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Showing items 11-13 of 13  (2 Page(s) Totally)
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Institution Date Title Author
國家衛生研究院 2020-12-18 Loss-of-function genomic variants highlight potential therapeutic targets for cardiovascular disease Nielsen, JB; Rom, O; Surakka, I; Graham, SE; Zhou, W; Roychowdhury, T; Fritsche, LG; Gagliano Taliun, SA; Sidore, C; Liu, Y; Gabrielsen, ME; Skogholt, AH; Wolford, B; Overton, W; Zhao, Y; Chen, J; Zhang, H; Hornsby, WE; Acheampong, A; Grooms, A; Schaefer, A; Zajac, GJM; Villacorta, L; Zhang, J; Brumpton, B; Løset, M; Rai, V; Lundegaard, PR; Olesen, MS; Taylor, KD; Palmer, ND; Chen, YD; Choi, SH; Lubitz, SA; Ellinor, PT; Barnes, KC; Daya, M; Rafaels, N; Weiss, ST; Lasky-Su, J; Tracy, RP; Vasan, RS; Cupples, LA; Mathias, RA; Yanek, LR; Becker, LC; Peyser, PA; Bielak, LF; Smith, JA; Aslibekyan, S; Hidalgo, BA; Arnett, DK; Irvin, MR; Wilson, JG; Musani, SK; Correa, A; Rich, SS; Guo, X; Rotter, JI; Konkle, BA; Johnsen, JM; Ashley-Koch, AE; Telen, MJ; Sheehan, VA; Blangero, J; Curran, JE; Peralta, JM; Montgomery, C; Sheu, WHH; Chung, RH; Schwander, K; Nouraie, SM; Gordeuk, VR; Zhang, Y; Kooperberg, C; Reiner, AP; Jackson, RD; Bleecker, ER; Meyers, DA; Li, X; Das, S; Yu, K; LeFaive, J; Smith, A; Blackwell, T; Taliun, D; Zollner, S; Forer, L; Schoenherr, S; Fuchsberger, C; Pandit, A; Zawistowski, M; Kheterpal, S; Brummett, CM; Natarajan, P; Schlessinger, D; Lee, S; Kang, HM; Cucca, F; Holmen, OL, .; et al.
國家衛生研究院 2020-10 Inherited causes of clonal haematopoiesis in 97,691 whole genomes Bick, AG;Weinstock, JS;Nandakumar, SK;Fulco, CP;Bao, EL;Zekavat, SM;Szeto, MD;Liao, XT;Leventhal, MJ;Nasser, J;Chang, K;Laurie, C;Burugula, BB;Gibson, CJ;Lin, AE;Taub, MA;Aguet, F;Ardlie, K;Mitchell, BD;Barnes, KC;Moscati, A;Fornage, M;Redline, S;Psaty, BM;Silverman, EK;Weiss, ST;Palmer, ND;Vasan, RS;Burchard, EG;Kardia, SLR;He, J;Kaplan, RC;Smith, NL;Arnett, DK;Schwartz, DA;Correa, A;de Andrade, M;Guo, XQ;Konkle, BA;Custer, B;Peralta, JM;Gui, HS;Meyers, DA;McGarvey, ST;Chen, IYD;Shoemaker, MB;Peyser, PA;Broome, JG;Gogarten, SM;Wang, FF;Wong, QN;Montasser, ME;Daya, M;Kenny, EE;North, KE;Launer, LJ;Cade, BE;Bis, JC;Cho, MH;Lasky-Su, J;Bowden, DW;Cupples, LA;Mak, ACY;Becker, LC;Smith, JA;Kelly, TN;Aslibekyan, S;Heckbert, SR;Tiwari, HK;Yang, IV;Heit, JA;Lubitz, SA;Johnsen, JM;Curran, JE;Wenzel, SE;Weeks, DE;Rao, DC;Darbar, D;Moon, JY;Tracy, RP;Buth, EJ;Rafaels, N;Loos, RJF;Durda, P;Liu, YM;Hou, LF;Lee, J;Kachroo, P;Freedman, BI;Levy, D;Bielak, LF;Hixson, JE;Floyd, JS;Whitsel, EA;Ellinor, PT;Irvin, MR;Fingerlin, TE;Raffield, LM;Armasu, SM;Wheeler, MM;et al.
國家衛生研究院 2020-09 Dynamic incorporation of multiple in silico functional annotations empowers rare variant association analysis of large whole-genome sequencing studies at scale Li, XH;Li, ZL;Zhou, HF;Gaynor, SM;Liu, YW;Chen, H;Sun, R;Dey, R;Arnett, DK;Aslibekyan, S;Ballantyne, CM;Bielak, LF;Blangero, J;Boerwinkle, E;Bowden, DW;Broome, JG;Conomos, MP;Correa, A;Cupples, LA;Curran, JE;Freedman, BI;Guo, XQ;Hindy, G;Irvin, MR;Kardia, SLR;Kathiresan, S;Khan, AT;Kooperberg, CL;Laurie, CC;Liu, XS;Mahaney, MC;Manichaikul, AW;Martin, LW;Mathias, RA;McGarvey, ST;Mitchell, BD;Montasser, ME;Moore, JE;Morrison, AC;O'Connell, JR;Palmer, ND;Pampana, A;Peralta, JM;Peyser, PA;Psaty, BM;Redline, S;Rice, KM;Rich, SS;Smith, JA;Tiwari, HK;Tsai, MCY;Vasan, RS;Wang, FF;Weeks, DE;Weng, ZP;Wilson, JG;Yanek, LR;Abe, N;Abe, N;Abecasis, GR;Aguet, F;Albert, C;Almasy, L;Alonso, A;Ament, S;Anderson, P;Anugu, P;Applebaum-Bowden, D;Ardlie, K;Arking, D;Arnett, DK;Ashley-Koch, A;Aslibekyan, S;Assimes, T;Auer, P;Avramopoulos, D;Barnard, J;Barnes, K;Barr, RG;Barron-Casella, E;Barwick, L;Beaty, T;Beck, G;Becker, D;Becker, L;Beer, R;Beitelshees, A;Benjamin, E;Benos, T;Bezerra, M;Bielak, LF;Bis, J;Blackwell, T;Blangero, J;Boerwinkle, E;Bowden, DW;Bowler, R;Brody, J;Broeckel, U;Broome, JG, et al.

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