Li Liu

Whole-genome sequencing combined RNA-sequencing analysis of patients with mutations in SET binding protein 1

H. Yao, Sihan Liu, Xiaojing Dong, 2022, Frontiers in Neuroscience.

Phases of the infinite U Hubbard model on square lattices.

S. White, E. Berg, S. Kivelson, 2011, Physical review letters.

Prenatal diagnosis identifies compound heterozygous variants in RYR1 that causes ultrasound abnormalities in a fetus

Yong-yi Ma, Xu Zhang, Xiaoduo Li, 2022, BMC Medical Genomics.

Case Report: Exome and RNA Sequencing Identify a Novel de novo Missense Variant in HNRNPK in a Chinese Patient With Au-Kline Syndrome

Xu Zhang, Sihan Liu, H. Yao, 2022, Frontiers in Genetics.

Expanding the mutational and clinical spectrum of Chinese intellectual disability patients with two novel CTCF variants

Sihan Liu, H. Yao, Xiaojing Dong, 2023, Frontiers in pediatrics.

Whole exome sequencing and transcriptome analysis in two unrelated patients with novel SET mutations

Li Liu, Bo-tao Tan, Xingyu Pan, 2023, Journal of Human Genetics.