Human Genome Epidemiology Literature Finder
Records 1 - 11 (of 11 Records) |
Query Trace: PBX4[original query] |
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Polymorphisms at newly identified lipid-associated loci are associated with blood lipids and cardiovascular disease in an Asian Malay population. Journal of lipid research 2009 Mar 50 (3): 514-20. Tai E Shyong, Sim Xue Ling, Ong Twee Hee, Wong Tien Yin, Saw Seang Mei, Aung Tin, Kathiresan Sekar, Orho-Melander Marju, Ordovas Jose M, Tan Jonathan T, Seielstad Ma |
Six new loci associated with blood low-density lipoprotein cholesterol, high-density lipoprotein cholesterol or triglycerides in humans.
Nature genetics 2008 Feb 40 (2): 189-97. Kathiresan Sekar, Melander Olle, Guiducci Candace, Surti Aarti, Burtt Noël P, Rieder Mark J, Cooper Gregory M, Roos Charlotta, Voight Benjamin F, Havulinna Aki S, Wahlstrand Björn, Hedner Thomas, Corella Dolores, Tai E Shyong, Ordovas Jose M, Berglund Göran, Vartiainen Erkki, Jousilahti Pekka, Hedblad Bo, Taskinen Marja-Riitta, Newton-Cheh Christopher, Salomaa Veikko, Peltonen Leena, Groop Leif, Altshuler David M, Orho-Melander Mar |
Large scale replication analysis of loci associated with lipid concentrations in a Japanese population. Journal of medical genetics 2009 Jun 46 (6): 370-4. Nakayama K, Bayasgalan T, Yamanaka K, Kumada M, Gotoh T, Utsumi N, Yanagisawa Y, Okayama M, Kajii E, Ishibashi S, Iwamoto S, |
Non-synonymous variants in pre-B cell leukemia homeobox (PBX) genes are associated with congenital heart defects. European journal of medical genetics 2012 Apr 55 (4): 235-7. Arrington Cammon B, Dowse Benjamin R, Bleyl Steven B, Bowles Neil |
Large-scale gene-centric meta-analysis across 39 studies identifies type 2 diabetes loci. American journal of human genetics 2012 Feb . Saxena R, Elbers CC, Guo Y, Peter I, Gaunt TR, Mega JL, Lanktree MB, Tare A, Castillo BA, Li YR, Johnson T, Bruinenberg M, Gilbert-Diamond D, Rajagopalan R, Voight BF, Balasubramanyam A, Barnard J, Bauer F, Baumert J, Bhangale T, Böhm BO, Braund PS, Burton PR, Chandrupatla HR, Clarke R, Cooper-Dehoff RM, Crook ED, Davey-Smith G, Day IN, de Boer A, de Groot MC, Drenos F, Ferguson J, Fox CS, Furlong CE, Gibson Q, Gieger C, Gilhuijs-Pederson LA, Glessner JT, Goel A, Gong Y, Grant SF, Grobbee DE, Hastie C, Humphries SE, Kim CE, Kivimaki M, Kleber M, Meisinger C, Kumari M, Langaee TY, Lawlor DA, Li M, Lobmeyer MT, Maitland-van der Zee AH, Meijs MF, Molony CM, Morrow DA, Murugesan G, Musani SK, Nelson CP, Newhouse SJ, O'Connell JR, Padmanabhan S, Palmen J, Patel SR, Pepine CJ, Pettinger M, Price TS, Rafelt S, Ranchalis J, Rasheed A, Rosenthal E, Ruczinski I, Shah S, Shen H, Silbernagel G, Smith EN, Spijkerman AW, Stanton A, Steffes MW, Thorand B, Trip M, van der Harst P, van der A DL, van Iperen EP, van Setten J, van Vliet-Ostaptchouk JV, Verweij N, Wolffenbuttel BH, Young T, Zafarmand MH, Zmuda JM, Boehnke M, Altshuler D, McCarthy M, Kao WH, Pankow JS, Cappola TP, Caulfield M, Dominiczak A, Shields DC, Bhatt D, Zhang L, Curtis SP, Danesh J, Casas JP, van der Schouw YT, Onland-Moret NC, Doevendans PA, Dorn GW, Farrall M, Fitzgerald GA, Hamsten A, Hegele R, Hingorani AD, Hofker MH, Huggins GS, Illig T, Jarvik GP, Johnson JA, Klungel OH, Knowler WC, Koenig W, März W, Meigs JB, Melander O, Munroe PB, Mitchell BD, Bielinski SJ, Rader DJ, Reilly MP, Rich SS, Rotter JI, Saleheen D, Samani NJ, Schadt EE, Shuldiner AR, Silverstein R, Kottke-Marchant K, Talmud PJ, Watkins H, Asselbergs F, de Bakker PI, McCaffery J, Wijmenga C, Sabatine MS, Wilson JG, Reiner A, Bowden DW, Hakonarson H, Siscovick DS, Keating BJ |
Impact of variants within seven candidate genes on statin treatment efficacy. Physiological research / Academia Scientiarum Bohemoslovaca 2012 61 (6): 609-17. Vrablík M, Hubá?ek J A, Dlouhá D, Lánská V, Rynekrová J, Zlatohlávek L, Prusíková M, Ceška R, Adámková |
Sex-specific association of rs16996148 SNP in the NCAN/CILP2/PBX4 and serum lipid levels in the Mulao and Han populations. Lipids in health and disease 2011 10 (1): 248. Yan Ting-Ting, Yin Rui-Xing, Li Qing, Huang Ping, Zeng Xiao-Na, Huang Ke-Ke, Aung Lynn Htet Htet, Wu Dong-Feng, Liu Cheng-Wu, Pan Shang-Li |
Systematic evaluation of coding variation identifies a candidate causal variant in TM6SF2 influencing total cholesterol and myocardial infarction risk. Nature genetics 2014 Apr 46 (4): 345-51. Holmen Oddgeir L, Zhang He, Fan Yanbo, Hovelson Daniel H, Schmidt Ellen M, Zhou Wei, Guo Yanhong, Zhang Ji, Langhammer Arnulf, Løchen Maja-Lisa, Ganesh Santhi K, Vatten Lars, Skorpen Frank, Dalen Håvard, Zhang Jifeng, Pennathur Subramaniam, Chen Jin, Platou Carl, Mathiesen Ellisiv B, Wilsgaard Tom, Njølstad Inger, Boehnke Michael, Chen Y Eugene, Abecasis Gonçalo R, Hveem Kristian, Willer Cristen |
A genome-wide study of lipid response to fenofibrate in Caucasians: a combined analysis of the GOLDN and ACCORD studies.
Pharmacogenetics and genomics 2016 Mar . Irvin Marguerite R, Rotroff Daniel M, Aslibekyan Stella, Zhi Degui, Hidalgo Bertha, Motsinger-Reif Alison, Marvel Skylar, Srinivasasainagendra Vinodh, Claas Steven A, Buse John B, Straka Robert J, Ordovas Jose M, Borecki Ingrid B, Guo Xiuqing, Chen Ida Y D, Rotter Jerome I, Wagner Michael J, Arnett Donna |
Genetic variants influencing lipid levels and risk of dyslipidemia in Chinese population. Journal of genetics 2017 Dec 96 (6): 985-992. Luo Huaichao, Zhang Xueping, Shuai Ping, Miao Yuanying, Ye Zimeng, Lin Yi |
Association of the NCAN-TM6SF2-CILP2-PBX4-SUGP1-MAU2 SNPs and gene-gene and gene-environment interactions with serum lipid levels. Aging 2020 6 12 (12): 11893-11913. Deng Guo-Xiong, Yin Rui-Xing, Guan Yao-Zong, Liu Chun-Xiao, Zheng Peng-Fei, Wei Bi-Liu, Wu Jin-Zhen, Miao L |
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