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Institution Date Title Author
國家衛生研究院 2021-03-11 Inherited causes of clonal haematopoiesis in 97,691 whole genomes[Erratum:Nature. 2020 Oct;586(7831):763-768.] Bick, AG; Weinstock, JS; Nandakumar, SK; Fulco, CP; Bao, EL; Zekavat, SM; Szeto, MD; Liao, X; Leventhal, MJ; Nasser, J; Chang, K; Laurie, C; Burugula, BB; Gibson, CJ; Niroula, A; 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, X; Konkle, BA; Custer, B; Peralta, JM; Gui, H; Meyers, DA; McGarvey, ST; Chen, IYD; Shoemaker, MB; Peyser, PA; Broome, JG; Gogarten, SM; Wang, FF; Wong, Q; 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, Y; Hou, L; 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, .; et al.
國家衛生研究院 2021-02-10 Sequencing of 53,831 diverse genomes from the NHLBI TOPMed Program Taliun, D; Harris, DN; Kessler, MD; Carlson, J; Szpiech, ZA; Torres, R; Taliun, SAG; Corvelo, A; Gogarten, SM; Kang, HM; Pitsillides, AN; LeFaive, J; Lee, SB; Tian, X; Browning, BL; Das, S; Emde, AK; Clarke, WE; Loesch, DP; Shetty, AC; Blackwell, TW; Smith, AV; Wong, Q; Liu, X; Conomos, MP; Bobo, DM; Aguet, F; Albert, C; Alonso, A; Ardlie, KG; Arking, DE; Aslibekyan, S; Auer, PL; Barnard, J; Barr, RG; Barwick, L; Becker, LC; Beer, RL; Benjamin, EJ; Bielak, LF; Blangero, J; Boehnke, M; Bowden, DW; Brody, JA; Burchard, EG; Cade, BE; Casella, JF; Chalazan, B; Chasman, DI; Chen, YDI; Cho, MH; Choi, SH; Chung, MK; Clish, CB; Correa, A; Curran, JE; Custer, B; Darbar, D; Daya, M; de Andrade, M; DeMeo, DL; Dutcher, SK; Ellinor, PT; Emery, LS; Eng, C; Fatkin, D; Fingerlin, T; Forer, L; Fornage, M; Franceschini, N; Fuchsberger, C; Fullerton, SM; Germer, S; Gladwin, MT; Gottlieb, DJ; Guo, X; Hall, ME; He, J; Heard-Costa, NL; Heckbert, SR; Irvin, MR; Johnsen, JM; Johnson, AD; Kaplan, R; Kardia, SLR; Kelly, T; Kelly, S; Kenny, EE; Kiel, DP; Klemmer, R; Konkle, BA; Kooperberg, C; Köttgen, A; Lange, LA; Lasky-Su, J; Levy, D; Lin, X; Lin, KH; Liu, C; Loos, RJF, .; 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.
國家衛生研究院 2017-09 Region-based association tests for sequencing data on survival traits Chien, LC;Bowden, DW;Chiu, YF
國家衛生研究院 2016-11 Association tests of multiple genetic variants for time-to-event traits Chiu, YF;Chien, LC;Bowden, DW
國家衛生研究院 2016-02 Generalization of rare variant association tests for longitudinal family studies Chien, LC;Hsu, FC;Bowden, DW;Chiu, YF

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