Wenjun Xia

发表

Research progress in pathogenic genes of hereditary non-syndromic mid-frequency deafness

Duan Ma, Wenjun Xia, Fei Liu, 2016, Frontiers of Medicine.

Exome Sequencing Identifies a Mutation in EYA4 as a Novel Cause of Autosomal Dominant Non-Syndromic Hearing Loss

Duan Ma, Zhaoxin Ma, Jiongjiong Hu, 2015, PloS one.

The Novel Pathogenic Mutation c.849dupT in BRCA2 Contributes to the Nonsense-Mediated mRNA Decay of BRCA2 in Familial Breast Cancer

Jichun Yang, Duan Ma, Ling-Yueh Hu, 2018, Journal of Breast Cancer.

Functional analysis of a de novo mutation c.1692 del A of the PHEX gene in a Chinese family with X-linked hypophosphataemic rickets

Jichun Yang, Duan Ma, Jin Zhang, 2019, Bone & joint research.

Grhl1 deficiency affects inner ear development in zebrafish.

Duan Ma, Zhaoxin Ma, Xu Wang, 2015, The International journal of developmental biology.

A novel loss-of-function heterozygous BRCA2 c.8946_8947delAG mutation found in a Chinese woman with family history of breast cancer

Jichun Yang, Duan Ma, Wenjing Jian, 2017, Journal of Cancer Research and Clinical Oncology.

Exome sequencing identifies a mutation in TMC1 as a novel cause of autosomal recessive nonsyndromic hearing loss

Duan Ma, Zhaoxin Ma, Zhenghua Zhu, 2016, Journal of Translational Medicine.

Mutations in TOP2B cause autosomal‐dominant hereditary hearing loss via inhibition of the PI3K‐Akt signalling pathway

Duan Ma, Zhaoxin Ma, Jin Zhang, 2019, FEBS letters.

Solute Carrier Family 26 Member a2 (slc26a2) Regulates Otic Development and Hair Cell Survival in Zebrafish

Weidong Tian, Duan Ma, Xu Wang, 2015, PloS one.

Epigenetic regulation of megakaryocytic and erythroid differentiation by PHF2 histone demethylase

Jichun Yang, Duan Ma, Y. Xiong, 2018, Journal of cellular physiology.

SLC44A4 mutation causes autosomal dominant hereditary postlingual non-syndromic mid-frequency hearing loss

Fei Liu, Duan Ma, Zhaoxin Ma, 2016, Human molecular genetics.

Novel TRRAP mutation causes autosomal dominant non‐syndromic hearing loss

Duan Ma, Zhaoxin Ma, Xu Wang, 2019, Clinical genetics.

Identification of ANLN as a new likely pathogenic gene of branchio‐otic syndrome in a three‐generation Chinese family

Zhaoxin Ma, Jiongjiong Hu, Wenjun Xia, 2018, Molecular genetics & genomic medicine.

New role of LRP5, associated with nonsyndromic autosomal‐recessive hereditary hearing loss

Duan Ma, Zhaoxin Ma, Xu Wang, 2017, Human mutation.

Down-regulation of msrb3 and destruction of normal auditory system development through hair cell apoptosis in zebrafish.

Fei Liu, Duan Ma, Xu Wang, 2015, International Journal of Developmental Biology.