Human Genome Epidemiology Literature Finder
Records 1 - 21 (of 21 Records) |
Query Trace: SERPINF1[original query] |
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Genetic variants in pigment epithelium-derived factor influence response of polypoidal choroidal vasculopathy to photodynamic therapy. Ophthalmology 2011 Jul 118 (7): 1408-15. Nakata Isao, Yamashiro Kenji, Yamada Ryo, Gotoh Norimoto, Nakanishi Hideo, Hayashi Hisako, Tsujikawa Akitaka, Otani Atsushi, Ooto Sotaro, Tamura Hiroshi, Saito Masaaki, Saito Kuniharu, Iida Tomohiro, Oishi Akio, Kurimoto Yasuo, Matsuda Fumihiko, Yoshimura Nagahi |
Association study of candidate gene polymorphisms and obesity in a young Mexican-American population from South Texas. Archives of medical research 2011 Aug 42 (6): 523-31. Duran-Gonzalez Jorge, Ortiz Ixiu, Gonzales Enrique, Ruiz Nicole, Ortiz Manti, Gonzalez Arthur, Sanchez Edna K, Curet Eugenia, Fisher-Hoch Susan, Rentfro Anne, Qu Huiqi, Nair Saraswat |
Common genetic variation in the SERPINF1 locus determines overall adiposity, obesity-related insulin resistance, and circulating leptin levels. PloS one 2012 7 (3): 3. Böhm A, Ordelheide AM, Machann J, Heni M, Ketterer C, Machicao F, Schick F, Stefan N, Fritsche A, Häring HU, Staiger H |
Polymorphisms in vascular endothelial growth factor receptor 2 are associated with better response rates to ranibizumab treatment in age-related macular degeneration. Ophthalmology 2014 Apr 121 (4): 905-10. Hermann Manuel M, van Asten Freekje, Muether Philipp S, Smailhodzic Dzenita, Lichtner Peter, Hoyng Carel B, Kirchhof Bernd, Grefkes Christian, den Hollander Anneke I, Fauser Sasc |
Normal bone density and fat mass in heterozygous SERPINF1 mutation carriers. The Journal of clinical endocrinology and metabolism 2014 Nov 99 (11): E2446-50. Al-Jallad Hadil, Palomo Telma, Moffatt Pierre, Roughley Peter, Glorieux Francis H, Rauch Fra |
Association between CFH, CFB, ARMS2, SERPINF1, VEGFR1 and VEGF polymorphisms and anatomical and functional response to ranibizumab treatment in neovascular age-related macular degeneration. Acta ophthalmologica 2017 Sep . Cobos Estefania, Recalde Sergio, Anter Jaouad, Hernandez-Sanchez Maria, Barreales Carla, Olavarrieta Leticia, Valverde Alicia, Suarez-Figueroa Marta, Cruz Fernando, Abraldes Maximino, Pérez-Pérez Julian, Fernández-Robredo Patricia, Arias Luis, García-Layana Alfre |
Extremely low level of serum pigment epithelium-derived factor is a special biomarker of Chinese osteogenesis imperfecta patients with SERPINF1 mutations. Clinica chimica acta; international journal of clinical chemistry 2018 Mar 478 216-221. Wang Jian-Yi, Li Lu-Jiao, Zhang Qian, Liu Yi, Lv Fang, Xu Xiao-Jie, Song Yu-Wen, Wang Ou, Jiang Yan, Xia Wei-Bo, Xing Xiao-Ping, Li M |
Analysis of Polymorphisms in Genes Differentially Expressed in the Enamel of Mice with Different Genetic Susceptibilities to Dental Fluorosis. Caries research 2018 8 53 (2): 228-233. Charone Senda, Küchler Erika Calvano, Leite Aline de Lima, Silva Fernandes Mileni, Taioqui Pelá Vinicius, Martini Tatiana, Brondino Bárbara Margarido, Magalhães Ana Carolina, Dionisio Thiago J, F Santos Carlos, Buzalaf Marília Afonso Rabe |
Genotype-phenotype correlation among Malaysian patients with osteogenesis imperfecta. Clinica chimica acta; international journal of clinical chemistry 2018 5 484 141-147. Mohd Nawawi Nadiah, Selveindran Nalini M, Rasat Rahmah, Chow Yock Ping, Abdul Latiff Zarina, Syed Zakaria Syed Zulkifli, Jamal Rahman, Abdul Murad Nor Azian, Abd Aziz Bilkis Ba |
Diagnostic strategies and genotype-phenotype correlation in a large Indian cohort of osteogenesis imperfecta. Bone 2018 3 110 368-377. Mrosk Julia, Bhavani Gandham SriLakshmi, Shah Hitesh, Hecht Jochen, Krüger Ulrike, Shukla Anju, Kornak Uwe, Girisha Katta Moh |
Genotype and malocclusion in patients with osteogenesis imperfecta. Orthodontics & craniofacial research 2018 2 21 (2): 71-77. Jabbour Z, Al-Khateeb A, Eimar H, Retrouvey J M, Rizkallah J, Glorieux F H, Rauch F, Tamimi |
Genetic Regulation of Pigment Epithelium-Derived Factor (PEDF): An Exome-Chip Association Analysis in Chinese Subjects With Type 2 Diabetes. Diabetes 2018 Oct . Cheung Chloe Y Y, Lee Chi-Ho, Tang Clara S, Xu Aimin, Au Ka-Wing, Fong Carol H Y, Ng Kelvin K K, Kwok Kelvin H M, Chow Wing-Sun, Woo Yu-Cho, Yuen Michele M A, Hai JoJo, Tan Kathryn C B, Lam Tai-Hing, Tse Hung-Fat, Sham Pak-Chung, Lam Karen S |
Osteogenesis imperfecta in Brazilian patients. Genetics and molecular biology 2019 8 42 (2): 344-350. Trancozo Maira, Moraes Marcos V D, Silva Dalila A, Soares Jéssica A M, Barbirato Clara, Almeida Márcio G, Santos Lígia R, Rebouças Maria R G O, Akel Akel N, Sipolatti Valentim, Nunes Vanda R R, Errera Flavia I V, Aguena Meire, Passos-Bueno Maria R, Paula Flavia |
Co-occurrence of heterozygous mutations in COL1A1 and SERPINF1 in a high-risk pregnancy complicated by osteogenesis imperfecta. Journal of genetics 2019 6 98 (2): . Ji Yunpeng, Ikram Aqsa, Ma Zhongren, Peppelenbosch Maikel P, Pan Qiuw |
Insufficient evidence for a role of SERPINF1 in otosclerosis. Molecular genetics and genomics : MGG 2019 4 294 (4): 1001-1006. Valgaeren Hanne, Sommen Manou, Beyens Matthias, Vandeweyer Geert, Schrauwen Isabelle, Schepers Anne, Schatteman Isabelle, Topsakal Vedat, Dhooge Ingeborg, Kunst Henricus, Zanetti Diego, Huber Alexander M, Hoischen Alexander, Fransen Erik, Van Camp G |
Genotypic and Phenotypic Analysis in Chinese Cohort With Autosomal Recessive Osteogenesis Imperfecta. Frontiers in genetics 2020 10 11 984. Li Shan, Cao Yixuan, Wang Han, Li Lulu, Ren Xiuzhi, Mi Huan, Wang Yanzhou, Guan Yun, Zhao Feiyue, Mao Bin, Yang Tao, You Yi, Guan Xin, Yang Yujiao, Zhang Xue, Zhao Xiu |
Genotype-Phenotype Relationship and Follow-up Analysis of a Chinese Cohort With Osteogenesis Imperfecta. Endocrine practice : official journal of the American College of Endocrinology and the American Association of Clinical Endocrinologists 2022 May . Wei Shuoshuo, Yao Yangyang, Shu Meng, Gao Ling, Zhao Jiajun, Li Tianyou, Wang Yanzhou, Xu Ch |
Genetic Factors Associated with Suicidal Behaviors and Alcohol Use Disorders in an American Indian Population. Research square 2023 7 . David Gilder, Rebecca Bernert, Katherine Karriker-Jaffe, Cindy Ehlers, Qian Pe |
Genotype-phenotype relationship and comparison between eastern and western patients with osteogenesis imperfecta. Journal of endocrinological investigation 2023 6 . X Lin, J Hu, B Zhou, Q Zhang, Y Jiang, O Wang, W Xia, X Xing, M |
Genetic variants and altered expression of SERPINF1 confer disease susceptibility in patients with otosclerosis. Journal of human genetics 2023 6 . Neha Singh, Kirtal Hansdah, Amal Bouzid, Chinmay Sundar Ray, Ashim Desai, Khirod Chandra Panda, Jyotish Chandra Choudhury, Adel Tekari, Saber Masmoudi, Puppala Venkat Ramchand |
Genetic factors associated with suicidal behaviors and alcohol use disorders in an American Indian population. Molecular psychiatry 2024 1 . Qian Peng, David A Gilder, Rebecca A Bernert, Katherine J Karriker-Jaffe, Cindy L Ehle |
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- Page last updated:Apr 22, 2024
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