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Search results
(1 - 24 of 114)
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Unravelling the mystery of migraine and cluster headache
KCNV2-associated retinopathy
The arrhythmogenic cardiomyopathy phenotype associated with PKP2 c.1211dup variant
Genome-wide association analysis identifies ancestry-specific genetic variation associated with acute response to metformin and glipizide in SUGAR-MGH
Geo-epidemiology of autoantibodies in rheumatoid arthritis
Geo-epidemiology of autoantibodies in rheumatoid arthritis
Genetics and life course epidemiology of cardiometabolic disease
Targeted DNA sequencing to identify genetic aberrations in glioblastoma that underlie venous thromboembolism; a cohort study
Implicating genes, pleiotropy, and sexual dimorphism at blood lipid loci through multi-ancestry meta-analysis
Mechanisms underlying mutational outcomes of DNA double-strand break repair
Pharmacogenetics-guided dalcetrapib therapy after an acute coronary syndrome
Towards solving the missing heritability in pharmacogenomics
Contralateral hearing loss in children with a unilateral enlarged vestibular aqueduct
The genomics of heart failure
"Omics" in traumatic brain injury: novel approaches to a complex disease
Facts of aggression
Genetic risk scores identify genetic aetiology of inflammatory bowel disease phenotypes
The polygenic and monogenic basis of paediatric fractures
Genetics of migraine aura: an update
Diversity in the globally intertwined giant barrel sponge species complex
Genetics in primary care: validating a tool to pre-symptomatically assess common disease risk using an Australian questionnaire on family history
Genetic and methodological aspects of statin-induced lipid response
The Early Growth Genetics (EGG) and EArly Genetics and Lifecourse Epidemiology (EAGLE) consortia: design, results and future prospects
Another Brick in the Wall: the role of the actinobacterial cell wall in antibiotic resistance, phylogeny and development
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