| Tumor mutation burden as a biomarker in resected non–small-cell lung cancer S Devarakonda, F Rotolo, MS Tsao, I Lanc, E Brambilla, A Masood, ... Journal of Clinical Oncology 36 (30), 2995-3006, 2018 | 249 | 2018 |
| Correlation of PD-L1 expression with tumor mutation burden and gene signatures for prognosis in early-stage squamous cell lung carcinoma H Yu, Z Chen, KV Ballman, MA Watson, R Govindan, I Lanc, DG Beer, ... Journal of Thoracic Oncology 14 (1), 25-36, 2019 | 91 | 2019 |
| Genomic profiling of lung adenocarcinoma in never-smokers S Devarakonda, Y Li, F Martins Rodrigues, S Sankararaman, H Kadara, ... Journal of Clinical Oncology 39 (33), 3747-3758, 2021 | 75 | 2021 |
| A multiple myeloma-specific capture sequencing platform discovers novel translocations and frequent, risk-associated point mutations in IGLL5 BS White, I Lanc, J O’Neal, H Gupta, RS Fulton, H Schmidt, C Fronick, ... Blood cancer journal 8 (3), 35, 2018 | 52 | 2018 |
| Adapting bioinformatics applications for heterogeneous systems: a case study I Lanc, P Bui, D Thain, S Emrich Proceedings of the second international workshop on Emerging computational …, 2011 | 16 | 2011 |
| Scripting distributed scientific workflows using Weaver P Bui, L Yu, A Thrasher, R Carmichael, I Lanc, P Donnelly, D Thain Concurrency and Computation: Practice and Experience 24 (15), 1685-1707, 2012 | 10 | 2012 |
| An unsupervised learning approach to assembly validation I Lanc, S Emrich 2013 IEEE 3rd International Conference on Computational Advances in Bio and …, 2013 | 3 | 2013 |
| Somatic mutations in mismatch repair pathway genes in non-small cell lung cancer. SH Devarakonda, A Masood, TM Johanns, I Lanc, L Du, B Ganesh, ... Journal of Clinical Oncology 34 (15_suppl), 11523-11523, 2016 | 2 | 2016 |
| Automated exposition of known and novel multiple myeloma genomic variants using a single sequencing platform B White, I Lanc, R Fulton, D Auclair, MH Tomasson US Patent 11,141,709, 2021 | | 2021 |
| Bioinformatics: What a Clinician Should Know I Lanc, A Danos Cancer Genomics for the Clinician, 43-66, 2019 | | 2019 |
| A Second Generation, Multiple Myeloma-Specific, Targeted Sequencing Platform for Detecting Translocations, Copy Number Alterations, and Single Nucleotide Variants BS White, I Lanc, D Auclair, R Fulton, MA Fiala, J King, G Ahmann, ... Blood 126 (23), 4207, 2015 | | 2015 |
| Novel methods for assembly validation and improvement I Lanc University of Notre Dame, 2014 | | 2014 |
