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Yanbao Xiang

Observed names: Yan-bao Xiang, Yan‐Bao Xiang
ORCID: 0000-0003-1105-8016
Observed ORCID: 0000-0003-1105-8016
OpenAlex ID: A5028034921
Mutation analysis of common deafness-causing genes among 506 patients with nonsyndromic hearing loss from Wenzhou city, China
2019 · Yan-bao Xiang, Shao-hua Tang, et al. · International Journal of Pediatric Otorhinolaryngology · 23
Skeleton Genetics: a comprehensive database for genes and mutations related to genetic skeletal disorders
2016 · Chong Chen, Yi Jiang, et al. · Database · 22
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Next‐generation sequencing identifies rare pathogenic and novel candidate variants in a cohort of Chinese patients with syndromic or nonsyndromic hearing loss
2020 · Yan‐Bao Xiang, Chen‐Yang Xu, et al. · Molecular Genetics & Genomic Medicine · 17
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PLPPR4 haploinsufficiency causes neurodevelopmental disorders by disrupting synaptic plasticity via mTOR signalling
2023 · Huanzheng Li, Qian Zhang, et al. · Journal of Cellular and Molecular Medicine · 10
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Genome-Wide Array Analysis Reveals Novel Genomic Regions and Candidate Gene for Intellectual Disability
2018 · Xiangnan Chen, Huanzheng Li, et al. · Molecular Diagnosis & Therapy · 7
Novel compound heterozygous synonymous and missense variants in the MYO7A gene identified by next‐generation sequencing in a Chinese family with nonsyndromic hearing loss
2022 · Yanbao Xiang, Chenyang Xu, et al. · Journal of Clinical Laboratory Analysis · 6
The variations in human orphan G protein‐coupled receptor QRFPR affect PI3K‐AKT‐mTOR signaling
2021 · Huanzheng Li, Ran Lou, et al. · Journal of Clinical Laboratory Analysis · 6
Genetic analysis and prenatal diagnosis of 20 Chinese families with oculocutaneous albinism
2020 · Chenyang Xu, Yanbao Xiang, et al. · Journal of Clinical Laboratory Analysis · 5
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Clinical application of chromosomal microarray analysis for fetuses with craniofacial malformations
2020 · Chenyang Xu, Yanbao Xiang, et al. · Molecular Cytogenetics · 5
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Saliva Sample‐Based Non‐Invasive Carrier Screening for Spinal Muscular Atrophy, Hereditary Hearing Loss, and Thalassemia in 13,926 Women of Reproductive Age From South Zhejiang
2025 · Chenyang Xu, Yanbao Xiang, et al. · Molecular Genetics & Genomic Medicine · 3
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[Mutation analysis and prenatal diagnosis for 12 families affected with hereditary hearing loss and enlarged vestibular aqueduct].
2017 · Yanbao Xiang, Huanzheng Li, et al. · PubMed · 3
Mutation analysis and prenatal diagnosis of a family with congenital contractural arachnodactyly
2021 · Lin Hu, Huanzheng Li, et al. · Molecular Genetics & Genomic Medicine · 2
[Genetic analysis of two novel variants in a Chinese pedigree affected with intellectual disorder].
2024 · Xiaoxiao Lyu, Chenyang Xu, et al. · PubMed · 1
Dynamics of Viral Load and Antibodies in First 8 Weeks of Infection by SARS-CoV-2: An Observational Cohort Study
2020 · Jianping Huang, Tingting Mao, et al. · SSRN Electronic Journal · 1
[Mutational analysis and prenatal diagnosis in a family affected with hypophosphatemic rickets].
2017 · Zhaotang Luan, Huanzheng Li, et al. · PubMed · 1
[Analysis of PKHD1 gene mutation in a family affected with infantile polycystic kidney disease].
2016 · Yanbao Xiang, Huanzheng Li, et al. · PubMed · 1
A Novel Intronic Variant Causes Aberrant Splicing of PCDH15 in a Family With Usher Syndrome Type 1F
2026 · Qifan Ma, Chenyang Xu, et al. · Molecular Genetics & Genomic Medicine
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[Analysis of ARID1B gene variants in two Chinese pedigrees with Coffin-Siris syndrome].
2022 · Yanbao Xiang, Ru Wan, et al. · PubMed
Prenatal molecular diagnosis for DMD/BMD families
2019 · Xu Chenyang, Yanbao Xiang, et al.
Correction to: Genome-Wide Array Analysis Reveals Novel Genomic Regions and Candidate Gene for Intellectual Disability
2018 · Xiangnan Chen, Huanzheng Li, et al. · Molecular Diagnosis & Therapy
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[Mutation analysis and prenatal diagnosis for 50 pedigrees affected with Duchenne/Becker muscular dystrophy].
2018 · Huanzheng Li, Chenyang Xu, et al. · PubMed
[SNP array analysis of three cases with partial 21q trisomy].
2017 · Lili Zhou, Chong Chen, et al. · PubMed
[Analysis of clinical phenotypes and GJB2 gene mutations in families affected with hearing loss from southern Zhejiang].
2017 · Chenyang Xu, Yanbao Xiang, et al. · PubMed
乳児(家系におけるpkhd1遺伝子突然変異の解析【jst・京大機械翻訳】
2016 · Yanbao Xiang, Huanzheng Li, et al. · Zhonghua yixue yichuanxue zazhi
Works count: 24
Citation count: 113
H-index: 6
I10-index: 4
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