On the use of dense SNP marker data for the identification of distant relative pairs von Sun, M., Jobling, M.A., Taliun, D., Pramstaller, P.P., Egeland, T., Sheehan, N.A.

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1000 Genomes-based meta-analysis identifies 10 novel loci for kidney function von Gorski, Mathias, Chu, Audrey Y., Li, Man, Nolte, Ilja M., Cocca, Massimiliano, Taliun, Daniel, Gomez, Felicia, Li, Yong, Tayo, Bamidele, Tin, Adrienne, Attia, John, Biffar, Reiner, Bochud, Murielle, Borecki, Ingrid, Bottinger, Erwin P., Chen, Ming-Huei, Ciullo, Marina, Coresh, Josef, Cornelis, Marilyn C., Curhan, Gary C., d’Adamo, Adamo Pio, Dehghan, Abbas, Dengler, Laura, Ding, Jingzhong, Eiriksdottir, Gudny, Enroth, Stefan, Esko, Tõnu, Franco, Oscar H., Gasparini, Paolo, Gieger, Christian, Girotto, Giorgia, Gudnason, Vilmundur, Gyllensten, Ulf, Harris, Tamara B., Helmer, Catherine, Höllerer, Simon, Hofer, Edith, Hofman, Albert, Holliday, Elizabeth G., Homuth, Georg, Huth, Cornelia, Hutri-Kähönen, Nina, Hwang, Shih-Jen, Imboden, Medea, Johansson, Åsa, Kähönen, Mika, König, Wolfgang, Kramer, Holly, Krämer, Bernhard K., Kumar, Ashish, Kutalik, Zoltan, Lambert, Jean-Charles, Launer, Lenore J., Lehtimäki, Terho, Navis, Gerjan, Swertz, Morris, Loos, Ruth J. F., Lu, Yingchang, Lyytikäinen, Leo-Pekka, McEvoy, Mark A., Meisinger, Christa, Meitinger, Thomas, Metspalu, Andres, Metzger, Marie, Mihailov, Evelin, Mitchell, Paul, Nauck, Matthias, Olden, Matthias, Pistis, Giorgio, Probst-Hensch, Nicole, Raitakari, Olli T., Ridker, Paul M., Rivadeneira, Fernando, Robino, Antonietta, Rosas, Sylvia E., Ruderfer, Douglas, Ruggiero, Daniela, Sala, Cinzia, Schmidt, Helena, Schmidt, Reinhold, Scott, Rodney J., Sedaghat, Sanaz, Smith, Albert V., Sorice, Rossella, Stengel, Benedicte, Stracke, Sylvia, Strauch, Konstantin, Toniolo, Daniela, Uitterlinden, Andre G., Ulivi, Sheila, Viikari, Jorma S., Völker, Uwe, Völzke, Henry, Vuckovic, Dragana, Waldenberger, Melanie, Yang, Qiong, Chasman, Daniel I., Tromp, Gerard, Heid, Iris M., Fuchsberger, Christian

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The Type 2 Diabetes Knowledge Portal: an open access genetic resource dedicated to type 2 diabetes and related traits von Costanzo, MC, Von Grotthuss, M, Massung, J, Jang, D, Caulkins, L, Koesterer, R, Gilbert, C, Welch, RP, Kudtarkar, P, Hoang, Q, Boughton, AP, Singh, P, Sun, Y, Duby, M, Moriondo, A, Nguyen, T, Smadbeck, P, Alexander, BR, Brandes, M, Carmichael, M, Dornbos, P, Green, T, Huellas-Bruskiewicz, KC, Ji, Y, Kluge, A, McMahon, AC, Mercader, JM, Ruebenacker, O, Sengupta, S, Spalding, D, Taliun, D, AMP-T2D Consortium, Smith, P, Thomas, MK, Akolkar, B, Brosnan, MJ, Cherkas, A, Chu, AY, Fauman, EB, Fox, CS, Kamphaus, TN, Miller, MR, Nguyen, L, Parsa, A, Reilly, DF, Ruetten, H, Wholley, D, Zaghloul, NA, Abecasis, GR, Altshuler, D, Keane, TM, McCarthy, MI, Gaulton, KJ, Florez, JC, Boehnke, M, Burtt, NP, Flannick, J

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Fine-mapping type 2 diabetes loci to single-variant resolution using high-density imputation and islet-specific epigenome maps von Mahajan, A, Taliun, D, Thurner, M, Robertson, NR, Torres, JM, Payne, AJ, Steinthorsdottir, V, Scott, RA, Grarup, N, Cook, JP, Wuttke, M, Sarnowski, C, Magill, R, Nano, J, Gieger, C, Trompet, S, Prins, BP, Guo, X, Bielak, LF, Below, JE, Bowden, DW, Chambers, JC, Kim, YJ, Ng, MCY, Petty, LE, Sim, X, Zhang, W, Brummett, CM, Kardt, K-UE, Kardia, SLR, Kronenberg, F, Lall, K, Liu, C-T, Locke, AE, Luan, J, Ntalla, L, Schoenherr, S, Schurmann, C, Yengo, L, Bottinger, EP, Brandslund, I, Christensen, C, Dedoussis, G, Florez, JC, Ford, I, France, OH, Frayling, TM, Giedraitis, V, Hackinger, S, Hattersley, AT, Herder, C, Jorgensen, ME, Jorgensen, T, Kriebel, J, Kuusisto, J, Ligthart, S, Linneberg, A, Mamakou, V, Meitinger, T, Mohlke, KL, Morris, AD, Nadkarni, G, Pankow, JS, Sattar, N, Stancakova, A, Strauch, K, Taylor, KD, Thorand, B, Thorleifsson, G, Tuomilehto, J, Witte, DR, Dupuis, J, Peyser, PA, Zeggini, E, Loos, RJF, Froguel, P, Ingelsson, E, Lind, L, Groop, L, Laakso, M, Collins, FS, Jukema, JW, Palmer, CNA, Grallert, H, Metspalu, A, Dehghan, A, Koettgen, A, Abecasis, GR, Meigs, JB, Rotter, J, Marchini, J, Pedersen, O, Hansen, T, Langenberg, C, Wareham, NJ, Stefansson, K, Gloyn, AL, Morris, AP, Boehnke, M, McCarthy, M

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Refining the accuracy of validated target identification through coding variant fine-mapping in type 2 diabetes von Mahajan, A, Kitajima, H, Rayner, NW, Lu, Y, Hu, Y, Cook, JP, Kim, YJ, Rybin, DV, Mueller-Nurasyid, M, Meidtner, K, Li-Gao, R, Li, J, An, P, Ligthart, S, Gustafsson, S, Lecoeur, C, Preuss, M, Highland, HM, Justice, AE, Marouli, E, Peloso, GM, Ahlqvist, E, Almgren, P, Amin, N, Bombieri, C, Brandslund, I, Brody, JA, Canouil, M, Eastwood, SV, Giedraitis, V, Han, S, Tybjaerg-Hansen, A, Isomaa, B, Jorgensen, T, Kim, B-J, Kim, SS, Koistinen, HA, Kriebel, J, Lall, K, Lehne, B, Linneberg, A, Liu, C-T, Liu, J, Mamakou, V, Ntalla, I, Rich, SS, Selvin, E, Small, KS, Surendran, P, Teslovich, TM, Thorand, B, Thorleifsson, G, Varbo, A, Witte, DR, Yajnik, P, Yao, J, Amouyel, P, Boeing, H, Chowdhury, R, Frossard, P, Harris, TB, Kathiresan, S, Kee, F, Langenberg, C, Launer, LJ, Lindgren, CM, Mannisto, S, Mohlke, KL, Morris, AD, Perola, M, Rasheed, A, Rosendaal, FR, Rosengren, AH, Sheu, WH-H, Sladek, R, Smith, BH, Bluher, M, Butterworth, AS, Chambers, JC, Franks, PW, Froguel, P, Groop, L, Ingelsson, E, Kardia, SLR, Karpe, F, Kooner, JS, Kottgen, A, Kuulasmaa, K, Lind, L, Loos, RJF, Rauramaa, R, Schulze, MB, Soranzo, N, Stefansson, K, Stumvoll, M, Thorsteinsdottir, U, Frayling, TM, Goodarzi, MO, Morris, AP, Rotter, JI

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A global reference for human genetic variation von Durbin, RM, Clark, AG, Donnelly, P, Green, ED, Knoppers, BM, Korbel, JO, Lee, C, Marth, GT, Fang, X, Jin, X, Li, G, Tang, M, Yin, Y, Zhang, D, Zhao, M, Toji, LH, Barker, J, Kelman, G, Radhakrishnan, R, Smirnov, D, James, T, Fulton, R, Ananiev, V, Beloslyudtsev, D, Cohen, R, O'Sullivan, C, Ponomarov, S, Shekhtman, E, Burton, J, Keane, TM, Stalker, J, Wong, B, Auton, A, Campbell, CL, Li, Q, Liu, B, Xie, Y, Ye, C, Alkan, C, Dal, E, Zhang, M, DePristo, MA, McCarroll, SA, Keinan, A, Sabeti, PC, Shlyakhter, I, Cox, A, Kahn, S, MacArthur, DG, Lek, M, Herwig, R, Lacroute, P, Halperin, E, Izatt, T, Sinari, SA, Squire, K, Gujral, M, Gignoux, CR, Kent, WJ, Ruiz-Linares, A, Kidd, JM, Caron, S, Scheller, C, Tan, A, Hodgkinson, A, Quitadamo, A, Mathieson, I, Tyler-Smith, C, Walter, K, Balasubramanian, S, Chen, J, Liu, J, Zhang, J, Meiers, S, Mills, RE, Nagaswamy, U, Yu, J, Dunham, I, Narechania, A, Poznik, GD, Coin, L, Mittelman, D, Ritchie, GR, Barnes, KC, Cai, H, Henn, B, Ossorio, PN, Tian, Z, Martinez-Cruzado, JC, Mathias, RA, Hennis, A, Watson, H, Asogun, D, Omoniwa, O, Kwiatkowski, D, Nguyen, TH, Kanneh, L, Vaydylevich, Y, Schloss, JA, Brooks, LD

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Linkage and association analysis of hyperthyrotropinaemia in an Alpine population reveal two novel loci on chromosomes 3q28-29 and 6q26-27 von Volpato, Claudia B, De Grandi, Alessandro, Gögele, Martin, Taliun, Daniel, Fuchsberger, Christian, Facheris, Maurizio F, Minelli, Cosetta, Pattaro, Cristian, Pramstaller, Peter P, Hicks, Andrew A

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Genome-wide analyses identify a role for SLC17A4 and AADAT in thyroid hormone regulation von Chaker, L., Groeneweg, S., Li, Y., Barbieri, C., Traglia, M., Akiyama, M., Appel, E.V.R., Arking, D.E., Arnold, A., Astrup, A., Beekman, M., Beilby, J.P., Bekaert, S., Boerwinkle, E., Brown, S.J., Buyzere, M. de, Ceresini, G., Cerqueira, C., Deelen, J., Eckardt, K.U., Ekici, A.B., Eriksson, J.G., Ferrrucci, L., Fiers, T., Fiorillo, E., Ford, I., Fox, C.S., Fuchsberger, C., Galesloot, T.E., Gieger, C., Gogele, M., Grandi, A. de, Grarup, N., Haljas, K., Hansen, T., Harris, S.E., Heemst, D. van, Heijer, M. den, Hicks, A.A., Hollander, W. den, Ittermann, T., Jing, J., Jukema, J.W., Kasbohm, E., Kaufman, J.M., Kloppenburg, M., Kronenberg, F., Kubo, M., Lahti, J., Lapauw, B., Li, S., Liewald, D.C.M., Lim, E.M., Linneberg, A., Marina, M., Matsuda, K., Medenwald, D., Meisinger, C., Meulenbelt, I., Meyer, T. de, Schwabedissen, H.E.M. zu, Mikolajczyk, R., Netea-Maier, R.T., Nolte, I.M., Pattaro, C., Petersmann, A., Porcu, E., Postmus, I., Pramstaller, P.P., Psaty, B.M., Ramos, Y.F.M., Rawal, R., Redmond, P., Rietzschel, E.R., Rivadeneira, F., Roef, G., Sala, C.F., Schlessinger, D., Slagboom, P.E., Soranzo, N., Spector, T.D., Stott, D.J., Taes, Y., Taliun, D., Thuesen, B., Tiller, D., Toniolo, D., Uitterlinden, A.G., Visser, W.E., Walsh, J.P., Wilson, S.G., Wolffenbuttel, B.H.R., Yang, Q., Zheng, H.F., Peeters, R.P., Naitza, S., Volzke, H., Sanna, S., Visser, T.J., Medici, M.

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Fine-mapping type 2 diabetes loci to single-variant resolution using high-density imputation and islet-specific epigenome maps von Mahajan, A., Taliun, D., Thurner, M., Torres, J.M., Rayner, N.W., Payne, A.J., Steinthorsdottir, V., Scott, R.A., Grarup, N., Cook, J.P., Schmidt, E.M., Wuttke, M., Sarnowski, C., Magill, R., Nano, J., Trompet, S., Lecoeur, C., Preuss, M.H., Prins, B.P., Guo, X.Q., Bielak, L.F., Below, J.E., Bowden, D.W., Chambers, J.C., Kim, Y.J., Ng, M.C.Y., Petty, L.E., Sim, X.L., Zhang, W.H., Bennett, A.J., Bork-Jensen, J., Brummett, C.M., Canouil, M., Fischer, K., Kardia, S.L.R., Kronenberg, F., Lall, K., Liu, C.T., Luan, J.A., Ntalla, L., Schonherr, S., Schurmann, C., Yengo, L., Bottinger, E.P., Brandslund, I., Christensen, C., Dedoussis, G., Florez, J.C., Ford, I., Frayling, T.M., Giedraitis, V., Hackinger, S., Hattersley, A.T., Herder, C., Ingelsson, M., Jorgensen, M.E., Jorgensen, T., Kuusisto, J., Ligthart, S., Lindgren, C.M., Linneberg, A., Lyssenko, V., Mamakou, V., Meitinger, T., Mohlke, K.L., Morris, A.D., Nadkarni, G., Pankow, J.S., Peters, A., Sattar, N., Stancakova, A., Strauch, K., Thorand, B., Thorleifsson, G., Thorsteinsdottir, U., Witte, D.R., Peyser, P.A., Zeggini, E., Loos, R.J.F., Froguel, P., Ingelsson, E., Lind, L., Groop, L., Laakso, M., Collins, F.S., Grallert, H., Metspalu, A., Kottgen, A., Abecasis, G.R., Meigs, J.B., Rotter, J.I., Marchini, J., Pedersen, O., Hansen, T., Langenberg, C., Stefansson, K., Gloyn, A.L., Morris, A.P., Boehnke, M., McCarthy, M.I.

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Refining the accuracy of validated target identification through coding variant fine-mapping in type 2 diabetes von Mahajan, A, Kitajima, H, Rayner, NW, Lu, Y, Hu, Y, Cook, JP, Kim, YJ, Rybin, DV, Mueller-Nurasyid, M, Meidtner, K, Li-Gao, R, Li, J, An, P, Ligthart, S, Gustafsson, S, Lecoeur, C, Preuss, M, Highland, HM, Justice, AE, Marouli, E, Peloso, GM, Ahlqvist, E, Almgren, P, Amin, N, Bombieri, C, Brandslund, I, Brody, JA, Canouil, M, Eastwood, SV, Giedraitis, V, de Haan, HG, Han, S, Tybjaerg-Hansen, A, Isomaa, B, Jorgensen, T, Kim, B-J, Kim, SS, Koistinen, HA, Kriebel, J, Lall, K, Lehne, B, Linneberg, A, Liu, C-T, Liu, J, Mamakou, V, Ntalla, I, Rich, SS, Small, KS, Surendran, P, Teslovich, TM, Thorand, B, Thorleifsson, G, Varbo, A, Witte, DR, Yajnik, P, Yao, J, Amouyel, P, Boeing, H, Chowdhury, R, Frossard, P, Harris, TB, Kathiresan, S, Kee, F, Langenberg, C, Launer, LJ, Lindgren, CM, Mannisto, S, Mohlke, KL, Morris, AD, Perola, M, Rasheed, A, Rosendaal, FR, Rosengren, AH, Sheu, WH-H, Sladek, R, Smith, BH, Bluher, M, Butterworth, AS, Chambers, JC, Franks, PW, Froguel, P, Groop, L, Ingelsson, E, Kardia, SLR, Karpe, F, Kooner, JS, Kottgen, A, Kuulasmaa, K, Lind, L, Loos, RJF, Rauramaa, R, Schulze, MB, Soranzo, N, Stefansson, K, Stumvoll, M, Thorsteinsdottir, U, Frayling, TM, Goodarzi, MO, Morris, AP, Rotter, JI

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A global reference for human genetic variation von Durbin, RM, Clark, AG, Donnelly, P, Green, ED, Knoppers, BM, Korbel, JO, Lee, C, Marth, GT, Fang, X, Jin, X, Li, G, Tang, M, Yin, Y, Zhao, M, Toji, LH, Barker, J, Kelman, G, Radhakrishnan, R, Smirnov, D, James, T, Fulton, R, Beloslyudtsev, D, Cohen, R, O'Sullivan, C, Ponomarov, S, Shekhtman, E, Burton, J, Keane, TM, Wong, B, Auton, A, Campbell, CL, Li, Q, Liu, B, Xie, Y, Ye, C, Alkan, C, Dal, E, Zhang, M, DePristo, MA, del Angel, G, McCarroll, SA, Keinan, A, Sabeti, PC, Shlyakhter, I, Cox, A, Kahn, S, MacArthur, DG, Lek, M, Herwig, R, Lacroute, P, Halperin, E, Izatt, T, Squire, K, Gujral, M, Gignoux, CR, Ruiz-Linares, A, Kidd, JM, Caron, S, Scheller, C, Tan, A, Hodgkinson, A, Quitadamo, A, Mathieson, I, Tyler-Smith, C, Walter, K, Balasubramanian, S, Chen, J, Liu, J, Zhang, J, Hall, I, Mills, RE, Dayama, G, Nelson, BJ, Ning, Z, Lu, J, Dunham, I, Mendez, FL, Poznik, GD, Ritchie, GR, Barnes, KC, Cai, H, Henn, B, Kaye, JS, Kent, A, Tian, Z, Wang, Y, Yang, H, Peltonen, L, Garcia-Montero, A, Dutil, J, Hennis, A, Watson, H, LaRocque, R, Tariyal, R, Joof, FS, Rockett, K, Kwiatkowski, D, Nguyen, TH, Kanneh, L, Poletti, G

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Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function von Pattaro, C, Chu, AY, Garnaas, M, Tin, A, Li, Y, Fox, CS, Dieffenbach, AK, Zonderman, AB, Wright, AF, Morrison, AC, Guessous, I, Hofman, A, Franke, A, Tonjes, A, Robino, A, Johansson, Å, Polasek, O, Demirkan, A, Kollerits, B, Krämer, BK, Peralta, CA, Hayward, C, Shaffer, CM, Sala, C, Van Duijn, CM, Toniolo, D, Cusi, D, Siscovick, DS, Ridker, PM, Grallert, H, Atkinson, EJ, Boerwinkle, E, Bottinger, EP, Kronenberg, F, Curhan, GC, Ehret, GB, Muntner, P, Coassin, S, Pistis, G, Gambaro, G, Eiriksdottir, G, Wichmann, HE, Campbell, H, Persico, I, Felix, JF, Divers, J, Lambert, JC, Faul, JD, Ding, J, Hirschhorn, JN, Chalmers, J, Endlich, K, Wallaschofski, H, Chen, MH, Ferrucci, L, Rao, M, ICBP Consortium, Pers, TH, Haun, M, Ciullo, M, McEvoy, MA, Woodward, M, Adam, M, Cocca, M, Johnson, AD, Nauck, M, Imboden, M, Pruijm, M, Evans, MK, Kähönen, M, Ko, YA, Bochud, M, Verweij, N, Gottesman, O, ECHOGen Consortium, Kovacs, P, Rettig, R, Middelberg, RP, Feitosa, MF, Enroth, S, Stengel, B, Hancock, SJ, Isaacs, A, Zeller, T, Lehtimäki, T, Nikopensius, T, Kramer, H, Emilsson, V, Igl, W, Koenig, W, D'Adamo, P, Loos, RJ, Pramstaller, PP, Parsa, A, O'Connell, JR, Susztak, K, Hamet, P, Böger, CA, Goessling, W, Chasman, DI

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Importance of different types of prior knowledge in selecting genome-wide findings for follow-up von Minelli, C, De Grandi, A, Weichenberger, CX, Gögele, M, Modenese, M, Attia, J, Barrett, JH, Boehnke, M, Borsani, G, Casari, G, Fox, CS, Freina, T, Hicks, AA, Marroni, F, Parmigiani, G, Pastore, A, Pattaro, C, Pfeufer, A, Ruggeri, F, Schwienbacher, C, Taliun, D, Pramstaller, PP, Domingues, FS, Thompson, JR

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Genome-wide association and functional follow-up reveals new loci for kidney function von Pattaro, C, Köttgen, A, Teumer, A, Garnaas, M, Böger, CA, Fuchsberger, C, Olden, M, Tin, A, Gao, X, O'Seaghdha, CM, Glazer, N, Isaacs, A, Liu, CT, O'Connell, JR, Tanaka, T, Johnson, AD, Gierman, HJ, Feitosa, M, Atkinson, EJ, Tönjes, A, Dehghan, A, Chouraki, V, Esko, T, Deshmukh, H, Chu, AY, Murgia, F, Pistis, G, CARDIoGRAM Consortium, ICBP Consortium, Launer, LJ, Eiriksdottir, G, Mitchell, BD, Rao, M, Hu, FB, Demirkan, A, Oostra, BA, Ding, J, Freedman, BI, Illig, T, Wichmann, HE, Zemunik, T, Boban, M, Minelli, C, Igl, W, Wild, SH, Campbell, H, Ellinghaus, D, Nöthlings, U, Jacobs, G, Biffar, R, Endlich, K, Homuth, G, Nauck, M, Völker, U, Völzke, H, Kovacs, P, Hofman, A, Uitterlinden, AG, Rivadeneira, F, Polasek, O, Hastie, N, Vitart, V, Wang, JJ, Ruggiero, D, Bergmann, S, Kähönen, M, Viikari, J, Nikopensius, T, Province, M, Ketkar, S, Giulianini, F, Portas, L, Buckley, BM, Adam, M, Sala, C, Metzger, M, Kim, SK, Vollenweider, P, Raitakari, O, Pirastu, M, Jukema, JW, Probst-Hensch, NM, Kronenberg, F, Toniolo, D, Gudnason, V, Coresh, J, Siscovick, DS, Van Duijn, CM, Curhan, GC, Rudan, I, Gyllensten, U, Wilson, JF, Rettig, R, Prokopenko, I, Witteman, JC, Hayward, C, Ridker, P, Heid, IM, Goessling, W, Chasman, DI

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GWAS of Hematuria von Gagliano Taliun, Sarah A, Sulem, Patrick, Sveinbjornsson, Gardar, Gudbjartsson, Daniel F, Stefansson, Kari, Paterson, Andrew D, Barua, Moumita

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GWAS for the composite traits of hematuria and albuminuria von Gagliano Taliun, Sarah A., Dinsmore, Ian R., Mirshahi, Tooraj, Chang, Alexander R., Paterson, Andrew D., Barua, Moumita

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Author Correction: GWAS for the composite traits of hematuria and albuminuria von Gagliano Taliun, Sarah A., Dinsmore, Ian R., Mirshahi, Tooraj, Chang, Alexander R., Paterson, Andrew D., Barua, Moumita

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Rare coding variants in ten genes confer substantial risk for schizophrenia von Singh, Tarjinder, Poterba, Timothy, Curtis, David, Akil, Huda, Al Eissa, Mariam, Barchas, Jack D., Bass, Nicholas, Bigdeli, Tim B., Breen, Gerome, Bromet, Evelyn J., Buckley, Peter F., Bunney, William E., Bybjerg-Grauholm, Jonas, Byerley, William F., Chapman, Sinéad B., Chen, Wei J., Churchhouse, Claire, Craddock, Nicholas, DeLisi, Lynn, Dodge, Sheila, Escamilla, Michael A., Eskelinen, Saana, Fanous, Ayman H., Faraone, Stephen V., Fiorentino, Alessia, Francioli, Laurent, Gabriel, Stacey B., Gage, Diane, Gagliano Taliun, Sarah A., Ganna, Andrea, Genovese, Giulio, Grove, Jakob, Hall, Mei-Hua, Heyne, Henrike O., Holi, Matti, Hougaard, David M., Howrigan, Daniel P., Huang, Hailiang, Hwu, Hai-Gwo, Kahn, René S., Kang, Hyun Min, Karczewski, Konrad J., Knowles, James A., Lee, Francis S., Lehrer, Douglas S., Lescai, Francesco, Marder, Stephen R., McCarroll, Steven A., McIntosh, Andrew M., Milani, Lili, Morley, Christopher P., Morris, Derek W., Mortensen, Preben Bo, Nordentoft, Merete, O’Brien, Niamh L., Olivares, Ana Maria, Ongur, Dost, Ouwehand, Willem H., Palmer, Duncan S., Paunio, Tiina, Quested, Digby, Rapaport, Mark H., Rees, Elliott, Rollins, Brandi, Satterstrom, F. Kyle, Schatzberg, Alan, Scolnick, Edward, Scott, Laura J., Sharp, Sally I., Sklar, Pamela, Smoller, Jordan W., Solomonson, Matthew, Stahl, Eli A., Stevens, Christine R., Suvisaari, Jaana, Watts, Nicholas A., Blackwood, Douglas H., Cohen, Bruce M., Corvin, Aiden P., Esko, Tõnu, Freimer, Nelson B., Glatt, Stephen J., Hultman, Christina M., McQuillin, Andrew, Palotie, Aarno, Pato, Carlos N., Pato, Michele T., Pulver, Ann E., St. Clair, David, Tsuang, Ming T., Vawter, Marquis P., Walters, James T., Werge, Thomas M., Ophoff, Roel A., Sullivan, Patrick F., Owen, Michael J., Boehnke, Michael, O’Donovan, Michael C., Neale, Benjamin M., Daly, Mark J.

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A global reference for human genetic variation von Auton, Adam, Brooks, Lisa D, Durbin, Richard M, Garrison, Erik P, Kang, Hyun Min, Korbel, Jan O, Marchini, Jonathan L, McCarthy, Shane, McVean, Gil A, Abecasis, Gonçalo R

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Refining the accuracy of validated target identification through coding variant fine-mapping in type 2 diabetes article von Mahajan, Anubha, Wessel, Jennifer, Willems, Sara M, Zhao, Wei, Robertson, Neil R, Chu, Audrey Y., Kravic, Jasmina, Ahlqvist, Emma, Rosengren, Anders, Groop, Leif, V Varga, Tibor, Franks, Paul, Almgren, Peter, Melander, Olle, Orho-Melander, Marju, McCarthy, Mark I.

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