BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

184 related articles for article (PubMed ID: 36481753)

  • 21. TOP-LD: A tool to explore linkage disequilibrium with TOPMed whole-genome sequence data.
    Huang L; Rosen JD; Sun Q; Chen J; Wheeler MM; Zhou Y; Min YI; Kooperberg C; Conomos MP; Stilp AM; Rich SS; Rotter JI; Manichaikul A; Loos RJF; Kenny EE; Blackwell TW; Smith AV; Jun G; Sedlazeck FJ; Metcalf G; Boerwinkle E; ; Raffield LM; Reiner AP; Auer PL; Li Y
    Am J Hum Genet; 2022 Jun; 109(6):1175-1181. PubMed ID: 35504290
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Whole-exome sequence analysis of anthropometric traits illustrates challenges in identifying effects of rare genetic variants.
    Young KL; Fisher V; Deng X; Brody JA; Graff M; Lim E; Lin BM; Xu H; Amin N; An P; Aslibekyan S; Fohner AE; Hidalgo B; Lenzini P; Kraaij R; Medina-Gomez C; Prokić I; Rivadeneira F; Sitlani C; Tao R; van Rooij J; Zhang D; Broome JG; Buth EJ; Heavner BD; Jain D; Smith AV; Barnes K; Boorgula MP; Chavan S; Darbar D; De Andrade M; Guo X; Haessler J; Irvin MR; Kalyani RR; Kardia SLR; Kooperberg C; Kim W; Mathias RA; McDonald ML; Mitchell BD; Peyser PA; Regan EA; Redline S; Reiner AP; Rich SS; Rotter JI; Smith JA; Weiss S; Wiggins KL; Yanek LR; Arnett D; Heard-Costa NL; Leal S; Lin D; McKnight B; Province M; van Duijn CM; North KE; Cupples LA; Liu CT
    HGG Adv; 2023 Jan; 4(1):100163. PubMed ID: 36568030
    [TBL] [Abstract][Full Text] [Related]  

  • 23. 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]  

  • 24. Monogenic and Polygenic Contributions to QTc Prolongation in the Population.
    Nauffal V; Morrill VN; Jurgens SJ; Choi SH; Hall AW; Weng LC; Halford JL; Austin-Tse C; Haggerty CM; Harris SL; Wong EK; Alonso A; Arking DE; Benjamin EJ; Boerwinkle E; Min YI; Correa A; Fornwalt BK; Heckbert SR; ; Kooperberg C; Lin HJ; J F Loos R; Rice KM; Gupta N; Blackwell TW; Mitchell BD; Morrison AC; Psaty BM; Post WS; Redline S; Rehm HL; Rich SS; Rotter JI; Soliman EZ; Sotoodehnia N; Lunetta KL; Ellinor PT; Lubitz SA;
    Circulation; 2022 May; 145(20):1524-1533. PubMed ID: 35389749
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Genome sequencing unveils a regulatory landscape of platelet reactivity.
    Keramati AR; Chen MH; Rodriguez BAT; Yanek LR; Bhan A; Gaynor BJ; Ryan K; Brody JA; Zhong X; Wei Q; ; Kammers K; Kanchan K; Iyer K; Kowalski MH; Pitsillides AN; Cupples LA; Li B; Schlaeger TM; Shuldiner AR; O'Connell JR; Ruczinski I; Mitchell BD; Faraday N; Taub MA; Becker LC; Lewis JP; Mathias RA; Johnson AD
    Nat Commun; 2021 Jun; 12(1):3626. PubMed ID: 34131117
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Whole Genome Sequencing Based Analysis of Inflammation Biomarkers in the Trans-Omics for Precision Medicine (TOPMed) Consortium.
    Jiang MZ; Gaynor SM; Li X; Van Buren E; Stilp A; Buth E; Wang FF; Manansala R; Gogarten SM; Li Z; Polfus LM; Salimi S; Bis JC; Pankratz N; Yanek LR; Durda P; Tracy RP; Rich SS; Rotter JI; Mitchell BD; Lewis JP; Psaty BM; Pratte KA; Silverman EK; Kaplan RC; Avery C; North K; Mathias RA; Faraday N; Lin H; Wang B; Carson AP; Norwood AF; Gibbs RA; Kooperberg C; Lundin J; Peters U; Dupuis J; Hou L; Fornage M; Benjamin EJ; Reiner AP; Bowler RP; Lin X; Auer PL; Raffield LM;
    bioRxiv; 2023 Sep; ():. PubMed ID: 37745480
    [TBL] [Abstract][Full Text] [Related]  

  • 27. 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]  

  • 28. 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]  

  • 29. Exploring quantitative traits-associated copy number deletions through reanalysis of UK10K consortium whole genome sequencing cohorts.
    Lee S; Kim J; Ohn JH
    BMC Genomics; 2023 Dec; 24(1):787. PubMed ID: 38110883
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Powerful and efficient SNP-set association tests across multiple phenotypes using GWAS summary data.
    Guo B; Wu B
    Bioinformatics; 2019 Apr; 35(8):1366-1372. PubMed ID: 30239606
    [TBL] [Abstract][Full Text] [Related]  

  • 31. The Value of Rare Genetic Variation in the Prediction of Common Obesity in European Ancestry Populations.
    Wang Z; Choi SW; Chami N; Boerwinkle E; Fornage M; Redline S; Bis JC; Brody JA; Psaty BM; Kim W; McDonald MN; Regan EA; Silverman EK; Liu CT; Vasan RS; Kalyani RR; Mathias RA; Yanek LR; Arnett DK; Justice AE; North KE; Kaplan R; Heckbert SR; de Andrade M; Guo X; Lange LA; Rich SS; Rotter JI; Ellinor PT; Lubitz SA; Blangero J; Shoemaker MB; Darbar D; Gladwin MT; Albert CM; Chasman DI; Jackson RD; Kooperberg C; Reiner AP; O'Reilly PF; Loos RJF
    Front Endocrinol (Lausanne); 2022; 13():863893. PubMed ID: 35592775
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Whole Genome Analysis of Venous Thromboembolism: the Trans-Omics for Precision Medicine Program.
    Seyerle AA; Laurie CA; Coombes BJ; Jain D; Conomos MP; Brody J; Chen MH; Gogarten SM; Beutel KM; Gupta N; Heckbert SR; Jackson RD; Johnson AD; Ko D; Manson JE; McKnight B; Metcalf GA; Morrison AC; Reiner AP; Sofer T; Tang W; Wiggins KL; ; Boerwinkle E; de Andrade M; Gabriel SB; Gibbs RA; Laurie CC; Psaty BM; Vasan RS; Rice K; Kooperberg C; Pankow JS; Smith NL; Pankratz N
    Circ Genom Precis Med; 2023 Apr; 16(2):e003532. PubMed ID: 36960714
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Structural variants and tandem repeats in the founder individuals of four F
    Blaj I; Tetens J; Bennewitz J; Thaller G; Falker-Gieske C
    BMC Genomics; 2022 Sep; 23(1):631. PubMed ID: 36057580
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Contribution of rare whole-genome sequencing variants to plasma protein levels and the missing heritability.
    Kierczak M; Rafati N; Höglund J; Gourlé H; Lo Faro V; Schmitz D; Ek WE; Gyllensten U; Enroth S; Ekman D; Nystedt B; Karlsson T; Johansson Å
    Nat Commun; 2022 May; 13(1):2532. PubMed ID: 35534486
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Whole genome sequencing of 4,787 individuals identifies gene-based rare variants in age-related macular degeneration.
    Kwong A; Zawistowski M; Fritsche LG; Zhan X; Bragg-Gresham J; Branham KE; Advani J; Othman M; Ratnapriya R; Teslovich TM; Stambolian D; Chew EY; Abecasis GR; Swaroop A
    Hum Mol Genet; 2024 Feb; 33(4):374-385. PubMed ID: 37934784
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Whole genome sequence analysis of pulmonary function and COPD in 19,996 multi-ethnic participants.
    Zhao X; Qiao D; Yang C; Kasela S; Kim W; Ma Y; Shrine N; Batini C; Sofer T; Taliun SAG; Sakornsakolpat P; Balte PP; Prokopenko D; Yu B; Lange LA; Dupuis J; Cade BE; Lee J; Gharib SA; Daya M; Laurie CA; Ruczinski I; Cupples LA; Loehr LR; Bartz TM; Morrison AC; Psaty BM; Vasan RS; Wilson JG; Taylor KD; Durda P; Johnson WC; Cornell E; Guo X; Liu Y; Tracy RP; Ardlie KG; Aguet F; VanDenBerg DJ; Papanicolaou GJ; Rotter JI; Barnes KC; Jain D; Nickerson DA; Muzny DM; Metcalf GA; Doddapaneni H; Dugan-Perez S; Gupta N; Gabriel S; Rich SS; O'Connor GT; Redline S; Reed RM; Laurie CC; Daviglus ML; Preudhomme LK; Burkart KM; Kaplan RC; Wain LV; Tobin MD; London SJ; Lappalainen T; Oelsner EC; Abecasis GR; Silverman EK; Barr RG; ; ; Cho MH; Manichaikul A
    Nat Commun; 2020 Oct; 11(1):5182. PubMed ID: 33057025
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Genetic architecture of quantitative traits in beef cattle revealed by genome wide association studies of imputed whole genome sequence variants: II: carcass merit traits.
    Wang Y; Zhang F; Mukiibi R; Chen L; Vinsky M; Plastow G; Basarab J; Stothard P; Li C
    BMC Genomics; 2020 Jan; 21(1):38. PubMed ID: 31931697
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Insights From a Large-Scale Whole-Genome Sequencing Study of Systolic Blood Pressure, Diastolic Blood Pressure, and Hypertension.
    Kelly TN; Sun X; He KY; Brown MR; Taliun SAG; Hellwege JN; Irvin MR; Mi X; Brody JA; Franceschini N; Guo X; Hwang SJ; de Vries PS; Gao Y; Moscati A; Nadkarni GN; Yanek LR; Elfassy T; Smith JA; Chung RH; Beitelshees AL; Patki A; Aslibekyan S; Blobner BM; Peralta JM; Assimes TL; Palmas WR; Liu C; Bress AP; Huang Z; Becker LC; Hwa CM; O'Connell JR; Carlson JC; Warren HR; Das S; Giri A; Martin LW; Craig Johnson W; Fox ER; Bottinger EP; Razavi AC; Vaidya D; Chuang LM; Chang YC; Naseri T; Jain D; Kang HM; Hung AM; Srinivasasainagendra V; Snively BM; Gu D; Montasser ME; Reupena MS; Heavner BD; LeFaive J; Hixson JE; Rice KM; Wang FF; Nielsen JB; Huang J; Khan AT; Zhou W; Nierenberg JL; Laurie CC; Armstrong ND; Shi M; Pan Y; Stilp AM; Emery L; Wong Q; Hawley NL; Minster RL; Curran JE; Munroe PB; Weeks DE; North KE; Tracy RP; Kenny EE; Shimbo D; Chakravarti A; Rich SS; Reiner AP; Blangero J; Redline S; Mitchell BD; Rao DC; Ida Chen YD; Kardia SLR; Kaplan RC; Mathias RA; He J; Psaty BM; Fornage M; Loos RJF; Correa A; Boerwinkle E; Rotter JI; Kooperberg C; Edwards TL; Abecasis GR; Zhu X; Levy D; Arnett DK; Morrison AC;
    Hypertension; 2022 Aug; 79(8):1656-1667. PubMed ID: 35652341
    [TBL] [Abstract][Full Text] [Related]  

  • 39. 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]  

  • 40. 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]  

    [Previous]   [Next]    [New Search]
    of 10.