Zhaoling Xuan

Mutational spectrum and risk stratification of intermediate-risk acute myeloid leukemia patients based on next-generation sequencing

Junbin Liang, Li-li Wang, A. Deng, 2016, Oncotarget.

Multicenter cross-sectional screening of the BRCA gene for Chinese high hereditary risk breast cancer populations.

R. Ling, N. Liao, Junbin Liang, 2018, Oncology letters.

Identification of a de novo fetal variant in osteogenesis imperfecta by targeted sequencing-based noninvasive prenatal testing

Junbin Liang, Juan Wang, Chongjian Chen, 2018, Journal of Human Genetics.

Germline mutations in 40 cancer susceptibility genes among Chinese patients with high hereditary risk breast cancer

R. Ling, N. Liao, Junbin Liang, 2018, International journal of cancer.

High resolution global chromosomal aberrations from spontaneous miscarriages revealed by low coverage whole genome sequencing.

Chong-Jian Chen, X. Kong, Juan Wang, 2018, European journal of obstetrics, gynecology, and reproductive biology.

Statistical Approach to Decreasing the Error Rate of Noninvasive Prenatal Aneuploid Detection caused by Maternal Copy Number Variation

J. Qiao, Yuan Wei, Dawei Li, 2015, Scientific Reports.

Identification of a de novo fetal variant in osteogenesis imperfecta by targeted sequencing-based noninvasive prenatal testing

Junbin Liang, Juan Wang, Chongjian Chen, 2018, Journal of Human Genetics.