Human Genome Epidemiology Literature Finder
|
Records 1 - 30 (of 267 Records) |
| Query Trace: Syndrome and MTHFR[original query] |
|---|
| 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 |
| A Genetic Association Study of MTHFR C677T Polymorphism with Risk of Metabolic Syndrome: A Systematic Review and Meta-Analysis. Galen medical journal 2021 9 8 e1472. Azizi Soheil, Shamshirian Amir, Alizadeh-Navaei Reza, Jafarpour Hamed, Asemi Zatollah, Tamtaji Omid Reza, Vaziri Mohammad Sadegh, Homayounfar Reza, Rezaei Shahmirzadi Arash, Alipoor Re |
| Early-Onset Schizophrenia: A Special Phenotype of the Disease Characterized by Increased MTHFR Polymorphisms and Aggravating Symptoms. Neuropsychiatric disease and treatment 2021 8 17 2511-2525. Wan Lin, Wei Ji |
| The Homocysteine and Metabolic Syndrome: A Mendelian Randomization Study. Nutrients 2021 8 13 (7): . Lee Ho-Sun, In Sanghwan, Park Taesu |
| Association of MTHFR C677T Polymorphism With Antipsychotic-Induced Change of Weight and Metabolism Index. Frontiers in psychiatry 2021 6 12 673715. Su Yi, Yan Hao, Guo Liangkun, Lu Tianlan, , Zhang Dai, Yue Weih |
| Potential environmental toxicant exposure, metabolizing gene variants and risk of PCOS-A systematic review. Reproductive toxicology (Elmsford, N.Y.) 2021 6 103 124-132. Sharma Priya, Bilkhiwal Nisha, Chaturvedi Pragya, Kumar Sachin, Khetarpal Pree |
| Homozygosity of the TT methylenetetrahydrofolate reductase C677T genotype is an independent long-term predictor of cardiac death in patients with premature myocardial infarction. Current medical research and opinion 2021 Apr 1. Rallidis Loukianos S, Kosmas Nikolaos, Stathopoulou Eleni, Rallidi Maria, Gialeraki Argy |
| Genetic Predictors for Sinusoidal Obstruction Syndrome-A Systematic Review. Journal of personalized medicine 2021 4 11 (5): . Waespe Nicolas, Strebel Sven, Jurkovic Mlakar Simona, Krajinovic Maja, Kuehni Claudia Elisabeth, Nava Tiago, Ansari Ma |
| Negative symptoms in schizophrenia: correlation with clinical and genetic factors. Pharmacogenomics 2021 4 22 (7): 389-399. Hajj Aline, Hallit Souheil, Chamoun Karam, Sacre Hala, Obeid Sahar, Haddad Chadia, Dollfus Sonia, Khabbaz Lydia Rabb |
| [Genotype and phenotype analysis of neonates with neonatal encephalopathy complicated with perinatal hypoxic event]. Zhonghua er ke za zhi = Chinese journal of pediatrics 2021 3 59 (4): 280-285. Xiao T T, Yang L, Wu B B, Peng X M, Wang H J, Cheng G Q, Wang L S, Cao Y, Hu L Y, Zhou W |
| One-carbon pathway and cognitive skills in children with Down syndrome. Scientific reports 2021 Feb 11 (1): 4225. Antonaros Francesca, Lanfranchi Silvia, Locatelli Chiara, Martelli Anna, Olivucci Giulia, Cicchini Elena, Carosi Diatricch Ludovica, Mannini Elisa, Vione Beatrice, Feliciello Agnese, Ramacieri Giuseppe, Onnivello Sara, Vianello Renzo, Vitale Lorenza, Pelleri Maria Chiara, Strippoli Pierluigi, Cocchi Guido, Pulina Francesca, Piovesan Allison, Caracausi Mar |
| Long acting aripiprazole influences cognitive functions in recent onset schizophrenia. Psychopharmacology 2021 Feb . Peitl Vjekoslav, Štefanovi? Mario, Orlovi? Ivona, Culej Jelena, Renduli? Ana, Mateši? Krunoslav, Karlovi? Dalib |
| Fibromyalgia: A Review of Related Polymorphisms and Clinical Relevance. Anais da Academia Brasileira de Ciencias 2021 11 93 (suppl 4): e20210618. Janssen Luísa P, Medeiros Liciane F, Souza Andressa DE, Silva Juliana |
| 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 |
| 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 |
| 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 |
- Page last reviewed:Feb 1, 2023
- Page last updated:Jun 02, 2023
- Content source: