Xue Z Liu

Professor

  • 5898 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

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
Deafness
Hearing Loss
Genes
Pedigree
Genome

Research Output 1993 2019

New Genotypes and Phenotypes in Patients with 3 Subtypes of Waardenburg Syndrome Identified by Diagnostic Next-Generation Sequencing

Li, W., Mei, L., Chen, H., Cai, X., Liu, Y., Men, M., Liu, X. Z., Yan, D., Ling, J., Feng, Y. & Dorszewska, J., Jan 1 2019, In : Neural Plasticity. 2019, 7143458.

Research output: Contribution to journalArticle

Open Access
Waardenburg Syndrome
Genotype
Phenotype
Melanosis
Amblyopia

Preclinical assessment of MEK1/2 inhibitors for neurofibromatosis type 2-associated schwannomas reveals differences in efficacy and drug resistance development

Fuse, M. A., Dinh, C. T., Vitte, J., Kirkpatrick, J., Mindos, T., Plati, S. K., Young, J. I., Huang, J., Carlstedt, A., Franco, M. C., Brnjos, K., Nagamoto, J., Petrilli, A. M., Copik, A. J., Soulakova, J. N., Bracho, O., Yan, D., Mittal, R., Shen, R., Telischi, F. F. & 5 othersMorrison, H., Giovannini, M., Liu, X. Z., Chang, L. S. & Fernandez-Valle, C., Mar 18 2019, In : Neuro-Oncology. 21, 4, p. 486-497 12 p.

Research output: Contribution to journalArticle

Neurofibromatosis 2
Neurilemmoma
Drug Resistance
Acoustic Neuroma
Neurofibromin 2

Role of microRNAs in inner ear development and hearing loss

Mittal, R., Liu, G., Polineni, S. P., Bencie, N., Yan, D. & Liu, X. Z., Feb 20 2019, In : Gene. 686, p. 49-55 7 p.

Research output: Contribution to journalReview article

Inner Ear
MicroRNAs
Hearing Loss
Inner Auditory Hair Cells
Research
1 Citation (Scopus)

A dominant variant in the PDE1C gene is associated with nonsyndromic hearing loss

Wang, L., Feng, Y., Yan, D., Qin, L., Grati, M., Mittal, R., Li, T., Sundhari, A. K., Liu, Y., Chapagain, P., Blanton, S. H., Liao, S. & Liu, X. Z., Jun 2 2018, (Accepted/In press) In : Human Genetics. p. 1-10 10 p.

Research output: Contribution to journalArticle

Phosphoric Diester Hydrolases
Exome
Inner Auditory Hair Cells
Genes
Genetic Heterogeneity

Amino acid 118 in the deafness causing (DFNA20/26) ACTG1 gene is a mutational hot spot

Wang, L., Yan, D., Qin, L., Li, T., Liu, H., Li, W., Mittal, R., Yong, F., Chapagain, P., Liao, S. & Liu, X. Z., Jun 1 2018, In : Gene Reports. 11, p. 264-269 6 p.

Research output: Contribution to journalArticle

Deafness
Hearing Loss
Amino Acids
Genes
Mutation