Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 107 Records) |
Query Trace: FOXE1[original query] |
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Mutation analysis of the NKX2.5 gene in Iranian pediatric patients with congenital hypothyroidism. Journal of pediatric endocrinology & metabolism : JPEM 2017 Jul . Khatami Mehri, Heidari Mohammad Mehdi, Tabesh Fatemeh, Ordooei Mahtab, Salehifar Zohr |
Replication confirms the association of loci in FOXE1, PDE8B, CAPZB and PDE10A with thyroid traits: a Genetics of Diabetes Audit and Research Tayside study (GoDARTS). Pharmacogenetics and genomics 2017 Jul . Soto-Pedre Enrique, Siddiqui Moneeza K, Doney Alex S, Palmer Colin N A, Pearson Ewan R, Leese Graham |
Genome-wide association and expression quantitative trait loci studies identify multiple susceptibility loci for thyroid cancer.
Nature communications 2017 Jul 8 15966. Son Ho-Young, Hwangbo Yul, Yoo Seong-Keun, Im Sun-Wha, Yang San Duk, Kwak Soo-Jung, Park Min Seon, Kwak Soo Heon, Cho Sun Wook, Ryu Jun Sun, Kim Jeongseon, Jung Yuh-Seog, Kim Tae Hyun, Kim Su-Jin, Lee Kyu Eun, Park Do Joon, Cho Nam Han, Sung Joohon, Seo Jeong-Sun, Lee Eun Kyung, Park Young Joo, Kim Jong- |
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 |
Genome-Wide Association Studies of Autoimmune Thyroid Diseases, Thyroid Function, and Thyroid Cancer. Endocrinology and metabolism (Seoul, Korea) 2018 6 33 (2): 175-184. Hwangbo Yul, Park Young J |
Exploration of the association between FOXE1 gene polymorphism and differentiated thyroid cancer: a meta-analysis. BMC medical genetics 2018 May 19 (1): 83. Chen Yong-Hui, Zhang Ying-Qia |
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 |
Does the Polymorphism in the Length of the Polyalanine Tract of FOXE1 Gene Influence the Risk of Thyroid Dysgenesis Occurrence? Journal of thyroid research 2017 2017 2793205. Pimentel Clebson Pantoja, Cortinhas-Alves Erik Artur, de Oliveira Edivaldo Herculano Correa, Santana-da-Silva Luiz Carl |
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 |
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 |
A systematic review and meta-analysis on protective role of forkhead box E1 (FOXE1) polymorphisms in susceptibility to non-syndromic cleft lip/palate. International orthodontics 2019 Jul . Imani Mohammad Moslem, Safaei Mohsen, Lopez-Jornet Pia, Sadeghi Maso |
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 |
Network-Based Analysis Reveals Association of FOXE1 Gene Polymorphisms in Thyroid Cancer Patients; A Case-Control Study in Southeast of Iran. Asian Pacific journal of cancer prevention : APJCP 2020 9 21 (9): 2771-2776. Mehrazin Ahmad, Safarpour Hossein, Davoudi Seyedeh Tahmineh, Parsamanesh Negin, Saeedi Farhad, Miri-Moghaddam Ebrah |
Pancreatic ductal adenocarcinomas from Mexican patients present a distinct genomic mutational pattern. Molecular biology reports 2020 6 47 (7): 5175-5184. Sanchez Paulina, Espinosa Magali, Maldonado Vilma, Barquera Rodrigo, Belem-Gabiño Nayeli, Torres Javier, Cravioto Adrian, Melendez-Zajgla Jor |
Association analysis of GWAS hits and non-syndromic cleft lip with/without palate with cleft alveolar in Han population of western China. International journal of clinical and experimental pathology 2020 11 13 (10): 2576-2585. Duan Shijun, Shi Jiayu, Shi Bing, Jia Zhongl |
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 |
Analysis of Mutation Spectra of 28 Pathogenic Genes Associated With Congenital Hypothyroidism in the Chinese Han Population. Frontiers in endocrinology 2021 12 695426. Huang Miao, Lu Xiyan, Dong Guoqing, Li Jianxu, Chen Chengcong, Yu Qiuxia, Li Mingzhu, Su Yuey |
Further Evidence That Defects in Main Thyroid Dysgenesis-Related Genes Are an Uncommon Etiology for Primary Congenital Hypothyroidism in Mexican Patients: Report of Rare Variants in FOXE1, NKX2-5 and TSHR. Children (Basel, Switzerland) 2021 6 8 (6): . Alcántara-Ortigoza Miguel Angel, Sánchez-Verdiguel Iraís, Fernández-Hernández Liliana, Enríquez-Flores Sergio, González-Núñez Aidy, Hernández-Martínez Nancy Leticia, Sánchez Carmen, González-Del Angel Ariad |
Molecular and clinical characteristics of congenital hypothyroidism in a large cohort study based on comprehensive thyroid transcription factor mutation screening in Henan. Clinica chimica acta; international journal of clinical chemistry 2021 3 518 162-169. Li Liangshan, Jia Chenlu, Li Xiaole, Wang Fang, Wang Yangang, Chen Yanping, Liu Shiguo, Zhao Deh |
The Contribution of Genetic Variants to the Risk of Papillary Thyroid Carcinoma in the Kazakh Population: Study of Common Single Nucleotide Polymorphisms and Their Clinicopathological Correlations. Frontiers in endocrinology 2020 11 543500. Mussazhanova Zhanna, Rogounovitch Tatiana I, Saenko Vladimir A, Krykpayeva Ainur, Espenbetova Maira, Azizov Bauyrzhan, Kondo Hisayoshi, Matsuda Katsuya, Kalmatayeva Zhanna, Issayeva Raushan, Yeleubayeva Zhanar, Madiyeva Madina, Mukanova Aray, Sandybayev Marat, Bolsynbekova Saltanat, Kozykenova Zhanna, Yamashita Shunichi, Nakashima Masahi |
Genetic Variants Associated with Thyroid Cancer Risk: Comprehensive Research Synopsis, Meta-Analysis, and Cumulative Epidemiological Evidence. Journal of oncology 2021 12 2021 9967599. Ran Ran, Tu Gang, Li Hui, Wang Hao, Mou Exian, Liu Caiya |
Screening of 23 candidate genes by next-generation sequencing of patients with permanent congenital hypothyroidism: novel variants in TG, TSHR, DUOX2, FOXE1, and SLC26A7. Journal of endocrinological investigation 2021 Nov . Acar S, Gürsoy S, Arslan G, Nalbanto?lu Ö, Hazan F, Köprülü Ö, Özkaya B, Özkan |
FOXE1 polymorphisms and chronic exposure to nitrates in drinking water cause metabolic dysfunction, thyroid abnormalities, and genotoxic damage in women. Genetics and molecular biology 2021 44 (3): e20210020. Gandarilla-Esparza Diana Dennys, Calleros-Rincón Esperanza Yasmin, Macias Hortensia Moreno, González-Delgado María Fernanda, Vargas Gonzalo García, Sustaita Jaime Duarte, González-Zamora Alberto, Ríos-Sánchez Efraín, Pérez-Morales Rebe |
Genetic predisposition of SNPs in miRNA-149 (rs2292832) and FOXE1 (rs3758249) in thyroid Cancer. Molecular biology reports 2021 10 48 (12): 7801-7809. Khan Rashida, Shaheen Humaira, Mansoor Qaisar, Abbasi Samina Asghar, Fatima Shazia, Ammar Ayesha, Baig Ruqia Mehmo |
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 |
Mutational screening of the TPO and DUOX2 genes in Argentinian children with congenital hypothyroidism due to thyroid dyshormonogenesis. Endocrine 2022 5 77 (1): 86-101. Molina Maricel F, Papendieck Patricia, Sobrero Gabriela, Balbi Viviana A, Belforte Fiorella S, Martínez Elena Bueno, Adrover Ezequiela, Olcese María C, Chiesa Ana, Miras Mirta B, González Verónica G, Pio Mauricio Gomes, González-Sarmiento Rogelio, Targovnik Héctor M, Rivolta Carina |
Mutation of Hashimoto's Thyroiditis and Papillary Thyroid Carcinoma Related Genes and the Screening of Candidate Genes. Frontiers in oncology 2022 1 11 813802. Zhang Lizhuo, Zhou Lingyan, Feng Qingqing, Li Qinglin, Ge Mingh |
Genetic markers for non-syndromic orofacial clefts in populations of European ancestry: a meta-analysis. Scientific reports 2022 1 12 (1): 1214. Slavec Lara, Karas Kuželi?ki Nataša, Locatelli Igor, Geršak Kseni |
The length of FOXE1 polyalanine tract in congenital hypothyroidism: Evidence for a pathogenic role from familial, molecular and cohort studies. Frontiers in endocrinology 2023 4 14 1127312. Grassi Elisa Stellaria, Rurale Giuditta, de Filippis Tiziana, Gentilini Davide, Carbone Erika, Coscia Francesca, Uraghi Sarah, Bullock Martyn, Clifton-Bligh Roderick J, Gupta Abhinav K, Persani Lu |
DNA Copy Number Alterations and Copy Neutral Loss of Heterozygosity in Adult Ph-Negative Acute B-Lymphoblastic Leukemia: Focus on the Genes Involved. International journal of molecular sciences 2023 12 24 (24): . Natalya Risinskaya, Maria Gladysheva, Abdulpatakh Abdulpatakhov, Yulia Chabaeva, Valeriya Surimova, Olga Aleshina, Anna Yushkova, Olga Dubova, Nikolay Kapranov, Irina Galtseva, Sergey Kulikov, Tatiana Obukhova, Andrey Sudarikov, Elena Parovichniko |
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- Page last updated:Jun 03, 2024
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