Large-scale, family-based, candidate gene association study of type 2 diabetes mellitus and abdominal obesity by Hirschhorn, J, Altshuler, D, Lindgren, C, Lane, C, Nemesh, J, Bolk, S, Sklar, P, Groop, L, Lander, E

Human genome sequence variation and the influence of gene history, mutation and recombination. by Reich, D, Schaffner, S, Daly, M, McVean, G, Mullikin, J, Higgins, J, Richter, D, Lander, E, Altshuler, D

Association Study of Lipoprotein (a) Genetic Markers, Traditional Risk Factors and Coronary Heart Disease in HIV-1-infected Patients by Lander eEgaña-Gorroño, Esteban eMartinez, Tuixent eEscribà, Marta eCalvo, Jose eGatell, Mireia eArnedo

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Detecting novel associations in large data sets. by Reshef, D, Reshef, Y, Finucane, H, Grossman, SR, McVean, G, Turnbaugh, P, Lander, E, Mitzenmacher, M, Sabeti, P

Application of high-throughout SNP genotyping to complex endocrine diseases. by Hirschorn, J, Altshuler, D, Sklar, P, Bolk, S, Lindblad, K, Lindgren, C, Lim, Y, Lane, C, Nemesh, J, Groop, L, Lander, E

Large-scale candidate gene association studies of type 2 diabetes. by Hirschhom, J, Altshuler, D, Lindgren, C, Klannemark, M, Daly, M, Vohl, M, Nemesh, J, Lane, C, Bolk, S, Hudson, T, Groop, L, Lander, E

Linkage disequilibrium at PPARG and other genes assessed with dense sets of SNPs.. by Hirschhorn, J, Altshuler, D, Daly, M, Lindgren, C, Burtt, N, Loomer, M, Villapakkam, A, Bolk, S, O'Donnell, C, Crews, J, Groop, L, Lander, E

A high-resolution linkage-disequilibrium map of the human major histocompatibility complex and first generation of tag single-nucleotide polymorphisms. by Miretti, M, Walsh, E, Ke, X, Delgado, M, Griffiths, M, Hunt, S, Morrison, J, Whittaker, P, Lander, E, Cardon, L, Bentley, DR, Rioux, J, Beck, S, Deloukas, P

Genomewide linkage analysis of stature in multiple populations reveals several regions with evidence of linkage to adult height. by Hirschhorn, J, Lindgren, C, Daly, M, Kirby, A, Schaffner, S, Burtt, N, Altshuler, D, Parker, A, Rioux, J, Platko, J, Gaudet, D, Hudson, T, Groop, L, Lander, E

Deuterostome phylogeny reveals monophyletic chordates and the new phylum Xenoturbellida. by Bourlat, S, Juliusdottir, T, Lowe, C, Freeman, R, Aronowicz, J, Kirschner, M, Lander, E, Thorndyke, M, Nakano, H, Kohn, AB, Heyland, A, Moroz, L, Copley, R, Telford, M

The common PPARgamma Pro12Ala polymorphism is associated with decreased risk of type 2 diabetes. by Altshuler, D, Hirschhorn, J, Klannemark, M, Lindgren, C, Vohl, M, Nemesh, J, Lane, C, Schaffner, S, Bolk, S, Brewer, C, Tuomi, T, Gaudet, D, Hudson, T, Daly, M, Groop, L, Lander, E

Gene expression profiling in skeletal muscle of subjects with different glycaemic tolerance. by Lindgren, C, Lehar, J, Hirschhorn, J, Vaag, A, Poulssen, P, Eriksson, K, Gaasenbeek, M, Ladd, C, Tamayo, P, Daly, M, Ridderstrale, M, Beck-Nielsen, H, Lander, E, Altshuler, D, Groop, L

Genomewide search for type 2 diabetes mellitus susceptibility loci in Finnish families: the Botnia study. by Lindgren, C, Mahtani, M, Widén, E, McCarthy, M, Daly, M, Kirby, A, Reeve, M, Kruglyak, L, Parker, A, Meyer, J, Almgren, P, Lehto, M, Kanninen, T, Tuomi, T, Groop, L, Lander, E

Two loci on chromosomes 2 and X for premature coronary heart disease identified in early- and late-settlement populations of Finland. by Pajukanta, P, Cargill, M, Viitanen, L, Nuotio, I, Kareinen, A, Perola, M, Terwilliger, J, Kempas, E, Daly, M, Lilja, H, Rioux, J, Brettin, T, Viikari, J, Rönnemaa, T, Laakso, M, Lander, E, Peltonen, L

Detecting recent positive selection in the human genome from haplotype structure. by Sabeti, P, Reich, D, Higgins, J, Levine, H, Richter, D, Schaffner, S, Gabriel, S, Platko, J, Patterson, N, McDonald, G, Ackerman, H, Campbell, S, Altshuler, D, Cooper, R, Kwiatkowski, D, Ward, R, Lander, E

Identifying recent adaptations in large-scale genomic data. by Grossman, SR, Andersen, K, Shlyakhter, I, Tabrizi, S, Winnicki, S, Yen, A, Park, D, Griesemer, D, Karlsson, E, Wong, S, Cabili, M, Adegbola, R, Bamezai, R, Hill, A, Vannberg, F, Rinn, J, Lander, E, Schaffner, S, Sabeti, P

PGC-1alpha-responsive genes involved in oxidative phosphorylation are coordinately downregulated in human diabetes. by Mootha, V, Lindgren, C, Eriksson, K, Subramanian, A, Sihag, S, Lehar, J, Puigserver, P, Carlsson, E, Ridderstråle, M, Laurila, E, Houstis, N, Daly, M, Patterson, N, Mesirov, J, Golub, T, Tamayo, P, Spiegelman, B, Lander, E, Hirschhorn, J, Altshuler, D, Groop, L

New models of collaboration in genome-wide association studies: the Genetic Association Information Network. by Manolio, T, Rodriguez, L, Brooks, L, Abecasis, G, Ballinger, D, Daly, M, Donnelly, P, Faraone, S, Frazer, K, Gabriel, S, Gejman, P, Guttmacher, A, Harris, E, Insel, T, Kelsoe, JR, Lander, E, McCowin, N, Mailman, MD, Nabel, E, Ostell, J, Pugh, E, Sherry, S, Sullivan, P, Thompson, J, Warram, J

Genome-wide detection and characterization of positive selection in human populations. by Sabeti, P, Varilly, P, Fry, B, Lohmueller, J, Hostetter, E, Cotsapas, C, Xie, X, Byrne, E, McCarroll, SA, Gaudet, R, Schaffner, S, Lander, E, Frazer, K, Ballinger, D, Cox, DR, Hinds, D, Stuve, L, Gibbs, R, Belmont, J, Boudreau, A, Hardenbol, P, Leal, S, Pasternak, S, Wheeler, D, Willis, T

Initial sequencing and analysis of the human genome. by Lander, E, Linton, L, Birren, B, Nusbaum, C, Zody, M, Baldwin, J, Devon, K, Dewar, K, Doyle, M, FitzHugh, W, Funke, R, Gage, D, Harris, K, Heaford, A, Howland, J, Kann, L, Lehoczky, J, LeVine, R, McEwan, P, McKernan, K, Meldrim, J, Mesirov, J, Miranda, C, Morris, W, Naylor, J