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Genome-wide association study of ulcerative colitis identifies three new susceptibility loci, including the HNF4A region
Genome-wide association study of CNVs in 16,000 cases of eight common diseases and 3,000 shared controls
Rare loss-of-function variants in SETD1A are associated with schizophrenia and developmental disorders.
Cell type specific novel lncRNAs and circRNAs in the BLUEPRINT haematopoietic transcriptomes atlas
Correction: Maps of Open Chromatin Guide the Functional Follow-Up of Genome-Wide Association Signals: Application to Hematological Traits
Platelet Genomics
Chromosome contacts in activated T cells identify autoimmune disease candidate genes
