Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 35 Records) |
Query Trace: GALNT2[original query] |
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A polygenic basis for four classical Fredrickson hyperlipoproteinemia phenotypes that are characterized by hypertriglyceridemia. Human molecular genetics 2009 Nov 18 (21): 4189-94. Hegele Robert A, Ban Matthew R, Hsueh Neil, Kennedy Brooke A, Cao Henian, Zou Guang Yong, Anand Sonia, Yusuf Salim, Huff Murray W, Wang Ji |
Biological, clinical and population relevance of 95 loci for blood lipids.
Nature 2010 Aug 466 (7307): 707-13. Teslovich Tanya M, Musunuru Kiran, Smith Albert V, Edmondson Andrew C, Stylianou Ioannis M, Koseki Masahiro, Pirruccello James P, Ripatti Samuli, Chasman Daniel I, Willer Cristen J, Johansen Christopher T, Fouchier Sigrid W, Isaacs Aaron, Peloso Gina M, Barbalic Maja, Ricketts Sally L, Bis Joshua C, Aulchenko Yurii S, Thorleifsson Gudmar, Feitosa Mary F, Chambers John, Orho-Melander Marju, Melander Olle, Johnson Toby, Li Xiaohui, Guo Xiuqing, Li Mingyao, Shin Cho Yoon, Jin Go Min, Jin Kim Young, Lee Jong-Young, Park Taesung, Kim Kyunga, Sim Xueling, Twee-Hee Ong Rick, Croteau-Chonka Damien C, Lange Leslie A, Smith Joshua D, Song Kijoung, Hua Zhao Jing, Yuan Xin, Luan Jian'an, Lamina Claudia, Ziegler Andreas, Zhang Weihua, Zee Robert Y L, Wright Alan F, Witteman Jacqueline C M, Wilson James F, Willemsen Gonneke, Wichmann H-Erich, Whitfield John B, Waterworth Dawn M, Wareham Nicholas J, Waeber Gérard, Vollenweider Peter, Voight Benjamin F, Vitart Veronique, Uitterlinden Andre G, Uda Manuela, Tuomilehto Jaakko, Thompson John R, Tanaka Toshiko, Surakka Ida, Stringham Heather M, Spector Tim D, Soranzo Nicole, Smit Johannes H, Sinisalo Juha, Silander Kaisa, Sijbrands Eric J G, Scuteri Angelo, Scott James, Schlessinger David, Sanna Serena, Salomaa Veikko, Saharinen Juha, Sabatti Chiara, Ruokonen Aimo, Rudan Igor, Rose Lynda M, Roberts Robert, Rieder Mark, Psaty Bruce M, Pramstaller Peter P, Pichler Irene, Perola Markus, Penninx Brenda W J H, Pedersen Nancy L, Pattaro Cristian, Parker Alex N, Pare Guillaume, Oostra Ben A, O'Donnell Christopher J, Nieminen Markku S, Nickerson Deborah A, Montgomery Grant W, Meitinger Thomas, McPherson Ruth, McCarthy Mark I, McArdle Wendy, Masson David, Martin Nicholas G, Marroni Fabio, Mangino Massimo, Magnusson Patrik K E, Lucas Gavin, Luben Robert, Loos Ruth J F, Lokki Marja-Liisa, Lettre Guillaume, Langenberg Claudia, Launer Lenore J, Lakatta Edward G, Laaksonen Reijo, Kyvik Kirsten O, Kronenberg Florian, König Inke R, Khaw Kay-Tee, Kaprio Jaakko, Kaplan Lee M, Johansson Asa, Jarvelin Marjo-Riitta, Janssens A Cecile J W, Ingelsson Erik, Igl Wilmar, Kees Hovingh G, Hottenga Jouke-Jan, Hofman Albert, Hicks Andrew A, Hengstenberg Christian, Heid Iris M, Hayward Caroline, Havulinna Aki S, Hastie Nicholas D, Harris Tamara B, Haritunians Talin, Hall Alistair S, Gyllensten Ulf, Guiducci Candace, Groop Leif C, Gonzalez Elena, Gieger Christian, Freimer Nelson B, Ferrucci Luigi, Erdmann Jeanette, Elliott Paul, Ejebe Kenechi G, Döring Angela, Dominiczak Anna F, Demissie Serkalem, Deloukas Panagiotis, de Geus Eco J C, de Faire Ulf, Crawford Gabriel, Collins Francis S, Chen Yii-der I, Caulfield Mark J, Campbell Harry, Burtt Noel P, Bonnycastle Lori L, Boomsma Dorret I, Boekholdt S Matthijs, Bergman Richard N, Barroso Inês, Bandinelli Stefania, Ballantyne Christie M, Assimes Themistocles L, Quertermous Thomas, Altshuler David, Seielstad Mark, Wong Tien Y, Tai E-Shyong, Feranil Alan B, Kuzawa Christopher W, Adair Linda S, Taylor Herman A, Borecki Ingrid B, Gabriel Stacey B, Wilson James G, Holm Hilma, Thorsteinsdottir Unnur, Gudnason Vilmundur, Krauss Ronald M, Mohlke Karen L, Ordovas Jose M, Munroe Patricia B, Kooner Jaspal S, Tall Alan R, Hegele Robert A, Kastelein John J P, Schadt Eric E, Rotter Jerome I, Boerwinkle Eric, Strachan David P, Mooser Vincent, Stefansson Kari, Reilly Muredach P, Samani Nilesh J, Schunkert Heribert, Cupples L Adrienne, Sandhu Manjinder S, Ridker Paul M, Rader Daniel J, van Duijn Cornelia M, Peltonen Leena, Abecasis Gonçalo R, Boehnke Michael, Kathiresan Sek |
Analysis of lipid pathway genes indicates association of sequence variation near SREBF1/TOM1L2/ATPAF2 with dementia risk. Human molecular genetics 2010 May 19 (10): 2068-78. Reynolds Chandra A, Hong Mun-Gwan, Eriksson Ulrika K, Blennow Kaj, Wiklund Fredrik, Johansson Boo, Malmberg Bo, Berg Stig, Alexeyenko Andrey, Grönberg Henrik, Gatz Margaret, Pedersen Nancy L, Prince Jonathan |
Investigation of variants identified in caucasian genome-wide association studies for plasma high-density lipoprotein cholesterol and triglycerides levels in Mexican dyslipidemic study samples. Circulation. Cardiovascular genetics 2010 Feb 3 (1): 31-8. Weissglas-Volkov Daphna, Aguilar-Salinas Carlos A, Sinsheimer Janet S, Riba Laura, Huertas-Vazquez Adriana, Ordoñez-Sánchez Maria L, Rodriguez-Guillen Rosario, Cantor Rita M, Tusie-Luna Teresa, Pajukanta Päi |
Triglyceride level modifying functional variants of GALTN2 and MLXIPL in patients with ischaemic stroke. European journal of neurology : the official journal of the European Federation of Neurological Societies 2010 Aug 17 (8): 1033-9. Polgár N, Járomi L, Csöngei V, Maász A, Sipeky C, Sáfrány E, Szabó M, Melegh |
Association of the GALNT2 gene polymorphisms and several environmental factors with serum lipid levels in the Mulao and Han populations. Lipids in health and disease 2011 10 (1): 160. Li Qing, Yin Rui-Xing, Yan Ting-Ting, Miao Lin, Cao Xiao-Li, Hu Xi-Jiang, Aung Lynn Htet Htet, Wu Dong-Feng, Wu Jin-Zhen, Lin Wei-Xio |
TLE1 modifies the effects of NOD2 in the pathogenesis of Crohn's disease. Gastroenterology 2011 Sep 141 (3): 972-981.e1-2. Nimmo Elaine R, Stevens Craig, Phillips Anne M, Smith Amanda, Drummond Hazel E, Noble Colin L, Quail Michael, Davies Gail, Aldhous Marian C, Wilson David C, Satsangi Ja |
Meta analysis of candidate gene variants outside the LPA locus with Lp(a) plasma levels in 14,500 participants of six White European cohorts. Atherosclerosis 2011 Aug 217 (2): 447-51. Zabaneh Delilah, Kumari Meena, Sandhu Manj, Wareham Nick, Wainwright Nick, Papamarkou Theodore, Hopewell Jemma, Clarke Robert, Li KaWah, Palmen Jutta, Talmud Philippa J, Kronenberg Florian, Lamina Claudia, Summerer Monika, Paulweber Bernhard, Price Jackie, Fowkes Gerry, Stewart Marlene, Drenos Fotios, Shah Sonia, Shah Tina, Casas Juan-Pablo, Kivimaki Mika, Whittaker John, Hingorani Aroon D, Humphries Steve |
Association of GWAS-based candidate genes with HDL-cholesterol levels before and after bariatric surgery in the Swedish obese subjects study. The Journal of clinical endocrinology and metabolism 2011 Jun 96 (6): E953-7. Sarzynski Mark A, Jacobson Peter, Rankinen Tuomo, Carlsson Björn, Sjöström Lars, Carlsson Lena M S, Bouchard Clau |
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 |
Segregation of LIPG, CETP, and GALNT2 mutations in Caucasian families with extremely high HDL cholesterol. PloS one 2012 7 (8): e37437. Tietjen Ian, Hovingh G Kees, Singaraja Roshni R, Radomski Chris, Barhdadi Amina, McEwen Jason, Chan Elden, Mattice Maryanne, Legendre Annick, Franchini Patrick L, Dubé Marie-Pierre, Kastelein John J P, Hayden Michael |
Phenome-wide association study (PheWAS) for detection of pleiotropy within the Population Architecture using Genomics and Epidemiology (PAGE) Network. PLoS genetics 2013 Jan 9 (1): 1. Pendergrass SA, Brown-Gentry K, Dudek S, Frase A, Torstenson ES, Goodloe R, Ambite JL, Avery CL, Buyske S, B?žková P, Deelman E, Fesinmeyer MD, Haiman CA, Heiss G, Hindorff LA, Hsu CN, Jackson RD, Kooperberg C, Le Marchand L, Lin Y, Matise TC, Monroe KR, Moreland L, Park SL, Reiner A, Wallace R, Wilkens LR, Crawford DC, Ritchie MD |
Evaluation of links between high-density lipoprotein genetics, functionality, and aortic valve stenosis risk in humans. Arteriosclerosis, thrombosis, and vascular biology 2014 Feb 34 (2): 457-62. Arsenault Benoit J, Dubé Marie-Pierre, Brodeur Mathieu R, de Oliveira Moraes Adriana Benjamin, Lavoie Véronique, Kernaleguen Anne-Elen, Guauque-Olarte Sandra, Mathieu Patrick, Pibarot Philippe, Messika-Zeitoun David, Bossé Yohan, Rhainds David, Rhéaume Eric, Tardif Jean-Clau |
Atenolol induced HDL-C change in the pharmacogenomic evaluation of antihypertensive responses (PEAR) study. PloS one 2013 8 (10): e76984. McDonough Caitrin W, Gillis Nancy K, Alsultan Abdullah, Chang Shin-Wen, Kawaguchi-Suzuki Marina, Lang Jason E, Shahin Mohamed Hossam A, Buford Thomas W, El Rouby Nihal M, Sá Ana C C, Langaee Taimour Y, Gums John G, Chapman Arlene B, Cooper-DeHoff Rhonda M, Turner Stephen T, Gong Yan, Johnson Julie |
Genome-wide association study of serum albumin:globulin ratio in Korean populations.
Journal of human genetics 2013 Mar 58 (3): 174-7. Hong Kyung-Won, Jin Hyun-Seok, Song Daesub, Kwak Hye-Kyoung, Kim Sung Soo, Kim Yeonju |
Adiposity significantly modifies genetic risk for dyslipidemia. Journal of lipid research 2014 Nov 55 (11): 2416-22. Cole Christopher B, Nikpay Majid, Lau Paulina, Stewart Alexandre F R, Davies Robert W, Wells George A, Dent Robert, McPherson Ru |
Identification of four novel genes contributing to familial elevated plasma HDL cholesterol in humans. Journal of lipid research 2014 Jun 55 (8): 1693-1701. Singaraja Roshni R, Tietjen Ian, Hovingh G Kees, Franchini Patrick L, Radomski Chris, Wong Kenny, vanHeek Margaret, Stylianou Ioannis M, Lin Linus, Wang Liangsu, Mitnaul Lyndon, Hubbard Brian, Winther Michael, Mattice Maryanne, Legendre Annick, Sherrington Robin, Kastelein John J, Akinsanya Karen, Plump Andrew, Hayden Michael |
Genome-wide association study on progression of carotid artery intima media thickness over 10 years in a Chinese cohort.
Atherosclerosis 2015 Nov 243 (1): 30-7. Xie Gaoqiang, Myint Phyo Kyaw, Voora Deepak, Laskowitz Daniel T, Shi Ping, Ren Fuxiu, Wang Hao, Yang Ying, Huo Yong, Gao Wei, Wu Yangfe |
Functional variants of lipid level modifier MLXIPL, GCKR, GALNT2, CILP2, ANGPTL3 and TRIB1 genes in healthy Roma and Hungarian populations. Pathology oncology research : POR 2015 Jul 21 (3): 743-9. Sumegi Katalin, Jaromi Luca, Magyari Lili, Kovesdi Erzsebet, Duga Balazs, Szalai Renata, Maasz Anita, Matyas Petra, Janicsek Ingrid, Melegh Be |
Association between the DOCK7, PCSK9 and GALNT2 Gene Polymorphisms and Serum Lipid levels. Scientific reports 2016 6 19079. Guo Tao, Yin Rui-Xing, Huang Feng, Yao Li-Mei, Lin Wei-Xiong, Pan Shang-Li |
HDL-cholesterol concentration in pregnant Chinese Han women of late second trimester associated with genetic variants in CETP, ABCA1, APOC3, and GALNT2. Oncotarget 2017 Aug 8 (34): 56737-56746. Cui Mingxuan, Li Wei, Ma Liangkun, Ping Fan, Liu Juntao, Wu Xueyan, Mao Jiangfeng, Wang Xi, Nie M |
Multiplexed Targeted Resequencing Identifies Coding and Regulatory Variation Underlying Phenotypic Extremes of High-Density Lipoprotein Cholesterol in Humans. Circulation. Genomic and precision medicine 2018 7 11 (7): e002070. Khetarpal Sumeet A, Babb Paul L, Zhao Wei, Hancock-Cerutti William F, Brown Christopher D, Rader Daniel J, Voight Benjamin |
Epigenome wide association study of SNP-CpG interactions on changes in triglyceride levels after pharmaceutical intervention: a GAW20 analysis. BMC proceedings 2018 10 12 (Suppl 9): 58. Veenstra Jenna, Kalsbeek Anya, Koster Karissa, Ryder Nathan, Bos Abbey, Huisman Jordan, VanderBerg Lucas, VanderWoude Jason, Tintle Nathan |
Quantile-dependent expressivity of postprandial lipemia. PloS one 2020 15 (2): e0229495. Williams Paul |
Quantile-Dependent Expressivity and Gene-Lifestyle Interactions Involving High-Density Lipoprotein Cholesterol. Lifestyle genomics 2020 12 14 (1): 1-19. Williams Paul |
GALNT2 Gene Variant rs4846914 Is Associated with Insulin and Insulin Resistance Depending on BMI in PCOS Patients: a Case-Control Study. Reproductive sciences (Thousand Oaks, Calif.) 2020 Nov . Chen Jinxin, Guan Linbo, Liu Hongwei, Liu Qingqing, Fan Ping, Bai Hu |
Genetic risk model for in-stent restenosis of second-and third-generation drug-eluting stents. iScience 2021 Sep 24 (9): 103082. Liu Yen-Wen, Huang Mu-Shiang, Hsu Ling-Wei, Chang Hsien-Yuan, Lee Cheng-Han, Lee Chi-Ying, Chen Dao-Peng, Li Yi-Heng, Chao Ting-Hsin, Su Pei-Fang, Shen Meng-Ru, Liu Ping-Y |
Maternal GALNT2 Variations Affect Blood Pressure, Atherogenic Index, and Fetal Growth, Depending on BMI in Gestational Diabetes Mellitus. Frontiers in endocrinology 2021 12 690229. Guan Linbo, Fan Ping, Liu Xinghui, Zhou Mi, Wu Yujie, Liu Rui, Liu Yu, Bai Hu |
Role of a novel mouse mutant of the Galnt2 gene in otitis media. Frontiers in neurology 2023 3 13 1054704. Ma Weijun, Li Heng, Hu Juan, Gao Ying, Lv Hui, Zhang Xiaotong, Zhang Qing, Xu Min, Cheng Yi |
Apolipoprotein-CIII O-Glycosylation, a Link between GALNT2 and Plasma Lipids. International journal of molecular sciences 2023 10 24 (19): . Annemieke Naber, Daniel Demus, Roderick Slieker, Simone Nicolardi, Joline W J Beulens, Petra J M Elders, Aloysius G Lieverse, Eric J G Sijbrands, Leen M 't Hart, Manfred Wuhrer, Mandy van Ho |
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