Publikationen von Andreas Tzschach

Fikret Erdogan, Reinhard Ullmann, Wei Chen, Marei Schubert, Sabine Adolph, Claus Hultschig, Vera M. Kalscheuer, Hans-Hilger Ropers, Christiane Spaich, and Andreas Tzschach, "Characterization of a 5.3 Mb deletion in 15q14 by Comparative Genomic Hybridization using a whole genome ”tiling path” BAC array in a girl with heart defect, cleft palate and developmental delay.," American Journal of Medical Genetics Part A 143 (2), 172-178 (2007).

Fikret Erdogan, Reinhard Ullmann, Wei Chen, Marei Schubert, Sabine Adolph, Claus Hultschig, Vera M. Kalscheuer, Hans-Hilger Ropers, Christiane Spaich, and Andreas Tzschach, "Characterization of a 5.3 Mb deletion in 15q14 by Comparative Genomic Hybridization using a whole genome ”tiling path” BAC array in a girl with heart defect, cleft palate and developmental delay.," American Journal of Medical Genetics Part A 143 (2), 172-178 (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).

Arjan P.M. de Brouwer, Helger G. Yntema, Tjitske Kleefstra, Dorien Lugtenberg, Astrid R. Oudakker, Bert B. A. de Vries, Hans van Bokhoven, Hilde van Esch, Suzanne G. M. Frints, Guy Froyen, Jean-Pierre Fryns, Martine Raynaud, Marie-Pierre Moizard, Nathalie Ronce, Anissa Bensalem, Claude Moraine, Karine Poirier, Laetitia Castelnau, Yoann Saillour, Thierry Bienvenu, Chérif Beldjord, Vincent des Portes, Jamel Chelly, Gillian Turner, Tod Fullston, Jozef Gecz, Andreas W. Kuss, Andreas Tzschach, Lars Riff Jensen, Steffen Lenzner, Vera M. Kalscheuer, Hans-Hilger Ropers, and Ben C.J. Hamel, "Mutation frequencies of X-linked mental retardation genes in families from the EuroMRX consortium," Human Mutation 28 (2), 207-208 (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).

Lars Riff Jensen, Steffen Lenzner, Bettina Mose, Kristine Freude, Andreas Tzschach, Wei Chen, Jean-Pierre Fryns, Jamel Chelly, Gillian Turner, Claude Moraine, Ben Hamel, Hans-Hilger Ropers, and Andreas walter Kuss, "X-linked mental retardation: a comprehensive molecular screen of 47 candidate genes from a 7.4 Mb interval in Xp11," European Journal of Human Genetics: EJHG ; the Official Journal of the European Society of Human Genetics 15 (1), 68-75 (2007).

Lars Riff Jensen, Steffen Lenzner, Bettina Mose, Kristine Freude, Andreas Tzschach, Wei Chen, Jean-Pierre Fryns, Jamel Chelly, Gillian Turner, Claude Moraine, Ben Hamel, Hans-Hilger Ropers, and Andreas walter Kuss, "X-linked mental retardation: a comprehensive molecular screen of 47 candidate genes from a 7.4 Mb interval in Xp11," European Journal of Human Genetics: EJHG ; the Official Journal of the European Society of Human Genetics 15 (1), 68-75 (2007).

Andreas Tzschach and Hans-Hilger Ropers, "Genetik der mentalen Retardierung.," Deutsches Ärzteblatt: Ärztliche Mitteilungen/Ausgabe A, Praxis-Ausgabe: Niedergelassene Ärzte 20 A, 1400-1405 (2007).

Andreas Tzschach, Maria Hoeltzenbein, Kirsten Hoffmann, Corinna Menzel, Alexander Beyer, Volker Ocker, Goetz Wurster, Martine Raynaud, Hans-Hilger Ropers, and Vear M. Kalscheuer, "Heterotaxy and cardiac defect in a girl with chromosome translocation t(X;1)(q26;p13.1) and involvement of ZIC3," European Journal of Human Genetics: EJHG ; the Official Journal of the European Society of Human Genetics 14 (12), 1317-1320 (2006).

Bartlomiej Budny, Wei Chen, Heymut Omran, Manfred Fliegauf, Andreas Tzschach, Marzena Wisniewska, Lars R. Jensen, Martine Raynaud, Sarah A. Shoichet, Magda Badura, Steffen Lenzner, Anna Latos-Bielenska, and Hans-Hilger Ropers, "A novel X-linked recessive mental retardation syndrome comprising macrocephaly and ciliary dysfunction is allelic to oral-facial-digital type I syndrome," Human Genetics 120 (2), 171-178 (2006).

Andreas Tzschach, Ines Krause-Plonka, Corinna Menzel, Andreas Knoblauch, Holger Toennies, Maria Hoeltzenbein, Michael Radke, Hans-Hilger Ropers, and Vera M. Kalscheuer, "Molecular cytogenetic analysis of a de novo interstitial chromosome 10q22 deletion," American Journal of Medical Genetics Part A 140 (10), 1108-1110 (2006).

Andreas Tzschach, Steffen Lenzner, Bettina Moser, Richard Reinhardt, Jamel Chelly, Jean-Pierre Fryns, Tjitske Kleefstra, Martine Raynaud, Gillian Turner, Hans-Hilger Ropers, Andreas Kuss, and Lars Riff Jensen, "Novel JARID1C/SMCX mutations in patients with X-linked mental retardation," Human Mutation 27 (4), 389-389 (2006).

Andreas Tzschach, Steffen Lenzner, Bettina Moser, Richard Reinhardt, Jamel Chelly, Jean-Pierre Fryns, Tjitske Kleefstra, Martine Raynaud, Gillian Turner, Hans-Hilger Ropers, Andreas Kuss, and Lars Riff Jensen, "Novel JARID1C/SMCX mutations in patients with X-linked mental retardation," Human Mutation 27 (4), 389-389 (2006).

Kai-Lin Yan, Xue-Jun Zhang, Zhi-Min Wang, Sen Yang, Guo-Long Zhang, Jian Wang, Feng-Li Xiao, Min Gao, Yong Cui, Jian-Jun Chen, Xing Fan, Liang-Dan Sun, Qing Xia, Kai-Yue Zhang, Zhen-Min Niu, Shi-Jie Xu, Andreas Tzschach, Hans-Hilger Ropers, Wei Huang, and Jian-Jun Liu, "A novel MGST2 non-synonymous mutation in a Chinese pedigree with psoriasis vulgaris," The Journal of Investigative Dermatology: Official Journal of the Society for Investigative Dermatology and the European Society for Dermatological Research 126 (5), 1003-1005 (2006).

Andreas Tzschach, Ines Krause-Plonka, Corinna Menzel, Vera M. Kalscheuer, Holger Toennies, Harry Scherthan, Andreas Knoblauch, Michael Radke, Hans-Hilger Ropes, and Maria Hoeltzenbein, "Molecular cytogenetic analysis of a de novo interstitial deletion 5q23.3q31.2 and its phenotypic consequences," American Journal of Medical Genetics 140 (5), 496-502 (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).

Andreas Tzschach and Hans-Hilger Ropers, "X-chromosomale Retardierung," Medizinische Genetik: : Mitteilungsblatt des Berufsverbandes Medizinische Genetik e.V. 2, 187-193 (2006).

Lars Riff Jensen, Marion Amende, Ulf Gurok, Bettina Moser, Verena Gimme, Andreas Tzschach, Andreas R. Janecke, Gholamali Tariverdian, Jamel Chelly, Jean-Pierre Fryns, Hilde Van Esch, Tjitske Kleefstra, Ben Hame, Claude Moraine, Jozef Gécz, Gillian Turner, Richard Reinhardt, Vera M. Kalscheuer, Hans-Hilger Ropers, and Steffen Lenzner, ": 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), 227-236 (2005).

Lars Riff Jensen, Marion Amende, Ulf Gurok, Bettina Moser, Verena Gimme, Andreas Tzschach, Andreas R. Janecke, Gholamali Tariverdian, Jamel Chelly, Jean-Pierre Fryns, Hilde Van Esch, Tjitske Kleefstra, Ben Hame, Claude Moraine, Jozef Gécz, Gillian Turner, Richard Reinhardt, Vera M. Kalscheuer, Hans-Hilger Ropers, and Steffen Lenzner, ": 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), 227-236 (2005).

Vera M. Kalscheuer, Kristine Freude, Luciana Musante, Lars R. Jensen, Helger G. Yntema, Jozef Gecz, Abdelaziz Sefiani, Kirsten Hoffmann, Bettina Moser, Stefan Haas, Ulf Gurok, Sebastian Haesler, Beatriz Aranda, Arpik Nshedjan, Andreas Tzschach, Nils Hartmann, Tim-Christoph Roloff, Sarah Shoichet, Olivier Hagens, Jiong Tao, Hans van Bokhoven, Gillian Turner, Jamel Chelly, Claude Moraine, Jean-Pierre Fryns, Ulrike Nuber, Maria Hoeltzenbein, Constance Scharff, Harry Scherthan, Steffen Lenzner, Ben C. J. Hamel, Susann Schweiger, and Hans-Hilger Ropers, "Mutations in the polyglutamine binding protein 1 gene cause X-linked mental retardation," Nature Genetics 35 (4), 313-315 (2003).