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"raffield lm"的相关文件
显示项目 1-11 / 11 (共1页)
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| 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
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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
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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 |
2024-10-09 |
Rare variant contribution to the heritability of coronary artery disease
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Rocheleau, G;Clarke, SL;Auguste, G;Hasbani, NR;Morrison, AC;Heath, AS;Bielak, LF;Iyer, KR;Young, EP;Stitziel, NO;Jun, G;Laurie, C;Broome, JG;Khan, AT;Arnett, DK;Becker, LC;Bis, JC;Boerwinkle, E;Bowden, DW;Carson, AP;Ellinor, PT;Fornage, M;Franceschini, N;Freedman, BI;Heard-Costa, NL;Hou, LF;Chen, YDI;Kenny, EE;Kooperberg, C;Kral, BG;Loos, RJF;Lutz, SM;Manson, JE;Martin, LW;Mitchell, BD;Nassir, R;Palmer, ND;Post, WS;Preuss, MH;Psaty, BM;Raffield, LM;Regan, EA;Rich, SS;Smith, JA;Taylor, KD;Yanek, LR;Young, KA;Anugu, P;Arnett, DK;Assimes, TL;Auer, P;Barwick, L;Becker, D;Becker, LC;Bielak, LF;Bis, JC;Boerwinkle, E;Bowden, DW;Broome, JG;Carson, AP;Carty, C;Castaldi, P;Chaffin, M;Chang, YC;Choi, SH;Chung, RH;Clarke, SL;Crandall, C;David, S;de las Fuentes, L;Deka, R;DeMeo, D;de Vries, PS;Do, R;Duan, Q;Eaton, C;Eaton, C;El Boueiz, A;Ellinor, PT;Fornage, M;Franceschini, N;Freedman, BI;Gao, SS;Gao, Y;Gass, M;Ghosh, A;Grine, D;Hall, M;Hasbani, NR;Heard-Costa, NL;Heath, AS;Hersh, C;Hobbs, B;Hou, LF;Hsiung, CA;Hung, YJ;Huston, H;Hwu, CM;Chen, YDI;Iyer, KR;Jackson, R;Johnsen, J;Jun, G;Kenny, EE;Khan, AT;Kooperberg, C;Kral, BG;Lange, C;Lange, E;Laurie, C;LeBoff, M;Lee, WJ;Li, Y;Liu, S;Liu, Y;Loos, RJF;Lutz, SM;Manson, JE;Martin, LW;Mathai, S;Mei, H;Miller, CL;Mitchell, BD;Morrison, AC;Naik, R;Naseri, T;Nassir, R;Neltner, B;Ochs-Balcom, H;Paik, DT;Palmer, ND;Parker, C;Perez, M;Peters, U;Peyser, PA;Phillips, LS;Post, WS;Becker, JP;Preuss, MH;Psaty, BM;Raffield, LM;Regan, EA;Reupena, MS;Rich, SS;Rocheleau, G;Roselli, C;Rotter, JI;Russell, P;Sabino, EC;Sandow, K;Schwander, K;Sciurba, F;Silver, B;Smith, JA;Smoller, S;Snively, B;Stitziel, NO;Storm, G;Sung, YJ;Tang, H;Taub, M;Taylor, KD;Tinker, L;Tirschwell, D;Tiwari, H;Vaidya, D;Vasan, RS;Walker, T;Wallace, R;Walts, A;Weng, LC;Yanek, LR;Yang, I;Young, EP;Young, KA;Zhao, SX;Hilliard, AT;Tcheandjieu, C;Peyser, PA;Vasan, RS;Rotte, JI;Miller, CL;Assimes, TL;de Vries, PS;Do, R |
| 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
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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
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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
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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 |
2023-01-26 |
Multi-ancestry transcriptome-wide association analyses yield insights into tobacco use biology and drug repurposing
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Chen, F;Wang, X;Jang, SK;Quach, BC;Weissenkampen, JD;Khunsriraksakul, C;Yang, L;Sauteraud, R;Albert, CM;Allred, NDD;Arnett, DK;Ashley-Koch, AE;Barnes, KC;Barr, RG;Becker, DM;Bielak, LF;Bis, JC;Blangero, J;Boorgula, MP;Chasman, DI;Chavan, S;Chen, YDI;Chuang, LM;Correa, A;Curran, JE;David, SP;Fuentes, L;Deka, R;Duggirala, R;Faul, JD;Garrett, ME;Gharib, SA;Guo, X;Hall, ME;Hawley, NL;He, J;Hobbs, BD;Hokanson, JE;Hsiung, CA;Hwang, SJ;Hyde, TM;Irvin, MR;Jaffe, AE;Johnson, EO;Kaplan, R;Kardia, SLR;Kaufman, JD;Kelly, TN;Kleinman, JE;Kooperberg, C;Lee, IT;Levy, D;Lutz, SM;Manichaikul, AW;Martin, LW;Marx, O;McGarvey, ST;Minster, RL;Moll, M;Moussa, KA;Naseri, T;North, KE;Oelsner, EC;Peralta, JM;Peyser, PA;Psaty, BM;Rafaels, N;Raffield, LM;Reupena, MS;Rich, SS;Rotter, JI;Schwartz, DA;Shadyab, AH;Sheu, WHH;Sims, M;Smith, JA;Sun, X;Taylor, KD;Telen, MJ;Watson, H;Weeks, DE;Weir, DR;Yanek, LR;Young, KA;Young, KL;Zhao, W;Hancock, DB;Jiang, B;Vrieze, S;Liu, DJ |
| 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
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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
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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. |
| 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.]
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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 |
2020-10 |
Inherited causes of clonal haematopoiesis in 97,691 whole genomes
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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. |
显示项目 1-11 / 11 (共1页)
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