Meierhofer, D.; Mayr, J. A.; Foetschl, U.; Berger, A.; Fink, K.; Schmeller, N.; Hacker, G. W.; Hauser-Kronberger, C.; Kofler, B.; Sperl, W.: Decrease of mitochondrial DNA content and energy metabolism in renal cell carcinoma. Carcinogenesis 25 (6), pp. 1005 - 1010 (2004)

Berger, A.; Mayr, J. A.; Meierhofer, D.; Fötschl, U.; Bittner, R.; Budka, H.; Grethen, C.; Huemer, M.; Kofler, B.; Sperl, W.: Severe depletion of mitochondrial DNA in spinal muscular atrophy. Acta Neuropathologica 105 (3), pp. 245 - 251 (2003)

Brunner, B.; Hornung, U.; Shan, Z.; Nanda, I.; Kondo, M.; Zend-Ajusch, E.; Haaf, T.; Ropers, H. H.; Shima, A.; Schmid, M. et al.; Kalscheuer, V. M.; Schartl, M.: Genomic organization and expression of the doublesex-related gene cluster in vertebrates and detection of putative regulatory regions for DMRT1. Genomics 77 (1-2), pp. 8 - 17 (2001)

Fritz, B.; Aslan, M.; Kalscheuer, V.; Ramsing, M.; Saar, K.; Fuchs, B.; Rehder, H.: Low incidence of UPD in spontaneous abortions beyond the 5th gestational week. Eur J Hum Genet 9 (12), pp. 910 - 6 (2001)

Mergenthaler, S.; Hitchins, M. P.; Blagitko-Dorfs, N.; Monk, D.; Wollmann, H. A.; Ranke, M. B.; Ropers, H. H.; Apostolidou, S.; Stanier, P.; Preece, M. A. et al.; Eggermann, T.; Kalscheuer, V. M.; Moore, G. E.: Conflicting reports of imprinting status of human GRB10 in developing brain: how reliable are somatic cell hybrids for predicting allelic origin of expression? Am J Hum Genet 68 (2), pp. 543 - 5 (2001)

Mergenthaler, S.; Sharp, A.; Ranke, M. B.; Kalscheuer, V. M.; Wollmann, H. A.; Eggermann, T.: Gene dosage analysis in Silver-Russell syndrome: use of quantitative competitive PCR and dual-color FISH to estimate the frequency of duplications in 7p11.2-p13. Genet Test 5 (3), pp. 261 - 6 (2001)

Sudbrak, R.; Wieczorek, G.; Nuber, U. A.; Mann, W.; Kirchner, R.; Erdogan, F.; Brown, C. J.; Wohrle, D.; Sterk, P.; Kalscheuer, V. M. et al.; Berger, W.; Lehrach, H.; Ropers, H. H.: X chromosome-specific cDNA arrays: identification of genes that escape from X-inactivation and other applications. Hum Mol Genet 10 (1), pp. 77 - 83 (2001)

Tonnies, H.; Stumm, M.; Wegner, R. D.; Chudoba, I.; Kalscheuer, V.; Neitzel, H.: Comparative genomic hybridization based strategy for the analysis of different chromosome imbalances detected in conventional cytogenetic diagnostics. Cytogenet Cell Genet 93 (3-4), pp. 188 - 94 (2001)

Volleth, M.; Stumm, M.; Mohnike, K.; Kalscheuer, V. M.; Jakubiczka, S.; Wieacker, P.: Preferential inactivation of a dupX(q23 --> q27-28) chromosome in a girl with mental retardation and dysmorphy. Hum Hered 52 (3), pp. 177 - 82 (2001)

Blagitko, N.; Mergenthaler, S.; Schulz, U.; Wollmann, H. A.; Craigen, W.; Eggermann, T.; Ropers, H. H.; Kalscheuer, V. M.: Human GRB10 is imprinted and expressed from the paternal and maternal allele in a highly tissue- and isoform-specific fashion. Hum Mol Genet 9 (11), pp. 1587 - 95 (2000)

Brunner, B.; Grutzner, F.; Yaspo, M. L.; Ropers, H. H.; Haaf, T.; Kalscheuer, V. M.: Molecular cloning and characterization of the Fugu rubripes MEST/COPG2 imprinting cluster and chromosomal localization in Fugu and Tetraodon nigroviridis. Chromosome Res 8 (6), pp. 465 - 76 (2000)

Mergenthaler, S.; Blagitko-Dorfs, N.; Wollmann, H. A.; Ranke, M. B.; Ropers, H. H.; Kalscheuer, V. M.; Eggermann, T.: Identification of two new polymorphisms (c2447-125A>G; c2532G>A) in the gamma 2-COP (COPG2) gene by screening of Silver-Russell syndrome patients. Hum Mutat 16 (1), p. 96 (2000)

Singh, A.; Henschel, S.; Sperling, K.; Kalscheuer, V.; Neitzel, H.: Differences in the meiotic pairing behavior of gonosomal heterochromatin between female and male Microtus agrestis: implications for the mechanism of heterochromatin amplification on the X and Y. Cytogenet Cell Genet 91 (1-4), pp. 253 - 60 (2000)

Blagitko, N.; Schulz, U.; Schinzel, A. A.; Ropers, H. H.; Kalscheuer, V. M.: gamma2-COP, a novel imprinted gene on chromosome 7q32, defines a new imprinting cluster in the human genome. Hum Mol Genet 8 (13), pp. 2387 - 96 (1999)

Brunner, B.; Todt, T.; Lenzner, S.; Stout, K.; Schulz, U.; Ropers, H. H.; Kalscheuer, V. M.: Genomic structure and comparative analysis of nine Fugu genes: conservation of synteny with human chromosome Xp22.2-p22.1. Genome Res 9 (5), pp. 437 - 48 (1999)

Krause, R.; Hemberger, M.; Himmelbauer, H.; Kalscheuer, V.; Fundele, R. H.: Identification and characterization of G90, a novel mouse RNA that lacks an extensive open reading frame. Gene 232 (1), pp. 35 - 42 (1999)

van de Wetering, R. A.; Gabreels-Festen, A. A.; Kremer, H.; Kalscheuer, V. M.; Gabreels, F. J.; Mariman, E. C.: Regulation and expression of the murine PMP22 gene. Mamm Genome 10 (4), pp. 419 - 22 (1999)

Neitzel, H.; Kalscheuer, V.; Henschel, S.; Digweed, M.; Sperling, K.: Beta-heterochromatin in mammals: evidence from studies in Microtus agrestis based on the extensive accumulation of L1 and non-L1 retroposons in the heterochromatin. Cytogenet Cell Genet 80 (1-4), pp. 165 - 72 (1998)

Riesewijk, A. M.; Blagitko, N.; Schinzel, A. A.; Hu, L.; Schulz, U.; Hamel, B. C.; Ropers, H. H.; Kalscheuer, V. M.: Evidence against a major role of PEG1/MEST in Silver-Russell syndrome. Eur J Hum Genet 6 (2), pp. 114 - 20 (1998)

Riesewijk, A. M.; Xu, Y. Q.; Schepens, M. T.; Mariman, E. M.; Polychronakos, C.; Ropers, H. H.; Kalscheuer, V. M.: Absence of an obvious molecular imprinting mechanism in a human fetus with monoallelic IGF2R expression. Biochem Biophys Res Commun 245 (1), pp. 272 - 7 (1998)