A hybrid micro-macroevolutionary approach to gene tree reconstruction von Durand, Dannie, Halldórsson, Bjarni V, Vernot, Benjamin

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Large-scale integration of the plasma proteome with genetics and disease von Ferkingstad, Egil, Sulem, Patrick, Atlason, Bjarni A., Sveinbjornsson, Gardar, Magnusson, Magnus I., Styrmisdottir, Edda L., Gunnarsdottir, Kristbjorg, Helgason, Agnar, Oddsson, Asmundur, Halldorsson, Bjarni V., Jensson, Brynjar O., Zink, Florian, Halldorsson, Gisli H., Masson, Gisli, Arnadottir, Gudny A., Katrinardottir, Hildigunnur, Juliusson, Kristinn, Magnusson, Magnus K., Magnusson, Olafur Th, Fridriksdottir, Run, Saevarsdottir, Saedis, Gudjonsson, Sigurjon A., Stacey, Simon N., Rognvaldsson, Solvi, Eiriksdottir, Thjodbjorg, Olafsdottir, Thorunn A., Steinthorsdottir, Valgerdur, Tragante, Vinicius, Ulfarsson, Magnus O., Stefansson, Hreinn, Jonsdottir, Ingileif, Holm, Hilma, Rafnar, Thorunn, Melsted, Pall, Saemundsdottir, Jona, Norddahl, Gudmundur L., Lund, Sigrun H., Gudbjartsson, Daniel F., Thorsteinsdottir, Unnur, Stefansson, Kari

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Approximation algorithms for the test cover problem von DE BONTRIDDER, K. M. J, HALLDORSSON, B. V, HALLDORSSON, M. M, HURKENS, C. A. J, LENSTRA, J. K, RAVI, R, STOUGIE, L

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An interior-point method for a class of saddle-point problems von HALLDORSSON, B. V, TÜTÜNÜ, R. H

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Local improvement algorithms for a path packing problem: A performance analysis based on linear programming von De Bontridder, K.M.J., Halldórsson, B.V., Halldórsson, M.M., Hurkens, C.A.J., Lenstra, J.K., Ravi, R., Stougie, L.

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Robustness of inference of haplotype block structure von Schwartz, Russell, Halldórsson, Bjarni V, Bafna, Vineet, Clark, Andrew G, Istrail, Sorin

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Impact of Genetics on Low Bone Mass in Adults von Sigurdsson, Gunnar, Halldorsson, Bjarni V, Styrkarsdottir, Unnur, Kristjansson, Kristleifur, Stefansson, Kari

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The Clark phaseable sample size problem: long-range phasing and loss of heterozygosity in GWAS von Halldórsson, Bjarni V, Aguiar, Derek, Tarpine, Ryan, Istrail, Sorin

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Variants in the LRP5 gene influence BMD both through common variants of small effect and rare mutations of large effect in osteoporotic families von Sigurdsson, G, Styrkarsdottir, U, Halldorsson, B.V, Stefansson, K

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Estrogen receptor genotypes and haplotypes associated with breast cancer risk von GOLD, Bert, KALUSH, Francis, HALLDORSSON, Bjarni V, WOODWORTH, Beth, WHITE, Thomas, CLARK, Andrew G, PARL, Fritz F, BRODER, Samuel, DEAN, Michael, OFFIT, Kenneth, BERGERON, Julie, SCOTT, Kevin, MITRA, Nandita, WILSON, Kelly, ELLIS, Nathan, HUANG, Helen, CHEN, Michael, LIPPERT, Ross

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Islands of Tractability for Parsimony Haplotyping von Sharan, R., Halldorsson, B.V., Istrail, S.

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Whole-Genome Shotgun Assembly and Comparison of Human Genome Assemblies von Istrail, Sorin, Sutton, Granger G., Florea, Liliana, Halpern, Aaron L., Mobarry, Clark M., Lippert, Ross, Walenz, Brian, Shatkay, Hagit, Dew, Ian, Miller, Jason R., Flanigan, Michael J., Edwards, Nathan J., Bolanos, Randall, Fasulo, Daniel, Halldorsson, Bjarni V., Hannenhalli, Sridhar, Turner, Russell, Yooseph, Shibu, Lu, Fu, Nusskern, Deborah R., Shue, Bixiong Chris, Zheng, Xiangqun Holly, Zhong, Fei, Delcher, Arthur L., Huson, Daniel H., Kravitz, Saul A., Mouchard, Laurent, Reinert, Knut, Remington, Karin A., Clark, Andrew G., Waterman, Michael S., Eichler, Evan E., Adams, Mark D., Hunkapiller, Michael W., Myers, Eugene W., Venter, J. Craig

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Optimal haplotype block-free selection of tagging SNPs for genome-wide association studies von Halldórsson, Bjarni V, Bafna, Vineet, Lippert, Ross, Schwartz, Russell, De La Vega, Francisco M, Clark, Andrew G, Istrail, Sorin

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Genome-wide association study identifies 74 loci associated with educational attainment von Rietveld, CA, Turley, P, Chen, G-B, Oskarsson, S, Hottenga, J-J, Jugessur, A, Kaakinen, MA, Kahonen, M, Kanoni, S, Keltigangas-Jarvinen, L, Kiemeney, LALM, Kraja, AT, Kroh, M, Kutalik, Z, Launer, LJ, Lebreton, MP, Loukola, A, Magi, R, Marioni, RE, Marques-Vidal, P, Meisinger, C, Meitinger, T, Milaneschi, Y, Milani, L, Montgomery, GW, Myhre, R, Nelson, CP, Paternoster, L, Raikkonen, K, Smith, BH, Smith, JA, Staessen, JA, Ahluwalia, TS, Tobin, MD, Van Rooij, FJA, Vinkhuyzen, AAE, Volzke, H, Vozzi, D, Attia, JR, Berger, K, Bertram, L, Bisgaard, H, Baumbach, C, Chabris, CF, Cusi, D, Dedoussis, GV, Van Duijn, CM, Gieger, C, Gratten, J, Hayward, C, Hinds, DA, Hoffmann, W, Iacono, WG, Jockel, K-H, Kaprio, J, Concas, MP, McGue, M, Pendleton, N, Derringer, J, Polasek, O, Schlessinger, D, Schmidt, R, Spector, TD, Thurik, AR, Timpson, NJ, Tung, JY, Uitterlinden, AG, Galesloot, TE, Wright, AF, Hofman, A, Laibson, DI, Yang, J, Koellinger, PD, Horikoshi, M, Kalafati, IP, Lahti, J, Van der Lee, SJ, De Leeuw, C, Lind, PA, Lindgren, K-O, Liu, T, Marten, J, Van der Most, PJ, Payton, A, Rueedi, R, Schmidt, B, St Pourcain, B, Teumer, A, Vuckovic, D, Westra, H-J, Zhao, W, Bakshi, A, Biino, G, Bonnelykke, K, Campbell, H, Demuth, I, Harris, TB, Heath, AC, Homuth, G, Horan, MA

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The linkage disequilibrium maps of three human chromosomes across four populations reflect their demographic history and a common underlying recombination pattern von De La Vega, Francisco M, Isaac, Hadar, Collins, Andrew, Scafe, Charles R, Halldórsson, Bjarni V, Su, Xiaoping, Lippert, Ross A, Wang, Yu, Laig-Webster, Marion, Koehler, Ryan T, Ziegle, Janet S, Wogan, Lewis T, Stevens, Junko F, Leinen, Kyle M, Olson, Sheri J, Guegler, Karl J, You, Xiaoqing, Xu, Lily H, Hemken, Heinz G, Kalush, Francis, Itakura, Mitsuo, Zheng, Yi, de Thé, Guy, O'Brien, Stephen J, Clark, Andrew G, Istrail, Sorin, Hunkapiller, Michael W, Spier, Eugene G, Gilbert, Dennis A

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Insights into the genetic architecture of osteoarthritis from stage 1 of the arcOGEN study von Panoutsopoulou, K, Southam, L, Wrayner, N, Zhai, G, Beazley, C, Thorleifsson, G, Arden, N K, Chapman, K, Deloukas, P, McCaskie, A, Ollier, W E R, Ralston, S H, Spector, T D, Valdes, A M, Wallis, G A, Arden, E, Battley, K, Blackburn, H, Blanco, F J, Bumpstead, S, Cupples, L A, Day-Williams, A G, Dixon, K, Doherty, S A, Esko, T, Evangelou, E, Felson, D, Gomez-Reino, J J, Gwilliam, R, Halldorsson, B V, Hauksson, V B, Ingvarsson, T, Jonsdottir, I, Jonsson, H, Keen, R, Kerkhof, H J M, Kloppenburg, M G, Koller, N, Lakenberg, N, Lane, N E, Metspalu, A, Meulenbelt, I, Nevitt, M C, Parimi, N, Potter, S C, Rego-Perez, I, Riancho, J A, Sherburn, K, Slagboom, P E, Stefansson, K, Styrkarsdottir, U, Sumillera, M, Swift, D, Thorsteinsdottir, U, Tsezou, A, Uitterlinden, A G, van Meurs, J B J, Watkins, B, Zmuda, J M, Zeggini, E, Loughlin, J, Ioannidis, John, Elliot, K S, Carr, A, Doherty, M, Wilkinson, J M, Gonzalez, A, Gordon, A, Hofman, A, Hunt, S E, Lee, A T, Wheeler, M, Mitchell, S, Zhu, Y, O'Neill, F

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Comparative Immunopeptidomics of Humans and Their Pathogens von Istrail, Sorin, Florea, Liliana, Halldórsson, Bjarni V., Kohlbacher, Oliver, Schwartz, Russell S., Yap, Von Bing, Yewdell, Jonathan W., Hoffman, Stephen L., Waterman, Michael S.

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Optimal Selection of SNP Markers for Disease Association Studies von Halldórsson, Bjarni V., Istrail, Sorin, De La Vega, Francisco M.

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A Survey of Computational Methods for Determining Haplotypes von Halldórsson, Bjarni V., Bafna, Vineet, Edwards, Nathan, Lippert, Ross, Yooseph, Shibu, Istrail, Sorin

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Invited: Algorithmic challenges in DNA sequencing and disease association von Halldorsson, B. V.

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