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Zeitschriftenartikel (119)

  1. 101.
    Zeitschriftenartikel
    Klopocki, E.; Schulze, H.; Strauß, G.; Ott, C.-E.; Hall, J.; Trotier, F.; Fleischhauer, S.; Greenhalgh, L.; Newbury-Ecob, R. A.; Neumann, L. M. et al.; Habenicht, R.; König, R.; Seemanova, E.; Megarbane, A.; Ropers, H.-H.; Ullmann, R.; Mundlos, S.: Complex inheritance pattern resembling autosomal recessive inheritance involving a microdeletion in thrombocytopenia-absent radius. American Journal of Human Genetics: AJHG / American Society of Human Genetics 80 (2), S. 232 - 240 (2007)
  2. 102.
    Zeitschriftenartikel
    Klopocki, E.; Schulze, H.; Strauß, G.; Ott, C.-E.; Hall, J.; Trotier, F.; Fleischhauer, S.; Greenhalgh, L.; Newbury-Ecob, R. A.; Neumann, L. M. et al.; Habenicht, R.; König, R.; Seemanova, E.; Megarbane, A.; Ropers, H.-H.; Ullmann, R.; Mundlos, S.: Complex inheritance pattern resembling autosomal recessive inheritance involving a microdeletion in thrombocytopenia-absent radius. American Journal of Human Genetics: AJHG / American Society of Human Genetics 80 (2), S. 232 - 240 (2007)
  3. 103.
    Zeitschriftenartikel
    Tzschach, A.; Menzel, C.; Erdogan, F.; Schubert, M.; Hoeltzenbein, M.; Barbi, G.; Petzenhauser, C.; Ropers, H.-H.; Ullmann, R.; Kalscheuer, V. M.: Characterization of a 16 Mb interstitial chromosome 7q21 deletion by tiling path array CGH. American Journal of Medical Genetics 143 A (4), S. 333 - 337 (2007)
  4. 104.
    Zeitschriftenartikel
    Kalscheuer, V. M.; FitzPatrick, D.; Tommerup, N.; Bugge, M.; Niebuhr, E.; Neumann, L. M.; Tzschach, A.; Shoichet, S. A.; Menzel, C.; Erdogan, F. et al.; Arkesteijn, G.; Ropers, H.-H.; Ullmann, R.: Mutations in Autism Susceptibility Candidate 2 (AUTS2) in patients with mental retardation. Human Genetics 121 (3-4), S. 501 - 509 (2007)
  5. 105.
    Zeitschriftenartikel
    Gratias, S.; Rieder, H.; Ullmann, R.; Klein-Hitpass, L.; Schneider, S.; Bölöni, R.; Kappler, M.; Lohmann, D. R.: Allelic loss in a minimal region on chromosome 16q24 is associated with vitreous seeding of retinoblastoma. Cancer Research: an Official Organ of the American Association for Cancer Research 67 (1), S. 408 - 416 (2007)
  6. 106.
    Zeitschriftenartikel
    Klopocki, E.; Neumann, L. M.; Tönnies, H.; Ropers, H.-H.; Mundlos, S.; Ullmann, R.: Ulnar-mammary syndrome with dysmorphic facies and mental retardation caused by a novel 1.28 Mb deletion encompassing the TBX3 gene. European Journal of Human Genetics: the Official Journal of the European Society of Human Genetics. 14 (121), S. 1274 - 1279 (2006)
  7. 107.
    Zeitschriftenartikel
    Klopocki, E.; Neumann, L. M.; Tönnies, H.; Ropers, H.-H.; Mundlos, S.; Ullmann, R.: Ulnar-mammary syndrome with dysmorphic facies and mental retardation caused by a novel 1.28 Mb deletion encompassing the TBX3 gene. European Journal of Human Genetics: the Official Journal of the European Society of Human Genetics. 14 (121), S. 1274 - 1279 (2006)
  8. 108.
    Zeitschriftenartikel
    Erdogan, F.; Chen, W.; Kirchhoff, M.; Kalscheuer, V. M.; Hultschig, C.; Müller, I.; Schulz, A.; Menzel, C.; Bryndorf, T.; Ropers, H.-H. et al.; Ullmann, R.: Impact of low copy repeats on the generation of balanced and unbalanced chromosomal aberrations in mental retardation. Cytogenetic and Genome Research 115 (3-4), S. 247 - 253 (2006)
  9. 109.
    Zeitschriftenartikel
    Erdogan, F.; Chen, W.; Kirchhoff, M.; Kalscheuer, V. M.; Hultschig, C.; Müller, I.; Schulz, A.; Menzel, C.; Bryndorf, T.; Ropers, H.-H. et al.; Ullmann, R.: Impact of low copy repeats on the generation of balanced and unbalanced chromosomal aberrations in mental retardation. Cytogenetic and Genome Research 115 (3-4), S. 247 - 253 (2006)
  10. 110.
    Zeitschriftenartikel
    Müller, D.; Klopocki, E.; Neumann, L. E.; Mundlos, S.; Taupitz, M.; Schulze, I.; Ropers, H.-H.; Querfeld, U.; Ullmann, R.: A complex phenotype with cystic renal disease. Kidney International: Official Journal of the International Society of Nephrology 70 (9), S. 1656 - 1660 (2006)
  11. 111.
    Zeitschriftenartikel
    Müller, D.; Klopocki, E.; Neumann, L. E.; Mundlos, S.; Taupitz, M.; Schulze, I.; Ropers, H.-H.; Querfeld, U.; Ullmann, R.: A complex phenotype with cystic renal disease. Kidney International: Official Journal of the International Society of Nephrology 70 (9), S. 1656 - 1660 (2006)
  12. 112.
    Zeitschriftenartikel
    Schwarzbraun, T.; Ullmann, R.; Schubert, M.; Ledinegg, M.; Ofner, L.; Windpassinger, C.; Wagner, K.; Kroisel, P. M.; Petek, E.: Characterisation of a de novo complex chromosome rearrangement (CCR) involving chromosomes 2 and 12, associated with mental retardation and impaired speech development. Cytogenetics and Genome Research 115 (1), S. 84 - 89 (2006)
  13. 113.
    Zeitschriftenartikel
    Klopocki, E.; Fiebig, B.; Robinson, P. N.; Tönnies, H.; Erdogan, F.; Ropers, H.-H.; Mundlos, S.; Ullmann, R.: A novel 8 Mb interstitial deletion of chromosome 8p12-p21.2. American Journal of Medical Genetics Part A 140A (8), S. 873 - 877 (2006)
  14. 114.
    Zeitschriftenartikel
    Garshasbi, M.; Motazacker, M. M.; Kahrizi, K.; Behjati, F.; Abedini, S. S.; Nieh, S. E.; Firouzabadi, S. G.; Becker, C.; Rüschendorf, F.; Nürnberg, P. et al.; Tzschach, A.; Vazifehmand, R.; Erdogan, F.; Ullmann, R.; Lenzner, S.; Kuss, A. W.; Ropers, H.-H.; Najmabadi, H.: SNP array-based homozygosity mapping reveals MCPH1 deletion in family with autosomal recessive mental retardation and mild microcephaly. Human Genetics 118 (6), S. 708 - 715 (2006)
  15. 115.
    Zeitschriftenartikel
    Chen, W.; Erdogan, F.; Ropers, H.-H.; Lenzner, S.; Ullmann, R.: : CGHPRO – a comprehensive data analysis tool for array CGH. BMC Bioinformatics 6 (1), S. 1471 - 2105 (2005)
  16. 116.
    Zeitschriftenartikel
    Petzmann, S.; Ullmann, R.; Halbwedl, I.; Popper, H. H.: Analysis of chromosome-11 aberrations in pulmonary and gastrointestinal carcinoids: an array comparative genomic hybridization-based study. Virchows Archiv: Official Journal of the European Society of Pathology 445 (2), S. 151 - 159 (2004)
  17. 117.
    Zeitschriftenartikel
    Ullmann, R.; Morbini, P.; Halbwedl, I.; Bongiovanni, M.; Gogg-Kammerer, M.; Papotti, M.; Gabor, S.; Renner, H.; Popper, H. H.: Protein expression profiles in adenocarcinomas and squamous cell carcinomas of the lung generated using tissue microarrays. Journal of Pathology: an Official Journal of the Pathological Society 203 (3), S. 798 - 807 (2004)
  18. 118.
    Zeitschriftenartikel
    Stacher, E.; Ullmann, R.; Halbwedl, I.; Gogg-Kammerer, M.; Boccon-Gibod, L.; Nicholson, A. G.; Sheppard, M. N.; Carvalho, L.; Franca, M. T.; MacSweeney, F. et al.; Morresi-Hauf, A.; Popper, H. H.: Atypical goblet cell hyperplasia in congenital cystic adenomatoid malformation as a possible preneoplasia for pulmonary adenocarcinoma in childhood: A genetic analysis. Human Pathology 35 (5), S. 565 - 570 (2004)
  19. 119.
    Zeitschriftenartikel
    Zatkova, A.; Ullmann, R.; Rouillard, J. M.; Lamb, B. J.; Kuick, R.; Hanash, S. M.; Schnittger, S.; Schoch, C.; Fonatsch, C.; Wimmer, K.: Distinct sequences on 11q13.5 and 11q23-24 are frequently coamplified with MLL in complexly organized 11q amplicons in AML/MDS patients. Genes Chromosomes Cancer 39 (4), S. 263 - 276 (2004)

Buchkapitel (2)

  1. 120.
    Buchkapitel
    Ullmann, R.: Array comparative genomic hybridization in pathology. In: Basic concepts of molecular pathology, S. 87 - 96 (Hg. Cagle, P. T.; Allen, T. C.). Springer, New York (2009)
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