| Profiling the HeLa S3 transcriptome using randomly primed cDNA and massively parallel short-read sequencing RD Morin, M Bainbridge, A Fejes, M Hirst, M Krzywinski, TJ Pugh, ... Biotechniques 45 (1), 81-94, 2008 | 597 | 2008 |
| Recurrent somatic DICER1 mutations in nonepithelial ovarian cancers A Heravi-Moussavi, MS Anglesio, SWG Cheng, J Senz, W Yang, ... New England Journal of Medicine 366 (3), 234-242, 2012 | 523 | 2012 |
| FindPeaks 3.1: a tool for identifying areas of enrichment from massively parallel short-read sequencing technology AP Fejes, G Robertson, M Bilenky, R Varhol, M Bainbridge, SJM Jones Bioinformatics 24 (15), 1729-1730, 2008 | 344 | 2008 |
| Mutations in EZH2 cause Weaver syndrome WT Gibson, RL Hood, SH Zhan, DE Bulman, AP Fejes, R Moore, ... The American Journal of Human Genetics 90 (1), 110-118, 2012 | 313 | 2012 |
| Genome-wide relationship between histone H3 lysine 4 mono-and tri-methylation and transcription factor binding AG Robertson, M Bilenky, A Tam, Y Zhao, T Zeng, N Thiessen, T Cezard, ... Genome research 18 (12), 1906-1917, 2008 | 233 | 2008 |
| A new algorithm for RNA secondary structure design M Andronescu, AP Fejes, F Hutter, HH Hoos, A Condon Journal of molecular biology 336 (3), 607-624, 2004 | 220 | 2004 |
| Evolution of an adenocarcinoma in response to selection by targeted kinase inhibitors SJM Jones, J Laskin, YY Li, OL Griffith, J An, M Bilenky, YS Butterfield, ... Genome biology 11, 1-12, 2010 | 205 | 2010 |
| Recurrent targets of aberrant somatic hypermutation in lymphoma AH Khodabakhshi, RD Morin, AP Fejes, AJ Mungall, KL Mungall, ... Oncotarget 3 (11), 1308, 2012 | 157 | 2012 |
| GPSM2 mutations cause the brain malformations and hearing loss in Chudley-McCullough syndrome D Doherty, AE Chudley, G Coghlan, GE Ishak, AM Innes, EG Lemire, ... The American Journal of Human Genetics 90 (6), 1088-1093, 2012 | 122 | 2012 |
| De novo motif identification improves the accuracy of predicting transcription factor binding sites in ChIP-Seq data analysis V Boeva, D Surdez, N Guillon, F Tirode, AP Fejes, O Delattre, E Barillot Nucleic acids research 38 (11), e126-e126, 2010 | 92 | 2010 |
| DNA methylation, genotype and gene expression: who is driving and who is along for the ride? MJ Jones, AP Fejes, MS Kobor Genome biology 14, 1-3, 2013 | 64 | 2013 |
| Gene expression profiling of oxidative stress response of C. elegans aging defective AMPK mutants using massively parallel transcriptome sequencing H Shin, H Lee, AP Fejes, DL Baillie, HS Koo, SJM Jones BMC research notes 4, 1-16, 2011 | 46 | 2011 |
| The VAAST Variant Prioritizer (VVP): ultrafast, easy to use whole genome variant prioritization tool S Flygare, EJ Hernandez, L Phan, B Moore, M Li, A Fejes, H Hu, K Eilbeck, ... Bmc Bioinformatics 19, 1-13, 2018 | 41 | 2018 |
| System and method for simulating the time-dependent behaviour of atomic and/or molecular systems subject to static or dynamic fields AP Fejes, JS Vieceli, S Rahnama, G Swaminathan US Patent App. 11/581,075, 2008 | 38 | 2008 |
| Shotgun proteomic analysis of a chromatophore-enriched preparation from the purple phototrophic bacterium Rhodopseudomonas palustris AP Fejes, EC Yi, DR Goodlett, JT Beatty Photosynthesis research 78, 195-203, 2003 | 28 | 2003 |
| System and method for modeling interactions AP Fejes, G Swaminathan, JS Vieceli US Patent 7,769,573, 2010 | 26 | 2010 |
| Human variation database: an open-source database template for genomic discovery AP Fejes, AH Khodabakhshi, I Birol, SJM Jones Bioinformatics 27 (8), 1155-1156, 2011 | 15 | 2011 |
| DaVIE: database for the visualization and integration of epigenetic data AP Fejes, MJ Jones, MS Kobor Frontiers in Genetics 5, 325, 2014 | 8 | 2014 |
| ChIP‐Seq: Mapping of Protein–DNA Interactions AP Fejes, SJM Jones Next Generation Genome Sequencing: Towards Personalized Medicine, 201-215, 2008 | 2 | 2008 |
| Drug Discovery in the bioinformatics Age G Duggan, A Fejes, C Ingram, M Salazar, M Sirski | 2 | 2000 |
Steven JonesBC Cancer, Simon Fraser University, University of British ColumbiaVerified email at bcgsc.ca
