Human Genome Epidemiology Literature Finder
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Records 1 - 19 (of 19 Records) |
| Query Trace: Mthfr[original query] |
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Polygenic prediction of preeclampsia and gestational hypertension.
Nature medicine 2023 5 29 (6): 1540-1549. Honigberg Michael C, Truong Buu, Khan Raiyan R, Xiao Brenda, Bhatta Laxmi, Vy Ha My T, Guerrero Rafael F, Schuermans Art, Selvaraj Margaret Sunitha, Patel Aniruddh P, Koyama Satoshi, Cho So Mi Jemma, Vellarikkal Shamsudheen Karuthedath, Trinder Mark, Urbut Sarah M, Gray Kathryn J, Brumpton Ben M, Patil Snehal, Zöllner Sebastian, Antopia Mariah C, Saxena Richa, Nadkarni Girish N, Do Ron, Yan Qi, Pe'er Itsik, Verma Shefali Setia, Gupta Rajat M, Haas David M, Martin Hilary C, van Heel David A, Laisk Triin, Natarajan Prade |
| Genome-wide association with bone mass and geometry in the Framingham Heart Study.
BMC medical genetics 2007 8 Suppl 1 S14. Kiel Douglas P, Demissie Serkalem, Dupuis Josée, Lunetta Kathryn L, Murabito Joanne M, Karasik Dav |
| Genome-wide significant predictors of metabolites in the one-carbon metabolism pathway.
Human molecular genetics 2009 Dec 18 (23): 4677-87. Hazra Aditi, Kraft Peter, Lazarus Ross, Chen Constance, Chanock Stephen J, Jacques Paul, Selhub Jacob, Hunter David |
| Genome-wide association study identifies eight loci associated with blood pressure.
Nature genetics 2009 Jun 41 (6): 666-76. Newton-Cheh Christopher, Johnson Toby, Gateva Vesela, Tobin Martin D, Bochud Murielle, Coin Lachlan, Najjar Samer S, Zhao Jing Hua, Heath Simon C, Eyheramendy Susana, Papadakis Konstantinos, Voight Benjamin F, Scott Laura J, Zhang Feng, Farrall Martin, Tanaka Toshiko, Wallace Chris, Chambers John C, Khaw Kay-Tee, Nilsson Peter, van der Harst Pim, Polidoro Silvia, Grobbee Diederick E, Onland-Moret N Charlotte, Bots Michiel L, Wain Louise V, Elliott Katherine S, Teumer Alexander, Luan Jian'an, Lucas Gavin, Kuusisto Johanna, Burton Paul R, Hadley David, McArdle Wendy L, , Brown Morris, Dominiczak Anna, Newhouse Stephen J, Samani Nilesh J, Webster John, Zeggini Eleftheria, Beckmann Jacques S, Bergmann Sven, Lim Noha, Song Kijoung, Vollenweider Peter, Waeber Gerard, Waterworth Dawn M, Yuan Xin, Groop Leif, Orho-Melander Marju, Allione Alessandra, Di Gregorio Alessandra, Guarrera Simonetta, Panico Salvatore, Ricceri Fulvio, Romanazzi Valeria, Sacerdote Carlotta, Vineis Paolo, Barroso Inês, Sandhu Manjinder S, Luben Robert N, Crawford Gabriel J, Jousilahti Pekka, Perola Markus, Boehnke Michael, Bonnycastle Lori L, Collins Francis S, Jackson Anne U, Mohlke Karen L, Stringham Heather M, Valle Timo T, Willer Cristen J, Bergman Richard N, Morken Mario A, Döring Angela, Gieger Christian, Illig Thomas, Meitinger Thomas, Org Elin, Pfeufer Arne, Wichmann H Erich, Kathiresan Sekar, Marrugat Jaume, O'Donnell Christopher J, Schwartz Stephen M, Siscovick David S, Subirana Isaac, Freimer Nelson B, Hartikainen Anna-Liisa, McCarthy Mark I, O'Reilly Paul F, Peltonen Leena, Pouta Anneli, de Jong Paul E, Snieder Harold, van Gilst Wiek H, Clarke Robert, Goel Anuj, Hamsten Anders, Peden John F, Seedorf Udo, Syvänen Ann-Christine, Tognoni Giovanni, Lakatta Edward G, Sanna Serena, Scheet Paul, Schlessinger David, Scuteri Angelo, Dörr Marcus, Ernst Florian, Felix Stephan B, Homuth Georg, Lorbeer Roberto, Reffelmann Thorsten, Rettig Rainer, Völker Uwe, Galan Pilar, Gut Ivo G, Hercberg Serge, Lathrop G Mark, Zelenika Diana, Deloukas Panos, Soranzo Nicole, Williams Frances M, Zhai Guangju, Salomaa Veikko, Laakso Markku, Elosua Roberto, Forouhi Nita G, Völzke Henry, Uiterwaal Cuno S, van der Schouw Yvonne T, Numans Mattijs E, Matullo Giuseppe, Navis Gerjan, Berglund Göran, Bingham Sheila A, Kooner Jaspal S, Connell John M, Bandinelli Stefania, Ferrucci Luigi, Watkins Hugh, Spector Tim D, Tuomilehto Jaakko, Altshuler David, Strachan David P, Laan Maris, Meneton Pierre, Wareham Nicholas J, Uda Manuela, Jarvelin Marjo-Riitta, Mooser Vincent, Melander Olle, Loos Ruth J F, Elliott Paul, Abecasis Gonçalo R, Caulfield Mark, Munroe Patricia |
| Genome-wide association study of vitamin B6, vitamin B12, folate, and homocysteine blood concentrations.
American journal of human genetics 2009 Mar . Tanaka T, Scheet P, Giusti B, Bandinelli S, Piras MG, Usala G, Lai S, Mulas A, Corsi AM, Vestrini A, Sofi F, Gori AM, Abbate R, Guralnik J, Singleton A, Abecasis GR, Schlessinger D, Uda M, Ferrucci L |
| Novel associations of CPS1, MUT, NOX4, and DPEP1 with plasma homocysteine in a healthy population: a genome-wide evaluation of 13 974 participants in the Women's Genome Health Study.
Circulation. Cardiovascular genetics 2009 Apr 2 (2): 142-50. Paré Guillaume, Chasman Daniel I, Parker Alexander N, Zee Robert R Y, Mälarstig Anders, Seedorf Udo, Collins Rory, Watkins Hugh, Hamsten Anders, Miletich Joseph P, Ridker Paul |
| Genome-wide association study of homocysteine levels in Filipinos provides evidence for CPS1 in women and a stronger MTHFR effect in young adults.
Human molecular genetics 2010 May 19 (10): 2050-8. Lange Leslie A, Croteau-Chonka Damien C, Marvelle Amanda F, Qin Li, Gaulton Kyle J, Kuzawa Christopher W, McDade Thomas W, Wang Yunfei, Li Yun, Levy Shawn, Borja Judith B, Lange Ethan M, Adair Linda S, Mohlke Karen |
| Genome-wide association analysis and fine mapping of NT-proBNP level provide novel insight into the role of the MTHFR-CLCN6-NPPA-NPPB gene cluster.
Human molecular genetics 2011 Apr 20 (8): 1660-71. Del Greco M Fabiola, Pattaro Cristian, Luchner Andreas, Pichler Irene, Winkler Thomas, Hicks Andrew A, Fuchsberger Christian, Franke Andre, Melville Scott A, Peters Annette, Wichmann H Erich, Schreiber Stefan, Heid Iris M, Krawczak Michael, Minelli Cosetta, Wiedermann Christian J, Pramstaller Peter |
| Common genetic loci influencing plasma homocysteine concentrations and their effect on risk of coronary artery disease.
The American journal of clinical nutrition 2013 Sep 98 (3): 668-76. van Meurs Joyce B J, Pare Guillaume, Schwartz Stephen M, Hazra Aditi, Tanaka Toshiko, Vermeulen Sita H, Cotlarciuc Ioana, Yuan Xin, Mälarstig Anders, Bandinelli Stefania, Bis Joshua C, Blom Henk, Brown Morris J, Chen Constance, Chen Yii-Der, Clarke Robert J, Dehghan Abbas, Erdmann Jeanette, Ferrucci Luigi, Hamsten Anders, Hofman Albert, Hunter David J, Goel Anuj, Johnson Andrew D, Kathiresan Sekar, Kampman Ellen, Kiel Douglas P, Kiemeney Lambertus A L M, Chambers John C, Kraft Peter, Lindemans Jan, McKnight Barbara, Nelson Christopher P, O'Donnell Christopher J, Psaty Bruce M, Ridker Paul M, Rivadeneira Fernando, Rose Lynda M, Seedorf Udo, Siscovick David S, Schunkert Heribert, Selhub Jacob, Ueland Per M, Vollenweider Peter, Waeber Gérard, Waterworth Dawn M, Watkins Hugh, Witteman Jacqueline C M, den Heijer Martin, Jacques Paul, Uitterlinden Andre G, Kooner Jaspal S, Rader Dan J, Reilly Muredach P, Mooser Vincent, Chasman Daniel I, Samani Nilesh J, Ahmadi Kourosh |
| Whole-exome SNP array identifies 15 new susceptibility loci for psoriasis.
Nature communications 2015 6 6793. Zuo Xianbo, Sun Liangdan, Yin Xianyong, Gao Jinping, Sheng Yujun, Xu Jinhua, Zhang Jianzhong, He Chundi, Qiu Ying, Wen Guangdong, Tian Hongqing, Zheng Xiaodong, Liu Shengxiu, Wang Wenjun, Li Weiran, Cheng Yuyan, Liu Longdan, Chang Yan, Wang Zaixing, Li Zenggang, Li Longnian, Wu Jianping, Fang Ling, Shen Changbing, Zhou Fusheng, Liang Bo, Chen Gang, Li Hui, Cui Yong, Xu Aie, Yang Xueqin, Hao Fei, Xu Limin, Fan Xing, Li Yuzhen, Wu Rina, Wang Xiuli, Liu Xiaoming, Zheng Min, Song Shunpeng, Ji Bihua, Fang Hong, Yu Jianbin, Sun Yongxin, Hui Yan, Zhang Furen, Yang Rongya, Yang Sen, Zhang Xuej |
| Genome-Wide Association Study of Loneliness Demonstrates a Role for Common Variation.
Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology 2016 Sep . Gao Jianjun, Davis Lea K, Hart Amy B, Sanchez-Roige Sandra, Han Lide, Cacioppo John T, Palmer Abraham |
| Genetic signatures of high-altitude adaptation in Tibetans.
Proceedings of the National Academy of Sciences of the United States of America 2017 04 114 (16): 4189-4194. Yang Jian, Jin Zi-Bing, Chen Jie, Huang Xiu-Feng, Li Xiao-Man, Liang Yuan-Bo, Mao Jian-Yang, Chen Xin, Zheng Zhili, Bakshi Andrew, Zheng Dong-Dong, Zheng Mei-Qin, Wray Naomi R, Visscher Peter M, Lu Fan, Qu J |
| 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 |
| Identification of three novel loci of ALDH2 Gene for Serum Folate levels in a Male Chinese Population by Genome-Wide Association Study.
Gene 2018 Jun . Deng Caiwang, Tang Shaomei, Huang Xiaoliang, Gao Jiamin, Tian Jiarong, Zhou Xianguo, Xie Yuanliang, Liao Ming, Mo Zengnan, Wang Qiuy |
| The 677C?T variant of MTHFR is the major genetic modifier of biomarkers of folate status in a young, healthy Irish population.
The American journal of clinical nutrition 2018 Dec 108 (6): 1334-1341. Shane Barry, Pangilinan Faith, Mills James L, Fan Ruzong, Gong Tingting, Cropp Cheryl D, Kim Yoonhee, Ueland Per M, Bailey-Wilson Joan E, Wilson Alexander F, Brody Lawrence C, Molloy Anne |
| Impact of natriuretic peptide polymorphisms on diastolic and metabolic function in a populational cohort: insights from the STANISLAS cohort.
ESC heart failure 2021 Nov . Xhaard Constance, Rouget Raphaël, Vodovar Nicolas, Le Floch Edith, Dandine-Roulland Claire, Wagner Sandra, Bacq-Daian Delphine, Thuillier Quentin, Boivin Jean-Marc, Branlant Christiane, Deleuze Jean-François, Behm-Ansmant Isabelle, Zannad Faiez, Rossignol Patrick, Girerd Nicol |
| Exome-Wide Association Study Identifies East Asian-Specific Missense Variant MTHFR C136T Influencing Homocysteine Levels in Chinese Populations RH: ExWAS of tHCY in a Chinese Population.
Frontiers in genetics 2021 12 717621. Liu Tianzi, Momin Mohetaboer, Zhou Huiyue, Zheng Qiwen, Fan Fangfang, Jia Jia, Liu Mengyuan, Bao Minghui, Li Jianping, Huo Yong, Liu Jialin, Zhang Yaning, Mao Xuemei, Han Xiao, Hu Zhiyuan, Zeng Changqing, Liu Fan, Zhang Y |
| Prominence of NUDT15 genetic variation associated with 6-mercaptopurine tolerance in a genome-wide association study of Japanese children with acute lymphoblastic leukaemia.
British journal of haematology 2022 Aug . Tanaka Yoichi, Urayama Kevin Y, Mori Makiko, Arakawa Yuki, Hasegawa Daisuke, Noguchi Yasushi, Yanagimachi Masakatsu, Keino Dai, Ota Setsuo, Akahane Koshi, Inukai Takeshi, Hangai Mayumi, Kawaguchi Takahisa, Takagi Masatoshi, Koh Katsuyoshi, Matsuda Fumihiko, Manabe Atsus |
| Genome-wide Association Study of Methotrexate-Induced Liver Injury in Rheumatoid Arthritis Patients.
Clinical pharmacology and therapeutics 2023 1 . Eektimmerman Frank, Swen Jesse J, den Broeder Alfons A, Hazes Johanna M W, Kurreeman Fina S, Verstappen Suzanne M M, Nair Nisha, Pawlik Andrzej, Nurmohamed Mike T, Dolžan Vita, Böhringer Stefan, Allaart Cornelia F, Guchelaar Henk-J |
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