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 | 868 | 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 | 151 | 2013 |
Methods and Systems for Identification of DNA Patterns through Spectral Analysis N Dimitrova, YH Cheung US Patent 8,189,892, 2012 | 103* | 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 | 83 | 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 | 63 | 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 | 61 | 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 | 38 | 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 | 23 | 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 | 12 | 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 App. 16/084,800, 2019 | 4 | 2019 |
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 | 4 | 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 |
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 |
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 |
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 | 1 | 2020 |
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 | 1 | 2019 |
20. Using blood-based gene expression profiling to assess responsiveness to immunotherapy of advanced non-small-cell lung cancer W Huang, J Wu, M Fanucchi, C Yin, YH Cheung, JT Fallon, N Dimitrova Cancer Genetics 233, S8, 2019 | 1 | 2019 |
Cross platform transformation of gene expression data YH Cheung, WFJ Verhaegh, N Dimitrova US Patent App. 15/518,257, 2017 | 1 | 2017 |
A parametric Bayesian method to test the association of rare variants Y Shen, YH Cheung, S Wang, I Pe'er 2011 IEEE International Conference on Bioinformatics and Biomedicine …, 2011 | 1 | 2011 |