Publikationen von Reinhard Ullmann

Eva Klopocki, Harald Schulze, Gabriele Strauß, Claus-Eric Ott, Judith Hall, Fabienne Trotier, Silke Fleischhauer, Lynn Greenhalgh, Ruth A. Newbury-Ecob, Luitgard M. Neumann, Rolf Habenicht, Rainer König, Eva Seemanova, André Megarbane, Hans-Hilger Ropers, Reinhard Ullmann, and Stefan Mundlos, "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), 232-240 (2007).

Eva Klopocki, Harald Schulze, Gabriele Strauß, Claus-Eric Ott, Judith Hall, Fabienne Trotier, Silke Fleischhauer, Lynn Greenhalgh, Ruth A. Newbury-Ecob, Luitgard M. Neumann, Rolf Habenicht, Rainer König, Eva Seemanova, André Megarbane, Hans-Hilger Ropers, Reinhard Ullmann, and Stefan Mundlos, "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), 232-240 (2007).

Andreas Tzschach, Corinna Menzel, Fikret Erdogan, Marei Schubert, Maria Hoeltzenbein, Gotthold Barbi, Christine Petzenhauser, Hans-Hilger Ropers, Reinhard Ullmann, and Vera M. Kalscheuer, "Characterization of a 16 Mb interstitial chromosome 7q21 deletion by tiling path array CGH.," American Journal of Medical Genetics 143 A (4), 333-337 (2007).

Vera M. Kalscheuer, David FitzPatrick, Niels Tommerup, Merete Bugge, Erik Niebuhr, Luitgard M. Neumann, Andreas Tzschach, Sarah A. Shoichet, Corinna Menzel, Fikret Erdogan, Ger Arkesteijn, Hans-Hilger Ropers, and Reinhard Ullmann, "Mutations in Autism Susceptibility Candidate 2 (AUTS2) in patients with mental retardation," Human Genetics 121 (3-4), 501-509 (2007).

Sandrine Gratias, Harald Rieder, Reinhard Ullmann, Ludger Klein-Hitpass, Stephanie Schneider, Réka Bölöni, Martin Kappler, and Dietmar R. Lohmann, "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), 408-416 (2007).

Eva Klopocki, Luitgard M. Neumann, Holger Tönnies, Hans-Hilger Ropers, Stefan Mundlos, and Reinhard Ullmann, "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), 1274-1279 (2006).

Eva Klopocki, Luitgard M. Neumann, Holger Tönnies, Hans-Hilger Ropers, Stefan Mundlos, and Reinhard Ullmann, "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), 1274-1279 (2006).

F. Erdogan, W. Chen, M. Kirchhoff, V. M. Kalscheuer, C. Hultschig, I. Müller, A. Schulz, C. Menzel, T. Bryndorf, H.-H. Ropers, and R. Ullmann, "Impact of low copy repeats on the generation of balanced and unbalanced chromosomal aberrations in mental retardation," Cytogenetic and Genome Research 115 (3-4), 247-253 (2006).

F. Erdogan, W. Chen, M. Kirchhoff, V. M. Kalscheuer, C. Hultschig, I. Müller, A. Schulz, C. Menzel, T. Bryndorf, H.-H. Ropers, and R. Ullmann, "Impact of low copy repeats on the generation of balanced and unbalanced chromosomal aberrations in mental retardation," Cytogenetic and Genome Research 115 (3-4), 247-253 (2006).

D. Müller, E. Klopocki, L. E. Neumann, Stefan Mundlos, M. Taupitz, I. Schulze, Hans-Hilger Ropers, U. Querfeld, and Reinhard Ullmann, "A complex phenotype with cystic renal disease," Kidney International: Official Journal of the International Society of Nephrology 70 (9), 1656-1660 (2006).

D. Müller, E. Klopocki, L. E. Neumann, Stefan Mundlos, M. Taupitz, I. Schulze, Hans-Hilger Ropers, U. Querfeld, and Reinhard Ullmann, "A complex phenotype with cystic renal disease," Kidney International: Official Journal of the International Society of Nephrology 70 (9), 1656-1660 (2006).

T. Schwarzbraun, Reinhard Ullmann, M Schubert, M. Ledinegg, L. Ofner, C. Windpassinger, K. Wagner, P. M. Kroisel, and E. Petek, "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), 84-89 (2006).

Eva Klopocki, Britta Fiebig, Peter N. Robinson, Holger Tönnies, Fikret Erdogan, Hans-Hilger Ropers, Stefan Mundlos, and Reinhard Ullmann, "A novel 8 Mb interstitial deletion of chromosome 8p12-p21.2," American Journal of Medical Genetics Part A 140A (8), 873-877 (2006).

Masoud Garshasbi, Mohammad Mahdi Motazacker, Kimia Kahrizi, Farkhondeh Behjati, Seyedeh Sedigheh Abedini, Sahar Esmaeeli Nieh, Saghar Ghasemi Firouzabadi, Christian Becker, Franz Rüschendorf, Peter Nürnberg, Andreas Tzschach, Reza Vazifehmand, Fikret Erdogan, Reinhard Ullmann, Steffen Lenzner, Andreas W. Kuss, Hans-Hilger Ropers, and Hossein Najmabadi, "SNP array-based homozygosity mapping reveals MCPH1 deletion in family with autosomal recessive mental retardation and mild microcephaly," Human Genetics 118 (6), 708-715 (2006).

Wei Chen, Fikret Erdogan, Hans-Hilger Ropers, Steffen Lenzner, and Reinhard Ullmann, ": CGHPRO – a comprehensive data analysis tool for array CGH," BMC Bioinformatics 6 (1), 1471-2105 (2005).

Susanna Petzmann, Reinhard Ullmann, Iris Halbwedl, and Helmut H. Popper, "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), 151-159 (2004).

Reinhard Ullmann, Patrizia Morbini, Iris Halbwedl, Massimo Bongiovanni, Margit Gogg-Kammerer, Mauro Papotti, Sabine Gabor, Heiko Renner, and Helmut Hans Popper, "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), 798-807 (2004).

Elvira Stacher, Reinhard Ullmann, Iris Halbwedl, Margit Gogg-Kammerer, Liliane Boccon-Gibod, Andrew G. Nicholson, Mary N. Sheppard, Lina Carvalho, Maria Teresa Franca, Fergus MacSweeney, Alicia Morresi-Hauf, and Helmut H. Popper, "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), 565-570 (2004).

Andrea Zatkova, Reinhard Ullmann, Jean Marie Rouillard, Barbara J. Lamb, Rork Kuick, Sam M. Hanash, Susanne Schnittger, Claudia Schoch, Christa Fonatsch, and Katharina Wimmer, "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), 263-276 (2004).

Reinhard Ullmann, "Array comparative genomic hybridization in pathology", in Basic concepts of molecular pathology, edited by Philip T. Cagle and Timothy Craig Allen (Springer, New York, 2009), pp. 87-96.