HuGE Literature Finder
Records
1
-
30
| Association of MTHFR gene C677T polymorphism with pregnancy outcome. European review for medical and pharmacological sciences 2023 1 27 (1): 166-171. Huang L-L, Tong J-R, Huang Y, Wei Y-N, Chen H-F, Chen Y, Su J-Y, Deng |
| 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 |
| Folate Pathway Gene Single Nucleotide Polymorphisms and Neural Tube Defects: A Systematic Review and Meta-Analysis. Journal of personalized medicine 2022 10 12 (10): . Almekkawi Ahmad K, AlJardali Marwa W, Daadaa Hicham M, Lane Alison L, Worner Ashley R, Karim Mohammad A, Scheck Adrienne C, Frye Richard |
| Lower plasma glutathione, choline, and betaine concentrations are associated with fatty liver in postmenopausal women. Nutrition research (New York, N.Y.) 2022 4 101 23-30. Muzsik-Kazimierska Agata, Szwengiel Artur, Nikrandt Grzegorz, Chmurzynska Aga |
| Maternal germline factors associated with aneuploid pregnancy loss: a systematic review. Human reproduction update 2021 . Blyth Ursula, Craciunas Laurentiu, Hudson Gavin, Choudhary Meenaks |
| Methylenetetrahydrofolate reductase gene polymorphisms are not associated with embryo chromosomal abnormalities and IVF outcomes. Systems biology in reproductive medicine 2021 May 1-11. Morales Ruth, Lledó Belén, Ortiz José A, Cascales Alba, Codina Helena, Rodríguez-Arnedo Adoración, Llácer Joaquin, Bernabeu Andrea, Bernabeu Rafa |
| 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 |
| Associations of Genetic Variants of Methylenetetrahydrofolate Reductase and Serum Folate Levels with Metabolic Parameters in Patients with Schizophrenia. International journal of environmental research and public health 2021 11 18 (21): . Chen Chun-Hsin, Chen Po-Yu, Chen Cynthia Yi-An, Chiu Chih-Chiang, Lu Mong-Liang, Huang Ming-Chyi, Lin Yen-Kuang, Chen Yi-H |
| Genetic risk factors for autism-spectrum disorders: a systematic review based on systematic reviews and meta-analysis. Journal of neural transmission (Vienna, Austria : 1996) 2021 6 128 (6): 717-734. Wei Hongyuan, Zhu Yunjiao, Wang Tianli, Zhang Xueqing, Zhang Kexin, Zhang Zhih |
| Hyperhomocysteinemia-related lung disease and hemolytic anemia with bone marrow features masquerading as myelodysplasia. American journal of blood research 2021 7 11 (3): 266-270. Yamanishi Masayoshi, Tamura Atsushi, Miyoshi Takashi, Imashuku Shinsa |
| Maternal Folic Acid Intake and Methylation Status of Genes Associated with Ventricular Septal Defects in Children: Case-Control Study. Nutrients 2021 7 13 (6): . González-Peña Sandra M, Calvo-Anguiano Geovana, Martínez-de-Villarreal Laura E, Ancer-Rodríguez Patricia R, Lugo-Trampe José J, Saldivar-Rodríguez Donato, Hernández-Almaguer María D, Calzada-Dávila Melissa, Guerrero-Orjuela Ligia S, Campos-Acevedo Luis |
| Morphometric and Nanomechanical Features of Platelets from Women with Early Pregnancy Loss Provide New Evidence of the Impact of Inherited Thrombophilia. International journal of molecular sciences 2021 8 22 (15): . Andreeva Tonya, Komsa-Penkova Regina, Langari Ariana, Krumova Sashka, Golemanov Georgi, Georgieva Galya B, Taneva Stefka G, Giosheva Ina, Mihaylova Nikolina, Tchorbanov Andrey, Todinova Svet |
| Stroke in Young Military Men With Heterozygous for MTHFR Gene Mutation or Factor V Leiden Gene Mutation Associated With Patent Foramen Ovale: Report of Two Cases and Therapeutic Strategy. Military medicine 2021 5 . Brisson Rodrigo Tavares, Arruda Josevânia Fulgêncio de Lima, Silva Liene Duarte, de Jesus Dilermando Leal Júnio, Zetola Viviane Flumignan, Kauffmann Nogueira Marcia Aparecida Camac |
| May the morphological findings in the first-trimester abortion materials be indicative of inherited thrombophilia? The journal of obstetrics and gynaecology research 2020 Aug . Kaymaz Esin, Gun Banu D, Genc Gunes C, Kokturk Furuzan, Ozmen Kaz?m |
| The Correlation Between Abnormal Uterine Artery Flow in the First Trimester and Genetic Thrombophilic Alteration: A Prospective Case-Controlled Pilot Study. Diagnostics (Basel, Switzerland) 2020 Aug 10 (9): . Vedmedovska Natalija, Bokucava Diana, Kivite-Urtane Anda, Rovite Vita, Zake-Nikitina Liene, Klovins Janis, Fodina Violeta, Donders Gilbert G |
| 3'UTR polymorphism of Thymidylate Synthase gene increased the risk of persistence of pre-neoplastic cervical lesions. BMC cancer 2020 4 20 (1): 323. Silva Nayara Nascimento Toledo, Santos Ana Carolina Silva, Nogueira Verlândia Mendes, Carneiro Cláudia Martins, Lima Angélica Alv |
| Maternal LINE-1 DNA Methylation and Congenital Heart Defects in Down Syndrome. Frontiers in genetics 2019 2 10 41. Babi? Božovi? Ivana, Stankovi? Aleksandra, Živkovi? Maja, Vranekovi? Jadranka, Mahulja-Stamenkovi? Vesna, Brajenovi?-Mili? Boja |
| Are Congenital Urinary Tract Abnormalities Linked to Maternal Methylenetetrahydrofolate Reductase Polymorphisms in Fetuses of Intentionally Terminated Pregnancies with Oligo- or Anhydramnios ? Fetal and pediatric pathology 2018 May 1-7. Beksac M Sinan, Beksac Alp Tuna, Buyukeren Melek, Tanacan Atakan, Bektas Hatice, Gucer Saf |
| Comparison of two groups for the apolipoprotein E polymorphisms by using next generation sequencing: The first group with three consecutive abortions and the second group with at most one abortion in three consecutive pregnancies. Gene 2018 May . Gumus Evr |
| Methylenetetrahydrofolate Reductase Polymorphisms and Pregnancy Outcome. Geburtshilfe und Frauenheilkunde 2018 9 78 (9): 871-878. Turgal Mert, Gumruk Fatma, Karaagaoglu Ergun, Beksac Mehmet Sin |
| Characteristics and Long-Term Prognosis of Patients =35 Years of Age with ST Segment Elevation Myocardial Infarction and "Normal or Near Normal" Coronary Arteries. The American journal of cardiology 2017 Jun . Rallidis Loukianos S, Gialeraki Argyri, Triantafyllis Andreas S, Tsirebolos Georgios, Liakos Georgios, Moutsatsou Paraskevi, Iliodromitis Efstathi |
| Associations of recurrent miscarriages with chromosomal abnormalities, thrombophilia allelic polymorphisms and/or consanguinity in Saudi Arabia. BMC medical genetics 2016 Oct 17 (Suppl 1): 69. Turki Rola F, Assidi Mourad, Banni Huda A, Zahed Hanan A, Karim Sajjad, Schulten Hans-Juergen, Abu-Elmagd Muhammad, Rouzi Abdulrahim A, Bajouh Osama, Jamal Hassan S, Al-Qahtani Mohammed H, Abuzenadah Adel |
| The efficacy of tissue factor -603A/G and +5466A>G polimorphisms at the development of venous thromboembolism in cancer patients. Experimental oncology 2016 Sep 38 (3): 187-90. Ero?lu A, Ceylan G G, Ozturk E, Yalcin A, Yalcin B, Karasoy |
| The incidence of severe intraventricular hemorrhage based on retrospective analysis of 35939 full-term newborns-report of two cases and review of literature. Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery 2016 Jul . Szpecht Dawid, Frydryszak Dagmara, Miszczyk Norbert, Szymankiewicz Marta, Gadzinowski Janu |
| Association between genetic polymorphisms in folate-related enzyme genes and infertile men with non-obstructive azoospermia. Systems biology in reproductive medicine 2015 Oct 61 (5): 286-92. Kim Shin Young, Lim Jung Wook, Kim Jin Woo, Park So Yeon, Seo Ju T |
| Variants in MTHFR gene and neural tube defects susceptibility in China. Metabolic brain disease 2015 Aug 30 (4): 1017-26. Wang Yongxin, Liu Yuan, Ji Wenyu, Qin Hu, Wu Hao, Xu Danshu, Turtuohut Tukebai, Wang Zenglia |
| A preliminary study of inherited thrombophilic risk factors in different clinical manifestations of venous thromboembolism in central Iran. The Indian journal of medical research 2015 Jul 142 (1): 46-52. Karimi Ali, Abolhasani Marziyeh, Hashemzadeh-Chaleshtori Morteza, Pourgheysari Bato |
| Association of Vitamin B12 Deficiency with Homozygosity of the TT MTHFR C677T Genotype, Hyperhomocysteinemia, and Endothelial Cell Dysfunction. The Israel Medical Association journal : IMAJ 2015 May 17 (5): 288-92. Shiran Avinoam, Remer Eric, Asmer Ihab, Karkabi Basheer, Zittan Eran, Cassel Aliza, Barak Mira, Rozenberg Orit, Karkabi Khaled, Flugelman Moshe |
| Analysis of MTHFR Gene C.677C>T and C.1298A>C Polymorphisms in Iranian Patients with Non-Syndromic Cleft Lip and Palate. Iranian journal of public health 2014 Jun 43 (6): 821-7. Jahanbin Arezoo, Hasanzadeh Nadia, Abdolhoseinpour Faraneh, Sadr-Nabavi Ariane, Raisolsadat Mohammad-Ali, Shamsian Khosro, Mohajertehran Farnaz, Kianifar Hamidre |
| Bladder exstrophy-epispadias complex and the role of methylenetetrahydrofolate reductase C677T polymorphism: A case control study. Journal of Indian Association of Pediatric Surgeons 0 21 (1): 28-32. Raman Venkat Shankar, Bajpai Minu, Ali Ab |
- Page last reviewed:Feb 1, 2023
- Page last updated:Mar 31, 2023
- Content source: