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Bernd Timmermann
Researcher at Max Planck Society
Publications - 161
Citations - 27435
Bernd Timmermann is an academic researcher from Max Planck Society. The author has contributed to research in topics: Gene & Genome. The author has an hindex of 45, co-authored 146 publications receiving 19299 citations. Previous affiliations of Bernd Timmermann include Max Delbrück Center for Molecular Medicine & University of Bergen.
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Journal ArticleDOI
Homeotic arm-to-leg transformation associated with genomic rearrangements at the PITX1 locus
Malte Spielmann,Francesco Brancati,Francesco Brancati,Peter Krawitz,Peter N. Robinson,Daniel M. Ibrahim,Daniel M. Ibrahim,Martin Franke,Jochen Hecht,Silke Lohan,Silke Lohan,Katarina Dathe,Anna Maria Nardone,Paola Ferrari,A. Landi,Lars Wittler,Bernd Timmermann,Danny Chan,Ulrich Mennen,Eva Klopocki,Stefan Mundlos,Stefan Mundlos +21 more
TL;DR: It is shown that Liebenberg syndrome, an autosomal-dominant upper-limb malformation, shows features of a homeotic limb transformation in which the arms have acquired morphological characteristics of a leg.
Journal ArticleDOI
Genome-wide tracking of dCas9-methyltransferase footprints
Christina Galonska,Jocelyn Charlton,Jocelyn Charlton,Alexandra L. Mattei,Alexandra L. Mattei,Alexandra L. Mattei,Julie Donaghey,Kendell Clement,Kendell Clement,Hongcang Gu,Arman W. Mohammad,Elena K. Stamenova,Davide Cacchiarelli,Sven Klages,Bernd Timmermann,Tobias Cantz,Hans R. Schöler,Andreas Gnirke,Michael J. Ziller,Alexander Meissner,Alexander Meissner,Alexander Meissner +21 more
TL;DR: The generation and use of an engineered, methylation depleted but maintenance competent mouse ES cell line is reported and a surprisingly ubiquitous nuclear activity of dCas9-methyltransferases is found, finding ubiquitous off-target activity within a highly methylated genome.
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Iranome: A catalog of genomic variations in the Iranian population.
Zohreh Fattahi,Maryam Beheshtian,Marzieh Mohseni,Hossein Poustchi,Erin Sellars,Sayyed Hossein Nezhadi,Amir Amini,Sanaz Arzhangi,Khadijeh Jalalvand,Peyman Jamali,Zahra Mohammadi,Behzad Davarnia,Pooneh Nikuei,Morteza Oladnabi,Akbar Mohammadzadeh,Elham Zohrehvand,Azim Nejatizadeh,Mohammad Shekari,Maryam Bagherzadeh,Ehsan Shamsi-Gooshki,Stefan T. Börno,Bernd Timmermann,Ali Akbar Haghdoost,Reza Najafipour,Hamid Reza Khorram Khorshid,Kimia Kahrizi,Reza Malekzadeh,Mohammad R. Akbari,Hossein Najmabadi +28 more
TL;DR: By presenting higher frequency for 37,384 novel or known rare variants, Iranome database can improve the power of molecular diagnosis and attainable clinical information makes this database a good resource for classifying pathogenicity of rare variants.
Journal ArticleDOI
Serial genomic inversions induce tissue-specific architectural stripes, gene misexpression and congenital malformations.
Katerina Kraft,Katerina Kraft,Katerina Kraft,Andreas Magg,Verena Heinrich,Christina Riemenschneider,Robert Schöpflin,Robert Schöpflin,Julia Markowski,Daniel M. Ibrahim,Daniel M. Ibrahim,Rocio Acuna-Hidalgo,Rocio Acuna-Hidalgo,Alexandra Despang,Alexandra Despang,Guillaume Andrey,Guillaume Andrey,Lars Wittler,Bernd Timmermann,Martin Vingron,Stefan Mundlos,Stefan Mundlos +21 more
TL;DR: It is shown that chromosomal inversions that relocate a limb enhancer can establish asymmetric stripes of the enhancer with downstream genes, resulting in ectopic gene expression and limb phenotypes, and architectural stripes are a frequent feature of developmental three-dimensional genome architecture often associated with active enhancers.
Journal ArticleDOI
A Y2H-seq approach defines the human protein methyltransferase interactome.
Mareike Weimann,Arndt Grossmann,Jonathan Woodsmith,Ziya Özkan,Petra Birth,David Meierhofer,Nouhad Benlasfer,Taras Valovka,Bernd Timmermann,Erich E. Wanker,Sascha Sauer,Ulrich Stelzl +11 more
TL;DR: A yeast two-hybrid interaction screening approach involving short-read second-generation sequencing with improved sensitivity and a quantitative scoring readout allowing rapid interaction validation to investigate enzymes involved in protein methylation, a largely unexplored post-translational modification.