127 papers found
Open Targets: a platform for therapeutic target identification and validation.
The ORFeome Collaboration: a genome-scale human ORF-clone resource
eFORGE: A Tool for Identifying Cell Type-Specific Signal in Epigenomic Data
Ensembl regulation resources
Genetic fine mapping and genomic annotation defines causal mechanisms at type 2 diabetes susceptibility loci
A global reference for human genetic variation
Using human genetics to make new medicines
Improved imputation of low-frequency and rare variants using the UK10K haplotype reference panel
The UK10K project identifies rare variants in health and disease
Where Next for Genetics and Genomics?
Linking rare and common disease: mapping clinical disease- phenotypes to ontologies in therapeutic target validation
Correction: Quantitative Genetics of CTCF Binding Reveal Local Sequence Effects and Different Modes of X-Chromosome Association
Whole-genome sequence-based analysis of thyroid function
FORGE: A tool to discover cell specific enrichments of GWAS associated SNPs in regulatory regions
Quantitative Genetics of CTCF Binding Reveal Local Sequence Effects and Different Modes of X-Chromosome Association
A rare variant in APOC3 is associated with plasma triglyceride and VLDL levels in Europeans
Reply to Brunet and Doolittle: Both selected effect and causal role elements can influence human biology and disease
Defining functional DNA elements in the human genome
Genomic and Phenotypic Characterization of a Wild Medaka Population: Towards the Establishment of an Isogenic Population Genetic Resource in Fish
Genome-wide meta-analysis identifies new susceptibility loci for migraine
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