Liangwei Mao

Wuhan, China

Last Updated: 09/26/2026

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Found 15 publications

Identification and functional characterization of ABCA4 gene variants in three patients with Stargardt disease or retinitis pigmentosa.

Identification and functional characterization of ABCA4 gene variants in three patients with Stargardt disease or retinitis pigmentosa.

Journal: Frontiers in genetics

Published: October 25, 2024

Genome surveillance of SARS-CoV-2 Omicron XBB subvariants in Wuhan in June 2023.

Genome surveillance of SARS-CoV-2 Omicron XBB subvariants in Wuhan in June 2023.

Journal: Archives of virology

Published: October 24, 2024

A rapid, sensitive, and high-throughput pathogen detection method and application of identifying pathogens based on multiplex PCR technology combined with capillary electrophoresis.

A rapid, sensitive, and high-throughput pathogen detection method and application of identifying pathogens based on multiplex PCR technology combined with capillary electrophoresis.

Journal: Diagnostic microbiology and infectious disease

Published: July 02, 2024

Clinical diagnosis of genetic disorders at both single-nucleotide and chromosomal levels based on BGISEQ-500 platform.

Clinical diagnosis of genetic disorders at both single-nucleotide and chromosomal levels based on BGISEQ-500 platform.

Journal: Human genome variation

Published: April 26, 2022

Cross-Sectional Study on the Gut Microbiome of Parkinson's Disease Patients in Central China.

Cross-Sectional Study on the Gut Microbiome of Parkinson's Disease Patients in Central China.

Journal: Frontiers in microbiology

Published: June 21, 2021

Novel missense variant in TTN cosegregating with familial atrioventricular block.

Novel missense variant in TTN cosegregating with familial atrioventricular block.

Journal: European journal of medical genetics

Published: May 14, 2019

Panel-based NGS reveals disease-causing mutations in hearing loss patients using BGISEQ-500 platform.

Panel-based NGS reveals disease-causing mutations in hearing loss patients using BGISEQ-500 platform.

Journal: Medicine

Published: March 22, 2019

Novel compound heterozygous mutations in OCA2 gene associated with non-syndromic oculocutaneous albinism in a Chinese Han patient: a case report.

Novel compound heterozygous mutations in OCA2 gene associated with non-syndromic oculocutaneous albinism in a Chinese Han patient: a case report.

Journal: BMC medical genetics

Published: February 05, 2019

Sub-Exome Target Sequencing in a Family With Syndactyly Type IV Due to a Novel Partial Duplication of the LMBR1 Gene: First Case Report in Fujian Province of China.

Sub-Exome Target Sequencing in a Family With Syndactyly Type IV Due to a Novel Partial Duplication of the LMBR1 Gene: First Case Report in Fujian Province of China.

Journal: Frontiers in genetics

Published: December 04, 2018

Targeted next-generation sequencing as a comprehensive test for Mendelian diseases: a cohort diagnostic study.

Targeted next-generation sequencing as a comprehensive test for Mendelian diseases: a cohort diagnostic study.

Journal: Scientific reports

Published: March 12, 2018

Application of an improved targeted next generation sequencing method to diagnose non‑syndromic mental retardation in one step: A case report.

Application of an improved targeted next generation sequencing method to diagnose non‑syndromic mental retardation in one step: A case report.

Journal: Molecular medicine reports

Published: October 18, 2017

Targeted next-generation sequencing identifies nine novel filaggrin gene variants in Chinese Han patients with ichthyosis vulgaris.

Targeted next-generation sequencing identifies nine novel filaggrin gene variants in Chinese Han patients with ichthyosis vulgaris.

Journal: The British journal of dermatology

Published: April 14, 2017

Showing 1-12 of 15

Last Updated: 09/26/2026