BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

170 related articles for article (PubMed ID: 22536414)

  • 1. Rare variants in ischemic stroke: an exome pilot study.
    Cole JW; Stine OC; Liu X; Pratap A; Cheng Y; Tallon LJ; Sadzewicz LK; Dueker N; Wozniak MA; Stern BJ; Meschia JF; Mitchell BD; Kittner SJ; O'Connell JR
    PLoS One; 2012; 7(4):e35591. PubMed ID: 22536414
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Rare and Coding Region Genetic Variants Associated With Risk of Ischemic Stroke: The NHLBI Exome Sequence Project.
    Auer PL; Nalls M; Meschia JF; Worrall BB; Longstreth WT; Seshadri S; Kooperberg C; Burger KM; Carlson CS; Carty CL; Chen WM; Cupples LA; DeStefano AL; Fornage M; Hardy J; Hsu L; Jackson RD; Jarvik GP; Kim DS; Lakshminarayan K; Lange LA; Manichaikul A; Quinlan AR; Singleton AB; Thornton TA; Nickerson DA; Peters U; Rich SS;
    JAMA Neurol; 2015 Jul; 72(7):781-8. PubMed ID: 25961151
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Exome Array Analysis of Early-Onset Ischemic Stroke.
    Jaworek T; Ryan KA; Gaynor BJ; McArdle PF; Stine OC; OConnor TD; Lopez H; Aparicio HJ; Gao Y; Lin X; Groves ML; Flaherty ML; Liu S; Yang Q; Wilson J; Seshadri S; Kittner SJ; Mitchell BD; Xu H; Cole JW
    Stroke; 2020 Nov; 51(11):3356-3360. PubMed ID: 32912094
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Exome Array Analysis of 9721 Ischemic Stroke Cases from the SiGN Consortium.
    Xu H; Nguyen K; Gaynor BJ; Ling H; Zhao W; McArdle PF; O'Connor TD; Stine OC; Ryan KA; Lynch M; Smith JA; Faul JD; Hu Y; Haessler JW; Fornage M; Kooperberg C; On Behalf Of The Trans-Omics For Precision Medicine TOPMed Stroke Working Group ; Perry JA; Hong CC; Cole JW; Pugh E; Doheny K; Kardia SLR; Weir DR; Kittner SJ; Mitchell BD;
    Genes (Basel); 2022 Dec; 14(1):. PubMed ID: 36672803
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Evaluating the breast cancer predisposition role of rare variants in genes associated with low-penetrance breast cancer risk SNPs.
    Li N; Rowley SM; Thompson ER; McInerny S; Devereux L; Amarasinghe KC; Zethoven M; Lupat R; Goode D; Li J; Trainer AH; Gorringe KL; James PA; Campbell IG
    Breast Cancer Res; 2018 Jan; 20(1):3. PubMed ID: 29316957
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Rare coding variation in paraoxonase-1 is associated with ischemic stroke in the NHLBI Exome Sequencing Project.
    Kim DS; Crosslin DR; Auer PL; Suzuki SM; Marsillach J; Burt AA; Gordon AS; Meschia JF; Nalls MA; Worrall BB; Longstreth WT; Gottesman RF; Furlong CE; Peters U; Rich SS; Nickerson DA; Jarvik GP;
    J Lipid Res; 2014 Jun; 55(6):1173-8. PubMed ID: 24711634
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Evolution and functional impact of rare coding variation from deep sequencing of human exomes.
    Tennessen JA; Bigham AW; O'Connor TD; Fu W; Kenny EE; Gravel S; McGee S; Do R; Liu X; Jun G; Kang HM; Jordan D; Leal SM; Gabriel S; Rieder MJ; Abecasis G; Altshuler D; Nickerson DA; Boerwinkle E; Sunyaev S; Bustamante CD; Bamshad MJ; Akey JM; ; ;
    Science; 2012 Jul; 337(6090):64-9. PubMed ID: 22604720
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Imputation-based assessment of next generation rare exome variant arrays.
    Martin AR; Tse G; Bustamante CD; Kenny EE
    Pac Symp Biocomput; 2014; ():241-52. PubMed ID: 24297551
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Whole-exome sequencing of over 4100 men of African ancestry and prostate cancer risk.
    Rand KA; Rohland N; Tandon A; Stram A; Sheng X; Do R; Pasaniuc B; Allen A; Quinque D; Mallick S; Le Marchand L; Kaggwa S; Lubwama A; ; ; Stram DO; Watya S; Henderson BE; Conti DV; Reich D; Haiman CA
    Hum Mol Genet; 2016 Jan; 25(2):371-81. PubMed ID: 26604137
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Phosphodiesterase 4D polymorphisms and the risk of cerebral infarction in a biracial population: the Stroke Prevention in Young Women Study.
    Song Q; Cole JW; O'Connell JR; Stine OC; Gallagher M; Giles WH; Mitchell BD; Wozniak MA; Stern BJ; Sorkin JD; McArdle PF; Naj AC; Xu Q; Gibbons GH; Kittner SJ
    Hum Mol Genet; 2006 Aug; 15(16):2468-78. PubMed ID: 16835261
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Association of frequent genetic variants in platelet activation pathway genes with large-vessel ischemic stroke in Polish population.
    Postula M; Janicki PK; Milanowski L; Pordzik J; Eyileten C; Karlinski M; Wylezol P; Solarska M; Czlonkowka A; Kurkowska-Jastrzebka I; Sugino S; Imamura Y; Mirowska-Guzel D
    Platelets; 2017 Jan; 28(1):66-73. PubMed ID: 27533483
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Exome sequencing and genetic testing for MODY.
    Johansson S; Irgens H; Chudasama KK; Molnes J; Aerts J; Roque FS; Jonassen I; Levy S; Lima K; Knappskog PM; Bell GI; Molven A; Njølstad PR
    PLoS One; 2012; 7(5):e38050. PubMed ID: 22662265
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Associations of NINJ2 sequence variants with incident ischemic stroke in the Cohorts for Heart and Aging in Genomic Epidemiology (CHARGE) consortium.
    Bis JC; DeStefano A; Liu X; Brody JA; Choi SH; Verhaaren BF; Debette S; Ikram MA; Shahar E; Butler KR; Gottesman RF; Muzny D; Kovar CL; Psaty BM; Hofman A; Lumley T; Gupta M; Wolf PA; van Duijn C; Gibbs RA; Mosley TH; Longstreth WT; Boerwinkle E; Seshadri S; Fornage M
    PLoS One; 2014; 9(6):e99798. PubMed ID: 24959832
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Exome sequencing of 75 individuals from multiply affected coeliac families and large scale resequencing follow up.
    Mistry V; Bockett NA; Levine AP; Mirza MM; Hunt KA; Ciclitira PJ; Hummerich H; Neuhausen SL; Simpson MA; Plagnol V; van Heel DA
    PLoS One; 2015; 10(1):e0116845. PubMed ID: 25635822
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Whole-exome sequencing identifies rare and low-frequency coding variants associated with LDL cholesterol.
    Lange LA; Hu Y; Zhang H; Xue C; Schmidt EM; Tang ZZ; Bizon C; Lange EM; Smith JD; Turner EH; Jun G; Kang HM; Peloso G; Auer P; Li KP; Flannick J; Zhang J; Fuchsberger C; Gaulton K; Lindgren C; Locke A; Manning A; Sim X; Rivas MA; Holmen OL; Gottesman O; Lu Y; Ruderfer D; Stahl EA; Duan Q; Li Y; Durda P; Jiao S; Isaacs A; Hofman A; Bis JC; Correa A; Griswold ME; Jakobsdottir J; Smith AV; Schreiner PJ; Feitosa MF; Zhang Q; Huffman JE; Crosby J; Wassel CL; Do R; Franceschini N; Martin LW; Robinson JG; Assimes TL; Crosslin DR; Rosenthal EA; Tsai M; Rieder MJ; Farlow DN; Folsom AR; Lumley T; Fox ER; Carlson CS; Peters U; Jackson RD; van Duijn CM; Uitterlinden AG; Levy D; Rotter JI; Taylor HA; Gudnason V; Siscovick DS; Fornage M; Borecki IB; Hayward C; Rudan I; Chen YE; Bottinger EP; Loos RJ; Sætrom P; Hveem K; Boehnke M; Groop L; McCarthy M; Meitinger T; Ballantyne CM; Gabriel SB; O'Donnell CJ; Post WS; North KE; Reiner AP; Boerwinkle E; Psaty BM; Altshuler D; Kathiresan S; Lin DY; Jarvik GP; Cupples LA; Kooperberg C; Wilson JG; Nickerson DA; Abecasis GR; Rich SS; Tracy RP; Willer CJ;
    Am J Hum Genet; 2014 Feb; 94(2):233-45. PubMed ID: 24507775
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Population-Specific Associations of Deleterious Rare Variants in Coding Region of P2RY1-P2RY12 Purinergic Receptor Genes in Large-Vessel Ischemic Stroke Patients.
    Janicki PK; Eyileten C; Ruiz-Velasco V; Sedeek KA; Pordzik J; Czlonkowska A; Kurkowska-Jastrzebska I; Sugino S; Imamura-Kawasawa Y; Mirowska-Guzel D; Postula M
    Int J Mol Sci; 2017 Dec; 18(12):. PubMed ID: 29232918
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. NOTCH3 variants and risk of ischemic stroke.
    Ross OA; Soto-Ortolaza AI; Heckman MG; Verbeeck C; Serie DJ; Rayaprolu S; Rich SS; Nalls MA; Singleton A; Guerreiro R; Kinsella E; Wszolek ZK; Brott TG; Brown RD; Worrall BB; Meschia JF
    PLoS One; 2013; 8(9):e75035. PubMed ID: 24086431
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Association Analysis of the Cubilin (CUBN) and Megalin (LRP2) Genes with ESRD in African Americans.
    Ma J; Guan M; Bowden DW; Ng MCY; Hicks PJ; Lea JP; Ma L; Gao C; Palmer ND; Freedman BI
    Clin J Am Soc Nephrol; 2016 Jun; 11(6):1034-1043. PubMed ID: 27197912
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Whole Exome Sequencing in Atrial Fibrillation.
    Lubitz SA; Brody JA; Bihlmeyer NA; Roselli C; Weng LC; Christophersen IE; Alonso A; Boerwinkle E; Gibbs RA; Bis JC; ; Cupples LA; Mohler PJ; Nickerson DA; Muzny D; Perez MV; Psaty BM; Soliman EZ; Sotoodehnia N; Lunetta KL; Benjamin EJ; Heckbert SR; Arking DE; Ellinor PT; Lin H
    PLoS Genet; 2016 Sep; 12(9):e1006284. PubMed ID: 27589061
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.