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臺灣學術機構典藏系統 (Taiwan Academic Institutional Repository, TAIR)
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Institution Date Title Author
國家衛生研究院 2025-09-09 Whole genome sequence analysis of low-density lipoprotein cholesterol across 246 K individuals Selvaraj, MS;Li, XH;Li, ZL;Van Buren, E;Haidermota, S;Postupaka, D;Hornsby, W;Bis, JC;Brody, JA;Cade, BE;Chung, RH;Curran, JE;Damrauer, SM;de las Fuentes, L;de Vries, PS;Duggirala, R;Freedman, BI;Graff, M;Guo, XQ;Hidalgo, BA;Hou, LF;Irvin, R;Judy, R;Kalyani, RR;Kelly, TN;Konigsberg, IR;Kral, BG;Kwee, LC;Levy, D;Li, CW;Manichaikul, AW;Martin, LW;Montasser, ME;Morrison, AC;Naseri, T;North, KE;O'Connell, JR;Palmer, ND;Peyser, PA;Reiner, AP;Shah, SH;Smit, RAJ;Smith, JA;Taylor, KD;Tiwari, H;Tsai, MY;Viali, S;Wang, Z;Wang, YX;Zhao, W;Arnett, DK;Blangero, J;Boerwinkle, E;Bowden, DW;Carlson, JC;Chen, YDI;Ellinor, PT;Fornage, M;He, J;Heard-Costa, N;Kaplan, RC;Kardia, SLR;Kooperberg, C;Kraus, WE;Lange, LA;Loos, RJF;Mitchell, BD;Psaty, BM;Rader, DJ;Redline, S;Rich, SS;Yanek, LR;Gibbs, R;Gabriel, S;Viaud-Martinez, KA;Dutcher, SK;Germer, S;Kim, R;Rotter, JI;Lin, XH;Peloso, GM;Natarajan, P; NT-OPMT Consortium
國家衛生研究院 2025-03-06 Sequencing in over 50,000 cases identifies coding and structural variation underlying atrial fibrillation risk Choi, SH; Jurgens, SJ; Xiao, L; Hill, MC; Haggerty, CM; Sveinbjörnsson, G; Morrill, VN; Marston, NA; Weng, LC; Pirruccello, JP; Arnar, DO; Gudbjartsson, DF; Mantineo, H; von Falkenhausen, AS; Natale, A; Tveit, A; Geelhoed, B; Roselli, C; Van Wagoner, DR; Darbar, D; Haase, D; Soliman, EZ; Davogustto, GE; Jun, G; Calkins, H; Anderson, JL; Brody, JA; Halford, JL; Barnard, J; Hokanson, JE; Smith, JD; Bis, JC; Young, K; Johnson, LSB; Risch, L; Gula, LJ; Kwee, LC; Chaffin, MD; Kühne, M; Preuss, M; Gupta, N; Nafissi, NA; Smith, NL; Nilsson, PM; van der Harst, P; Wells, QS; Judy, RL; Schnabel, RB; Johnson, R; Smit, RAJ; Gabriel, S; Knight, S; Furukawa, T; Blackwell, TW; Nauffal, V; Wang, X; Min, YI; Yoneda, ZT; Laksman, ZWM; Bezzina, CR; Alonso, A; Psaty, BM; Albert, CM; Arking, DE; Roden, DM; Chasman, DI; Rader, DJ; Conen, D; McManus, DD; Fatkin, D; Benjamin, EJ; Boerwinkle, E; Marcus, GM; Christophersen, IE; Smith, JG; Roberts, JD; Raffield, LM; Shoemaker, MB; Cho, MH; Cutler, MJ; Rienstra, M; Chung, MK; Olesen, MS; Sinner, MF; Sotoodehnia, N; Kirchhof, P; Loos, RJF; Nazarian, S; Mohanty, S; Damrauer, SM; Kaab, S; Heckbert, SR; Redline, S; Shah, SH; Tanaka, T; Ebana, Y; Holm, H; Stefansson, K; Ruff, CT; Sabatine, MS, .; et al.
國家衛生研究院 2025-02-07 A statistical framework for multi-trait rare variant analysis in large-scale whole-genome sequencing studies Li, XH;Chen, H;Selvaraj, MS;Van Buren, E;Zhou, HF;Wang, YX;Sun, R;McCaw, ZR;Yu, Z;Jiang, MZ;DiCorpo, D;Gaynor, SM;Dey, R;Arnett, DK;Benjamin, EJ;Bis, JC;Blangero, J;Boerwinkle, E;Bowden, DW;Brody, JA;Cade, BE;Carson, AP;Carlson, JC;Chami, N;Chen, YDI;Curran, JE;de Vries, PS;Fornage, M;Franceschini, N;Freedman, BI;Gu, C;Heard-Costa, NL;He, J;Hou, LF;Hung, YJ;Irvin, MR;Kaplan, RC;Kardia, SLR;Kelly, TN;Konigsberg, I;Kooperberg, C;Kral, BG;Li, CW;Li, Y;Lin, HH;Liu, CT;Loos, RJF;Mahaney, MC;Martin, LW;Mathias, RA;Mitchell, BD;Montasser, ME;Morrison, AC;Naseri, T;North, KE;Palmer, ND;Peyser, PA;Psaty, BM;Redline, S;Reiner, AP;Rich, SS;Sitlani, CM;Smith, JA;Taylor, KD;Tiwari, HK;Vasan, RS;Viali, S;Wang, Z;Wessel, J;Yanek, LR;Yu, B;Dupuis, J;Meigs, JB;Auer, PL;Raffield, LM;Manning, AK;Rice, KM;Rotter, JI;Peloso, GM;Natarajan, P;Li, ZL;Liu, ZH;Lin, XH;Abe, N;Abecasis, G;Aguet, F;Albert, C;Almasy, L;Alonso, A;Ament, S;Anderson, P;Anugu, P;Applebaum-Bowden, D;Ardlie, K;Arking, D;Ashley-Koch, A;Aslibekyan, S;Assimes, T;Avramopoulos, D;Ayas, N, .;al, et
國家衛生研究院 2024-05-30 Machine learning models for predicting blood pressure phenotypes by combining multiple polygenic risk scores Hrytsenko, Y;Shea, B;Elgart, M;Kurniansyah, N;Lyons, G;Morrison, AC;Carson, AP;Haring, B;Mitchell, BD;Psaty, BM;Jaeger, BC;Gu, CC;Kooperberg, C;Levy, D;Lloyd-Jones, D;Choi, E;Brody, JA;Smith, JA;Rotter, JI;Moll, M;Fornage, M;Simon, N;Castaldi, P;Casanova, R;Chung, RH;Kaplan, R;Loos, RJF;Kardia, SLR;Rich, SS;Redline, S;Kelly, T;O'Connor, T;Zhao, W;Kim, W;Guo, X;Ida Chen, YD;Sofer, T
國家衛生研究院 2023-12-14 Machine learning models for blood pressure phenotypes combining multiple polygenic risk scores Hrytsenko, Y;Shea, B;Elgart, M;Kurniansyah, N;Lyons, G;Morrison, AC;Carson, AP;Haring, B;Mitchel, BD;Psaty, BM;Jaeger, BC;Gu, CC;Kooperberg, C;Levy, D;Lloyd-Jones, D;Choi, E;Brody, JA;Smith, JA;Rotter, JI;Moll, M;Fornage, M;Simon, N;Castaldi, P;Casanova, R;Chung, RH;Kaplan, R;Loos, RJF;Kardia, SLR;Rich, SS;Redline, S;Kelly, T;O'Connor, T;Zhao, W;Kim, W;Guo, X;Der Ida Chen, Y;Sofer, T
國家衛生研究院 2023-10-05 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, YDI;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, WHH;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
國家衛生研究院 2023-06-29 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
國家衛生研究院 2023-04-12 Aberrant activation of TCL1A promotes stem cell expansion in clonal haematopoiesis Weinstock, JS;Gopakumar, J;Burugula, BB;Uddin, MM;Jahn, N;Belk, JA;Bouzid, H;Daniel, B;Miao, Z;Ly, N;Mack, TM;Luna, SE;Prothro, KP;Mitchell, SR;Laurie, CA;Broome, JG;Taylor, KD;Guo, XQ;Sinner, MF;von Falkenhausen, AS;Kaab, S;Shuldiner, AR;O'Connell, JR;Lewis, JP;Boerwinkle, E;Barnes, KC;Chami, N;Kenny, EE;Loos, RJF;Fornage, M;Hou, LF;Lloyd-Jones, DM;Redline, S;Cade, BE;Psaty, BM;Bis, JC;Brody, JA;Silverman, EK;Yun, JH;Qiao, DD;Palmer, ND;Freedman, BI;Bowden, DW;Cho, MH;DeMeo, DL;Vasan, RS;Yanek, LR;Becker, LC;Kardia, SLR;Peyser, PA;He, J;Rienstra, M;Van der Harst, P;Kaplan, R;Heckbert, SR;Smith, NL;Wiggins, KL;Arnett, DK;Irvin, MR;Tiwari, H;Cutler, MJ;Knight, S;Muhlestein, JB;Correa, A;Raffield, LM;Gao, Y;de Andrade, M;Rotter, JI;Rich, SS;Tracy, RP;Konkle, BA;Johnsen, JM;Wheeler, MM;Smith, JG;Melander, O;Nilsson, PM;Custer, BS;Duggirala, R;Curran, JE;Blangero, J;McGarvey, S;Williams, LK;Xiao, SJ;Yang, M;Gu, CC;Chen, YDI;Lee, WJ;Marcus, GM;Kane, JP;Pullinger, CR;Shoemaker, MB;Darbar, D;Roden, DM;Albert, C;Kooperberg, C;Zhou, Y;Manson, JE;Desai, P;Johnson, AD;Mathias, RA, .;et al.
國家衛生研究院 2022-12-23 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;Abe, N;Abecasis, G;Aguet, F;Albert, C;Almasy, L;Alonso, A;Ament, S;Anderson, P;Anugu, P;Applebaum-Bowden, D;Ardlie, K;Dan, A;Ashley-Koch, A;Aslibekyan, S;Assimes, T;Auer, P;Avramopoulos, D;Ayas, N;Balasubramanian, A;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;Blackwell, T;Blue, N;Bowler, R;Broeckel, U;Broome, J;Brown, D;Bunting, K;Burchard, E;Bustamante, C;Buth, E;Cardwell, J;Carey, V, .;et al.
國家衛生研究院 2022-10-27 A framework for detecting noncoding rare-variant associations of large-scale whole-genome sequencing studies Li, Z;Li, X;Zhou, H;Gaynor, SM;Selvaraj, MS;Arapoglou, T;Quick, C;Liu, Y;Chen, H;Sun, R;Dey, R;Arnett, DK;Auer, PL;Bielak, LF;Bis, JC;Blackwell, TW;Blangero, J;Boerwinkle, E;Bowden, DW;Brody, JA;Cade, BE;Conomos, MP;Correa, A;Cupples, LA;Curran, JE;de Vries, PS;Duggirala, R;Franceschini, N;Freedman, BI;Göring, HHH;Guo, X;Kalyani, RR;Kooperberg, C;Kral, BG;Lange, LA;Lin, BM;Manichaikul, A;Manning, AK;Martin, LW;Mathias, RA;Meigs, JB;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;Smith, JA;Taylor, KD;Taub, MA;Vasan, RS;Weeks, DE;Wilson, JG;Yanek, LR;Zhao, W;Abe, N;Abecasis, G;Aguet, F;Albert, C;Almasy, L;Alonso, A;Ament, S;Anderson, P;Anugu, P;Applebaum-Bowden, D;Ardlie, K;Arking, D;Ashley-Koch, A;Aslibekyan, S;Assimes, T;Avramopoulos, D;Ayas, N;Balasubramanian, A;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;Blue, N;Bowler, R;Broeckel, U;Broome, J;Brown, D, .; et al.

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