| Genetic diagnosis of Mendelian disorders via RNA sequencing LS Kremer, DM Bader, C Mertes, R Kopajtich, G Pichler, A Iuso, TB Haack, ... Nature Communications 8, 2017 | 577 | 2017 |
| A beginners guide to SNP calling from high-throughput DNA-sequencing data A Altmann, P Weber, D Bader, M Preuß, EB Binder, B Müller-Myhsok Human genetics 131 (10), 1541-1554, 2012 | 200 | 2012 |
| OUTRIDER: A statistical method for detecting aberrantly expressed genes in RNA sequencing data F Brechtmann, C Mertes, A Matusevičiūtė, VA Yépez, Ž Avsec, M Herzog, ... The American Journal of Human Genetics 103 (6), 907-917, 2018 | 185 | 2018 |
| Biallelic Mutations in NBAS Cause Recurrent Acute Liver Failure with Onset in Infancy TB Haack, C Staufner, MG Köpke, BK Straub, S Kölker, C Thiel, ... The American Journal of Human Genetics 97 (1), 163-169, 2015 | 136 | 2015 |
| Re-Annotator: Annotation Pipeline for Microarray Probe Sequences J Arloth, DM Bader, S Röh, A Altmann PloS one 10 (10), e0139516, 2015 | 118 | 2015 |
| Negative feedback buffers effects of regulatory variants DM Bader, S Wilkening, G Lin, MM Tekkedil, K Dietrich, LM Steinmetz, ... Molecular systems biology 11 (1), 785, 2015 | 43 | 2015 |
| Rare variants in TMEM132D in a case–control sample for panic disorder C Quast, A Altmann, P Weber, J Arloth, D Bader, A Heck, H Pfister, ... American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 159 …, 2012 | 30 | 2012 |
| Functional coding variants in SLC6A15, a possible risk gene for major depression C Quast, S Cuboni, D Bader, A Altmann, P Weber, J Arloth, S Röh, ... PloS one 8 (7), e68645, 2013 | 20 | 2013 |
| Re-Annotator: Annotation Pipeline for Microarrays J Arloth, DM Bader, S Röh, A Altmann bioRxiv, 019596, 2015 | 2 | 2015 |
| Consequences of DNA variation on gene regulation and human disease via RNA sequencing DM Bader lmu, 2017 | | 2017 |
