| Identification and analysis of functional elements in 1% of the human genome by the ENCODE pilot project ENCODE Project Consortium Nature 447 (7146), 799, 2007 | 4812 | 2007 |
| Total RNA sequencing reveals nascent transcription and widespread co-transcriptional splicing in the human brain A Ameur, A Zaghlool, J Halvardson, A Wetterbom, U Gyllensten, ... Nature structural & molecular biology 18 (12), 1435, 2011 | 224 | 2011 |
| Ultra-deep sequencing of mouse mitochondrial DNA: mutational patterns and their origins A Ameur, JB Stewart, C Freyer, E Hagström, M Ingman, NG Larsson, ... PLoS genetics 7 (3), e1002028, 2011 | 149 | 2011 |
| Butyrate mediates decrease of histone acetylation centered on transcription start sites and down-regulation of associated genes A Rada-Iglesias, S Enroth, A Ameur, CM Koch, GK Clelland, ... Genome research 17 (6), 708-719, 2007 | 122 | 2007 |
| Endocan is a VEGF-A and PI3K regulated gene with increased expression in human renal cancer E Rennel, S Mellberg, A Dimberg, L Petersson, J Botling, A Ameur, ... Experimental cell research 313 (7), 1285-1294, 2007 | 114 | 2007 |
| Genetic adaptation of fatty-acid metabolism: a human-specific haplotype increasing the biosynthesis of long-chain omega-3 and omega-6 fatty acids A Ameur, S Enroth, Å Johansson, G Zaboli, W Igl, ACV Johansson, ... The American Journal of Human Genetics 90 (5), 809-820, 2012 | 111 | 2012 |
| Global and unbiased detection of splice junctions from RNA-seq data A Ameur, A Wetterbom, L Feuk, U Gyllensten Genome biology 11 (3), R34, 2010 | 104 | 2010 |
| Whole-genome maps of USF1 and USF2 binding and histone H3 acetylation reveal new aspects of promoter structure and candidate genes for common human disorders A Rada-Iglesias, A Ameur, P Kapranov, S Enroth, J Komorowski, ... Genome research 18 (3), 380-392, 2008 | 95 | 2008 |
| Binding sites for metabolic disease related transcription factors inferred at base pair resolution by chromatin immunoprecipitation and genomic microarrays A Rada-Iglesias, O Wallerman, C Koch, A Ameur, S Enroth, G Clelland, ... Human molecular genetics 14 (22), 3435-3447, 2005 | 91 | 2005 |
| Transcriptional profiling reveals a critical role for tyrosine phosphatase VE-PTP in regulation of VEGFR2 activity and endothelial cell morphogenesis S Mellberg, A Dimberg, F Bahram, M Hayashi, E Rennel, A Ameur, ... The FASEB Journal 23 (5), 1490-1502, 2009 | 88 | 2009 |
| Data-driven unbiased curation of the TP53 tumor suppressor gene mutation database and validation by ultradeep sequencing of human tumors K Edlund, O Larsson, A Ameur, I Bunikis, U Gyllensten, B Leroy, ... Proceedings of the National Academy of Sciences 109 (24), 9551-9556, 2012 | 80 | 2012 |
| Combinatorial control of gene expression by the three yeast repressors Mig1, Mig2 and Mig3 JO Westholm, N Nordberg, E Murén, A Ameur, J Komorowski, H Ronne BMC genomics 9 (1), 601, 2008 | 71 | 2008 |
| Identification of novel genetic causes of Rett syndrome-like phenotypes F Lopes, M Barbosa, A Ameur, G Soares, J de Sá, AI Dias, G Oliveira, ... Journal of medical genetics 53 (3), 190-199, 2016 | 70 | 2016 |
| Welander Distal Myopathy Caused by an Ancient Founder Mutation in TIA1 Associated with Perturbed Splicing J Klar, M Sobol, A Melberg, K Mäbert, A Ameur, ACV Johansson, L Feuk, ... Human mutation 34 (4), 572-577, 2013 | 69 | 2013 |
| Single molecule real-time (SMRT) sequencing comes of age: applications and utilities for medical diagnostics S Ardui, A Ameur, JR Vermeesch, MS Hestand Nucleic acids research 46 (5), 2159-2168, 2018 | 68 | 2018 |
| Differential binding and co-binding pattern of FOXA1 and FOXA3 and their relation to H3K4me3 in HepG2 cells revealed by ChIP-seq M Motallebipour, A Ameur, MSR Bysani, K Patra, O Wallerman, J Mangion, ... Genome biology 10 (11), R129, 2009 | 57 | 2009 |
| The LCB data warehouse A Ameur, V Yankovski, S Enroth, O Spjuth, J Komorowski Bioinformatics 22 (8), 1024-1026, 2006 | 47 | 2006 |
| SweGen: a whole-genome data resource of genetic variability in a cross-section of the Swedish population A Ameur, J Dahlberg, P Olason, F Vezzi, R Karlsson, M Martin, J Viklund, ... European Journal of Human Genetics 25 (11), 1253, 2017 | 40 | 2017 |
| Intratumoral genome diversity parallels progression and predicts outcome in pediatric cancer LH Mengelbier, J Karlsson, D Lindgren, A Valind, H Lilljebjörn, C Jansson, ... Nature communications 6, 6125, 2015 | 39 | 2015 |
| Determination of the obesity-associated gene variants within the entire FTO gene by ultra-deep targeted sequencing in obese and lean children MS Almén, M Rask-Andersen, JA Jacobsson, A Ameur, I Kalnina, ... International journal of obesity 37 (3), 424, 2013 | 39 | 2013 |
