|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
|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
|Methods and Systems for Identification of DNA Patterns through Spectral Analysis|
N Dimitrova, YH Cheung
US Patent 8,189,892, 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
|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
|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
|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
|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
|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
|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
|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
|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
|α Tree in Sensor Network|
YH Cheung, N Maxemchuk
New York Metro Area Networking Workshop (NYMAN), 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
|Using k-mers for rapid quality control of sequencing data without alignment|
J Wu, YH Cheung
US Patent App. 16/177,684, 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
|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
|Interactive precision medicine explorer for genomic abberations and treatment options|
YH Cheung, N Dimitrova, JM De Bont
US Patent App. 15/964,180, 2018
|Cross platform transformation of gene expression data|
YH Cheung, WFJ Verhaegh, N Dimitrova
US Patent App. 15/518,257, 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