Get started
Author

Xiaolan Gao

Clinical, biochemical, and molecular analysis of combined methylmalonic acidemia and hyperhomocysteinemia (cblC type) in China
2010 · Fei Wang, Lianshu Han, et al. · Journal of Inherited Metabolic Disease · 86
Factors associated with unplanned extubation in the Intensive Care Unit for adult patients: A systematic review and meta-analysis
2018 · Zhong-Ping Ai, Xiao-Lan Gao, et al. · Intensive and Critical Care Nursing · 76
Analysis of the IDS Gene in 38 Patients with Hunter Syndrome: The c.879G>A (p.Gln293Gln) Synonymous Variation in a Female Create Exonic Splicing
2011 · Huiwen Zhang, Jing Li, et al. · PLoS ONE · 56
PDF
Pentagalloyl Glucose: A Review of Anticancer Properties, Molecular Targets, Mechanisms of Action, Pharmacokinetics, and Safety Profile
2023 · Chengli Wen, Nathupakorn Dechsupa, et al. · Molecules · 45
PDF
Spectrum Analysis of Common Inherited Metabolic Diseases in Chinese Patients Screened and Diagnosed by Tandem Mass Spectrometry
2014 · Lianshu Han, Feng Han, et al. · Journal of Clinical Laboratory Analysis · 43
Simultaneous Use of Hypertonic Saline and IV Furosemide for Fluid Overload: A Systematic Review and Meta-Analysis
2021 · Chang Liu, Zhiyong Peng, et al. · Critical Care Medicine · 38
An interpretable machine learning model for predicting 28-day mortality in patients with sepsis-associated liver injury
2024 · Chengli Wen, Xu Zhang, et al. · PLoS ONE · 35
Clinical, biochemical, and genotype‐phenotype correlations of 118 patients with Niemann‐Pick disease Types A/B
2021 · Jiayue Hu, Gustavo H.B. Maegawa, et al. · Human Mutation · 35
PDF
Analysis of genetic mutations in Chinese patients with systemic primary carnitine deficiency
2014 · Lianshu Han, Fei Wang, et al. · European Journal of Medical Genetics · 35
Discrepancy between perceptions and acceptance of clinical decision support Systems: implementation of artificial intelligence for vancomycin dosing
2023 · Xinyan Liu, Erin F. Barreto, et al. · BMC Medical Informatics and Decision Making · 26
PDF
Use of Ambroxol as Therapy for Gaucher Disease
2023 · Xia Zhan, Huiwen Zhang, et al. · JAMA Network Open · 25
PDF
Deaths from COPD in patients with cancer: a population-based study
2021 · Yongqiang Zheng, Yan Huang, et al. · Aging · 24
Identification of predominant GNPTAB gene mutations in Eastern Chinese patients with mucolipidosis II/III and a prenatal diagnosis of mucolipidosis II
2018 · Yu Wang, Jun Ye, et al. · Acta Pharmacologica Sinica · 23
PDF
Screening of 1.17 million newborns for inborn errors of metabolism using tandem mass spectrometry in Shanghai, China: A 19-year report
2023 · Lili Hao, Lili Liang, et al. · Molecular Genetics and Metabolism · 22
Newborn screening of maple syrup urine disease and the effect of early diagnosis
2023 · Ting Chen, Deyun Lu, et al. · Clinica Chimica Acta · 21
Biochemical, molecular and outcome analysis of eight chinese asymptomatic individuals with methyl malonic acidemia detected through newborn screening
2015 · Lianshu Han, Shengnan Wu, et al. · American Journal of Medical Genetics Part A · 19
[Diagnosis of inborn errors of metabolism using tandem mass spectrometry and gas chromatography mass spectrometry].
2008 · Lian-Shu Han, Jun Ye, et al. · PubMed · 17
[Analysis of gene mutations in Chinese patients with methylmalonic acidemia and homocysteinemia].
2009 · Fei Wang, Lian-shu Han, et al. · PubMed · 16
[A pilot study of selective screening for high risk children with inborn error of metabolism using tandem mass spectrometry in China].
2004 · Xue-fan Gu, Lian-shu Han, et al. · PubMed · 16
Changing trends and influencing factors of the quality of life of chemotherapy patients with breast cancer
2017 · Zhong-Ping Ai, Xiao-Lan Gao, et al. · Chinese Nursing Research · 15
PDF
[Application of tandem mass spectrometry in diagnosis of organic acidemias].
2005 · Lian-shu Han, Xiao-lan Gao, et al. · PubMed · 15
Extracorporeal membrane oxygenation and acute kidney injury: a single-center retrospective cohort
2023 · Xiaolan Gao, Jacob Ninan, et al. · Scientific Reports · 14
PDF
[Studies on the clinical manifestation and SLC25A13 gene mutation of Chinese patients with neonatal intrahepatic cholestasis caused by citrin deficiency].
2010 · Ya-zhi Xing, Wen-juan Qiu, et al. · PubMed · 14
Eight novel mutations in the ABCD1 gene and clinical characteristics of 25 Chinese patients with X-linked adrenoleukodystrophy
2015 · Shan-Shan Chu, Jun Ye, et al. · World Journal of Pediatrics · 13
Clinical, biochemical, and molecular genetic characteristics of patients with primary carnitine deficiency identified by newborn screening in Shanghai, China
2022 · Siyu Chang, Yi Yang, et al. · Frontiers in Genetics · 12
PDF
Works count: 79
Citation count: 922
H-index: 17
I10-index: 29
Year
Topic
Type