosome

Common genetic variation in multiple metabolic pathways influences susceptibility to low HDL-cholesterol and coronary heart disease

Common variants at 9p21 and 8q22 are associated with increased susceptibility to optic nerve degeneration in glaucoma

Common variants near CAV1 and CAV2 are associated with primary open-angle glaucoma in Caucasians from the USA ⬇️

Detectable clonal mosaicism from birth to old age and its relationship to cancer

Enhancing the power of genetic association studies through the use of silver standard cases derived from electronic medical records

Evaluating genetic risk for prostate cancer among Japanese and Latinos

Feasibility of High-Throughput Genome-Wide Genotyping using DNA from Stored Buccal Cell Samples

Gene-environment interaction effects on the development of immune responses in the 1st year of life

Genetic variants associated with the white blood cell count in 13,923 subjects in the eMERGE Network

Genetic variants at 2q24 are associated with susceptibility to type 2 diabetes

Genetic variants in ABO blood group region, plasma soluble E-selectin levels and risk of type 2 diabetes

Genetic variation associated with circulating monocyte count in the eMERGE Network

Genetic variation in immunoregulatory pathways and atopic phenotypes in infancy

Genetics of rheumatoid arthritis contributes to biology and drug discovery

Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants

Genome-wide association scan in women with systemic lupus erythematosus identifies susceptibility variants in ITGAM, PXK, KIAA1542 and other loci

Genome-wide association study identifies polymorphisms in LEPR as determinants of plasma soluble leptin receptor levels

Genome-wide association study identifies polymorphisms in LEPR as determinants of plasma soluble leptin receptor levels

Genome-wide association study identifies variants at the IL18-BCO2 locus associated with interleukin-18 levels

Genome-wide association study in a high-risk isolate for multiple sclerosis reveals associated variants in STAT3 gene

Genome-wide joint meta-analysis of SNP and SNP-by-smoking interaction identifies novel loci for pulmonary function

Genomic, Transcriptomic, and Lipidomic Profiling Highlights the Role of Inflammation in Individuals With Low High-density Lipoprotein Cholesterol

Identification of HKDC1 and BACE2 as genes influencing glycemic traits during pregnancy through genome-wide association studies

Incidental genetic findings in randomized clinical trials: recommendations from the Genomics and Randomized Trials Network (GARNET).

Integration of sequence data from a Consanguineous family with genetic data from an outbred population identifies PLB1 as a candidate rheumatoid arthritis risk gene

Is 'forward' the same as 'plus'?…and other adventures in SNP allele nomenclature

Lack of association between the Trp719Arg polymorphism in kinesin-like protein-6 and coronary artery disease in 19 case-control studies

Limited clinical utility of a genetic risk score for the prediction of fracture risk in elderly subjects

Linkage analysis identifies a locus for plasma von Willebrand factor undetected by genome-wide association

Mapping of multiple susceptibility variants within the MHC region for 7 immune-mediated diseases

New susceptibility loci associated with kidney disease in type 1 diabetes

Pitfalls of merging GWAS data: lessons learned in the eMERGE network and quality control procedures to maintain high data quality

Quality control and quality assurance in genotypic data for genome-wide association studies

Quality control procedures for genome-wide association studies

Return of individual research results from genome-wide association studies: experience of the Electronic Medical Records and Genomics (eMERGE) Network

The Gene, Environment Association Studies consortium (GENEVA): maximizing the knowledge obtained from GWAS by collaboration across studies of multiple conditions

The chromosome 3q25 genomic region is associated with measures of adiposity in newborns in a multi-ethnic genome-wide association study