Human Genome Epidemiology Literature Finder
Records 1 - 22 (of 22 Records) |
Query Trace: MTHFD1L[original query] |
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A common variant in MTHFD1L is associated with neural tube defects and mRNA splicing efficiency. Human mutation 2009 Dec 30 (12): 1650-6. Parle-McDermott Anne, Pangilinan Faith, O'Brien Kirsty K, Mills James L, Magee Alan M, Troendle James, Sutton Marie, Scott John M, Kirke Peadar N, Molloy Anne M, Brody Lawrence |
Common genetic polymorphisms in moyamoya and atherosclerotic disease in Europeans. Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery 2011 Feb 27 (2): 245-52. Roder Constantin, Peters Vera, Kasuya Hidetoshi, Nishizawa Tsutomu, Takehara Yayoi, Berg Daniela, Schulte Claudia, Khan Nadia, Tatagiba Marcos, Krischek Bor |
Dementia revealed: novel chromosome 6 locus for late-onset Alzheimer disease provides genetic evidence for folate-pathway abnormalities.
PLoS genetics 2010 Sep 6 (9): e1001130. Naj Adam C, Beecham Gary W, Martin Eden R, Gallins Paul J, Powell Eric H, Konidari Ioanna, Whitehead Patrice L, Cai Guiqing, Haroutunian Vahram, Scott William K, Vance Jeffery M, Slifer Michael A, Gwirtsman Harry E, Gilbert John R, Haines Jonathan L, Buxbaum Joseph D, Pericak-Vance Margaret |
Comparative analysis of genome-wide association studies signals for lipids, diabetes, and coronary heart disease: Cardiovascular Biomarker Genetics Collaboration. European heart journal 2012 Feb 33 (3): 393-407. Angelakopoulou Aspasia, Shah Tina, Sofat Reecha, Shah Sonia, Berry Diane J, Cooper Jackie, Palmen Jutta, Tzoulaki Ioanna, Wong Andrew, Jefferis Barbara J, Maniatis Nikolas, Drenos Fotios, Gigante Bruna, Hardy Rebecca, Laxton Ross C, Leander Karin, Motterle Anna, Simpson Iain A, Smeeth Liam, Thomson Andy, Verzilli Claudio, Kuh Diana, Ireland Helen, Deanfield John, Caulfield Mark, Wallace Chris, Samani Nilesh, Munroe Patricia B, Lathrop Mark, Fowkes F Gerry R, Marmot Michael, Whincup Peter H, Whittaker John C, de Faire Ulf, Kivimaki Mika, Kumari Meena, Hypponen Elina, Power Chris, Humphries Steve E, Talmud Philippa J, Price Jackie, Morris Richard W, Ye Shu, Casas Juan P, Hingorani Aroon |
The MTHFD1L gene rs11754661 marker is associated with susceptibility to Alzheimer's disease in the Chinese Han population. Journal of the neurological sciences 2011 Sep 308 (1-2): 32-4. Ren Ru-Jing, Wang Li-Ling, Fang Rong, Liu Li-Hua, Wang Ying, Tang Hui-Dong, Deng Yu-Lei, Xu Wei, Wang Gang, Chen Sheng- |
Association of SNP rs17465637 on chromosome 1q41 and rs599839 on 1p13.3 with myocardial infarction in an American caucasian population. Annals of human genetics 2011 Jul 75 (4): 475-82. Wang Annabel Z, Li Lin, Zhang Bin, Shen Gong-Qing, Wang Qing Kenne |
The MTHFD1L gene rs11754661 marker is not associated with Alzheimer's disease in a sample of the Spanish population. Journal of Alzheimer's disease : JAD 2011 25 (1): 47-50. Ramírez-Lorca Reposo, Boada Mercé, Antúnez Carmen, López-Arrieta Jesús, Moreno-Rey Concha, Hernández Isabel, Marín Juan, Gayán Javier, González-Pérez Antonio, Alegret Montserrat, Tárraga Lluis, Real Luis M, Ruiz Agust |
Folate network genetic variation, plasma homocysteine, and global genomic methylation content: a genetic association study. BMC medical genetics 2011 12 (1): 150. Wernimont Susan M, Clark Andrew G, Stover Patrick J, Wells Martin T, Litonjua Augusto A, Weiss Scott T, Gaziano J Michael, Tucker Katherine L, Baccarelli Andrea, Schwartz Joel, Bollati Valentina, Cassano Patricia |
Association of genetic variants and incident coronary heart disease in multiethnic cohorts: the PAGE study. Circulation. Cardiovascular genetics 2011 Dec 4 (6): 661-72. Franceschini Nora, Carty Cara, B?zková Petra, Reiner Alex P, Garrett Tiana, Lin Yi, Vöckler Jens-S, Hindorff Lucia A, Cole Shelley A, Boerwinkle Eric, Lin Dan-Yu, Bookman Ebony, Best Lyle G, Bella Jonathan N, Eaton Charles, Greenland Philip, Jenny Nancy, North Kari E, Taverna Darin, Young Alicia M, Deelman Ewa, Kooperberg Charles, Psaty Bruce, Heiss Gerar |
Investigation of 95 variants identified in a genome-wide study for association with mortality after acute coronary syndrome. BMC medical genetics 2011 12 127. Morgan Thomas M, House John A, Cresci Sharon, Jones Philip, Allayee Hooman, Hazen Stanley L, Patel Yesha, Patel Riyaz S, Eapen Danny J, Waddy Salina P, Quyyumi Arshed A, Kleber Marcus E, März Winfried, Winkelmann Bernhard R, Boehm Bernhard O, Krumholz Harlan M, Spertus John |
Genotyping of a tri-allelic polymorphism by a novel melting curve assay in MTHFD1L: an association study of nonsyndromic Cleft in Ireland. BMC medical genetics 2012 13 (1): 29. Minguzzi Stefano, Molloy Anne M, Peadar Kirke, Mills James, Scott John M, Troendle James, Pangilinan Faith, Brody Lawrence, Parle-McDermott An |
Replication of the MTHFD1L gene association with late-onset Alzheimer's disease in a Northern Han Chinese population. Journal of Alzheimer's disease : JAD 2012 29 (3): 521-5. Ma Xiao-Ying, Yu Jin-Tai, Wu Zhong-Chen, Zhang Qun, Liu Qiu-Yan, Wang Hui-Fu, Wang Wei, Tan L |
Large scale association analysis identifies three susceptibility loci for coronary artery disease. PloS one 2011 6 (12): e29427. Saade Stephanie, Cazier Jean-Baptiste, Ghassibe-Sabbagh Michella, Youhanna Sonia, Badro Danielle A, Kamatani Yoichiro, Hager Jörg, Yeretzian Joumana S, El-Khazen Georges, Haber Marc, Salloum Angelique K, Douaihy Bouchra, Othman Raed, Shasha Nabil, Kabbani Samer, Bayeh Hamid El, Chammas Elie, Farrall Martin, Gauguier Dominique, Platt Daniel E, Zalloua Pierre A, |
Genetic polymorphism rs6922269 in the MTHFD1L gene is associated with survival and baseline active vitamin B12 levels in post-acute coronary syndromes patients. PloS one 2014 9 (3): e89029. Palmer Barry R, Slow Sandy, Ellis Katrina L, Pilbrow Anna P, Skelton Lorraine, Frampton Chris M, Palmer Suetonia C, Troughton Richard W, Yandle Tim G, Doughty Rob N, Whalley Gillian A, Lever Michael, George Peter M, Chambers Stephen T, Ellis Chris, Richards A Mark, Cameron Vicky |
Rs6922269 marker at the MTHFD1L gene predict cardiovascular mortality in males after acute coronary syndrome. Molecular biology reports 2015 Aug 42 (8): 1289-93. Hubacek J A, Stan?k V, Gebauerová M, Poledne R, Aschermann M, Skalická H, Matoušková J, Kruger A, P?ni?ka M, Hrabáková H, Veselka J, Hájek P, Lánská V, Adámková V, Pit?ha |
A family-based study of gene variants and maternal folate and choline in neuroblastoma: a report from the Children's Oncology Group. Cancer causes & control : CCC 2016 Aug . Mazul Angela L, Siega-Riz Anna Maria, Weinberg Clarice R, Engel Stephanie M, Zou Fei, Carrier Kathryn S, Basta Patricia V, Vaksman Zalman, Maris John M, Diskin Sharon J, Maxen Charlene, Naranjo Arlene, Olshan Andrew |
Distinct effects of folate pathway genes MTHFR and MTHFD1L on ruminative response style: a potential risk mechanism for depression. Translational psychiatry 2016 6 e745. Eszlari N, Kovacs D, Petschner P, Pap D, Gonda X, Elliott R, Anderson I M, Deakin J F W, Bagdy G, Juhasz |
A Genome-Wide Association Study and Complex Network Identify Four Core Hub Genes in Bipolar Disorder. International journal of molecular sciences 2017 Dec 18 (12): . Xie Zengyan, Yang Xianyan, Deng Xiaoya, Ma Mingyue, Shu Kunxi |
Influence of SH2B3, MTHFD1L, GGCX, and ITGB3 Gene Polymorphisms on theVariability on Warfarin Dosage Requirements and Susceptibility to CVD in the Jordanian Population. Journal of personalized medicine 2020 9 10 (3): . Al-Eitan Laith N, Almasri Ayah Y, Khasawneh Rame H, Alghamdi Mansour |
Association of the PSRC1 rs599839 Variant with Coronary Artery Disease in a Mexican Population. Medicina (Kaunas, Lithuania) 2020 8 56 (9): . Rodríguez-Arellano Martha Eunice, Solares-Tlapechco Jacqueline, Costa-Urrutia Paula, Cárdenas-Hernández Helios, Vallejo-Gómez Marajael, Granados Julio, Salas-Padilla Serg |
Genetic Variants in One-Carbon Metabolism Pathway Predict Survival Outcomes of Early-Stage Non-Small Cell Lung Cancer. Oncology 2020 Aug 1-8. Do Sook Kyung, Choi Sun Ha, Lee Shin Yup, Choi Jin Eun, Kang Hyo-Gyoung, Hong Mi Jeong, Kim Ji Hyun, Baek Sun Ah, Lee Jang Hyuck, Lee Won Kee, Do Young Woo, Lee Eung Bae, Shin Kyung Min, Jeong Ji Yun, Lee Yong Hoon, Seo Hyewon, Yoo Seung Soo, Lee Jaehee, Cha Seung Ick, Kim Chang Ho, Seok Yangki, Cho Sukki, Jheon Sanghoon, Park Jae Yo |
Vitamin B-related Gene Polymorphisms and Cardiovascular Disease. Endocrine, metabolic & immune disorders drug targets 2022 3 22 (10): 979-984. Katsa Maria Efthymia, Gil Andrea Paola Roj |
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- Page last updated:Apr 22, 2024
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