Human Genome Epidemiology Literature Finder
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Records 1 - 27 (of 27 Records) |
| Query Trace: Disease and CGA[original query] |
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| A prospective study of paraoxonase gene Q/R192 polymorphism and severity, progression and regression of coronary atherosclerosis, plasma lipid levels, clinical events and response to fluvastatin. Atherosclerosis 2001 Feb 154 (3): 633-40. Turban S, Fuentes F, Ferlic L, Brugada R, Gotto A M, Ballantyne C M, Marian A |
| Relationship between a novel polymorphism of lipoprotein lipase gene and coronary heart disease. Chinese medical journal 2002 May 115 (5): 677-80. Su Zhiguang, Zhang Sizhong, Hou Yiping, Zhang Li, Liao Linchuan, Xiao Cuiyi |
| Plasma fibrinogen concentration predicts the risk of myocardial infarction differently in various parts of Europe: effects of beta-fibrinogen genotype and environmental factors. The HIFMECH Study. Thrombosis and haemostasis 2004 Dec 92 (6): 1240-9. Mannila Maria Nastase, Silveira Angela, Hawe Emma, Eriksson Per, Aillaud Marie Françoise, Juhan-Vague Irene, Yudkin John, Margaglione Maurizio, di Minno Giovanni, Mussoni Luciana, Tremoli Elena, Humphries Steve, Hamsten Anders, |
| Parathyroid hormone gene polymorphism and sporadic idiopathic hypoparathyroidism. The Journal of clinical endocrinology and metabolism 2004 Oct 89 (10): 4840-5. Goswami Ravinder, Mohapatra Trilochan, Gupta Nandita, Rani Rajni, Tomar Neeraj, Dikshit Anupam, Sharma Ram Kum |
| SNP 668C (-44) alters a NF-kappaB1 putative binding site in non-coding strand of human beta-defensin 1 (DEFB1) and is associated with lepromatous leprosy. Infection, genetics and evolution : journal of molecular epidemiology and evolutionary genetics in infectious diseases 2009 Jul 9 (4): 617-25. Prado-Montes de Oca Ernesto, Velarde-Félix Jesús Salvador, Ríos-Tostado Juan José, Picos-Cárdenas Verónica Judith, Figuera Luis Eduar |
| The APOE polymorphism in Alzheimer's disease patients with neuropsychiatric symptoms and syndromes. International journal of geriatric psychiatry 2011 Oct 26 (10): 1062-70. D'Onofrio Grazia, Panza Francesco, Seripa Davide, Sancarlo Daniele, Paris Francesco, Cascavilla Leandro, Urbano Maria, Gravina Carolina, Fontana Andrea, Solfrizzi Vincenzo, Pellegrini Fabio, Pilotto Alber |
| Study on the relationship between TSHR gene and thyroid diseases. Cell biochemistry and biophysics 2011 Nov 61 (2): 377-82. Shao Li, Jiang Hua, Liang Jun, Niu Xianping, Teng Lili, Zhang H |
| Common polymorphisms in the P-selectin gene in women with recurrent spontaneous abortions. Gene 2011 Dec . Dendana M, Hizem S, Magddoud K, Messaoudi S, Zammiti W, Nouira M, Almawi WY, Mahjoub T |
| Two-stage association study in Chinese Han identifies two independent associations in CCR1/CCR3 locus as candidate for Behçet's disease susceptibility. Human genetics 2012 Jul . Hou S, Xiao X, Li F, Jiang Z, Kijlstra A, Yang P |
| Osteoprotegerin CGA haplotype protection against cerebrovascular complications in anti-CCP negative patients with rheumatoid arthritis. PloS one 2014 9 (9): e106823. Genre Fernanda, López-Mejías Raquel, García-Bermúdez Mercedes, Castañeda Santos, González-Juanatey Carlos, Llorca Javier, Corrales Alfonso, Ubilla Begoña, Miranda-Filloy José A, Pina Trinitario, Gómez-Vaquero Carmen, Rodríguez-Rodríguez Luis, Fernández-Gutiérrez Benjamín, Balsa Alejandro, Pascual-Salcedo Dora, López-Longo Francisco J, Carreira Patricia, Blanco Ricardo, González-Álvaro Isidoro, Martín Javier, González-Gay Miguel |
| The (G>A) rs11573191 polymorphism of PLA2G5 gene is associated with premature coronary artery disease in the Mexican Mestizo population: the genetics of atherosclerotic disease Mexican study. BioMed research international 2014 2014 931361. Vargas-Alarcón Gilberto, Posadas-Romero Carlos, Villarreal-Molina Teresa, Alvarez-León Edith, Angeles-Martinez Javier, Soto María Elena, Monroy-Muñoz Irma, Juárez Juan Gabriel, Sánchez-Ramírez Carlos Jerges, Ramirez-Bello Julian, Ramírez-Fuentes Silvestre, Fragoso José Manuel, Rodríguez-Pérez José Manu |
| Clinical utility of chromogranin A in SDHx-related paragangliomas. European journal of clinical investigation 2014 Apr 44 (4): 365-71. Zuber Samuel, Wesley Robert, Prodanov Tamara, Eisenhofer Graeme, Pacak Karel, Kantorovich Vita |
| A Subset of Cerebrospinal Fluid Proteins from a Multi-Analyte Panel Associated with Brain Atrophy, Disease Classification and Prediction in Alzheimer's Disease. PloS one 2015 10 (8): e0134368. Khan Wasim, Aguilar Carlos, Kiddle Steven J, Doyle Orla, Thambisetty Madhav, Muehlboeck Sebastian, Sattlecker Martina, Newhouse Stephen, Lovestone Simon, Dobson Richard, Giampietro Vincent, Westman Eric, Simmons Andrew, |
| Vascular Endothelial Growth Factor Receptor-2 Polymorphisms Have Protective Effect against the Development of Tendinopathy in Volleyball Athletes. PloS one 2016 11 (12): e0167717. Salles José Inácio, Duarte Maria Eugenia Leite, Guimarães João Matheus, Lopes Lucas Rafael, Vilarinho Cardoso Jessica, Aguiar Diego Pinheiro, Machado Neto João Olyntho, Machado Daniel Escorsim, Perini Jamila Alessand |
| Association of CD28 and CTLA4 haplotypes with susceptibility to primary Sjögren's syndrome in Mexican population. Journal of clinical laboratory analysis 2018 Jul e22620. López-Villalobos Erika Fabiola, Carrillo-Ballesteros Francisco Josué, Muñoz-Valle José Francisco, Palafox-Sánchez Claudia Azucena, Valle Yeminia, Orozco-Barocio Gerardo, Oregon-Romero Edi |
| Polymorphisms and haplotypes in the promoter of the TNF-? gene are associated with disease severity of severe fever with thrombocytopenia syndrome in Chinese Han population. PLoS neglected tropical diseases 2018 Jun 12 (6): e0006547. Xing Bo, Li Xiao-Kun, Zhang Shao-Fei, Lu Qing-Bin, Du Juan, Zhang Pan-He, Yang Zhen-Dong, Cui Ning, Guo Chen-Tao, Cao Wu-Chun, Zhang Xiao-Ai, Liu W |
| Analysis of miR-29 Serum Levels in Patients with Neuroendocrine Tumors-Results from an Exploratory Study. Journal of clinical medicine 2020 9 9 (9): . Özdirik Burcin, Stueven Anna K, Mohr Raphael, Geisler Lukas, Wree Alexander, Knorr Jana, Demir Münevver, Vucur Mihael, Loosen Sven H, Benz Fabian, Reiss Markus, Wiedenmann Bertram, Tacke Frank, Jann Henning, Hellberg Teresa, Roderburg Christo |
| Association of CYP19A1 and CYP1A2 genetic polymorphisms with type 2 diabetes mellitus risk in the Chinese Han population. Lipids in health and disease 2020 Aug 19 (1): 187. Yang Yafeng, Wang Pi |
| Polymorphisms of IRAK1 Gene on X Chromosome Is Associated with Hashimoto Thyroiditis in Korean Children. Endocrinology 2020 6 161 (8): . Shin Hye-Ri, Cho Won Kyoung, Baek In-Cheol, Lee Na Yeong, Lee Yoon Ji, Kim Seul Ki, Ahn Moon Bae, Suh Byung-Kyu, Kim Tai-G |
| Biases in arginine codon usage correlate with genetic disease risk. Genetics in medicine : official journal of the American College of Medical Genetics 2020 May . Schulze Katharina V, Hanchard Neil A, Wangler Michael |
| Novel genetic characteristics in low-grade fetal adenocarcinoma of the lung. Thoracic cancer 2021 8 12 (20): 2789-2795. Zhang Shuyang, Yin Huihui, Zhang Jing, Yang Lu, Yang Guangjian, Jia Jia, Jiao Yuchen, Ying Jianming, Wang Y |
| Clinicopathological and molecular characteristics of the alpha-fetoprotein-producing gastric cancer: emphasis on two major subtypes. APMIS : acta pathologica, microbiologica, et immunologica Scandinavica 2021 12 130 (3): 169-180. Lu Jun, Jin Mulan, Zhou Xiang, Chen Xin, Shao Yang, Jiang Xingr |
| Genetic Variants in METTL14 are Associated with the Risk of Acute Lymphoblastic Leukemia in Southern Chinese Children: A Five-Center Case-Control Study. Cancer management and research 2021 12 13 9189-9200. Luo Ailing, Yang Lihua, Li Ming, Cai Mansi, Huang Amin, Liu Xiaodan, Yang Xu, Yan Yaping, Wang Xueliang, Wu Xuedong, Huang Ke, Huang Libin, Liu Shanshan, Xu Ling, Liu Xiaopi |
| A novel pathogenic variant of ARMC5 in a patient with primary bilateral macronodular adrenal hyperplasia: a case report. BMC endocrine disorders 2022 8 22 (1): 211. Wang Wei, Wei Fe |
| Prevalence of Selected Single-Nucleotide Variants in Patients with Neuroendocrine Tumors-Potential Clinical Relevance. Journal of clinical medicine 2022 10 11 (19): . Kurzy?ska Anna, Pach Dorota, Skalniak Anna El?bieta, Stefa?ska Agnieszka, Opali?ska Marta, Przybylik-Mazurek Elwira, Hubalewska-Dydejczyk Alic |
| Investigation of the relationship between IL17A, IL17F and ILR1N polymorphisms and COVID-19 severity: The predictive role of IL17A rs2275913 polymorphism in the clinical course of COVID-19. International journal of immunogenetics 2023 4 . Cakmak Genc Gunes, Karakas Celik Sevim, Yilmaz Busra, Piskin Nihal, Altinsoy Bulent, Dursun Ahm |
| Association Study of CACNA1D, KCNJ11, KCNQ1, and CACNA1E Single-Nucleotide Polymorphisms with Type 2 Diabetes Mellitus. International journal of molecular sciences 2024 9 25 (17): . Juan Daniel Díaz-García, Margarita Leyva-Leyva, Fabiola Sánchez-Aguillón, Mercedes Piedad de León-Bautista, Abel Fuentes-Venegas, Alfredo Torres-Viloria, Erika Karina Tenorio-Aguirre, Sara Luz Morales-Lázaro, Angélica Olivo-Díaz, Ricardo González-Ramír |
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