Now showing items 1-4 of 4

    • Discovery and fine mapping of serum protein loci through transethnic meta-analysis 

      Franceschini N; van Rooij FJ; Prins BP; Feitosa MF; Karakas M; Eckfeldt JH; Folsom AR; Kopp J; Vaez A; Andrews JS; Baumert J; Boraska V; Broer L; Hayward C; Ngwa JS; Okada Y; Polasek O; Westra HJ; Wang YA; Del Greco M F; Glazer NL; Kapur K; Kema IP; Lopez LM; Schillert A; Smith AV; Winkler CA; Zgaga L; LifeLines Cohort Study; Bandinelli S; Bergmann S; Boban M; Bochud M; Chen YD; Davies G; Dehghan A; Ding J; Doering A; Durda JP; Ferrucci L; Franco OH; Franke L; Gunjaca G; Hofman A; Hsu FC; Kolcic I; Kraja A; Kubo M; Lackner KJ; Launer L; Loehr LR; Li G; Meisinger C; Nakamura Y; Schwienbacher C; Starr JM; Takahashi A; Torlak V; Uitterlinden AG; Vitart V; Waldenberger M; Wild PS; Kirin M; Zeller T; Zemunik T; Zhang Q; Ziegler A; Blankenberg S; Boerwinkle E; Borecki IB; Campbell H; Deary IJ; Frayling TM; Gieger C; Harris TB; Hicks AA; Koenig W; O' Donnell CJ; Fox CS; Pramstaller PP; Psaty BM; Reiner AP; Rotter JI; Rudan I; Snieder H; Tanaka T; van Duijn CM; Vollenweider P; Waeber G; Wilson JF; Witteman JC; Wolffenbuttel BH; Wright AF; Wu Q; Liu Y; Jenny NS; North KE; Felix JF; Alizadeh BZ; Cupples LA; Perry JR; Morris AP (2012)
      Many disorders are associated with altered serum protein concentrations, including malnutrition, cancer, and cardiovascular, kidney, and inflammatory diseases. Although these protein concentrations are highly heritable, ...
    • Discovery and fine mapping of serum protein loci through transethnic meta-analysis 

      Franceschini N; van Rooij FJ; Prins BP; Feitosa MF; Karakas M; Eckfeldt JH; Folsom AR; Kopp J; Vaez A; Andrews JS; Baumert J; Boraska V; Broer L; Hayward C; Ngwa JS; Okada Y; Polasek O; Westra HJ; Wang YA; Del Greco M F; Glazer NL; Kapur K; Kema IP; Lopez LM; Schillert A; Smith AV; Winkler CA; Zgaga L; LifeLines Cohort Study; Bandinelli S; Bergmann S; Boban M; Bochud M; Chen YD; Davies G; Dehghan A; Ding J; Doering A; Durda JP; Ferrucci L; Franco OH; Franke L; Gunjaca G; Hofman A; Hsu FC; Kolcic I; Kraja A; Kubo M; Lackner KJ; Launer L; Loehr LR; Li G; Meisinger C; Nakamura Y; Schwienbacher C; Starr JM; Takahashi A; Torlak V; Uitterlinden AG; Vitart V; Waldenberger M; Wild PS; Kirin M; Zeller T; Zemunik T; Zhang Q; Ziegler A; Blankenberg S; Boerwinkle E; Borecki IB; Campbell H; Deary IJ; Frayling TM; Gieger C; Harris TB; Hicks AA; Koenig W; O' Donnell CJ; Fox CS; Pramstaller PP; Psaty BM; Reiner AP; Rotter JI; Rudan I; Snieder H; Tanaka T; van Duijn CM; Vollenweider P; Waeber G; Wilson JF; Witteman JC; Wolffenbuttel BH; Wright AF; Wu Q; Liu Y; Jenny NS; North KE; Felix JF; Alizadeh BZ; Cupples LA; Perry JR; Morris AP (2012)
      Many disorders are associated with altered serum protein concentrations, including malnutrition, cancer, and cardiovascular, kidney, and inflammatory diseases. Although these protein concentrations are highly heritable, ...
    • KCND3 potassium channel gene variant confers susceptibility to electrocardiographic early repolarization pattern 

      Teumer A; Trenkwalder T; Kessler T; Jamshidi Y; van den Berg ME; Kaess B; Nelson CP; Bastiaenen R; De Bortoli M; Rossini A; Deisenhofer I; Stark K; Assa S; Braund PS; Cabrera C; Dominiczak AF; Gögele M; Hall LM; Ikram MA; Kavousi M; Lackner KJ; Müller C; Münzel T; Nauck M; Padmanabhan S; Pfeiffer N; Spector TD; Uitterlinden AG; Verweij N; Völker U; Warren HR; Zafar M; Felix SB; Kors JA; Snieder H; Munroe PB; Pattaro C; Fuchsberger C; Schmidt G; Nolte IM; Schunkert H; Pramstaller P; Wild PS; van der Harst P; Stricker BH; Schnabel RB; Samani NJ; Hengstenberg C; Dörr M; Behr ER; Reinhard W (2019)
      BACKGROUND The presence of an early repolarization pattern (ERP) on the surface ECG is associated with risk of ventricular fibrillation and sudden cardiac death. Family studies have shown that ERP is a highly heritable ...
    • Large-scale genome-wide analysis identifies genetic variants associated with cardiac structure and function 

      Wild PS; Felix JF; Schillert A; Teumer A; Chen MH; Leening MJG; Völker U; Großmann V; Brody JA; Irvin MR; Shah SJ; Pramana S; Lieb W; Schmidt R; Stanton AV; Malzahn D; Smith AV; Sundström J; Minelli C; Ruggiero D; Lyytikäinen LP; Tiller D; Smith JG; Monnereau C; Di Tullio MR; Musani SK; Morrison AC; Pers TH; Morley M; Kleber ME; Aragam J; Benjamin EJ; Bis JC; Bisping E; Broeckel U; Cheng S; Deckers JW; Del Greco M F; Edelmann F; Fornage M; Franke L; Friedrich N; Harris TB; Hofer E; Hofman A; Huang J; Hughes AD; Kähönen M; Investigators K; Kruppa J; Lackner KJ; Lannfelt L; Laskowski R; Launer LJ; Leosdottir M; Lin H; Lindgren CM; Loley C; MacRae CA; Mascalzoni D; Mayet J; Medenwald D; Morris AP; Müller C; Müller-Nurasyid M; Nappo S; Nilsson PM; Nuding S; Nutile T; Peters A; Pfeufer A; Pietzner D; Pramstaller PP; Raitakari OT; Rice KM; Rivadeneira F; Rotter JI; Ruohonen ST; Sacco RL; Samdarshi TE; Schmidt H; Sharp ASP; Shields DC; Sorice R; Sotoodehnia N; Stricker BH; Surendran P; Thom S; Töglhofer AM; Uitterlinden AG; Wachter R; Völzke H; Ziegler A; Münzel T; März W; Cappola TP; Hirschhorn JN; Mitchell GF; Smith NL; Fox ER; Dueker ND; Jaddoe VWV; Melander O; Russ M; Lehtimäki T; Ciullo M; Hicks AA; Lind L; Gudnason V; Pieske B; Barron AJ; Zweiker R; Schunkert H; Ingelsson E; Liu K; Arnett DK; Psaty BM; Blankenberg S; Larson MG; Felix SB; Franco OH; Zeller T; Vasan RS; Dörr M (2017)
      BACKGROUND: Understanding the genetic architecture of cardiac structure and function may help to prevent and treat heart disease. This investigation sought to identify common genetic variations associated with inter-individual ...