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Exome sequencing provides additional evidence for the involvement of ARHGAP29 in Mendelian orofacial clefting and extends the phenotypic spectrum to isolated cleft palate.
Liu H, Busch T, Eliason S, Anand D, Bullard S, Gowans LJJ, Nidey N, Petrin A, Augustine-Akpan EA, Saadi I, Dunnwald M, Lachke SA, Zhu Y, Adeyemo A, Amendt B, Roscioli T, Cornell R, Murray J, Butali A. Liu H, et al. Among authors: butali a. Birth Defects Res. 2017 Jan 20;109(1):27-37. doi: 10.1002/bdra.23596. Birth Defects Res. 2017. PMID: 28029220 Free PMC article.
Study protocol for a pilot quasi-experimental study on oral health education for nurses and community health workers in Nigeria.
Oladayo AM, Lawal FB, Sofola OO, Uti OG, Oyapero A, Aborisade A, Stewart B, Daep CA, Hines D, Beard J, Dedeke A, Fagbule OF, Williams AT, Uchendu OC, Ohiare K, Adedire AO, Yahya-Imam AA, Adeniji OI, Mele AB, Baffa AS, Adetula I, Lawal TA, Oke GA, Butali A. Oladayo AM, et al. Among authors: butali a. Front Public Health. 2024 Jun 7;12:1398869. doi: 10.3389/fpubh.2024.1398869. eCollection 2024. Front Public Health. 2024. PMID: 38912270 Free PMC article.
Global Health Mentorship: Challenges and Opportunities for Equitable Partnership.
Bain LE, Mbouamba Yankam B, Kong JD, Claude Nkfusai N, Badru OA, Ebuenyi ID, Butali A, Adjei NK, Adeagbo O. Bain LE, et al. Among authors: butali a. BMJ Glob Health. 2023 Nov;8(11):e013751. doi: 10.1136/bmjgh-2023-013751. BMJ Glob Health. 2023. PMID: 37984896 Free PMC article. No abstract available.
Replication of genome wide association identified candidate genes confirm the role of common and rare variants in PAX7 and VAX1 in the etiology of nonsyndromic CL(P).
Butali A, Suzuki S, Cooper ME, Mansilla AM, Cuenco K, Leslie EJ, Suzuki Y, Niimi T, Yamamoto M, Ayanga G, Erkhembaatar T, Furukawa H, Fujiwawa K, Imura H, Petrin AL, Natsume N, Beaty TH, Marazita ML, Murray JC. Butali A, et al. Am J Med Genet A. 2013 May;161A(5):965-72. doi: 10.1002/ajmg.a.35749. Epub 2013 Mar 5. Am J Med Genet A. 2013. PMID: 23463464 Free PMC article.
Novel IRF6 mutations in families with Van Der Woude syndrome and popliteal pterygium syndrome from sub-Saharan Africa.
Butali A, Mossey PA, Adeyemo WL, Eshete MA, Gaines LA, Even D, Braimah RO, Aregbesola BS, Rigdon JV, Emeka CI, James O, Ogunlewe MO, Ladeinde AL, Abate F, Hailu T, Mohammed I, Gravem PE, Deribew M, Gesses M, Adeyemo AA, Murray JC. Butali A, et al. Mol Genet Genomic Med. 2014 May;2(3):254-60. doi: 10.1002/mgg3.66. Epub 2014 Jan 27. Mol Genet Genomic Med. 2014. PMID: 24936515 Free PMC article.
Rare functional variants in genome-wide association identified candidate genes for nonsyndromic clefts in the African population.
Butali A, Mossey P, Adeyemo W, Eshete M, Gaines L, Braimah R, Aregbesola B, Rigdon J, Emeka C, Olutayo J, Ogunlewe O, Ladeinde A, Abate F, Hailu T, Mohammed I, Gravem P, Deribew M, Gesses M, Adeyemo A, Marazita M, Murray J. Butali A, et al. Am J Med Genet A. 2014 Oct;164A(10):2567-71. doi: 10.1002/ajmg.a.36691. Epub 2014 Jul 31. Am J Med Genet A. 2014. PMID: 25081408 Free PMC article.
111 results