BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

208 related articles for article (PubMed ID: 37802043)

  • 21. Rare coding variants in 35 genes associate with circulating lipid levels-A multi-ancestry analysis of 170,000 exomes.
    Hindy G; Dornbos P; Chaffin MD; Liu DJ; Wang M; Selvaraj MS; Zhang D; Park J; Aguilar-Salinas CA; Antonacci-Fulton L; Ardissino D; Arnett DK; Aslibekyan S; Atzmon G; Ballantyne CM; Barajas-Olmos F; Barzilai N; Becker LC; Bielak LF; Bis JC; Blangero J; Boerwinkle E; Bonnycastle LL; Bottinger E; Bowden DW; Bown MJ; Brody JA; Broome JG; Burtt NP; Cade BE; Centeno-Cruz F; Chan E; Chang YC; Chen YI; Cheng CY; Choi WJ; Chowdhury R; Contreras-Cubas C; Córdova EJ; Correa A; Cupples LA; Curran JE; Danesh J; de Vries PS; DeFronzo RA; Doddapaneni H; Duggirala R; Dutcher SK; Ellinor PT; Emery LS; Florez JC; Fornage M; Freedman BI; Fuster V; Garay-Sevilla ME; García-Ortiz H; Germer S; Gibbs RA; Gieger C; Glaser B; Gonzalez C; Gonzalez-Villalpando ME; Graff M; Graham SE; Grarup N; Groop LC; Guo X; Gupta N; Han S; Hanis CL; Hansen T; He J; Heard-Costa NL; Hung YJ; Hwang MY; Irvin MR; Islas-Andrade S; Jarvik GP; Kang HM; Kardia SLR; Kelly T; Kenny EE; Khan AT; Kim BJ; Kim RW; Kim YJ; Koistinen HA; Kooperberg C; Kuusisto J; Kwak SH; Laakso M; Lange LA; Lee J; Lee J; Lee S; Lehman DM; Lemaitre RN; Linneberg A; Liu J; Loos RJF; Lubitz SA; Lyssenko V; Ma RCW; Martin LW; Martínez-Hernández A; Mathias RA; McGarvey ST; McPherson R; Meigs JB; Meitinger T; Melander O; Mendoza-Caamal E; Metcalf GA; Mi X; Mohlke KL; Montasser ME; Moon JY; Moreno-Macías H; Morrison AC; Muzny DM; Nelson SC; Nilsson PM; O'Connell JR; Orho-Melander M; Orozco L; Palmer CNA; Palmer ND; Park CJ; Park KS; Pedersen O; Peralta JM; Peyser PA; Post WS; Preuss M; Psaty BM; Qi Q; Rao DC; Redline S; Reiner AP; Revilla-Monsalve C; Rich SS; Samani N; Schunkert H; Schurmann C; Seo D; Seo JS; Sim X; Sladek R; Small KS; So WY; Stilp AM; Tai ES; Tam CHT; Taylor KD; Teo YY; Thameem F; Tomlinson B; Tsai MY; Tuomi T; Tuomilehto J; Tusié-Luna T; Udler MS; van Dam RM; Vasan RS; Viaud Martinez KA; Wang FF; Wang X; Watkins H; Weeks DE; Wilson JG; Witte DR; Wong TY; Yanek LR; ; ; ; Kathiresan S; Rader DJ; Rotter JI; Boehnke M; McCarthy MI; Willer CJ; Natarajan P; Flannick JA; Khera AV; Peloso GM
    Am J Hum Genet; 2022 Jan; 109(1):81-96. PubMed ID: 34932938
    [TBL] [Abstract][Full Text] [Related]  

  • 22. 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]  

  • 23. Leveraging linkage evidence to identify low-frequency and rare variants on 16p13 associated with blood pressure using TOPMed whole genome sequencing data.
    He KY; Li X; Kelly TN; Liang J; Cade BE; Assimes TL; Becker LC; Beitelshees AL; Bress AP; Chang YC; Chen YI; de Vries PS; Fox ER; Franceschini N; Furniss A; Gao Y; Guo X; Haessler J; Hwang SJ; Irvin MR; Kalyani RR; Liu CT; Liu C; Martin LW; Montasser ME; Muntner PM; Mwasongwe S; Palmas W; Reiner AP; Shimbo D; Smith JA; Snively BM; Yanek LR; Boerwinkle E; Correa A; Cupples LA; He J; Kardia SLR; Kooperberg C; Mathias RA; Mitchell BD; Psaty BM; Vasan RS; Rao DC; Rich SS; Rotter JI; Wilson JG; ; Chakravarti A; Morrison AC; Levy D; Arnett DK; Redline S; Zhu X
    Hum Genet; 2019 Feb; 138(2):199-210. PubMed ID: 30671673
    [TBL] [Abstract][Full Text] [Related]  

  • 24. 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]  

  • 25. Identification of putative causal loci in whole-genome sequencing data via knockoff statistics.
    He Z; Liu L; Wang C; Le Guen Y; Lee J; Gogarten S; Lu F; Montgomery S; Tang H; Silverman EK; Cho MH; Greicius M; Ionita-Laza I
    Nat Commun; 2021 May; 12(1):3152. PubMed ID: 34035245
    [TBL] [Abstract][Full Text] [Related]  

  • 26. 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]  

  • 27. 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 KE; 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;
    Hum Mol Genet; 2024 May; ():. PubMed ID: 38747556
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Key variants via the Alzheimer's Disease Sequencing Project whole genome sequence data.
    Wang Y; Sarnowski C; Lin H; Pitsillides AN; Heard-Costa NL; Choi SH; Wang D; Bis JC; Blue EE; ; Boerwinkle E; De Jager PL; Fornage M; Wijsman EM; Seshadri S; Dupuis J; Peloso GM; DeStefano AL;
    Alzheimers Dement; 2024 May; 20(5):3290-3304. PubMed ID: 38511601
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Practical Approaches for Whole-Genome Sequence Analysis of Heart- and Blood-Related Traits.
    Morrison AC; Huang Z; Yu B; Metcalf G; Liu X; Ballantyne C; Coresh J; Yu F; Muzny D; Feofanova E; Rustagi N; Gibbs R; Boerwinkle E
    Am J Hum Genet; 2017 Feb; 100(2):205-215. PubMed ID: 28089252
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Integrating DNA sequencing and transcriptomic data for association analyses of low-frequency variants and lipid traits.
    Yang T; Wu C; Wei P; Pan W
    Hum Mol Genet; 2020 Feb; 29(3):515-526. PubMed ID: 31919517
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Mining the LIPG allelic spectrum reveals the contribution of rare and common regulatory variants to HDL cholesterol.
    Khetarpal SA; Edmondson AC; Raghavan A; Neeli H; Jin W; Badellino KO; Demissie S; Manning AK; DerOhannessian SL; Wolfe ML; Cupples LA; Li M; Kathiresan S; Rader DJ
    PLoS Genet; 2011 Dec; 7(12):e1002393. PubMed ID: 22174694
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Allelic Heterogeneity at the CRP Locus Identified by Whole-Genome Sequencing in Multi-ancestry Cohorts.
    Raffield LM; Iyengar AK; Wang B; Gaynor SM; Spracklen CN; Zhong X; Kowalski MH; Salimi S; Polfus LM; Benjamin EJ; Bis JC; Bowler R; Cade BE; Choi WJ; Comellas AP; Correa A; Cruz P; Doddapaneni H; Durda P; Gogarten SM; Jain D; Kim RW; Kral BG; Lange LA; Larson MG; Laurie C; Lee J; Lee S; Lewis JP; Metcalf GA; Mitchell BD; Momin Z; Muzny DM; Pankratz N; Park CJ; Rich SS; Rotter JI; Ryan K; Seo D; Tracy RP; Viaud-Martinez KA; Yanek LR; Zhao LP; Lin X; Li B; Li Y; Dupuis J; Reiner AP; Mohlke KL; Auer PL; ;
    Am J Hum Genet; 2020 Jan; 106(1):112-120. PubMed ID: 31883642
    [TBL] [Abstract][Full Text] [Related]  

  • 33. A genome-wide association study for blood lipid phenotypes in the Framingham Heart Study.
    Kathiresan S; Manning AK; Demissie S; D'Agostino RB; Surti A; Guiducci C; Gianniny L; Burtt NP; Melander O; Orho-Melander M; Arnett DK; Peloso GM; Ordovas JM; Cupples LA
    BMC Med Genet; 2007 Sep; 8 Suppl 1(Suppl 1):S17. PubMed ID: 17903299
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Analysis with the exome array identifies multiple new independent variants in lipid loci.
    Kanoni S; Masca NG; Stirrups KE; Varga TV; Warren HR; Scott RA; Southam L; Zhang W; Yaghootkar H; Müller-Nurasyid M; Couto Alves A; Strawbridge RJ; Lataniotis L; An Hashim N; Besse C; Boland A; Braund PS; Connell JM; Dominiczak A; Farmaki AE; Franks S; Grallert H; Jansson JH; Karaleftheri M; Keinänen-Kiukaanniemi S; Matchan A; Pasko D; Peters A; Poulter N; Rayner NW; Renström F; Rolandsson O; Sabater-Lleal M; Sennblad B; Sever P; Shields D; Silveira A; Stanton AV; Strauch K; Tomaszewski M; Tsafantakis E; Waldenberger M; Blakemore AI; Dedoussis G; Escher SA; Kooner JS; McCarthy MI; Palmer CN; ; Hamsten A; Caulfield MJ; Frayling TM; Tobin MD; Jarvelin MR; Zeggini E; Gieger C; Chambers JC; Wareham NJ; Munroe PB; Franks PW; Samani NJ; Deloukas P
    Hum Mol Genet; 2016 Sep; 25(18):4094-4106. PubMed ID: 27466198
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Genome-wide association study of blood lipids in Indians confirms universality of established variants.
    Bandesh K; Prasad G; Giri AK; Kauser Y; Upadhyay M; ; Basu A; Tandon N; Bharadwaj D
    J Hum Genet; 2019 Jun; 64(6):573-587. PubMed ID: 30911093
    [TBL] [Abstract][Full Text] [Related]  

  • 36. 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]  

  • 37. eSCAN: scan regulatory regions for aggregate association testing using whole-genome sequencing data.
    Yang Y; Sun Q; Huang L; Broome JG; Correa A; Reiner A; ; Raffield LM; Yang Y; Li Y
    Brief Bioinform; 2022 Jan; 23(1):. PubMed ID: 34882196
    [TBL] [Abstract][Full Text] [Related]  

  • 38. 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]  

  • 39. Sequencing Analysis at 8p23 Identifies Multiple Rare Variants in DLC1 Associated with Sleep-Related Oxyhemoglobin Saturation Level.
    Liang J; Cade BE; He KY; Wang H; Lee J; Sofer T; Williams S; Li R; Chen H; Gottlieb DJ; Evans DS; Guo X; Gharib SA; Hale L; Hillman DR; Lutsey PL; Mukherjee S; Ochs-Balcom HM; Palmer LJ; Rhodes J; Purcell S; Patel SR; Saxena R; Stone KL; Tang W; Tranah GJ; Boerwinkle E; Lin X; Liu Y; Psaty BM; Vasan RS; Cho MH; Manichaikul A; Silverman EK; Barr RG; Rich SS; Rotter JI; Wilson JG; ; ; Redline S; Zhu X
    Am J Hum Genet; 2019 Nov; 105(5):1057-1068. PubMed ID: 31668705
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Whole genome analysis of plasma fibrinogen reveals population-differentiated genetic regulators with putative liver roles.
    Huffman JE; Nicolas J; Hahn J; Heath AS; Raffield LM; Yanek LR; Brody JA; Thibord F; Almasy L; Bartz TM; Bielak LF; Bowler RP; Carrasquilla GD; Chasman DI; Chen MH; Emmert DB; Ghanbari M; Haessle J; Hottenga JJ; Kleber ME; Le NQ; Lee J; Lewis JP; Li-Gao R; Luan J; Malmberg A; Mangino M; Marioni RE; Martinez-Perez A; Pankratz N; Polasek O; Richmond A; Rodriguez BA; Rotter JI; Steri M; Suchon P; Trompet S; Weiss S; Zare M; Auer P; Cho MH; Christofidou P; Davies G; de Geus E; Deleuze JF; Delgado GE; Ekunwe L; Faraday N; Gögele M; Greinacher A; He G; Howard T; Joshi PK; Kilpeläinen TO; Lahti J; Linneberg A; Naitza S; Noordam R; Paüls-Vergés F; Rich SS; Rosendaal FR; Rudan I; Ryan KA; Souto JC; van Rooij FJ; Wang H; Zhao W; Becker LC; Beswick A; Brown MR; Cade BE; Campbell H; Cho K; Crapo JD; Curran JE; de Maat MP; Doyle M; Elliott P; Floyd JS; Fuchsberger C; Grarup N; Guo X; Harris SE; Hou L; Kolcic I; Kooperberg C; Menni C; Nauck M; O'Connell JR; Orrù V; Psaty BM; Räikkönen K; Smith JA; Soria JM; Stott DJ; van Hylckama Vlieg A; Watkins H; Willemsen G; Wilson P; Ben-Shlomo Y; Blangero J; Boomsma D; Cox SR; Dehghan A; Eriksson JG; Fiorillo E; Fornage M; Hansen T; Hayward C; Ikram MA; Jukema JW; Kardia SL; Lange LA; März W; Mathias RA; Mitchell BD; Mook-Kanamori DO; Morange PE; Pedersen O; Pramstaller PP; Redline S; Reiner A; Ridker PM; Silverman EK; Spector TD; Völker U; Wareham N; Wilson JF; Yao J; ; ; Trégouët DA; Johnson AD; Wolberg AS; de Vries PS; Sabater-Lleal M; Morrison AC; Smith NL
    medRxiv; 2023 Jun; ():. PubMed ID: 37398003
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 11.