Human Genome Epidemiology Literature Finder
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Records 1 - 30 (of 279 Records) |
| Query Trace: Syndrome and MTHFR[original query] |
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| MEDTEC Students against Coronavirus: Investigating the Role of Hemostatic Genes in the Predisposition to COVID-19 Severity. Journal of personalized medicine 2021 Nov 11 (11): . Cappadona Claudio, Paraboschi Elvezia Maria, Ziliotto Nicole, Bottaro Sandro, Rimoldi Valeria, Gerussi Alessio, Azimonti Andrea, Brenna Daniele, Brunati Andrea, Cameroni Charlotte, Campanaro Giovanni, Carloni Francesca, Cavadini Giacomo, Ciravegna Martina, Composto Antonio, Converso Giuseppe, Corbella Pierluigi, D'Eugenio Davide, Dal Rì Giovanna, Di Giorgio Sofia Maria, Grondelli Maria Chiara, Guerrera Lorenza, Laffoucriere Georges, Lando Beatrice, Lopedote Leandro, Maizza Benedetta, Marconi Elettra, Mariola Carlotta, Matronola Guia Margherita, Menga Luca Maria, Montorsi Giulia, Papatolo Antonio, Patti Riccardo, Profeta Lorenzo, Rebasti Vera, Smidili Alice, Tarchi Sofia Maria, Tartaglia Francesco Carlo, Tettamanzi Gaia, Tinelli Elena, Stuani Riccardo, Bolchini Cristiana, Pattini Linda, Invernizzi Pietro, Degenhardt Frauke, Franke Andre, Duga Stefano, Asselta Rosan |
| Investigation on factors associated with ovarian cancer: an umbrella review of systematic review and meta-analyses. Journal of ovarian research 2021 11 14 (1): 153. Tanha Kiarash, Mottaghi Azadeh, Nojomi Marzieh, Moradi Marzieh, Rajabzadeh Rezvan, Lotfi Samaneh, Janani Lei |
| Identification of genetic variants related to metabolic syndrome by next-generation sequencing. Diabetology & metabolic syndrome 2022 Aug 14 (1): 119. Lee Sanghoo, Kim Seol-A, Hong Jeonghoon, Kim Yejin, Hong Gayeon, Baik SaeYun, Choi Kyeonghwan, Lee Mi-Kyeong, Lee Kyoung-Ry |
| Comprehensive Thrombophilia Evaluation in Cerebral Venous Thrombosis: A Single Center Cross Sectional Study. Indian journal of hematology & blood transfusion : an official journal of Indian Society of Hematology and Blood Transfusion 2022 6 38 (3): 522-528. Kumar Rajiv, Vinny Pulikottil Wilson, Nair Vishnu G, Jakku Raje |
| The role of methylenetetrahydrofolate reductase C677T gene polymorphism as a risk factor for coronary artery disease: a cross-sectional study in the Sidoarjo Regional General Hospital. The Pan African medical journal 2022 41 212. Sugijo Hairudi, Sargowo Djanggan, Widjajanto Edi, Romdoni Rochm |
| Genetic Polymorphisms in a Familial Hypercholesterolemia Population from North-Eastern Europe. Journal of personalized medicine 2022 3 12 (3): . Ma?taleru Alexandra, Cojocariu Sabina Alexandra, Oancea Andra, Constantin Maria Magdalena Leon, Roca Mihai, Zota Ioana M?d?lina, Abdulan Irina, Rusu Cristina, Popescu Roxana, Antoci Lucian Mihai, Ciobanu Cristian Gabriel, Costache Alexandru Dan, Cojocaru Elena, Mitu Flor |
| Association of MTHFR 677C?>?T gene polymorphism with neonatal defects: a meta-analysis of 81444 subjects. Journal of obstetrics and gynaecology : the journal of the Institute of Obstetrics and Gynaecology 2022 3 42 (6): 1811-1822. Li Juan, Feng Danqin, He Shiwei, Yang Hua, Su Zhiying, Ye Huimi |
| Role of folate metabolizing genes and homocysteine in mothers of Down syndrome children. Tzu chi medical journal 2022 12 34 (4): 456-461. Kaur Amandeep, Kaur Anup |
| Maternal Inherited Thrombophilia in Monochorionic Twin Pregnancy with Twin-Twin Transfusion Syndrome. Journal of clinical medicine 2022 12 11 (23): . Giannubilo Stefano R, Fiorelli Alessia, Marzioni Daniela, Tossetta Giovanni, Capogrosso Giulia, Ciavattini Andr |
| Folic acid inhibits 5-methyltetrahydrofolate transport across the blood-cerebrospinal fluid barrier: Clinical biochemical data from two cases. JIMD reports 2022 11 63 (6): 529-535. Akiyama Tomoyuki, Kuki Ichiro, Kim Kiyohiro, Yamamoto Naohiro, Yamada Yumi, Igarashi Kazuya, Ishihara Tomohiko, Hatano Yuya, Kobayashi Katsuhi |
| Genetic Determinants of Cardiovascular Disease: The Endothelial Nitric Oxide Synthase 3 (eNOS3), Krüppel-Like Factor-14 (KLF-14), Methylenetetrahydrofolate Reductase (MTHFR), MiRNAs27a and Their Association with the Predisposition and Susceptibility to Coronary Artery Disease. Life (Basel, Switzerland) 2022 11 12 (11): . Mir Rashid, Elfaki Imadeldin, Javid Jamsheed, Barnawi Jameel, Altayar Malik A, Albalawi Salem Owaid, Jalal Mohammed M, Tayeb Faris J, Yousif Aadil, Ullah Mohammad Fahad, AbuDuhier Faisel |
| Different effects of maternal homocysteine concentration, MTHFR and MTRR genetic polymorphisms on the occurrence of fetal aneuploidy. Reproductive biomedicine online 2022 Jul . Guo Qian-Nan, Wang Ling, Liu Zheng-Yan, Wang Hong-Dan, Wang Li, Long Jian-Gang, Liao Shi-X |
| Optimisation of individual cardiovascular risk assessment in a German coronary artery disease cohort using a commercial test for genetic polymorphisms - a pilot study. Acta cardiologica 2022 Oct 1-11. Krohn Jona B, Neubauer Clemens, Fischer Simon, Oberkanins Christian, Katus Hugo A, Gleissner Christian |
| Association between MTHFR C677T and A1298C gene polymorphisms and maternal risk for Down syndrome: A protocol for systematic review and/or meta-analysis. Medicine 2022 1 101 (3): e28293. Ginani Carla Talita Azevedo, Luz Jefferson Romáryo Duarte da, Silva Saulo Victor E, Coppedè Fabio, Almeida Maria das Graç |
| Associations between AGT, MTHFR, and VEGF gene polymorphisms and preeclampsia in the Chinese population. Placenta 2022 1 118 38-45. Ding Guifeng, Li Yan, Gao Jianrong, Wang Wenxia, Wang Huijuan, Bai Guiq |
| Cerebral sinuses thrombosis prior to the diagnosis of acute lymphoblastic leukemia in a child: A case report. SAGE open medical case reports 2022 10 2050313X221117337. Sherief Laila M, Zakaria Marwa, Soliman Basma K, Kamal Naglaa M, Alharthi Sultan A, Abosabie Sara As, Abdelazeem Mahmo |
| Association of C677T and A1298C polymorphisms of the MTHFR gene with maternal risk for Down syndrome: a meta-analysis of case-control studies. Mutation research. Reviews in mutation research 2023 9 108470. Carla Talita Azevedo Ginani, Jefferson Romáryo Duarte da Luz, Kleyton Santos de Medeiros, Ayane Cristine Alves Sarmento, Fabio Coppedè, Maria das Graças Almei |
| Prothrombotic states in portal vein thrombosis and Budd-Chiari syndrome in India: A systematic review and meta-analysis. Indian journal of gastroenterology : official journal of the Indian Society of Gastroenterology 2023 8 . Suprabhat Giri, Sumaswi Angadi, Jijo Varghese, Sridhar Sundaram, Sukanya Bhrugumal |
| A Potential Strategy for Atherosclerosis Prevention in Modernizing China - Hyperhomocysteinemia, MTHFR C677T Polymorphism and Air Pollution (PM2.5) on Atherogenesis in Chinese Adults. The journal of nutrition, health & aging 2023 2 27 (2): 134-141. Kwok C Y T, Poon Y K P, Chook P, Guo D S, Lin C Q, Yin Y H, Celermajer D S, Woo K |
| Heavy metals and genetic variations in folate metabolism pathway: A gene-environment interaction. Indian journal of public health 2023 11 67 (3): 477-479. Amandeep Kaur, Mohan Jairath, Anupam Ka |
| MTHFR C677T and A1298C polymorphism's effect on risk of colorectal cancer in Lynch syndrome. Scientific reports 2023 11 13 (1): 18783. Mariann Unhjem Wiik, Mia Negline, Vidar Beisvåg, Matthew Clapham, Elizabeth Holliday, Nuria Dueñas, Joan Brunet, Marta Pineda, Nuria Bonifaci, Stefan Aretz, Hannah Klinkhammer, Isabel Spier, Claudia Perne, Andreas Mayr, Laura Valle, Jan Lubinski, Wenche Sjursen, Rodney J Scott, Bente A Talseth-Palm |
| Methylenetetrahydrofolate Reductase 677T Allele Is a Risk Factor for Arterial Thrombosis in Chinese Han Patients with Antiphospholipid Syndrome. Biomedicines 2023 1 11 (1): . Tang Zihan, Shi Hui, Liu Honglei, Cheng Xiaobing, Su Yutong, Ye Junna, Sun Yue, Hu Qiongyi, Chi Huihui, Zhou Zhuochao, Jia Jinchao, Meng Jianfen, Wang Mengyan, Wang Fan, Teng Jialin, Yang Chengde, Liu Tingti |
| Co-Occurring Methylenetetrahydrofolate Reductase (MTHFR) rs1801133 and rs1801131 Genotypes as Associative Genetic Modifiers of Clinical Severity in Rett Syndrome. Brain sciences 2024 7 14 (7): . Jatinder Singh, Georgina Wilkins, Ella Goodman-Vincent, Samiya Chishti, Ruben Bonilla Guerrero, Leighton McFadden, Zvi Zahavi, Paramala Santo |
| Folate and Vitamin B12 Levels in Chilean Women with PCOS and Their Association with Metabolic Outcomes. Nutrients 2024 6 16 (12): . Matías Carrasco-Cabezas, Taís Silveira Assmann, Paz Martínez, Leslie Cerpa, Susan Calfunao, Bárbara Echiburú, Manuel Maliqueo, Nicolás Crisosto, Francisca Salas-Pér |
| Analysis of Genes Involved in Oxidative Stress and Iron Metabolism in Heart Failure: A Step Forward in Risk Stratification. Cureus 2024 6 16 (5): e60707. Pedro X Silva, Laura Aguiar, Marcos Gaspar, Paula Faustino, Luiz M Falcão, Mário Barbosa, Manuel Bicho, Ângela Inác |
| MTHFR 677C>T and 1298A>C Variants in Mothers of Infants with Down Syndrome from Western Mexico. Genetic testing and molecular biomarkers 2024 5 . Yaneris Maibeth Romero-Bolaño, Lucina Bobadilla-Morales, Alfredo Corona-Rivera, Idalid Cuero-Quezada, Jennifer Santana-Hernández, Christian Peña-Padilla, Alejandro Brukman-Jiménez, Mireya Orozco-Vela, Natalia Navia-Espinoza, Jorge Román Corona-Rive |
| The risk profiles of pregnancy-related cerebral venous thrombosis: a retrospective study in a comprehensive hospital. BMC neurology 2024 5 24 (1): 182. Shaoying Wang, Ming Yao, Nan Hu, Juntao Liu, Bin Pe |
| Effects of MTHFR C677T polymorphism on homocysteine and vitamin D in women with polycystic ovary syndrome. Gene 2024 4 919 148504. Jinyan Zhao, Xianghong Li, Qing Ch |
| Dual rare genetic diseases in five pediatric patients: insights from next-generation diagnostic methods. Orphanet journal of rare diseases 2024 4 19 (1): 159. Yupeng Liu, Xue Ma, Zhehui Chen, Ruxuan He, Yao Zhang, Hui Dong, Yanyan Ma, Tongfei Wu, Qiao Wang, Yuan Ding, Xiyuan Li, Dongxiao Li, Jinqing Song, Mengqiu Li, Ying Jin, Jiong Qin, Yanling Ya |
| The effect of hereditary thrombophilia on recurrent pregnancy loss: a retrospective cohort study. BMC pregnancy and childbirth 2024 11 24 (1): 719. Hasan Berkan Sayal, Mehmet Sinan Beks |
- Page last reviewed:Feb 1, 2024
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