BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

319 related articles for article (PubMed ID: 24026423)

  • 1. A genome- and phenome-wide association study to identify genetic variants influencing platelet count and volume and their pleiotropic effects.
    Shameer K; Denny JC; Ding K; Jouni H; Crosslin DR; de Andrade M; Chute CG; Peissig P; Pacheco JA; Li R; Bastarache L; Kho AN; Ritchie MD; Masys DR; Chisholm RL; Larson EB; McCarty CA; Roden DM; Jarvik GP; Kullo IJ
    Hum Genet; 2014 Jan; 133(1):95-109. PubMed ID: 24026423
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Integrative Genomic Analysis Reveals Four Protein Biomarkers for Platelet Traits.
    Lee DH; Yao C; Bhan A; Schlaeger T; Keefe J; Rodriguez BAT; Hwang SJ; Chen MH; Levy D; Johnson AD
    Circ Res; 2020 Oct; 127(9):1182-1194. PubMed ID: 32781905
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Genetics of platelet traits in ischaemic stroke: focus on mean platelet volume and platelet count.
    Vasudeva K; Munshi A
    Int J Neurosci; 2019 May; 129(5):511-522. PubMed ID: 30371123
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Platelet-Related Variants Identified by Exomechip Meta-analysis in 157,293 Individuals.
    Eicher JD; Chami N; Kacprowski T; Nomura A; Chen MH; Yanek LR; Tajuddin SM; Schick UM; Slater AJ; Pankratz N; Polfus L; Schurmann C; Giri A; Brody JA; Lange LA; Manichaikul A; Hill WD; Pazoki R; Elliot P; Evangelou E; Tzoulaki I; Gao H; Vergnaud AC; Mathias RA; Becker DM; Becker LC; Burt A; Crosslin DR; Lyytikäinen LP; Nikus K; Hernesniemi J; Kähönen M; Raitoharju E; Mononen N; Raitakari OT; Lehtimäki T; Cushman M; Zakai NA; Nickerson DA; Raffield LM; Quarells R; Willer CJ; Peloso GM; Abecasis GR; Liu DJ; ; Deloukas P; Samani NJ; Schunkert H; Erdmann J; ; ; Fornage M; Richard M; Tardif JC; Rioux JD; Dube MP; de Denus S; Lu Y; Bottinger EP; Loos RJ; Smith AV; Harris TB; Launer LJ; Gudnason V; Velez Edwards DR; Torstenson ES; Liu Y; Tracy RP; Rotter JI; Rich SS; Highland HM; Boerwinkle E; Li J; Lange E; Wilson JG; Mihailov E; Mägi R; Hirschhorn J; Metspalu A; Esko T; Vacchi-Suzzi C; Nalls MA; Zonderman AB; Evans MK; Engström G; Orho-Melander M; Melander O; O'Donoghue ML; Waterworth DM; Wallentin L; White HD; Floyd JS; Bartz TM; Rice KM; Psaty BM; Starr JM; Liewald DC; Hayward C; Deary IJ; Greinacher A; Völker U; Thiele T; Völzke H; van Rooij FJ; Uitterlinden AG; Franco OH; Dehghan A; Edwards TL; Ganesh SK; Kathiresan S; Faraday N; Auer PL; Reiner AP; Lettre G; Johnson AD
    Am J Hum Genet; 2016 Jul; 99(1):40-55. PubMed ID: 27346686
    [TBL] [Abstract][Full Text] [Related]  

  • 5. A meta-analysis and genome-wide association study of platelet count and mean platelet volume in african americans.
    Qayyum R; Snively BM; Ziv E; Nalls MA; Liu Y; Tang W; Yanek LR; Lange L; Evans MK; Ganesh S; Austin MA; Lettre G; Becker DM; Zonderman AB; Singleton AB; Harris TB; Mohler ER; Logsdon BA; Kooperberg C; Folsom AR; Wilson JG; Becker LC; Reiner AP
    PLoS Genet; 2012; 8(3):e1002491. PubMed ID: 22423221
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Leveraging Genome and Phenome-Wide Association Studies to Investigate Genetic Risk of Acute Lymphoblastic Leukemia.
    Semmes EC; Vijayakrishnan J; Zhang C; Hurst JH; Houlston RS; Walsh KM
    Cancer Epidemiol Biomarkers Prev; 2020 Aug; 29(8):1606-1614. PubMed ID: 32467347
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Genetically determined serum urate levels and cardiovascular and other diseases in UK Biobank cohort: A phenome-wide mendelian randomization study.
    Li X; Meng X; He Y; Spiliopoulou A; Timofeeva M; Wei WQ; Gifford A; Yang T; Varley T; Tzoulaki I; Joshi P; Denny JC; Mckeigue P; Campbell H; Theodoratou E
    PLoS Med; 2019 Oct; 16(10):e1002937. PubMed ID: 31626644
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Phenome-wide association study (PheWAS) for detection of pleiotropy within the Population Architecture using Genomics and Epidemiology (PAGE) Network.
    Pendergrass SA; Brown-Gentry K; Dudek S; Frase A; Torstenson ES; Goodloe R; Ambite JL; Avery CL; Buyske S; Bůžková 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
    PLoS Genet; 2013; 9(1):e1003087. PubMed ID: 23382687
    [TBL] [Abstract][Full Text] [Related]  

  • 9. A novel variant on chromosome 7q22.3 associated with mean platelet volume, counts, and function.
    Soranzo N; Rendon A; Gieger C; Jones CI; Watkins NA; Menzel S; Döring A; Stephens J; Prokisch H; Erber W; Potter SC; Bray SL; Burns P; Jolley J; Falchi M; Kühnel B; Erdmann J; Schunkert H; Samani NJ; Illig T; Garner SF; Rankin A; Meisinger C; Bradley JR; Thein SL; Goodall AH; Spector TD; Deloukas P; Ouwehand WH
    Blood; 2009 Apr; 113(16):3831-7. PubMed ID: 19221038
    [TBL] [Abstract][Full Text] [Related]  

  • 10. An integrative functional genomics framework for effective identification of novel regulatory variants in genome-phenome studies.
    Zhao J; Cheng F; Jia P; Cox N; Denny JC; Zhao Z
    Genome Med; 2018 Jan; 10(1):7. PubMed ID: 29378629
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Whole genome sequence analysis of platelet traits in the NHLBI Trans-Omics for Precision Medicine (TOPMed) initiative.
    Little A; Hu Y; Sun Q; Jain D; Broome J; Chen MH; Thibord F; McHugh C; Surendran P; Blackwell TW; Brody JA; Bhan A; Chami N; de Vries PS; Ekunwe L; Heard-Costa N; Hobbs BD; Manichaikul A; Moon JY; Preuss MH; Ryan K; Wang Z; Wheeler M; Yanek LR; Abecasis GR; Almasy L; Beaty TH; Becker LC; Blangero J; Boerwinkle E; Butterworth AS; Choquet H; Correa A; Curran JE; Faraday N; Fornage M; Glahn DC; Hou L; Jorgenson E; Kooperberg C; Lewis JP; Lloyd-Jones DM; Loos RJF; Min YI; Mitchell BD; Morrison AC; Nickerson DA; North KE; O'Connell JR; Pankratz N; Psaty BM; Vasan RS; Rich SS; Rotter JI; Smith AV; Smith NL; Tang H; Tracy RP; Conomos MP; Laurie CA; Mathias RA; Li Y; Auer PL; ; Thornton T; Reiner AP; Johnson AD; Raffield LM
    Hum Mol Genet; 2022 Feb; 31(3):347-361. PubMed ID: 34553764
    [TBL] [Abstract][Full Text] [Related]  

  • 12. GWAS and PheWAS of red blood cell components in a Northern Nevadan cohort.
    Read RW; Schlauch KA; Elhanan G; Metcalf WJ; Slonim AD; Aweti R; Borkowski R; Grzymski JJ
    PLoS One; 2019; 14(6):e0218078. PubMed ID: 31194788
    [TBL] [Abstract][Full Text] [Related]  

  • 13. The SH2B3 and KCNK5 loci may be implicated in regulation of platelet count, volume, and maturity.
    Christiansen MK; Larsen SB; Nyegaard M; Neergaard-Petersen S; Würtz M; Grove EL; Hvas AM; Jensen HK; Kristensen SD
    Thromb Res; 2017 Oct; 158():86-92. PubMed ID: 28865245
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Multivariate Genome-wide Association Analysis of a Cytokine Network Reveals Variants with Widespread Immune, Haematological, and Cardiometabolic Pleiotropy.
    Nath AP; Ritchie SC; Grinberg NF; Tang HH; Huang QQ; Teo SM; Ahola-Olli AV; Würtz P; Havulinna AS; Santalahti K; Pitkänen N; Lehtimäki T; Kähönen M; Lyytikäinen LP; Raitoharju E; Seppälä I; Sarin AP; Ripatti S; Palotie A; Perola M; Viikari JS; Jalkanen S; Maksimow M; Salmi M; Wallace C; Raitakari OT; Salomaa V; Abraham G; Kettunen J; Inouye M
    Am J Hum Genet; 2019 Dec; 105(6):1076-1090. PubMed ID: 31679650
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Phenome-wide functional dissection of pleiotropic effects highlights key molecular pathways for human complex traits.
    Shikov AE; Skitchenko RK; Predeus AV; Barbitoff YA
    Sci Rep; 2020 Jan; 10(1):1037. PubMed ID: 31974475
    [TBL] [Abstract][Full Text] [Related]  

  • 16. A phenome-wide association study (PheWAS) in the Population Architecture using Genomics and Epidemiology (PAGE) study reveals potential pleiotropy in African Americans.
    Pendergrass SA; Buyske S; Jeff JM; Frase A; Dudek S; Bradford Y; Ambite JL; Avery CL; Buzkova P; Deelman E; Fesinmeyer MD; Haiman C; Heiss G; Hindorff LA; Hsu CN; Jackson RD; Lin Y; Le Marchand L; Matise TC; Monroe KR; Moreland L; North KE; Park SL; Reiner A; Wallace R; Wilkens LR; Kooperberg C; Ritchie MD; Crawford DC
    PLoS One; 2019; 14(12):e0226771. PubMed ID: 31891604
    [TBL] [Abstract][Full Text] [Related]  

  • 17. A methodology for multivariate phenotype-based genome-wide association studies to mine pleiotropic genes.
    Park SH; Lee JY; Kim S
    BMC Syst Biol; 2011; 5 Suppl 2(Suppl 2):S13. PubMed ID: 22784570
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Pleiotropy within gene variants associated with nonalcoholic fatty liver disease and traits of the hematopoietic system.
    Pirola CJ; Salatino A; Sookoian S
    World J Gastroenterol; 2021 Jan; 27(4):305-320. PubMed ID: 33584064
    [TBL] [Abstract][Full Text] [Related]  

  • 19. A genome-wide association study identifies three loci associated with mean platelet volume.
    Meisinger C; Prokisch H; Gieger C; Soranzo N; Mehta D; Rosskopf D; Lichtner P; Klopp N; Stephens J; Watkins NA; Deloukas P; Greinacher A; Koenig W; Nauck M; Rimmbach C; Völzke H; Peters A; Illig T; Ouwehand WH; Meitinger T; Wichmann HE; Döring A
    Am J Hum Genet; 2009 Jan; 84(1):66-71. PubMed ID: 19110211
    [TBL] [Abstract][Full Text] [Related]  

  • 20. eMERGE Phenome-Wide Association Study (PheWAS) identifies clinical associations and pleiotropy for stop-gain variants.
    Verma A; Verma SS; Pendergrass SA; Crawford DC; Crosslin DR; Kuivaniemi H; Bush WS; Bradford Y; Kullo I; Bielinski SJ; Li R; Denny JC; Peissig P; Hebbring S; De Andrade M; Ritchie MD; Tromp G
    BMC Med Genomics; 2016 Aug; 9 Suppl 1(Suppl 1):32. PubMed ID: 27535653
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 16.