Publikationen von Reinhard Ullmann

S. Jakubiczka, C. Schröder, Reinhard Ullmann, M. Volleth, S. Ledig, E. Gilberg, P. Kroisel, and P. P. Wieacker, "Translocation and Deletion around SOX9 in a Patient with Acampomelic Campomelic Dysplasia and Sex Reversal.," Sexual Development: Genetics, Molecular Biology, Evolution, Endocrinology, Embryology, and Pathology of Sex Determination and Differentiation 4 (3), 143-149 (2010).

Andreas Tzschach, Corinna Menzel, Fikret Erdogan, Erman Salih Istifli, Martin Rieger, Angela Ovens-Raeder, Alfons Macke, Hans-Hilger Ropers, Reinhard Ullmann, and Vera M. Kalscheuer, "Characterization of an interstitial 4q32 deletion in a patient with mental retardation and a complex chromosome rearrangement.," American Journal of Medical Genetics. Part A. 152A (4), 1008-1012 (2010).

K.-P. Lesch, S. Selch, T. J. Renner, C. Jacob, T. T. Nguyen, T. Hahn, M. Romanos, S. Walitza, S. Shoichet, A. Dempfle, M. Heine, A. Boreatti-Hümmer, J. Romanos, S. Gross-Lesch, H. Zerlaut, T. Wultsch, S. Heinzel, M. Fassnacht, A. Fallgatter, B. Allolio, H. Schäfer, A. A Warnke, A . Reif, Hans-Hilger Ropers, and Reinhard Ullmann, "Genome-wide copy number variation analysis in attention-deficit/hyperactivity disorder: association with neuropeptide Y gene dosage in an extended pedigree1," Molecular Psychiatry , 1-13 (2010).

Andreas Tzschach, Anne-Marie Bisgaard, Maria Kirchhoff, Luitgard M. Graul-Neumann, Heidemarie Neitzel, Stephanie Page, Alischo Ahmed, Ines Müller, Fikret Erdogan, Hans-Hilger Ropers, Vera M. Kalscheuer, and Reinhard Ullmann, "Chromosome aberrations involving 10q22: report of three overlapping interstitial deletions and a balanced translocation disrupting C10orf11.," European Journal of Human Genetics: EJHG 18 (3), 291-295 (2010).

Andreas Tzschach, Anne-Marie Bisgaard, Maria Kirchhoff, Luitgard M. Graul-Neumann, Heidemarie Neitzel, Stephanie Page, Alischo Ahmed, Ines Müller, Fikret Erdogan, Hans-Hilger Ropers, Vera M. Kalscheuer, and Reinhard Ullmann, "Chromosome aberrations involving 10q22: report of three overlapping interstitial deletions and a balanced translocation disrupting C10orf11.," European Journal of Human Genetics: EJHG 18 (3), 291-295 (2010).

Vivien Boldt, Elvira Stacher, Iris Halbwedl, Helmut Popper, Claus Hultschig, Farid Moinfar, Reinhard Ullmann, and Fattaneh A. Tavassoli, "Positioning of necrotic lobular intraepithelial neoplasias (LIN, grade3) within the sequence of breast carcinoma progression.," Genes Chromosomes Cancer 49 (5), 463-470 (2010).

Vivien Boldt, Elvira Stacher, Iris Halbwedl, Helmut Popper, Claus Hultschig, Farid Moinfar, Reinhard Ullmann, and Fattaneh A. Tavassoli, "Positioning of necrotic lobular intraepithelial neoplasias (LIN, grade3) within the sequence of breast carcinoma progression.," Genes Chromosomes Cancer 49 (5), 463-470 (2010).

Dorien Lugtenberg, Luiz Zangrande-Vieira, Maria Kirchhoff, Annabel C. Whibley, Astrid R. Oudakker, Susanne Kjaergaard, Angela M. Vianna-Morgante, Tjitske Kleefstra, Mariken Ruiter, Fernanda S. Jehee, Reinhard Ullmann, Charles E. Schwartz, Michael Stratton, F. Lucy Raymond, Joris A. Veltman, Terry Vrijenhoek, Rolph Pfundt, Janneke H.M. Schuurs-Hoeijmakers, Jayne Y. Hehir-Kwa, Guy Froyen, Jamel Chelly, Hans-Hilger Ropers, Claude Moraine, Jozef Gècz, Jeroen Knijnenburg, Sarina G. Kant, Ben C.J. Hamel, Carla Rosenberg, Hans van Bokhoven, and Arjan P.M. de Brouwer, "Recurrent deletion of ZNF630 at Xp11.23 is not associated with mental retardation.," American Journal of Medical Genetics. Part A. 152A (3), 638-645 (2010).

Andishe Attarbaschi, Markus Pisecker, Andrea Inthal, Georg Mann, Dasa Janousek, Michael Dworzak, Ulrike Pötschger, Reinhard Ullmann, Martin Schrappe, Helmut Gadner, Oskar A. Haas, Renate Panzer-Grümayer, and Sabine Strehl, "Prognostic relevance of TLX3 (HOX11L2) expression in childhood T-cell acute lymphoblastic leukaemia treated with Berlin–Frankfurt–Münster (BFM) protocols containing early and late re-intensification elements," British Journal of Hematology 148 (2), 293-300 (2010).

Wei Chen, Reinhard Ullmann, Claudia Langnick, Corinna Menzel, Zofia Wotschofsky, Hao Hu, Andreas Döring, Yuhui Hu, Hui Kang, Andreas Tzschach, Maria Hoeltzenbein, Heidemarie Neitzel, Susanne Markus, Eberhard Wiedersberg, Gerd Kistner, Conny M. A. van Ravenswaaij-Arts, Tjitske Kleefstra, Vera M. Kalscheuer, and Hans-Hilger Ropers, "Breakpoint analysis of balanced chromosome rearrangements by next-generation paired-end sequencing," European Journal of Human Genetics (2010).

Jennifer Haensel, Nicolai Kohlschmidt, Susanne Pitz, Annerose Keilmann, Martin Zenker, Reinhard Ullmann, Thomas Haaf, and Oliver Bartsch, "Case report supporting that the Barber-Say and ablepharon macrostomia syndromes could represent one disorder," American Journal of Medical Genetics Part A 149 (10), 2236-2240 (2009).

Yvonne Hilhorst-Hofstee, Zeynep Tümer, Peter Born, Jeroen Knijnenburg, Kerstin Hansson, Vindhya Yatawara, Jesper Steensberg, Reinhard Ullmann, Ger Arkesteijn, Niels Tommerup, and Lars Allan Larsen, "Molecular characterization of two patients with de novo interstitial deletions in 4q22-q24," American Journal of Medical Genetics Part A 149 (8), 1830-1833 (2009).

Juliane Najm, Denise Horn, Isabella Wimplinger, Jeffrey A. Golden, Victor V. Chizhikov, Jyotsna Sudi, Susan L. Christian, Reinhard Ullmann, Alma Kuechler, Carola A. Haas, Armin Flubacher, Lawrence R. Charnas, Gökhan Uyanik, Ulrich Frank, Eva Klopocki, William B. Dobyns, and Kerstin Kutsche, "Mutations of CASK cause an X-linked brain malformation phenotype with microcephaly and hypoplasia of the brainstem and cerebellum," Nature Genetics 40 (9), 1065-1067 (2009).

Litu Zhang, Zeynep Tümer, Kjeld Møllgård, Gotthold Barbi, Eva Rossier, Eske Bendsen, Rikke Steensbjerre Møller, Reinhard Ullmann, Jian He, Nickolas Papadopoulos, Niels Tommerup, and Lars Allan Larsen, "Characterization of a t(5;8)(q31;q21) translocation in a patient with mental retardation and congenital heart disease: implications for involvement of RUNX1T1 in human brain and heart development," European Journal of Human Genetics 17 (8), 1010-1018 (2009).

Ariana Kariminejad, Roxana Kariminejad, Andreas Tzschach, Reinhard Ullmann, Alisho Ahmed, Alaleh Asghari-Roodsari, Shadab Salehpour, Fariba Afroozan, Hans-Hilger Ropers, and Mohammad Hasan Kariminejad, "Craniosynostosis in a patient with 2q37.3 deletion 5q34 duplication: Association of extra copy of MSX2 with craniosynostosis," American Journal of Medical Genetics Part A 149 (7), 1544-1549 (2009).

Klemens Raile, Eva Klopocki, Martin Holder, Theda Wessel, Angela Galler, Dorothee Deiss, Dominik Müller, Thomas Riebel, Denise Horn, Monika Maringa, Jürgen Weber, Reinhard Ullmann, and Annette Grüters, "Expanded clinical spectrum in hepatocyte nuclear factor 1B-maturity-onset diabetes of the young," Journal of Clinical Endocrinology & Metabolism 94 (7), 2658-2664 (2009).

Sarah A Shoichet, Stefan Waibel, Sonja Endruhn, Anne D. Sperfeld, Brita Vorwerk, Ines Mümlller, Fikret Erdogan, Albert C. Ludolph, Hans-Hilger Ropers, and Reinhard Ullmann, "Identification of candidate genes for sporadic amyotrophic lateral sclerosis by array comparative genomic hybridization," Amyotrophic Lateral Sclerosis 10 (3), 162-169 (2009).

A. Tzschach, C. Ramel, A. Kron, B. Seipel, C. Wüster, U. Cordes, T. Liehr, M. Hoeltzenbein, C. Menzel, H.-H. Ropers, R. Ullmann, V. Kalscheuer, J. Decker, and D. Steinberger, "Hypergonadotropic hypogonadism in a patient with inv ins (2;4)," International Journal of Andrology 32 (3), 226-230 (2009).

Andrea Zatkova, Sylvia Merk, Melanie Wendehack, Martin Bilban, Eva Maria Muzik, Artur Muradyan, Claudia Haferlach, Torsten Haferlach, Katharina Wimmer, Christa Fonatsch, and Reinhard Ullmann, "AML/MDS with 11q/MLL amplification show characteristic gene expression signature and interplay of DNA copy number changes," Genes, Chromosomes and Cancer 48 (6), 510-520 (2009).

Andreas Tzschach, Luitgard M. Graul-Neumann, Kateryna Konrat, Reyk Richter, Grit Ebert, Reinhard Ullmann, and Heidemarie Neitzel, "Interstitial deletion 2p11.2-p12: Report of a patient with mental retardation and review of the literature," American Journal of Medical Genetics Part A 149 (2), 242-245 (2009).