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Showing items 1-7 of 7 (1 Page(s) Totally)
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| 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 |
2023-08-22 |
Whole genome sequencing analysis of body mass index identifies novel african ancestry-specific risk allele
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Zhang, X; Brody, JA; Graff, M; Highland, HM; Chami, N; Xu, H; Wang, Z; Ferrier, K; Chittoor, G; Josyula, NS; Li, X; Li, Z; Allison, MA; Becker, DM; Bielak, LF; Bis, JC; Boorgula, MP; Bowden, DW; Broome, JG; Buth, EJ; Carlson, CS; Chang, KM; Chavan, S; Chiu, YF; Chuang, LM; Conomos, MP; DeMeo, DL; Du, M; Duggirala, R; Eng, C; Fohner, AE; Freedman, BI; Garrett, ME; Guo, X; Haiman, C; Heavner, BD; Hidalgo, B; Hixson, JE; Ho, YL; Hobbs, BD; Hu, D; Hui, Q; Hwu, CM; Jackson, RD; Jain, D; Kalyani, RR; Kardia, SLR; Kelly, TN; Lange, EM; LeNoir, M; Li, C; Marchand, LL; McDonald, MN; McHugh, CP; Morrison, AC; Naseri, T; O'Connell, J; O'Donnell, CJ; Palmer, ND; Pankow, JS; Perry, JA; Peters, U; Preuss, MH; Rao, DC; Regan, EA; Reupena, SM; Roden, DM; Rodriguez-Santana, J; Sitlani, CM; Smith, JA; Tiwari, HK; Vasan, RS; Wang, Z; Weeks, DE; Wessel, J; Wiggins, KL; Wilkens, LR; Wilson, PWF; Yanek, LR; Yoneda, ZT; Zhao, W; Zöllner, S; Arnett, DK; Ashley-Koch, AE; Barnes, KC; Blangero, J; Boerwinkle, E; Burchard, EG; Carson, AP; Chasman, DI; Chen, YI; Curran, JE; Fornage, M; Gordeuk, VR; He, J; Heckbert, SR; Hou, L; Irvin, MR; Kooperberg, C; Minster, RL, .; et al. |
| 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 |
2022-06-29 |
Development and validation of a trans-ancestry polygenic risk score for type 2 diabetes in diverse populations
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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.]
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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. |
| 國家衛生研究院 |
2020-09 |
Dynamic incorporation of multiple in silico functional annotations empowers rare variant association analysis of large whole-genome sequencing studies at scale
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Li, XH;Li, ZL;Zhou, HF;Gaynor, SM;Liu, YW;Chen, H;Sun, R;Dey, R;Arnett, DK;Aslibekyan, S;Ballantyne, CM;Bielak, LF;Blangero, J;Boerwinkle, E;Bowden, DW;Broome, JG;Conomos, MP;Correa, A;Cupples, LA;Curran, JE;Freedman, BI;Guo, XQ;Hindy, G;Irvin, MR;Kardia, SLR;Kathiresan, S;Khan, AT;Kooperberg, CL;Laurie, CC;Liu, XS;Mahaney, MC;Manichaikul, AW;Martin, LW;Mathias, RA;McGarvey, ST;Mitchell, BD;Montasser, ME;Moore, JE;Morrison, AC;O'Connell, JR;Palmer, ND;Pampana, A;Peralta, JM;Peyser, PA;Psaty, BM;Redline, S;Rice, KM;Rich, SS;Smith, JA;Tiwari, HK;Tsai, MCY;Vasan, RS;Wang, FF;Weeks, DE;Weng, ZP;Wilson, JG;Yanek, LR;Abe, N;Abe, N;Abecasis, GR;Aguet, F;Albert, C;Almasy, L;Alonso, A;Ament, S;Anderson, P;Anugu, P;Applebaum-Bowden, D;Ardlie, K;Arking, D;Arnett, DK;Ashley-Koch, A;Aslibekyan, S;Assimes, T;Auer, P;Avramopoulos, D;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;Bielak, LF;Bis, J;Blackwell, T;Blangero, J;Boerwinkle, E;Bowden, DW;Bowler, R;Brody, J;Broeckel, U;Broome, JG, et al. |
Showing items 1-7 of 7 (1 Page(s) Totally)
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