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 *

188 related articles for article (PubMed ID: 24889828)

  • 1. Validated context-dependent associations of coronary heart disease risk with genotype variation in the chromosome 9p21 region: the Atherosclerosis Risk in Communities study.
    Lusk CM; Dyson G; Clark AG; Ballantyne CM; Frikke-Schmidt R; Tybjærg-Hansen A; Boerwinkle E; Sing CF
    Hum Genet; 2014 Sep; 133(9):1105-16. PubMed ID: 24889828
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Effect of 9p21 genetic variation on coronary heart disease is not modified by other risk markers. The Atherosclerosis Risk in Communities (ARIC) Study.
    Folsom AR; Nambi V; Pankow JS; Tang W; Farbakhsh K; Yamagishi K; Boerwinkle E
    Atherosclerosis; 2012 Oct; 224(2):435-9. PubMed ID: 22935634
    [TBL] [Abstract][Full Text] [Related]  

  • 3. The 9p21 susceptibility locus for coronary artery disease and the severity of coronary atherosclerosis.
    Chen SN; Ballantyne CM; Gotto AM; Marian AJ
    BMC Cardiovasc Disord; 2009 Jan; 9():3. PubMed ID: 19173706
    [TBL] [Abstract][Full Text] [Related]  

  • 4. A genetic variant on chromosome 9p21 and incident heart failure in the ARIC study.
    Yamagishi K; Folsom AR; Rosamond WD; Boerwinkle E;
    Eur Heart J; 2009 May; 30(10):1222-8. PubMed ID: 19329499
    [TBL] [Abstract][Full Text] [Related]  

  • 5. The relationship between diastolic blood pressure and coronary artery calcification is dependent on single nucleotide polymorphisms on chromosome 9p21.3.
    Kim DS; Smith JA; Bielak LF; Wu CY; Sun YV; Sheedy PF; Turner ST; Peyser PA; Kardia SL
    BMC Med Genet; 2014 Sep; 15():89. PubMed ID: 25185447
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Impact of adding a single allele in the 9p21 locus to traditional risk factors on reclassification of coronary heart disease risk and implications for lipid-modifying therapy in the Atherosclerosis Risk in Communities study.
    Brautbar A; Ballantyne CM; Lawson K; Nambi V; Chambless L; Folsom AR; Willerson JT; Boerwinkle E
    Circ Cardiovasc Genet; 2009 Jun; 2(3):279-85. PubMed ID: 20031596
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Genetic variants in loci 1p13 and 9p21 and fatal coronary heart disease in a Norwegian case-cohort study.
    Jansen MD; Knudsen GP; Myhre R; Høiseth G; Mørland J; Næss Ø; Tambs K; Magnus P
    Mol Biol Rep; 2014 May; 41(5):2733-43. PubMed ID: 24728607
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Replication of the association of chromosomal region 9p21.3 with generalized aggressive periodontitis (gAgP) using an independent case-control cohort.
    Ernst FD; Uhr K; Teumer A; Fanghänel J; Schulz S; Noack B; Gonzales J; Reichert S; Eickholz P; Holtfreter B; Meisel P; Linden GJ; Homuth G; Kocher T
    BMC Med Genet; 2010 Aug; 11():119. PubMed ID: 20696043
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Factor XIIIA Val34Leu polymorphism does not predict risk of coronary heart disease: The Atherosclerosis Risk in Communities (ARIC) Study.
    Aleksic N; Ahn C; Wang YW; Juneja H; Folsom AR; Boerwinkle E; Wu KK
    Arterioscler Thromb Vasc Biol; 2002 Feb; 22(2):348-52. PubMed ID: 11834540
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Chromosome 9p21 and ABCA1 Genetic Variants and Their Interactions on Coronary Heart Disease and Ischemic Stroke in a Chinese Han Population.
    Cao XL; Yin RX; Huang F; Wu JZ; Chen WX
    Int J Mol Sci; 2016 Apr; 17(4):586. PubMed ID: 27096864
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Association of Chromosome 9p21 With Subsequent Coronary Heart Disease Events.
    Patel RS; Schmidt AF; Tragante V; McCubrey RO; Holmes MV; Howe LJ; Direk K; Åkerblom A; Leander K; Virani SS; Kaminski KA; Muehlschlegel JD; Dubé MP; Allayee H; Almgren P; Alver M; Baranova EV; Behlouli H; Boeckx B; Braund PS; Breitling LP; Delgado G; Duarte NE; Dufresne L; Eriksson N; Foco L; Gijsberts CM; Gong Y; Hartiala J; Heydarpour M; Hubacek JA; Kleber M; Kofink D; Kuukasjärvi P; Lee VV; Leiherer A; Lenzini PA; Levin D; Lyytikäinen LP; Martinelli N; Mons U; Nelson CP; Nikus K; Pilbrow AP; Ploski R; Sun YV; Tanck MWT; Tang WHW; Trompet S; van der Laan SW; van Setten J; Vilmundarson RO; Viviani Anselmi C; Vlachopoulou E; Boerwinkle E; Briguori C; Carlquist JF; Carruthers KF; Casu G; Deanfield J; Deloukas P; Dudbridge F; Fitzpatrick N; Gigante B; James S; Lokki ML; Lotufo PA; Marziliano N; Mordi IR; Muhlestein JB; Newton Cheh C; Pitha J; Saely CH; Samman-Tahhan A; Sandesara PB; Teren A; Timmis A; Van de Werf F; Wauters E; Wilde AAM; Ford I; Stott DJ; Algra A; Andreassi MG; Ardissino D; Arsenault BJ; Ballantyne CM; Bergmeijer TO; Bezzina CR; Body SC; Bogaty P; de Borst GJ; Brenner H; Burkhardt R; Carpeggiani C; Condorelli G; Cooper-DeHoff RM; Cresci S; de Faire U; Doughty RN; Drexel H; Engert JC; Fox KAA; Girelli D; Hagström E; Hazen SL; Held C; Hemingway H; Hoefer IE; Hovingh GK; Johnson JA; de Jong PA; Jukema JW; Kaczor MP; Kähönen M; Kettner J; Kiliszek M; Klungel OH; Lagerqvist B; Lambrechts D; Laurikka JO; Lehtimäki T; Lindholm D; Mahmoodi BK; Maitland-van der Zee AH; McPherson R; Melander O; Metspalu A; Pepinski W; Olivieri O; Opolski G; Palmer CN; Pasterkamp G; Pepine CJ; Pereira AC; Pilote L; Quyyumi AA; Richards AM; Sanak M; Scholz M; Siegbahn A; Sinisalo J; Smith JG; Spertus JA; Stewart AFR; Szczeklik W; Szpakowicz A; Ten Berg JM; Thanassoulis G; Thiery J; van der Graaf Y; Visseren FLJ; Waltenberger J; ; Van der Harst P; Tardif JC; Sattar N; Lang CC; Pare G; Brophy JM; Anderson JL; März W; Wallentin L; Cameron VA; Horne BD; Samani NJ; Hingorani AD; Asselbergs FW
    Circ Genom Precis Med; 2019 Apr; 12(4):e002471. PubMed ID: 30897348
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Genetic variants of chromosome 9p21.3 region associated with coronary artery disease and premature coronary artery disease in an Asian Indian population.
    Kalpana B; Murthy DK; Balakrishna N; Aiyengar MT
    Indian Heart J; 2019; 71(3):263-271. PubMed ID: 31543200
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Resequencing and clinical associations of the 9p21.3 region: a comprehensive investigation in the Framingham heart study.
    Johnson AD; Hwang SJ; Voorman A; Morrison A; Peloso GM; Hsu YH; Thanassoulis G; Newton-Cheh C; Rogers IS; Hoffmann U; Freedman JE; Fox CS; Psaty BM; Boerwinkle E; Cupples LA; O'Donnell CJ
    Circulation; 2013 Feb; 127(7):799-810. PubMed ID: 23315372
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Evaluation of association between common genetic variants on chromosome 9p21 and coronary artery disease in Turkish population.
    Çakmak HA; Bayoğlu B; Durmaz E; Can G; Karadağ B; Cengiz M; Vural VA; Yüksel H
    Anatol J Cardiol; 2015 Mar; 15(3):196-203. PubMed ID: 25333979
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Repeated replication and a prospective meta-analysis of the association between chromosome 9p21.3 and coronary artery disease.
    Schunkert H; Götz A; Braund P; McGinnis R; Tregouet DA; Mangino M; Linsel-Nitschke P; Cambien F; Hengstenberg C; Stark K; Blankenberg S; Tiret L; Ducimetiere P; Keniry A; Ghori MJ; Schreiber S; El Mokhtari NE; Hall AS; Dixon RJ; Goodall AH; Liptau H; Pollard H; Schwarz DF; Hothorn LA; Wichmann HE; König IR; Fischer M; Meisinger C; Ouwehand W; Deloukas P; Thompson JR; Erdmann J; Ziegler A; Samani NJ;
    Circulation; 2008 Apr; 117(13):1675-84. PubMed ID: 18362232
    [TBL] [Abstract][Full Text] [Related]  

  • 16. The relationship between polymorphisms on chromosome 9p21 and age of onset of coronary heart disease in black and white women.
    Beckie TM; Groër MW; Beckstead JW
    Genet Test Mol Biomarkers; 2011 Jun; 15(6):435-42. PubMed ID: 21375403
    [TBL] [Abstract][Full Text] [Related]  

  • 17. The Correlation Between 9p21 Chromosome rs4977574 Polymorphism Genotypes and the Development of Coronary Artery Heart Disease.
    Tang O; Lv J; Cheng Y; Qin F
    Cardiovasc Toxicol; 2017 Apr; 17(2):185-189. PubMed ID: 27240780
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Association of genetic variation on chromosome 9p21 with susceptibility and progression of atherosclerosis: a population-based, prospective study.
    Ye S; Willeit J; Kronenberg F; Xu Q; Kiechl S
    J Am Coll Cardiol; 2008 Jul; 52(5):378-84. PubMed ID: 18652946
    [TBL] [Abstract][Full Text] [Related]  

  • 19. The 9p21 genetic variant is additive to carotid intima media thickness and plaque in improving coronary heart disease risk prediction in white participants of the Atherosclerosis Risk in Communities (ARIC) Study.
    Nambi V; Boerwinkle E; Lawson K; Brautbar A; Chambless L; Franeschini N; North KE; Virani SS; Folsom AR; Ballantyne CM
    Atherosclerosis; 2012 May; 222(1):135-7. PubMed ID: 22349088
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Sequence variants on chromosome 9p21.3 confer risk for atherosclerotic stroke.
    Gschwendtner A; Bevan S; Cole JW; Plourde A; Matarin M; Ross-Adams H; Meitinger T; Wichmann E; Mitchell BD; Furie K; Slowik A; Rich SS; Syme PD; MacLeod MJ; Meschia JF; Rosand J; Kittner SJ; Markus HS; Müller-Myhsok B; Dichgans M;
    Ann Neurol; 2009 May; 65(5):531-9. PubMed ID: 19475673
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.