Identification and Analysis of Co-Occurrence Networks with NetCutter

Por Müller, Heiko, Mancuso, Francesco
Publicado em 2008

Topological Properties of Co-Occurrence Networks in Published Gene Expression Signatures

Por Muller, Heiko, Acquati, Francesco
Publicado em 2008

The MI bundle: enabling network and structural biology in genome visualization tools

Por Céol, Arnaud, Müller, Heiko
Publicado no Bioinformatics (2015)

Mining published lists of cancer related microarray experiments: Identification of a gene expression signature having a critical role in cell-cycle control

Por Finocchiaro, Giacomo, Mancuso, Francesco, Muller, Heiko
Publicado em 2005

IsomiRage: From Functional Classification to Differential Expression of miRNA Isoforms

Por Muller, Heiko, Marzi, Matteo Jacopo, Nicassio, Francesco
Publicado em 2014

SMITH: a LIMS for handling next-generation sequencing workflows

Por Venco, Francesco, Vaskin, Yuriy, Ceol, Arnaud, Muller, Heiko
Publicado no BMC Bioinformatics (2014)

Graph-based identification of cancer signaling pathways from published gene expression signatures using PubLiME

Por Finocchiaro, Giacomo, Mancuso, Francesco Mattia, Cittaro, Davide, Muller, Heiko
Publicado em 2007

Clinical Utility of Creatinine- and Cystatin C–Based Definition of Renal Function for Risk Prediction of Primary Cardiovascular Events in Patients With Diabetes

Por Schöttker, Ben, Herder, Christian, Müller, Heiko, Brenner, Hermann, Rothenbacher, Dietrich
Publicado em 2012

Cross-sectional and longitudinal changes in DNA methylation with age: an epigenome-wide analysis revealing over 60 novel age-associated CpG sites

Por Florath, Ines, Butterbach, Katja, Müller, Heiko, Bewerunge-Hudler, Melanie, Brenner, Hermann
Publicado em 2014

AnnotateGenomicRegions: a web application

Por Zammataro, Luca, DeMolfetta, Rita, Bucci, Gabriele, Ceol, Arnaud, Muller, Heiko
Publicado em 2014

Genome and network visualization facilitates the analyses of the effects of drugs and mutations on protein-protein and drug-protein networks

Por Céol, Arnaud, Verhoef, Lisette G. G. C., Wade, Mark, Muller, Heiko
Publicado no BMC Bioinformatics (2016)

Localizing hotspots of antisense transcription

Por Finocchiaro, Giacomo, Carro, Maria Stella, Francois, Stephanie, Parise, Paola, DiNinni, Valentina, Muller, Heiko
Publicado em 2007

8-Oxo-7,8-dihydroguanine in DNA does not constitute a barrier to transcription, but is converted into transcription-blocking damage by OGG1

Por Kitsera, Nataliya, Stathis, Dimitrios, Lühnsdorf, Bork, Müller, Heiko, Carell, Thomas, Epe, Bernd, Khobta, Andriy
Publicado em 2011

Proinflammatory Cytokines, Adiponectin, and Increased Risk of Primary Cardiovascular Events in Diabetic Patients With or Without Renal Dysfunction: Results from the ESTHER study

Por Schöttker, Ben, Herder, Christian, Rothenbacher, Dietrich, Roden, Michael, Kolb, Hubert, Müller, Heiko, Brenner, Hermann
Publicado em 2013

CDC25A Phosphatase Is a Target of E2F and Is Required for Efficient E2F-Induced S Phase

Por Vigo, Elena, Müller, Heiko, Prosperini, Elena, Hateboer, Guus, Cartwright, Peter, Moroni, Maria Cristina, Helin, Kristian
Publicado em 1999

DNA repair gene polymorphisms and risk of chronic atrophic gastritis: a case-control study

Por Frank, Bernd, Müller, Heiko, Weck, Melanie Nicole, Klopp, Norman, Illig, Thomas, Raum, Elke, Brenner, Hermann
Publicado em 2011

VCF.Filter: interactive prioritization of disease-linked genetic variants from sequencing data

Por Müller, Heiko, Jimenez-Heredia, Raul, Krolo, Ana, Hirschmugl, Tatjana, Dmytrus, Jasmin, Boztug, Kaan, Bock, Christoph
Publicado no Nucleic Acids Res (2017)

Columba: an integrated database of proteins, structures, and annotations

Por Trißl, Silke, Rother, Kristian, Müller, Heiko, Steinke, Thomas, Koch, Ina, Preissner, Robert, Frömmel, Cornelius, Leser, Ulf
Publicado em 2005

Patient Blood Management Implementation Strategies and Their Effect on Physicians' Risk Perception, Clinical Knowledge and Perioperative Practice – the Frankfurt Experience

Por Fischer, Dania P., Zacharowski, Kai D., Müller, Markus M., Geisen, Christof, Seifried, Erhard, Müller, Heiko, Meybohm, Patrick
Publicado no Transfus Med Hemother (2015)

LowMACA: exploiting protein family analysis for the identification of rare driver mutations in cancer

Por Melloni, Giorgio E. M., de Pretis, Stefano, Riva, Laura, Pelizzola, Mattia, Céol, Arnaud, Costanza, Jole, Müller, Heiko, Zammataro, Luca
Publicado no BMC Bioinformatics (2016)