These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

215 related articles for article (PubMed ID: 22702842)

  • 1. Genome-wide association study validation identifies novel loci for atherosclerotic cardiovascular disease.
    Chen X; Li S; Yang Y; Yang X; Liu Y; Liu Y; Hu W; Jin L; Wang X
    J Thromb Haemost; 2012 Aug; 10(8):1508-14. PubMed ID: 22702842
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Association of two polymorphisms in the FADS1/FADS2 gene cluster and the risk of coronary artery disease and ischemic stroke.
    Yang Q; Yin RX; Cao XL; Wu DF; Chen WX; Zhou YJ
    Int J Clin Exp Pathol; 2015; 8(6):7318-31. PubMed ID: 26261632
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Common and Rare Genetic Variation in CCR2, CCR5, or CX3CR1 and Risk of Atherosclerotic Coronary Heart Disease and Glucometabolic Traits.
    Golbus JR; Stitziel NO; Zhao W; Xue C; Farrall M; McPherson R; Erdmann J; Deloukas P; Watkins H; Schunkert H; Samani NJ; Saleheen D; Kathiresan S; Reilly MP;
    Circ Cardiovasc Genet; 2016 Jun; 9(3):250-8. PubMed ID: 27013693
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Identification of CELSR1 as a susceptibility gene for ischemic stroke in Japanese individuals by a genome-wide association study.
    Yamada Y; Fuku N; Tanaka M; Aoyagi Y; Sawabe M; Metoki N; Yoshida H; Satoh K; Kato K; Watanabe S; Nozawa Y; Hasegawa A; Kojima T
    Atherosclerosis; 2009 Nov; 207(1):144-9. PubMed ID: 19403135
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Genomic variant in CAV1 increases susceptibility to coronary artery disease and myocardial infarction.
    Chen S; Wang X; Wang J; Zhao Y; Wang D; Tan C; Fa J; Zhang R; Wang F; Xu C; Huang Y; Li S; Yin D; Xiong X; Li X; Chen Q; Tu X; Yang Y; Xia Y; Xu C; Wang QK
    Atherosclerosis; 2016 Mar; 246():148-156. PubMed ID: 26775120
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Genetic variants associated with myocardial infarction and the risk factors in Chinese population.
    Wang Y; Wang L; Liu X; Zhang Y; Yu L; Zhang F; Liu L; Cai J; Yang X; Wang X
    PLoS One; 2014; 9(1):e86332. PubMed ID: 24475106
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Association study of polymorphisms in the ABO gene with ischemic stroke in the Chinese population.
    Ling X; Zheng Y; Tao J; Zheng Z; Chen L
    BMC Neurol; 2016 Aug; 16(1):146. PubMed ID: 27542834
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Validation of the association of genetic variants on chromosome 9p21 and 1q41 with myocardial infarction in a Japanese population.
    Hiura Y; Fukushima Y; Yuno M; Sawamura H; Kokubo Y; Okamura T; Tomoike H; Goto Y; Nonogi H; Takahashi R; Iwai N
    Circ J; 2008 Aug; 72(8):1213-7. PubMed ID: 18654002
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Minor allele C of chromosome 1p32 single nucleotide polymorphism rs11206510 confers risk of ischemic stroke in the Chinese Han population.
    Xu C; Wang F; Wang B; Li X; Li C; Wang D; Xiong X; Wang P; Lu Q; Wang X; Yang Q; Yin D; Huang Y; Ji L; Wang N; Chen S; Cheng X; Liao Y; Ma X; Su D; Chen G; Xia H; Shi L; Tu X; Wang QK
    Stroke; 2010 Aug; 41(8):1587-92. PubMed ID: 20576952
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Significant Association between OPG/TNFRSF11B Variant and Common Complex Ischemic Stroke.
    Xiong X; Naji DH; Wang B; Zhao Y; Wang J; Wang D; Zhang Y; Li S; Chen S; Huang Y; Yang Q; Wang X; Yin D; Tu X; Chen Q; Ma X; Xu C; Wang QK
    J Stroke Cerebrovasc Dis; 2018 Jun; 27(6):1683-1691. PubMed ID: 29501268
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Associations of lipid levels susceptibility loci with coronary artery disease in Chinese population.
    Wang XB; Han YD; Cui NH; Gao JJ; Yang J; Huang ZL; Zhu Q; Zheng F
    Lipids Health Dis; 2015 Jul; 14():80. PubMed ID: 26209006
    [TBL] [Abstract][Full Text] [Related]  

  • 12. A polymorphism in the ABCG1 promoter is functionally associated with coronary artery disease in a Chinese Han population.
    Xu Y; Wang W; Zhang L; Qi LP; Li LY; Chen LF; Fang Q; Dang AM; Yan XW
    Atherosclerosis; 2011 Dec; 219(2):648-54. PubMed ID: 21722899
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Identification of PTCSC3 as a Novel Locus for Large-Vessel Ischemic Stroke: A Genome-Wide Association Study.
    Lee TH; Ko TM; Chen CH; Lee MT; Chang YJ; Chang CH; Huang KL; Chang TY; Lee JD; Chang KC; Yang JT; Wen MS; Wang CY; Chen YT; Hsieh CS; Chou SY; Liu YM; Chen HW; Liao HT; Wang CW; Chen SP; Lu LS; Chen YT; Wu JY
    J Am Heart Assoc; 2016 Mar; 5(3):e003003. PubMed ID: 27025970
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Interaction of type 2 diabetes mellitus with chromosome 9p21 rs10757274 polymorphism on the risk of myocardial infarction: a case-control study in Chinese population.
    Zhang LW; Li JP; Duan FF; Liu ZK; Zhan SY; Hu YH; Jiang J; Zhang Y; Huo Y; Chen DF
    BMC Cardiovasc Disord; 2014 Nov; 14():170. PubMed ID: 25430018
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Apolipoprotein(a) genetic sequence variants associated with systemic atherosclerosis and coronary atherosclerotic burden but not with venous thromboembolism.
    Helgadottir A; Gretarsdottir S; Thorleifsson G; Holm H; Patel RS; Gudnason T; Jones GT; van Rij AM; Eapen DJ; Baas AF; Tregouet DA; Morange PE; Emmerich J; Lindblad B; Gottsäter A; Kiemeny LA; Lindholt JS; Sakalihasan N; Ferrell RE; Carey DJ; Elmore JR; Tsao PS; Grarup N; Jørgensen T; Witte DR; Hansen T; Pedersen O; Pola R; Gaetani E; Magnadottir HB; Wijmenga C; Tromp G; Ronkainen A; Ruigrok YM; Blankensteijn JD; Mueller T; Wells PS; Corral J; Soria JM; Souto JC; Peden JF; Jalilzadeh S; Mayosi BM; Keavney B; Strawbridge RJ; Sabater-Lleal M; Gertow K; Baldassarre D; Nyyssönen K; Rauramaa R; Smit AJ; Mannarino E; Giral P; Tremoli E; de Faire U; Humphries SE; Hamsten A; Haraldsdottir V; Olafsson I; Magnusson MK; Samani NJ; Levey AI; Markus HS; Kostulas K; Dichgans M; Berger K; Kuhlenbäumer G; Ringelstein EB; Stoll M; Seedorf U; Rothwell PM; Powell JT; Kuivaniemi H; Onundarson PT; Valdimarsson E; Matthiasson SE; Gudbjartsson DF; Thorgeirsson G; Quyyumi AA; Watkins H; Farrall M; Thorsteinsdottir U; Stefansson K
    J Am Coll Cardiol; 2012 Aug; 60(8):722-9. PubMed ID: 22898070
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Multiethnic meta-analysis of genome-wide association studies in >100 000 subjects identifies 23 fibrinogen-associated Loci but no strong evidence of a causal association between circulating fibrinogen and cardiovascular disease.
    Sabater-Lleal M; Huang J; Chasman D; Naitza S; Dehghan A; Johnson AD; Teumer A; Reiner AP; Folkersen L; Basu S; Rudnicka AR; Trompet S; Mälarstig A; Baumert J; Bis JC; Guo X; Hottenga JJ; Shin SY; Lopez LM; Lahti J; Tanaka T; Yanek LR; Oudot-Mellakh T; Wilson JF; Navarro P; Huffman JE; Zemunik T; Redline S; Mehra R; Pulanic D; Rudan I; Wright AF; Kolcic I; Polasek O; Wild SH; Campbell H; Curb JD; Wallace R; Liu S; Eaton CB; Becker DM; Becker LC; Bandinelli S; Räikkönen K; Widen E; Palotie A; Fornage M; Green D; Gross M; Davies G; Harris SE; Liewald DC; Starr JM; Williams FM; Grant PJ; Spector TD; Strawbridge RJ; Silveira A; Sennblad B; Rivadeneira F; Uitterlinden AG; Franco OH; Hofman A; van Dongen J; Willemsen G; Boomsma DI; Yao J; Swords Jenny N; Haritunians T; McKnight B; Lumley T; Taylor KD; Rotter JI; Psaty BM; Peters A; Gieger C; Illig T; Grotevendt A; Homuth G; Völzke H; Kocher T; Goel A; Franzosi MG; Seedorf U; Clarke R; Steri M; Tarasov KV; Sanna S; Schlessinger D; Stott DJ; Sattar N; Buckley BM; Rumley A; Lowe GD; McArdle WL; Chen MH; Tofler GH; Song J; Boerwinkle E; Folsom AR; Rose LM; Franco-Cereceda A; Teichert M; Ikram MA; Mosley TH; Bevan S; Dichgans M; Rothwell PM; Sudlow CL; Hopewell JC; Chambers JC; Saleheen D; Kooner JS; Danesh J; Nelson CP; Erdmann J; Reilly MP; Kathiresan S; Schunkert H; Morange PE; Ferrucci L; Eriksson JG; Jacobs D; Deary IJ; Soranzo N; Witteman JC; de Geus EJ; Tracy RP; Hayward C; Koenig W; Cucca F; Jukema JW; Eriksson P; Seshadri S; Markus HS; Watkins H; Samani NJ; ; ; ; ; ; Wallaschofski H; Smith NL; Tregouet D; Ridker PM; Tang W; Strachan DP; Hamsten A; O'Donnell CJ
    Circulation; 2013 Sep; 128(12):1310-24. PubMed ID: 23969696
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Association analysis of the IL-17F His161Arg polymorphism in myocardial infarction.
    Pei F; Han Y; Zhang X; Yan C; Huang M; Deng J; Kang J
    Coron Artery Dis; 2009 Dec; 20(8):513-7. PubMed ID: 19838108
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Adiponectin Gene Polymorphism and Ischemic Stroke Subtypes in a Chinese Population.
    Li S; Lu N; Li Z; Jiao B; Wang H; Yang J; Yu T
    J Stroke Cerebrovasc Dis; 2017 May; 26(5):944-951. PubMed ID: 27913202
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Loci associated with ischaemic stroke and its subtypes (SiGN): a genome-wide association study.
    ;
    Lancet Neurol; 2016 Feb; 15(2):174-184. PubMed ID: 26708676
    [TBL] [Abstract][Full Text] [Related]  

  • 20. A genome-wide association study identifies PLCL2 and AP3D1-DOT1L-SF3A2 as new susceptibility loci for myocardial infarction in Japanese.
    Hirokawa M; Morita H; Tajima T; Takahashi A; Ashikawa K; Miya F; Shigemizu D; Ozaki K; Sakata Y; Nakatani D; Suna S; Imai Y; Tanaka T; Tsunoda T; Matsuda K; Kadowaki T; Nakamura Y; Nagai R; Komuro I; Kubo M
    Eur J Hum Genet; 2015 Mar; 23(3):374-80. PubMed ID: 24916648
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 11.