Human Genome Epidemiology Literature Finder
Records 1 - 8 (of 8 Records) |
Query Trace: PRMT8[original query] |
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Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts.
Nature genetics 2009 Jan 41 (1): 47-55. Aulchenko Yurii S, Ripatti Samuli, Lindqvist Ida, Boomsma Dorret, Heid Iris M, Pramstaller Peter P, Penninx Brenda W J H, Janssens A Cecile J W, Wilson James F, Spector Tim, Martin Nicholas G, Pedersen Nancy L, Kyvik Kirsten Ohm, Kaprio Jaakko, Hofman Albert, Freimer Nelson B, Jarvelin Marjo-Riitta, Gyllensten Ulf, Campbell Harry, Rudan Igor, Johansson Asa, Marroni Fabio, Hayward Caroline, Vitart Veronique, Jonasson Inger, Pattaro Cristian, Wright Alan, Hastie Nick, Pichler Irene, Hicks Andrew A, Falchi Mario, Willemsen Gonneke, Hottenga Jouke-Jan, de Geus Eco J C, Montgomery Grant W, Whitfield John, Magnusson Patrik, Saharinen Juha, Perola Markus, Silander Kaisa, Isaacs Aaron, Sijbrands Eric J G, Uitterlinden Andre G, Witteman Jacqueline C M, Oostra Ben A, Elliott Paul, Ruokonen Aimo, Sabatti Chiara, Gieger Christian, Meitinger Thomas, Kronenberg Florian, Döring Angela, Wichmann H-Erich, Smit Johannes H, McCarthy Mark I, van Duijn Cornelia M, Peltonen Leena, |
Dense genotyping of candidate gene loci identifies variants associated with high-density lipoprotein cholesterol. Circulation. Cardiovascular genetics 2011 Apr 4 (2): 145-55. Edmondson Andrew C, Braund Peter S, Stylianou Ioannis M, Khera Amit V, Nelson Christopher P, Wolfe Megan L, Derohannessian Stephanie L, Keating Brendan J, Qu Liming, He Jing, Tobin Martin D, Tomaszewski Maciej, Baumert Jens, Klopp Norman, Döring Angela, Thorand Barbara, Li Mingyao, Reilly Muredach P, Koenig Wolfgang, Samani Nilesh J, Rader Daniel |
Association between genetic variants in DNA and histone methylation and telomere length. PloS one 2012 7 (7): 7. Kim S, Parks CG, Xu Z, Carswell G, Deroo LA, Sandler DP, Taylor JA |
Insight in glioma susceptibility through an analysis of 6p22.3, 12p13.33-12.1, 17q22-23.2 and 18q23 SNP genotypes in familial and non-familial glioma. Human genetics 2012 Sep 131 (9): 1507-17. Liu Yanhong, Melin Beatrice S, Rajaraman Preetha, Wang Zhaoming, Linet Martha, Shete Sanjay, Amos Christopher I, Lau Ching C, Scheurer Michael E, Tsavachidis Spiridon, Armstrong Georgina N, Houlston Richard S, Hosking Fay J, Claus Elizabeth B, Barnholtz-Sloan Jill, Lai Rose, Il'yasova Dora, Schildkraut Joellen, Sadetzki Siegal, Johansen Christoffer, Bernstein Jonine L, Olson Sara H, Jenkins Robert B, LaChance Daniel, Vick Nicholas A, Wrensch Margaret, Davis Faith, McCarthy Bridget J, Andersson Ulrika, Thompson Patricia A, Chanock Stephen, , Bondy Melissa |
Mutations in protein N-arginine methyltransferases are not the cause of FTLD-FUS. Neurobiology of aging 2013 Sep 34 (9): 2235.e11-3. Ravenscroft Thomas A, Baker Matt C, Rutherford Nicola J, Neumann Manuela, Mackenzie Ian R, Josephs Keith A, Boeve Bradley F, Petersen Ronald, Halliday Glenda M, Kril Jillian, van Swieten John C, Seeley William W, Dickson Dennis W, Rademakers Ro |
Identification of Key Genes and Pathways Associated with RUNX1 Mutations in Acute Myeloid Leukemia Using Bioinformatics Analysis. Medical science monitor : international medical journal of experimental and clinical research 2018 Oct 24 7100-7108. Zhu Fangxiao, Huang Rui, Li Jing, Liao Xiwen, Huang Yumei, Lai Yongro |
Associations of BRAP polymorphisms with the risk of alcohol dependence and scores on the Alcohol Use Disorders Identification Test. Neuropsychiatric disease and treatment 2019 15 83-94. Kim Jee Wook, Choe Young Min, Shin Joong-Gon, Park Byung Lae, Shin Hyung-Doo, Choi Ihn-Geun, Lee Boung Ch |
Screening and identifying a novel M-MDSCs-related gene signature for predicting prognostic risk and immunotherapeutic responses in patients with lung adenocarcinoma. Frontiers in genetics 2023 1 13 989141. Wang Geng-Chong, Zhou Mi, Zhang Yan, Cai Hua-Man, Chiang Seok-Theng, Chen Qi, Han Tian-Zhen, Li Rong-X |
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