Human Genome Epidemiology Literature Finder
Neurological Disorders
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Records 1 - 30 (of 82 Records) |
| Query Trace: Neural Tube Defects[original query] |
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| DNA methylation aberrations rather than polymorphisms of FZD3 gene increase the risk of spina bifida in a high-risk region for neural tube defects. Birth defects research. Part A, Clinical and molecular teratology 2015 Jan 103 (1): 37-44. Shangguan Shaofang, Wang Li, Chang Shaoyan, Lu Xiaoling, Wang Zhen, Wu Lihua, Wang Jianhua, Wang Xiuwei, Guan Zhen, Bao Yihua, Zhao Huizhi, Zou Jizhen, Niu Bo, Zhang Ti |
| Variants in maternal COMT and MTHFR genes and risk of neural tube defects in offspring. Metabolic brain disease 2015 Apr 30 (2): 507-13. Liu Jufen, Zhang Yali, Jin Lei, Li Guoxing, Wang Linlin, Bao Yanping, Fu Yunting, Li Zhiwen, Zhang Le, Ye Rongwei, Ren Aig |
| Association of neural tube defects in children of mothers with MTHFR 677TT genotype and abnormal carbohydrate metabolism risk: a case-control study. Genetics and molecular research : GMR 2014 13 (1): 2200-7. Cadenas-Benitez N M, Yanes-Sosa F, Gonzalez-Meneses A, Cerrillos L, Acosta D, Praena-Fernandez J M, Neth O, Gomez de Terreros I, Ybot-González |
| C677T mutation in methylenetetrahydrofolate reductase gene and neural tube defects: should Japanese women undergo gene screening before pregnancy? Congenital anomalies 2014 Feb 54 (1): 30-4. Kondo Atsuo, Fukuda Hiromi, Matsuo Takuya, Shinozaki Keiko, Okai Iku |
| Identification of novel CELSR1 mutations in spina bifida. PloS one 2014 9 (3): e92207. Lei Yunping, Zhu Huiping, Yang Wei, Ross M Elizabeth, Shaw Gary M, Finnell Richard |
| Paternal transmission of MTHFD1 G1958A variant predisposes to neural tube defects in the offspring. Developmental medicine and child neurology 2015 Sep . Prasoona Kattekola R, Sunitha Tella, Srinadh Buragadda, Deepika Madireddy L N, Kumari Tiruvatturu M, Jyothy Ak |
| Role of the planar cell polarity gene Protein tyrosine kinase 7 in neural tube defects in humans. Birth defects research. Part A, Clinical and molecular teratology 2015 Sep . Wang Mingqin, De Marco Patrizia, Merello Elisa, Drapeau Pierre, Capra Valeria, Kibar Zo |
| Heme oxygenase-1 promoter polymorphisms and risk of spina bifida. Birth defects research. Part A, Clinical and molecular teratology 2015 Sep 103 (9): 741-6. Fujioka Kazumichi, Yang Wei, Wallenstein Matthew B, Zhao Hui, Wong Ronald J, Stevenson David K, Shaw Gary |
| Functional variant in methionine synthase reductase intron-1 is associated with pleiotropic congenital malformations. Molecular and cellular biochemistry 2015 Sep 407 (1-2): 51-6. Cheng Haiqin, Li Huili, Bu Zhaoli, Zhang Qin, Bai Baoling, Zhao Hong, Li Ren-Ke, Zhang Ting, Xie J |
| Sonic Hedgehog Signaling Affected by Promoter Hypermethylation Induces Aberrant Gli2 Expression in Spina Bifida. Molecular neurobiology 2015 Oct . Lu Xiao-Lin, Wang Li, Chang Shao-Yan, Shangguan Shao-Fang, Wang Zhen, Wu Li-Hua, Zou Ji-Zhen, Xiao Ping, Li Rui, Bao Yi-Hua, Qiu Z-Y, Zhang Ti |
| Analysis of polymorphisms of genes associated with folate-mediated one-carbon metabolism and neural tube defects in Chinese Han Population. Birth defects research. Part A, Clinical and molecular teratology 2016 Mar . Piao Wei, Guo Jin, Bao Yihua, Wang Fang, Zhang Ting, Huo Junsheng, Zhang Kunl |
| Interaction between Maternal and Paternal SHMT1 C1420T Predisposes to Neural Tube Defects in the Fetus: Evidence from Case-Control and Family-Based Triad Approaches. Birth defects research 2017 8 109 (13): 1020-1029. K Rebekah Prasoona, Tella Sunitha, Buragadda Srinadh, Tiruvatturu Muni Kumari, Akka Jyot |
| An Inframe Trinucleotide Deletion in MTRR Exon 1 is Associated with the Risk of Spina Bifida. Neuromolecular medicine 2017 Jul . Zhang Jun, Dai Xiao-Lu, Liu Gui-Cen, Wang Juan, Ren Xue-Yi, Jin Mu-Hua, Mi Nan-Nan, Wang Shu-Q |
| A targeted sequencing panel identifies rare damaging variants in multiple genes in the cranial neural tube defect, anencephaly. Clinical genetics 2017 12 93 (4): 870-879. Ishida M, Cullup T, Boustred C, James C, Docker J, English C, , Lench N, Copp A J, Moore G E, Greene N D E, Stanier |
| Using Human 'Experiments of Nature' to Predict Drug Safety Issues: An Example with PCSK9 Inhibitors. Drug safety 2017 11 41 (3): 303-311. Jerome Rebecca N, Pulley Jill M, Roden Dan M, Shirey-Rice Jana K, Bastarache Lisa A, R Bernard Gordon, B Ekstrom Leeland, Lancaster William J, Denny Joshua |
| Dominant negative GPR161 rare variants are risk factors of human spina bifida. Human molecular genetics 2018 9 28 (2): 200-208. Kim Sung-Eun, Lei Yunping, Hwang Sun-Hee, Wlodarczyk Bogdan J, Mukhopadhyay Saikat, Shaw Gary M, Ross M Elizabeth, Finnell Richard |
| Polymorphism rs1052536 in Base Excision Repair Gene Is a Risk Factor in a High-Risk Area of Neural Tube Defects in China. Medical science monitor : international medical journal of experimental and clinical research 2018 Jul 24 5015-5026. Li Guannan, Wang Xin, Wang Xiuwei, Guan Zhen, Guo Jin, Wang Fang, Zhang Jianzhao, Niu Bo, Zhang Ting, Wang Jianhua, Yang Ji |
| Maternal association and influence of DHFR 19?bp deletion variant predisposes foetus to anencephaly susceptibility: a family-based triad study. Biomarkers : biochemical indicators of exposure, response, and susceptibility to chemicals 2018 Apr 1-19. Prasoona K R, Sunitha T, Srinadh B, Muni Kumari T, Jyothy |
| Digenic variants of planar cell polarity genes in human neural tube defect patients. Molecular genetics and metabolism 2018 3 124 (1): 94-100. Wang Linlin, Xiao Yanhui, Tian Tian, Jin Lei, Lei Yunping, Finnell Richard H, Ren Aig |
| [THE DIFFERENTIATED APPROACH TO PREVENTION OF NEURAL TUBE DEFECTS IN CHILDREN]. Georgian medical news 2018 2 (274): 52-59. Kotova N, Maichuk V, Fedorenko |
| Genetic and functional analysis of SHROOM1-4 in a Chinese neural tube defect cohort. Human genetics 2018 Feb . Chen Zhongzhong, Kuang Lele, Finnell Richard H, Wang Hongy |
| Genetic variants in GRHL3 and risk for neural tube defects: A case-control and case-parent triad/control study. Birth defects research 2019 Jul . Yang Wenlei, Xiao Yanhui, Tian Tian, Jin Lei, Wang Linlin, Ren Aig |
| Variants identified in PTK7 associated with neural tube defects. Molecular genetics & genomic medicine 2019 Jan e584. Lei Yunping, Kim Sung-Eun, Chen Zhongzhong, Cao Xuanye, Zhu Huiping, Yang Wei, Shaw Gary M, Zheng Yufang, Zhang Ting, Wang Hong-Yan, Finnell Richard |
| Association of Fetal MTHFR C677T Polymorphism with Susceptibility to Neural Tube Defects: A Systematic Review and Update Meta-Analysis. Fetal and pediatric pathology 2020 Jun 1-17. Tabatabaei Razieh Sadat, Fatahi-Meibodi Neda, Meibodi Bahare, Javaheri Atiyeh, Abbasi Hajar, Hadadan Amaneh, Bahrami Reza, Mirjalili Seyed Reza, Karimi-Zarchi Mojgan, Neamatzadeh Hosse |
| Eph and Ephrin Variants in Malaysian Neural Tube Defect Families. Genes 2022 6 13 (6): . Mohd-Zin Siti Waheeda, Tan Amelia Cheng Wei, Atroosh Wahib M, Thong Meow-Keong, Azizi Abu Bakar, Greene Nicholas D E, Abdul-Aziz Noraishah Myd |
| Genomic architecture of fetal central nervous system anomalies using whole-genome sequencing. NPJ genomic medicine 2022 May 7 (1): 31. Yang Ying, Zhao Sheng, Sun Guoqiang, Chen Fang, Zhang Tongda, Song Jieping, Yang Wenzhong, Wang Lin, Zhan Nianji, Yang Xiaohong, Zhu Xia, Rao Bin, Yin Zhenzhen, Zhou Jing, Yan Haisheng, Huang Yushan, Ye Jingyu, Huang Hui, Cheng Chen, Zhu Shida, Guo Jian, Xu Xun, Chen Xinl |
| Genetic Effects of ITPK1 Polymorphisms on the Risk of Neural Tube Defects: a Population-Based Study. Reproductive sciences (Thousand Oaks, Calif.) 2022 11 . Guan Zhen, Liang Yingchao, Zhu ZhiQiang, Yang Aiyun, Li Shen, Wang Xiuwei, Wang Jianh |
| Family-base rare variant association analysis in Saudi Arabian hydrocephalus subjects using whole exome sequencing. Journal of neurosurgical sciences 2023 5 . Ahmed Ammar, Dalal K Bubshait, Abdulrazaq Al Ojan, Shuroq A Alshari, Cyril Cyrus, Rawan Alanazi, Mohammed A Al Ghamdi, Brendan J Keating, Abdulrahman Al-Anazi, Noorah H Al Qahtani, Amein K Al-A |
| Genetic mutations in ribosomal biogenesis gene TCOF1 identified in human neural tube defects. Molecular genetics & genomic medicine 2023 2 e2150. Wang Fang, Cheng Haiqin, Zhang Qin, Guo J |
| Association between the MTHFR (rs1801133) gene variation and serum trace elements levels (Copper and Zinc) in individuals diagnosed with neural tube defects. Clinica chimica acta; international journal of clinical chemistry 2024 7 562 119856. Nitish Kumar Singh, Sarita Choudhary, Sangeeta Rai, Abhay Kumar Yadav, Royana Sin |
- Page last reviewed:Feb 1, 2024
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