Herskin, M. S., Kobek-Kjeldager, C., Kaiser, M. Ø., Thodberg, K., Jensen, L. D., Chen, G., Zhang, G., Rong, L. & Foldager, L., (2022).
Krav til indvendig højde ved transport af smågrise, No. 2020-0096886, 15 p., Jul 05, 2022.
Hernandez-de Sosa, N.
, Athanasiadis, G., Malouf, J., Laiz, A., Muñoz-Marin, A. M., Herrera, S., Farrerons, J., Soria, J. M. & Casademont, J. (2016).
Genetic Contribution of Femoral Neck Bone Geometry to the Risk of Developing Osteoporosis: A Family-Based Study.
P L o S One,
11(5), Article 0154833.
https://doi.org/10.1371/journal.pone.0154833
Hernández-Castellano, L. E., Sørensen, M. T., Foldager, L., Herskin, M. S., Gross, J. J., Bruckmaier, R. M.
& Larsen, M. (2023).
Effects of feeding level, milking frequency, and single injection of cabergoline on blood metabolites, hormones, and minerals around dry-off in dairy cows.
Journal of Dairy Science,
106(4), 2919-2932.
https://doi.org/10.3168/jds.2022-22648
Herbsleb, M., Andersen, T. T., Wiuf, C. & Ørntoft, T. F. (2006).
Identification of New Transcriptional Correlations in Cancer Using Array Databases and Functional In Vitro Studies , presented at PhD Annual Day, Graduate School of Health, University of Aarhus.. Poster session presented at
Identification of New Transcriptional Correlations in Cancer Using Array Databases and Functional In Vitro Studies , presented at PhD Annual Day, Graduate School of Health, University of Aarhus..
Herbsleb, M., Birkenkamp-Demtröder, K., Andersen, T. T., Wiuf, C., Hein, A.-M. K., Ørntoft, T. F. & Andersen, L. D. (2008).
Increased cell motility and invasion upon knockdown of lipolysis stimulated lipoprotein receptor (LSR) in SW780 bladder cancer cells.
B M C Medical Genomics,
1.
https://doi.org/10.1186/1755-8794-1-31
Herbsleb, M., Christensen, O. F., Thykjaer, T., Wiuf, C., Borre, M., Ørntoft, T. F. & Dyrskjøt, L. (2008).
Bioinformatic identification of FGF, p38-MAPK, and calcium signalling pathways associated with carcinoma in situ in the urinary bladder.
B M C Cancer,
8, 37.
https://doi.org/10.1186/1471-2407-8-37
Herbsleb, M., Birkenkamp-Demtroder, K., Thykjaer, T.
, Wiuf, C., Hein, A.-M. K., Orntoft, T. F. & Andersen, L. D. (2008).
Increased cell motility and invasion upon knockdown of lipolysis stimulated lipoprotein receptor (LSR) in SW780 bladder cancer cells.
B M C Medical Genomics,
1, 31.
https://doi.org/10.1186/1755-8794-1-31
Heinz, J. L., Swagemakers, S. M. A., von Hofsten, J., Helleberg, M.
, Thomsen, M. M., De Keukeleere, K., de Boer, J. H.
, Ilginis, T., Verjans, G. M. G. M., van Hagen, P. M., van der Spek, P. J.
& Mogensen, T. H. (2023).
Whole exome sequencing of patients with varicella-zoster virus and herpes simplex virus induced acute retinal necrosis reveals rare disease-associated genetic variants.
Frontiers in Molecular Neuroscience,
16, Article 1253040.
https://doi.org/10.3389/fnmol.2023.1253040
Hein, J.
, Wiuf, C., Møller, M., Knudsen, B. & Wibling, G. (2000).
Statistical alignment: computational properties, homology testing and goodness-of-fit.
J. Mol. Biol.,
302(1), 265-279.
https://doi.org/10.1006/jmbi.2000.4061
Hedegaard, J., Thorsen, K., Lund, M. K., Hein, A.-M. K., Hamilton-Dutoit, S. J., Vang, S., Nordentoft, I., Birkenkamp-Demtröder, K., Kruhøffer, M., Hager, H., Knudsen, B., Andersen, C. L., Sørensen, K. D., Pedersen, J. S., Orntoft, T. F. & Dyrskjøt, L. (2014).
Next-generation sequencing of RNA and DNA isolated from paired fresh-frozen and formalin-fixed paraffin-embedded samples of human cancer and normal tissue.
PLOS ONE,
9(5), e98187.
https://doi.org/10.1371/journal.pone.0098187
Hebsgaard, MB.
, Wiuf, C., Gilbert, MTP., Glenner, H. & Willerslev, E. (2007).
Evaluating Neandertal genetics and phylogeny.
J. Mol. Evol.,
64, 50-60.
https://doi.org/10.1007/s00239-006-0017-y
Hayeck, T. J., Busby, G. B., Chun, S., Lewis, A. C. F., Roberts, M. C.
& Vilhjálmsson, B. J. (2023).
Polygenic Risk Scores: Genomes to Risk Prediction.
Clinical Chemistry,
69(6), 551–557.
https://doi.org/10.1093/clinchem/hvad049
Haudry, A., Cenci, A., Ravel, C.
, Bataillon, T., Brunel, D., Poncet, C., Hochu, I., Poirier, S., Santoni, S., Glemin, S. & David, J. (2007).
Grinding up Wheat: a Massive Loss of Nucleotide Diversity Since Domestication.
Molecular Biology and Evolution,
24(7), 1506-1517.
https://doi.org/10.1093/molbev/msm077
Hauberg, M. E., Holm-Nielsen, M. H., Mattheisen, M., Askou, A. L., Grove, J., Børglum, A. D. & Corydon, T. J. (2016).
Schizophrenia risk variants affecting microRNA function and site-specific regulation of NT5C2 by miR-206.
European neuropsychopharmacology : the journal of the European College of Neuropsychopharmacology,
26(9), 1522-6.
https://doi.org/10.1016/j.euroneuro.2016.06.014
Hansen, AJ., Mitchell, D.
, Wiuf, C., Paniker, L., Brand, TB., Binladen, J., Gilichinsky, DA., Rønn, R. & Willerslev, E. (2006).
Crosslinks rather than Strand Breaks Determine Access to Ancient DNA Sequences from Frozen Sediments.
Genetics,
173, 1175-1179.
https://doi.org/10.1534/genetics.106.057349
Hansen, AJ., Willerslev, E.
, Wiuf, C., Mourier, T. & Arctander, P. (2001).
Statistical evidence for miscoding lesions in ancient DNA templates.
Mol. Biol. Evol.,
18, 262-265.
Hansen, S. K., Vestergaard, M., Thøgersen, L., Schiøtt, B., Nielsen, N. C. & Vosegaard, T. (2014).
Lipid Dynamics Studied by Calculation of 31P Solid-State NMR Spectra Using Ensembles from Molecular Dynamics Simulations.
Journal of Physical Chemistry Part B: Condensed Matter, Materials, Surfaces, Interfaces & Biophysical,
118(19), 5119-5129.
https://doi.org/10.1021/jp5000304
Hansen, M. C., Nyvold, C. G., Roug, A. S., Kjeldsen, E., Villesen, P., Nederby, L. & Hokland, P. (2015).
Nature and nurture: a case of transcending haematological pre-malignancies in a pair of monozygotic twins adding possible clues on the pathogenesis of B-cell proliferations.
British Journal of Haematology,
169(3), 391–400.
https://doi.org/10.1111/bjh.13305
Hansen, M. C., Nederby, L., Roug, A., Villesen, P., Kjeldsen, E., Nyvold, C. G. & Hokland, P. (2015).
Novel scripts for improved annotation and selection of variants from whole exome sequencing in cancer research.
MethodsX,
2, 145-53.
https://doi.org/10.1016/j.mex.2015.03.003
Hansen, E. K. B., Fredsøe, J. H., Okholm, T. L. H., Ulhøi, B. P., Klingenberg, S., Jensen, J. B., Kjems, J., Bouchelouche, K., Borre, M., Damgaard, C. K., Pedersen, J. S., Kristensen, L. S. & Sørensen, K. D. (2022).
The transcriptional landscape and biomarker potential of circular RNAs in prostate cancer.
Genome Medicine,
14(1), Article 8.
https://doi.org/10.1186/s13073-021-01009-3
Hansen, N. P., Kristensen, T., Johansen, M., Wiking, L., Poulsen, N. A., Hellwing, A. L. F., Foldager, L., Jensen, S. K., Larsen, L. B. & Weisbjerg, M. R. (2022).
Effects on feed intake, milk production, and methane emission in dairy cows fed silage or fresh grass with concentrate or fresh grass harvested at early or late maturity stage without concentrate.
Journal of Dairy Science,
105(10), 8036-8053.
https://doi.org/10.3168/jds.2022-21885
Hannon, E.
, Schendel, D., Ladd-Acosta, C.
, Grove, J., Hansen, C. S., Andrews, S. V., Hougaard, D. M., Bresnahan, M.
, Mors, O., Hollegaard, M. V., Bækvad-Hansen, M., Hornig, M.
, Mortensen, P. B., Børglum, A. D., Werge, T.
, Pedersen, M. G., Nordentoft, M., Buxbaum, J., Daniele Fallin, M. ... iPSYCH-Broad ASD Group (Mette Nyegaard, Per Qvist, Jane Hvarregaard Christensen - members of -) (2018).
Elevated polygenic burden for autism is associated with differential DNA methylation at birth.
Genome Medicine,
10(1), Article 19.
https://doi.org/10.1186/s13073-018-0527-4
Hannon, E.
, Schendel, D., Ladd-Acosta, C.
, Grove, J., Hansen, C. S., Hougaard, D. M., Bresnahan, M.
, Mors, O., Hollegaard, M. V., Bækvad-Hansen, M., Hornig, M.
, Mortensen, P. B., Børglum, A. D., Werge, T.
, Pedersen, M. G., Nordentoft, M., Buxbaum, J. D., Fallin, M. D., Bybjerg-Grauholm, J. ... Mill, J. (2019).
Variable DNA methylation in neonates mediates the association between prenatal smoking and birth weight.
Philosophical Transactions of the Royal Society B: Biological Sciences,
374(1770), Article 20180120.
https://doi.org/10.1098/rstb.2018.0120
Hanghøj, K., Seguin, A., Schubert, M.
, Madsen, T., Pedersen, J. S., Willerslev, E. & Orlando, L. (2016).
Fast, accurate and automatic ancient nucleosome and methylation maps with epiPALEOMIX.
Molecular Biology and Evolution,
33(12), 3284-3298.
https://doi.org/10.1093/molbev/msw184
Gusev, A., Lee, S. H., Trynka, G., Finucane, H.
, Vilhjálmsson, B. J., Xu, H., Zang, C., Ripke, S., Bulik-Sullivan, B., Stahl, E., Kähler, A. K., Hultman, C. M., Purcell, S. M., McCarroll, S. A., Daly, M., Pasaniuc, B., Sullivan, P. F., Neale, B. M., Wray, N. R. ... Schizophrenia Working Group of the Psychiatric Genomics Consortium (Manuel Mattheisen and Jakob Grove, members) (2014).
Partitioning Heritability of Regulatory and Cell-Type-Specific Variants across 11 Common Diseases.
American Journal of Human Genetics,
95(5), 535-52.
https://doi.org/10.1016/j.ajhg.2014.10.004
Gupta, V., Markmann, K., Pedersen, C. N. S., Stougaard, J. & Andersen, S. U. (2012).
shortran: A pipeline for small RNA-seq data analysis.
Bioinformatics,
28(20), 2698-2700.
https://doi.org/10.1093/bioinformatics/bts496
Guo, Y.-L.
, Bechsgaard, J. S., Slotte, T., Neuffer, B., Lascoux, M., Weigel, D.
& Schierup, M. H. (2009).
Recent speciation of Capsella rubella from Capsella grandiflora, associated with loss of self-incompatibility and an extreme bottleneck.
Proceedings of the National Academy of Sciences,
106(13), 5246-51.
https://doi.org/10.1073/pnas.0808012106
Guillemet, M., Chabas, H., Nicot, A., Gatchich, F., Ortega-Abboud, E., Buus, C.
, Hindhede, L., Rousseau, G. M.
, Bataillon, T., Moineau, S. & Gandon, S. (2022).
Competition and coevolution drive the evolution and the diversification of CRISPR immunity.
Nature Ecology & Evolution,
6(10), 1480-1488.
https://doi.org/10.1038/s41559-022-01841-9
Gruening, B., Sallou, O., Moreno, P., da Veiga Leprevost, F., Ménager, H.
, Søndergaard, D., Röst, H., Sachsenberg, T., O'connor, B., Madeira, F., Del Angel, V. D., Crusoe, M. R., Varma, S., Blankenberg, D., Jimenez, R. C., BioContainers Community & Perez-Riverol, Y. (2019).
Recommendations for the packaging and containerizing of bioinformatics software: [version 2; peer review: 2 approved, 1 approved with reservations].
F1000Research,
7, Article 742.
https://doi.org/10.12688/f1000research.15140.2
Grove, J., Demontis, D., Hollegaard, M. V., Pedersen, C. B., Ørntoft, T. F., Yolken, R., Didriksen, M., Hougaard, D.
, Wiuf, C. H., Mors, O., Mortensen, P. B. & Børglum, A. (2011).
Genome-Wide Significant Interaction by Cytomegalovirus with Respect to Risk of Schizophrenia. Poster session presented at XIX World Congress on Psychiatric Genetics, Washington DC, United States.
Grove, J., Foldager, L., Demontis, D., Hollegaard, M. V.
, Pedersen, C. B., Yolken, R. H., Hougaard, D. M.
, Mors, O., Mortensen, P. B., The Psychiatric Genomics Consortium – Schizophrenia
& Børglum, A. (2013).
Interaction between polygenic scores for schizophrenia and infection by herpes simples virus 1 and 2. Poster session presented at XXIst World Congress of Psychiatric Genetics, Boston, United States.