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

por Kappelmann, Nils, Müller-Myhsok, Bertram, Kopf-Beck, Johannes
Publicado 2021

Meta analysis of whole-genome linkage scans with data uncertainty: an application to Parkinson's disease

por Rosenberger, Albert, Sharma, Manu, Müller-Myhsok, Bertram, Gasser, Thomas, Bickeböller, Heike
Publicado 2007

Systematic Review of Functional MRI Applications for Psychiatric Disease Subtyping

por Miranda, Lucas, Paul, Riya, Pütz, Benno, Koutsouleris, Nikolaos, Müller-Myhsok, Bertram
Publicado 2021

Epistasis detection on quantitative phenotypes by exhaustive enumeration using GPUs

por Kam-Thong, Tony, Pütz, Benno, Karbalai, Nazanin, Müller−Myhsok, Bertram, Borgwardt, Karsten
Publicado 2011

Mitochondrial haplogroup U is associated with a reduced risk to develop exfoliation glaucoma in the German population

por Wolf, Christiane, Gramer, Eugen, Müller-Myhsok, Bertram, Pasutto, Francesca, Wissinger, Bernd, Weisschuh, Nicole
Publicado 2010

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

por Gampawar, Piyush, Saba, Yasaman, Werner, Ulrike, Schmidt, Reinhold, Müller-Myhsok, Bertram, Schmidt, Helena
Publicado 2019

DNA-methylation dynamics across short-term, exposure-containing CBT in patients with panic disorder

por Moser, Sylvain, Martins, Jade, Czamara, Darina, Lange, Jennifer, Müller-Myhsok, Bertram, Erhardt, Angelika
Publicado 2022

Creating sparser prediction models of treatment outcome in depression: a proof-of-concept study using simultaneous feature selection and hyperparameter tuning

por Rost, Nicolas, Brückl, Tanja M., Koutsouleris, Nikolaos, Binder, Elisabeth B., Müller-Myhsok, Bertram
Publicado 2022

Genome and transcriptome profiling of spontaneous preterm birth phenotypes

por Gupta, Juhi K., Care, Angharad, Goodfellow, Laura, Alfirevic, Zarko, Müller-Myhsok, Bertram, Alfirevic, Ana
Publicado 2022

Publisher Correction: Genome and transcriptome profiling of spontaneous preterm birth phenotypes

por Gupta, Juhi K., Care, Angharad, Goodfellow, Laura, Alfirevic, Zarko, Müller‑Myhsok, Bertram, Alfirevic, Ana
Publicado 2022

Evaluation of nine candidate genes in patients with normal tension glaucoma: a case control study

por Wolf, Christiane, Gramer, Eugen, Müller-Myhsok, Bertram, Pasutto, Francesca, Reinthal, Eva, Wissinger, Bernd, Weisschuh, Nicole
Publicado 2009

vipR: variant identification in pooled DNA using R

por Altmann, Andre, Weber, Peter, Quast, Carina, Rex-Haffner, Monika, Binder, Elisabeth B., Müller-Myhsok, Bertram
Publicado 2011

Efficient branch-and-bound techniques for two-locus association mapping

por Klotzbücher, Karin, Kobayashi, Yasushi, Shervashidze, Nino, Stegle, Oliver, Müller-Myhsok, Bertram, Weigel, Detlef, Borgwardt, Karsten
Publicado 2011

Evidence for the Late MMN as a Neurophysiological Endophenotype for Dyslexia

por Neuhoff, Nina, Bruder, Jennifer, Bartling, Jürgen, Warnke, Andreas, Remschmidt, Helmut, Müller-Myhsok, Bertram, Schulte-Körne, Gerd
Publicado 2012

A different view on fine-scale population structure in Western African populations

por Chaichoompu, Kridsadakorn, Abegaz, Fentaw, Cavadas, Bruno, Fernandes, Verónica, Müller-Myhsok, Bertram, Pereira, Luísa, Van Steen, Kristel
Publicado 2019

Genes from Chagas Susceptibility Loci That Are Differentially Expressed in T. cruzi-Resistant Mice Are Candidates Accounting for Impaired Immunity

por Graefe, Sebastian E. B., Streichert, Thomas, Budde, Birgit S., Nürnberg, Peter, Steeg, Christiane, Müller-Myhsok, Bertram, Fleischer, Bernhard
Publicado 2006

Association of a specific haplotype across the genes MMP1 and MMP3 with radiographic joint destruction in rheumatoid arthritis

por Dörr, Sylvia, Lechtenböhmer, Nadine, Rau, Rolf, Herborn, Gertraud, Wagner, Ulf, Müller-Myhsok, Bertram, Hansmann, Ingo, Keyszer, Gernot
Publicado 2004

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

por Zhou, Jiayan, Passero, Kristin, Palmiero, Nicole E., Müller-Myhsok, Bertram, Kleber, Marcus E., Maerz, Winfried, Hall, Molly A.
Publicado 2020

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

por Faber, Hans, Kurtoic, Dunja, Krishnamoorthy, Gurumoorthy, Weber, Peter, Pütz, Benno, Müller-Myhsok, Bertram, Weber, Frank, Andlauer, Till F. M.
Publicado 2020

Metabolic profiling of maternal serum of women at high-risk of spontaneous preterm birth using NMR and MGWAS approach

por Gupta, Juhi K., Care, Angharad, Goodfellow, Laura, Alfirevic, Zarko, Lian, Lu-Yun, Müller-Myhsok, Bertram, Alfirevic, Ana, Phelan, Marie M.
Publicado 2021