Wenjun Xia

Shanghai, 200032, China

Last Updated: 09/26/2026

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Found 20 publications

Evaluation of three obturation techniques in 3D-printed models of oval canals with standardized prepared morphology: a micro-CT study.

Evaluation of three obturation techniques in 3D-printed models of oval canals with standardized prepared morphology: a micro-CT study.

Journal: BMC oral health

Published: July 21, 2025

Root canal treatment planning by automatic tooth and root canal segmentation in dental CBCT with deep multi-task feature learning.

Root canal treatment planning by automatic tooth and root canal segmentation in dental CBCT with deep multi-task feature learning.

Journal: Medical image analysis

Published: May 29, 2022

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

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

Journal: Bone & joint research

Published: September 21, 2019

Novel TRRAP mutation causes autosomal dominant non-syndromic hearing loss.

Novel TRRAP mutation causes autosomal dominant non-syndromic hearing loss.

Journal: Clinical genetics

Published: April 09, 2019

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

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

Journal: FEBS letters

Published: April 06, 2019

Impact of Graphene Exposure on Microbial Activity and Community Ecosystem in Saliva.

Impact of Graphene Exposure on Microbial Activity and Community Ecosystem in Saliva.

Journal: ACS applied bio materials

Published: January 22, 2019

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

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

Journal: Molecular genetics & genomic medicine

Published: July 06, 2018

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

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

Journal: Journal of breast cancer

Published: March 18, 2018

Selective Transformation of β-Lactam Antibiotics by Peroxymonosulfate: Reaction Kinetics and Nonradical Mechanism.

Selective Transformation of β-Lactam Antibiotics by Peroxymonosulfate: Reaction Kinetics and Nonradical Mechanism.

Journal: Environmental science & technology

Published: January 03, 2018

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

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

Journal: Human molecular genetics

Published: September 02, 2017

Epigenetic regulation of megakaryocytic and erythroid differentiation by PHF2 histone demethylase.

Epigenetic regulation of megakaryocytic and erythroid differentiation by PHF2 histone demethylase.

Journal: Journal of cellular physiology

Published: July 24, 2017

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

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

Journal: Human mutation

Published: December 28, 2016

Showing 1-12 of 20

Last Updated: 09/26/2026