Yuanlong Yan

Five novel globin gene mutations identified in five Chinese families by next‐generation sequencing

Zhiyu Peng, J. Zhang, Jing He, 2021, Molecular genetics & genomic medicine.

Analysis of deletional hereditary persistence of fetal hemoglobin/δβ‐thalassemia and δ‐globin gene mutations in Southerwestern China

Tonghua Yang, P. Li, Jie Zhang, 2019, Molecular genetics & genomic medicine.

[Genetic and clinical study of three Chinese pedigrees with Fabry disease].

Xiao-xia Liu, Yuan Yang, Zhang-Xue Hu, 2013, Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics.

Molecular epidemiology, pathogenicity, and structural analysis of haemoglobin variants in the Yunnan province population of Southwestern China

Peng Li, Jie Zhang, Hong Chen, 2019, Scientific Reports.

Combined analysis of genome-wide-linked susceptibility loci to Kawasaki disease in Han Chinese

Q. Peng, D. Tao, Yongxin Ma, 2013, Human Genetics.

Genome-Wide Loci Linked to Non-Obstructive Azoospermia Susceptibility May Be Independent of Reduced Sperm Production in Males with Normozoospermia1

D. Tao, Yongxin Ma, Yunqiang Liu, 2015, Biology of reproduction.

A significant effect of the TSPY1 copy number on spermatogenesis efficiency and the phenotypic expression of the gr/gr deletion.

D. Tao, Yongxin Ma, Yunqiang Liu, 2013, Human molecular genetics.

TSPY1 suppresses USP7-mediated p53 function and promotes spermatogonial proliferation

Q. Dong, Yunqiang Liu, Mohan Liu, 2018, Cell Death & Disease.

Epigenetic modifications promote the expression of the orphan nuclear receptor NR0B1 in human lung adenocarcinoma cells

Yi-lu Lu, D. Tao, Yongxin Ma, 2016, Oncotarget.

Combined analysis of genome-wide-linked susceptibility loci to Kawasaki disease in Han Chinese

Q. Peng, D. Tao, Yongxin Ma, 2013, Human Genetics.

TSPY1 suppresses USP7-mediated p53 function and promotes spermatogonial proliferation

Q. Dong, Yunqiang Liu, Mohan Liu, 2018, Cell Death & Disease.