| Identification and analysis of functional elements in 1% of the human genome by the ENCODE pilot project Management Group Liefer Laura A. 51 Wetterstrand Kris A. 51 Good Peter J. 51 ... nature 447 (7146), 799-816, 2007 | 6107 | 2007 |
| 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 | 739 | 2018 |
| 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), 1435-1440, 2011 | 389 | 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 | 271 | 2011 |
| 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 | 270 | 2012 |
| 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 | 216 | 2016 |
| 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), 1253-1260, 2017 | 204 | 2017 |
| 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 | 187 | 2007 |
| Single-molecule sequencing: towards clinical applications A Ameur, WP Kloosterman, MS Hestand Trends in biotechnology 37 (1), 72-85, 2019 | 181 | 2019 |
| 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 | 168 | 2007 |
| 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 | 127 | 2009 |
| 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 | 123 | 2008 |
| Genome-wide association analyses of physical activity and sedentary behavior provide insights into underlying mechanisms and roles in disease prevention Z Wang, A Emmerich, NJ Pillon, T Moore, D Hemerich, MC Cornelis, ... Nature genetics 54 (9), 1332-1344, 2022 | 122 | 2022 |
| 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, 1-15, 2008 | 121 | 2008 |
| CRISPR-Cas9 induces large structural variants at on-target and off-target sites in vivo that segregate across generations I Höijer, A Emmanouilidou, R Östlund, R van Schendel, S Bozorgpana, ... Nature communications 13 (1), 1-10, 2022 | 120 | 2022 |
| 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 | 117 | 2013 |
| Global and unbiased detection of splice junctions from RNA-seq data A Ameur, A Wetterbom, L Feuk, U Gyllensten Genome biology 11, 1-9, 2010 | 115 | 2010 |
| 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 | 108 | 2012 |
| 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 | 94 | 2005 |
| Detailed analysis of HTT repeat elements in human blood using targeted amplification‐free long‐read sequencing I Höijer, YC Tsai, TA Clark, P Kotturi, N Dahl, EL Stattin, ML Bondeson, ... Human Mutation 39 (9), 1262-1272, 2018 | 90 | 2018 |
