BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

291 related articles for article (PubMed ID: 30639324)

  • 1. Efficient Variant Set Mixed Model Association Tests for Continuous and Binary Traits in Large-Scale Whole-Genome Sequencing Studies.
    Chen H; Huffman JE; Brody JA; Wang C; Lee S; Li Z; Gogarten SM; Sofer T; Bielak LF; Bis JC; Blangero J; Bowler RP; Cade BE; Cho MH; Correa A; Curran JE; de Vries PS; Glahn DC; Guo X; Johnson AD; Kardia S; Kooperberg C; Lewis JP; Liu X; Mathias RA; Mitchell BD; O'Connell JR; Peyser PA; Post WS; Reiner AP; Rich SS; Rotter JI; Silverman EK; Smith JA; Vasan RS; Wilson JG; Yanek LR; ; ; Redline S; Smith NL; Boerwinkle E; Borecki IB; Cupples LA; Laurie CC; Morrison AC; Rice KM; Lin X
    Am J Hum Genet; 2019 Feb; 104(2):260-274. PubMed ID: 30639324
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Whole-genome association analyses of sleep-disordered breathing phenotypes in the NHLBI TOPMed program.
    Cade BE; Lee J; Sofer T; Wang H; Zhang M; Chen H; Gharib SA; Gottlieb DJ; Guo X; Lane JM; Liang J; Lin X; Mei H; Patel SR; Purcell SM; Saxena R; Shah NA; Evans DS; Hanis CL; Hillman DR; Mukherjee S; Palmer LJ; Stone KL; Tranah GJ; ; Abecasis GR; Boerwinkle EA; Correa A; Cupples LA; Kaplan RC; Nickerson DA; North KE; Psaty BM; Rotter JI; Rich SS; Tracy RP; Vasan RS; Wilson JG; Zhu X; Redline S;
    Genome Med; 2021 Aug; 13(1):136. PubMed ID: 34446064
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Rare variants in long non-coding RNAs are associated with blood lipid levels in the TOPMed whole-genome sequencing study.
    Wang Y; Selvaraj MS; Li X; Li Z; Holdcraft JA; Arnett DK; Bis JC; Blangero J; Boerwinkle E; Bowden DW; Cade BE; Carlson JC; Carson AP; Chen YI; Curran JE; de Vries PS; Dutcher SK; Ellinor PT; Floyd JS; Fornage M; Freedman BI; Gabriel S; Germer S; Gibbs RA; Guo X; He J; Heard-Costa N; Hildalgo B; Hou L; Irvin MR; Joehanes R; Kaplan RC; Kardia SL; Kelly TN; Kim R; Kooperberg C; Kral BG; Levy D; Li C; Liu C; Lloyd-Jone D; Loos RJ; Mahaney MC; Martin LW; Mathias RA; Minster RL; Mitchell BD; Montasser ME; Morrison AC; Murabito JM; Naseri T; O'Connell JR; Palmer ND; Preuss MH; Psaty BM; Raffield LM; Rao DC; Redline S; Reiner AP; Rich SS; Ruepena MS; Sheu WH; Smith JA; Smith A; Tiwari HK; Tsai MY; Viaud-Martinez KA; Wang Z; Yanek LR; Zhao W; ; Rotter JI; Lin X; Natarajan P; Peloso GM
    Am J Hum Genet; 2023 Oct; 110(10):1704-1717. PubMed ID: 37802043
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Diversity of variant alleles encoding Kidd, Duffy, and Kell antigens in individuals with sickle cell disease using whole genome sequencing data from the NHLBI TOPMed Program.
    Dinardo CL; Oliveira TGM; Kelly S; Ashley-Koch A; Telen M; Schmidt LC; Castilho S; Melo K; Dezan MR; Wheeler MM; Johnsen JM; Nickerson DA; Jain D; Custer B; Pereira AC; Sabino EC;
    Transfusion; 2021 Feb; 61(2):603-616. PubMed ID: 33231305
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Whole-genome sequencing association analysis of quantitative red blood cell phenotypes: The NHLBI TOPMed program.
    Hu Y; Stilp AM; McHugh CP; Rao S; Jain D; Zheng X; Lane J; Méric de Bellefon S; Raffield LM; Chen MH; Yanek LR; Wheeler M; Yao Y; Ren C; Broome J; Moon JY; de Vries PS; Hobbs BD; Sun Q; Surendran P; Brody JA; Blackwell TW; Choquet H; Ryan K; Duggirala R; Heard-Costa N; Wang Z; Chami N; Preuss MH; Min N; Ekunwe L; Lange LA; Cushman M; Faraday N; Curran JE; Almasy L; Kundu K; Smith AV; Gabriel S; Rotter JI; Fornage M; Lloyd-Jones DM; Vasan RS; Smith NL; North KE; Boerwinkle E; Becker LC; Lewis JP; Abecasis GR; Hou L; O'Connell JR; Morrison AC; Beaty TH; Kaplan R; Correa A; Blangero J; Jorgenson E; Psaty BM; Kooperberg C; Walton RT; Kleinstiver BP; Tang H; Loos RJF; Soranzo N; Butterworth AS; Nickerson D; Rich SS; Mitchell BD; Johnson AD; Auer PL; Li Y; Mathias RA; Lettre G; Pankratz N; Laurie CC; Laurie CA; Bauer DE; Conomos MP; Reiner AP;
    Am J Hum Genet; 2021 May; 108(5):874-893. PubMed ID: 33887194
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Powerful, scalable and resource-efficient meta-analysis of rare variant associations in large whole genome sequencing studies.
    Li X; Quick C; Zhou H; Gaynor SM; Liu Y; Chen H; Selvaraj MS; Sun R; Dey R; Arnett DK; Bielak LF; Bis JC; Blangero J; Boerwinkle E; Bowden DW; Brody JA; Cade BE; Correa A; Cupples LA; Curran JE; de Vries PS; Duggirala R; Freedman BI; Göring HHH; Guo X; Haessler J; Kalyani RR; Kooperberg C; Kral BG; Lange LA; Manichaikul A; Martin LW; McGarvey ST; Mitchell BD; Montasser ME; Morrison AC; Naseri T; O'Connell JR; Palmer ND; Peyser PA; Psaty BM; Raffield LM; Redline S; Reiner AP; Reupena MS; Rice KM; Rich SS; Sitlani CM; Smith JA; Taylor KD; Vasan RS; Willer CJ; Wilson JG; Yanek LR; Zhao W; ; Rotter JI; Natarajan P; Peloso GM; Li Z; Lin X
    Nat Genet; 2023 Jan; 55(1):154-164. PubMed ID: 36564505
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Whole genome sequence analyses of eGFR in 23,732 people representing multiple ancestries in the NHLBI trans-omics for precision medicine (TOPMed) consortium.
    Lin BM; Grinde KE; Brody JA; Breeze CE; Raffield LM; Mychaleckyj JC; Thornton TA; Perry JA; Baier LJ; de Las Fuentes L; Guo X; Heavner BD; Hanson RL; Hung YJ; Qian H; Hsiung CA; Hwang SJ; Irvin MR; Jain D; Kelly TN; Kobes S; Lange L; Lash JP; Li Y; Liu X; Mi X; Musani SK; Papanicolaou GJ; Parsa A; Reiner AP; Salimi S; Sheu WH; Shuldiner AR; Taylor KD; Smith AV; Smith JA; Tin A; Vaidya D; Wallace RB; Yamamoto K; Sakaue S; Matsuda K; Kamatani Y; Momozawa Y; Yanek LR; Young BA; Zhao W; Okada Y; Abecasis G; Psaty BM; Arnett DK; Boerwinkle E; Cai J; Yii-Der Chen I; Correa A; Cupples LA; He J; Kardia SL; Kooperberg C; Mathias RA; Mitchell BD; Nickerson DA; Turner ST; Vasan RS; Rotter JI; Levy D; Kramer HJ; Köttgen A; Nhlbi Trans-Omics For Precision Medicine TOPMed Consortium ; TOPMed Kidney Working Group ; Rich SS; Lin DY; Browning SR; Franceschini N
    EBioMedicine; 2021 Jan; 63():103157. PubMed ID: 33418499
    [TBL] [Abstract][Full Text] [Related]  

  • 8. A novel rare variants association test for binary traits in family-based designs via copulas.
    Dossa HRG; Bureau A; Maziade M; Lakhal-Chaieb L; Oualkacha K
    Stat Methods Med Res; 2023 Nov; 32(11):2096-2122. PubMed ID: 37832140
    [TBL] [Abstract][Full Text] [Related]  

  • 9. A unified method for rare variant analysis of gene-environment interactions.
    Lim E; Chen H; Dupuis J; Liu CT
    Stat Med; 2020 Mar; 39(6):801-813. PubMed ID: 31799744
    [TBL] [Abstract][Full Text] [Related]  

  • 10. A statistical framework for powerful multi-trait rare variant analysis in large-scale whole-genome sequencing studies.
    Li X; Chen H; Selvaraj MS; Van Buren E; Zhou H; Wang Y; Sun R; McCaw ZR; Yu Z; Arnett DK; Bis JC; Blangero J; Boerwinkle E; Bowden DW; Brody JA; Cade BE; Carson AP; Carlson JC; Chami N; Chen YI; Curran JE; de Vries PS; Fornage M; Franceschini N; Freedman BI; Gu C; Heard-Costa NL; He J; Hou L; Hung YJ; Irvin MR; Kaplan RC; Kardia SLR; Kelly T; Konigsberg I; Kooperberg C; Kral BG; Li C; Loos RJF; Mahaney MC; Martin LW; Mathias RA; Minster RL; Mitchell BD; Montasser ME; Morrison AC; Palmer ND; Peyser PA; Psaty BM; Raffield LM; Redline S; Reiner AP; Rich SS; Sitlani CM; Smith JA; Taylor KD; Tiwari H; Vasan RS; Wang Z; Yanek LR; Yu B; ; Rice KM; Rotter JI; Peloso GM; Natarajan P; Li Z; Liu Z; Lin X
    bioRxiv; 2023 Nov; ():. PubMed ID: 37961350
    [TBL] [Abstract][Full Text] [Related]  

  • 11. A variational Bayes discrete mixture test for rare variant association.
    Logsdon BA; Dai JY; Auer PL; Johnsen JM; Ganesh SK; Smith NL; Wilson JG; Tracy RP; Lange LA; Jiao S; Rich SS; Lettre G; Carlson CS; Jackson RD; O'Donnell CJ; Wurfel MM; Nickerson DA; Tang H; Reiner AP; Kooperberg C;
    Genet Epidemiol; 2014 Jan; 38(1):21-30. PubMed ID: 24482836
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Optimal unified approach for rare-variant association testing with application to small-sample case-control whole-exome sequencing studies.
    Lee S; Emond MJ; Bamshad MJ; Barnes KC; Rieder MJ; Nickerson DA; ; Christiani DC; Wurfel MM; Lin X
    Am J Hum Genet; 2012 Aug; 91(2):224-37. PubMed ID: 22863193
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Efficient gene-environment interaction tests for large biobank-scale sequencing studies.
    Wang X; Lim E; Liu CT; Sung YJ; Rao DC; Morrison AC; Boerwinkle E; Manning AK; Chen H
    Genet Epidemiol; 2020 Nov; 44(8):908-923. PubMed ID: 32864785
    [TBL] [Abstract][Full Text] [Related]  

  • 14. BinomiRare: A robust test for association of a rare genetic variant with a binary outcome for mixed models and any case-control proportion.
    Sofer T; Lee J; Kurniansyah N; Jain D; Laurie CA; Gogarten SM; Conomos MP; Heavner B; Hu Y; Kooperberg C; Haessler J; Vasan RS; Cupples LA; Coombes BJ; Seyerle A; Gharib SA; Chen H; O'Connell JR; Zhang M; Gottlieb DJ; Psaty BM; Longstreth WT; Rotter JI; Taylor KD; Rich SS; Guo X; Boerwinkle E; Morrison AC; Pankow JS; Johnson AD; Pankratz N; ; Reiner AP; Redline S; Smith NL; Rice KM; Schifano ED
    HGG Adv; 2021 Jul; 2(3):. PubMed ID: 34337551
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Rare variants in long non-coding RNAs are associated with blood lipid levels in the TOPMed Whole Genome Sequencing Study.
    Wang Y; Selvaraj MS; Li X; Li Z; Holdcraft JA; Arnett DK; Bis JC; Blangero J; Boerwinkle E; Bowden DW; Cade BE; Carlson JC; Carson AP; Chen YI; Curran JE; de Vries PS; Dutcher SK; Ellinor PT; Floyd JS; Fornage M; Freedman BI; Gabriel S; Germer S; Gibbs RA; Guo X; He J; Heard-Costa N; Hildalgo B; Hou L; Irvin MR; Joehanes R; Kaplan RC; Kardia SL; Kelly TN; Kim R; Kooperberg C; Kral BG; Levy D; Li C; Liu C; Lloyd-Jone D; Loos RJ; Mahaney MC; Martin LW; Mathias RA; Minster RL; Mitchell BD; Montasser ME; Morrison AC; Murabito JM; Naseri T; O'Connell JR; Palmer ND; Preuss MH; Psaty BM; Raffield LM; Rao DC; Redline S; Reiner AP; Rich SS; Ruepena MS; Sheu WH; Smith JA; Smith A; Tiwari HK; Tsai MY; Viaud-Martinez KA; Wang Z; Yanek LR; Zhao W; ; Rotter JI; Lin X; Natarajan P; Peloso GM
    medRxiv; 2023 Jun; ():. PubMed ID: 37425772
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Robust rare variant association testing for quantitative traits in samples with related individuals.
    Jiang D; McPeek MS
    Genet Epidemiol; 2014 Jan; 38(1):10-20. PubMed ID: 24248908
    [TBL] [Abstract][Full Text] [Related]  

  • 17. A framework for detecting noncoding rare-variant associations of large-scale whole-genome sequencing studies.
    Li Z; Li X; Zhou H; Gaynor SM; Selvaraj MS; Arapoglou T; Quick C; Liu Y; Chen H; Sun R; Dey R; Arnett DK; Auer PL; Bielak LF; Bis JC; Blackwell TW; Blangero J; Boerwinkle E; Bowden DW; Brody JA; Cade BE; Conomos MP; Correa A; Cupples LA; Curran JE; de Vries PS; Duggirala R; Franceschini N; Freedman BI; Göring HHH; Guo X; Kalyani RR; Kooperberg C; Kral BG; Lange LA; Lin BM; Manichaikul A; Manning AK; Martin LW; Mathias RA; Meigs JB; Mitchell BD; Montasser ME; Morrison AC; Naseri T; O'Connell JR; Palmer ND; Peyser PA; Psaty BM; Raffield LM; Redline S; Reiner AP; Reupena MS; Rice KM; Rich SS; Smith JA; Taylor KD; Taub MA; Vasan RS; Weeks DE; Wilson JG; Yanek LR; Zhao W; ; ; Rotter JI; Willer CJ; Natarajan P; Peloso GM; Lin X
    Nat Methods; 2022 Dec; 19(12):1599-1611. PubMed ID: 36303018
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Control for Population Structure and Relatedness for Binary Traits in Genetic Association Studies via Logistic Mixed Models.
    Chen H; Wang C; Conomos MP; Stilp AM; Li Z; Sofer T; Szpiro AA; Chen W; Brehm JM; Celedón JC; Redline S; Papanicolaou GJ; Thornton TA; Laurie CC; Rice K; Lin X
    Am J Hum Genet; 2016 Apr; 98(4):653-66. PubMed ID: 27018471
    [TBL] [Abstract][Full Text] [Related]  

  • 19. An evaluation of approaches for rare variant association analyses of binary traits in related samples.
    Chen MH; Pitsillides A; Yang Q
    Sci Rep; 2021 Feb; 11(1):3145. PubMed ID: 33542345
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Sequencing of 53,831 diverse genomes from the NHLBI TOPMed Program.
    Taliun D; Harris DN; Kessler MD; Carlson J; Szpiech ZA; Torres R; Taliun SAG; Corvelo A; Gogarten SM; Kang HM; Pitsillides AN; LeFaive J; Lee SB; Tian X; Browning BL; Das S; Emde AK; Clarke WE; Loesch DP; Shetty AC; Blackwell TW; Smith AV; Wong Q; Liu X; Conomos MP; Bobo DM; Aguet F; Albert C; Alonso A; Ardlie KG; Arking DE; Aslibekyan S; Auer PL; Barnard J; Barr RG; Barwick L; Becker LC; Beer RL; Benjamin EJ; Bielak LF; Blangero J; Boehnke M; Bowden DW; Brody JA; Burchard EG; Cade BE; Casella JF; Chalazan B; Chasman DI; Chen YI; Cho MH; Choi SH; Chung MK; Clish CB; Correa A; Curran JE; Custer B; Darbar D; Daya M; de Andrade M; DeMeo DL; Dutcher SK; Ellinor PT; Emery LS; Eng C; Fatkin D; Fingerlin T; Forer L; Fornage M; Franceschini N; Fuchsberger C; Fullerton SM; Germer S; Gladwin MT; Gottlieb DJ; Guo X; Hall ME; He J; Heard-Costa NL; Heckbert SR; Irvin MR; Johnsen JM; Johnson AD; Kaplan R; Kardia SLR; Kelly T; Kelly S; Kenny EE; Kiel DP; Klemmer R; Konkle BA; Kooperberg C; Köttgen A; Lange LA; Lasky-Su J; Levy D; Lin X; Lin KH; Liu C; Loos RJF; Garman L; Gerszten R; Lubitz SA; Lunetta KL; Mak ACY; Manichaikul A; Manning AK; Mathias RA; McManus DD; McGarvey ST; Meigs JB; Meyers DA; Mikulla JL; Minear MA; Mitchell BD; Mohanty S; Montasser ME; Montgomery C; Morrison AC; Murabito JM; Natale A; Natarajan P; Nelson SC; North KE; O'Connell JR; Palmer ND; Pankratz N; Peloso GM; Peyser PA; Pleiness J; Post WS; Psaty BM; Rao DC; Redline S; Reiner AP; Roden D; Rotter JI; Ruczinski I; Sarnowski C; Schoenherr S; Schwartz DA; Seo JS; Seshadri S; Sheehan VA; Sheu WH; Shoemaker MB; Smith NL; Smith JA; Sotoodehnia N; Stilp AM; Tang W; Taylor KD; Telen M; Thornton TA; Tracy RP; Van Den Berg DJ; Vasan RS; Viaud-Martinez KA; Vrieze S; Weeks DE; Weir BS; Weiss ST; Weng LC; Willer CJ; Zhang Y; Zhao X; Arnett DK; Ashley-Koch AE; Barnes KC; Boerwinkle E; Gabriel S; Gibbs R; Rice KM; Rich SS; Silverman EK; Qasba P; Gan W; ; Papanicolaou GJ; Nickerson DA; Browning SR; Zody MC; Zöllner S; Wilson JG; Cupples LA; Laurie CC; Jaquish CE; Hernandez RD; O'Connor TD; Abecasis GR
    Nature; 2021 Feb; 590(7845):290-299. PubMed ID: 33568819
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 15.