Evaluation of the Performance of AmpliSeq and SureSelect Exome Sequencing Libraries for Ion Proton

by Piyush Gampawar, Yasaman Saba, Ulrike Werner, Reinhold Schmidt, Bertram Müller-Myhsok, Bertram Müller-Myhsok, Bertram Müller-Myhsok, Helena Schmidt
Published 2019-09-01

Adapting the randomised controlled trial (RCT) for precision medicine: introducing the nested-precision RCT (npRCT)

by Nils Kappelmann, Bertram Müller-Myhsok, Johannes Kopf-Beck
Published 2021-01-01

Gene Expression in Spontaneous Experimental Autoimmune Encephalomyelitis Is Linked to Human Multiple Sclerosis Risk Genes

by Hans Faber, Dunja Kurtoic, Gurumoorthy Krishnamoorthy, Peter Weber, Benno Pütz, Bertram Müller-Myhsok, Bertram Müller-Myhsok, Frank Weber, Till F. M. Andlauer, Till F. M. Andlauer
Published 2020-09-01

Evidence for the late MMN as a neurophysiological endophenotype for dyslexia.

by Nina Neuhoff, Jennifer Bruder, Jürgen Bartling, Andreas Warnke, Helmut Remschmidt, Bertram Müller-Myhsok, Gerd Schulte-Körne
Published 2012-01-01

Genes from Chagas susceptibility loci that are differentially expressed in T. cruzi-resistant mice are candidates accounting for impaired immunity.

by Sebastian E B Graefe, Thomas Streichert, Birgit S Budde, Peter Nürnberg, Christiane Steeg, Bertram Müller-Myhsok, Bernhard Fleischer
Published 2006-01-01

Investigation of gene-gene interactions in cardiac traits and serum fatty acid levels in the LURIC Health Study.

by Jiayan Zhou, Kristin Passero, Nicole E Palmiero, Bertram Müller-Myhsok, Marcus E Kleber, Winfried Maerz, Molly A Hall
Published 2020-01-01

Investigation of gene-gene interactions in cardiac traits and serum fatty acid levels in the LURIC Health Study

by Jiayan Zhou, Kristin Passero, Nicole E. Palmiero, Bertram Müller-Myhsok, Marcus E. Kleber, Winfried Maerz, Molly A. Hall, Heming Wang
Published 2020-01-01

Clinically apparent and occult metastasized seminoma: almost indistinguishable on the transcriptional level.

by Christian G Ruf, Matthias Port, Hans-Ulrich Schmelz, Walter Wagner, Felix Müller, Sven Senf, Cord Matthies, Bertram Müller-Myhsok, Viktor Meineke, Michael Abend
Published 2014-01-01

Genetic Markers for PTSD Risk and Resilience Among Survivors of the World Trade Center Attacks

by Casey Sarapas, Guiqing Cai, Linda M. Bierer, Julia A. Golier, Sandro Galea, Marcus Ising, Theo Rein, James Schmeidler, Bertram Müller-Myhsok, Manfred Uhr, Florian Holsboer, Joseph D. Buxbaum, Rachel Yehuda
Published 2011-01-01

Children with ADHD symptoms have a higher risk for reading, spelling and math difficulties in the GINIplus and LISAplus cohort studies.

by Darina Czamara, Carla M T Tiesler, Gabriele Kohlböck, Dietrich Berdel, Barbara Hoffmann, Carl-Peter Bauer, Sibylle Koletzko, Beate Schaaf, Irina Lehmann, Olf Herbarth, Andrea von Berg, Bertram Müller-Myhsok, Gerd Schulte-Körne, Joachim Heinrich
Published 2013-01-01

PTGER4 expression-modulating polymorphisms in the 5p13.1 region predispose to Crohn's disease and affect NF-κB and XBP1 binding sites.

by Jürgen Glas, Julia Seiderer, Darina Czamara, Giulia Pasciuto, Julia Diegelmann, Martin Wetzke, Torsten Olszak, Christiane Wolf, Bertram Müller-Myhsok, Tobias Balschun, Jean-Paul Achkar, M Ilyas Kamboh, Andre Franke, Richard H Duerr, Stephan Brand
Published 2012-01-01

The NOD2 single nucleotide polymorphisms rs2066843 and rs2076756 are novel and common Crohn's disease susceptibility gene variants.

by Jürgen Glas, Julia Seiderer, Cornelia Tillack, Simone Pfennig, Florian Beigel, Matthias Jürgens, Torsten Olszak, Rüdiger P Laubender, Maria Weidinger, Bertram Müller-Myhsok, Burkhard Göke, Thomas Ochsenkühn, Peter Lohse, Julia Diegelmann, Darina Czamara, Stephan Brand
Published 2010-01-01

Connecting Anxiety and Genomic Copy Number Variation: A Genome-Wide Analysis in CD-1 Mice.

by Julia Brenndörfer, André Altmann, Regina Widner-Andrä, Benno Pütz, Darina Czamara, Erik Tilch, Tony Kam-Thong, Peter Weber, Monika Rex-Haffner, Thomas Bettecken, Andrea Bultmann, Bertram Müller-Myhsok, Elisabeth E Binder, Rainer Landgraf, Ludwig Czibere
Published 2015-01-01

Evidence for STAT4 as a common autoimmune gene: rs7574865 is associated with colonic Crohn's disease and early disease onset.

by Jürgen Glas, Julia Seiderer, Melinda Nagy, Christoph Fries, Florian Beigel, Maria Weidinger, Simone Pfennig, Wolfram Klein, Jörg T Epplen, Peter Lohse, Matthias Folwaczny, Burkhard Göke, Thomas Ochsenkühn, Julia Diegelmann, Bertram Müller-Myhsok, Darina Roeske, Stephan Brand
Published 2010-01-01

CEACAM6 gene variants in inflammatory bowel disease.

by Jürgen Glas, Julia Seiderer, Christoph Fries, Cornelia Tillack, Simone Pfennig, Maria Weidinger, Florian Beigel, Torsten Olszak, Ulrich Lass, Burkhard Göke, Thomas Ochsenkühn, Christiane Wolf, Peter Lohse, Bertram Müller-Myhsok, Julia Diegelmann, Darina Czamara, Stephan Brand
Published 2011-01-01

Possible associations of NTRK2 polymorphisms with antidepressant treatment outcome: findings from an extended tag SNP approach.

by Johannes M Hennings, Martin A Kohli, Darina Czamara, Maria Giese, Anne Eckert, Christiane Wolf, Angela Heck, Katharina Domschke, Volker Arolt, Bernhard T Baune, Sonja Horstmann, Tanja Brückl, Torsten Klengel, Andreas Menke, Bertram Müller-Myhsok, Marcus Ising, Manfred Uhr, Susanne Lucae
Published 2013-01-01

A hypomorphic vasopressin allele prevents anxiety-related behavior.

by Mirjam Bunck, Ludwig Czibere, Charlotte Horvath, Cornelia Graf, Elisabeth Frank, Melanie S Kessler, Chris Murgatroyd, Bertram Müller-Myhsok, Mariya Gonik, Peter Weber, Benno Pütz, Patrik Muigg, Markus Panhuysen, Nicolas Singewald, Thomas Bettecken, Jan M Deussing, Florian Holsboer, Dietmar Spengler, Rainer Landgraf
Published 2009-01-01

SKP2 attenuates autophagy through Beclin1-ubiquitination and its inhibition reduces MERS-Coronavirus infection

by Nils C. Gassen, Daniela Niemeyer, Doreen Muth, Victor M. Corman, Silvia Martinelli, Alwine Gassen, Kathrin Hafner, Jan Papies, Kirstin Mösbauer, Andreas Zellner, Anthony S. Zannas, Alexander Herrmann, Florian Holsboer, Ruth Brack-Werner, Michael Boshart, Bertram Müller-Myhsok, Christian Drosten, Marcel A. Müller, Theo Rein
Published 2019-12-01

Rare variants in PLXNA4 and Parkinson's disease.

by Eva C Schulte, Immanuel Stahl, Darina Czamara, Daniel C Ellwanger, Sebastian Eck, Elisabeth Graf, Brit Mollenhauer, Alexander Zimprich, Peter Lichtner, Dietrich Haubenberger, Walter Pirker, Thomas Brücke, Benjamin Bereznai, Maria J Molnar, Annette Peters, Christian Gieger, Bertram Müller-Myhsok, Claudia Trenkwalder, Juliane Winkelmann
Published 2013-01-01

Genetic regulatory effects modified by immune activation contribute to autoimmune disease associations

by Sarah Kim-Hellmuth, Matthias Bechheim, Benno Pütz, Pejman Mohammadi, Yohann Nédélec, Nicholas Giangreco, Jessica Becker, Vera Kaiser, Nadine Fricker, Esther Beier, Peter Boor, Stephane E. Castel, Markus M. Nöthen, Luis B. Barreiro, Joseph K. Pickrell, Bertram Müller-Myhsok, Tuuli Lappalainen, Johannes Schumacher, Veit Hornung
Published 2017-08-01