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Boonen, S. E.; Stahl, D.; Kreiborg, S.; Rosenberg, T.; Kalscheuer, V.; Larsen, L. A.; Tommerup, N.; Brondum-Nielsen, K.; Tumer, Z.: Delineation of an interstitial 9q22 deletion in basal cell nevus syndrome. Am J Med Genet A 132A (3), pp. 324 - 8 (2005)

Erkel, C.; Kemnitz, D.; Kube, M.; Ricke, P.; Chin, K.-J.; Dedysh, S.; Reinhardt, R.; Conrad, R.; Liesack, W.: Retrieval of first genome data for rice cluster I methanogens by a combination of cultivation and molecular techniques. FEMS Microbiology Ecology 53 (2), pp. 187 - 204 (2005)

Foerster, J.; Nolte, I.; Junge, J.; Bruinenberg, M.; Schweiger, S.; Spaar, K.; van der Steege, G.; Ehlert, C.; Mulder, M.; Kalscheuer, V.: Haplotype sharing analysis identifies a retroviral dUTPase as candidate susceptibility gene for psoriasis. The Journal of Investigative Dermatology: an International Journal for Research in Cutaneous Biology 124 (1), pp. 99 - 102 (2005)

Gupta, S.; Vingron, M.; Haas, S. A.: T-STAG: resource and web-interface for tissue-specific transcripts and genes. Nucleic Acids Research 33 ((Web Server Issue)), pp. W654 - W658 (2005)

Jensen, L. R.; Amende, M.; Gurok, U.; Moser, B.; Gimme, V.; Tzschach, A.; Janecke, A. R.; Tariverdian, G.; Chelly, J.; Fryns, J.-P. et al.; Van Esch, H.; Kleefstra, T.; Hame, B.; Moraine, C.; Gécz, J.; Turner, G.; Reinhardt, R.; Kalscheuer, V. M.; Ropers, H.-H.; Lenzner, S.: : Mutations in the JARID1C gene, which is involved in transcriptional regulation and chromatin remodeling, cause X-linked mental retardation. American Journal of Human Genetics 76 (2), pp. 227 - 236 (2005)

Jensen, L. R.; Amende, M.; Gurok, U.; Moser, B.; Gimme, V.; Tzschach, A.; Janecke, A. R.; Tariverdian, G.; Chelly, J.; Fryns, J.-P. et al.; Van Esch, H.; Kleefstra, T.; Hame, B.; Moraine, C.; Gécz, J.; Turner, G.; Reinhardt, R.; Kalscheuer, V. M.; Ropers, H.-H.; Lenzner, S.: : Mutations in the JARID1C gene, which is involved in transcriptional regulation and chromatin remodeling, cause X-linked mental retardation. American Journal of Human Genetics 76 (2), pp. 227 - 236 (2005)

Kreutzberger, J.: Proteinchip-Diagnose von Neisseria meningitidis-Infektionen. Laborwelt 6 (3), pp. 18 - 21 (2005)

Markowetz, F.; Spang, R.: Molecular diagnosis: classification, model selection, and performance evaluation. Methods of Information in Medicine 44 (3), pp. 438 - 443 (2005)

Michael, M.; Dieterich, C.; Vingron, M.: SITEBLAST-rapid and sensitive local alignment of genomic sequences employing motif anchors. Bioinformatics 21 (9), pp. 2093 - 2094 (2005)

Nino-Soto, M.I.; Nuber, U. A.; Basrur, P.K.; Ropers, H.-H.; King, W.A.: Differences in the pattern of X-linked gene expression between fetal bovine muscle and fibroblast cultures derived from the same muscle biopsies. Cytogenetic and Genome Research 111 (1), pp. 57 - 64 (2005)

Rabus, R.; Kube, M.; Heider, J.; Beck, A.; Heitmann, K.; Widdel, F.; Reinhardt, R.: The genome sequence of an anaerobic aromatic-degrading denitrifying bacterium, strain EbN1. Archives of Microbiology 183 (1), pp. 27 - 36 (2005)

Ropers, H.-H.; Hamel, B. C. J.: X-linked mental retardation. Nature Reviews Genetics 6 (1), pp. 46 - 57 (2005)

Schröder, G.; Savvides, S. N.; Waksman, G.; Lanka, E.: Type IV secretion machinery. Forschungsbericht 200539-3 200539-3, pp. 179 - 221 (2005)

So, J.; Suckow, V.; Kijas, Z.; Kalscheuer, V. M.; Moser, B.; Winter, J.; Baars, M.; Firth, H.; Lunt, P.; Hamel, B. et al.; Meinecke, P.; Moraine, C.; Odent, S.; Schinzel, A.; van der Smagt, J.J.; Devriendt, K.; Albrecht, B.; Gillessen-Kaesbach, G.; van der Burgt, I.; Petrij, F.; Faivre, L.; McGaughran, J.; McKenzie, F.; Opitz, J. M.; Cox, T.; Schweiger, S.: Mild phenotypes in a series of patients with Opitz GBBB syndrome with MID1 mutations. American Journal of Medical Genetics: Part A 132 (1), pp. 1 - 7 (2005)

So, J.; Suckow, V.; Kijas, Z.; Kalscheuer, V. M.; Moser, B.; Winter, J.; Baars, M.; Firth, H.; Lunt, P.; Hamel, B. et al.; Meinecke, P.; Moraine, C.; Odent, S.; Schinzel, A.; van der Smagt, J.J.; Devriendt, K.; Albrecht, B.; Gillessen-Kaesbach, G.; van der Burgt, I.; Petrij, F.; Faivre, L.; McGaughran, J.; McKenzie, F.; Opitz, J. M.; Cox, T.; Schweiger, S.: Mild phenotypes in a series of patients with Opitz GBBB syndrome with MID1 mutations. American Journal of Medical Genetics: Part A 132 (1), pp. 1 - 7 (2005)

Sueltmann, H.; von Heydebreck, A.; Huber, W.; Kuner, R.; Buness, A.; Vogt, M.; Gunawan, B.; Vingron, M.; Fuezesi, L.; Poustka, A.: Gene Expression in Kidney Cancer Is Associated with Cytogenetic Abnormalities, Metastasis Formation, and Patient Survival. Clinical Cancer Research 11 (2 Pt 1), pp. 646 - 655 (2005)

Toedling, J.; Schmeier, S.; Heinig, M.; Georgi, B.; Roepcke, S.: MACAT--microarray chromosome analysis tool. Bioinformatics 21 (9), pp. 2112 - 2113 (2005)

Trachtulec, Z.; Mihola, O.; Vlcek, C.; Himmelbauer, H.; Pacces, V.: Positional cloning of the Hybrid sterility 1 gene: fine genetic mapping and evaluation of two candidate genes. Biological Journal of the Linnean Society 84, pp. 637 - 641 (2005)

Tumer, Z.; Henriksen, A. M.; Bache, I.; Brixen, K.; Kalscheuer, V.; Illum, N.; Rasmussen, K.; Larsen, L. A.; Tommerup, N.: Eponymous Jacobsen syndrome: mapping the breakpoints of the original family suggests an association between the distal 1.1 Mb of chromosome 21 and osteoporosis in Down syndrome. Am J Med Genet A 135 (3), pp. 339 - 41 (2005)