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Showing items 1-10 of 10 (1 Page(s) Totally)
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| 國家衛生研究院 |
2025-09-09 |
Whole genome sequence analysis of low-density lipoprotein cholesterol across 246 K individuals
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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 |
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 |
2022-10-11 |
Whole genome sequence analysis of blood lipid levels in >66,000 individuals
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Selvaraj, MS;Li, X;Li, Z;Pampana, A;Zhang, DY;Park, J;Aslibekyan, S;Bis, JC;Brody, JA;Cade, BE;Chuang, LM;Chung, RH;Curran, JE;de Las Fuentes, L;de Vries, PS;Duggirala, R;Freedman, BI;Graff, M;Guo, X;Heard-Costa, N;Hidalgo, B;Hwu, CM;Irvin, MR;Kelly, TN;Kral, BG;Lange, L;Li, X;Lisa, M;Lubitz, SA;Manichaikul, AW;Michael, P;Montasser, ME;Morrison, AC;Naseri, T;O'Connell, JR;Palmer, ND;Peyser, PA;Reupena, MS;Smith, JA;Sun, X;Taylor, KD;Tracy, RP;Tsai, MY;Wang, Z;Wang, Y;Bao, W;Wilkins, JT;Yanek, LR;Zhao, W;Arnett, DK;Blangero, J;Boerwinkle, E;Bowden, DW;Chen, YI;Correa, A;Cupples, LA;Dutcher, SK;Ellinor, PT;Fornage, M;Gabriel, S;Germer, S;Gibbs, R;He, J;Kaplan, RC;Kardia, SLR;Kim, R;Kooperberg, C;Loos, RJF;Viaud-Martinez, KA;Mathias, RA;McGarvey, ST;Mitchell, BD;Nickerson, D;North, KE;Psaty, BM;Redline, S;Reiner, AP;Vasan, RS;Rich, SS;Willer, C;Rotter, JI;Rader, DJ;Lin, X;Peloso, GM;Natarajan, P |
| 國家衛生研究院 |
2021-04-12 |
Chromosome Xq23 is associated with lower atherogenic lipid concentrations and favorable cardiometabolic indices
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Natarajan, P;Pampana, A;Graham, SE;Ruotsalainen, SE;Perry, JA;de Vries, PS;Broome, JG;Pirruccello, JP;Honigbere, MC;Aragam, K;Wolford, B;Brody, JA;Antonacci-Fulton, L;Arden, M;Aslibekyan, S;Assimes, TL;Ballantyne, CM;Bielak, LF;Bisl, JC;Cade, BE;Do, R;Doddapaneni, H;Emery, LS;Hung, YJ;Irvin, MR;Khan, AT;Lange, L;Lee, J;Lemaitre, RN;Martin, LW;Metcalf, G;Montasser, ME;Moon, JY;Muzny, D;Connell, JRO;Palmer, ND;Peralta, JM;Peyser, PA;Stilp, AM;Tsai, M;Wang, FF;Weeks, DE;Yanek, LR;Wilson, JG;Abecasis, G;Arnett, DK;Becker, LC;Blangercy, J;Boerwinkle, E;Bowden, DW;Chang, YC;Chen, YDI;Choi, WJ;Correa, A;Curran, JE;Daly, MJ;DutcherE, SK;Ellinor, PT;Fornage, M;Freedman, BI;Gabriel, S;Germer, S;Gibbs, RA;He, J;Hveem, K;Jarvik, GP;Kaplan, RC;Kardia, SLR;Kennyn, E;Kim, RW;Kooperberg, C;Laurie, CC;Lee, S;Lloyd-Jones, DM;Loos, RJF;Lubitz, SA;Mathias, RA;Martinez, KAV;McGarvey, ST;Mitche, BD;Nickerson, DA;North, KE;Palotie, A;Park, CJ;Psat, YBM;Rao, DC;Redline, S;Reiner, AP;Seo, D;Seo, JS;Smith, AV;Tracy, RP;Kathiresan, S;Cupples, LA;Rotten, JI;Morrison, AC;Rich, SS;Ripatti, S;Wilier, C;Peloso, GM, .;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 |
2021-02-10 |
Sequencing of 53,831 diverse genomes from the NHLBI TOPMed Program
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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 |
2020-12-18 |
Loss-of-function genomic variants highlight potential therapeutic targets for cardiovascular disease
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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. |
Showing items 1-10 of 10 (1 Page(s) Totally)
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