Publikationen von Wei Chen

Andreas Walter Kuss and Wei Chen, "MicroRNAs in brain function and disease," Current Neurology and Neuroscience Reports 8 (3), 190-197 (2008).

Marc R Friedländer, Wei Chen, Catherine Adamidi, Jonas Maaskola, Ralf Einspanier, Signe Knespel, and Nikolaus Rajewsky, "Discovering microRNAs from deep sequencing data using miRDeep," Nature Biotechnology 26 (4), 407-415 (2008).

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).

Ingrid E. Scheffer, Samantha J. Turner, Leanne M. Dibbens, Marta A. Bayly, Kathryn Friend, Bree Hodgson, Linda Burrows, Marie Shaw, Wei Chen, Reinhard Ullmann, Hans-Hilger Ropers, Pierre Szepetowski, Eric Haan, Aziz Mazarib, Zaid Afawi, Miriam Y. Neufeld, P. Ian Andrews, Geoffrey Wallace, Sara Kivity, Dorit Lev, Tally Lerman-Sagie, Christopher P. Derry, Amos D. Korczyn, Jozef Gecz, John C. Mulley, and Samuel F. Berkovic, "Epilepsy and mental retardation limited to females: an under-recognized disorder," Brain 131 (4), 918-927 (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).

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).

Wei Chen, Lars R Jensen, Jozef Gecz, Jean-Pierre Fryns, Claude Moraine, Arjan de Brouwer, Jamel Chelly, Bettina Moser, Hans-Hilger Ropers, and Andreas W. Kuss, "Mutation screening of brain-expressed X-chromosomal miRNA genes in 464 patients with nonsyndromic X-linked mental retardation," European Journal of Human Genetics: EJHG ; the Official Journal of the European Society of Human Genetics 15 (3), 375-378 (2007).

Wei Chen, Lars R Jensen, Jozef Gecz, Jean-Pierre Fryns, Claude Moraine, Arjan de Brouwer, Jamel Chelly, Bettina Moser, Hans-Hilger Ropers, and Andreas W. Kuss, "Mutation screening of brain-expressed X-chromosomal miRNA genes in 464 patients with nonsyndromic X-linked mental retardation," European Journal of Human Genetics: EJHG ; the Official Journal of the European Society of Human Genetics 15 (3), 375-378 (2007).

Hossein Najmabadi, Mohammad Mahdi Motazacker, Masoud Garshasbi, Kimia Kahrizi, Andreas Tzschach, Wei Chen, Farkhondeh Behjati, Valeh Hadavi, Sahar Esmaeeli Nieh, Seyedeh Sedigheh Abedini, Reza Vazifehmand, Saghar Ghasemi Firouzabadi, Payman Jamali, Masoumeh Falah, Seyed Morteza Seifati, Annette Grüters, Steffen Lenzner, Lars R. Jensen, Franz Rüschendorf, Andreas W. Kuss, and Hans-Hilger Ropers, "Homozygosity mapping in consanguineous families reveals extreme heterogeneity of non-syndromic autosomal recessive mental retardation and identifies 8 novel gene loci.," Human Genetics 121 (1), 43-48 (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).

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).

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).

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).

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).

Wei Chen, Development and application of CGHPRO, a novel software package for retrieving, handling and analysing array CGH data, PhD Thesis, Freie Universität, 2006.