Publikationen von F. Erdogan

R. Kariminejad, A. Lind-Thomsen, Z. Tumer, F. Erdogan, H. H. Ropers, N. Tommerup, R. Ullmann, and R. S. Moller, "High frequency of rare copy number variants affecting functionally related genes in patients with structural brain malformations," Hum Mutat 32 (12), 1427-35 (2011).

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).

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).

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).

Wei Chen, Vera Kalscheuer, Andreas Tzschach, Corinna Menzel, Reinhard Ullmann, Marcel Holger Schulz, Fikret Erdogan, Li Na, Zofia Kijas, Ger Arkesteijn, Isidora Lopez Pajares, Margret Goetz-Sothmann, Uwe Heinrich, Imma Rost, Andreas Dufke, Ute Grasshoff, Birgitta Glaeser, Martin Vingron, and H. Hilger Ropers, "Mapping translocation breakpoints by next-generation sequencing," Genome Research 18 (7), 1143-1149 (2008).

George Kirov, Dilihan Gumus, Wei Chen, Nadine Norton, Lyudmila Georgieva, Murat Sari, Michael C. O’Donovan, Fikret Erdogan, Michael J. Owen, Hans-Hilger Ropers, and Reinhard Ullmann, "Comparative genome hybridization suggests a role for NRXN1 and APBA2 in schizophrenia," Human Molecular Genetics 17 (3), 458-465 (2008).

Andreas Tzschach, Christina Kelbova, Sabine Weidensee, Hartmut Peters, Hans-Hilger Ropers, Reinhard Ullmann, Fikret Erdogan, Jan Jurkatis, Corinna Menzel, Vera M. Kalscheuer, and Stephanie Demuth, "Blepharophimosis-ptosis, epicanthus inversus syndrome in a girl with chromosome translocation t(2;3) (q33;q23)," Ophthalmic Genetics 29 (1), 37-40 (2008).

Joanna Walczak-Sztulpa, Marzena Wisniewska, Anna Latos-Bielenska, Maja Linné, Christina Kelbova, Britta Belitz, Lutz Pfeiffer, Vera M. Kalscheuer, Fikret Erdogan, Andreas W. Kuss, Hans-Hilger Ropers, Reinhard Ullmann, and Andreas Tzschach, "Chromosome deletions in 13q33-34: Report of four patients and review of the literature," American Journal of Medical Genetics Part A 146 (3), 337-342 (2008).

F. Erdogan, J. M. Belloso, K. D. Ajbro, M. Guitart, Hans Hilger. Ropers, N. Tommerup, Reinhard Ullmann, Z. Tümer, and L. A. Larsen, "Fine mapping of a de novo interstitial 10q22-q23 duplication in a patient with congenital heart disease and microcephaly," European Journal of Medical Genetics 51 (1), 81-86 (2008).

Andreas Tzschach, Wei Chen, Fikret Erdogan, Adelheid Hoeller, Hans-Hilger Ropers, Claudio Castellan, Reinhard Ullmann, and Albert Schinzel, "Characterization of Interstitial Xp duplications in two families by tiling path array CGH. American Journal of Medical Genetics," American Journal of Medical Genetics Part A 146A (2), 197-203 (2008).

O. Bartsch, Z. Vlccaronková, Fikret Erdogan, Reinhard Ullmann, D. Novotná, M. Spiegel, V. Beyer, Thomas Haaf, U. Zechner, and E. Seemanová, "Two independent chromosomal rearrangements, a very small (550 kb) duplication of the 7q subtelomeric region and an atypical 17q11.2 (NF1) microdeletion, in a girl with neurofibromatosis," Cytogenetic and Genome Research 119 (1 - 2), 158-64 (2007).

Reinhard Ullmann, Gillian Turner, Maria Kirchhoff, Wei Chen, Bruce Tonge, Carla Rosenberg, Michael Field, Angela M. Vianna-Morgante, Louise Christie, Ana C. Krepischi-Santos, Lynn Banna, Avril V. Brereton, Alyssa Hill, Anne-Marie Bisgaard, Ines Müller, Claus Hultschig, Fikret Erdogan, Georg Wieczorek, and Hans-Hilger Ropers, "Array CGH identifies reciprocal 16p13.1 duplications and deletions that predispose to autism and/or mental retardation," Human Mutation: Variation, Databases, and Disease 28 (7), 674-682 (2007).

Reinhard Ullmann, Gillian Turner, Maria Kirchhoff, Wei Chen, Bruce Tonge, Carla Rosenberg, Michael Field, Angela M. Vianna-Morgante, Louise Christie, Ana C. Krepischi-Santos, Lynn Banna, Avril V. Brereton, Alyssa Hill, Anne-Marie Bisgaard, Ines Müller, Claus Hultschig, Fikret Erdogan, Georg Wieczorek, and Hans-Hilger Ropers, "Array CGH identifies reciprocal 16p13.1 duplications and deletions that predispose to autism and/or mental retardation," Human Mutation: Variation, Databases, and Disease 28 (7) (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).

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).

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).

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).