Xianghong Shan

A mouse model of aniridia reveals the in vivo downstream targets of Pax6 driving iris and ciliary body development in the eye.

C. Gregory‐Evans, X. Shan, Xia Wang, 2017, Biochimica et biophysica acta. Molecular basis of disease.

Loss‐of‐function mutations in KIF14 cause severe microcephaly and kidney development defects in humans and zebrafish

S. Saunier, J. Roume, C. Jeanpierre, 2018, Human molecular genetics.

Focused Magnetic Stem Cell Targeting to the Retina Using Superparamagnetic Iron Oxide Nanoparticles

U. Häfeli, P. Soema, O. L. Moritz, 2012, Cell transplantation.

RNA-based therapies in animal models of Leber congenital amaurosis causing blindness

K. Gregory-Evans, C. Gregory‐Evans, X. Shan, 2020, Precision clinical medicine.

Efficacy of Postnatal In Vivo Nonsense Suppression Therapy in a Pax6 Mouse Model of Aniridia

K. Gregory-Evans, C. Gregory‐Evans, K. Wasan, 2017, Molecular therapy. Nucleic acids.

Pax2 regulates a fadd-dependent molecular switch that drives tissue fusion during eye development.

J. Ngai, K. Gregory-Evans, C. Gregory‐Evans, 2012, Human molecular genetics.

Identifying candidate genes for 2p15p16.1 microdeletion syndrome using clinical, genomic, and functional analysis.

M. Nowaczyk, A. Lehman, B. Maranda, 2016, JCI insight.