L. Zhang

Common genetic variants on 1p13.2 associate with risk of autism

Z. Hu, D. St. Clair, Y. Hu, 2014, Molecular Psychiatry.

Exome sequencing identifies UPF3B as the causative gene for a Chinese non‐syndrome mental retardation pedigree

Y. Zheng, K. Xia, Z. Xiong, 2013, Clinical genetics.

Novel FLG mutations associated with ichthyosis vulgaris in the Chinese population

K. Xia, Z. Xiong, L. Zhang, 2012, Clinical and experimental dermatology.

Meiotic recombination break points resolve at high rates at the 5' end of a maize coding sequence.

P. Schnable, L. Zhang, A. Hsia, 1995, The Plant cell.

Characterization of a TIR-NBS-LRR gene associated with downy mildew resistance in grape.

Y. Zhu, L. Zhang, Z. Cui, 2015, Genetics and molecular research : GMR.

Novel mutations in mevalonate kinase cause disseminated superficial actinic porokeratosis

D. Tian, K. Xia, Z. Xiong, 2019, The British journal of dermatology.