FINEMAP-miss: Fine-mapping genome-wide association studies with missing genotype information Read more about FINEMAP-miss: Fine-mapping genome-wide association studies with missing genotype information
Quantifying risk modifiers of hereditary hemochromatosis using genomic and electronic health record data Read more about Quantifying risk modifiers of hereditary hemochromatosis using genomic and electronic health record data
PCSK9 and breast cancer survival: a Mendelian Randomization study Read more about PCSK9 and breast cancer survival: a Mendelian Randomization study
A genomic-led strategy to anticipate drug safety effects Read more about A genomic-led strategy to anticipate drug safety effects
Expanded map of genomic imprinting reveals insight into human disease Read more about Expanded map of genomic imprinting reveals insight into human disease
Germline Variants Influence Chronic Liver Disease Progression through Distinct Pathways Read more about Germline Variants Influence Chronic Liver Disease Progression through Distinct Pathways
The Genetics of Fibromyalgia and its Relationships to Psychiatric and Medical Traits Read more about The Genetics of Fibromyalgia and its Relationships to Psychiatric and Medical Traits
Triangulating cross-carcinoma GWAS delineates shared programs and disease-specific drivers Read more about Triangulating cross-carcinoma GWAS delineates shared programs and disease-specific drivers
Genetic liability to meniscus degeneration and its comorbidity patterns: a phenome-wide association study in the UK Biobank Read more about Genetic liability to meniscus degeneration and its comorbidity patterns: a phenome-wide association study in the UK Biobank
Protective PLCG2 variants associate with a delayed onset of Alzheimer's disease among heterozygous APOE ε4 carriers Read more about Protective PLCG2 variants associate with a delayed onset of Alzheimer's disease among heterozygous APOE ε4 carriers