Chao Lu

The Personal Genome Project Canada: findings from whole genome sequences of the inaugural 56 participants

Daniele Merico, Marc Fiume, John Wei, 2018, Canadian Medical Association Journal.

A Discovery Resource of Rare Copy Number Variations in Individuals with Autism Spectrum Disorder

John Wei, S. Scherer, D. Merico, 2012, G3: Genes | Genomes | Genetics.

A large data resource of genomic copy number variation across neurodevelopmental disorders

J. R. MacDonald, John Wei, S. Scherer, 2019, npj Genomic Medicine.

Microarray profiles of human basal cell carcinoma: insights into tumor growth and behavior.

N. Solish, A. Mamelak, Chao Lu, 2005, Journal of dermatological science.

A high-resolution copy-number variation resource for clinical and population genetics

Pingzhao Hu, John Wei, Christian R Marshall, 2014, Genetics in Medicine.

A large data resource of genomic copy number variation across neurodevelopmental disorders

John Wei, S. Scherer, D. Merico, 2019, npj Genomic Medicine.

A common IL-13 Arg130Gln single nucleotide polymorphism among Chinese atopy patients with allergic rhinitis

Chao Lu, Li-sheng Yu, Z. Xing, 2003, Human Genetics.

Improving the scaling normalization for high-density oligonucleotide GeneChip expression microarrays

Chao Lu, Chao Lu, 2004, BMC Bioinformatics.