Publikationen von Bernd Timmermann

Florian Mertes, Björn Lichtner, Heiner Kuhl, Mirjam Blattner , Jörg Otte, Wasco Wruck, Bernd Timmermann, Hans Lehrach, and James Adjaye, "Combined ultra-low input mRNA and whole-genome sequencing of human embryonic stem cells," BMC Genomics 16, 16:925 (2015).

Imke Satzger, Lena Marks, Martin Kerick, Sven Klages, Carola Berking, Rudolf Herbst, Bernward Völker, Vivien Schacht, Bernd Timmermann, and Ralf Gutzmer, "Allele frequencies of BRAFV600 mutations in primary melanomas and matched metastases and their relevance for BRAF inhibitor therapy in metastatic melanoma," Oncotarget 2015, 5634 (2015).

Peter H. Sudmant, Tobias Rausch, Eugene J. Gardner, Robert E. Handsaker, Alexej Abyzov, John Huddleston, The 1000 Genomes Project Consortium, Bernd Timmermann, Ralf Herwig, and Hans Lehrach, "An integrated map of structural variation in 2,504 human genomes," Nature 526 (7571), 75-81 (2015).

The 1000 Genome Project Consortium, Hans Lehrach, Vyacheslav Amstislavskiy, Matthias Lienhard, Florian Mertes, Marc Sultan, Bernd Timmermann, Marie-Laure Yaspo, and Ralf Herwig, "A global reference for human genetic variation," Nature 526 (7571), 68-74 (2015).

Sandra Milena Bernal Ulloa, Julia Heinzmann, Doris Herrmann, Bernd Timmermann, Ulrich Baulain, Rudolf Großfeld, Mike Diederich, Andrea Lucas-Hahn, and Heiner Niemann, "Effects of different oocyte retrieval and in vitro maturation systems on bovine embryo development and quality," Zygote 23 (3), 367-377 (2015).

Darío G. Lupiáñez, Katerina Kraft, Verena Heinrich, Peter Krawitz, Francesco Brancati, Eva Klopocki, Denise Horn, Hülya Kayserili, John M. Opitz, Renata Laxova, Fernando Santos-Simarro, Brigitte Gilbert-Dussardier, Lars Wittler, Marina Borschiwer, Stefan A. Haas, Marco Osterwalder, Martin Franke, Bernd Timmermann, Jochen Hecht, Malte Spielmann, Axel Visel, and Stefan Mundlos, "Disruptions of Topological Chromatin Domains Cause Pathogenic Rewiring of Gene-Enhancer Interactions," Cell 161 (5), 1012-1025 (2015).

Reinhard Seifert, Melanie Flick, Wolfgang Bönigk, Luis Alvarez, Christian Trötschel, Ansgar Poetsch, Astrid Müller, Normann Goodwin, Patric Pelzer, Nachiket D. Kashikar, Elisabeth Kremmer, Jan Jikeli, Bernd Timmermann, Heiner Kuhl, Dmitry Fridman, Florian Windler, U. Benjamin Kaupp, and Timo Strünker, "The CatSper channel controls chemosensation in sea urchin sperm," EMBO Journal 34 (3), 379-392 (2015).

Carolina Frankl-Vilches, Heiner Kuhl, Martin Werber, Sven Klages, Martin Kerick, Antje Bakker, Edivaldo H. C. de Oliveira, Christina Reusch, Floriana Capuano, Jakob Vowinckel, Stefan Leitner, Markus Ralser, Bernd Timmermann, and Manfred Gahr, "Using the canary genome to decipher the evolution of hormone-sensitive gene regulation in seasonal singing birds," Genome Biology: Biology for the Post-Genomic Era 16 (1), 16:19 (2015).

Thomas Willems, Melissa Gymrek, Gareth Highnam, Consortium The 1000 Genomes Project, Ralf Herwig, Hans Lehrach, Ralf Sudbrak, Bernd Timmermann, David Mittelman, and Yaniv Erlich, "The landscape of human STR variation," Genome Research 24 (11), 1894-1904 (2014).

P. M. Krawitz, D. Schiska, U. Krüger, S. Appelt, V. Heinrich, D. Parkhomchuk, B. Timmermann, J. M. Millan, P. N. Robinson, S. Mundlos, J. Hecht, and M. Gross, "Screening for single nucleotide variants, small indels and exon deletions with a next-generation sequencing based gene panel approach for Usher syndrome," Molecular Genetics and Genomic Medicine 2 (5), 393-401 (2014).

V. Colonna, Q. Ayub, Y. Chen, L. Pagani, P. Luisi, M. Pybus, E. Garrison, Y. Xue, C. Tyler-Smith, Consortium 1000 Genomes Project, R. Sudbrak, M. Albrecht, V. Amstislavskiy, T. A. Borodina, A. Dahl, A. Davydov, R. Herwig, P. Marquardt, F. Mertes, W. Nietfeld, D. Parkhomchuk, A. V. Soldatov, B. Timmermann, M. Tolzmann, H. Lehrach, and M. L. Yaspo, "Human genomic regions with exceptionally high levels of population differentiation identified from 911 whole-genome sequences," Genome Biology: Biology for the Post-Genomic Era 15 (6), R88 (2014).

Marcel Grunert, Cornelia Dorn, Markus Schueler, Ilona Dunkel, Jenny Schlesinger, Siegrun Mebus, Vladimir Alexi-Meskishvili, Andreas Perrot, Katharina Wassilew, Bernd Timmermann, Roland Hetzer, Felix Berger, and Silke R. Sperling, "Rare and Private Variations in Neural Crest, Apoptosis and Sarcomere Genes Define the Polygenic Background of Isolated Tetralogy of Fallot," Human Molecular Genetics 23 (12), 3115-3128 (2014).

O. Delaneau, J. Marchini, Consortium 1000 Genomes Project, H. Lehrach, R. Sudbrak, V. S. Amstislavskiy, M. Lienhard, F. Mertes, M. Sultan, B. Timmermann, M. L. Yaspo, and R. Herwig, "Integrating sequence and array data to create an improved 1000 Genomes Project haplotype reference panel," Nature Communications 5, 5:3934 (2014).

M. Draaken, F. Baudisch, B. Timmermann, H. Kuhl, M. Kerick, J. Proske, L. Wittler, T. Pennimpede, A. K. Ebert, W. Rösch, R. Stein, E. Bartels, C. von Lowtzow, T. M. Boemers, S. Herms, J. P. Gearhart, Y. Lakshmanan, C. C. Kockum, G. Holmdahl, G. Läckgren, A. Nordenskjöld, S. A. Boyadjiev, B. G. Herrmann, M. M. Nöthen, M. Ludwig, and H. Reutter, "Classic bladder exstrophy: Frequent 22q11.21 duplications and definition of a 414 kb phenocritical region," Birth Defects Research Part A: Clinical and Molecular Teratology 100 (6), 512-517 (2014).

Martin Werber, Lars Wittler, Bernd Timmermann, Phillip Grote, and Bernhard G. Herrmann, "The tissue-specific transcriptomic landscape of the mid-gestational mouse embryo," Development 141 (11), 2325-2330 (2014).

M. Hussong, S. Börno, M. Kerick, A. Wunderlich, A. Franz, H. Sültmann, B. Timmermann, H. Lehrach, M. Hirsch-Kauffmann, and M. R. Schweiger, "The bromodomain protein BRD4 regulates the KEAP1/NRF2-dependent oxidative stress response," Cell Death and Disease 5, 5:e1195 (2014).

M. Hussong, S. T. Börno, M. Kerick, A. Wunderlich, A. Franz, H. Sültmann, B. Timmermann, H. Lehrach, M. Hirsch-Kauffmann, and M. R. Schweiger, "The bromodomain protein BRD4 regulates the KEAP1/NRF2 dependent oxidative stress response," Cell Death and Disease 2014 (5), e1195 (2014).

Alexej Abyzov, Rebecca Iskow, Omer Gokcumen, David W. Radke, Suganthi Balasubramanian, Baikang Pei, Lukas Habegger, Consortium 1000 Genomes Project, Bernd Timmermann, Charles Lee, and Mark Gerstein, "Analysis of variable retroduplications in human populations suggests coupling of retrotransposition to cell division," Genome Research 23 (12), 2042-2052 (2013).

Daniel Ibrahim, Peter Hansen, Christian Rödelsperger, Asita C. Stiege, Sandra C. Doelken, Denise Horn, Marten Jäger, Catrin Janetzki, Peter Krawitz, Gundula Leschik, Florian Wagner, Till Scheuer, Mareen Schmidt-von Kegler, Petra Seemann, Bernd Timmermann, Peter N. Robinson, Stefan Mundlos, and Jochen Hecht, "Distinct global shifts in genomic binding profiles of limb malformation associated HOXD13 mutations," Genome Research 23 (12), 2091-2102 (2013).

E. Khurana, Y. Fu, V. Colonna, X. J. Mu, H. M. Kang, T. Lappalainen, A. Sboner, L. Lochovsky, J. Chen, A. Harmanci, J. Das, A. Abyzov, S. Balasubramanian, K. Beal, D. Chakravarty, D. Challis, Y. Chen, D. Clarke, L. Clarke, F. Cunningham, U. S. Evani, P. Flicek, R. Fragoza, E. Garrison, R. Gibbs, Z. H. Gumus, J. Herrero, N. Kitabayashi, Y. Kong, K. Lage, V. Liluashvili, S. M. Lipkin, D. G. MacArthur, G. Marth, D. Muzny, T. H. Pers, G. R. Ritchie, J. A. Rosenfeld, C. Sisu, X. Wei, M. Wilson, Y. Xue, F. Yu, Consortium 1000 Genomes Project, H. Lehrach, R. Sudbrak, M. W. Albrecht, V. Amstislavskiy, T. A. Borodina, M. Lienhard, F. Mertes, M. Sultan, B. Timmermann, M. L. Yaspo, E. T. Dermitzakis, H. Yu, M. A. Rubin, C. Tyler-Smith, and M. Gerstein, "Integrative annotation of variants from 1092 humans: application to cancer genomics," Science 342 (6154), 1235587-1235587 (2013).