Y. Cheung

发表

Variants in GATA4 are a rare cause of familial and sporadic congenital diaphragmatic hernia

W. Chung, Yufeng Shen, M. Arkovitz, 2013, Human Genetics.

De novo mutations in histone modifying genes in congenital heart disease

Murim Choi, Hongyu Zhao, Alexander E. Lopez, 2013, Nature.

A recurrent PDGFRB mutation causes familial infantile myofibromatosis.

W. Chung, R. Gibbs, A. Berghuis, 2013, American journal of human genetics.

Whole‐Exome sequencing identifies novel LEPR mutations in individuals with severe early onset obesity

Yufeng Shen, Y. Cheung, J. Yanovski, 2014, Obesity.

A Fast and Noise‐Resilient Approach to Detect Rare‐Variant Associations With Deep Sequencing Data for Complex Disorders

Shuang Wang, Yee Him Cheung, Gao Wang, 2012, Genetic epidemiology.

Conditional meta-analysis stratifying on detailed HLA genotypes identifies a novel type 1 diabetes locus around TCF19 in the MHC

J. Watkinson, D. Anastassiou, Y. Cheung, 2010, Human Genetics.

Analysis and visualization of DNA spectrograms: open possibilities for the genome research

Michael Q. Zhang, Nevenka Dimitrova, Yee Him Cheung, 2006, MM '06.

Variants in GATA4 are a rare cause of familial and sporadic congenital diaphragmatic hernia

W. Chung, Yufeng Shen, M. Arkovitz, 2013, Human Genetics.

Whole exome sequencing identifies de novo mutations in GATA6 associated with congenital diaphragmatic hernia

G. Carvill, H. Mefford, W. Chung, 2014, Journal of Medical Genetics.

Whole exome sequencing identi fi es de novo mutations in GATA 6 associated with congenital diaphragmatic hernia

G. Carvill, H. Mefford, W. Chung, 2013 .

A Fast and Noise‐Resilient Approach to Detect Rare‐Variant Associations With Deep Sequencing Data for Complex Disorders

Gao T. Wang, S. Leal, Y. Cheung, 2012, Genetic epidemiology.

A parametric Bayesian method to test the association of rare variants

Yufeng Shen, Shuang Wang, Itsik Pe'er, 2011, 2011 IEEE International Conference on Bioinformatics and Biomedicine Workshops (BIBMW).