Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 101 Records) |
Query Trace: Spina bifida[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 |
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 |
Association between maternal single nucleotide polymorphisms in genes regulating glucose metabolism and risk for neural tube defects in offspring. Birth defects research. Part A, Clinical and molecular teratology 2015 Jun 103 (6): 471-8. Fu Yunting, Wang Lin-lin, Yi Deqing, Jin Lei, Liu Jufen, Zhang Yali, Ren Aig |
[Methylenetetrahydrofolate reductase polymorphisms as risk factors for myelomeningocele]. Revista médica de Chile 2014 May 142 (5): 587-92. Pardo Rosa, Suazo José, Castillo Silvia, Vargas Marcela, Zalavari Andrea, Santos José Luis, Blanco Rafael, Rotter Karin, Solar Margarita, Tapia E |
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 |
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 |
Genetic variation associated with the occurrence and progression of neurological disorders. Neurotoxicology 2016 Oct . Little Julian, Barakat-Haddad Caroline, Martino Rosemary, Pringsheim Tamara, Tremlett Helen, McKay Kyla A, van Lieshout Pascal, Walsh Stephanie J, Gomes James, Krewski Dani |
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 |
Genetic variation in biotransformation enzymes, air pollution exposures, and risk of spina bifida. American journal of medical genetics. Part A 2018 May 176 (5): 1055-1090. Padula Amy M, Yang Wei, Schultz Kathleen, Lurmann Fred, Hammond S Katharine, Shaw Gary |
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 |
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 |
Systems biology analysis of human genomes points to key pathways conferring spina bifida risk. Proceedings of the National Academy of Sciences of the United States of America 2021 12 118 (51): . Aguiar-Pulido Vanessa, Wolujewicz Paul, Martinez-Fundichely Alexander, Elhaik Eran, Thareja Gaurav, Abdel Aleem Alice, Chalhoub Nader, Cuykendall Tawny, Al-Zamer Jamel, Lei Yunping, El-Bashir Haitham, Musser James M, Al-Kaabi Abdulla, Shaw Gary M, Khurana Ekta, Suhre Karsten, Mason Christopher E, Elemento Olivier, Finnell Richard H, Ross M Elizabe |
Myelomeningocele genotype-phenotype correlation findings in cilia, HH, PCP, and WNT signaling pathways. Birth defects research 2021 Jan . Ortiz-Cruz Gabriela, Aguayo-Gómez Adolfo, Luna-Muñoz Leonora, Muñoz-Téllez Luis A, Mutchinick Osvaldo |
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 |
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 |
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 |
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 |
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- Page last updated:May 13, 2024
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