How genetic risk contributes to autoimmune liver disease

por Ellinghaus, David
Publicado 2022

EagleImp: fast and accurate genome-wide phasing and imputation in a single tool

por Wienbrandt, Lars, Ellinghaus, David
Publicado 2022

LTRharvest, an efficient and flexible software for de novo detection of LTR retrotransposons

por Ellinghaus, David, Kurtz, Stefan, Willhoeft, Ute
Publicado 2008

Reference-Based Haplotype Phasing with FPGAs

por Wienbrandt, Lars, Kässens, Jan Christian, Ellinghaus, David
Publicado 2020

BIGwas: Single-command quality control and association testing for multi-cohort and biobank-scale GWAS/PheWAS data

por Kässens, Jan Christian, Wienbrandt, Lars, Ellinghaus, David
Publicado 2021

Current software for genotype imputation

por Ellinghaus, David, Schreiber, Stefan, Franke, Andre, Nothnagel, Michael
Publicado 2009

MAGScoT: a fast, lightweight and accurate bin-refinement tool

por Rühlemann, Malte Christoph, Wacker, Eike Matthias, Ellinghaus, David, Franke, Andre
Publicado 2022

A benchmark of hemoglobin blocking during library preparation for mRNA-Sequencing of human blood samples

por Uellendahl-Werth, Florian, Wolfien, Markus, Franke, Andre, Wolkenhauer, Olaf, Ellinghaus, David
Publicado 2020

Opportunities and challenges of whole-genome and -exome sequencing

por Petersen, Britt-Sabina, Fredrich, Broder, Hoeppner, Marc P., Ellinghaus, David, Franke, Andre
Publicado 2017

LitDB - Keeping Track of Research Papers From Your Institute Made Simple

por Bethune, Jörn, Kraemer, Lars, Thomsen, Ingo, Keller, Andreas, Ellinghaus, David, Franke, Andre
Publicado 2017

Vy-PER: eliminating false positive detection of virus integration events in next generation sequencing data

por Forster, Michael, Szymczak, Silke, Ellinghaus, David, Hemmrich, Georg, Rühlemann, Malte, Kraemer, Lars, Mucha, Sören, Wienbrandt, Lars, Stanulla, Martin, Franke, Andre
Publicado 2015

Genetic risk factors predict disease progression in Crohn’s disease patients of the Swiss inflammatory bowel disease cohort

por Ditrich, Felicitas, Blümel, Sena, Biedermann, Luc, Fournier, Nicolas, Rossel, Jean-Benoit, Ellinghaus, David, Franke, Andre, Stange, Eduard F., Rogler, Gerhard, Scharl, Michael
Publicado 2020

VarWatch—A stand-alone software tool for variant matching

por Fredrich, Broder, Schmöhl, Marcus, Junge, Olaf, Gundlach, Sven, Ellinghaus, David, Pfeufer, Arne, Bettecken, Thomas, Siddiqui, Roman, Franke, Andre, Wienker, Thomas F., Hoeppner, Marc P., Krawczak, Michael
Publicado 2019

Male-specific association between MT-ND4 11719 A/G polymorphism and ulcerative colitis: a mitochondria-wide genetic association study

por Dankowski, Theresa, Schröder, Torsten, Möller, Steffen, Yu, Xinhua, Ellinghaus, David, Bär, Florian, Fellermann, Klaus, Lehnert, Hendrik, Schreiber, Stefan, Franke, Andre, Sina, Christian, Ibrahim, Saleh M., König, Inke R.
Publicado 2016

Genome-wide association analysis for chronic venous disease identifies EFEMP1 and KCNH8 as susceptibility loci

por Ellinghaus, Eva, Ellinghaus, David, Krusche, Petra, Greiner, Aljoscha, Schreiber, Claudia, Nikolaus, Susanna, Gieger, Christian, Strauch, Konstantin, Lieb, Wolfgang, Rosenstiel, Philip, Frings, Norbert, Fiebig, Andreas, Schreiber, Stefan, Franke, Andre
Publicado 2017

The MUC5B Promoter Polymorphism Associates With Severe COVID-19 in the European Population

por van Moorsel, Coline H. M., van der Vis, Joanne J., Duckworth, Anna, Scotton, Chris J., Benschop, Claudia, Ellinghaus, David, Ruven, Henk J. T., Quanjel, Marian J. R., Grutters, Jan C.
Publicado 2021

Local genetic variation of inflammatory bowel disease in Basque population and its effect in risk prediction

por Garcia-Etxebarria, Koldo, Merino, Olga, Gaite-Reguero, Adrián, Rodrigues, Pedro M., Herrarte, Amaia, Etxart, Ane, Ellinghaus, David, Alonso-Galan, Horacio, Franke, Andre, Marigorta, Urko M., Bujanda, Luis, D’Amato, Mauro
Publicado 2022

Sex differences in the genetics of sarcoidosis across European and African ancestry populations

por Xiong, Ying, Kullberg, Susanna, Garman, Lori, Pezant, Nathan, Ellinghaus, David, Vasila, Vasiliki, Eklund, Anders, Rybicki, Benjamin A., Iannuzzi, Michael C., Schreiber, Stefan, Müller-Quernheim, Joachim, Montgomery, Courtney G., Grunewald, Johan, Padyukov, Leonid, Rivera, Natalia V.
Publicado 2023

Genetic background of high blood pressure is associated with reduced mortality in premature neonates

por Göpel, Wolfgang, Müller, Mirja, Rabe, Heike, Borgmann, Johannes, Rausch, Tanja K, Faust, Kirstin, Kribs, Angela, Dötsch, Jörg, Ellinghaus, David, Härtel, Christoph, Roll, Claudia, Szabo, Miklos, Nürnberg, Peter, Franke, Andre, König, Inke R, Turner, Mark A, Herting, Egbert
Publicado 2020

From next-generation sequencing alignments to accurate comparison and validation of single-nucleotide variants: the pibase software

por Forster, Michael, Forster, Peter, Elsharawy, Abdou, Hemmrich, Georg, Kreck, Benjamin, Wittig, Michael, Thomsen, Ingo, Stade, Björn, Barann, Matthias, Ellinghaus, David, Petersen, Britt-Sabina, May, Sandra, Melum, Espen, Schilhabel, Markus B., Keller, Andreas, Schreiber, Stefan, Rosenstiel, Philip, Franke, Andre
Publicado 2013