Publications

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Asmussen, S. & Hobolth, A. (2012). Markov bridges, bisection and variance reduction. In L. Plaskota & H. Wozniakowski (Eds.), Monte Carlo and Quasi-Monte Carlo Methods 2010 (pp. 3-22). Springer. https://doi.org/10.1007/978-3-642-27440-4_1

Foldager, L., Steffensen, R. N., Thiel, S., Als, T. D., Nielsen, H. J., Nordentoft, M., Mortensen, P. B., Mors, O. & Jensenius, J. C. (2012). MBL and MASP-2 concentrations in serum and MBL2 promoter polymorphisms are associated to schizophrenia. Acta Neuropsychiatrica, 24(4), 199-207. https://doi.org/10.1111/j.1601-5215.2011.00618.x

Ehlers, B. K., Grøndahl, E., Ronfort, J. & Bataillon, T. (2012). "Ménage à trois": the presence/absence of thyme shapes the mutualistic interaction between the host plant Medicago truncatula (Fabaceae) and its symbiotic bacterium Sinorhizobium meliloti. Ecology and Evolution, 2(7), 1676-81. https://doi.org/10.1002/ece3.270

Alsner, J., Toustrup, K., Sørensen, B. S., Wiuf, C. H., Nordsmark, M. & Overgaard, J. (2012). Method for determining clinically relevant hypoxia in cancer. (Patent No. WO/2012/146259).

Saetre, P., Grove, J., Børglum, A., Mors, O., Werge, T. M., Andreassen, O. A., Vares, M., Agartz, I., Terenius, L. & Jönsson, E. G. (2012). Methylenetetrahydrofolate reductase (MTHFR) C677T polymorphism and age at onset of schizophrenia: no consistent evidence for an association in the Nordic population. American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 159B(8).

Kraft, J. F., Vestergaard, M., Schiøtt, B. & Thøgersen, L. (2012). Modeling the Self-assembly and Stability of DHPC Micelles using Atomic Resolution and Coarse Grained MD Simulations. Journal of Chemical Theory and Computation, 8(5), 1556–1569. https://doi.org/10.1021/ct200921u

Siuda, I. A. (2012). Modelling Protein Dynamics on the Microsecond Time Scale: Problems and Solutions. Aarhus University, Faculty of Science and Technology.

Agerbo, E., Mortensen, P. B., Wiuf, C., Pedersen, M. S., McGrath, J., Hollegaard, M. V., Nørgaard-Pedersen, B., Hougaard, D. M., Mors, O. & Pedersen, C. B. (2012). Modelling the contribution of family history and variation in single nucleotide polymorphisms to risk of schizophrenia: A Danish national birth cohort-based study. Schizophrenia Research, 134(2-3), 246-52. https://doi.org/10.1016/j.schres.2011.10.025

Tuni, C., Goodacre, S., Bechsgaard, J. S. & Bilde, T. (2012). Moderate multiple parentage and low genetic variation reduces the potential for genetic incompatibility avoidance despite high risk of inbreeding. PLoS One, 7(1), e29636. https://doi.org/10.1371/journal.pone.0029636

Thomsen, P. F., Kielgast, J., Iversen, L. L., Wiuf, C. H., Rasmussen, M., Gilbert, M. T. P., Orlando, L. A. A. & Willerslev, E. (2012). Monitoring endangered freshwater biodiversity using environmental DNA. Molecular Ecology, 21(11), 2565-2573. https://doi.org/10.1111/j.1365-294X.2011.05418.x

Abdallah, M., Larsen, N., Mortensen, E. L., Atladóttir, H. Ó., Nørgaard-Pedersen, B., Bonefeld-Jørgensen, E. C., Grove, J. & Hougaard, D. M. (2012). Neonatal levels of cytokines and risk of autism spectrum disorders: An exploratory register-based historic birth cohort study utilizing the Danish Newborn Screening Biobank. Journal of Neuroimmunology, 252, 75-82. https://doi.org/10.1016/j.jneuroim.2012.07.013

Mattila, T., Bechsgaard, J. S., Hansen, T., Schierup, M. H. & Bilde, T. (2012). Ortholog genes identified by transcriptome sequencing in the spider genus Stegodyphus. BMC Genomics, 13(70). https://doi.org/10.1186/1471-2164-13-70

Miller, W., Schuster, S. C., Welch, A. J., Ratan, A., Bedoya-Reina, O. C., Zhao, F., Kim, H. L., Burhans, R. C., Drautz, D. I., Wittekindt, N. E., Tomsho, L. P., Ibarra-Laclette, E., Herrera-Estrella, L., Peacock, E., Farley, S., Sage, G. K., Rode, K., Obbard, M., Montiel, R. ... Lindqvist, C. (2012). Polar and brown bear genomes reveal ancient admixture and demographic footprints of past climate change. Proceedings of the National Academy of Sciences (PNAS). https://doi.org/10.1073/pnas.1210506109

Sükösd, Z., Knudsen, B., Kjems, J. & Pedersen, C. N. S. (2012). PPfold 3.0: fast RNA secondary structure prediction using phylogeny and auxiliary data. Bioinformatics, 28(20), 2691-2692. https://doi.org/10.1093/bioinformatics/bts488

Kjeldsen, K. U., Bataillon, T., Pinel, N., De Mita, S., Lund, M. B., Panitz, F., Bendixen, C., Stahl, D. A. & Schramm, A. (2012). Purifying selection and molecular adaptation in the genome of Verminephrobacter, the heritable symbiotic bacteria of earthworms. Genome Biology and Evolution, 4(3), 307-315. https://doi.org/10.1093/gbe/evs014

Kong, A., Frigge, M. L., Masson, G., Besenbacher, S., Sulem, P., Magnusson, G., Gudjonsson, S. A., Sigurdsson, A., Jonasdottir, A., Jonasdottir, A., Wong, W. S. W., Sigurdsson, G., Walters, G. B., Steinberg, S., Helgason, H., Thorleifsson, G., Gudbjartsson, D. F., Helgason, A., Magnusson, O. T. ... Stefansson, K. (2012). Rate of de novo mutations and the importance of father's age to disease risk. Nature, 488(7412), 471-5. https://doi.org/10.1038/nature11396

Feliu, E., Knudsen, M. & Wiuf, C. H. (2012). Signaling Cascades: Consequences of Varying Substrate and Phosphatase Levels. Advances in Experimental Medicine and Biology, 736, 81-94. https://doi.org/10.1007/978-1-4419-7210-1_4

Dai, N., Foldager, L., Gallego, J. A., Hack, L. M., Ji, Y., Lett, T. A. P., Liu, B., Loken, E. K., Mandelli, L., Mehta, D., Power, R. A., Sprooten, E., Stephens, S. H., Paska, A. V., Yan, J., Zai, C. C., Zai, G., Zhang-James, Y., O'Shea, A. & DeLisi, L. E. (2012). Summaries from the XIX World Congress of Psychiatric Genetics, Washington, DC, September 10-14 2011. American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 159B(1), 128-129. https://doi.org/10.1002/ajmg.b.32017

Prüfer, K., Munch, K., Hellmann, I., Akagi, K., Miller, J. R., Walenz, B., Koren, S., Sutton, G., Kodira, C., Winer, R., Knight, J. R., Mullikin, J. C., Meader, S. J., Ponting, C. P., Lunter, G., Higashino, S., Hobolth, A., Dutheil, J., Karakoç, E. ... Pääbo, S. (2012). The bonobo genome compared with the chimpanzee and human genomes. Nature, 486(7404), 527-31. https://doi.org/10.1038/nature11128

Jensen, K., Kristensen, L. M. & Mailund, T. (2012). The sweep-line state space exploration method. Theoretical Computer Science, 429, 169–179. https://doi.org/10.1016/j.tcs.2011.12.036

Musgaard, M., Thøgersen, L., Schiøtt, B. & Tajkhorshid, E. (2012). Tracing Cytoplasmic Ca²⁺ Ion and Water Access Points in the Ca²⁺-ATPase. Biophysical Journal, 102(2), 268-277. https://doi.org/10.1016/j.bpj.2011.12.009

Hilker, R., Sickinger, C., Pedersen, C. N. S. & Stoye, J. (2012). UniMoG - A unifying framework for genomic distance calculation and sorting based DCJ. Bioinformatics, 28(19), 2509-2511. https://doi.org/10.1093/bioinformatics/bts440

Mailund, T., Halager, A. E. & Westergaard, M. (2012). Using colored Petri nets to construct coalescent hidden markov models: Automatic translation from demographic specifications to efficient inference methods. Lecture Notes in Computer Science, 7347, 32-50. https://doi.org/10.1007/978-3-642-31131-4_3

Djernes, J. K., Gulmann, N. C., Foldager, L., Olesen, F. & Munk-Jørgensen, P. (2011). 13 year follow up of morbidity, mortality and use of health services among elderly depressed patients and general elderly populations. The Australian & New Zealand Journal of Psychiatry, 45(8), 654-662. https://doi.org/10.3109/00048674.2011.589368

Laurila, K., Øster, B., Andersen, C. L., Lamy, P., Orntoft, T., Yli-Harja, O. & Wiuf, C. (2011). A Beta-Mixture Model for Dimensionality Reduction, Sample Classification and Analysis. BMC Bioinformatics, 12(1), 215. https://doi.org/10.1186/1471-2105-12-215

Nielsen, J. (2011). A Coarse-to-Fine Approach to Computing the k-best Viterbi Paths. Lecture Notes in Computer Science, 6661, 376-387. https://doi.org/10.1007/978-3-642-21458-5_32

Nielsen, J. & Sand, A. (2011). Algorithms for a parallel implementation of Hidden Markov Models with a small state space. In 2011 IEEE IPDPS Workshops & PhD Forum (pp. 447-454). IEEE Computer Society Press. https://doi.org/10.1109/IPDPS.2011.181

Abdallah, M., Larsen, N., Grove, J., Nørgaard-Pedersen, B., Hougaard, D. M. & Mortensen, E. L. (2011). Amniotic Fluid Chemokines Levels and Autism Spectrum Disorders, a study utilizing a Danish historic birth cohort. Abstract from World Congress of Epidemiology, Edinburgh, United Kingdom.

Feliu, E., Knudsen, M., Andersen, L. N. & Wiuf, C. H. (2011). An Algebraic Approach to Signaling Cascades with n Layers. Bulletin of Mathematical Biology, 74(1), 45-72. https://doi.org/10.1007/s11538-011-9658-0

Penner, R., Knudsen, M., Wiuf, C. H. & Andersen, J. E. (2011). An Algebro-Topological Description of Protein Domain Structure. PLoS One. https://doi.org/10.1371/journal.pone.0019670

Lamy, P., Grove, J. & Wiuf, C. (2011). A review of software for microarray genotyping. Human Genomics (Online), 5(4), 304-9.

Demontis, D., Nyegaard, M., Buttenschøn, H. N., Hedemand, A., Pedersen, C. B., Grove, J., Flint, T. J., Nordentoft, M., Werge, T., Hougaard, D. M., Sørensen, K. M., Yolken, R. H., Mors, O., Børglum, A. D. & Mortensen, P. B. (2011). Association of GRIN1 and GRIN2A-D With schizophrenia and genetic interaction with maternal herpes simplex virus-2 infection affecting disease risk. American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 156(8), 913-922. https://doi.org/10.1002/ajmg.b.31234

Nielsen, J., Kristensen, A. K., Mailund, T. & Pedersen, C. N. S. (2011). A sub-cubic time algorithm for computing the quartet distance between two general trees. Algorithms for Molecular Biology, 6(15). https://doi.org/10.1186/1748-7188-6-15

Abdallah, M., Grove, J. & David M. Hougaard, Bent Nørgaard-Pedersen, Fuad Ibrahimov, Erik L. Mortensen (2011). Autism spectrum disorders and maternal serum alpha-fetoprotein levels during pregnancy. Poster session presented at 10th World Congress of Biological Psychiatry, Prague, Czech Republic.

Abdallah, M., Grove, J., Hougaard, D. M., Nørgaard-Pedersen, B., Ibrahimov, F. & Mortensen, E. L. (2011). Autism Spectrum Disorders and Maternal Serum α-Fetoprotein Levels During Pregnancy. The Canadian Journal of Psychiatry, 56(12).

Steinberg, S., de Jong, S., Andreassen, O. A., Werge, T., Børglum, A. D., Mors, O., Mortensen, P. B., Gustafsson, O., Costas, J., Pietiläinen, O. P. H., Demontis, D., Papiol, S., Huttenlocher, J., Mattheisen, M., Breuer, R., Vassos, E., Giegling, I., Fraser, G., Walker, N. ... Irish Schizophrenia Genomics Consortium (2011). Common Variants at VRK2 and TCF4 Conferring Risk of Schizophrenia. Human Molecular Genetics, 20(20), 4076-81. https://doi.org/10.1093/hmg/ddr325

Locke, D. P., Hillier, L. W., Warren, W. C., Yang, S.-P., Wang, Z., Chinwalla, A. T., Minx, P., Mitreva, M., Cook, L., Delehaunty, K. D., Fronick, C., Schmidt, H., Fulton, L. A., Fulton, R. S., Nelson, J. O., Magrini, V., Pohl, C., Graves, T. A., Markovic, C. ... de Jong, P. J. (2011). Comparative and demographic analysis of orang-utan genomes. Nature, 469, 529-533. https://doi.org/10.1038/nature09687

Fei, G., Luo, Y., Li, S., Li, J., Lin, L., Nielsen, A. L., Sørensen, C. B., Vajta, G., Wang, J., Zhang, X., Du, Y., Yang, H. & Bolund, L. (2011). Comparison of gene expression and genome-wide DNA methylation profiling between phenotypically normal cloned pigs and conventionally bred controls. PLoS One, 6(10), e25901. https://doi.org/10.1371/journal.pone.0025901

Tataru, P. C. & Hobolth, A. (2011). Comparison of methods for calculating conditional expectations of sufficient statistics for continuous time Markov chains. BMC Bioinformatics, 12(1), 465. https://doi.org/10.1186/1471-2105-12-465

Reinert, T., Modin, C., Mansilla Castano, F., Lamy, P., Wojdacz, T. K., Hansen, L. L., Wiuf, C., Borre, M., Andersen, L. D. & Ørntoft, T. F. (2011). Comprehensive genome methylation analysis in bladder cancer;identification and validation of novel methylated genes and application of these as urinary tumor markers. Clinical Cancer Research. https://doi.org/10.1158/1078-0432.CCR-10-2659

Dalby, R. B., Elfving, B., Plougmann, P. H., Foldager, L., Rosenberg, R. & Videbech, P. (2011). Correlations between brain-derived neurotrophic factor (BDNF), vascular endothelial growth factor (VEGF), and vascular risk factors in late-onset major depression. Poster session presented at IBRO 8th World Congress of Neuroscience, Firenze, Italy.

Bataillon, T., Zhang, T. & Kassen, R. (2011). Cost of Adaptation and Fitness Effects of Beneficial Mutations in Pseudomonas fluorescens. Genetics, 189(3), 939-949. https://doi.org/10.1534/genetics.111.130468

Abdallah, M., Larsen, N., Grove, J., Nørgaard-Pedersen, B., Mortensen, E. L. & Hougaard, D. M. (2011). Cytokine Levels In Amniotic Fluid: a Marker of Maternal Immune Activation. Abstract from International Meeting for Autism Research (IMFAR 2011), San Diego, CA, United States.

Mapendano, C. K., Preker, P., Villesen, P., Prokop, A., Piatkowski, J., Schierup, M. H. & Jensen, T. H. (2011). Depletion of the RNA exosome triggers hypermethylation of human promoters.. Abstract from Third EMBO meeting on 'Chromatin and Epigenetics, Heidelberg, Germany.

Buttenschøn, H. N., Elfving, B., Foldager, L., Plougmann, P. H., Andersen, J. H., Bonde, J. P., Grynderup, M., Hansen, A. M., Kolstad, H., Kærgaard, A., Kærlev, L., Mikkelsen, S., Thomsen, J. F., Børglum, A., Wegener, G. & Mors, O. (2011). Depression og Val66Met polymorfien påvirker serum BDNF niveauet. Poster session presented at Psykiatriens 6. Forskningsdag, Risskov, Denmark.

Gao, F., Li, S., Lin, L., Li, J., Luo, Y., Zhang, X., Nielsen, A. L. & Bolund, L. (2011). DNA methylation in peripheral blood cells of pigs cloned by somatic cell nuclear transfer. Cellular Reprogramming, 13(4), 307-14. https://doi.org/10.1089/cell.2010.0099, https://doi.org/10.1089/cell.2010.0099

Simonsen, M. (2011). Efficient algorithms for tree reconstruction and prediction of molecular interactions. Department of Computer Science, Aarhus University.

Nielsen, J. (2011). Engineering Algorithms for Finding Patterns in Biological Data.

Furrow, R., Christiansen, F. & Feldman, M. (2011). Environment-sensitive Epigenetics and the Heritability of Complex Diseases. Genetics, 189(4), 1377-1387. https://doi.org/10.1534/genetics.111.131912

Displaying results 851 to 900 out of 1420

Revised 13.01.2026

Palle Villesen