|
"weiss st"的相關文件
顯示項目 1-5 / 5 (共1頁)
1
每頁顯示[10|25|50]項目
| 國家衛生研究院 |
2022-06-29 |
Development and validation of a trans-ancestry polygenic risk score for type 2 diabetes in diverse populations
|
Ge, T;Irvin, MR;Patki, A;Srinivasasainagendra, V;Lin, YF;Tiwari, HK;Armstrong, ND;Benoit, B;Chen, CY;Choi, KW;Cimino, JJ;Davis, BH;Dikilitas, O;Etheridge, B;Feng, YA;Gainer, V;Huang, H;Jarvik, GP;Kachulis, C;Kenny, EE;Khan, A;Kiryluk, K;Kottyan, L;Kullo, IJ;Lange, C;Lennon, N;Leong, A;Malolepsza, E;Miles, AD;Murphy, S;Namjou, B;Narayan, R;O'Connor, MJ;Pacheco, JA;Perez, E;Rasmussen-Torvik, LJ;Rosenthal, EA;Schaid, D;Stamou, M;Udler, MS;Wei, WQ;Weiss, ST;Ng, MCY;Smoller, JW;Lebo, MS;Meigs, JB;Limdi, NA;Karlson, EW |
| 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 |
2020-12-18 |
Loss-of-function genomic variants highlight potential therapeutic targets for cardiovascular disease
|
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. |
| 國家衛生研究院 |
2019-12 |
Whole genome sequencing identifies CRISPLD2 as a lung function gene in children with asthma
|
Kachroo, P;Hecker, J;Chawes, BL;Ahluwalia, TS;Cho, MH;Qiao, DD;Kelly, RS;Chu, SH;Virkud, YV;Huang, MN;Barnes, KC;Burchard, EG;Eng, C;Hu, DL;Celedon, JC;Daya, M;Levin, AM;Gui, HS;Williams, LK;Forno, E;Mak, ACY;Avila, L;Soto-Quiros, ME;Cloutier, MM;Acosta-Perez, E;Canino, G;Bonnelykke, K;Bisgaard, H;Raby, BA;Lange, C;Weiss, ST;Lasky-Su, JA;et al. |
顯示項目 1-5 / 5 (共1頁)
1
每頁顯示[10|25|50]項目
|
