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Xiaohui Gong

Transcription factor ISL1 is essential for pacemaker development and function
2015 · Xingqun Liang, Qingquan Zhang, et al. · Journal of Clinical Investigation · 126
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Histological and ultrastructural changes of the colon in dextran sodium sulfate‑induced mouse colitis
2020 · Xiaojuan Xu, Sisi Lin, et al. · Experimental and Therapeutic Medicine · 47
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Temporal requirements for ISL1 in sympathetic neuron proliferation, differentiation, and diversification
2018 · Qingquan Zhang, Ru Huang, et al. · Cell Death and Disease · 42
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Long non-coding RNA MALAT1 protects preterm infants with bronchopulmonary dysplasia by inhibiting cell apoptosis
2017 · Cheng Cai, Jiajun Qiu, et al. · BMC Pulmonary Medicine · 41
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Long Non Coding RNA SNHG16 Facilitates Proliferation, Migration, Invasion and Autophagy of Neuroblastoma Cells via Sponging miR-542-3p and Upregulating ATG5 Expression
2020 · Yi Wen, Xiaohui Gong, et al. · OncoTargets and Therapy · 31
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Novel PITX2c loss-of-function mutations associated with complex congenital heart disease
2014 · DONG WEI, XIAO-HUI GONG, et al. · International Journal of Molecular Medicine · 31
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Application of Next-Generation Sequencing for Genetic Diagnosis in Neonatal Intensive Care Units: Results of a Multicenter Study in China
2020 · Tianwen Zhu, Xiaohui Gong, et al. · Frontiers in Genetics · 23
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Loss of Protein Function Causing Severe Phenotypes of Female-Restricted Wieacker Wolff Syndrome due to a Novel Nonsense Mutation in the ZC4H2 Gene
2022 · Jing-Jing Sun, Qin Cai, et al. · Genes · 12
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Primary immunodeficiency‐related genes in neonatal intensive care unit patients with various genetic immune abnormalities: a multicentre study in China
2021 · Tianwen Zhu, Xiaohui Gong, et al. · Clinical & Translational Immunology · 10
LINC00037 Inhibits Proliferation of Renal Cell Carcinoma Cells in an Epidermal Growth Factor Receptor-Dependent Way
2018 · Xiaohui Gong, Xianjin Du, et al. · Cellular Physiology and Biochemistry · 10
Microdeletion and Microduplication Analysis of Chinese Conotruncal Defects Patients with Targeted Array Comparative Genomic Hybridization
2013 · Xiaohui Gong, Xi Wu, et al. · PLoS ONE · 10
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Expression of ILK in renal stroma is essential for multiple aspects of renal development
2018 · Xiaohui Gong, Xiaoxia Guo, et al. · American Journal of Physiology-Renal Physiology · 8
Clinical features, management, and prognosis of Bacillus cereus sepsis in premature neonates
2023 · Na Li, Yunlin Shen, et al. · Medicine · 7
A Case of Sepsis Due to Carbapenem-Resistant Klebsiella pneumoniae in an Extremely Low-Birth Weight Infant Treated with Trimethoprim–Sulfamethoxazole
2021 · Bowen Weng, Xiaoyue Zhang, et al. · Infection and Drug Resistance · 7
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A Chinese newborn with Zellweger syndrome and compound heterozygous mutations novel in the PEX1 gene: a case report and literature review
2021 · Pei Lu, Li Ma, et al. · Translational Pediatrics · 6
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Trends in the antimicrobial susceptibility among Chinese neonates from 2012 to 2021: a multicenter study
2024 · Zhanghua Yin, Jintong Tan, et al. · Antimicrobial Resistance and Infection Control · 5
Pseudohypoaldosteronism type 1b in fraternal twins of a Chinese family: report of two cases and literature review
2023 · Zhen Gao, Jingjing Sun, et al. · Archives of Endocrinology and Metabolism · 5
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The temporal requirements for Isl1 in sympathetic neuron proliferation, differentiation and diversification
2017 · Qingquan Zhang, Ru Huang, et al. · Mechanisms of Development · 4
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Continuous renal replacement therapy in neonates with multiple organ dysfunction syndrome: clinical utilization effects and outcomes
2025 · Xiaoyun Chu, Jinglin Xu, et al. · The Italian Journal of Pediatrics/Italian journal of pediatrics · 3
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Generation of an induced pluripotent stem cell line (OGHFUi001-A) from a type 1 early infantile epileptic encephalopathy with ARX mutation
2021 · Nan Jia, Xiaohui Gong, et al. · Stem Cell Research · 3
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[Identification of a homozygous ASS1 mutation in a child with citrullinemia type Ⅰ with high-melting curve method].
2018 · Jingjing Sun, Yunlin Shen, et al. · PubMed · 3
Generation of an isogenic gene-corrected iPSC line (OGHFUi001-A-1) from a type 1 early infantile epileptic encephalopathy (EIEE1) patient with a hemizygous R330L mutation in the ARX gene
2022 · Xiaohui Gong, Zhangqian Zheng, et al. · Stem Cell Research · 2
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Two Congenital Myasthenic Syndrome Patients Due to Mutations in COLQ Gene and the Consequence Protein Defect Prediction
2022 · Qiting Zhang, Qianqian Sha, et al. · Heliyon · 2
Two novel variants in PLOD1 causing hydrocephalus in female newborn with kyphoscoliotic Ehlers-Danlos syndrome
2021 · Yingchun Zhao, Jingjing Sun, et al. · European Journal of Medical Genetics · 2
[Maple syrup urine disease caused by two novel BCKDHB gene mutations in a Chinese neonate].
2015 · Yunlin Shen, Xiaohui Gong, et al. · PubMed · 2
Works count: 42
Citation count: 444
H-index: 10
I10-index: 11
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