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2017 1
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21 results

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Page 1
Trio-based GWAS identifies novel associations and subtype-specific risk factors for cleft palate.
Robinson K, Mosley TJ, Rivera-González KS, Jabbarpour CR, Curtis SW, Adeyemo WL, Beaty TH, Butali A, Buxó CJ, Cutler DJ, Epstein MP, Gowans LJJ, Hecht JT, Murray JC, Shaw GM, Uribe LM, Weinberg SM, Brand H, Marazita ML, Lipinski RJ, Leslie EJ. Robinson K, et al. HGG Adv. 2023 Aug 25;4(4):100234. doi: 10.1016/j.xhgg.2023.100234. eCollection 2023 Oct 12. HGG Adv. 2023. PMID: 37719664 Free PMC article.
Dental anomaly detection using intraoral photos via deep learning.
Ragodos R, Wang T, Padilla C, Hecht JT, Poletta FA, Orioli IM, Buxó CJ, Butali A, Valencia-Ramirez C, Restrepo Muñeton C, Wehby GL, Weinberg SM, Marazita ML, Moreno Uribe LM, Howe BJ. Ragodos R, et al. Sci Rep. 2022 Jul 8;12(1):11577. doi: 10.1038/s41598-022-15788-1. Sci Rep. 2022. PMID: 35804050 Free PMC article.
Author Correction: Dental anomaly detection using intraoral photos via deep learning.
Ragodos R, Wang T, Padilla C, Hecht JT, Poletta FA, Orioli IM, Buxó CJ, Butali A, Valencia-Ramirez C, Muñeton CR, Wehby GL, Weinberg SM, Marazita ML, Moreno Uribe LM, Howe BJ. Ragodos R, et al. Sci Rep. 2022 Aug 8;12(1):13541. doi: 10.1038/s41598-022-17668-0. Sci Rep. 2022. PMID: 35941160 Free PMC article. No abstract available.
Trio-based GWAS identifies novel associations and subtype-specific risk factors for cleft palate.
Robinson K, Mosley TJ, Rivera-González KS, Jabbarpour CR, Curtis SW, Adeyemo WL, Beaty TH, Butali A, Buxó CJ, Cutler DJ, Epstein MP, Gowans LJ, Hecht JT, Murray JC, Shaw GM, Uribe LM, Weinberg SM, Brand H, Marazita ML, Lipinski RJ, Leslie EJ. Robinson K, et al. medRxiv [Preprint]. 2023 Apr 6:2023.03.01.23286642. doi: 10.1101/2023.03.01.23286642. medRxiv. 2023. Update in: HGG Adv. 2023 Aug 25;4(4):100234. doi: 10.1016/j.xhgg.2023.100234 PMID: 37066311 Free PMC article. Updated. Preprint.
Clinically actionable secondary findings in 130 triads from sub-Saharan African families with non-syndromic orofacial clefts.
Oladayo A, Gowans LJJ, Awotoye W, Alade A, Busch T, Naicker T, Eshete MA, Adeyemo WL, Hetmanski JB, Zeng E, Adamson O, Adeleke C, Li M, Sule V, Kayali S, Olotu J, Mossey PA, Obiri-Yeboah S, Buxo CJ, Beaty T, Taub M, Donkor P, Marazita ML, Odukoya O, Adeyemo AA, Murray JC, Prince A, Butali A. Oladayo A, et al. Mol Genet Genomic Med. 2023 Oct;11(10):e2237. doi: 10.1002/mgg3.2237. Epub 2023 Jul 26. Mol Genet Genomic Med. 2023. PMID: 37496383 Free PMC article.
Genome scan reveals several loci associated with torus palatinus.
Lee MK, El Sergani AM, Herrick N, Green RM, Padilla C, Buxó CJ, Long RE, Valencia-Ramirez C, Muñeton CPR, Moreno Uribe LM, Adeyemo WL, Butali A, Marazita ML, Shaffer JR, Weinberg SM. Lee MK, et al. Orthod Craniofac Res. 2025 Feb;28(1):159-165. doi: 10.1111/ocr.12857. Epub 2024 Sep 18. Orthod Craniofac Res. 2025. PMID: 39291419 Free PMC article.
Mutations in Van Der Woude Families From Ethiopia.
Eshete M, Alade A, Abate F, Mossey PA, Awotoye WA, Busch T, Hailu A, Demissie Y, Butali A. Eshete M, et al. J Craniofac Surg. 2022 Mar-Apr 01;33(2):e138-e140. doi: 10.1097/SCS.0000000000008142. J Craniofac Surg. 2022. PMID: 34643600 Free PMC article.
Tooth Agenesis Patterns in Orofacial Clefting Using Tooth Agenesis Code: A Meta-Analysis.
Howe BJ, Pendleton C, Withanage MHH, Childs CA, Zeng E, van Wijk A, Hermus R, Padilla C, Hecht JT, Poletta FA, Orioli IM, Buxó-Martínez CJ, Deleyiannis F, Vieira AR, Butali A, Valencia-Ramirez C, Restrepo Muñeton C, Wehby GL, Weinberg SM, Marazita ML, Moreno Uribe LM, Xie XJ. Howe BJ, et al. Dent J (Basel). 2022 Jul 5;10(7):128. doi: 10.3390/dj10070128. Dent J (Basel). 2022. PMID: 35877402 Free PMC article. Review.
Genetic Analyses of Enamel Hypoplasia in Multiethnic Cohorts.
Alotaibi RN, Howe BJ, Moreno Uribe LM, Sanchez C, Deleyiannis FWB, Padilla C, Poletta FA, Orioli IM, Buxó CJ, Wehby GL, Vieira AR, Murray J, Valencia-Ramírez C, Restrepo Muñeton CP, Long RE, Shaffer JR, Reis SE, Weinberg SM, Neiswanger K, McNeil DW, Marazita ML. Alotaibi RN, et al. Hum Hered. 2022 Feb 16;87(2):34-50. doi: 10.1159/000522642. Online ahead of print. Hum Hered. 2022. PMID: 35172313 Free PMC article.
Non-random distribution of deleterious mutations in the DNA and protein-binding domains of IRF6 are associated with Van Der Woude syndrome.
Alade AA, Buxo-Martinez CJ, Mossey PA, Gowans LJJ, Eshete MA, Adeyemo WL, Naicker T, Awotoye WA, Adeleke C, Busch T, Toraño AM, Bello CA, Soto M, Soto M, Ledesma R, Marquez M, Cordero JF, Lopez-Del Valle LM, Salcedo MI, Debs N, Li M, Petrin A, Olotu J, Aldous C, Olutayo J, Ogunlewe MO, Abate F, Hailu T, Muhammed I, Gravem P, Deribew M, Gesses M, Hassan M, Pape J, Adeniyan OA, Obiri-Yeboah S, Arthur FKN, Oti AA, Olatosi O, Miller SE, Donkor P, Dunnwald MM, Marazita ML, Adeyemo AA, Murray JC, Butali A. Alade AA, et al. Mol Genet Genomic Med. 2020 Aug;8(8):e1355. doi: 10.1002/mgg3.1355. Epub 2020 Jun 17. Mol Genet Genomic Med. 2020. PMID: 32558391 Free PMC article. Review.
21 results