Human Genome Epidemiology Literature Finder
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Records 1 - 24 (of 24 Records) |
| Query Trace: Disease and FGF23[original query] |
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| A study of the association between serum bone-specific alkaline phosphatase and serum phosphorus concentration or dietary phosphorus intake. Journal of nutritional science and vitaminology 2012 58 (6): 442-5. Haraikawa Mayu, Tanabe Rieko, Sogabe Natsuko, Sugimoto Aoi, Kawamura Yuka, Michigami Toshimi, Hosoi Takayuki, Goseki-Sone Mas |
| Fibroblast growth factor 23 (FGF23) gene polymorphism in children with Kawasaki syndrome (KS) and susceptibility to cardiac abnormalities. Italian journal of pediatrics 2013 39 (1): 69. Falcini Fernanda, Rigante Donato, Masi Laura, Covino Marcello, Franceschelli Francesco, Leoncini Gigliola, Tarantino Giusyda, Matucci Cerinic Marco, Brandi Maria Lui |
| [Association of FGF23 gene polymorphism with Kawasaki disease and coronary artery lesions]. Zhongguo dang dai er ke za zhi = Chinese journal of contemporary pediatrics 2015 Oct 17 (10): 1107-11. Geng Ya-Nan, Zhang Hong-Y |
| Combined sequence and sequence-structure based methods for analyzing FGF23, CYP24A1 and VDR genes. Meta gene 2016 Sep 9 26-36. Nagamani Selvaraman, Singh Kh Dhanachandra, Muthusamy Karthikey |
| Ecto-5' -Nucleotidase CD73 (NT5E), vitamin D receptor and FGF23 gene polymorphisms may play a role in the development of calcific uremic arteriolopathy in dialysis patients - Data from the German Calciphylaxis Registry. PloS one 2017 12 (2): e0172407. Rothe Hansjörg, Brandenburg Vincent, Haun Margot, Kollerits Barbara, Kronenberg Florian, Ketteler Markus, Wanner Christo |
| The Roles of Genetic Factors in Kawasaki Disease: A Systematic Review and Meta-analysis of Genetic Association Studies. Pediatric cardiology 2017 Nov . Xie Xiaochuan, Shi Xiaohan, Liu Meil |
| Assessing known chronic kidney disease associated genetic variants in Saudi Arabian populations. BMC nephrology 2018 Apr 19 (1): 88. Cyrus Cyril, Al-Mueilo Samir, Vatte Chittibabu, Chathoth Shahanas, Li Yun R, Qutub Hatem, Al Ali Rudaynah, Al-Muhanna Fahad, Lanktree Matthew B, Alkharsah Khaled Riyad, Al-Rubaish Abdullah, Kim-Mozeleski Brian, Keating Brendan, Al Ali Ame |
| Outcome of adult patients with X-linked hypophosphatemia caused by PHEX gene mutations. Journal of inherited metabolic disease 2018 2 41 (5): 865-876. Chesher Douglas, Oddy Michael, Darbar Ulpee, Sayal Parag, Casey Adrian, Ryan Aidan, Sechi Annalisa, Simister Charlotte, Waters Aoife, Wedatilake Yehani, Lachmann Robin H, Murphy Elai |
| Association of klotho gene polymorphism and the regulation of calcium-phosphate metabolism disorders in patients with end-stage renal disease. Nephrology (Carlton, Vic.) 2018 Dec . Zeng Qing-Ya, Xia Zhi-Yin, Tong Yan-Shan, Sun Liang, Mou Hong-Bin, Chen Rui, Bi Guang-Yu, Liu Chang-H |
| [Mutation analysis of four pedigrees affected with hypophosphatemic rickets through targeted next-generation sequencing]. Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics 2018 10 35 (5): 638-643. Bai Ying, Liu Ning, Shao Mingwei, Qin Guijun, Gao Xu, Kong Xiangdo |
| Exonic variants of genes related to the vitamin D signaling pathway in the families of familial multiple sclerosis using whole-exome next generation sequencing. Brain and behavior 2019 3 9 (4): e01272. Pytel Vanesa, Matías-Guiu Jordi A, Torre-Fuentes Laura, Montero-Escribano Paloma, Maietta Paolo, Botet Javier, Álvarez Sara, Gómez-Pinedo Ulises, Matías-Guiu Jor |
| Fibroblast Growth Factor 23 Genotype and Cardiovascular Disease in Patients Undergoing Hemodialysis. American journal of nephrology 2019 Jan 49 (2): 125-132. Schwantes-An Tae-Hwi, Liu Sai, Stedman Margaret, Decker Brian S, Wetherill Leah, Edenberg Howard J, Vatta Matteo, Foroud Tatiana M, Chertow Glenn M, Moe Sharon |
| Interactions between FGF23 and Genotype in Autosomal Dominant Polycystic Kidney Disease. Kidney360 2020 12 1 (7): 648-656. Grau Laura, Gitomer Berenice, McNair Bryan, Wolf Myles, Harris Peter, Brosnahan Godela, Torres Vicente, Steinman Theodore, Yu Alan, Chapman Arlene, Chonchol Michel, Nowak Kristen |
| Investigating the causal effect of fibroblast growth factor 23 on osteoporosis and cardiometabolic disorders: A Mendelian randomization study. Bone 2020 Nov 115777. Yokomoto-Umakoshi Maki, Umakoshi Hironobu, Miyazawa Takashi, Ogata Masatoshi, Sakamoto Ryuichi, Ogawa Yoshihi |
| Genetically Predicted Fibroblast Growth Factor 23 and Major Cardiovascular Diseases, Their Risk Factors, Kidney Function, and Longevity: A Two-Sample Mendelian Randomization Study. Frontiers in genetics 2021 12 699455. Liang Ying, Luo Shan, Schooling C Mary, Au Yeung Shiu L |
| Prognostic Value of Fibroblast Growth Factor 23 in Autosomal Dominant Polycystic Kidney Disease. Kidney international reports 2021 4 6 (4): 953-961. El Ters Mireille, Lu Pengcheng, Mahnken Jonathan D, Stubbs Jason R, Zhang Shiqin, Wallace Darren P, Grantham Jared J, Chapman Arlene B, Torres Vicente E, Harris Peter C, Bae Kyongtae Ty, Landsittel Douglas P, Rahbari-Oskoui Frederic F, Mrug Michal, Bennett William M, Yu Alan S |
| Age and genotype dependent erythropoietin protection in COVID-19. World journal of stem cells 2021 11 13 (10): 1513-1529. Papadopoulos Konstantinos I, Sutheesophon Warachaya, Manipalviratn Somjate, Aw Tar-Cho |
GWAS meta-analysis followed by Mendelian randomization revealed potential control mechanisms for circulating ?-Klotho levels.
Human molecular genetics 2021 9 31 (5): 792-802. Gergei Ingrid, Zheng Jie, Andlauer Till F M, Brandenburg Vincent, Mirza-Schreiber Nazanin, Müller-Myhsok Bertram, Krämer Bernhard K, Richard Daniel, Falk Louise, Movérare-Skrtic Sofia, Ohlsson Claes, Davey Smith George, März Winfried, Voelkl Jakob, Tobias Jonathan |
| Molecular Landscape and Prognostic Biomarker Analysis of Advanced Pancreatic Cancer and Predictors of Treatment Efficacy of AG Chemotherapy. Frontiers in oncology 2022 12 844527. Du Juan, Qiu Xin, Lu Changchang, Zhu Yahui, Kong Weiwei, Xu Mian, Zhang Xin, Tang Min, Chen Jun, Li Qi, Li Aimei, He Jian, Gu Qing, Wang Lei, Qiu Yudong, Liu Baor |
| Assessment of Surrogate Markers for Cardiovascular Disease in Familial Mediterranean Fever-Related Amyloidosis Patients Homozygous for M694V Mutation in MEFV Gene. Life (Basel, Switzerland) 2022 5 12 (5): . Sahin Sezgin, Romano Micol, Guzel Ferhat, Piskin David, Poddighe Dimitri, Sezer Siren, Kasapcopur Ozgur, Appleton C Thomas, Yilmaz Ilker, Demirkaya Erk |
| Genetic Variants Associated With Mineral Metabolism Traits in Chronic Kidney Disease. The Journal of clinical endocrinology and metabolism 2022 May . Laster Marciana L, Rowan Bryce, Chen Hua-Chang, Schwantes-An Tae-Hwi, Sheng Xin, Friedman Peter A, Ikizler T Alp, Sinshiemer Janet S, Ix Joachim H, Susztak Katalin, de Boer Ian H, Kestenbaum Bryan, Hung Adriana, Moe Sharon M, Perwad Farzana, Robinson-Cohen Cassian |
| MIF rs755622 and IL6 rs1800795 Are Implied in Genetic Susceptibility to End-Stage Renal Disease (ESRD). Genes 2022 2 13 (2): . Guarneri Marco, Scola Letizia, Giarratana Rosa Maria, Bova Manuela, Carollo Caterina, Vaccarino Loredana, Calandra Leonardo, Lio Domenico, Balistreri Carmela Rita, Cottone Santi |
| Advanced hepatocellular carcinoma treated by transcatheter arterial chemoembolization with drug-eluting beads plus lenvatinib versus sorafenib, a propensity score matching retrospective study. American journal of cancer research 2022 1 11 (12): 6107-6118. Xue Miao, Wu Yanqin, Zhu Bowen, Zou Xinhua, Fan Wenzhe, Li Jiapi |
| Serum Fibroblast Growth Factor 23 and FGF23 Gene Variants in Patients with Type 2 Diabetes and Essential Hypertension. Association with Chronic Kidney Disease. Archives of medical research 2023 3 . Mendoza-Carrera Francisco, Farías-Basulto Alfonso, Gómez-García Erika F, Cortés-Sanabria Laura, Cueto-Manzano Alfonso Martin, Rizo-de la Torre Lourdes Del Carmen, Leal-Cortés Caridad |
- Page last reviewed:Feb 1, 2024
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