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| 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 |
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
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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. |
Showing items 1-5 of 5 (1 Page(s) Totally)
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