Human Genome Epidemiology Literature Finder
Records 1 - 17 (of 17 Records) |
Query Trace: ARHGAP29[original query] |
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Expression and mutation analyses implicate ARHGAP29 as the etiologic gene for the cleft lip with or without cleft palate locus identified by genome-wide association on chromosome 1p22. Birth defects research. Part A, Clinical and molecular teratology 2012 Nov 94 (11): 934-42. Leslie Elizabeth J, Mansilla M Adela, Biggs Leah C, Schuette Kristi, Bullard Steve, Cooper Margaret, Dunnwald Martine, Lidral Andrew C, Marazita Mary L, Beaty Terri H, Murray Jeffrey |
Further evidence suggesting a role for variation in ARHGAP29 variants in nonsyndromic cleft lip/palate. Birth defects research. Part A, Clinical and molecular teratology 2014 Sep 100 (9): 679-85. Letra Ariadne, Maili Lorena, Mulliken John B, Buchanan Edward, Blanton Susan H, Hecht Jacqueline |
Rare functional variants in genome-wide association identified candidate genes for nonsyndromic clefts in the African population. American journal of medical genetics. Part A 2014 Oct 164A (10): 2567-71. Butali Azeez, Mossey Peter, Adeyemo Wasiu, Eshete Mekonen, Gaines Lauren, Braimah Ramat, Aregbesola Babatunde, Rigdon Jennifer, Emeka Christian, Olutayo James, Ogunlewe Olugbenga, Ladeinde Akinola, Abate Fikre, Hailu Taye, Mohammed Ibrahim, Gravem Paul, Deribew Milliard, Gesses Mulualem, Adeyemo Adebowale, Marazita Mary, Murray Jeffr |
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 |
Identification of functional variants for cleft lip with or without cleft palate in or near PAX7, FGFR2, and NOG by targeted sequencing of GWAS loci. American journal of human genetics 2015 Mar 96 (3): 397-411. Leslie Elizabeth J, Taub Margaret A, Liu Huan, Steinberg Karyn Meltz, Koboldt Daniel C, Zhang Qunyuan, Carlson Jenna C, Hetmanski Jacqueline B, Wang Hang, Larson David E, Fulton Robert S, Kousa Youssef A, Fakhouri Walid D, Naji Ali, Ruczinski Ingo, Begum Ferdouse, Parker Margaret M, Busch Tamara, Standley Jennifer, Rigdon Jennifer, Hecht Jacqueline T, Scott Alan F, Wehby George L, Christensen Kaare, Czeizel Andrew E, Deleyiannis Frederic W-B, Schutte Brian C, Wilson Richard K, Cornell Robert A, Lidral Andrew C, Weinstock George M, Beaty Terri H, Marazita Mary L, Murray Jeffrey |
Association Studies and Direct DNA Sequencing Implicate Genetic Susceptibility Loci in the Etiology of Nonsyndromic Orofacial Clefts in Sub-Saharan African Populations. Journal of dental research 2016 Jul . Gowans L J J, Adeyemo W L, Eshete M, Mossey P A, Busch T, Aregbesola B, Donkor P, Arthur F K N, Bello S A, Martinez A, Li M, Augustine-Akpan E A, Deressa W, Twumasi P, Olutayo J, Deribew M, Agbenorku P, Oti A A, Braimah R, Plange-Rhule G, Gesses M, Obiri-Yeboah S, Oseni G O, Olaitan P B, Abdur-Rahman L, Abate F, Hailu T, Gravem P, Ogunlewe M O, Buxó C J, Marazita M L, Adeyemo A A, Murray J C, Butali |
Impact of rare variants in ARHGAP29 to the etiology of oral clefts: role of loss-of-function vs missense variants. Clinical genetics 2016 Jun . Savastano Clarice P, Brito Luciano A, Faria Ágatha C, Setó-Salvia Núria, Peskett Emma, Musso Camila M, Alvizi Lucas, Ezquina Suzana A M, James Chela, GOSgene , Beales Philip, Lees Melissa, Moore Gudrun E, Stanier Philip, Passos-Bueno Maria Ri |
A multi-ethnic genome-wide association study identifies novel loci for non-syndromic cleft lip with or without cleft palate on 2p24.2, 17q23 and 19q13. Human molecular genetics 2016 Mar . Leslie Elizabeth J, 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, Lidral Andrew C, Valencia-Ramirez Luz Consuelo, Lopez-Palacio Ana Maria, Rivera Valencia Dora, Arcos-Burgos Mauricio, Czeizel Andrew E, Field L Leigh, Padilla Carmencita D, Cutiongco-de la Paz Eva Maria C, Deleyiannis Frederic, Christensen Kaare, Munger Ronald G, Lie Rolv T, Wilcox Allen, Romitti Paul A, 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, Abate Fikre, Koruyucu Mine, Seymen Figen, Ma Lian, Enríquez de Salamanca Javier, Weinberg Seth, Moreno Lina, Murray Jeffrey C, Marazita Mary |
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 |
A novel splicing mutation of ARHGAP29 is associated with nonsyndromic cleft lip with or without cleft palate. The journal of maternal-fetal & neonatal medicine : the official journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians 2020 7 35 (13): 2499-2506. Yu Qiuxia, Deng Qiong, Fu Fang, Li Ru, Zhang Wenwen, Wan Junhui, Yang Xin, Wang Dan, Li Fucheng, Wu Shaoqing, Li Jian, Li Dongzhi, Liao C |
Gene-gene interactions between BMP4 and ARHGAP29 among non-syndromic cleft lip only (NSCLO) trios from western Han Chinese population. International journal of clinical and experimental pathology 2020 13 (2): 295-301. Wang Yiru, Shi Jiayu, Zheng Qian, Shi Bing, Jia Zhongl |
The SNP rs560426 Within ABCA4-ARHGAP29 Locus and the Risk of Nonsyndromic Oral Clefts. The Cleft palate-craniofacial journal : official publication of the American Cleft Palate-Craniofacial Association 2020 Jan 1055665619899764. Wu-Chou Yah-Huei, Chen Kuo-Ting Philip, Lu Yi-Chieh, Lin Yin-Ting, Chang Hsien-Fang, Lo Lun-J |
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 |
Targeted re-sequencing on 1p22 among non-syndromic orofacial clefts from Han Chinese population. Frontiers in genetics 2022 9 13 947126. Li Mu-Jia, Shi Jia-Yu, Zhang Bi-He, Chen Qian-Ming, Shi Bing, Jia Zhong-L |
Genetic Variants Associated With Subjective Cognitive Decline in Patients With Migraine.
Frontiers in aging neuroscience 2022 14 860604. Yeh Po-Kuan, Liang Chih-Sung, Tsai Chia-Lin, Lin Yu-Kai, Lin Guan-Yu, Tsai Chia-Kuang, Tsai Ming-Chen, Liu Yi, Tai Yueh-Ming, Hung Kuo-Sheng, Yang Fu-C |
Identification of novel susceptibility genes for non-syndromic cleft lip with or without cleft palate using NGS-based multigene panel testing. Molecular genetics and genomics : MGG 2022 Jul . D?browska Justyna, Biedziak Barbara, Szponar-?urowska Anna, Budner Margareta, Jagodzi?ski Pawe? P, P?oski Rafa?, Mostowska Adrian |
Identification of Novel Risk Variants of Non-Syndromic Cleft Palate by Targeted Gene Panel Sequencing. Journal of clinical medicine 2023 3 12 (5): . D?browska Justyna, Biedziak Barbara, Bogdanowicz Agnieszka, Mostowska Adrian |
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- Page last updated:Apr 22, 2024
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