BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

244 related articles for article (PubMed ID: 36220816)

  • 1. Whole genome sequence analysis of blood lipid levels in >66,000 individuals.
    Selvaraj MS; Li X; Li Z; Pampana A; Zhang DY; Park J; Aslibekyan S; Bis JC; Brody JA; Cade BE; Chuang LM; Chung RH; Curran JE; de Las Fuentes L; de Vries PS; Duggirala R; Freedman BI; Graff M; Guo X; Heard-Costa N; Hidalgo B; Hwu CM; Irvin MR; Kelly TN; Kral BG; Lange L; Li X; Lisa M; Lubitz SA; Manichaikul AW; Michael P; Montasser ME; Morrison AC; Naseri T; O'Connell JR; Palmer ND; Peyser PA; Reupena MS; Smith JA; Sun X; Taylor KD; Tracy RP; Tsai MY; Wang Z; Wang Y; Bao W; Wilkins JT; Yanek LR; Zhao W; Arnett DK; Blangero J; Boerwinkle E; Bowden DW; Chen YI; Correa A; Cupples LA; Dutcher SK; Ellinor PT; Fornage M; Gabriel S; Germer S; Gibbs R; He J; Kaplan RC; Kardia SLR; Kim R; Kooperberg C; Loos RJF; Viaud-Martinez KA; Mathias RA; McGarvey ST; Mitchell BD; Nickerson D; North KE; Psaty BM; Redline S; Reiner AP; Vasan RS; Rich SS; Willer C; Rotter JI; Rader DJ; Lin X; ; Peloso GM; Natarajan P
    Nat Commun; 2022 Oct; 13(1):5995. PubMed ID: 36220816
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Deep-coverage whole genome sequences and blood lipids among 16,324 individuals.
    Natarajan P; Peloso GM; Zekavat SM; Montasser M; Ganna A; Chaffin M; Khera AV; Zhou W; Bloom JM; Engreitz JM; Ernst J; O'Connell JR; Ruotsalainen SE; Alver M; Manichaikul A; Johnson WC; Perry JA; Poterba T; Seed C; Surakka IL; Esko T; Ripatti S; Salomaa V; Correa A; Vasan RS; Kellis M; Neale BM; Lander ES; Abecasis G; Mitchell B; Rich SS; Wilson JG; Cupples LA; Rotter JI; Willer CJ; Kathiresan S;
    Nat Commun; 2018 Aug; 9(1):3391. PubMed ID: 30140000
    [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. Low coverage whole genome sequencing enables accurate assessment of common variants and calculation of genome-wide polygenic scores.
    Homburger JR; Neben CL; Mishne G; Zhou AY; Kathiresan S; Khera AV
    Genome Med; 2019 Nov; 11(1):74. PubMed ID: 31771638
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Targeted exonic sequencing of GWAS loci in the high extremes of the plasma lipids distribution.
    Patel AP; Peloso GM; Pirruccello JP; Johansen CT; Dubé JB; Larach DB; Ban MR; Dallinge-Thie GM; Gupta N; Boehnke M; Abecasis GR; Kastelein JJ; Hovingh GK; Hegele RA; Rader DJ; Kathiresan S
    Atherosclerosis; 2016 Jul; 250():63-8. PubMed ID: 27182959
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. 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]  

  • 8. Dynamic Scan Procedure for Detecting Rare-Variant Association Regions in Whole-Genome Sequencing Studies.
    Li Z; Li X; Liu Y; Shen J; Chen H; Zhou H; Morrison AC; Boerwinkle E; Lin X
    Am J Hum Genet; 2019 May; 104(5):802-814. PubMed ID: 30982610
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Coding-sequence variants are associated with blood lipid levels in 14,473 Chinese.
    Lu X; Li J; Li H; Chen Y; Wang L; He M; Wang Y; Sun L; Hu Y; Huang J; Wang F; Liu X; Chen S; Yu K; Yang X; Mo Z; Lin X; Wu T; Gu D
    Hum Mol Genet; 2016 Sep; 25(18):4107-4116. PubMed ID: 27516387
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Translating genetic association of lipid levels for biological and clinical application.
    Crone B; Krause AM; Hornsby WE; Willer CJ; Surakka I
    Cardiovasc Drugs Ther; 2021 Jun; 35(3):617-626. PubMed ID: 33604704
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Recent developments in genome and exome-wide analyses of plasma lipids.
    Lange LA; Willer CJ; Rich SS
    Curr Opin Lipidol; 2015 Apr; 26(2):96-102. PubMed ID: 25692345
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Rare non-coding variants are associated with plasma lipid traits in a founder population.
    Igartua C; Mozaffari SV; Nicolae DL; Ober C
    Sci Rep; 2017 Nov; 7(1):16415. PubMed ID: 29180722
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Deep coverage whole genome sequences and plasma lipoprotein(a) in individuals of European and African ancestries.
    Zekavat SM; Ruotsalainen S; Handsaker RE; Alver M; Bloom J; Poterba T; Seed C; Ernst J; Chaffin M; Engreitz J; Peloso GM; Manichaikul A; Yang C; Ryan KA; Fu M; Johnson WC; Tsai M; Budoff M; Vasan RS; Cupples LA; Rotter JI; Rich SS; Post W; Mitchell BD; Correa A; Metspalu A; Wilson JG; Salomaa V; Kellis M; Daly MJ; Neale BM; McCarroll S; Surakka I; Esko T; Ganna A; Ripatti S; Kathiresan S; Natarajan P;
    Nat Commun; 2018 Jul; 9(1):2606. PubMed ID: 29973585
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Whole-exome sequencing identifies novel protein-altering variants associated with serum apolipoprotein and lipid concentrations.
    Sandholm N; Hotakainen R; Haukka JK; Jansson Sigfrids F; Dahlström EH; Antikainen AA; Valo E; Syreeni A; Kilpeläinen E; Kytölä A; Palotie A; Harjutsalo V; Forsblom C; Groop PH;
    Genome Med; 2022 Nov; 14(1):132. PubMed ID: 36419110
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. Polygenic link between blood lipids and amyotrophic lateral sclerosis.
    Chen X; Yazdani S; Piehl F; Magnusson PKE; Fang F
    Neurobiol Aging; 2018 Jul; 67():202.e1-202.e6. PubMed ID: 29685649
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Multiple associated variants increase the heritability explained for plasma lipids and coronary artery disease.
    Tada H; Won HH; Melander O; Yang J; Peloso GM; Kathiresan S
    Circ Cardiovasc Genet; 2014 Oct; 7(5):583-7. PubMed ID: 25170055
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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]  

  • 19. The causal effects of lipid traits on kidney function in Africans: bidirectional and multivariable Mendelian-randomization study.
    Kintu C; Soremekun O; Kamiza AB; Kalungi A; Mayanja R; Kalyesubula R; Bagaya S B; Jjingo D; Fabian J; Gill D; Nyirenda M; Nitsch D; Chikowore T; Fatumo S
    EBioMedicine; 2023 Apr; 90():104537. PubMed ID: 37001235
    [TBL] [Abstract][Full Text] [Related]  

  • 20. HDL Cholesterol, LDL Cholesterol, and Triglycerides as Risk Factors for CKD: A Mendelian Randomization Study.
    Lanktree MB; Thériault S; Walsh M; Paré G
    Am J Kidney Dis; 2018 Feb; 71(2):166-172. PubMed ID: 28754456
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 13.