HuGE Literature Finder
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| Association analysis of SNPs in GRHL3, FAF1, and KCNJ2 with NSCPO sub-phenotypes in Han Chinese. Oral diseases 2021 7 28 (8): 2204-2214. Sun Jia-Lin, Shi Jia-Yu, Yin Bin, Lin Yan-Song, Shi Bing, Jia Zhong-L |
| Novel GRHL3 Variants in a South African Cohort With Cleft Lip and Palate. The Cleft palate-craniofacial journal : official publication of the American Cleft Palate-Craniofacial Association 2021 8 59 (9): 1125-1130. Naicker Thirona, Adeleke Chinyere C, Alade Azeez, Mossey Peter A, Awotoye Waheed A, Busch Tamara D, Li Mary, Olotu Joy, Gowans Lord J J, Aldous Colleen, Butali Aze |
Pleiotropy method reveals genetic overlap between orofacial clefts at multiple novel loci from GWAS of multi-ethnic trios.
PLoS genetics 2021 7 17 (7): e1009584. Ray Debashree, Venkataraghavan Sowmya, Zhang Wanying, Leslie Elizabeth J, Hetmanski Jacqueline B, Weinberg Seth M, Murray Jeffrey C, Marazita Mary L, Ruczinski Ingo, Taub Margaret A, Beaty Terri |
| Machine learning in prediction of genetic risk of nonsyndromic oral clefts in the Brazilian population. Clinical oral investigations 2020 Jul . Machado Renato Assis, de Oliveira Silva Carolina, Martelli-Junior Hercílio, das Neves Lucimara Teixeira, Coletta Ricardo |
| Exploring GRHL3 polymorphisms and SNP-SNP interactions in the risk of non-syndromic oral clefts in the Brazilian population. Oral diseases 2019 Sep . Azevedo Camilla de Marchi Sanches, Machado Renato Assis, Martelli-Júnior Hercílio, Reis Silvia Regina de Almeida, Persuhn Darlene Camati, Coletta Ricardo D, Rangel Ana Lúcia Carrinho Ayro |
| Threonine 454 phosphorylation in Grainyhead-like 3 is important for its function and regulation by the p38 MAPK pathway. Biochimica et biophysica acta. Molecular cell research 2018 4 1865 (7): 1002-1011. Krzywinska Ewa, Zorawski Marek Dominick, Taracha Agnieszka, Kotarba Grzegorz, Kikulska Agnieszka, Mlacki Michal, Kwiatkowska Katarzyna, Wilanowski Toma |
| Loss-of-Function GRHL3 Variants Detected in African Patients with Isolated Cleft Palate. Journal of dental research 2017 Sep 22034517729819. Eshete M A, Liu H, Li M, Adeyemo W L, Gowans L J J, Mossey P A, Busch T, Deressa W, Donkor P, Olaitan P B, Aregbesola B S, Braimah R O, Oseni G O, Oginni F, Audu R, Onwuamah C, James O, Augustine-Akpan E, Rahman L A, Ogunlewe M O, Arthur F K N, Bello S A, Agbenorku P, Twumasi P, Abate F, Hailu T, Demissie Y, Hailu A, Plange-Rhule G, Obiri-Yeboah S, Dunnwald M M, Gravem P E, Marazita M L, Adeyemo A A, Murray J C, Cornell R A, Butali |
| Candidate Genes for Nonsyndromic Cleft Palate Detected by Exome Sequencing. Journal of dental research 2017 Aug 22034517722761. Hoebel A K, Drichel D, van de Vorst M, Böhmer A C, Sivalingam S, Ishorst N, Klamt J, Gölz L, Alblas M, Maaser A, Keppler K, Zink A M, Dixon M J, Dixon J, Hemprich A, Kruse T, Graf I, Dunsche A, Schmidt G, Daratsianos N, Nowak S, Aldhorae K A, Nöthen M M, Knapp M, Thiele H, Gilissen C, Reutter H, Hoischen A, Mangold E, Ludwig K |
| Association study between Van der Woude Syndrome causative gene GRHL3 and nonsyndromic cleft lip with or without cleft palate in a Chinese cohort. Gene 2016 Apr . Wang Yirui, Sun Yimin, Huang Yongqing, Pan Yongchu, Jia Zhonglin, Ma Lijuan, Ma Lan, Lan Feifei, Zhou Yuxi, Shi Jiayu, Yang Xiong, Zhang Lei, Jiang Hongbing, Jiang Min, Yin Aihua, Cheng Jing, Wang Lin, Yang Yinxue, Shi Bi |
| A Genome-wide Association Study of Nonsyndromic Cleft Palate Identifies an Etiologic Missense Variant in GRHL3.
American journal of human genetics 2016 Mar . Leslie Elizabeth J, Liu Huan, Carlson Jenna C, Shaffer John R, Feingold Eleanor, Wehby George, Laurie Cecelia A, Jain Deepti, Laurie Cathy C, Doheny Kimberly F, McHenry Toby, Resick Judith, Sanchez Carla, Jacobs Jennifer, Emanuele Beth, Vieira Alexandre R, Neiswanger Katherine, Standley Jennifer, Czeizel Andrew E, Deleyiannis Frederic, Christensen Kaare, Munger Ronald G, Lie Rolv T, Wilcox Allen, Romitti Paul A, Field L Leigh, Padilla Carmencita D, Cutiongco-de la Paz Eva Maria C, Lidral Andrew C, Valencia-Ramirez Luz Consuelo, Lopez-Palacio Ana Maria, Valencia Dora Rivera, Arcos-Burgos Mauricio, Castilla Eduardo E, Mereb Juan C, Poletta Fernando A, Orioli Iêda M, Carvalho Flavia M, Hecht Jacqueline T, Blanton Susan H, Buxó Carmen J, Butali Azeez, Mossey Peter A, Adeyemo Wasiu L, James Olutayo, Braimah Ramat O, Aregbesola Babatunde S, Eshete Mekonen A, Deribew Milliard, Koruyucu Mine, Seymen Figen, Ma Lian, de Salamanca Javier Enríquez, Weinberg Seth M, Moreno Lina, Cornell Robert A, Murray Jeffrey C, Marazita Mary |
| Sequencing the GRHL3 Coding Region Reveals Rare Truncating Mutations and a Common Susceptibility Variant for Nonsyndromic Cleft Palate. American journal of human genetics 2016 Mar . Mangold Elisabeth, Böhmer Anne C, Ishorst Nina, Hoebel Ann-Kathrin, Gültepe Pinar, Schuenke Hannah, Klamt Johanna, Hofmann Andrea, Gölz Lina, Raff Ruth, Tessmann Peter, Nowak Stefanie, Reutter Heiko, Hemprich Alexander, Kreusch Thomas, Kramer Franz-Josef, Braumann Bert, Reich Rudolf, Schmidt Gül, Jäger Andreas, Reiter Rudolf, Brosch Sibylle, Stavusis Janis, Ishida Miho, Seselgyte Rimante, Moore Gudrun E, Nöthen Markus M, Borck Guntram, Aldhorae Khalid A, Lace Baiba, Stanier Philip, Knapp Michael, Ludwig Kerstin |
| Lack of Association between Missense Variants in GRHL3 (rs2486668 and rs545809) and Susceptibility to Non-Syndromic Orofacial Clefts in a Han Chinese Population. PloS one 2016 11 (7): e0159940. He Miao, Bian Zhu |
| Association of Nucleotide Variants of GRHL3, IRF6, NAT2, SDC2, BCL3, and PVRL1 Genes with Nonsyndromic Cleft Lip With/Without Cleft Palate in Multigenerational Families: A Retrospective Study. Contemporary clinical dentistry 0 12 (2): 138-142. Neela Praveen Kumar, Gosla Srinivas Reddy, Husain Akhter, Mohan Vasavi, Thumoju Sravya, Rajeshwari B |
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- Page last updated:Mar 28, 2023
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