Xue Z Liu

Professor

  • 6200 Citations
1993 …2023
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  • 18 Similar Profiles
Hearing Loss Medicine & Life Sciences
Deafness Medicine & Life Sciences
Mutation Medicine & Life Sciences
Usher Syndromes Medicine & Life Sciences
Genes Medicine & Life Sciences
Sensorineural Hearing Loss Medicine & Life Sciences
Hearing Medicine & Life Sciences
Inner Ear Medicine & Life Sciences

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Projects 2000 2023

1-Phosphatidylinositol 4-Kinase
Acoustic Neuroma
Neurofibromin 2
Schwann Cells
Neurofibromatosis 2
Otolaryngology
Research
Hearing Disorders
Communication Disorders
National Institute on Deafness and Other Communication Disorders (U.S.)
Clinical Medicine
Patient Care
Deafness
Hearing Loss
Genes
Deafness
Molecular Biology
Hearing Loss
Genes
Mutation
Hearing Loss
Molecular Biology
Genes
Deafness
Dominant Genes

Research Output 1993 2019

A novel ABHD12 nonsense variant in Usher syndrome type 3 family with genotype-phenotype spectrum review

Li, T., Feng, Y., Liu, Y., He, C., Liu, J., Chen, H., Deng, Y., Li, M., Li, W., Song, J., Niu, Z., Sang, S., Wen, J., Men, M., Chen, X., Li, J., Liu, X. Z. & Ling, J., Jul 1 2019, In : Gene. 704, p. 113-120 8 p.

Research output: Contribution to journalArticle

Usher Syndromes
Genotype
Phenotype
Deaf-Blind Disorders
Exome

Correction: ClinGen expert clinical validity curation of 164 hearing loss gene–disease pairs (Genetics in Medicine, (2019), 10.1038/s41436-019-0487-0)

on behalf of the ClinGen Hearing Loss Clinical Domain Working Group, Jan 1 2019, (Accepted/In press) In : Genetics in Medicine.

Research output: Contribution to journalComment/debate

Open Access
Hearing Loss
Medicine
Open Access
Induced Pluripotent Stem Cells
Audition
Stem cells
Hearing Loss
Oligonucleotides

Extrusion pump ABCC1 was first linked with nonsyndromic hearing loss in humans by stepwise genetic analysis

Li, M., Mei, L., He, C., Chen, H., Cai, X., Liu, Y., Tian, R., Tian, Q., Song, J., Jiang, L., Liu, C., Wu, H., Li, T., Liu, J., Li, X., Yi, Y., Yan, D., Blanton, S. H., Hu, Z., Liu, X. Z. & 3 others, Li, J., Ling, J. & Feng, Y., Jan 1 2019, In : Genetics in Medicine.

Research output: Contribution to journalArticle

Cochlea
Medical Genetics
Fluorescent Antibody Technique
Stria Vascularis
Exome
Genetic Testing
Hearing Loss
Tongue
Hearing
Newborn Infant