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Yali Zhao

Observed names: Ya-Li ZHAO, Ya-Li Zhao, Ya-li Zhao, Zhao Ya-li, Zhao Ya–li, Zhao, Ya-Li
Observed institutions: Beijing Tongren Hospital, Capital Medical University, Chinese Academy of Medical Sciences & Peking Union Medical College, Wellcome Sanger Institute, Chinese PLA General Hospital, UNSW Sydney, Lianyungang Maternal and Children’s Hospital, St George Hospital, Hainan 301 Hospital, Beijing Municipal Education Commission, Second Affiliated Hospital of Anhui Medical University, Chinese People's Liberation Army, Institute of Basic Medical Sciences of the Chinese Academy of Medical Sciences, Tsinghua University
ORCID: 0000-0002-3785-6668
Observed ORCID: 0000-0002-3785-6668
OpenAlex ID: A5100946331
Human Y Chromosome Base-Substitution Mutation Rate Measured by Direct Sequencing in a Deep-Rooting Pedigree
2009 · Yali Xue, Qiuju Wang, et al. · Current Biology · 217
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Mutations in apoptosis-inducing factor cause X-linked recessive auditory neuropathy spectrum disorder
2015 · Liang Zong, Jing Guan, et al. · Journal of Medical Genetics · 119
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A Novel DFNA36 Mutation in TMC1 Orthologous to the Beethoven (Bth) Mouse Associated with Autosomal Dominant Hearing Loss in a Chinese Family
2014 · Yali Zhao, Dayong Wang, et al. · PLoS ONE · 71
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Exome Sequencing and Linkage Analysis Identified Tenascin-C (TNC) as a Novel Causative Gene in Nonsyndromic Hearing Loss
2013 · Yali Zhao, Feifan Zhao, et al. · PLoS ONE · 64
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Clinical and molecular analysis of a four-generation Chinese family with aminoglycoside-induced and nonsyndromic hearing loss associated with the mitochondrial 12S rRNA C1494T mutation
2005 · Qiuju Wang, Qing-Zhong Li, et al. · Biochemical and Biophysical Research Communications · 55
Keratin 14 Point Mutations at Codon 119 of Helix 1A Resulting in Different Epidermolysis Bullosa Simplex Phenotypes
2001 · Rebecca E. Cummins, Sandra Klingberg, et al. · Journal of Investigative Dermatology · 44
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Targeted High-Throughput Sequencing Identifies Pathogenic Mutations in KCNQ4 in Two Large Chinese Families with Autosomal Dominant Hearing Loss
2014 · Hongyang Wang, Yali Zhao, et al. · PLoS ONE · 32
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Genetic Basis of Y-Linked Hearing Impairment
2013 · Qiuju Wang, Yali Xue, et al. · The American Journal of Human Genetics · 27
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Identification of Two Disease-causing Genes TJP2 and GJB2 in a Chinese Family with Unconditional Autosomal Dominant Nonsyndromic Hereditary Hearing Impairment
2015 · Hong-Yang Wang, Ya-Li Zhao, et al. · Chinese Medical Journal · 25
Identification of gene biomarkers with expression profiles in patients with allergic rhinitis
2022 · Yun Hao, Boqian Wang, et al. · Allergy Asthma and Clinical Immunology · 23
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SIX2 haploinsufficiency causes conductive hearing loss with ptosis in humans
2016 · Jing Guan, Dayong Wang, et al. · Journal of Human Genetics · 18
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Health literacy and falls among community-dwelling older people in China: is there a sex difference?
2024 · Shaojie Li, Jingjing Wang, et al. · Aging Clinical and Experimental Research · 17
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A common variant of the cardiomyopathy associated 5 gene (CMYA5) is associated with schizophrenia in Chinese population
2011 · Ming Li, Xiong-jian Luo, et al. · Schizophrenia Research · 15
HLA‐DRB1*08:03:02 and HLA‐DQB1*06:01:01 are associated with house dust mite–sensitive allergic rhinitis in Chinese subjects
2016 · Yanming Zhao, Yali Zhao, et al. · International Forum of Allergy & Rhinology · 14
HLA‐II genes are associated with outcomes of specific immunotherapy for allergic rhinitis
2019 · Yanming Zhao, Yali Zhao, et al. · International Forum of Allergy & Rhinology · 12
Phenotype–Genotype Correlation in 295 Chinese Deaf Subjects with Biallelic Causative Mutations in the GJB2 Gene
2011 · Fei-Fan Zhao, Yu-Bin Ji, et al. · Genetic Testing and Molecular Biomarkers · 12
Variant analysis in Chinese families with hereditary hemorrhagic telangiectasia
2019 · Yali Zhao, Yuan Zhang, et al. · Molecular Genetics & Genomic Medicine · 11
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Analysis of a Large-Scale Screening of Mitochondrial DNA m.1555A>G Mutation in 2417 Deaf–Mute Students in Northwest of China
2010 · Yu-Fen Guo, Xiao-Wen Liu, et al. · Genetic Testing and Molecular Biomarkers · 10
Variant of PBX2 gene in the 6p21.3 asthma susceptibility locus is associated with allergic rhinitis in Chinese subjects
2016 · Yali Zhao, Yuan Zhang, et al. · International Forum of Allergy & Rhinology · 8
Immune cell related signature predicts prognosis in esophageal squamous cell carcinoma based on single-cell and bulk-RNA sequencing
2024 · Xian Wang, Wei Peng, et al. · Frontiers in Oncology · 6
Identification of rare variants of allergic rhinitis based on whole genome sequencing and gene expression profiling: A preliminary investigation in four families
2019 · Yuan Zhang, Jingyun Li, et al. · World Allergy Organization Journal · 6
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Clue to a New Deafness Gene: A Large Chinese Nonsyndromic Hearing Loss Family Linked to DFNA4
2012 · Liang Zong, Chunye Lu, et al. · Journal of genetics and genomics/Journal of Genetics and Genomics · 6
Integrating newborn genetic screening with traditional screening to improve newborn screening
2025 · Shuai Men, Zhiwei Wang, et al. · The Journal of Maternal-Fetal & Neonatal Medicine · 3
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The large Chinese family with Y-linked hearing loss revisited: Clinical investigation
2008 · Qiu-Ju Wang, Shao-Qi Rao, et al. · Acta Oto-Laryngologica · 3
Screening of GJB2 mutations in Chinese population
2007 · Han Ming-kun, Han Dong-yi, et al. · Journal of Otology · 3
Works count: 38
Citation count: 828
H-index: 14
I10-index: 18
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