Qian Han

Exome sequencing reveals a de novo PRKG1 mutation in a sporadic patient with aortic dissection

Wei Zhou, Wei Zhou, Q. Cao, 2018, BMC Medical Genetics.

Identification of a missense mutation of COL3A1 in a Chinese family with atypical Ehlers-Danlos syndrome using targeted next-generation sequencing

Chang-jian Liu, Min Zhou, Zhao Liu, 2016, Molecular medicine reports.

Whole exome sequencing reveals a stop-gain mutation of PKD2 in an autosomal dominant polycystic kidney disease family complicated with aortic dissection

Wei Zhou, Q. Cao, Weimin Zhou, 2018, BMC Medical Genetics.

Increased METTL3-mediated m6A methylation inhibits embryo implantation by repressing HOXA10 expression in recurrent implantation failure

Wei Zhou, Bin Yu, Lingyun Xu, 2021, Reproductive Biology and Endocrinology.

Extensive serum biomarker analysis in the prethrombotic state of recurrent spontaneous abortion

Jingshang Wang, C. Yin, Qian Han, 2021, Journal of cellular and molecular medicine.

Whole exome sequencing identifies FBN1 mutations in two patients with early-onset type B aortic dissection

Chang-jian Liu, Xitai Sun, Min Zhou, 2017, Molecular medicine reports.