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Author

Yuan Lyu

Observed name: Yuan Lv
Observed institutions: Peking University, Sheng Jing Hospital, Northern Jiangsu People's Hospital, Peking University Third Hospital, Shenyang Women and Infants Hospital, China Medical University
ORCID: 0000-0002-9752-9220
Observed ORCID: 0000-0002-9752-9220
OpenAlex ID: A5101632471
Rare De Novo IGF2 Variant on the Paternal Allele in a Patient With Silver–Russell Syndrome
2019 · Chun-Ling Xia, Yuan Lyu, et al. · Frontiers in Genetics · 11
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Melatonin Protects Against Cocaine‐Induced Blood−Brain Barrier Dysfunction and Cognitive Impairment by Regulating miR‐320a‐Dependent GLUT1 Expression
2024 · Jia‐Yi Wei, Hui Liu, et al. · Journal of Pineal Research · 10
Case Report: Compound Heterozygous Phosphatidylinositol-Glycan Biosynthesis Class N (PIGN) Mutations in a Chinese Fetus With Hypotonia-Seizures Syndrome 1
2020 · Shi-qi Xiao, Mei-hui Li, et al. · Frontiers in Genetics · 8
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ALG3-CDG: lethal phenotype and novel variants in Chinese siblings
2020 · Yue Bian, Chong Qiao, et al. · Journal of Human Genetics · 8
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Case Report: Novel Heterozygous DFNA5 Splicing Variant Responsible for Autosomal Dominant Non-syndromic Hearing Loss in a Chinese Family
2020 · Xi Chen, Bao-Long Jia, et al. · Frontiers in Genetics · 7
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Chinese Fetal Growth: A Multicenter Cohort Study Based on Fetal Ultrasound Measurements
2021 · Xiaoli Gong, Tianchen Wu, et al. · Maternal-Fetal Medicine · 4
Radiological and histopathological features of short rib‑polydactyly syndrome type III and identification of two novel DYNC2H1 variants
2021 · Chun-Ling Xia, Shi-Qi Xiao, et al. · Molecular Medicine Reports · 4
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[Analysis of prenatal phenotype and pathogenetic variant in a fetus with Papillorenal syndrome].
2020 · Jie Li, Shaowei Yin, et al. · PubMed · 3
Application of single-sperm sequencing in a male with Marfan syndrome: a case report and a literature review
2021 · Chuang Li, Feifei Zhou, et al. · Journal of Genetics · 2
The Role of PDZ Binding Kinase as a Potential Prognostic and Diagnostic Biomarker in Ovarian Cancer
2021 · Chuang Li, Yuan Lyu, et al. · Cancer Biotherapy and Radiopharmaceuticals · 2
[Diagnosis of a fetus with atelosteogenesis type 2 through combined prenatal ultrasonography and whole exome sequencing].
2020 · Jie Li, Yilin Meng, et al. · PubMed · 2
Comprehensive analyses reveal three-gene signatures in ovarian cancer
2020 · Chuang Li, Yuan Lyu, et al. · 2
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[Phenotype-genotype analysis and detection of gene variant in six families with osteogenesis imperfecta].
2020 · Rui Hou, Chuang Li, et al. · PubMed · 2
[Clinical feature and pathogenic analysis of a fetus with split hand-foot malformation].
2020 · Chuang Li, Yuan Lyu, et al. · PubMed · 2
[Clinical manifestation and genetic analysis of a child with early infantile epileptic encephalopathy 42].
2021 · Yan Ran, Yuan Lyu, et al. · PubMed · 1
[Application of single sperm sequencing for preimplantation genetic testing of male patient with achondroplasia].
2020 · Yuan Lyu, Chuang Li, et al. · PubMed · 1
[Clinical phenotype and genotype analysis of the family with the Usher syndrome].
2020 · Changliang Lin, Yuan Lyu, et al. · PubMed · 1
[Mutation analysis in a large Chinese pedigree affected with preaxial polydactyly II].
2019 · Zhitao Zhang, Yuan Lyu, et al. · PubMed · 1
Prenatal exome sequencing of fetuses with central nervous system anomalies based on prenatal ultrasound and magnetic resonance imaging diagnosis: A retrospective cohort study with a systematic review and meta‐analysis
2026 · Jia Yao, Yan Wang, et al. · Acta Obstetricia Et Gynecologica Scandinavica
[A case of complex structural variants in the Xq28 region diagnosed by whole genome sequencing].
2025 · Yulai Yang, Chuang Li, et al. · PubMed
Identification of a Novel Compound Heterozygous Mutation of PHGDH in Neu–Laxova Syndrome
2022 · Huan Li, Wen-Qian Yu, et al. · Research Square
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[Clinical characterization and genetic testing for a patient with creatine deficiency syndrome 1].
2022 · Shu Xyu, Chen Xu, et al. · PubMed
[Identification of pathogenic variant and preimplantation genetic testing for a Chinese family affected with osteogenesis imperfecta].
2022 · Chuang Li, Rui Hou, et al. · PubMed
[Clinical feature and genetic analysis of a fetus with autosomal recessive polycystic kidney disease].
2021 · Shu Xyu, Chen Xyu, et al. · PubMed
[Preliminary study on the application of third-generation sequencing technology for the detection of chromosomal aneuploidies].
2021 · Yuan Lyu, Chuang Li, et al. · PubMed
Works count: 29
Citation count: 71
H-index: 5
I10-index: 2
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