{"database":"biostudies-literature","file_versions":[],"scores":null,"additional":{"submitter":["Richard D"],"funding":["NICHD NIH HHS","NIDDK NIH HHS","NHGRI NIH HHS","NIAMS NIH HHS"],"pagination":["15-32.e24"],"full_dataset_link":["https://www.ebi.ac.uk/biostudies/studies/S-EPMC11724752"],"repository":["biostudies-literature"],"omics_type":["Unknown"],"volume":["188(1)"],"pubmed_abstract":["Underlying variation in height are regulatory changes to chondrocytes, cartilage cells comprising long-bone growth plates. Currently, we lack knowledge on epigenetic regulation and gene expression of chondrocytes sampled across the human skeleton, and therefore we cannot understand basic regulatory mechanisms controlling height biology. We first rectify this issue by generating extensive epigenetic and transcriptomic maps from chondrocytes sampled from different growth plates across developing human skeletons, discovering novel regulatory networks shaping human bone/joint development. Next, using these maps in tandem with height genome-wide association study (GWAS) signals, we disentangle the regulatory impacts that skeletal element-specific versus global-acting variants have on skeletal g"],"journal":["Cell"],"pubmed_title":["Functional genomics of human skeletal development and the patterning of height heritability."],"pmcid":["PMC11724752"],"funding_grant_id":["R01 AR073821","R01 AR081274","R24 HD000836","T32 HG002295","R01 DK075787"],"pubmed_authors":["Vedantam S","Yengo L","GIANT Consortium","Bartell E","Hirschhorn J","Muthuirulan P","Young M","Marouli E","Capellini TD","Richard D"],"additional_accession":[]},"is_claimable":false,"name":"Functional genomics of human skeletal development and the patterning of height heritability.","description":"Underlying variation in height are regulatory changes to chondrocytes, cartilage cells comprising long-bone growth plates. Currently, we lack knowledge on epigenetic regulation and gene expression of chondrocytes sampled across the human skeleton, and therefore we cannot understand basic regulatory mechanisms controlling height biology. We first rectify this issue by generating extensive epigenetic and transcriptomic maps from chondrocytes sampled from different growth plates across developing human skeletons, discovering novel regulatory networks shaping human bone/joint development. Next, using these maps in tandem with height genome-wide association study (GWAS) signals, we disentangle the regulatory impacts that skeletal element-specific versus global-acting variants have on skeletal g","dates":{"release":"2025-01-01T00:00:00Z","publication":"2025 Jan","modification":"2026-06-06T19:54:34.181Z","creation":"2026-06-04T03:12:41.754Z"},"accession":"S-EPMC11724752","cross_references":{"pubmed":["39549696"],"doi":["10.1016/j.cell.2024.10.040"]}}