Danhua H. Liu

Zhengzhou, China

Last Updated: 09/26/2026

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Found 13 publications

Selective loss and transcriptional reprogramming of Nox4+ GABAergic neurons in the trigeminal nucleus caudalis of NTG-induced chronic migraine model.

Selective loss and transcriptional reprogramming of Nox4+ GABAergic neurons in the trigeminal nucleus caudalis of NTG-induced chronic migraine model.

Journal: The journal of headache and pain

Published: August 28, 2025

Novel compound heterozygous pathogenic variants in the SLC3A1 gene in a Chinese family with cystinuria.

Novel compound heterozygous pathogenic variants in the SLC3A1 gene in a Chinese family with cystinuria.

Journal: BMC medical genomics

Published: October 08, 2023

Case report: Clinical and genetic analysis of a family with nonsyndromic auditory neuropathy.

Case report: Clinical and genetic analysis of a family with nonsyndromic auditory neuropathy.

Journal: Frontiers in pediatrics

Published: July 28, 2022

An accessible insight into genetic findings for transplantation recipients with suspected genetic kidney disease.

An accessible insight into genetic findings for transplantation recipients with suspected genetic kidney disease.

Journal: NPJ genomic medicine

Published: January 20, 2021

Increased diagnosis of enlarged vestibular aqueduct by multiplex PCR enrichment and next-generation sequencing of the SLC26A4 gene.

Increased diagnosis of enlarged vestibular aqueduct by multiplex PCR enrichment and next-generation sequencing of the SLC26A4 gene.

Journal: Molecular genetics & genomic medicine

Published: January 20, 2021

High Genetic Heterogeneity in Chinese Patients With Waardenburg Syndrome Revealed by Next-Generation Sequencing.

High Genetic Heterogeneity in Chinese Patients With Waardenburg Syndrome Revealed by Next-Generation Sequencing.

Journal: Frontiers in genetics

Published: December 18, 2020

Missense Variant of Endoplasmic Reticulum Region of WFS1 Gene Causes Autosomal Dominant Hearing Loss without Syndromic Phenotype.

Missense Variant of Endoplasmic Reticulum Region of WFS1 Gene Causes Autosomal Dominant Hearing Loss without Syndromic Phenotype.

Journal: BioMed research international

Published: November 24, 2020

Auditory Neuropathy Spectrum Disorder (ANSD)-Clinical Characteristics and Pathogenic Variant Analysis of Three Nonsyndromic Deafness Families.

Auditory Neuropathy Spectrum Disorder (ANSD)-Clinical Characteristics and Pathogenic Variant Analysis of Three Nonsyndromic Deafness Families.

Journal: BioMed research international

Published: October 01, 2020

Study on syndromic deafness caused by novel pattern of compound heterozygous variants in the CDH23 gene

Study on syndromic deafness caused by novel pattern of compound heterozygous variants in the CDH23 gene

Journal: Zhonghua er bi yan hou tou jing wai ke za zhi = Chinese journal of otorhinolaryngology head and neck surgery

Published: September 11, 2020

Treacher Collins syndrome: Clinical report and retrospective analysis of Chinese patients.

Treacher Collins syndrome: Clinical report and retrospective analysis of Chinese patients.

Journal: Molecular genetics & genomic medicine

Published: August 29, 2020

Dynamics of binding ability prediction between spike protein and human ACE2 reveals the adaptive strategy of SARS-CoV-2 in humans.

Dynamics of binding ability prediction between spike protein and human ACE2 reveals the adaptive strategy of SARS-CoV-2 in humans.

Journal: Scientific reports

Published: July 01, 2020

Early truncation of the N-terminal variable region of EYA4 gene causes dominant hearing loss without cardiac phenotype.

Early truncation of the N-terminal variable region of EYA4 gene causes dominant hearing loss without cardiac phenotype.

Journal: Molecular genetics & genomic medicine

Published: May 02, 2020

Showing 1-12 of 13

Last Updated: 09/26/2026