Human Genome Epidemiology Literature Finder
Reproductive and Child Health
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Records 1 - 30 (of 349 Records) |
| Query Trace: Neural Tube Defects Or Spina Bifida Or Anencephaly[original query] |
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| Associations between prenatal exposure to cadmium and lead with neural tube defect risks are modified by single-nucleotide polymorphisms of fetal MTHFR and SOD2: a case-control study. Environmental health : a global access science source 2021 Jun 20 (1): 66. Liu Mengyuan, Yu Jinhui, Su Zaiming, Sun Ying, Liu Yaqiong, Xie Qing, Li Zhiwen, Wang Linlin, Zhang Jie, Jin Lei, Ren Aig |
| MTHFR C677T and A1298C variants in Mexican Mestizo infants with neural tube defects from Western Mexico. Congenital anomalies 2021 May . Aranda-Sánchez Cristian Irela, Bobadilla-Morales Lucina, Corona-Rivera Alfredo, Cuero-Quezada Idalid, Santana-Hernández Jennifer, Baldomero-López Alejandra, Romero-Bolaño Yaneris M, Peña-Padilla Christian, Corona-Rivera Jorge Rom |
| Effects of Periconceptional Multivitamin Supplementation on Folate and Homocysteine Levels Depending on Genetic Variants of Methyltetrahydrofolate Reductase in Infertile Japanese Women. Nutrients 2021 4 13 (4): . Kuroda Keiji, Horikawa Takashi, Gekka Yoko, Moriyama Azusa, Nakao Kazuki, Juen Hiroyasu, Takamizawa Satoru, Ojiro Yuko, Nakagawa Koji, Sugiyama Rikika |
| Genome-wide investigation identifies a rare copy-number variant burden associated with human spina bifida. Genetics in medicine : official journal of the American College of Medical Genetics 2021 Mar . Wolujewicz Paul, Aguiar-Pulido Vanessa, AbdelAleem Alice, Nair Vidya, Thareja Gaurav, Suhre Karsten, Shaw Gary M, Finnell Richard H, Elemento Olivier, Ross M Elizabe |
| Genetic Polymorphisms in DNA Repair Gene APE1/Ref-1 and the Risk of Neural Tube Defects in a High-Risk Area of China. Reproductive sciences (Thousand Oaks, Calif.) 2021 Mar . Wang Xiuwei, Yue Huixuan, Li Shen, Guo Jin, Guan Zhen, Zhu Zhiqiang, Niu Bo, Zhang Ting, Wang Jianh |
| 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 |
| Scribble Controls Social Motivation Behavior through the Regulation of the ERK/Mnk1 Pathway. Cells 2022 5 11 (10): . Moreau Maïté M, Pietropaolo Susanna, Ezan Jérôme, Robert Benjamin J A, Miraux Sylvain, Maître Marlène, Cho Yoon, Crusio Wim E, Montcouquiol Mireille, Sans Nathal |
| 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 |
| 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 |
| Pathogenic/likely pathogenic copy number variations and regions of homozygosity in fetal central nervous system malformations. Archives of gynecology and obstetrics 2022 12 . Zhi Yunxiao, Liu Ling, Cui Shihong, Li Ying, Chen Xiaolin, Che Jia, Han Xiao, Zhao Lanl |
| Study on the relationship between genetic polymorphism of reductive folic acid carrier and the risk of neural tube defects. Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery 2022 12 . Yang Xusen, Fan Guofeng, Wang Zengliang, Li Shaoshan, Qin Hu, Wang Yun, Ma Xiaohu, Ji Wenyu, Wang Yongx |
| 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 |
| Single nucleotide polymorphisms of PCP pathway related genes participate in the occurrence and development of neural tube defect. Molecular genetics & genomic medicine 2022 11 11 (1): e2094. Liu Yan, Dong Liang, Zhi Xiufang, Liu Yang, Zhao Linsheng, Xu Xiaowei, Wang Lu, Zheng Jie, Pu Linjie, Gu Chunyu, Shu Jianbo, Cai Chunqu |
| 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 |
| Whole exome sequencing identifies potential candidate genes for spina bifida derived from mouse models. American journal of medical genetics. Part A 2022 1 188 (5): 1355-1367. Wang Chunyan, Seltzsam Steve, Zheng Bixia, Wu Chen-Han Wilfred, Nicolas-Frank Camille, Yousef Kirollos, Au Kit Sing, Mann Nina, Pantel Dalia, Schneider Sophia, Schierbaum Luca, Kitzler Thomas M, Connaughton Dervla M, Mao Youying, Dai Rufeng, Nakayama Makiko, Kari Jameela A, El Desoky Sherif, Shalaby Mohammed, Eid Loai A, Awad Hazem S, Tasic Velibor, Mane Shrikant M, Lifton Richard P, Baum Michelle A, Shril Shirlee, Estrada Carlos R, Hildebrandt Friedhe |
| Polymorphisms in Maternal Selected Folate Metabolism-Related Genes in Neural Tube Defect-Affected Pregnancy. Advanced biomedical research 2023 8 12 160. Winner K Dewelle, Daniel S Melka, Abenezer T Aklilu, Mahlet Y Gebremariam, Markos A Alemayehu, Dawit H Alemayehu, Tamrayehu S Woldemichael, Solomon G Geb |
| The evolution of folate supplementation - from one size for all to personalized, precision, poly-paths. Journal of translational internal medicine 2023 7 11 (2): 128-137. Qiangqiang He, Jianping |
| 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 |
| Metabolic Analysis of Methylenetetrahydrofolate Reductase Single Nucleotide Polymorphisms (MTHFR 677C<T and MTHFR 1298A<C), Serum Folate and Vitamin B12 in Neural Tube Defects. Indian journal of clinical biochemistry : IJCB 2023 5 38 (3): 305-315. Mohammed H Hassan, Mohamed A Raslan, Mena Tharwat, Hala M Sakhr, Eslam El-Sayed El-Khateeb, Shimaa Fathy Sakr, Hesham H Ameen, Ali R Hamd |
| Polymorphisms of placental iodothyronine deiodinase genes in a rural area of Northern China with high prevalence of neural tube defects. Human heredity 2023 3 . Wang Fang, Gu Yan-Hong, Guo Jin, Bao YiHua, Qiu ZhiYong, Zheng Ping, Ushijima Masaru, Matsuura Masaaki, Zhang Ti |
| 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 |
| MTHFR C677T and MTR A2756G Gene Polymorphism in Neural Tube Defect Patients and Its Association with Red Blood Cell Folate Level in Eastern Indian Population. Journal of Indian Association of Pediatric Surgeons 2023 1 27 (6): 699-706. Kumari Rekha, Kumar Santosh, Thakur Vinit Kumar, Singh Kalpana, Kumar Ud |
| Influence of different forms of folic acid supplementation on pregnancy outcomes under various exposure factors. Technology and health care : official journal of the European Society for Engineering and Medicine 2024 9 . Jie Song, Ruihong Lan, Dahua Yin, Ling Wang, Humin Go |
| Maternal arsenic exposure modifies associations between arsenic, folate and arsenic metabolism gene variants, and spina bifida risk: A case?control study in Bangladesh. Environmental research 2024 8 261 119714. Chih-Fu Wei, Gwen Tindula, Sudipta Kumer Mukherjee, Xingyan Wang, Sheikh Muhammad Ekramullah, D M Arman, Md Joynul Islam, Mubinul Azim, Asifur Rahman, Shamantha Afreen, Md Ziaddin, Benjamin C Warf, Marc G Weisskopf, David C Christiani, Liming Liang, Maitreyi Mazumd |
| 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 |
| Association between UCP2 gene 3'UTR I/D and A55V polymorphisms and neural tube defects susceptibility: systematic review, meta-analysis, and trial sequential analysis. Frontiers in neurology 2024 7 15 1411184. Haokun Tian, Zhen Guan, Shen Li, Jianhua Wa |
| Docosahexaenoic acid, eicosapentaenoic acid, arachidonic acid, and neural tube defects in Tunisian population. Birth defects research 2024 6 116 (6): e2372. Kaouther Nasri, Nadia Ben Jamaa, Soumeya Siala Gaigi, Moncef Feki, Raja Marrakc |
| Association of MTHFR (C677T, A1298C) and MTRR A66G polymorphisms with fatty acids profile and risk of neural tube defects. Birth defects research 2024 5 116 (5): e2333. Kaouther Nasri, Nadia Ben Jamaa, Soumeya Siala Gaigi, Moncef Feki, Raja Marrakc |
| Identification and Functional Analysis of Rare HECTD1 Missense Variants in Human Neural Tube Defects. Research square 2024 1 . Elias Oxman, Huili Li, Hong-Yan Wang, Irene Zo |
| Bayesian polygenic risk estimation approach to nuclear families with discordant sib-pairs for myelomeningocele. PloS one 2025 1 19 (12): e0316378. Adolfo Aguayo-Gómez, Leonora Luna-Muñoz, Yevgeniya Svyryd, Luis Ángel Muñoz-Téllez, Osvaldo M Mutchini |
- Page last reviewed:Feb 1, 2024
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