Showing 1 - 11 results of 11 for search 'Iotchkova, V', query time: 0.03s
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Bayesian methods for multivariate phenotype analysis in genome-wide association studies by Iotchkova, V
Published 2013Thesis -
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Network inference in matrix-variate Gaussian models with non-independent noise by Dahl, A, Hore, V, Iotchkova, V, Marchini, J
Published 2013Journal article -
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A multiple phenotype imputation method for genetic studies by Dahl, A, Iotchkova, V, Baud, A, Johansson, Å, Gyllensten, U, Soranzo, N, Mott, R, Kranis, A, Marchini, J
Published 2016Journal article -
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eFORGE: A Tool for Identifying Cell Type-Specific Signal in Epigenomic Data by Breeze, C, Paul, D, van Dongen, J, Butcher, L, Ambrose, J, Barrett, J, Lowe, R, Rakyan, V, Iotchkova, V, Frontini, M, Downes, K, Ouwehand, W, Laperle, J, Jacques, P, Bourque, G, Bergmann, A, Siebert, R, Vellenga, E, Saeed, S, Matarese, F, Martens, J, Stunnenberg, H, Teschendorff, A, Herrero, J, Birney, E, Dunham, I, Beck, S
Published 2016Journal article -
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Mechanisms of progression of myeloid preleukemia to transformed myeloid leukemia in children with Down syndrome by Labuhn, M, Perkins, K, Matzk, S, Varghese, L, Garnett, C, Papaemmanuil, E, Metzner, M, Kennedy, A, Amstislavskiy, V, Risch, T, Bhayadia, R, Samulowski, D, Hernandez, D, Stoilova, B, Iotchkova, V, Oppermann, U, Scheer, C, Yoshida, K, Schwarzer, A, Taub, J, Crispino, J, Weiss, M, Hayashi, A, Taga, T, Ito, E, Ogawa, S, Reinhardt, D, Yaspo, M, Campbell, P, Roberts, I, Constantinescu, S, Vyas, P, Heckl, D, Klusmann, J
Published 2019Journal article -
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Low-frequency variation in TP53 has large effects on head circumference and intracranial volume by Haworth, S, Shapland, CY, Hayward, C, Prins, BP, Felix, JF, Medina-Gomez, C, Rivadeneira, F, Wang, C, Ahluwalia, TS, Vrijheid, M, Guxens, M, Sunyer, J, Tachmazidou, I, Walter, K, Iotchkova, V, Jackson, A, Cleal, L, Huffmann, J, Min, JL, Sass, L, Timmers, PRHJ, Smith, G, Fisher, SE, Wilson, JF, Cole, TJ, Fernandez-Orth, D, Bønnelykke, K, Bisgaard, H, Pennell, CE, Jaddoe, VWV, Dedoussis, G, Timpson, N, Zeggini, E, Vitart, V, St Pourcain, B, UK10K consortium, Bhattacharya, S
Published 2019Journal article -
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Discovery and refinement of genetic loci associated with cardiometabolic risk using dense imputation maps by Iotchkova, V, Huang, J, Morris, J, Jain, D, Barbieri, C, Walter, K, Min, J, Chen, L, Astle, W, Cocca, M, Deelen, P, Elding, H, Farmaki, A, Franklin, C, Franberg, M, Gaunt, T, Hofman, A, Jiang, T, Kleber, M, Lachance, G, Luan, J, Malerba, G, Matchan, A, Mead, D, Memari, Y, Ntalla, I, Panoutsopoulou, K, Pazoki, R, Perry, J, Rivadeneira, F, Sabater-Lleal, M, Sennblad, B, Shin, S, Southam, L, Traglia, M, van Dijk, F, van Leeuwen, E, Zaza, G, Zhang, W, Amin, N, Butterworth, A, Chambers, J, Dedoussis, G, Dehghan, A, Franco, O, Franke, L, Frontini, M, Gambaro, G, Gasparini, P, Hamsten, A, Issacs, A, Kooner, J, Kooperberg, C, Langenberg, C, Marz, W, Scott, R, Swertz, M, Toniolo, D, Uitterlinden, A, van Duijn, C, Watkins, H, Zeggini, E, Maurano, M, Timpson, N, Reiner, A, Auer, P, Soranzo, N
Published 2016Journal article -
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Genetic Drivers of Epigenetic and Transcriptional Variation in Human Immune Cells by Chen, L, Ge, B, Casale, FP, Vasquez, L, Kwan, T, Garrido-Martín, D, Watt, S, Yan, Y, Kundu, K, Ecker, S, Datta, A, Richardson, D, Burden, F, Mead, D, Mann, AL, Fernandez, JM, Rowlston, S, Wilder, SP, Farrow, S, Shao, X, Lambourne, JJ, Redensek, A, Albers, CA, Amstislavskiy, V, Ashford, S, Berentsen, K, Bomba, L, Bourque, G, Bujold, D, Busche, S, Caron, M, Chen, S-H, Cheung, W, Delaneau, O, Dermitzakis, ET, Elding, H, Colgiu, I, Bagger, FO, Flicek, P, Habibi, E, Iotchkova, V, Janssen-Megens, E, Kim, B, Lehrach, H, Lowy, E, Mandoli, A, Matarese, F, Maurano, MT, Morris, JA, Pancaldi, V, Pourfarzad, F, Rehnstrom, K, Rendon, A, Risch, T, Sharifi, N, Simon, M-M, Sultan, M, Valencia, A, Walter, K, Wang, S-Y, Frontini, M, Antonarakis, SE, Clarke, L, Yaspo, M-L, Beck, S, Guigo, R, Rico, D, Martens, JHA, Ouwehand, WH, Kuijpers, TW, Paul, DS, Stunnenberg, HG, Stegle, O, Downes, K, Pastinen, T, Soranzo, N
Published 2016Journal article -
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The allelic landscape of human blood cell trait variation and links to common complex disease by Astle, WJ, Elding, H, Jiang, T, Allen, D, Ruklisa, D, Mann, AL, Mead, D, Bouman, H, Riveros-Mckay, F, Kostadima, MA, Lambourne, JJ, Sivapalaratnam, S, Downes, K, Kundu, K, Bomba, L, Berentsen, K, Bradley, JR, Daugherty, LC, Delaneau, O, Freson, K, Garner, SF, Grassi, L, Guerrero, J, Haimel, M, Janssen-Megens, EM, Kaan, A, Kamat, M, Kim, B, Mandoli, A, Marchini, J, Martens, JH, Meacham, S, Megy, K, O'Connell, J, Petersen, R, Sharifi, N, Sheard, SM, Staley, JR, Tuna, S, van der Ent, M, Walter, K, Wang, SY, Wheeler, E, Wilder, SP, Iotchkova, V, Moore, C, Sambrook, J, Stunnenberg, HG, Di Angelantonio, E, Kaptoge, S, Kuijpers, TW, Carrillo-de-Santa-Pau, E, Juan, D, Rico, D, Valencia, A, Chen, L, Ge, B, Vasquez, L, Kwan, T, Garrido-Martín, D, Watt, S, Yang, Y, Guigo, R, Beck, S, Paul, DS, Pastinen, T, Bujold, D, Bourque, G, Frontini, M, Danesh, J, Roberts, DJ, Ouwehand, WH, Butterworth, AS, Soranzo, N
Published 2016Journal article