HuGE Literature Finder
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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 |
| Association between forkhead box E1 polymorphisms and risk of non-syndromic cleft lip with or without cleft palate: A meta-analysis. Orthodontics & craniofacial research 2020 Jan . Xiao Wen-Lin, Jia Kai-Ning, Yu Guo, Zhao Ni |
| 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 |
| MicroRNA-655-3p and microRNA-497-5p inhibit cell proliferation in cultured human lip cells through the regulation of genes related to human cleft lip. BMC medical genomics 2019 May 12 (1): 70. Gajera Mona, Desai Neha, Suzuki Akiko, Li Aimin, Zhang Musi, Jun Goo, Jia Peilin, Zhao Zhongming, Iwata Junic |
| Association of low-frequency genetic variants in regulatory regions with nonsyndromic orofacial clefts. American journal of medical genetics. Part A 2019 Mar 179 (3): 467-474. Shaffer John R, LeClair Jessica, Carlson Jenna C, Feingold Eleanor, Buxó Carmen J, Christensen Kaare, Deleyiannis Frederic W B, Field L Leigh, Hecht Jacqueline T, Moreno Lina, Orioli Ieda M, Padilla Carmencita, Vieira Alexandre R, Wehby George L, Murray Jeffrey C, Weinberg Seth M, Marazita Mary L, Leslie Elizabeth |
| Association of SNP rs1867277 in FOXE1 Gene and Cleft Lip with or without Cleft Palate in a Han Chinese Population. Fetal and pediatric pathology 2018 Mar 1-6. Xie Liang, Deng Ying, Yuan Yumei, Tan Xiong, Liu Lijun, Li Nana, Deng Changfei, Liu Hanmin, Dai |
| A Population-Based Study of Effects of Genetic Loci on Orofacial Clefts. Journal of dental research 2017 Oct 96 (11): 1322-1329. Moreno Uribe L M, Fomina T, Munger R G, Romitti P A, Jenkins M M, Gjessing H K, Gjerdevik M, Christensen K, Wilcox A J, Murray J C, Lie R T, Wehby G |
| Genome-wide meta-analyses of nonsyndromic orofacial clefts identify novel associations between FOXE1 and all orofacial clefts, and TP63 and cleft lip with or without cleft palate.
Human genetics 2017 Mar 136 (3): 275-286. Leslie Elizabeth J, Carlson Jenna C, Shaffer John R, Butali Azeez, Buxó Carmen J, Castilla Eduardo E, Christensen Kaare, Deleyiannis Fred W B, Leigh Field L, Hecht Jacqueline T, Moreno Lina, Orioli Ieda M, Padilla Carmencita, Vieira Alexandre R, Wehby George L, Feingold Eleanor, Weinberg Seth M, Murray Jeffrey C, Beaty Terri H, Marazita Mary |
| Identification of 16q21 as a modifier of nonsyndromic orofacial cleft phenotypes. Genetic epidemiology 2017 11 41 (8): 887-897. Carlson Jenna C, Standley Jennifer, Petrin Aline, Shaffer John R, Butali Azeez, Buxó Carmen J, Castilla Eduardo, Christensen Kaare, Deleyiannis Frederic W-D, Hecht Jacqueline T, Field L Leigh, Garidkhuu Ariuntuul, Moreno Uribe Lina M, Nagato Natsume, Orioli Ieda M, Padilla Carmencita, Poletta Fernando, Suzuki Satoshi, Vieira Alexandre R, Wehby George L, Weinberg Seth M, Beaty Terri H, Feingold Eleanor, Murray Jeffrey C, Marazita Mary L, Leslie Elizabeth |
| Genetic variation of FOXE1 and risk for orofacial clefts in a California population. American journal of medical genetics. Part A 2016 Sep . Lammer Edward J, Mohammed Nebil, Iovannisci David M, Ma Chen, Lidral Andrew C, Shaw Gary |
| Association between FOXE1 and non-syndromic orofacial clefts in a northeastern Chinese population. The British journal of oral & maxillofacial surgery 2015 Oct 53 (8): 705-10. Liu Kun, Lu Yongping, Ai Lisi, Jiao Boqiang, Yu Jiantao, Zhang Bin, Liu Qia |
| Investigation of genetic factors underlying typical orofacial clefts: mutational screening and copy number variation. Journal of human genetics 2015 Jan 60 (1): 17-25. Simioni Milena, Araujo Tânia Kawasaki, Monlleo Isabella Lopes, Maurer-Morelli Cláudia Vianna, Gil-da-Silva-Lopes Vera Lúc |
| Exploratory genotype-phenotype correlations of facial form and asymmetry in unaffected relatives of children with non-syndromic cleft lip and/or palate. Journal of anatomy 2014 Jun 224 (6): 688-709. Miller Steven F, Weinberg Seth M, Nidey Nichole L, Defay David K, Marazita Mary L, Wehby George L, Moreno Uribe Lina |
| Strong association of variants around FOXE1 and orofacial clefting. Journal of dental research 2014 Apr 93 (4): 376-81. Ludwig K U, Böhmer A C, Rubini M, Mossey P A, Herms S, Nowak S, Reutter H, Alblas M A, Lippke B, Barth S, Paredes-Zenteno M, Muñoz-Jimenez S G, Ortiz-Lopez R, Kreusch T, Hemprich A, Martini M, Braumann B, Jäger A, Pötzsch B, Molloy A, Peterlin B, Hoffmann P, Nöthen M M, Rojas-Martinez A, Knapp M, Steegers-Theunissen R P, Mangold |
| FOXE1 mutations in Thai patients with oral clefts. Genetics research 2013 Nov . Srichomthong C, Ittiwut R, Siriwan P, Suphapeetiporn K, Shotelersuk V |
| Search for genetic modifiers of IRF6 and genotype-phenotype correlations in Van der Woude and popliteal pterygium syndromes. American journal of medical genetics. Part A 2013 Oct 161A (10): 2535-44. Leslie Elizabeth J, Mancuso Jennifer L, Schutte Brian C, Cooper Margaret E, Durda Kate M, L'heureux Jamie, Zucchero Theresa M, Marazita Mary L, Murray Jeffrey |
| Confirming genes influencing risk to cleft lip with/without cleft palate in a case-parent trio study. Human genetics 2013 Jul 132 (7): 771-81. Beaty T H, Taub M A, Scott A F, Murray J C, Marazita M L, Schwender H, Parker M M, Hetmanski J B, Balakrishnan P, Mansilla M A, Mangold E, Ludwig K U, Noethen M M, Rubini M, Elcioglu N, Ruczinski |
| Association of candidate genes with nonsyndromic clefts in Honduran and Colombian populations. The Laryngoscope 2012 Sep 122 (9): 2082-7. Lennon Christen J, Birkeland Andrew C, Nuñez José Arturo Pacheco, Su Gloria H, Lanzano Patricia, Guzman Edwin, Celis Katrina, Eisig Sidney B, Hoffman David, Rendon Maria Teresa Guerra, Ostos Henry, Chung Wendy K, Haddad Jose |
| Variation in FGF1, FOXE1, and TIMP2 genes is associated with nonsyndromic cleft lip with or without cleft palate. Birth defects research. Part A, Clinical and molecular teratology 2011 Apr 91 (4): 218-25. Nikopensius Tiit, Kempa Inga, Ambrozaityt? Laima, Jagomägi Triin, Saag Mare, Matulevi?ien? Aušra, Utkus Algirdas, Krjutškov Kaarel, Tammekivi Veronika, Piekuse Linda, Akota Ilze, Barkane Biruta, Krumina Astrida, Klovins Janis, Lace Baiba, Ku?inskas Vaidutis, Metspalu Andr |
| Association between genetic variants of reported candidate genes or regions and risk of cleft lip with or without cleft palate in the polish population. Birth defects research. Part A, Clinical and molecular teratology 2010 Jul 88 (7): 538-45. Mostowska Adrianna, Hozyasz Kamil K, Wojcicki Piotr, Biedziak Barbara, Paradowska Patrycja, Jagodzinski Pawel |
| FOXE1 association with both isolated cleft lip with or without cleft palate, and isolated cleft palate. Human molecular genetics 2009 Dec 18 (24): 4879-96. Moreno Lina M, Mansilla Maria Adela, Bullard Steve A, Cooper Margaret E, Busch Tamara D, Machida Junichiro, Johnson Marla K, Brauer David, Krahn Katherine, Daack-Hirsch Sandy, L'heureux Jamie, Valencia-Ramirez Consuelo, Rivera Dora, López Ana Maria, Moreno Manuel A, Hing Anne, Lammer Edward J, Jones Marilyn, Christensen Kaare, Lie Rolv T, Jugessur Astanand, Wilcox Allen J, Chines Peter, Pugh Elizabeth, Doheny Kim, Arcos-Burgos Mauricio, Marazita Mary L, Murray Jeffrey C, Lidral Andrew |
| Altered binding of MYF-5 to FOXE1 promoter in non-syndromic and CHARGE-associated cleft palate. Journal of oral pathology & medicine : official publication of the International Association of Oral Pathologists and the American Academy of Oral Pathology 2009 Jan 38 (1): 18-23. Venza Mario, Visalli Maria, Venza Isabella, Torino Claudia, Tripodo Barbara, Melita Rocco, Teti Dia |
| FOXE1 gene mutation screening by multiplex PCR/DHPLC in CHARGE syndrome and syndromic and non-syndromic cleft palate. Journal of chromatography. B, Analytical technologies in the biomedical and life sciences 2006 May 836 (1-2): 39-46. Venza Mario, Visalli Maria, Venza Isabella, Torino Claudia, Saladino Rita, Teti Dia |
| Medical sequencing of candidate genes for nonsyndromic cleft lip and palate. PLoS genetics 2005 Dec 1 (6): e64. Vieira Alexandre R, Avila Joseph R, Daack-Hirsch Sandra, Dragan Ecaterina, Félix Têmis M, Rahimov Fedik, Harrington Jill, Schultz Rebecca R, Watanabe Yoriko, Johnson Marla, Fang Jennifer, O'Brien Sarah E, Orioli Iêda M, Castilla Eduardo E, Fitzpatrick David R, Jiang Rulang, Marazita Mary L, Murray Jeffrey |
| A novel loss-of-function mutation in TTF-2 is associated with congenital hypothyroidism, thyroid agenesis and cleft palate. Human molecular genetics 2002 Aug 11 (17): 2051-9. Castanet Mireille, Park Soo-Mi, Smith Aaron, Bost Michel, Léger Juliane, Lyonnet Stanislas, Pelet Anna, Czernichow Paul, Chatterjee Krishna, Polak Mich |
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- Page last updated:Mar 31, 2023
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