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 *

172 related articles for article (PubMed ID: 28642624)

  • 1. Whole Exome Sequencing to Identify Genetic Variants Associated with Raised Atherosclerotic Lesions in Young Persons.
    Hixson JE; Jun G; Shimmin LC; Wang Y; Yu G; Mao C; Warren AS; Howard TD; Heide RSV; Van Eyk J; Wang Y; Herrington DM
    Sci Rep; 2017 Jun; 7(1):4091. PubMed ID: 28642624
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. Common variants in the periostin gene influence development of atherosclerosis in young persons.
    Hixson JE; Shimmin LC; Montasser ME; Kim DK; Zhong Y; Ibarguen H; Follis J; Malcom G; Strong J; Howard T; Langefeld C; Liu Y; Rotter JI; Johnson C; Herrington D
    Arterioscler Thromb Vasc Biol; 2011 Jul; 31(7):1661-7. PubMed ID: 21474826
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Exome Sequencing Identifies Genetic Variants Associated with Circulating Lipid Levels in Mexican Americans: The Insulin Resistance Atherosclerosis Family Study (IRASFS).
    Gao C; Tabb KL; Dimitrov LM; Taylor KD; Wang N; Guo X; Long J; Rotter JI; Watanabe RM; Curran JE; Blangero J; Langefeld CD; Bowden DW; Palmer ND
    Sci Rep; 2018 Apr; 8(1):5603. PubMed ID: 29618726
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Global DNA methylation and risk of subclinical atherosclerosis in young adults: the Pathobiological Determinants of Atherosclerosis in Youth (PDAY) study.
    Bressler J; Shimmin LC; Boerwinkle E; Hixson JE
    Atherosclerosis; 2011 Dec; 219(2):958-62. PubMed ID: 22015179
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Whole exome sequencing of extreme age-related macular degeneration phenotypes.
    Sardell RJ; Bailey JN; Courtenay MD; Whitehead P; Laux RA; Adams LD; Fortun JA; Brantley MA; Kovach JL; Schwartz SG; Agarwal A; Scott WK; Haines JL; Pericak-Vance MA
    Mol Vis; 2016; 22():1062-76. PubMed ID: 27625572
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Large-scale gene-centric analysis identifies novel variants for coronary artery disease.
    IBC 50K CAD Consortium
    PLoS Genet; 2011 Sep; 7(9):e1002260. PubMed ID: 21966275
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Identification of STXBP2 as a novel susceptibility locus for myocardial infarction in Japanese individuals by an exome-wide association study.
    Yamada Y; Sakuma J; Takeuchi I; Yasukochi Y; Kato K; Oguri M; Fujimaki T; Horibe H; Muramatsu M; Sawabe M; Fujiwara Y; Taniguchi Y; Obuchi S; Kawai H; Shinkai S; Mori S; Arai T; Tanaka M
    Oncotarget; 2017 May; 8(20):33527-33535. PubMed ID: 28380445
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Population-based identity-by-descent mapping combined with exome sequencing to detect rare risk variants for schizophrenia.
    Harold D; Connolly S; Riley BP; Kendler KS; McCarthy SE; McCombie WR; Richards A; Owen MJ; O'Donovan MC; Walters J; ; ; Donohoe G; Gill M; Corvin A; Morris DW
    Am J Med Genet B Neuropsychiatr Genet; 2019 Apr; 180(3):223-231. PubMed ID: 30801977
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Exome sequence analysis identifies rare coding variants associated with a machine learning-based marker for coronary artery disease.
    Petrazzini BO; Forrest IS; Rocheleau G; Vy HMT; Márquez-Luna C; Duffy Á; Chen R; Park JK; Gibson K; Goonewardena SN; Malick WA; Rosenson RS; Jordan DM; Do R
    Nat Genet; 2024 Jul; 56(7):1412-1419. PubMed ID: 38862854
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Admixture mapping of coronary artery calcification in African Americans from the NHLBI family heart study.
    Gomez F; Wang L; Abel H; Zhang Q; Province MA; Borecki IB
    BMC Genet; 2015 Apr; 16():42. PubMed ID: 25902833
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Common and Rare Variants Genetic Association Analysis of Circulating Neutrophil Extracellular Traps.
    Donkel SJ; Portilla Fernández E; Ahmad S; Rivadeneira F; van Rooij FJA; Ikram MA; Leebeek FWG; de Maat MPM; Ghanbari M
    Front Immunol; 2021; 12():615527. PubMed ID: 33717105
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Analysis of potential protein-modifying variants in 9000 endometriosis patients and 150000 controls of European ancestry.
    Sapkota Y; Vivo I; Steinthorsdottir V; Fassbender A; Bowdler L; Buring JE; Edwards TL; Jones S; O D; Peterse D; Rexrode KM; Ridker PM; Schork AJ; Thorleifsson G; Wallace LM; ; Kraft P; Morris AP; Nyholt DR; Edwards DRV; Nyegaard M; D'Hooghe T; Chasman DI; Stefansson K; Missmer SA; Montgomery GW
    Sci Rep; 2017 Sep; 7(1):11380. PubMed ID: 28900119
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Exome sequencing identifies novel genetic variants associated with varicose veins.
    Zhang DD; He XY; Yang L; Wu BS; Fu Y; Liu WS; Guo Y; Fei CJ; Kang JJ; Feng JF; Cheng W; Tan L; Yu JT
    PLoS Genet; 2024 Jul; 20(7):e1011339. PubMed ID: 38980841
    [TBL] [Abstract][Full Text] [Related]  

  • 15. A linkage and exome study of multiplex families with bipolar disorder implicates rare coding variants of ANK3 and additional rare alleles at 10q11-q21.
    Toma C; Shaw AD; Heath A; Pierce KD; Mitchell PB; Schofield PR; Fullerton JM
    J Psychiatry Neurosci; 2021 Mar; 46(2):E247-E257. PubMed ID: 33729739
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Mapping gene and gene pathways associated with coronary artery disease: a CARDIoGRAM exome and multi-ancestry UK biobank analysis.
    Hariharan P; Dupuis J
    Sci Rep; 2021 Aug; 11(1):16461. PubMed ID: 34385509
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Whole-exome imputation of sequence variants identified two novel alleles associated with adult body height in African Americans.
    Du M; Auer PL; Jiao S; Haessler J; Altshuler D; Boerwinkle E; Carlson CS; Carty CL; Chen YD; Curtis K; Franceschini N; Hsu L; Jackson R; Lange LA; Lettre G; Monda KL; ; Nickerson DA; Reiner AP; Rich SS; Rosse SA; Rotter JI; Willer CJ; Wilson JG; North K; Kooperberg C; Heard-Costa N; Peters U
    Hum Mol Genet; 2014 Dec; 23(24):6607-15. PubMed ID: 25027330
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Whole-genome sequencing study of serum peptide levels: the Atherosclerosis Risk in Communities study.
    de Vries PS; Yu B; Feofanova EV; Metcalf GA; Brown MR; Zeighami AL; Liu X; Muzny DM; Gibbs RA; Boerwinkle E; Morrison AC
    Hum Mol Genet; 2017 Sep; 26(17):3442-3450. PubMed ID: 28854705
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Analysis of Whole Exome Sequencing with Cardiometabolic Traits Using Family-Based Linkage and Association in the IRAS Family Study.
    Tabb KL; Hellwege JN; Palmer ND; Dimitrov L; Sajuthi S; Taylor KD; Ng MC; Hawkins GA; Chen YI; Brown WM; McWilliams D; Williams A; Lorenzo C; Norris JM; Long J; Rotter JI; Curran JE; Blangero J; Wagenknecht LE; Langefeld CD; Bowden DW
    Ann Hum Genet; 2017 Mar; 81(2):49-58. PubMed ID: 28067407
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Genetic Regulation of Atherosclerosis-Relevant Phenotypes in Human Vascular Smooth Muscle Cells.
    Aherrahrou R; Guo L; Nagraj VP; Aguhob A; Hinkle J; Chen L; Yuhl Soh J; Lue D; Alencar GF; Boltjes A; van der Laan SW; Farber E; Fuller D; Anane-Wae R; Akingbesote N; Manichaikul AW; Ma L; Kaikkonen MU; Björkegren JLM; Önengüt-Gümüşcü S; Pasterkamp G; Miller CL; Owens GK; Finn A; Navab M; Fogelman AM; Berliner JA; Civelek M
    Circ Res; 2020 Dec; 127(12):1552-1565. PubMed ID: 33040646
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.