{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2025,11,12]],"date-time":"2025-11-12T10:06:01Z","timestamp":1762941961901,"version":"3.45.0"},"reference-count":8,"publisher":"Walter de Gruyter GmbH","issue":"10","content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":[],"published-print":{"date-parts":[[2025,10,27]]},"DOI":"10.1515\/jpem-2025-0295","type":"journal-article","created":{"date-parts":[[2025,8,26]],"date-time":"2025-08-26T05:56:46Z","timestamp":1756187806000},"page":"1111-1113","source":"Crossref","is-referenced-by-count":0,"title":["<i>ANKS1B<\/i>\n                    is a potential candidate gene for short stature and failure to thrive in children"],"prefix":"10.1515","volume":"38","author":[{"ORCID":"https:\/\/orcid.org\/0000-0002-5949-6421","authenticated-orcid":false,"given":"Pankaj","family":"Prasun","sequence":"first","affiliation":[{"name":"Department of Pediatrics, Division of Genetics , American Family Children\u2019s Hospital Madison , Madison , USA"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Rebecca C.","family":"Pulvermacher","sequence":"additional","affiliation":[{"name":"Department of Pediatrics, Division of Genetics , American Family Children\u2019s Hospital Madison , Madison , USA"}],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"374","published-online":{"date-parts":[[2025,8,27]]},"reference":[{"key":"2025111210012236759_j_jpem-2025-0295_ref_001","doi-asserted-by":"crossref","unstructured":"Jee, YH, Andrade, AC, Baron, J, Nilsson, O. Genetics of short stature. Endocrinol Metab Clin N Am. 2017; 46:259-81. https:\/\/doi.org\/10.1016\/j.ecl.2017.01.001.","DOI":"10.1016\/j.ecl.2017.01.001"},{"key":"2025111210012236759_j_jpem-2025-0295_ref_002","doi-asserted-by":"crossref","unstructured":"Carbonell, AU, Cho, CH, Tindi, JO, Counts, PA, Bates, JC, Erdjument-Bromage, H, et al.. Haploinsufficiency in the ANKS1B gene encoding AIDA-1 leads to a neurodevelopmental syndrome. Nat Commun. 2019; 10:3529. https:\/\/doi.org\/10.1038\/s41467-019-11437-w.","DOI":"10.1038\/s41467-019-11437-w"},{"key":"2025111210012236759_j_jpem-2025-0295_ref_003","doi-asserted-by":"crossref","unstructured":"Foreman, J, Perrett, D, Mazaika, E, Hunt, SE, Ware, JS, Firth, HV. DECIPHER: improving genetic diagnosis through dynamic integration of genomic and clinical data. Annu Rev Genom Hum Genet 2023; 24:151-76. https:\/\/doi.org\/10.1146\/annurev-genom-102822-100509.","DOI":"10.1146\/annurev-genom-102822-100509"},{"key":"2025111210012236759_j_jpem-2025-0295_ref_004","doi-asserted-by":"crossref","unstructured":"Smith, FJ, Irvine, AD, Terron-Kwiatkowski, A, Sandilands, A, Campbell, LE, Zhao, Y, et al.. Loss-of-function mutations in the gene encoding filaggrin cause ichthyosis vulgaris. Nat Genet. 2006; 38:337-42. https:\/\/doi.org\/10.1038\/ng1743.","DOI":"10.1038\/ng1743"},{"key":"2025111210012236759_j_jpem-2025-0295_ref_005","doi-asserted-by":"crossref","unstructured":"Croteau-Chonka, DC, Marvelle, AF, Lange, EM, Lee, NR, Adair, LS, Lange, LA, et al.. Genome-wide association study of anthropometric traits and evidence of interactions with age and study year in Filipino women. Obesity. 2011; 19:1019-27. https:\/\/doi.org\/10.1038\/oby.2010.256.","DOI":"10.1038\/oby.2010.256"},{"key":"2025111210012236759_j_jpem-2025-0295_ref_006","doi-asserted-by":"crossref","unstructured":"Lee, SI, Kim, SK, Kang, SW. Genetic variants associated with body mass index changes in Korean adults: the anseong and ansan cohorts of the Korean genome and epidemiology study. Curr Issues Mol Biol. 2024; 46:9074-81. https:\/\/doi.org\/10.3390\/cimb46080536.","DOI":"10.3390\/cimb46080536"},{"key":"2025111210012236759_j_jpem-2025-0295_ref_007","doi-asserted-by":"crossref","unstructured":"Cho, CH, Deyneko, IV, Cordova-Martinez, D, Vazquez, J, Maguire, AS, Diaz, JR, et al.. ANKS1B encoded AIDA-1 regulates social behaviors by controlling oligodendrocyte function. Nat Commun. 2023; 14:8499. https:\/\/doi.org\/10.1038\/s41467-023-43438-1.","DOI":"10.1038\/s41467-023-43438-1"},{"key":"2025111210012236759_j_jpem-2025-0295_ref_008","doi-asserted-by":"crossref","unstructured":"B\u00f8nnelykke, K, Pipper, CB, Tavendale, R, Palmer, CN, Bisgaard, H. Filaggrin gene variants and atopic diseases in early childhood assessed longitudinally from birth. Pediatr Allergy Immunol. 2010; 21:954-61. https:\/\/doi.org\/10.1111\/j.1399-3038.2010.01073.x.","DOI":"10.1111\/j.1399-3038.2010.01073.x"}],"container-title":["Journal of Pediatric Endocrinology and Metabolism"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/www.degruyterbrill.com\/document\/doi\/10.1515\/jpem-2025-0295\/xml","content-type":"application\/xml","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/www.degruyterbrill.com\/document\/doi\/10.1515\/jpem-2025-0295\/pdf","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2025,11,12]],"date-time":"2025-11-12T10:02:45Z","timestamp":1762941765000},"score":1,"resource":{"primary":{"URL":"https:\/\/www.degruyterbrill.com\/document\/doi\/10.1515\/jpem-2025-0295\/html"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2025,8,27]]},"references-count":8,"journal-issue":{"issue":"10","published-online":{"date-parts":[[2025,6,13]]},"published-print":{"date-parts":[[2025,10,27]]}},"alternative-id":["10.1515\/jpem-2025-0295"],"URL":"https:\/\/doi.org\/10.1515\/jpem-2025-0295","relation":{},"ISSN":["0334-018X","2191-0251"],"issn-type":[{"type":"print","value":"0334-018X"},{"type":"electronic","value":"2191-0251"}],"subject":[],"published":{"date-parts":[[2025,8,27]]}}}