| Human genome sequencing using unchained base reads on self-assembling DNA nanoarrays R Drmanac, AB Sparks, MJ Callow, AL Halpern, NL Burns, BG Kermani, ... Science 327 (5961), 78-81, 2010 | 1587 | 2010 |
| Diverse somatic mutation patterns and pathway alterations in human cancers Z Kan, BS Jaiswal, J Stinson, V Janakiraman, D Bhatt, HM Stern, P Yue, ... Nature 466 (7308), 869-873, 2010 | 1233 | 2010 |
| The PIK3CA gene is mutated with high frequency in human breast cancers KE Bachman, P Argani, Y Samuels, N Silliman, J Ptak, S Szabo, ... Cancer biology & therapy 3 (8), 772-775, 2004 | 889 | 2004 |
| Mutational analysis of the tyrosine phosphatome in colorectal cancers Z Wang, D Shen, DW Parsons, A Bardelli, J Sager, S Szabo, J Ptak, ... Science 304 (5674), 1164-1166, 2004 | 652 | 2004 |
| Contribution of bone marrow–derived endothelial cells to human tumor vasculature BA Peters, LA Diaz Jr, K Polyak, L Meszler, K Romans, EC Guinan, ... Nature medicine 11 (3), 261-262, 2005 | 645 | 2005 |
| Oncogenic ERBB3 mutations in human cancers BS Jaiswal, NM Kljavin, EW Stawiski, E Chan, C Parikh, S Durinck, ... Cancer cell 23 (5), 603-617, 2013 | 417 | 2013 |
| Accurate whole-genome sequencing and haplotyping from 10 to 20 human cells BA Peters, BG Kermani, AB Sparks, O Alferov, P Hong, A Alexeev, Y Jiang, ... Nature 487 (7406), 190-195, 2012 | 406 | 2012 |
| Methods and compositions for long fragment read sequencing R Drmanac, BA Peters, A Alexeev, P Hong US Patent 8,592,150, 2013 | 398 | 2013 |
| Somatic mutations in p85α promote tumorigenesis through class IA PI3K activation BS Jaiswal, V Janakiraman, NM Kljavin, S Chaudhuri, HM Stern, W Wang, ... Cancer cell 16 (6), 463-474, 2009 | 346 | 2009 |
| Truncating mutations of MAGEL2 cause Prader-Willi phenotypes and autism CP Schaaf, ML Gonzalez-Garay, F Xia, L Potocki, KW Gripp, B Zhang, ... Nature genetics 45 (11), 1405-1408, 2013 | 340 | 2013 |
| Genetic alterations and oncogenic pathways associated with breast cancer subtypes X Hu, HM Stern, L Ge, C O'Brien, L Haydu, CD Honchell, PM Haverty, ... Molecular cancer research 7 (4), 511-522, 2009 | 289 | 2009 |
| TGS-GapCloser: a fast and accurate gap closer for large genomes with low coverage of error-prone long reads M Xu, L Guo, S Gu, O Wang, R Zhang, BA Peters, G Fan, X Liu, X Xu, ... GigaScience 9 (9), giaa094, 2020 | 269 | 2020 |
| A public resource facilitating clinical use of genomes MP Ball, JV Thakuria, AW Zaranek, T Clegg, AM Rosenbaum, X Wu, ... Proceedings of the National Academy of Sciences 109 (30), 11920-11927, 2012 | 234 | 2012 |
| Efficient and unique cobarcoding of second-generation sequencing reads from long DNA molecules enabling cost-effective and accurate sequencing, haplotyping, and de novo assembly O Wang, R Chin, X Cheng, MKY Wu, Q Mao, J Tang, Y Sun, E Anderson, ... Genome research 29 (5), 798-808, 2019 | 216 | 2019 |
| Multiple tagging of individual long DNA fragments R Drmanac, BA Peters, A Alexeev US Patent 9,328,382, 2016 | 201 | 2016 |
| Deep RNA sequencing analysis of readthrough gene fusions in human prostate adenocarcinoma and reference samples S Nacu, W Yuan, Z Kan, D Bhatt, CS Rivers, J Stinson, BA Peters, ... BMC medical genomics 4, 1-22, 2011 | 197 | 2011 |
| Processing and analysis of complex nucleic acid sequence data R Drmanac, BA Peters, BG Kermani US Patent 9,524,369, 2016 | 157 | 2016 |
| Distinguishing cancer-associated missense mutations from common polymorphisms JS Kaminker, Y Zhang, A Waugh, PM Haverty, B Peters, D Sebisanovic, ... Cancer research 67 (2), 465-473, 2007 | 140 | 2007 |
| Sequencing Small Amounts of Complex Nucleic Acids R Drmanac, BA Peters, BG Kermani US Patent App. 13/448,279, 2013 | 131 | 2013 |
| Pharmacologic and Toxicologic Evaluation of C. novyi-NT Spores LA Diaz Jr, I Cheong, CA Foss, X Zhang, BA Peters, N Agrawal, ... Toxicological Sciences 88 (2), 562-575, 2005 | 131 | 2005 |
