Dissociation between saliency signals and activity in early visual cortex von Betz, Torsten, Wilming, Niklas, Bogler, Carsten, Haynes, John-Dylan, König, Peter

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P-10 Flexible sensorimotor linkage during decision-making in changing environments von Hagena, K., van den Brink, R.L., Wilming, N., Murphy, P.R., Büchel, C., Donner, T.H.

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FV 3 Large-scale informational connectivity tracks flexible sensory-motor mapping rules in the human brain von van den Brink, R., Hagena, K., Wilming, N., Murphy, P., Büchel, C., Donner, T.

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P-106 Spontaneous pupil fluctuations differentiate progressive supranuclear palsy patients from healthy controls von Hagena, K., Meyke, M., Zeitschel, M., Wilming, N., Engel, A.K., Gerloff, C., Moll, C., Donner, T., Gulberti, A., Pötter-Nerger, M.

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Learning and Adaptation of Sensorimotor Contingencies: Prism-Adaptation, a Case Study von Kootstra, Gert, Wilming, Niklas, Schmidt, Nico M., Djurfeldt, Mikael, Kragic, Danica, König, Peter

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Mouse Genome Database (MGD) 2019 von Bult, Carol J, Blake, Judith A, Smith, Cynthia L, Kadin, James A, Richardson, Joel E

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Genetic analysis of completely sequenced disease-associated MHC haplotypes identifies shuffling of segments in recent human history von Traherne, James A, Horton, Roger, Roberts, Anne N, Miretti, Marcos M, Hurles, Matthew E, Stewart, C Andrew, Ashurst, Jennifer L, Atrazhev, Alexey M, Coggill, Penny, Palmer, Sophie, Almeida, Jeff, Sims, Sarah, Wilming, Laurens G, Rogers, Jane, de Jong, Pieter J, Carrington, Mary, Elliott, John F, Sawcer, Stephen, Todd, John A, Trowsdale, John, Beck, Stephan

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Complete MHC haplotype sequencing for common disease gene mapping von Stewart, C Andrew, Horton, Roger, Allcock, Richard J N, Ashurst, Jennifer L, Atrazhev, Alexey M, Coggill, Penny, Dunham, Ian, Forbes, Simon, Halls, Karen, Howson, Joanna M M, Humphray, Sean J, Hunt, Sarah, Mungall, Andrew J, Osoegawa, Kazutoyo, Palmer, Sophie, Roberts, Anne N, Rogers, Jane, Sims, Sarah, Wang, Yu, Wilming, Laurens G, Elliott, John F, de Jong, Pieter J, Sawcer, Stephen, Todd, John A, Trowsdale, John, Beck, Stephan

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Mouse Genome Database (MGD)-2017: community knowledge resource for the laboratory mouse von Blake, Judith A, Eppig, Janan T, Kadin, James A, Richardson, Joel E, Smith, Cynthia L, Bult, Carol J

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Analysis of the mouse transcriptome based on functional annotation of 60,770 full-length cDNAs von Okazaki, Y, Furuno, M, Kasukawa, T, Adachi, J, Bono, H, Kondo, S, Nikaido, I, Osato, N, Saito, R, Suzuki, H, Yamanaka, I, Kiyosawa, H, Yagi, K, Tomaru, Y, Hasegawa, Y, Nogami, A, Schönbach, C, Gojobori, T, Baldarelli, R, Hill, D P, Bult, C, Hume, D A, Quackenbush, J, Schriml, L M, Kanapin, A, Matsuda, H, Batalov, S, Beisel, K W, Blake, J A, Bradt, D, Brusic, V, Chothia, C, Corbani, L E, Cousins, S, Dalla, E, Dragani, T A, Fletcher, C F, Forrest, A, Frazer, K S, Gaasterland, T, Gariboldi, M, Gissi, C, Godzik, A, Gough, J, Grimmond, S, Gustincich, S, Hirokawa, N, Jackson, I J, Jarvis, E D, Kanai, A, Kawaji, H, Kawasawa, Y, Kedzierski, R M, King, B L, Konagaya, A, Kurochkin, I V, Lee, Y, Lenhard, B, Lyons, P A, Maglott, D R, Maltais, L, Marchionni, L, McKenzie, L, Miki, H, Nagashima, T, Numata, K, Okido, T, Pavan, W J, Pertea, G, Pesole, G, Petrovsky, N, Pillai, R, Pontius, J U, Qi, D, Ramachandran, S, Ravasi, T, Reed, J C, Reed, D J, Reid, J, Ring, B Z, Ringwald, M, Sandelin, A, Schneider, C, Semple, C A M, Setou, M, Shimada, K, Sultana, R, Takenaka, Y, Taylor, M S, Teasdale, R D, Tomita, M, Verardo, R, Wagner, L, Wahlestedt, C, Wang, Y, Watanabe, Y, Wells, C, Wilming, L G, Wynshaw-Boris, A, Yanagisawa, M

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Mouse Genome Informatics: an integrated knowledgebase system for the laboratory mouse von Baldarelli, Richard M, Smith, Cynthia L, Ringwald, Martin, Richardson, Joel E, Bult, Carol J

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Variation analysis and gene annotation of eight MHC haplotypes: The MHC Haplotype Project von Horton, Roger, Gibson, Richard, Coggill, Penny, Miretti, Marcos, Allcock, Richard J, Almeida, Jeff, Forbes, Simon, Gilbert, James G. R, Halls, Karen, Harrow, Jennifer L, Hart, Elizabeth, Howe, Kevin, Jackson, David K, Palmer, Sophie, Roberts, Anne N, Sims, Sarah, Stewart, C. Andrew, Traherne, James A, Trevanion, Steve, Wilming, Laurens, Rogers, Jane, de Jong, Pieter J, Elliott, John F, Sawcer, Stephen, Todd, John A, Trowsdale, John, Beck, Stephan

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By-passing fluctuation theorems with a catalyst von Boes, P., Gallego, R., Ng, N. H. Y., Eisert, J., Wilming, H.

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Functional annotation of a full-length mouse cDNA collection von Sakamoto, N, Batalov, S, Izawa, M, Kohtsuki, S, Sato, K, Schönbach, C, Kasukawa, T, Shibata, K, Okido, T, Baldarelli, R, Matsuda, H, Matsuo, Y, Itoh, M, Gissi, C, Saito, R, Hume, D. A, Arakawa, T, Gojobori, T, Kochiwa, H, Boffelli, D, Kawaji, H, Aizawa, K, Storch, K.-F, Fukuda, S, Ring, B, Kadota, K, Rodriguez, I, Wynshaw-Boris, A, Saito, T, Kuehl, P, Wagner, L, Fukunishi, Y, Brownstein, M. J, Washio, T, Okazaki, Y, Fleischmann, W, Ringwald, M, Mazzarelli, J, Mombaerts, P, Sasaki, H, Schriml, L. M, Suzuki, H, Bult, C, King, B, Kondo, S, Carninci, P, Wilming, L, Weitz, C, Lee, N. H, Seya, T, Nishi, K, Pesole, G, Furuno, M, Nikaido, I, Toyo-oka, K, Hayashizaki, Y, Quackenbush, J, Wang, K. H, Bono, H, Hasegawa, Y, Barsh, G, Gariboldi, M, Gustincich, S, Adachi, J, Ishii, Y, Mashima, J, Hofmann, M, Ashburner, M, Shibata, Y, Yoshida, K, Lyons, P, Lewis, S, Shinagawa, A, Hill, D, Kawai, J, Tomita, M, Marchionni, L, Kiyosawa, H, Staubli, F, Suzuki, R, Bojunga, N, Nordone, P, Fletcher, C, Whittaker, C, Yoshino, M, Konno, H, Sakai, K, de Bonaldo, M. F, Hara, A, Casavant, T, Aono, H, Fujita, M, Yamanaka, I, Blake, J, Gaasterland, T, Kamiya, M

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A novel member of the transmembrane serine/threonine kinase receptor family is specifically expressed in the gonads and in mesenchymal cells adjacent to the mullerian duct von BAARENDS, W. M, VAN HELMOND, M. J. L, THEMMEN, A. P. N, GROOTEGOED, J, POST, M, VAN DER SCHOOT, P. J. C. M, HOOGERBRUGGE, J. W, DE WINTER, J. P, UILENBROEK, J. T. J, KARELS, B, WILMING, L. G, MEIJERS, J. H. C

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The DNA sequence and biological annotation of human chromosome 1 von Martin, S, Pelan, S, Chapman, J. C, Cobley, V, Grocock, R, Kaul, R, Hunt, S. E, Sims, S, Mistry, S, Bye, J, Frankish, A, Peck, A. I, Pearce, A. V, White, S, Hall, R. E, Burton, J, Frankland, J, Ambrose, K. D, Hunter, G, Van Helmond, Z, Errington, H, Mashreghi-Mohammadi, M, McLaren, S, Deadman, R, Kimberley, A. M, Holmes, S, Jones, M. C, French, L, Garnett, J, Phillimore, B. J, Ross, M. T, Sehra, H. K, Hubbard, T, Brown, A. J, Ainscough, R, Parker, A, McLay, K. E, O'Dell, C. N, Williams, H, Durbin, R, Isherwood, J, Plumb, R, Andrews, T. D, Dunn, M, Earthrowl, M, Glithero, R. J, Ghori, M. R. J, Subramanian, S, Babbage, A. K, Atkinson, A, Harrow, J, Gilby, L. M, Skuce, C. D, Lawlor, S, Howden, P. J, Bray-Allen, S, Zhou, Y, Rouse, G, Matthews, L, Lovell, J, Gillett, W, Bailey, J, Sycamore, N, Wallis, J. M, Griffiths-Jones, S, James, R, Almeida, J. P, Kershaw, J. K, Loveland, J, Carter, N. P, Swarbreck, D, Wooster, R, Rogers, J, McVean, G, Joy, A, Kibukawa, M, M oore, M. J. F, Grafham, D. V, Beck, S, Ashwell, R. I. S, Lush, M. J, Shownkeen, R, Corby, N, Harrison, E. S. I, King, A, Bird, C. P, Lyne, R, Anderson, F, Phillips, K, Scott, C. E, Woodfine, K, Bethel, G, Coville, G. J, Aubin, K, Howe, K. L, Buckley, D, Ellington, A. G, Barlow, K. F, Raymond, C, Lloyd, C

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The DNA sequence of human chromosome 22 von Bruskiewich, R, Bailey, J, Bates, K. N, Beasley, O, Blakey, S, Buck, D, Burgess, J, Burton, J, Clark, G, Cobley, V, Collier, R. E, Davis, J, Dockree, C, Durbin, R. M, Fey, J. M, Garner, A. A, Goward, M. E, Grafham, D, Griffiths, M. N, Hall, C, Hall, R, Heathcott, R. W, Ho, S, Hunt, S. E, Jones, M. C, Laird, G. K, Leversha, M. A, McCann, O. T, McClay, J, Milne, S. A, Mortimore, B. J, Pavitt, R, Pearce, A. V, Pearson, D, Phillimore, B. J, Ramsey, Y, Rogers, L, Ross, M. T, Skuce, C. D, Smalley, S, Steward, C. A, Swann, R. M, Vaudin, M, Wallis, J. M, Whiteley, M. N, Willey, D, Williams, S, Wilmer, T. E, Wilming, L, Wright, C. L, Bentley, D. R, Rogers, J, Minoshima, S, Kawasaki, K, Asakawa, S, Kudoh, J, Shintani, A, Shibuya, K, Yoshizaki, Y, Mitsuyama, S, Do, A, Do, T, Dorman, A, Fang, F, Kenton, S, Lewis, J, Lin, S.-P, Loh, P, Phan, S, Ray, L, Ren, Q, Sloan, D, Song, L, White, J, Wu, H, Yao, Z, Zhan, M, Chissoe, S, Murray, J, Minx, P, Fulton, R, Johnson, D, Bentley, D, Bradshaw, H, Bourne, S, Du, Z, Kemp, K, Latreille, P, Scheet, P, Wohldmann, P, Korf, I, Mardis, E, Wilson, R, Emanuel, B. S, Johnson, A, Kedra, D, Fransson, I, Tapia, I, Bruder, C. E, O'Brien, K. P

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The DNA sequence and analysis of human chromosome 6 von Mungall, A. J, Beck, S, Palmer, S. A, Edwards, C. A, Jones, M. C, Horton, R, Scott, C. E, Clamp, M. E, Milne, S, Almeida, J. P, Babbage, A. K, Bagguley, C. L, Bailey, J, Banerjee, R, Barker, D. J, Barlow, K. F, Beasley, H, Beasley, O, Bird, C. P, Blakey, S, Bray-Allen, S, Brown, A. J, Brown, J. Y, Burton, J, Chapman, J. C, Clark, S. Y, Clark, G, Clee, C. M, Clegg, S, Collier, R. E, Collins, J. E, Corby, N. R, Coville, G. J, Earthrowl, M. E, Ellington, A. E, Evans, K. A, Francis, M. D, Garner, P, Garnett, J, Gillson, C. J, Grafham, D. V, Grant, M, Gribble, S, Griffiths, C, Hall, R, Halls, K. S, Heathcott, R, Howden, P. J, Howell, G. R, Huckle, E, Humphray, S. J, Humphries, M. D, Hunt, A. R, Johnson, C. M, Joy, A. A, Kay, M, Kimberley, A. M, Laird, G. K, Lawlor, S, Leongamornlert, D. A, Lloyd, C. R, Lovell, J, Mashreghi-Mohammadi, M, Maslen, G. L, McCann, O. T, McLaren, S. J, McLay, K, McMurray, A, Novik, K. L, Overton-Larty, E. K, Parker, A, Patel, R, Phillimore, B, Phillips, S, Plumb, R. W, Ranby, S. A, Rice, C. M, Sheridan, E, Skuce, C. D, Smith, S, Spraggon, L, Squares, S. L, Tamlyn-Hall, G, Tester, J, Thorpe, A, Tromans, A, Wallis, J. M, West, A. P, White, S. S, Whitehead, S. L, Whittaker, H, Wild, A, Wilmer, T. E, Wood, J. M, Wray, P. W, Younger, R. M, Coulson, A, Hubbard, T, Sulston, J. E, Rogers, J

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The DNA sequence and biological annotation of human chromosome 1 von Gregory, S. G, Swarbreck, D, Howe, K. L, Woodfine, K, Spencer, C. C. A, Searle, S, Zhou, Y, Kokocinski, F, McDonald, L, Evans, R, Phillips, K, Atkinson, A, Jones, C, Andrews, T. D, Lloyd, C, Ainscough, R, Almeida, J. P, Ambrose, K. D, Anderson, F, Andrew, R. W, Ashwell, R. I. S, Aubin, K, Bagguley, C. L, Bailey, J, Banerjee, R, Beasley, H, Bethel, G, Bray-Allen, S, Brown, A. J, Bryant, S. P, Buckley, D, Burford, D. C, Burrill, W. D. H, Bye, J, Carder, C, Chapman, J. C, Clark, S. Y, Collier, R. E, Corby, N, Coville, G. J, Dhami, P, Dovey, O, Ellington, A. G, Frankish, A, Gay, L, Ghori, M. R. J, Gilby, L. M, Gillett, W, Grocock, R, Hammond, S, Harrison, E. S. I, Holmes, S, Holt, K, Howden, P. J, Hunt, A. R, Hunt, S. E, Hunter, G, James, R, Johnson, C, Johnson, D, Kershaw, J. K, Kibukawa, M, Laird, G, Lawlor, S, Lovell, J, Lush, M. J, Mashreghi-Mohammadi, M, Milne, S, Mistry, S, oore, M. J. F. M, Nickerson, T, Palmeiri, A, Parker, A, Pearce, A. V, Pelan, S, Phelps, K, Phillimore, B. J, Porter, K. M, Rajan, J, Raymond, C, Rouse, G, Saenphimmachak, C, Shownkeen, R, Sims, S, Skuce, C. D, Smith, M, Sycamore, N, Tracey, A, Van Helmond, Z, White, S, Wilming, L, Wray, P. W, Wu, Z, Sulston, J. E, Hubbard, T, Carter, N. P, McVean, G, Harrow, J, Beck, S, Bentley, D. R

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Genetic analysis of completely sequenced disease-associated MHC haplotypes identifies shuffling of segments in recent human history von James A Traherne, Roger Horton, Anne N Roberts, Marcos M Miretti, Matthew E Hurles, C Andrew Stewart, Jennifer L Ashurst, Alexey M Atrazhev, Penny Coggill, Sophie Palmer, Jeff Almeida, Sarah Sims, Laurens G Wilming, Jane Rogers, Pieter J de Jong, Mary Carrington, John F Elliott, Stephen Sawcer, John A Todd, John Trowsdale, Stephan Beck

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