Jianing Gu

发表

Identification and functional characterization of KLF5 as a novel disease gene responsible for familial dilated cardiomyopathy.

Cui-Mei Zhao, Ying-Jia Xu, Yi-Qing Yang, 2019, European journal of medical genetics.

Complex renal cysts combined with hemorrhage during crizotinib treatment for ALK-rearranged lung adenocarcinoma.

X. Niu, Ling Yang, Jianing Gu, 2021, Cancer treatment and research communications.

Association Between METS-IR and Prehypertension or Hypertension Among Normoglycemia Subjects in Japan: A Retrospective Study

Jianing Gu, Jie Liu, Dan Liu, 2022, Frontiers in Endocrinology.

Identification of BMP10 as a Novel Gene Contributing to Dilated Cardiomyopathy

Ling Yang, Ying-Jia Xu, Yi-Qing Yang, 2023, Diagnostics.

SOX7 loss-of-function variation as a cause of familial congenital heart disease.

Ri-tai Huang, S. Xue, X. Qiu, 2022, American journal of translational research.

Detection and functional characterization of a novel MEF2A variation responsible for familial dilated cardiomyopathy

M. Zhang, Cui-Mei Zhao, Ruo-Gu Li, 2020, Clinical chemistry and laboratory medicine.

VEZF1 loss-of-function mutation underlying familial dilated cardiomyopathy.

X. Qiu, Ying-Jia Xu, Yi-Qing Yang, 2023, European journal of medical genetics.

ISL1 loss-of-function variation causes familial atrial fibrillation.

X. Qiu, Ying-Jia Xu, Yi-Qing Yang, 2020, European journal of medical genetics.

Identification and Functional Characterization of an ISL1 Mutation Predisposing to Dilated Cardiomyopathy

Ying-Jia Xu, Yi-Qing Yang, Qi Qiao, 2018, Journal of Cardiovascular Translational Research.