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5 Most Recent Publications
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Identification of common variants influencing risk of the tauopathy progressive supranuclear palsy
(Article)
Hoglinger, G. Melhem, N.M. Swieten, J.C. van Pahwa, R. Pezzoli, G. Pickering-Brown, S. Poewe, W. Rabano, A. Rajput, A. Reich, S.G. Respondek, G. Roeber, S. Rohrer, J.D. Heutink, P. Ross, O.A. Rossor, M. Sacilotto, G. Seeley, W.W. Seppi, K. Silveira-Moriyama, L. Spina, S. Srulijes, K. St. George-Hyslop, P. Stamelou, M. Wszolek, Z.K. Standaert, D.G. Tesei, S. Tourtellotte, W.W. Trenkwalder, C. Troakes, C. Trojanowski, J.Q. Troncoso, J.C. Deerlin, V.M. Vonsattel, J.P.G. Wenning, G.K. Uitti, R.J. White, C.L. Winter, P. Zarow, C. Zecchinelli, A.L. Antonini, A. Vandrovcova, J. Hurtig, H.I. Gross, R.G. Maetzler, W. Goldwurm, S. Tolosa, E. Dickson, D. Borroni, B. Pastor, P. Cantwell, L.B. Han, M.R. Dillman, A. Brug, M.P. van der Gibbs, J. Cookson, M.R. Hernandez, D.G. Singleton, A. Sleiman, P.M.A. Farrer, M.J. Yu, C.-E. Golbe, L.I. Revesz, T. Hardy, J. Lees, A.J. Devlin, B. Hakonarson, H. Müller, U. Schellenberg, G.D. Wang, L.-S. Albin, R.L. Alonso, E. Apfelbacher, M. Arnold, S.E. Avila, J. Beach, T.G. Beecher, S. Berg, D. Bird, T.D. Bogdanovic, N. Klei, L. Boon, A.J.W. Bordelon, Y. Brice, A. Budka, H. Canesi, M. Chiu, W.Z. Cilia, R. Colosimo, C. Deyn, P.P. de Yebenes, J.G. de Rademakers, R. Donker Kaat, L. Duara, R. Durr, A. Engelborghs, S. Fabbrini, G. Finch, N.A. Flook, R. Frosch, M.P. Gaig, C. Galasko, D. Silva, R. de Gasser, T. Gearing, M. Geller, E.T. Ghetti, B. Graff-Radford, N.R. Grossman, M. Hall, D.A. Hazrati, L.-N. Höllerhage, M. Jankovic, J. Litvan, I. Juncos, J.L. Karydas, A. Kretzschmar, H.A. Leber, I. Lee, V.M.Y. Lieberman, A.P. Lyons, K.E. Mariani, C. Masliah, E. Massey, L.A. Riley, D.E. McLean, C.A. Meucci, N. Miller, B.L. Mollenhauer, B. Möller, J.C. Morris, H. O'Sullivan, S.S. Oertel, W. Ottaviani, D. Padovani, A. |
2011-07-01
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Genetic variants influencing circulating lipid levels and risk of coronary artery disease
(Article)
Waterworth, D. Ricketts, S.L. Luan, J. Ashford, S. Wheeler, E. Young, E.H. Hadley, D. Thompson, J.R. Braund, P.S. Johnson, T. Struchalin, M.V. Surakka, I. Song, K. Luben, R.N. Khaw, K-T. Rodwell, S.A. Loos, R.J.F. Boekholdt, S.M. Inouye, M. Deloukas, P. Elliott, P. Schlessinger, D. Sanna, S. Chen, L. Scuteri, A. Jackson, A.U. Mohlke, K.L. Tuomilehto, J. Roberts, R. Stewart, A. Kesaniemi, Y.A. Mahley, R. Grundy, S.M. McArdle, W.L. Zhao, J.H. Cardon, L. Waeber, G. Vollenweider, P. Chambers, J.C. Boehnke, M. Abecasis, G.R. Salomaa, V. Järvelin, M.R. Ruokonen, A. Barroso, I. Ripatti, S. Epstein, S.E. Hakonarson, H. Rader, D.J. Reilly, M.P. Witteman, J.C.M. Hall, A.S. Samani, N.J. Strachan, D.P. Barter, P. Tikka-Kleemola, P. Aulchenko, Y.S. Kooner, J.S. Peltonen, L. Wareham, N.J. McPherson, R. Mooser, V. Sandhu, M.S. Zhang, W. Yuan, X. Lim, N. |
2010-11-01
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A locus on 19p13 modifies risk of breast cancer in BRCA1 mutation carriers and is associated with hormone receptor-negative breast cancer in the general population
(Article)
Antoniou, A.C. Wang, X. Ghoussaini, M. Caldes, T. Hoya, M. de La Singer, C.F. Fink-Retter, A. Greene, M.H. Mai, P.L. Loud, J.T. Guidugli, L. Lindor, N.M. Hansen, T.V.O. Barrowdale, D. Nielsen, F.C. Blanco, I. Lazaro, C. Garber, J. Ramus, S.J. Gayther, S.A. Phelan, C. Narod, S. Szabo, C. Benitez, J. Peock, S. Osorio, A. Nevanlinna, H. Heikkinen, T. Caligo, M.A. Beattie, M.S. Hamman, U. Godwin, A.K. Montagna, M. Casella, C. Neuhausen, S.L. Cook, M. Karlan, B.Y. Tung, N. Toland, A.E. Weitzel, J. Olopade, P. Simard, J. Soucy, P. Rubinstein, W.S. Arason, A. Rennert, G. Oliver, C. Martin, N.G. Montgomery, G.W. Chang-Claude, J. Flesch-Janys, D. Brauch, H. Severi, G. Baglietto, L. Cox, A. Cross, S.S. Miron, P. Frost, D. Gerty, S.M. Tapper, W. Yannoukakos, D. Fountzilas, G. Fasching, P.A. Beckmann, M.W. Dos Santos Silva, I. Peto, J. Lambrechts, D. Paridaens, R. Eccles, D. Rüdiger, T. Försti, A. Winqvist, R. Pylkäs, K. Diasio, R.B. Lee, A.M. Eckel-Passow, J. Vachon, C. Blows, F. Driver, K. Evans, D.G. Dunning, A.M. Pharaoh, P.D.P. Offit, K. Pankratz, V.S. Hakonarson, H. Chenevix-Trench, G. Easton, D.F. Couch, F.J. Eeles, R. Izatt, L. Fredericksen, Z. Chu, C. Douglas, F. Paterson, J. Stoppa-Lyonnet, D. Houdayer, C. Mazoyer, S. Giraud, S. Lassett, C. Remenieras, A. Caron, O. McGuffog, L. Hardouin, A. Berthet, P. Hogervorst, F.B.L. Rookus, M.A. Jager, A. Ouweland, A.M.W. van den Hoogerbrugge, N. Luijt, R.B. van der Meijers-Heijboer, H. G'mez García, E.B. Tarrell, R. Devilee, P. Vreeswijk, M.P. Lubinski, J. Jakubowska, A. Gronwald, J. Huzarski, T. Byrski, T. G'rski, B. Cybulski, C. Spurdle, A.B. Sinilnikova, O. Holland, H. Goldgar, D. John, E.M. Hopper, J. Southey, M.C. Buys, S.S. Daly, M.B. Terry, M-B. Schmutzler, R.K. Wappenschmidt, B. Healey, S. Engel, C. Meindl, A. Preisler-Adams, S. Arnold, N. Niederacher, D. Sutter, C. Domchek, S.M. Nathanson, K.L. Rebbeck, T.R. Blum, J.L. Morrison, J. Piedmonte, M. Rodriguez, G.C. Wakeley, K. Boggess, J.F. Basil, J. Blank, S.V. Friedman, E. Kaufman, B. Laitman, Y. Milgrom, R. kartsonaki, C. Andrulis, I.L. Glendon, G. Ozcelik, H. Kirchhoff, T. Vijai, J. Gaudet, M.M. Altshuler, D. Guiducci, C. Loman, N. Harbst, K. Lesnick, T. Rantala, J. Ehrencona, H. Gerdes, A-M. Thomassen, M. Sunde, L. Peterlongo, P. Manoukian, S. Bonanni, B. Viel, A. Radice, P. |
2010-10-01
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Variants in ADCY5 and near CCNL1 are associated with fetal growth and birth weight
(Article)
Freathy, R.M. Mook-Kanamori, D.O. Lange, L.A. Bradfield, J.P. Kerkhof, M. Marsh, J.A. Mägi, R. Chen, C. Lyon, H.N. Kirin, M. Adair, L.S. Aulchenko, Y.S. Sovio, U. Bennett, A.J. Borja, J.B. Bouatia-Naji, N. Charoen, P. Coin, L. Cousminer, D.L. Geus, E.J.C. de Deloukas, P. Elliott, P. Evans, D.M. Prokopenko, I. Froguel, P. Glaser, B. Groves, C.J. Hartikainen, A.L. Hassanali, N. Hirschhorn, J.N. Hofman, A. Holly, J.M.P. Hyppönen, E. Kanoni, S. Timpson, N. Knight, B.A. Laitinen, J. Lindgren, C.M. McArdle, W.L. O'Reilly, P.F. Pennell, C.E. Postma, D.S. Pouta, A. Ramasamy, A. Rayner, N.W. Berry, D. Ring, S.M. Rivadeneira Ramirez, F. Shields, B.M. Strachan, D.P. Surakka, I. Taanila, A. Tiesler, C. Uitterlinden, A.G. Tikka-Kleemola, P. Wijga, A. Warrington, N. Willemsen, G.A.H.M. Zhang, H. Zhao, J.H. Wilson, J.F. Steegers-Theunissen, R.P.M. Hattersley, A.T. Hagen, K. Peltonen, L. Mohlke, K.L. Grant, S.F. Widen, E. Hakonarson, H. Koppelman, G.H. Dedoussis, G.V. Heinrich, J. Gillman, M.W. Palmer, C. Frayling, T.M. Boomsma, D.I. Smith, G.D. Power, C. Hottenga, J.J. Jaddoe, V.W.V. Jarvelin, M.R. McCarthy, M.I. Kaakinen, M. |
2010-05-01
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Common variants at 7p21 are associated with frontotemporal lobar degeneration with TDP-43 inclusions
(Article)
Deerlin, V.M. Sleiman, P.M.A. Arnold, S.E. Mann, D. Pickering-Brown, S. Seelaar, H. Heutink, P. Swieten, J.C. van Murrell, J.R. Ghetti, B. Spina, S. Grafman, J. Martinez-Lage, M. Hodges, J. Spillantini, M.G. Gilman, S. Lieberman, A.P. Kaye, J.A. Woltjer, R.L. Bigio, E.H. Mesulam, M. Al-Sarraj, S. Troakes, C. Chen-Plotkin, A. Rosenberg, R.N. White, C.L. Ferrer, I. Lladó, A. Neumann, H.A.M. Kretzschmar, H.A. Hulette, C. Welsh-Bohmer, K.A. Miller, B.L. Alzualde, A. Wang, L. Munain, A.L. de McKee, A.C. Gearing, M. Levey, A.I. Lah, J.J. Hardy, J. Rohrer, J.D. Lashley, T. Mackenzie, I.R.A. Feldman, H.H. Graff-Radford, N.R. Hamilton, R.L. Dekosky, S.T. Zee, J. van der Kumar-Singh, S. Broeckhoven, C. van Mayeux, R. Vonsattel, J.P. Troncoso, J.C. Kril, J.J. Kwok, J.B.J. Dickson, D. Halliday, G.M. Bird, T.D. Ince, P.G. Shaw, P.J. Cairns, N.J. Morris, J.C. McLean, C.A. DeCarli, C. Ellis, W.G. Freeman, S.H. Rademakers, R. Frosch, M.P. Growdon, J.H. Perl, D.P. Sano, M. Bennett, D.A. Schneider, J.A. Beach, T.G. Reiman, E.M. Woodruff, B.K. Cummings, J.F. Boeve, B. Vinters, H.V. Miller, C.A. Chui, H. Alafuzoff, I. Hartikainen, P. Seilhean, D. Galasko, D. Masliah, E. Cotman, C.W. Tũón, M.T. Grossman, M. Martínez, M.C.C. Munoz, D.G. Carroll, S.L. Marson, D. Riederer, P.F. Bogdanovic, N. Schellenberg, G.D. Hakonarson, H. Trojanowski, J.Q. Lee, V.M.Y. |
2010-03-01
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