| De novo mutations in histone-modifying genes in congenital heart disease S Zaidi, M Choi, H Wakimoto, L Ma, J Jiang, JD Overton, ... Nature 498 (7453), 220-223, 2013 | 950 | 2013 |
| A recurrent PDGFRB mutation causes familial infantile myofibromatosis YH Cheung, T Gayden, PM Campeau, CA LeDuc, D Russo, VH Nguyen, ... The American Journal of Human Genetics 92 (6), 996-1000, 2013 | 157 | 2013 |
| Methods and Systems for Identification of DNA Patterns through Spectral Analysis N Dimitrova, YH Cheung US Patent 8,189,892, 2012 | 120* | 2012 |
| Variants in GATA4 are a rare cause of familial and sporadic congenital diaphragmatic hernia L Yu, J Wynn, YH Cheung, Y Shen, GB Mychaliska, TM Crombleholme, ... Human genetics 132, 285-292, 2013 | 88 | 2013 |
| Whole‐Exome sequencing identifies novel LEPR mutations in individuals with severe early onset obesity R Gill, YH Cheung, Y Shen, P Lanzano, NM Mirza, S Ten, NK Maclaren, ... Obesity 22 (2), 576-584, 2014 | 69 | 2014 |
| Whole exome sequencing identifies de novo mutations in GATA6 associated with congenital diaphragmatic hernia L Yu, JT Bennett, J Wynn, GL Carvill, YH Cheung, Y Shen, GB Mychaliska, ... Journal of medical genetics 51 (3), 197-202, 2014 | 67 | 2014 |
| Conditional meta-analysis stratifying on detailed HLA genotypes identifies a novel type 1 diabetes locus around TCF19 in the MHC YH Cheung, J Watkinson, D Anastassiou Human genetics 129, 161-176, 2011 | 42 | 2011 |
| A fast and noise‐resilient approach to detect rare‐variant associations with deep sequencing data for complex disorders YH Cheung, G Wang, SM Leal, S Wang Genetic Epidemiology 36 (7), 675-685, 2012 | 25 | 2012 |
| Analysis and visualization of DNA spectrograms: open possibilities for the genome research N Dimitrova, YH Cheung, M Zhang Proceedings of the 14th ACM international conference on Multimedia, 1017-1024, 2006 | 15 | 2006 |
| Relevance feedback to improve the performance of clustering model that clusters patients with similar profiles together V Agrawal, AR Mankovich, N Dimitrova, N Banerjee, YH Cheung, ... US Patent 11,854,694, 2023 | 6 | 2023 |
| Cohort explorer for visualizing comprehensive sample relationships through multi-modal feature variations YH Cheung, Y Mao, N Dimitrova, N Banerjee, JM De Bont, ... US Patent App. 15/973,775, 2018 | 5 | 2018 |
| Telescopic data compression in dense sensor networks that support fire-fighters YH Cheung, NF Maxemchuk IEEE GLOBECOM 2007-IEEE Global Telecommunications Conference, 914-919, 2007 | 4 | 2007 |
| Blood-based gene expression profiling to reveal potential response biomarkers for immunotherapy in advanced lung cancer. J Wu, W Huang, C Yin, YH Cheung, D Abrams, JT Fallon, N Dimitrova, ... Journal of Clinical Oncology 38 (15_suppl), e15155-e15155, 2020 | 3 | 2020 |
| Tumor functional mutation and epitope loads as improved predictive biomarkers for immunotherapy response YH Cheung, AR Mankovich, J Wu, N Dimitrova US Patent App. 17/050,642, 2021 | 2 | 2021 |
| Using k-mers for rapid quality control of sequencing data without alignment J Wu, YH Cheung US Patent App. 16/177,684, 2019 | 2 | 2019 |
| Gene expression profiles of peripheral blood mononuclear cells from patients with advanced non-small cell lung cancer treated with anti-PD-1 monoclonal antibodies. J Wu, YH Cheung, W Huang, C Yin, JT Fallon, N Dimitrova, MP Fanucchi Journal of Clinical Oncology 37 (15_suppl), e14107-e14107, 2019 | 2 | 2019 |
| Interactive precision medicine explorer for genomic abberations and treatment options YH Cheung, N Dimitrova, JM De Bont US Patent App. 15/964,180, 2018 | 2 | 2018 |
| α Tree in Sensor Network YH Cheung, N Maxemchuk New York Metro Area Networking Workshop (NYMAN), 2003 | 2 | 2003 |
| Genomic information compression by configurable machine learning-based arithmetic coding S Chandak, YH Cheung US Patent App. 18/015,089, 2023 | 1 | 2023 |
| Method and system using integrative multi-omic data analysis for evaluating the functional impacts of genomic variants YH Cheung, J Wu, N Dimitrova US Patent App. 17/780,037, 2022 | 1 | 2022 |
