Cordell HJ

Latest

Contribution of global rare copy-number variants to the risk of sporadic congenital heart disease
A genome-wide association study identifies SERPINB10, CRLF3, STX7, LAMP3, IFNG-AS1, and KRT80 as risk loci contributing to cutaneous leishmaniasis in Brazil
Investigation of genetically regulated gene expression and response to treatment in rheumatoid arthritis highlights an association between IL18RAP expression and treatment response
A genome-wide association study highlights a regulatory role for IFNG-AS1 contributing to cutaneous leishmaniasis in Brazil
Marked variation in heritability estimates of left ventricular mass depending on modality of measurement
A case–control genome wide association study of substance use disorder (SUD) identifies novel variants on chromosome 7p14.1 in patients from the United Arab Emirates (UAE)
Prediction of treatment response in rheumatoid arthritis patients using genome-wide SNP data
Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits
Using penalized regression to predict phenotype from SNP data
Novel blood pressure locus and gene discovery using genome-wide association study and expression data sets from blood and the kidney
A comparison of methods for inferring causal relationships between genotype and phenotype using additional biological measurements
Genome-wide analysis identifies 12 loci influencing human reproductive behavior
Using gene expression data to identify causal pathways between genotype and phenotype in a complex disease: Application to Genetic Analysis Workshop 19
A variant in the BACH2 gene is associated with susceptibility to autoimmune Addison's disease in humans
A comparison of methods for inferring causal relationships between genotype and phenotype using multi‐omics data
Increased power for detection of parent-of-origin effects via the use of haplotype estimation
Association between C677T polymorphism of methylene tetrahydrofolate reductase and congenital heart disease
Genome-wide association study of multiple congenital heart disease phenotypes identifies a susceptibility locus for atrial septal defect at chromosome 4p16
Genome-wide association study identifies loci on 12q24 and 13q32 associated with tetralogy of fallot
Aetiological role of folate deficiency in congenital cardiovascular malformation: Evidence from 'mendelian randomisation' and meta-analysis
A common variant in the PTPN11 gene contributes to the risk of tetralogy of fallot
Investigation of maternal effects, maternal-fetal interactions and parent-of-origin effects (imprinting), using mothers and their offspring
Penalized-regression-based multimarker genotype analysis of Genetic Analysis Workshop 17 data
Investigation of maternal effects, maternal-foetal interactions and parent-of-origin effects (imprinting), using mothers and their offspring