{"type": "root", "children": [{"type": "p", "children": [{"type": "t", "text": "\n Although both studies investigated the genetic architecture underlying facial and anthropometric traits (1,2), neither abstract provides explicit details regarding the functional role of LINC01432. As a long non‐coding RNA, LINC01432 may be implicated in gene regulatory processes; however, no specific associations, mechanistic insights, or phenotypic contributions of LINC01432 were discussed in the reported genome‐wide association analyses. Further targeted investigations would be required to elucidate its molecular function and potential impact on human morphological variation.\n "}]}, {"type": "t", "text": "\n "}, {"type": "p", "children": [{"type": "t", "text": "\n Citation (1):"}, {"type": "fg", "children": [{"type": "fg_f", "ref": "1"}]}, {"type": "t", "text": "  |  \n Citation (2):."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "2"}]}, {"type": "t", "text": ""}]}, {"type": "rg", "children": [{"type": "r", "ref": 1, "children": [{"type": "t", "text": "Kaustubh Adhikari, Macarena Fuentes-Guajardo, Mirsha Quinto-Sánchez, et al. "}, {"type": "b", "children": [{"type": "t", "text": "A genome-wide association scan implicates DCHS2, RUNX2, GLI3, PAX1 and EDAR in human facial variation."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Nat Commun (2016)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1038/ncomms11616"}], "href": "https://doi.org/10.1038/ncomms11616"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "27193062"}], "href": "https://pubmed.ncbi.nlm.nih.gov/27193062"}]}, {"type": "r", "ref": 2, "children": [{"type": "t", "text": "Iván Galván-Femenía, Mireia Obón-Santacana, David Piñeyro, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Multitrait genome association analysis identifies new susceptibility genes for human anthropometric variation in the GCAT cohort."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "J Med Genet (2018)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1136/jmedgenet-2018-105437"}], "href": "https://doi.org/10.1136/jmedgenet-2018-105437"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "30166351"}], "href": "https://pubmed.ncbi.nlm.nih.gov/30166351"}]}]}]}