Publikationen von W. Chen

H. Hu, S. A. Haas, J. Chelly, H. Van Esch, M. Raynaud, A. P. M. de Brouwer, S. Weinert, G. Froyen, S. G. M. Frints, F. Laumonnier, T. Zemojtel, M. I. Love, H. Richard, A.-K. Emde, M. Bienek, C. Jensen, M. Hambrock, U. Fischer, C. Langnick, M. Feldkamp, W. Wissink-Lindhout, N. Lebrun, L. Castelnau, J. Rucci, R. Montjean, O. Dorseuil, P. Billuart, T. Stuhlmann, M. Shaw, M. A. Corbett, A. Gardner, S. Willis-Owen, C. Tan, K. L. Friend, S. Belet, K. E. P. van Roozendaal, M. Jimenez-Pocquet, M.-P. Moizard, N. Ronce, R. Sun, S. O'Keeffe, R. Chenna, A. van Bömmel, J. Göke, A. Hackett, M. Field, L. Christie, J. Boyle, E. Haan, J. Nelson, G. Turner, G. Baynam, G. Gillessen-Kaesbach, U. Müller, D. Steinberger, B. Budny, M. Badura-Stronka, A. Latos-Bieleńska, L. B. Ousager, P. Wieacker, G. Rodríguez Criado, M.-L. Bondeson, G. Annerén, A. Dufke, M. Cohen, L. Van Maldergem, C. Vincent-Delorme, B. Echenne, B. Simon-Bouy, T. Kleefstra, M. Willemsen, J.-P. Fryns, K. Devriendt, R. Ullmann, M. Vingron, K. Wrogemann, T. F. Wienker, A. Tzschach, H. van Bokhoven, J. Gecz, T. J. Jentsch, W. Chen, H.-H. Ropers, and V. M. Kalscheuer, "X-exome sequencing of 405 unresolved families identifies seven novel intellectual disability genes," Molecular Psychiatry 21 (1), 133-148 (2016).

A. P. de Brouwer, S. B. Nabuurs, I. E. Verhaart, A. R. Oudakker, R. Hordijk, H. G. Yntema, J. M. Hordijk-Hos, K. Voesenek, B. B. de Vries, T. van Essen, W. Chen, H. Hu, J. Chelly, J. T. den Dunnen, V. M. Kalscheuer, A. M. Aartsma-Rus, B. C. Hamel, H. van Bokhoven, and T. Kleefstra, "A 3-base pair deletion, c.9711_9713del, in DMD results in intellectual disability without muscular dystrophy," European journal of human genetics 22 (4), 480-485 (2014).

Y. Wang, A. Gogol-Doring, H. Hu, S. Frohler, Y. Ma, M. Jens, J. Maaskola, Y. Murakawa, C. Quedenau, M. Landthaler, V. Kalscheuer, D. Wieczorek, Y. Wang, Y. Hu, and W. Chen, "Integrative analysis revealed the molecular mechanism underlying RBM10-mediated splicing regulation," EMBO Molecular Medicine 5 (9), 1431-1442 (2013).

M. N. Bainbridge, H. Hu, D. M. Muzny, L. Musante, J. R. Lupski, B. H. Graham, W. Chen, K. W. Gripp, K. Jenny, T. F. Wienker, Y. Yang, V. R. Sutton, R. A. Gibbs, and H. H. Ropers, "De novo truncating mutations in ASXL3 are associated with a novel clinical phenotype with similarities to Bohring-Opitz syndrome," Genome Medicine 5 (2), 5:11-5:11 (2013).

H. Hu, K. Eggers, W. Chen, M. Garshasbi, M. M. Motazacker, K. Wrogemann, K. Kahrizi, A. Tzschach, M. Hosseini, I. Bahman, T. Hucho, M. Muhlenhoff, R. Gerardy-Schahn, H. Najmabadi, H. H. Ropers, and A. W. Kuss, "ST3GAL3 mutations impair the development of higher cognitive functions," Am J Hum Genet 89 (3), 407-14 (2011).

L. R. Jensen, W. Chen, B. Moser, B. Lipkowitz, C. Schroeder, L. Musante, A. Tzschach, V. M. Kalscheuer, I. Meloni, M. Raynaud, H. van Esch, J. Chelly, A. P. de Brouwer, A. Hackett, S. van der Haar, W. Henn, J. Gecz, O. Riess, M. Bonin, R. Reinhardt, H. H. Ropers, and A. W. Kuss, "Hybridisation-based resequencing of 17 X-linked intellectual disability genes in 135 patients reveals novel mutations in ATRX, SLC6A8 and PQBP1," Eur J Hum Genet 19 (6), 717-20 (2011).

K. Kahrizi, C. H. Hu, M. Garshasbi, S. S. Abedini, S. Ghadami, R. Kariminejad, R. Ullmann, W. Chen, H. H. Ropers, A. W. Kuss, H. Najmabadi, and A. Tzschach, "Next generation sequencing in a family with autosomal recessive Kahrizi syndrome (OMIM 612713) reveals a homozygous frameshift mutation in SRD5A3," Eur J Hum Genet 19 (1), 115-7 (2011).

H. Najmabadi, H. Hu, M. Garshasbi, T. Zemojtel, S. S. Abedini, W. Chen, M. Hosseini, F. Behjati, S. Haas, P. Jamali, A. Zecha, M. Mohseni, L. Puttmann, L. N. Vahid, C. Jensen, L. A. Moheb, M. Bienek, F. Larti, I. Mueller, R. Weissmann, H. Darvish, K. Wrogemann, V. Hadavi, B. Lipkowitz, S. Esmaeeli-Nieh, D. Wieczorek, R. Kariminejad, S. G. Firouzabadi, M. Cohen, Z. Fattahi, I. Rost, F. Mojahedi, C. Hertzberg, A. Dehghan, A. Rajab, M. J. Banavandi, J. Hoffer, M. Falah, L. Musante, V. Kalscheuer, R. Ullmann, A. W. Kuss, A. Tzschach, K. Kahrizi, and H. H. Ropers, "Deep sequencing reveals 50 novel genes for recessive cognitive disorders," Nature 478 (7367), 57-63 (2011).

Kimia Kahrizi, Cougar Hao Hu, Masoud Garshasbi, Seyedeh Sedigheh Abedini, Shirin Ghadami, Roxana Kariminejad, Reinhard Ullmann, Wei Chen, Hans-Hilger Ropers, Andreas W. Kuss, Hossein Najmabadi, and Andreas Tzschach, "Next generation sequencing in a family with autosomal recessive Kahrizi syndrome (OMIM 612713) reveals a homozygous frameshift mutation in SRD5A3.," European Journal of Human Genetics 19, 115-117 (2010).

Shahaf Peleg, Farahnaz Sananbenesi, Athanasios Zovoilis, Susanne Burkhardt, Sanaz Bahari-Javan, Roberto Carlos Agis-Balboa, Perla Cota, Jessica Lee Wittnam, Andreas Gogol-Doering, Lennart Opitz, Gabriella Salinas-Riester, Markus Dettenhofer, Hui Kang, Laurent Farinelli, Wei Chen, and André Fischer, "Altered Histone Acetylation Is Associated with Age-Dependent Memory Impairment in Mice.," Science 328 (5979), 753-756 (2010).

Yuting Liu, Wenchao Hu, Haifang Wang, Minghua Lu, Chunxuan Shao, Corinna Menzel, Zheng Yan, Ying Li, Sen Zhao, Philipp Khaitovich, Mofang Liu, Wei Chen, Brian M. Barnes, and Jun Yan, "Genomic Analysis of miRNAs in an Extreme Mammalian Hibernator, the Arctic Ground Squirrel.," Physiological Genomics 42A (1), 39-51 (2010).

Soroush Sharbati, Marc R. Friedländer, Jutta Sharbati, Lena Hoeke, Wei Chen, Andreas Keller, Peer F. Stähler, Nikolaus Rajewsky, and Ralf Einspanier, "Deciphering the porcine intestinal microRNA transcriptome.," BMC Genomics 11, e275-e275 (2010).

Hao Hu, Klaus Wrogemann, Vera M. Kalscheuer, Andreas Tzschach, Hugues Richard, Stefan A. Haas, Corinna Menzel, Melanie Bienek, Guy Froyen, Martine Raynaud, Hans Van Bokhoven, Jamel Chelly, Hans-Hilger Ropers, and Wei Chen, "Erratum to: Mutation screening in 86 known X-linked mental retardation genes by droplet-based multiplex PCR and massive parallel sequencing.," The Hugo Journal 3 (1-4), 83-83 (2010).

Ivana Grabundzija, Markus Irgang, Lajos Mátés Lajos Mátés, Eyayu Belay, Janka Matrai, Andreas Gogol-Döring, Koichi Kawakami, Wei Chen, Patricia Ruiz, Marinee K. L. Chuah, Thierry VandenDriessche, Zsuzsanna Izsvák, and Zoltán Ivics, "Comparative Analysis of Transposable Element Vector Systems in Human Cells.," Molecular Therapy: the Journal of the American Society of Gene Therapy 18 (6), 1200-1209 (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).

Marlon Stoeckius, Jonas Maaskola, Teresa Colombo, Hans-Peter Rahn, Marc R. Friedländer, Na Li, Wei Chen, Fabio Piano, and Nikolaus Rajewsky, "Large-scale sorting of C. elegans embryos reveals the dynamics of small RNA expression," Nature Methods 6, 745-751 (2009).

Hai Yang Hu, Zheng Yan, Ying Xu, Hao Hu, Corinna Menzel, Yan Hong Zhou, Wei Chen, and Philipp Khaitovich, "Sequence features associated with microRNA strand selection in humans and flies," BMC Genomics 10, 413-413 (2009).

Xing Fu, Ning Fu, Song Guo, Zheng Yan, Ying Xu, Hao Hu, Corinna Menzel, Wei Chen, Yixue Li, Rong Zeng, and Philipp Khaitovich, "Estimating accuracy of RNA-Seq and microarrays with proteomics," BMC Genomics 10, 161-161 (2009).

Christine Ender, Azra Krek, Marc R. Friedländer, Michaela Beitzinger, Lasse Weinmann, Wei Chen, Sébastien Pfeffer, Nikolaus Rajewsky, and Gunter Meister, "A human snoRNA with microRNA-like functions," Molecular Cell 32 (4), 519-528 (2008).

F Erdogan, L A Larsen, L Zhang, Z Tümer, N Tommerup, Wei Chen, J R Jacobsen, M Schubert, J Jurkatis, Andreas Tzschach, Hans Hilger Ropers, and Reinhard Ullmann, "High frequency of submicroscopic genomic aberrations detected by tiling path array CGH in patients with isolated congenital heart disease," Journal of Medical Genetics 11, 705-709 (2008).