Zhong Ren

Exome sequencing in amyotrophic lateral sclerosis identifies risk genes and pathways

Brittany N. Lasseigne, W. Chung, D. Goldstein, 2015, Science.

Germline De Novo Mutations in GNB1 Cause Severe Neurodevelopmental Disability, Hypotonia, and Seizures.

J. Rosenfeld, I. Scheffer, H. Mefford, 2016, American journal of human genetics.

Diagnostic Utility of Exome Sequencing for Kidney Disease

Chunhua Weng, Krzysztof Kiryluk, Jai Radhakrishnan, 2019, The New England journal of medicine.

Annotating pathogenic non-coding variants in genic regions

Zhong Ren, Kelly Schoch, Slavé Petrovski, 2017, Nature Communications.