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A Genome-wide Association Study of Nonsyndromic Cleft Palate Identifies an Etiologic Missense Variant in GRHL3.
Leslie EJ, Liu H, Carlson JC, Shaffer JR, Feingold E, Wehby G, Laurie CA, Jain D, Laurie CC, Doheny KF, McHenry T, Resick J, Sanchez C, Jacobs J, Emanuele B, Vieira AR, Neiswanger K, Standley J, Czeizel AE, Deleyiannis F, Christensen K, Munger RG, Lie RT, Wilcox A, Romitti PA, Field LL, Padilla CD, Cutiongco-de la Paz EM, Lidral AC, Valencia-Ramirez LC, Lopez-Palacio AM, Valencia DR, Arcos-Burgos M, Castilla EE, Mereb JC, Poletta FA, Orioli IM, Carvalho FM, Hecht JT, Blanton SH, Buxó CJ, Butali A, Mossey PA, Adeyemo WL, James O, Braimah RO, Aregbesola BS, Eshete MA, Deribew M, Koruyucu M, Seymen F, Ma L, de Salamanca JE, Weinberg SM, Moreno L, Cornell RA, Murray JC, Marazita ML. Leslie EJ, et al. Among authors: butali a. Am J Hum Genet. 2016 Apr 7;98(4):744-54. doi: 10.1016/j.ajhg.2016.02.014. Epub 2016 Mar 24. Am J Hum Genet. 2016. PMID: 27018472 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.
DNA methylation effects on Van der Woude Syndrome phenotypic variability.
Seaberg A, Awotoye W, Qian F, Dunlay L, Butali A, Murray J, Moreno-Uribe L, Petrin A. Seaberg A, et al. Among authors: butali a. medRxiv [Preprint]. 2023 Dec 6:2023.11.04.23298094. doi: 10.1101/2023.11.04.23298094. medRxiv. 2023. PMID: 37961322 Free PMC article. Preprint.
CACNA1S mutation-associated dental anomalies: A calcium channelopathy.
Kantaputra P, Butali A, Eliason S, Chalkley C, Nakornchai S, Bongkochwilawan C, Kawasaki K, Kumchiang A, Ngamphiw C, Tongsima S, Ketudat Cairns JR, Olsen B, Intachai W, Ohazama A, Tucker AS, Amendt BA. Kantaputra P, et al. Among authors: butali a. Oral Dis. 2024 Apr;30(3):1350-1359. doi: 10.1111/odi.14551. Epub 2023 Mar 13. Oral Dis. 2024. PMID: 36825457
An overview of cleft care in Nigeria.
Butali A, Adeyemo WL. Butali A, et al. Niger Postgrad Med J. 2011 Jun;18(2):151-3. Niger Postgrad Med J. 2011. PMID: 21670785 Review.
Genetic studies in the Nigerian population implicate an MSX1 mutation in complex oral facial clefting disorders.
Butali A, Mossey PA, Adeyemo WL, Jezewski PA, Onwuamah CK, Ogunlewe MO, Ugboko VI, Adejuyigbe O, Adigun AI, Abdur-Rahman LO, Onah II, Audu RA, Idigbe EO, Mansilla MA, Dragan EA, Petrin AL, Bullard SA, Uduezue AO, Akpata O, Osaguona AO, Olasoji HO, Ligali TO, Kejeh BM, Iseh KR, Olaitan PB, Adebola AR, Efunkoya E, Adesina OA, Oluwatosin OM, Murray JC; NigeriaCRAN Collaboration. Butali A, et al. Cleft Palate Craniofac J. 2011 Nov;48(6):646-53. doi: 10.1597/10-133. Epub 2011 Jul 8. Cleft Palate Craniofac J. 2011. PMID: 21740177 Free PMC article.
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.
103 results