Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 94 Records) |
Query Trace: TCN2[original query] |
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Novel Susceptibility Loci for Moyamoya Disease Revealed by a Genome-Wide Association Study.
Stroke 2018 Jan 49 (1): 11-18. Duan Lian, Wei Ling, Tian Yanghua, Zhang Zhengshan, Hu Panpan, Wei Qiang, Liu Sugang, Zhang Jun, Wang Yuyang, Li Desheng, Yang Weizhong, Zong Rui, Xian Peng, Han Cong, Bao Xiangyang, Zhao Feng, Feng Jie, Liu Wei, Cao Wuchun, Zhou Guoping, Zhu Chunyan, Yu Fengqiong, Yang Weimin, Meng Yu, Wang Jingye, Chen Xianwen, Wang Yu, Shen Bing, Zhao Bing, Wan Jinghai, Zhang Fengyu, Zhao Gang, Xu Aimin, Zhang Xuejun, Liu Jianjun, Zuo Xianbo, Wang K |
Associations Between MTR A2756G, MTRR A66G, and TCN2 C776G Polymorphisms and Risk of Nonsyndromic Cleft Lip With or Without Cleft Palate: A Meta-Analysis. Genetic testing and molecular biomarkers 2018 Jul . Lei Wei, Xia Yinlan, Wu Yang, Fu Gang, Ren Ais |
Discovery of 4 exonic and 1 intergenic novel susceptibility loci for leprosy. Clinical genetics 2018 May . Wang Z, Mi Z, Wang H, Sun L, Yu G, Fu X, Wang C, Bao F, Yue Z, Zhao Q, Wang N, Cheng X, Liu H, Zhang |
Evaluation of transcobalamin II rs1801198 and transcobalamin II receptor rs2336573 gene polymorphisms in recurrent spontaneous abortion. Journal of obstetrics and gynaecology : the journal of the Institute of Obstetrics and Gynaecology 2018 Mar 1-4. Hashemi Mohammad, Mokhtari Mojgan, Yazdani-Shahrbabaki Vajiheh, Danesh Hiva, Bizhani Fatemeh, Taheri Mohs |
Exome-wide analyses identify low-frequency variant in CYP26B1 and additional coding variants associated with esophageal squamous cell carcinoma. Nature genetics 2018 Jan . Chang Jiang, Zhong Rong, Tian Jianbo, Li Jiaoyuan, Zhai Kan, Ke Juntao, Lou Jiao, Chen Wei, Zhu Beibei, Shen Na, Zhang Yi, Zhu Ying, Gong Yajie, Yang Yang, Zou Danyi, Peng Xiating, Zhang Zhi, Zhang Xuemei, Huang Kun, Wu Tangchun, Wu Chen, Miao Xiaoping, Lin Dongx |
Association Study of Polymorphisms in Genes Relevant to Vitamin B12 and Folate Metabolism with Childhood Autism Spectrum Disorder in a Han Chinese Population. Medical science monitor : international medical journal of experimental and clinical research 2018 Jan 24 370-376. Zhang Zengyu, Yu Lianfang, Li Sufang, Liu J |
Exome sequencing of cases with neural tube defects identifies candidate genes involved in one-carbon/vitamin B12 metabolisms and Sonic Hedgehog pathway. Human genetics 2019 May . Renard Emeline, Chéry Céline, Oussalah Abderrahim, Josse Thomas, Perrin Pascal, Tramoy Denise, Voirin Jimmy, Klein Olivier, Leheup Bruno, Feillet François, Guéant-Rodriguez Rosa-Maria, Guéant Jean-Lou |
Genetic polymorphisms of the cobalamin transport system are associated with idiopathic recurrent implantation failure. Journal of assisted reproduction and genetics 2019 May . Park Han Sung, Kim Jung Oh, An Hui Jeong, Ryu Chang Soo, Ko Eun Ju, Kim Young Ran, Ahn Eun Hee, Lee Woo Sik, Kim Ji Hyang, Kim Nam Ke |
Folate/homocysteine metabolism and lung cancer risk among smokers. PloS one 2019 14 (4): e0214462. Stanislawska-Sachadyn Anna, Borzyszkowska Joanna, Krzeminski Michal, Janowicz Alicja, Dziadziuszko Rafal, Jassem Jacek, Rzyman Witold, Limon Janu |
Association of single nucleotide polymorphisms of MTHFR, TCN2, RNF213 with susceptibility to hypertension and blood pressure. Bioscience reports 2019 Dec . Liu Shan, Liu Mengwei, Li Qian, Liu Xiuping, Wang Yue, Mambiya Michael, Zhang Kaili, Yang Luping, Zhang Qian, Shang Mengke, Zeng Fanxin, Nie Fangfang, Liu Wanya |
Association between oral cleft and transcobalamin 2 polymorphism in a sample study from Nassiriya, Iraq. International journal of immunopathology and pharmacology 0 33 2058738419855571. Carinci Francesco, Palmieri Annalisa, Scapoli Luca, Cura Francesca, Abenavoli Fabio, Giannì Aldo Bruno, Russillo Antonio, Docimo Raffaella, Martinelli Marcel |
Non-syndromic cleft palate: Association analysis on three gene polymorphisms of the folate pathway in Asian and Italian populations. International journal of immunopathology and pharmacology 2019 10 33 2058738419858572. Carinci Francesco, Palmieri Annalisa, Scapoli Luca, Cura Francesca, Borelli Francesco, Morselli Paolo Giovanni, Nouri Nayereh, Abdali Hossein, Gianni Aldo Bruno, Russillo Antonio, Docimo Raffaella, Martinelli Marcel |
Exome Chip Analysis of 14,026 Koreans Reveals Known and Newly Discovered Genetic Loci Associated with Type 2 Diabetes Mellitus.
Diabetes & metabolism journal 2020 Jul . Cho Seong Beom, Jang Jin Hwa, Chung Myung Guen, Kim Sang Che |
Maternal folate, one-carbon metabolism and pregnancy outcomes. Maternal & child nutrition 2020 Jul e13064. Jankovic-Karasoulos Tanja, Furness Denise L, Leemaqz Shalem Y, Dekker Gustaaf A, Grzeskowiak Luke E, Grieger Jessica A, Andraweera Prabha H, McCullough Dylan, McAninch Dale, McCowan Lesley M, Bianco-Miotto Tina, Roberts Claire |
3'-UTR Polymorphisms of Vitamin B-Related Genes Are Associated with Osteoporosis and Osteoporotic Vertebral Compression Fractures (OVCFs) in Postmenopausal Women. Genes 2020 Jun 11 (6): . Ahn Tae-Keun, Kim Jung Oh, An Hui Jeong, Park Han Sung, Choi Un Yong, Sohn Seil, Kim Kyoung-Tae, Kim Nam Keun, Han In- |
The Effect of Interactions between Folic Acid Supplementation and One Carbon Metabolism Gene Variants on Small-for-Gestational-Age Births in the Screening for Pregnancy Endpoints (SCOPE) Cohort Study. Nutrients 2020 Jun 12 (6): . Bulloch Rhodi E, Wall Clare R, McCowan Lesley M E, Taylor Rennae S, Roberts Claire T, Thompson John M |
Relationship between cobalt transporter II gene rs9606756 site mutant and serum homocysteine level and recurrent cerebral infarction in young and middle-aged people. Minerva medica 2020 Mar . Liu Jing, Jiang Yan, Liu Deshui, Zhang Hao, Chen Tuantuan, Zhang Guangping, Liu Hongbin, DU Shu, Lin Zaihong, Jin Yan, Li Xiaoh |
One-carbon metabolism and global DNA methylation in mothers of individuals with Down syndrome. Human cell 2021 8 34 (6): 1671-1681. Mendes Cristiani Cortez, Zampieri Bruna Lancia, Arantes Lidia Maria Rebolho Batista, Melendez Matias Eliseo, Biselli Joice Matos, Carvalho André Lopes, Eberlin Marcos Nogueira, Riccio Maria Francesca, Vannucchi Hélio, Carvalho Valdemir Melechco, Goloni-Bertollo Eny Maria, Pavarino Érika Cristi |
Genetic Polymorphisms in Enzymes Involved in One-Carbon Metabolism and Anti-epileptic Drug Monotherapy on Homocysteine Metabolism in Patients With Epilepsy. Frontiers in neurology 2021 6 12 683275. Zhu Shaofang, Ni Guanzhong, Sui Lisen, Zhao Yiran, Zhang Xiaoxu, Dai Qilin, Chen Aohan, Lin Wanrong, Li Yinchao, Huang Min, Zhou Liem |
Folate metabolizing gene polymorphisms and genetic vulnerability to preterm birth in Korean women. Genes & genomics 2021 May . Kwon Bit Na, Lee Noo Ri, Kim Hyung Jun, Kang Yun Dan, Kim Jong Soo, Park Jin Wan, Jin Han J |
Whole exome sequencing, a hypothesis-free approach to investigate recurrent early miscarriage. Reproductive biomedicine online 2021 3 42 (4): 789-798. Gourhant Lenaick, Bocher Ozvan, De Saint Martin Luc, Ludwig Thomas E, Boland Anne, Deleuze Jean F, Merviel Philippe, Dupré Pierre F, Lemarié Catherine A, Couturaud Francis, Le Maréchal Cédric, Génin Emmanuelle, Pasquier Elisabe |
Associations between Genetic Variants and Blood Biomarkers of One-Carbon Metabolism in Postmenopausal Women from the Women's Health Initiative Observational Study. The Journal of nutrition 2021 12 152 (4): 1099-1106. Cheng Ting-Yuan David, Ilozumba Mmadili N, Balavarca Yesilda, Neuhouser Marian L, Miller Joshua W, Beresford Shirley A A, Zheng Yingye, Song Xiaoling, Duggan David J, Toriola Adetunji T, Bailey Lynn B, Green Ralph, Caudill Marie A, Ulrich Cornelia |
[Clinical and genetic analysis of a child with transcobalamin II deficiency]. Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics 2021 10 38 (10): 993-996. Yang Chunlan, Wang Xiaodong, Wang Chunjing, Zhang Xiaoling, Li Yue, Yu Yue, Liu Si |
Homocysteine levels, genetic background, and cognitive impairment in Parkinson's disease. Journal of neurology 2022 9 270 (1): 477-485. Periñán María Teresa, Macías-García Daniel, Jesús Silvia, Martín-Rodríguez Juan Francisco, Muñoz-Delgado Laura, Jimenez-Jaraba Maria Valle, Buiza-Rueda Dolores, Bonilla-Toribio Marta, Adarmes-Gómez Astrid Daniela, Gómez-Garre Pilar, Mir Pab |
Vitamin B12 Transport Genes and Nonsyndromic Cleft Lip With or Without Cleft Palate in Chile. Reproductive sciences (Thousand Oaks, Calif.) 2022 4 29 (10): 2921-2926. Suazo José, Salamanca Carlos, Cáceres-Rojas Gabriela, González-Hormazábal Patricio, Pantoja Roberto, Leiva Noemi, Pardo Ro |
An Assessment of Selected Molecular and Biochemical Markers of the Folate Pathway as Potential Risk Factors for Fetal Trisomy 21 during the First Trimester of Pregnancy in the Polish Population. Journal of clinical medicine 2022 3 11 (5): . Zió?kowska Katarzyna, Tobo?a-Wróbel Kinga, Pietryga Marek, Kasprzak Gra?yna, Jamsheer Aleksander, Wysocka E |
Clinical relevance of vitamin B12 level and vitamin B12 metabolic gene variation in pulmonary tuberculosis. Frontiers in immunology 2022 13 947897. Zhang Tian-Ping, Li Rui, Wang Li-Jun, Tang Fei, Li Hong-Mi |
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 |
Associations between Genetic Variants and Blood Biomarkers of One-Carbon Metabolism in Postmenopausal Women from the Women's Health Initiative Observational Study. The Journal of nutrition 2023 3 152 (4): 1099-1106. Cheng Ting-Yuan David, Ilozumba Mmadili N, Balavarca Yesilda, Neuhouser Marian L, Miller Joshua W, Beresford Shirley A A, Zheng Yingye, Song Xiaoling, Duggan David J, Toriola Adetunji T, Bailey Lynn B, Green Ralph, Caudill Marie A, Ulrich Cornelia |
Gene-Folic Acid Interactions and Risk of Conotruncal Heart Defects: Results from the National Birth Defects Prevention Study. Genes 2023 1 14 (1): . Webber Daniel M, Li Ming, MacLeod Stewart L, Tang Xinyu, Levy Joseph W, Karim Mohammad A, Erickson Stephen W, Hobbs Charlotte A, The National Birth Defects Prevention Stud |
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- Page last updated:Apr 22, 2024
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