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Affymetrix/Cold Spring Harbor Laboratory (2009). Post-transcriptional processing generates a diversity of 5[prime]-modified long and short RNAs Nature, 457:1028--1032.
Armour, JA (2009). Human genetics: Sharp focus on the variable genome Nature, 461:735--736.
Bikard, D, Patel, D, Le Mette, C, Giorgi, V, Camilleri, C, Bennett, MJ, and Loudet, O (2009). Divergent Evolution of Duplicate Genes Leads to Genetic Incompatibilities Within A. thaliana Science, 323:623--626.
Boerjan, W and Vuylsteke, M (2009). Integrative genetical genomics in Arabidopsis Nat Genet, 41:144--145.
Cahan, P, Li, Y, Izumi, M, and Graubert, TA (2009). The impact of copy number variation on local gene expression in mouse hematopoietic stem and progenitor cells Nat Genet, advanced online publication.
Charlesworth, B (2009). Fundamental concepts in genetics: Effective population size and patterns of molecular evolution and variation Nat Rev Genet, 10:195--205.
Conrad, DF, Pinto, D, Redon, R, Feuk, L, Gokcumen, O, Zhang, Y, Aerts, J, Andrews, TD, Barnes, C, Campbell, P, Fitzgerald, T, Hu, M, Ihm, CH, Kristiansson, K, MacArthur, DG, MacDonald, JR, Onyiah, I, Pang, AW, Robson, S, Stirrups, K, Valsesia, A, Walter, K, Wei, J, Tyler-Smith, C, Carter, NP, Lee, C, Scherer, SW, and Hurles, ME (2009). Origins and functional impact of copy number variation in the human genome Nature, advance online publication.
Coop, G, Pickrell, JK, Novembre, J, Kudaravalli, S, Li, J, Absher, D, Myers, RM, Cavalli-Sforza, LL, Feldman, MW, and Pritchard, JK (2009). The Role of Geography in Human Adaptation PLoS Genet, 5:e1000500.
Cordell, HJ (2009). Detecting gene-gene interactions that underlie human diseases Nat Rev Genet, 10:392--404.
Dean, MD and Nachman, MW (2009). Faster fertilization rate in conspecific versus heterospecific matings in house mice. Evolution, 63(1):20-8.
Duret, L (2009). Mutation Patterns in the Human Genome: More Variable Than Expected PLoS Biology, 7:e28 EP -.
Fu, J, Keurentjes, JJ, Bouwmeester, H, America, T, Verstappen, FW, Ward, JL, Beale, MH, de Vos, RC, Dijkstra, M, Scheltema, RA, Johannes, F, Koornneef, M, Vreugdenhil, D, Breitling, R, and Jansen, RC (2009). System-wide molecular evidence for phenotypic buffering in Arabidopsis Nat Genet, 41:166--167.
Gerke, J, Lorenz, K, and Cohen, B (2009). Genetic interactions between transcription factors cause natural variation in yeast. Science, 323(5913):498-501.
Gusev, A, Lowe, JK, Stoffel, M, Daly, MJ, Altshuler, D, Breslow, JL, Friedman, JM, and Pe'er, I (2009). Whole population, genome-wide mapping of hidden relatedness Genome Research, 19:318--326.
Henrichsen, CN, Vinckenbosch, N, Zollner, S, Chaignat, E, Pradervand, S, Schutz, F, Ruedi, M, Kaessmann, H, and Reymond, A (2009). Segmental copy number variation shapes tissue transcriptomes Nat Genet, advanced online publication.
Hodgkinson, A, Ladoukakis, E, and Eyre-Walker, A (2009). Cryptic Variation in the Human Mutation Rate PLoS Biology, 7:e27 EP -.
Irizarry, RA, Wu, H, and Feinberg, AP (2009). A species-generalized probabilistic model-based definition of CpG islands. Mamm Genome.
Lincoln, MR, Ramagopalan, SV, Chao, MJ, Herrera, BM, DeLuca, GC, Orton, S, Dyment, DA, Sadovnick, AD, and Ebers, GC (2009). Epistasis among HLA-DRB1, HLA-DQA1, and HLA-DQB1 loci determines multiple sclerosis susceptibility Proceedings of the National Academy of Sciences, 106:7542--7547.
Lister, R and Ecker, JR (2009). Finding the fifth base: Genome-wide sequencing of cytosine methylation Genome Research, 19:959--966.
Lister, R, Pelizzola, M, Dowen, RH, Hawkins, RD, Hon, G, Tonti-Filippini, J, Nery, JR, Lee, L, Ye, Z, Ngo, Q, Edsall, L, Antosiewicz-Bourget, J, Stewart, R, Ruotti, V, Millar, AH, Thomson, JA, Ren, B, and Ecker, JR (2009). Human DNA methylomes at base resolution show widespread epigenomic differences Nature, advance online publication.
Madsen, BE and Browning, SR (2009). A Groupwise Association Test for Rare Mutations Using a Weighted Sum Statistic PLoS Genet, 5:e1000384.
Malone, CD and Hannon, GJ (2009). Small RNAs as Guardians of the Genome Cell, 136:656--668.
Manenti, G, Galvan, A, Pettinicchio, A, Trincucci, G, Spada, E, Zolin, A, Milani, S, Gonzalez-Neira, A, and Dragani, TA (2009). Mouse Genome-Wide Association Mapping Needs Linkage Analysis to Avoid False-Positive Loci PLoS Genetics, 5:e1000331.
Neher, RA and Shraiman, BI (2009). Competition between recombination and epistasis can cause a transition from allele to genotype selection Proceedings of the National Academy of Sciences.
Pickrell, JK, Coop, G, Novembre, J, Kudaravalli, S, Li, JZ, Absher, D, Srinivasan, BS, Barsh, GS, Myers, RM, Feldman, MW, and Pritchard, JK (2009). Signals of recent positive selection in a worldwide sample of human populations Genome Research, 19:826--837.
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