BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

168 related articles for article (PubMed ID: 30828643)

  • 1. The Genetic Sphygmomanometer: an argument for routine genome-wide genotyping in the population and a new view on its use to inform clinical practice.
    Timpson NJ; Dudbridge F
    Wellcome Open Res; 2018; 3():138. PubMed ID: 30828643
    [TBL] [Abstract][Full Text] [Related]  

  • 2. The future of Cochrane Neonatal.
    Soll RF; Ovelman C; McGuire W
    Early Hum Dev; 2020 Nov; 150():105191. PubMed ID: 33036834
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Genomic prediction in contrast to a genome-wide association study in explaining heritable variation of complex growth traits in breeding populations of Eucalyptus.
    Müller BSF; Neves LG; de Almeida Filho JE; Resende MFR; Muñoz PR; Dos Santos PET; Filho EP; Kirst M; Grattapaglia D
    BMC Genomics; 2017 Jul; 18(1):524. PubMed ID: 28693539
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Regional heritability mapping and genome-wide association identify loci for complex growth, wood and disease resistance traits in Eucalyptus.
    Resende RT; Resende MD; Silva FF; Azevedo CF; Takahashi EK; Silva-Junior OB; Grattapaglia D
    New Phytol; 2017 Feb; 213(3):1287-1300. PubMed ID: 28079935
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Improved Genetic Profiling of Anthropometric Traits Using a Big Data Approach.
    Canela-Xandri O; Rawlik K; Woolliams JA; Tenesa A
    PLoS One; 2016; 11(12):e0166755. PubMed ID: 27977676
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Inferring the Nature of Missing Heritability in Human Traits Using Data from the GWAS Catalog.
    López-Cortegano E; Caballero A
    Genetics; 2019 Jul; 212(3):891-904. PubMed ID: 31123044
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Describing the genetic architecture of epilepsy through heritability analysis.
    Speed D; O'Brien TJ; Palotie A; Shkura K; Marson AG; Balding DJ; Johnson MR
    Brain; 2014 Oct; 137(Pt 10):2680-9. PubMed ID: 25063994
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Genome-wide Association Identifies Novel Etiological Insights Associated with Parkinson's Disease in African and African Admixed Populations.
    Rizig M; Bandres-Ciga S; Makarious MB; Ojo O; Crea PW; Abiodun O; Levine KS; Abubakar S; Achoru C; Vitale D; Adeniji O; Agabi O; Koretsky MJ; Agulanna U; Hall DA; Akinyemi R; Xie T; Ali M; Shamim EA; Ani-Osheku I; Padmanaban M; Arigbodi O; Standaert DG; Bello A; Dean M; Erameh C; Elsayed I; Farombi T; Okunoye O; Fawale M; Billingsley KJ; Imarhiagbe F; Jerez PA; Iwuozo E; Baker B; Komolafe M; Malik L; Nwani P; Daida K; Nwazor E; Miano-Burkhardt A; Nyandaiti Y; Fang ZH; Obiabo Y; Kluss JH; Odeniyi O; Hernandez D; Odiase F; Tayebi N; Ojini F; Sidranksy E; Onwuegbuzie G; D'Souza AM; Osaigbovo G; Berhe B; Osemwegie N; Reed X; Oshinaike O; Leonard H; Otubogun F; Alvarado CX; Oyakhire S; Ozomma S; Samuel S; Taiwo F; Wahab K; Zubair Y; Iwaki H; Kim JJ; Morris HR; Hardy J; Nalls M; Heilbron K; Norcliffe-Kaufmann L; ; Blauwendraat C; Houlden H; Singleton A; Okubadejo N
    medRxiv; 2023 May; ():. PubMed ID: 37398408
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Heritability and GWAS Studies for Monocyte-Lymphocyte Ratio.
    Lin BD; Willemsen G; Fedko IO; Jansen R; Penninx B; de Geus E; Kluft C; Hottenga J; Boomsma DI
    Twin Res Hum Genet; 2017 Apr; 20(2):97-107. PubMed ID: 28193307
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Comparison of selective genotyping strategies for prediction of breeding values in a population undergoing selection.
    Boligon AA; Long N; Albuquerque LG; Weigel KA; Gianola D; Rosa GJ
    J Anim Sci; 2012 Dec; 90(13):4716-22. PubMed ID: 23372045
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Transethnic Genome-Wide Association Study Provides Insights in the Genetic Architecture and Heritability of Long QT Syndrome.
    Lahrouchi N; Tadros R; Crotti L; Mizusawa Y; Postema PG; Beekman L; Walsh R; Hasegawa K; Barc J; Ernsting M; Turkowski KL; Mazzanti A; Beckmann BM; Shimamoto K; Diamant UB; Wijeyeratne YD; Kucho Y; Robyns T; Ishikawa T; Arbelo E; Christiansen M; Winbo A; Jabbari R; Lubitz SA; Steinfurt J; Rudic B; Loeys B; Shoemaker MB; Weeke PE; Pfeiffer R; Davies B; Andorin A; Hofman N; Dagradi F; Pedrazzini M; Tester DJ; Bos JM; Sarquella-Brugada G; Campuzano Ó; Platonov PG; Stallmeyer B; Zumhagen S; Nannenberg EA; Veldink JH; van den Berg LH; Al-Chalabi A; Shaw CE; Shaw PJ; Morrison KE; Andersen PM; Müller-Nurasyid M; Cusi D; Barlassina C; Galan P; Lathrop M; Munter M; Werge T; Ribasés M; Aung T; Khor CC; Ozaki M; Lichtner P; Meitinger T; van Tintelen JP; Hoedemaekers Y; Denjoy I; Leenhardt A; Napolitano C; Shimizu W; Schott JJ; Gourraud JB; Makiyama T; Ohno S; Itoh H; Krahn AD; Antzelevitch C; Roden DM; Saenen J; Borggrefe M; Odening KE; Ellinor PT; Tfelt-Hansen J; Skinner JR; van den Berg MP; Olesen MS; Brugada J; Brugada R; Makita N; Breckpot J; Yoshinaga M; Behr ER; Rydberg A; Aiba T; Kääb S; Priori SG; Guicheney P; Tan HL; Newton-Cheh C; Ackerman MJ; Schwartz PJ; Schulze-Bahr E; Probst V; Horie M; Wilde AA; Tanck MWT; Bezzina CR
    Circulation; 2020 Jul; 142(4):324-338. PubMed ID: 32429735
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Genome-Wide Association and Regional Heritability Mapping of Plant Architecture, Lodging and Productivity in
    Resende RT; de Resende MDV; Azevedo CF; Fonseca E Silva F; Melo LC; Pereira HS; Souza TLPO; Valdisser PAMR; Brondani C; Vianello RP
    G3 (Bethesda); 2018 Jul; 8(8):2841-2854. PubMed ID: 29967054
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Assessment of whole-genome regression for type II diabetes.
    Vazquez AI; Klimentidis YC; Dhurandhar EJ; Veturi YC; Paérez-Rodríguez P
    PLoS One; 2015; 10(4):e0123818. PubMed ID: 25885636
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Genetic heritability of ischemic stroke and the contribution of previously reported candidate gene and genomewide associations.
    Bevan S; Traylor M; Adib-Samii P; Malik R; Paul NL; Jackson C; Farrall M; Rothwell PM; Sudlow C; Dichgans M; Markus HS
    Stroke; 2012 Dec; 43(12):3161-7. PubMed ID: 23042660
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Heritability in the genome-wide association era.
    Zaitlen N; Kraft P
    Hum Genet; 2012 Oct; 131(10):1655-64. PubMed ID: 22821350
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Implementation of genome-wide complex trait analysis to quantify the heritability in multiple myeloma.
    Mitchell JS; Johnson DC; Litchfield K; Broderick P; Weinhold N; Davies FE; Gregory WA; Jackson GH; Kaiser M; Morgan GJ; Houlston RS
    Sci Rep; 2015 Jul; 5():12473. PubMed ID: 26208354
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Methodological Considerations in Estimation of Phenotype Heritability Using Genome-Wide SNP Data, Illustrated by an Analysis of the Heritability of Height in a Large Sample of African Ancestry Adults.
    Chen F; He J; Zhang J; Chen GK; Thomas V; Ambrosone CB; Bandera EV; Berndt SI; Bernstein L; Blot WJ; Cai Q; Carpten J; Casey G; Chanock SJ; Cheng I; Chu L; Deming SL; Driver WR; Goodman P; Hayes RB; Hennis AJ; Hsing AW; Hu JJ; Ingles SA; John EM; Kittles RA; Kolb S; Leske MC; Millikan RC; Monroe KR; Murphy A; Nemesure B; Neslund-Dudas C; Nyante S; Ostrander EA; Press MF; Rodriguez-Gil JL; Rybicki BA; Schumacher F; Stanford JL; Signorello LB; Strom SS; Stevens V; Van Den Berg D; Wang Z; Witte JS; Wu SY; Yamamura Y; Zheng W; Ziegler RG; Stram AH; Kolonel LN; Le Marchand L; Henderson BE; Haiman CA; Stram DO
    PLoS One; 2015; 10(6):e0131106. PubMed ID: 26125186
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Genome-wide association studies and polygenic risk scores for skin cancer: clinically useful yet?
    Roberts MR; Asgari MM; Toland AE
    Br J Dermatol; 2019 Dec; 181(6):1146-1155. PubMed ID: 30908599
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Multitrait genome association analysis identifies new susceptibility genes for human anthropometric variation in the GCAT cohort.
    Galván-Femenía I; Obón-Santacana M; Piñeyro D; Guindo-Martinez M; Duran X; Carreras A; Pluvinet R; Velasco J; Ramos L; Aussó S; Mercader JM; Puig L; Perucho M; Torrents D; Moreno V; Sumoy L; de Cid R
    J Med Genet; 2018 Nov; 55(11):765-778. PubMed ID: 30166351
    [TBL] [Abstract][Full Text] [Related]  

  • 20.
    ; ; . PubMed ID:
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 9.