Sfoglia per Rivista NATURE GENETICS
Discovery and refinement of genetic loci associated with cardiometabolic risk using dense imputation maps
2016-01-01 Iotchkova, Valentina; Huang, Jie; Morris, John A; Jain, Deepti; Barbieri, Caterina; Walter, Klaudia; Min, Josine L; Chen, Lu; Astle, William; Cocca, Massimilian; Deelen, Patrick; Elding, Heather; Farmaki, Aliki Eleni; Franklin, Christopher S; Franberg, Mattias; Gaunt, Tom R; Hofman, Albert; Jiang, Tao; Kleber, Marcus E; Lachance, Genevieve; Luan, Jian'An; Malerba, Giovanni; Matchan, Angela; Mead, Daniel; Memari, Yasin; Ntalla, Ioanna; Panoutsopoulou, Kalliope; Pazoki, Raha; Perry, John R. B; Rivadeneira, Fernando; Sabater Lleal, Maria; Sennblad, Bengt; Shin, So Youn; Southam, Lorraine; Traglia, Michela; van Dijk, Freerk; van Leeuwen, Elisabeth M; Zaza, Gianluigi; Zhang, Weihua; Amin, Najaf; Butterworth, Adam; Chambers, John C; Dedoussis, George; Dehghan, Abbas; Franco, Oscar H; Franke, Lude; Frontini, Mattia; Gambaro, Giovanni; Gasparini, Paolo; Hamsten, Anders; Issacs, Aaron; Kooner, Jaspal S; Kooperberg, Charles; Langenberg, Claudia; Marz, Winfried; Scott, Robert A; Swertz, Morris A; Toniolo, Daniela; Uitterlinden, Andre G; van Duijn, Cornelia M; Watkins, Hugh; Zeggini, Eleftheria; Maurano, Mathew T; Timpson, Nicholas J; Reiner, Alexander P; Auer, Paul L; Soranzo, Nicole
Monovalent cation leaks in human red cells caused by single amino-acid substitutions in the transport domain of the band 3 chloride-bicarbonate exchanger, AE1.
2005-01-01 Bruce, Lj; Robinson, Hc; Guizouarn, H; Borgese, F; Harrison, P; King, Mj; Goede, Js; Coles, Se; Gore, Dm; Lutz, Hu; Ficarella, R; Layton, Dm; Iolascon, Achille; Ellory, Jc; Stewart, Gw
Multiple common variants for celiac disease influencing immune gene expression
2010-01-01 Dubois, Pc; Trynka, G; Franke, L; Hunt, Ka; Romanos, J; Curtotti, A; Zhernakova, A; Heap, Ga; Adány, R; Aromaa, A; Bardella, Mt; van den Berg, Lh; Bockett, Na; de la Concha, Eg; Dema, B; Fehrmann, Rs; Fernández-Arquero, M; Fiatal, S; Grandone, E; Green, Pm; Groen, Hj; Gwilliam, R; Houwen, Rh; Hunt, Se; Kaukinen, K; Kelleher, D; Korponay-Szabo, I; Kurppa, K; Macmathuna, P; Mäki, M; Mazzilli, Mc; Mccann, Ot; Mearin, Ml; Mein, Ca; Mirza, Mm; Mistry, V; Mora, B; Morley, Ki; Mulder, Cj; Murray, Ja; Núñez, C; Oosterom, E; Ophoff, Ra; Polanco, I; Peltonen, L; Platteel, M; Rybak, A; Salomaa, V; Schweizer, Jj; Sperandeo, Mp; Tack, Gj; Turner, G; Veldink, Jh; Verbeek, Wh; Weersma, Rk; Wolters, Vm; Urcelay, E; Cukrowska, B; Greco, L; Neuhausen, Sl; Mcmanus, R; Barisani, D; Deloukas, P; Barrett, Jc; Saavalainen, P; Wijmenga, C; van Heel, Da
Mutations in MYH9 result in the May-Hegglin anomaly and Fechtner and Sebastian syndromes. The May-Heggllin/Fechtner Syndrome Consortium.
2000-01-01 Seri, M; Cusano, R; Gangarossa, S; Caridi, G; Bordo, D; LO NIGRO, C; Ghiggeri, Gm; Ravazzolo, R; Savino, M; DEL VECCHIO, M; D'Apolito, M; Iolascon, Achille; Zelante, Ll; Savoia, A; Balduini, Cl; Noris, P; Magrini, U; Belletti, S; Heath, Ke; Babcock, M; Glucksman, Mj; Aliprandis, E; Bizzaro, N; Desnick, Rj; Martignetti, J. A.
| Titolo | Data di pubblicazione | Autore(i) | File |
|---|---|---|---|
| Discovery and refinement of genetic loci associated with cardiometabolic risk using dense imputation maps | 1-gen-2016 | Iotchkova, Valentina; Huang, Jie; Morris, John A; Jain, Deepti; Barbieri, Caterina; Walter, Klaudia; Min, Josine L; Chen, Lu; Astle, William; Cocca, Massimilian; Deelen, Patrick; Elding, Heather; Farmaki, Aliki Eleni; Franklin, Christopher S; Franberg, Mattias; Gaunt, Tom R; Hofman, Albert; Jiang, Tao; Kleber, Marcus E; Lachance, Genevieve; Luan, Jian'An; Malerba, Giovanni; Matchan, Angela; Mead, Daniel; Memari, Yasin; Ntalla, Ioanna; Panoutsopoulou, Kalliope; Pazoki, Raha; Perry, John R. B; Rivadeneira, Fernando; Sabater Lleal, Maria; Sennblad, Bengt; Shin, So Youn; Southam, Lorraine; Traglia, Michela; van Dijk, Freerk; van Leeuwen, Elisabeth M; Zaza, Gianluigi; Zhang, Weihua; Amin, Najaf; Butterworth, Adam; Chambers, John C; Dedoussis, George; Dehghan, Abbas; Franco, Oscar H; Franke, Lude; Frontini, Mattia; Gambaro, Giovanni; Gasparini, Paolo; Hamsten, Anders; Issacs, Aaron; Kooner, Jaspal S; Kooperberg, Charles; Langenberg, Claudia; Marz, Winfried; Scott, Robert A; Swertz, Morris A; Toniolo, Daniela; Uitterlinden, Andre G; van Duijn, Cornelia M; Watkins, Hugh; Zeggini, Eleftheria; Maurano, Mathew T; Timpson, Nicholas J; Reiner, Alexander P; Auer, Paul L; Soranzo, Nicole | |
| Monovalent cation leaks in human red cells caused by single amino-acid substitutions in the transport domain of the band 3 chloride-bicarbonate exchanger, AE1. | 1-gen-2005 | Bruce, Lj; Robinson, Hc; Guizouarn, H; Borgese, F; Harrison, P; King, Mj; Goede, Js; Coles, Se; Gore, Dm; Lutz, Hu; Ficarella, R; Layton, Dm; Iolascon, Achille; Ellory, Jc; Stewart, Gw | |
| Multiple common variants for celiac disease influencing immune gene expression | 1-gen-2010 | Dubois, Pc; Trynka, G; Franke, L; Hunt, Ka; Romanos, J; Curtotti, A; Zhernakova, A; Heap, Ga; Adány, R; Aromaa, A; Bardella, Mt; van den Berg, Lh; Bockett, Na; de la Concha, Eg; Dema, B; Fehrmann, Rs; Fernández-Arquero, M; Fiatal, S; Grandone, E; Green, Pm; Groen, Hj; Gwilliam, R; Houwen, Rh; Hunt, Se; Kaukinen, K; Kelleher, D; Korponay-Szabo, I; Kurppa, K; Macmathuna, P; Mäki, M; Mazzilli, Mc; Mccann, Ot; Mearin, Ml; Mein, Ca; Mirza, Mm; Mistry, V; Mora, B; Morley, Ki; Mulder, Cj; Murray, Ja; Núñez, C; Oosterom, E; Ophoff, Ra; Polanco, I; Peltonen, L; Platteel, M; Rybak, A; Salomaa, V; Schweizer, Jj; Sperandeo, Mp; Tack, Gj; Turner, G; Veldink, Jh; Verbeek, Wh; Weersma, Rk; Wolters, Vm; Urcelay, E; Cukrowska, B; Greco, L; Neuhausen, Sl; Mcmanus, R; Barisani, D; Deloukas, P; Barrett, Jc; Saavalainen, P; Wijmenga, C; van Heel, Da | |
| Mutations in MYH9 result in the May-Hegglin anomaly and Fechtner and Sebastian syndromes. The May-Heggllin/Fechtner Syndrome Consortium. | 1-gen-2000 | Seri, M; Cusano, R; Gangarossa, S; Caridi, G; Bordo, D; LO NIGRO, C; Ghiggeri, Gm; Ravazzolo, R; Savino, M; DEL VECCHIO, M; D'Apolito, M; Iolascon, Achille; Zelante, Ll; Savoia, A; Balduini, Cl; Noris, P; Magrini, U; Belletti, S; Heath, Ke; Babcock, M; Glucksman, Mj; Aliprandis, E; Bizzaro, N; Desnick, Rj; Martignetti, J. A. |
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