| An integrated map of genetic variation from 1,092 human genomes 1000 Genomes Project Consortium Nature 491 (7422), 56, 2012 | 5840 | 2012 |
| A global reference for human genetic variation 1000 Genomes Project Consortium Nature 526 (7571), 68, 2015 | 4192 | 2015 |
| Driver mutations in histone H3. 3 and chromatin remodelling genes in paediatric glioblastoma J Schwartzentruber, A Korshunov, XY Liu, DTW Jones, E Pfaff, K Jacob, ... Nature 482 (7384), 226, 2012 | 1390 | 2012 |
| Mapping copy number variation by population-scale genome sequencing RE Mills, K Walter, C Stewart, RE Handsaker, K Chen, C Alkan, A Abyzov, ... Nature 470 (7332), 59-65, 2011 | 938 | 2011 |
| An integrated map of structural variation in 2,504 human genomes PH Sudmant, T Rausch, EJ Gardner, RE Handsaker, A Abyzov, ... Nature 526 (7571), 75, 2015 | 866 | 2015 |
| DELLY: structural variant discovery by integrated paired-end and split-read analysis T Rausch, T Zichner, A Schlattl, AM Stütz, V Benes, JO Korbel Bioinformatics 28 (18), i333-i339, 2012 | 741 | 2012 |
| Dissecting the genomic complexity underlying medulloblastoma DTW Jones, N Jäger, M Kool, T Zichner, B Hutter, M Sultan, YJ Cho, ... Nature 488 (7409), 100, 2012 | 624 | 2012 |
| Genome Sequencing of Pediatric Medulloblastoma Links Catastrophic DNA Rearrangements with TP53 Mutations T Rausch, DTW Jones, M Zapatka, AM Stütz, T Zichner, J Weischenfeldt, ... Cell 148 (1), 59-71, 2012 | 572 | 2012 |
| Genome sequencing of SHH medulloblastoma predicts genotype-related response to smoothened inhibition M Kool, DTW Jones, N Jäger, PA Northcott, TJ Pugh, V Hovestadt, ... Cancer cell 25 (3), 393-405, 2014 | 393 | 2014 |
| The genomic and transcriptomic landscape of a HeLa cell line JJM Landry, PT Pyl, T Rausch, T Zichner, MM Tekkedil, AM Stütz, A Jauch, ... G3: Genes, Genomes, Genetics 3 (8), 1213-1224, 2013 | 341 | 2013 |
| Assembly and diploid architecture of an individual human genome via single-molecule technologies M Pendleton, R Sebra, AWC Pang, A Ummat, O Franzen, T Rausch, ... Nature methods 12 (8), 780, 2015 | 305 | 2015 |
| SeqAn an efficient, generic C++ library for sequence analysis A Döring, D Weese, T Rausch, K Reinert BMC bioinformatics 9 (1), 11, 2008 | 302 | 2008 |
| Recurrent mutation of the ID3 gene in Burkitt lymphoma identified by integrated genome, exome and transcriptome sequencing J Richter, M Schlesner, S Hoffmann, M Kreuz, E Leich, B Burkhardt, ... Nature genetics 44 (12), 1316, 2012 | 287 | 2012 |
| Integrative genomic analyses reveal an androgen-driven somatic alteration landscape in early-onset prostate cancer J Weischenfeldt, R Simon, L Feuerbach, K Schlangen, D Weichenhan, ... Cancer cell 23 (2), 159-170, 2013 | 249 | 2013 |
| Integrating sequence and array data to create an improved 1000 Genomes Project haplotype reference panel O Delaneau, J Marchini, GA McVean, P Donnelly, G Lunter, JL Marchini, ... Nature communications 5, 3934, 2014 | 182 | 2014 |
| RazerS—fast read mapping with sensitivity control D Weese, AK Emde, T Rausch, A Döring, K Reinert Genome Research 19 (9), 1646-1654, 2009 | 182 | 2009 |
| The landscape of genomic alterations across childhood cancers SN Gröbner, BC Worst, J Weischenfeldt, I Buchhalter, K Kleinheinz, ... Nature 555 (7696), 321, 2018 | 145 | 2018 |
| Bioconda: sustainable and comprehensive software distribution for the life sciences B Grüning, R Dale, A Sjödin, BA Chapman, J Rowe, CH Tomkins-Tinch, ... Nature methods 15 (7), 475, 2018 | 111 | 2018 |
| Whole-exome sequencing links caspase recruitment domain 11 (CARD11) inactivation to severe combined immunodeficiency J Greil, T Rausch, T Giese, OR Bandapalli, V Daniel, I Bekeredjian-Ding, ... Journal of Allergy and Clinical Immunology, 2013 | 92 | 2013 |
| Segment-based multiple sequence alignment T Rausch, AK Emde, D Weese, A Döring, C Notredame, K Reinert Bioinformatics 24 (16), i187-i192, 2008 | 69 | 2008 |
Jan KorbelPrincipal Investigator, Senior Scientist, European Molecular Biology Laboratory (EMBL)Verified email at embl.de