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university association study department health medicine institute research lung function table function disease genome-wide variant genetic effect center epidemiology blood region stage pressure school control london science hospital genet result centre population netherland 1/fvc genome-wide association study blood pressure fev 1 fev 1/fvc locus finland australia material sample dpp 6 genomic individual germany number nature risk score division intron health sciences erasmus universiteit rotterdam genome-wide association studies dpp 6 locus hypertension european ancestry meta-analysi analysis smoker washington ancestry nipa 1 allele stage 1 analyses expression groningen height european sclerosis signal consortium singapore trait amyotrophic smoking genome-wide screen 10−1 score
3 Most Recent Publications
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Genome-wide association and large-scale follow up identifies 16 new loci influencing lung function
(Article)
Artigas, M.S. Loth, D.W. Albrecht, E. Vonk, J.M. Wannamethee, S.G. Whincup, P.H. Wijmenga, C. Williams, O.D. Wong, A. Mangino, M. Marciante, K. McArdle, W.L. Meibohm, B. Jackson, C.M. Morrison, A.C. North, K.E. Omenaas, E. Palmer, L.J. Pietilainen, K.H. Pin, I. Polasek, O. Pouta, A. Psaty, B.M. Hartikainen, A.L. Evans, D.M. Rantanen, T. Ripatti, S. Rotter, J.I. Rudan, I. Rudnicka, A.R. Schulz, H. Shin, S.-Y. Spector, T.D. Surakka, I. Vitart, V. Cadby, G. Völzke, H. Wareham, N.J. Warrington, N. Wichmann, H.E. Wild, S.H. Wilk, J.B. Wjst, M. Wright, A.F. Zgaga, L. Zemunik, T. Fornage, M. Pennell, C.E. Nyberg, F. Kuh, D. Holloway, J.W. Boezen, H.M. Lawlor, D.A. Probst-Hensch, N. Kaprio, J. Wilson, J.F. Hayward, C. Manichaikul, A. Kähönen, M. Heinrich, J. Musk, A.W. Jarvis, D.L. Gläser, S. Järvelin, M.R. Barroso, I. Stricker, B.H.Ch. Elliott, P. O'Connor, G.T. Lopez, L.M. Strachan, D.P. London, S.J. Hall, I.P. Gudnason, V. Tobin, M.D. Johnson, T. Aldrich, M.C. Aspelund, T. Wain, L.V. Campbell, H. Cassano, P.A. Couper, D. Eiriksdottir, G. Franceschini, N. Garcia, M. Gieger, C. Gislason, G.K. Grkovic, I. Hammond, C.J. Gharib, S.A. Hancock, D.B. Harris, T.B. Ramasamy, A. Heckbert, S.R. Heliovaara, M. Homuth, G. Hysi, P.G. James, A.L. Jankovic, S. Joubert, B.R. Obeidat, M. Karrasch, S. Klopp, N. Koch, B. Kritchevsky, S.B. Launer, L.J. Liu, Y. Loehr, L.R. Lohman, K. Loos, R.J.F. Lumley, T. Tang, W. Al Balushi, K.A. Ang, W.Q. Barr, R.G. Beilby, J.P. Blakey, J.D. Boban, M. Boraska, V. Brisman, J. Britton, J.R. Brusselle, G.G. Zhai, G. Cooper, C. Curjuric, I. Dahgam, S. Deary, I.J. Ebrahim, S. Eijgelsheim, M. Francks, C. Gaysina, D. Granell, R. Gu, X. Zhao, J.H. Hankinson, J.L. Hardy, R. Henderson, J. Henry, A. Hingorani, A. Hofman, A. Holt, P.G. Hui, J. Hunter, M.L. Imboden, M. Smith, A.V. Jameson, K. Kerr, S.M. Kolcic, I. Kronenberg, F. Marchini, J. McKeever, T. Morris, A.D. Olin, A.-C. Porteous, D.J. Postma, D.S. Huffman, J.E. Rich, S.S. Ring, S.M. Rivadeneira Ramirez, F. Rochat, T. Sayer, A.A. Sayers, I. Sly, P.D. Sood, A. Starr, J.M. Uitterlinden, A.G. |
2011-11-01
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Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk
(Article)
Ehret, G.B. Munroe, P. Pihur, V. Hopewell, J. Ongen, H. Dreisbach, A.W. Li, Y. Hunter Young, J. Bis, J.C. Kähönen, M. Viikari, J. Lee, N.R. Chen, M-H. Vollenweider, P. Olden, M. Pattaro, C. Hoffman Bolton, J.A. Köttgen, A. Bergmann, S. Mooser, V. Chaturvedi, N. Frayling, T.M. Islam, M. Jafar, T.H. O'Reilly, P.F. Erdmann, J. Kulkarni, S.R. Bornstein, S.R. Gräßler, J. Groop, L. Voight, B.F. Kettunen, J. Howard, P. Taylor, A. Guarrera, S. Amin, N. Ricceri, F. Emilsson, V. Plump, A.S. Khaw, K-T. Weder, A.B. Hunt, S.C. Sun, Y.V. Bergman, R.N. Collins, F.S. Bonnycastle, L.L. Bragg-Gresham, J.L. Scott, L.J. Stringham, H.M. Peltonen, L. Perola, M. Vartiainen, E. Brand, S.-M. Staessen, J.A. Wang, Y.A. Burton, P.R. Soler Artigas, M. Teumer, A. Dong, Y. Snieder, H. Zhu, H. Lohman, K. Rudock, M.E. Heckbert, S.R. Wiggins, K.L. Doumatey, A. Shriner, D. Veldre, G. Glazer, N.L. Viigimaa, M. Kinra, S. Prabhakaran, D. Tripathy, V. Langefeld, C.D. Rosengren, A. Thelle, D.S. Maria Corsi, A. Singleton, A. Forrester, T. Launer, L.J. Hilton, G. McKenzie, C.A. Salako, T. Iwai, N. Kita, Y. Ogihara, T. Ohkubo, T. Okamura, T. Ueshima, H. Umemura, S. Hua Zhao, J. Eyheramendy, S. Meitinger, T. Wichmann, H.E. Shin Cho, Y. Kim, H.-L. Sehmi, J.S. Hedblad, B. Nilsson, P. Davey-Smith, G. Wong, A. Aulchenko, Y.S. Narisu, N. Stancáková, A. Raffel, L.J. Yao, J. Kathiresan, S. O'Donnell, C.J. Schwartz, S.M. Arfan Ikram, M. Longstreth Jr, W.T. Mosley, T.H. Rice, K.M. Heath, S.C. Seshadri, S. Shrine, N.R.G. Wain, L.V. Morken, M.A. Swift, A.J. Laitinen, J. Prokopenko, I. Zitting, P. Humphries, S.E. Danesh, J. Sõber, S. Rasheed, A. Goel, A. Hamsten, A. Watkins, H. Gilst, W.H. van Janipalli, C.S. Radha Mani, K. Yajnik, C. Hofman, A. Mattace-Raso, F.U.S. Parsa, A. Oostra, B.A. Demirkan, A. Isaacs, A. Rivadeneira Ramirez, F. Lakatta, E. Orrù, M. Scuteri, A. Ala-Korpela, M. Kangas, A.J. Lyytikäinen, L.-P. Luan, J. Soininen, P. Tukiainen, T. Würtz, P. Twee-Hee Ong, R. Dörr, M. Kroemer, H.K. Völker, U. Völzke, H. Galan, P. Hercberg, S. Arora, P. Lathrop, G.M. Zelenika, D. Deloukas, P. Mangino, M. Spector, T.D. Zhai, G. Meschia, J.F. Nalls, M.A. Sharma, P. Terzic, J. Dehghan, A. Kranthi Kumar, M.V. Denniff, M. Zukowska-Szczechowska, E. Wagenknecht, L.E. Gerald R. Fowkes, F. Charchar, F.J. Schwarz, P.E.H. Hayward, C. Guo, X. Rotimi, C. Zhang, F. Bots, M.L. Samani, N.J. Polasek, O. Talmud, P.J. Nyberg, F. Kuh, D. Laan, M. Hveem, K. Schouw, Y.T. van der Casas, J.P. Lucas, G. Mohlke, K.L. Vineis, P. Raitakari, O. Ganesh, S.K. Shyong Tai, E. Laakso, M. Rao, D.C. Harris, T.B. Morris, R.W. Dominiczak, A. Hicks, A.A. Kivimaki, M. Marmot, M. Miki, T. Saleheen, D. Chandak, G.R. Coresh, J. Navis, G. Salomaa, V. Han, B.-G. Kooner, J.S. Jackson, A.U. Melander, O. Ridker, P.M. Bandinelli, S. Gyllensten, U. Wright, A.F. Wilson, J.F. Ferrucci, L. Farrall, M. Tuomilehto, J. Pramstaller, P.P. Bochud, M. Peden, J. Elosua, R. Soranzo, N. Sijbrands, E.J.G. Altshuler, D. Loos, R.J.F. Shuldiner, A.R. Gieger, C. Meneton, P. Uitterlinden, A.G. Wareham, N.J. Tanaka, T. Gudnason, V. Rotter, J.I. Rettig, R. Uda, M. Strachan, D.P. Witteman, J.C.M. Hartikainen, A.L. Beckmann, J.S. Boerwinkle, E. Vasan, R.S. Wild, S.H. Boehnke, M. Larson, M.G. Järvelin, M.R. Psaty, B.M. Elliott, P. Tikka-Kleemola, P. Newton-Cheh, C. Levy, D. Caulfield, M. Abecasis, G.R. Rudan, I. Adair, L.S. Bakker, S.J.L. Barroso, I. Igl, W. Milaneschi, Y. Parker, A.N. Fava, C. Chambers, J.C. Fox, E.R. Johnson, A.D. Kumari, M. Jin Go, M. Harst, P. van der Hong Linda Kao, W. Sjögren, M. Vinay, D.G. Alexander, M. Tabara, Y. Shaw-Hawkins, S. Whincup, P.H. Chasman, D.I. Liu, Y. Shi, G. Kuusisto, J. Tayo, B. Seielstad, M. Sim, X. Hoang Nguyen, K.-D. Lehtimäki, T. Matullo, G. Wu, Y. Smith, A.V. Gaunt, T.R. Charlotte Onland-Moret, N. Cooper, M.N. Platou, C. Org, E. Hardy, R. Dahgam, S. Palmen, J. Vitart, V. Braund, P.S. Tobin, M.D. Kuznetsova, T. Uiterwaal, C.S.P.M. Adeyemo, A. Palmas, W. Campbell, H. Ludwig, B. Tomaszewski, M. Tzoulaki, I. Palmer, N.D. Aspelund, T. Verwoert, G.C. Garcia, M. Chang, Y.-P.C. O´Connell, J.R. Steinle, N.I. Grobbee, D.E. Arking, D.E. Kardia, S.L. Morrison, A.C. Hernandez, D.G. Najjar, S.S. Hwang, S.J. McArdle, W.L. Hadley, D. Brown, M.J. Connell, J. Hingorani, A. Day, I.N.M. Lawlor, D.A. Beilby, J.P. Lawrence, R.W. Clarke, R. |
2011-10-06
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A large genome scan for rare CNVs in amyotrophic lateral sclerosis
(Article)
Blauw, H.M. Al-Chalabi, A. Slot, R.V. Strengman, E. Estrada Gil, J.K. Rivadeneira Ramirez, F. Hofman, A. Uitterlinden, A.G. Kiemeney, L.A.L.M. Vermeulen, S.H.H.M. Birve, A. Waibel, S. Andersen, P.M. Meyer, T. Cronin, S. Mclaughlin, R.L. Hardiman, O. Sapp, P.C. Tobin, M.D. Wain, L.V. Tomik, B. Slowik, A. Lemmens, R. Vught, P.W. van Rujescu, D. Schulte, C. Gasser, T. Brown Jr, R.H. Landers, J.E. Robberecht, W. Ludolph, A.C. Ophoff, R.A. Veldink, J.H. Berg, L.H. van den Diekstra, F.P. Es, M.A. van Saris, C.G. Groen, E.J. Rheenen, W. van Koppers, M. |
2010-08-04
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