Human Genome Epidemiology Literature Finder
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Records 1 - 30 (of 36 Records) |
| Query Trace: Disease and MTHFD1[original query] |
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| A common variant in MTHFD1L is associated with neural tube defects and mRNA splicing efficiency. Human mutation 2009 Dec 30 (12): 1650-6. Parle-McDermott Anne, Pangilinan Faith, O'Brien Kirsty K, Mills James L, Magee Alan M, Troendle James, Sutton Marie, Scott John M, Kirke Peadar N, Molloy Anne M, Brody Lawrence |
| Xenobiotic and folate pathway gene polymorphisms and risk of childhood acute lymphoblastic leukaemia in Javanese children. Hematological oncology 2011 Sep 29 (3): 116-23. Chan Jason Yong-Sheng, Ugrasena Dewa G, Lum Danny Wai-Kiong, Lu Yi, Yeoh Allen Eng-J |
| Polymorphisms within the folate pathway predict folate concentrations but are not associated with disease activity in rheumatoid arthritis patients on methotrexate. Pharmacogenetics and genomics 2010 Jun 20 (6): 367-76. Stamp Lisa K, Chapman Peter T, O'Donnell John L, Zhang Mei, James Jill, Frampton Christopher, Barclay Murray L, Kennedy Martin A, Roberts Rebecca |
| Association analysis of CbetaS 844ins68 and MTHFD1 G1958A polymorphisms with Alzheimer's disease in Chinese. Journal of neural transmission (Vienna, Austria : 1996) 2010 Apr 117 (4): 499-503. Bi Xiu-Hua, Zhao Hua-Lu, Zhang Zhen-Xin, Liu Qian, Zhang Jun- |
| Germline genetic polymorphisms may influence chemotherapy response and disease outcome in osteosarcoma: a pilot study. Cancer 2012 Apr 118 (7): 1856-67. Windsor Rachael E, Strauss Sandra J, Kallis Constantinos, Wood Nicholas E, Whelan Jeremy |
| Polymorphic variants of genes involved in homocysteine metabolism in celiac disease. Molecular biology reports 2012 Mar 39 (3): 3123-30. Hozyasz Kamil K, Mostowska Adrianna, Szaflarska-Poplawska Anna, Lianeri Margarita, Jagodzinski Pawel |
| MTHFD1 G1958A, BHMT G742A, TC2 C776G and TC2 A67G polymorphisms and head and neck squamous cell carcinoma risk. Molecular biology reports 2012 Feb 39 (2): 887-93. da Silva Lidia Maria Rebolho Batista, Galbiatti Ana Lívia Silva, Ruiz Mariangela Torreglosa, Raposo Luiz Sérgio, Maniglia José Victor, Pavarino Erika Cristina, Goloni-Bertollo Eny Mar |
| Head and neck carconogenesis: impact of MTHFD1 G1958A polymorphism. Revista da Associação Médica Brasileira (1992) 0 57 (2): 194-9. Silva Lidia Maria Rebolho Batista da, Silva Jéssika Nunes Gomes da, Galbiatti Ana Lívia Silva, Succi Maysa, Ruiz Mariangela Torreglosa, Raposo Luiz Sérgio, Maniglia José Víctor, Pavarino-Bertelli Erika Cristina, Goloni-Bertollo Eny Mar |
| Polymorphic variants of folate and choline metabolism genes and the risk of endometriosis-associated infertility. European journal of obstetrics, gynecology, and reproductive biology 2011 Jul 157 (1): 67-72. Szczepa?ska Malgorzata, Mostowska Adrianna, Wirstlein Przemyslaw, Lianeri Margarita, Marianowski Piotr, Skrzypczak Jana, Jagodzi?ski Pawe? |
| Clinical pharmacogenetic model to predict response of MTX monotherapy in patients with established rheumatoid arthritis after DMARD failure. Pharmacogenomics 2012 Jul 13 (9): 9. Fransen J, Kooloos WM, Wessels JA, Huizinga TW, Guchelaar HJ, van Riel PL, Barrera P |
| Head and neck cancer: genetic polymorphisms and folate metabolism. Brazilian journal of otorhinolaryngology 2012 Feb 78 (1): 132-9. Galbiatti Ana Lívia Silva, Ruiz Mariangela Torreglosa, Maniglia José Victor, Raposo Luis Sérgio, Pavarino-Bertelli Erika Cristina, Goloni-Bertollo Eny Mar |
| Investigation of homocysteine-pathway-related variants in essential hypertension. International journal of hypertension 2012 2012 190923. Fowdar Javed Y, Lason Marta V, Szvetko Attila L, Lea Rodney A, Griffiths Lyn |
| Roles of genetic polymorphisms in the folate pathway in childhood acute lymphoblastic leukemia evaluated by Bayesian relevance and effect size analysis. PloS one 2013 8 (8): e69843. Lautner-Csorba Orsolya, Gézsi András, Erdélyi Dániel J, Hullám Gábor, Antal Péter, Semsei Ágnes F, Kutszegi Nóra, Kovács Gábor, Falus András, Szalai Csa |
| MTHFR rs1801133 C>T polymorphism is associated with an increased risk of tetralogy of Fallot. Biomedical reports 2014 Mar 2 (2): 172-176. Huang Jianbing, Mei Ju, Jiang Lianyong, Jiang Zhaolei, Liu Hao, Ding Fangb |
| Association between MTHFD1 polymorphisms and neural tube defect susceptibility. Journal of the neurological sciences 2015 Jan 348 (1-2): 188-94. Meng Jingjing, Han Lei, Zhuang |
| [G894T (NOS3) and G1958A (MTHFD1) gene polymorphisms and risk of ischemic heart disease in Yucatan, Mexico]. Clínica e investigación en arteriosclerosis : publicación oficial de la Sociedad Española de Arteriosclerosis 0 27 (2): 64-73. García-González Igrid, Solís-Cárdenas Alberto de Jesús, Flores-Ocampo Jorge A, Alejos-Mex Ricardo, Herrera-Sánchez Luis Fernando, González-Herrera Lizbeth Josefi |
| Association of genetic polymorphisms of de novo nucleotide biosynthesis with increased CHD susceptibility in the northern Chinese population. Clinical genetics 2016 Sep . Jiang Yu-Chao, Kuang Le-Le, Sun Shu-Na, Duan Wen-Yuan, Qiao Bin, Wang Hong-Y |
| Relationship Between Polymorphisms in Methotrexate Pathway Genes and Outcome of Methotrexate Treatment in a Cohort of 119 Patients with Juvenile Idiopathic Arthritis. The Journal of rheumatology 2017 Jun . Zajc Avramovi? Mojca, Dolžan Vita, Toplak Nataša, Accetto Meta, Lusa Lara, Av?in Tad |
| Evidence of gene-gene interactions between MTHFD1 and MTHFR in relation to anterior encephalocele susceptibility in Northeast India. Birth defects research 2017 Apr 109 (6): 432-444. Dutta Hemonta Kr, Borbora Debasish, Baruah Mauchumi, Narain Kanw |
| MTHFR and MTHFD1 gene polymorphisms are not associated with pseudoexfoliation syndrome in South Indian population. International ophthalmology 2017 Mar . Gopalakrishnan Prakadeeswari, Haripriya Aravind, Sundaresan Periasa |
| Identification and validation of mA RNA methylation regulators with clinical prognostic value in Papillary thyroid cancer. Cancer cell international 2020 20 203. Wang Xinyi, Fu Xiaorui, Zhang Junjia, Xiong Chengfeng, Zhang Shuyong, Lv Yunx |
| Polymorphism of genes involved in methotrexate pathway: Predictors of response to methotrexate therapy in Indian rheumatoid arthritis patients. International journal of rheumatic diseases 2021 Mar . Singh Ankita, Gangadharan Harikrishnan, Gupta Vikas, Patro Pradeepta S, Misra Ramnath, Aggarwal Ami |
| [Association of maternal MTHFD1 and MTHFD2 gene polymorphisms with congenital heart disease in offspring]. Zhongguo dang dai er ke za zhi = Chinese journal of contemporary pediatrics 2022 7 24 (7): 797-805. Chen Qian, Huang Peng, Song Xin-Li, Liu Yi-Ping, Sun Meng-Ting, Wang Ting-Ting, Zhang Sen-Mao, Qin Jia- |
| A Common Polymorphism in the MTHFD1 Gene Is a Modulator of Risk of Congenital Heart Disease. Journal of cardiovascular development and disease 2022 May 9 (6): . Karas Kuželi?ki Nataša, Šmid Alenka, Vidmar Golja Maša, Kek Tina, Geršak Borut, Mazi? Uroš, Mlinari?-Raš?an Irena, Geršak Kseni |
| Folate Related Pathway Gene Analysis Reveals a Novel Metabolic Variant Associated with Alzheimer's Disease with a Change in Metabolic Profile. Metabolites 2022 6 12 (6): . Miyan Jaleel, Buttercase Charlotte, Beswick Emma, Miyan Salma, Moshkdanian Ghazaleh, Naz Nai |
| Association of MTHFD1 gene polymorphisms and maternal smoking with risk of congenital heart disease: a hospital-based case-control study. BMC pregnancy and childbirth 2022 Jan 22 (1): 88. Song Xinli, Li Qiongxuan, Diao Jingyi, Li Jinqi, Li Yihuan, Zhang Senmao, Zhao Lijuan, Chen Letao, Wei Jianhui, Shu Jing, Liu Yiping, Sun Mengting, Huang Peng, Wang Tingting, Qin Jia |
| Association of Maternal Folate Intake and Offspring MTHFD1 and MTHFD2 Genes with Congenital Heart Disease. Nutrients 2023 8 15 (16): . Hanjun Liu, Jun Ou, Yige Chen, Qian Chen, Manjun Luo, Tingting Wang, Jiabi Q |
| Multiple genetic variants involved in both autoimmunity and autoinflammation detected in Chinese patients with sporadic Meniere's disease: a preliminary study. Frontiers in neurology 2023 6 14 1159658. Jing Zou, Guoping Zhang, Hongbin Li, Zikai Zhao, Qing Zhang, Ilmari Pyykkö, Antti Mäkit |
| Doubly bi-allelic variants of MTHFR and MTHFD1 in a Chinese patient with hyperhomocysteinemia and failure of folic acid therapy. Frontiers in genetics 2023 1 13 964990. Liu Yu-Xing, Ding Man-Hua, Sheng Yue, Sun Meng-Fei, Liu Lv, Zhang Ya |
| Congenital Heart Disease and Genetic Changes in Folate/Methionine Cycles. Genes 2024 7 15 (7): . Nataša Karas Kuželi?ki, Bojan Dolj |
- Page last reviewed:Feb 1, 2024
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