Yongli Guo

Yongli Guo, Yongbo Yu, Jie Lu, 2017, Growth hormone & IGF research : official journal of the Growth Hormone Research Society and the International IGF Research Society.

Cyclooxygenase‐2 Gly587Arg variant is associated with differential enzymatic activity and risk of esophageal squamous‐cell carcinoma

W. Tan, D. Lin, Yongli Guo, 2009, Molecular carcinogenesis.

All-trans-retinoic acid antagonizes the hedgehog pathway by inducing patched

E. Dmitrovsky, Yongli Guo, S. Fiering, 2014, Cancer biology & therapy.

A multi-omics annotation platform for rare disease to benefit precision medicine

Tieliu Shi, Jinmeng Jia, Zhongxin An, 2018, SCIENTIA SINICA Vitae.

Socioeconomic inequalities in cancer incidence and access to health services among children and adolescents in China: a cross-sectional study

R. Zheng, Yongli Guo, Yue Xi, 2022, The Lancet.

Effects of COVID-19-targeted nonpharmaceutical interventions on children's respiratory admissions in China: a national multicenter time series study

Yongli Guo, X. Ni, Xin-yu Wang, 2022, International Journal of Infectious Diseases.

A somatic mutation in PIK3CD unravels a novel candidate gene for lymphatic malformation

W. Wang, Yongli Guo, X. Ni, 2021, Orphanet Journal of Rare Diseases.

Aberrant Topological Properties of Brain Functional Network in Children with Obstructive Sleep Apnea Derived from Resting-State fMRI

Yongli Guo, Zhifei Xu, X. Ni, 2022, Brain Topography.

Predictive Significance of Enhanced Level of Angiogenesis and Tissue Neutrophils for Antrochoanal Polyps Recurrence in Children

Yongli Guo, Jie Lu, Shujing Han, 2020, Ear, nose, & throat journal.

Application of Gastroscopy in the Diagnosis of Congenital Pyriform Sinus Fistula in Children

Yongli Guo, Yuzhu He, Yongbo Yu, 2021, Frontiers in Pediatrics.

Sequencing XMET genes to promote genotype-guided risk assessment and precision medicine

W. Xiao, Tieliu Shi, Leming Shi, 2019, Science China Life Sciences.

Identification of potential pathogenic mutations in Chinese children with first branchial cleft anomalies detected by whole‐exome sequencing

Min Chen, Yongli Guo, Yongbo Yu, 2021, Pediatric investigation.

Two novel mutations of PAX3 and SOX10 were characterized as genetic causes of Waardenburg Syndrome

Min Chen, Yongli Guo, Yongbo Yu, 2020, Molecular genetics & genomic medicine.

The efficacy and safety of montelukast in children with obstructive sleep apnea: a systematic review and meta-analysis.

Yongli Guo, Zhifei Xu, X. Ni, 2020, Sleep medicine.

A six-nucleotide insertion-deletion polymorphism in the CASP8 promoter is associated with susceptibility to multiple cancers

Changqing Zeng, Yang Gao, Qingrun Zhang, 2007, Nature Genetics.

Cross Protective Mucosal Immunity Mediated by Memory Th17 Cells against Streptococcus pneumoniae Lung Infection

Yongli Guo, Gregory F. Sonnenberg, X. Ni, 2016, Mucosal Immunology.

Progresses in clinical studies on antiviral therapies for COVID‐19—Experience and lessons in design of clinical trials

Yongli Guo, G. Zhaori, Chunyan Liu, 2020, Pediatric investigation.

Identification of functional genetic variants in cyclooxygenase-2 and their association with risk of esophageal cancer.

B. Ning, W. Tan, D. Lin, 2005, Gastroenterology.

UBE1L causes lung cancer growth suppression by targeting cyclin D1

E. Dmitrovsky, Yongli Guo, L. Sempere, 2008, Molecular Cancer Therapeutics.

causes lung cancer growth suppression by targeting cyclin D 1

E. Dmitrovsky, Yongli Guo, L. Sempere, 2008 .

eRAM: encyclopedia of rare disease annotations for precision medicine

Wei Li, Xin Li, Yue Ming, 2017, Nucleic Acids Res..

lncRNA SNHG16 is associated with proliferation and poor prognosis of pediatric neuroblastoma

Yongli Guo, Yongbo Yu, Jie Lu, 2019, International journal of oncology.

Two Compound Heterozygous Were Identified in SLC26A4 Gene in Two Chinese Families With Enlarged Vestibular Aqueduct

Feng Chen, Yongli Guo, Yongbo Yu, 2018, Clinical and experimental otorhinolaryngology.

MYC-associated protein X binding with the variant rs72780850 in RNA helicase DEAD box 1 for susceptibility to neuroblastoma

Yongli Guo, Yongbo Yu, Jie Lu, 2020, Science China Life Sciences.

Evidence for the Ubiquitin Protease UBP43 as an Antineoplastic Target

E. Dmitrovsky, A. Andrew, Yongli Guo, 2012, Molecular Cancer Therapeutics.

Candidate Gene Association Analysis of Neuroblastoma in Chinese Children Strengthens the Role of LMO1

Yongli Guo, Jie Lu, Shujing Han, 2015, PloS one.

Single nucleotide polymorphism rs11669203 in TGFBR3L is associated with the risk of neuroblastoma in a Chinese population

B. Ning, Dianke Yu, Yongli Guo, 2016, Tumor Biology.

Comparing Histone Deacetylase Inhibitor Responses in Genetically Engineered Mouse Lung Cancer Models and a Window of Opportunity Trial in Patients with Lung Cancer

E. Dmitrovsky, Yongli Guo, Hua Li, 2013, Molecular Cancer Therapeutics.

Deep Learning-Based Multi-Omics Data Integration Reveals Two Prognostic Subtypes in High-Risk Neuroblastoma

Tieliu Shi, Li Zhang, Yongli Guo, 2018, Front. Genet..

A Novel Germline Compound Heterozygous Mutation of BRCA2 Gene Associated With Familial Peripheral Neuroblastic Tumors in Two Siblings

Tieliu Shi, Yongli Guo, Min Xu, 2021, Frontiers in Genetics.

Application of genome analysis strategies in the clinical testing for pediatric diseases

Weida Tong, Huixiao Hong, Baitang Ning, 2018, Pediatric investigation.

Cigarette smoking strongly modifies the association of complement factor H variant and the risk of lung cancer.

Dianke Yu, Yongli Guo, Xuemei Zhang, 2012, Cancer epidemiology.

Functional genetic variations in cytotoxic T-lymphocyte antigen 4 and susceptibility to multiple types of cancer.

Hongbing Shen, W. Tan, D. Lin, 2008, Cancer research.

Haplotypes in Matrix Metalloproteinase Gene Cluster on Chromosome 11q22 Contribute to the Risk of Lung Cancer Development and Progression

Changqing Zeng, Yang Gao, Qingrun Zhang, 2006, Clinical Cancer Research.

Genetic polymorphisms in cell cycle regulatory genes MDM2 and TP53 are associated with susceptibility to lung cancer

Wen Tan, Dongxin Lin, Xiaoping Miao, 2006, Human mutation.

MicroRNA hsa-miR-25-3p suppresses the expression and drug induction of CYP2B6 in human hepatocytes.

B. Ning, Dianke Yu, Yongli Guo, 2016, Biochemical pharmacology.

The role of P53 and MDM2 polymorphisms in the risk of esophageal squamous cell carcinoma.

W. Tan, D. Lin, Zhihua Liu, 2005, Cancer research.

Interaction of P53 Arg72Pro and MDM2 T309G polymorphisms and their associations with risk of gastric cardia cancer.

Wen Tan, Dianke Yu, Dongxin Lin, 2007, Carcinogenesis.

Wnt signaling pathway upregulates DNMT1 to trigger NHERF1 promoter hypermethylation in colon cancer.

Yongli Guo, M. Wang, Hua Zhu, 2018, Oncology reports.

Involvement of microRNAs in lung cancer biology and therapy.

E. Dmitrovsky, M. Korc, S. Kauppinen, 2011, Translational research : the journal of laboratory and clinical medicine.

A brief introduction to the FUTang Updating medical REcords (FUTURE) database

Yongli Guo, G. Feng, X. Ni, 2021, Pediatric investigation.

Detection of FOXO1 break-apart status by fluorescence in situ hybridization in atypical alveolar rhabdomyosarcoma

Yongli Guo, Jin Shi, X. Ni, 2017, Science China Life Sciences.

Whole Genome Sequencing Identifies Novel Compound Heterozygous Lysosomal Trafficking Regulator Gene Mutations Associated with Autosomal Recessive Chediak-Higashi Syndrome

Tieliu Shi, F. Chen, Yongli Guo, 2017, Scientific Reports.

Combined low tracheotomy and rigid bronchoscopy to remove an irregular tracheal foreign body

Yongli Guo, X. Ni, Jie Zhang, 2018, Pediatric investigation.

Whole-Genome Sequencing Identifies a Novel Variation of WAS Gene Coordinating With Heterozygous Germline Mutation of APC to Enhance Hepatoblastoma Oncogenesis

Tieliu Shi, Yongli Guo, Yongbo Yu, 2018, Front. Genet..

PedAM: a database for Pediatric Disease Annotation and Medicine

Yue Ming, Xin Li, Wei Li, 2017, Nucleic Acids Res..

Efficacy and safety of oral sildenafil in treatment of pediatric head and neck lymphatic malformations

Yongli Guo, Yuzhu He, Yue Liu, 2017, Acta oto-laryngologica.

Efficacy of Initial Sirolimus Therapy for 27 Patients with Intractable Lymphatic Malformations

Yongli Guo, Xiaoling Cheng, X. Ni, 2021, The Laryngoscope.

The MDM2 promoter SNP285C/309G haplotype diminishes Sp1 transcription factor binding and reduces risk for breast and ovarian cancer in Caucasians.

Dongxin Lin, Peter Devilee, Caroline Seynaeve, 2011, Cancer cell.

The Role of P 53 and MDM 2 Polymorphisms in the Risk of Esophageal Squamous Cell Carcinoma

W. Tan, D. Lin, Zhihua Liu, 2005 .

FASL –844C polymorphism is associated with increased activation-induced T cell death and risk of cervical cancer

W. Tan, D. Lin, Yifeng Zhou, 2005, The Journal of experimental medicine.

Primary cardiac CIC‐rearranged undifferentiated sarcoma in an infant

Yongli Guo, Yeran Yang, X. Yao, 2021, Pediatric investigation.

Distribution of selected characteristics by case-control status in multiple types of cancer association analysis Variable Northern Chinese population Lung cancer

Hongbing Shen, W. Tan, D. Lin, 2008 .

Multiple microRNAs function as self-protective modules in acetaminophen-induced hepatotoxicity in humans

W. Xiao, Tieliu Shi, Leming Shi, 2018, Archives of Toxicology.

MiR-20a-5p suppresses tumor proliferation by targeting autophagy-related gene 7 in neuroblastoma

Yongli Guo, Yongbo Yu, Jie Lu, 2018, Cancer Cell International.

Genotype-phenotype correlations of Berardinelli-Seip congenital lipodystrophy and novel candidate genes prediction

Tieliu Shi, Jinmeng Jia, Yongli Guo, 2020, Orphanet Journal of Rare Diseases.

Functional polymorphisms in FAS and FASL contribute to increased apoptosis of tumor infiltration lymphocytes and risk of breast cancer

W. Tan, D. Lin, Yifeng Zhou, 2006 .

RRS1 gene expression involved in the progression of papillary thyroid carcinoma

Xin Li, Feng Chen, Yongli Guo, 2018, Cancer Cell International.

Characterization of the Blood and Cerebrospinal Fluid Microbiome in Children with Bacterial Meningitis and Its Potential Correlation with Inflammation

Xiangyin Kong, Yongli Guo, Landian Hu, 2021, mSystems.

A group of sclerosing epithelioid fibrosarcomas with low-level amplified EWSR1-CREB3L1 fusion gene in children.

Yongli Guo, Yongbo Yu, X. Yao, 2021, Pathology, research and practice.

DCX and CRABP2 are candidate genes for differential diagnosis between pre‐chemotherapy embryonic and alveolar rhabdomyosarcoma in pediatric patients

Yongli Guo, X. Ni, J. Tai, 2021, Pediatric investigation.

Disease characteristics and neuropathological changes associated with cognitive dysfunction in obstructive sleep apnea

Yongli Guo, X. Ni, Yue Qiu, 2021, Pediatric investigation.

Bioinformatics analysis to screen key genes in papillary thyroid carcinoma

Yongli Guo, Yongbo Yu, Jie Lu, 2019, Oncology letters.

CO2 laser cauterization approach to congenital pyriform sinus fistula.

Ya-mei Zhang, Yongli Guo, G. Feng, 2017, Journal of pediatric surgery.

Response to inhibition of smoothened in diverse epithelial cancer cells that lack smoothened or patched 1 mutations

E. Dmitrovsky, Patricia Greninger, J. Settleman, 2012, International journal of oncology.

Clinical and surgical outcome differences on the basis of pathology category in cervical neuroblastic tumors.

Yongli Guo, Jihang Sun, Yan Su, 2022, Journal of pediatric surgery.

Deafness gene mutations in newborns in Beijing

Yongli Guo, Jie Lu, Jin Shi, 2016, Acta oto-laryngologica.

Functional Genetic Variants of TNFSF15 and Their Association with Gastric Adenocarcinoma: A Case-Control Study

Dianke Yu, Kan Zhai, Yongli Guo, 2014, PloS one.

Correlation between BRAFV600E mutation and clinicopathological features in pediatric papillary thyroid carcinoma

Yongli Guo, X. Ni, H. Qin, 2017, Science China Life Sciences.

Clinical relevance of BCOR internal tandem duplication and TP53 aberration in clear cell sarcoma of the kidney.

Yongli Guo, Yongbo Yu, Huanmin Wang, 2022, Human pathology.

Modulation of ALDH5A1 and SLC22A7 by microRNA hsa-miR-29a-3p in human liver cells.

Lei Guo, B. Ning, Dianke Yu, 2015, Biochemical pharmacology.

Correlation between TERT C228T and clinic-pathological features in pediatric papillary thyroid carcinoma

Yongli Guo, Yongbo Yu, X. Ni, 2019, Science China Life Sciences.

Identification of Functional Genetic Variants in and Their Association With Risk of Esophageal Cancer

B. Ning, W. Tan, X. Miao, 2005 .

Clinical features and survival of Chinese children with trilateral retinoblastoma during 2006-2019: A retrospective multicenter study.

Yongli Guo, X. Ni, M. Jin, 2020, American journal of ophthalmology.

The Impacts of Obstructive Sleep Apnea Severity on Brain White Matter Integrity and Cognitive Functions in Children: A Diffusion Tensor Imaging Study

J Zhang, Yongli Guo, Huifang Huang, 2021, Nature and science of sleep.

Facial Feature as Predictor for Early-Persistence OSAS After Adenotonsillectomy in Children With Moderate to Severe OSAS

Yi Lei, Li Zheng, Jun Tai, 2020, IT Professional.

NSS_A_329408 2125..2135

Yongli Guo, Huifang Huang, Yue Liu, 2021 .

Clinical analysis of surgical treatment for head and neck lymphatic malformations in children: a series of 128 cases

Ya-mei Zhang, Yongli Guo, Yuzhu He, 2019, Acta oto-laryngologica.

MicroRNA-365a-3p promotes tumor growth and metastasis in laryngeal squamous cell carcinoma.

Yongli Guo, Yongbo Yu, Jie Lu, 2016, Oncology reports.

Identification of functional genetic variants in cyclooxygenase-2 and their association with risk of esophageal cancer.

B. Ning, W. Tan, D. Lin, 2005, Gastroenterology.

Genetic variant in CASP3 affects promoter activity and risk of esophageal squamous cell carcinoma

Dianke Yu, Yongli Guo, Xuemei Zhang, 2012, Cancer science.

Reply to ”A promoter polymorphism in the CASP8 gene is not associated with cancer risk”

Changqing Zeng, Yang Gao, Qingrun Zhang, 2008, Nature Genetics.

Effects of obstructive sleep apnoea severity on neurocognitive and brain white matter alterations in children according to sex: a tract-based spatial statistics study.

Ya-mei Zhang, Yongli Guo, Yue Liu, 2020, Sleep medicine.

The optimal surgical approach for papillary thyroid carcinoma with pathological n1 metastases: An analysis from the SEER database

Yongli Guo, X. Ni, Wei Wang, 2019, The Laryngoscope.

Erratum to “The Feasibility of Xpert MTB/RIF Testing to Detect Rifampicin Resistance among Childhood Tuberculosis for Prevalence Surveys in Northern China”

Yongli Guo, Yanlin Zhao, Jie Lu, 2017, BioMed research international.

The MDM2 promoter SNP285C/309G haplotype diminishes Sp1 transcription factor binding and reduces risk for breast and ovarian cancer in Caucasians.

P. Lønning, A. Børresen-Dale, David Evans, 2011, Cancer cell.

Detection of FOXO1 break-apart status by fluorescence in situ hybridization in atypical alveolar rhabdomyosarcoma

Jie Zhang, Jun Tai, Feng Chen, 2017, Science China Life Sciences.