Xiaolan Gao

896 total citations
69 papers, 572 citations indexed

About

Xiaolan Gao is a scholar working on Clinical Biochemistry, Molecular Biology and Physiology. According to data from OpenAlex, Xiaolan Gao has authored 69 papers receiving a total of 572 indexed citations (citations by other indexed papers that have themselves been cited), including 33 papers in Clinical Biochemistry, 25 papers in Molecular Biology and 20 papers in Physiology. Recurrent topics in Xiaolan Gao's work include Metabolism and Genetic Disorders (33 papers), Folate and B Vitamins Research (14 papers) and Mitochondrial Function and Pathology (12 papers). Xiaolan Gao is often cited by papers focused on Metabolism and Genetic Disorders (33 papers), Folate and B Vitamins Research (14 papers) and Mitochondrial Function and Pathology (12 papers). Xiaolan Gao collaborates with scholars based in China, United States and Peru. Xiaolan Gao's co-authors include Xuefan Gu, Wenjuan Qiu, Lianshu Han, Huiwen Zhang, Jun Ye, Xiaolei Zhao, Yu Wang, Yafen Zhang, Jun Ye and Yu Wang and has published in prestigious journals such as SHILAP Revista de lepidopterología, PLoS ONE and Scientific Reports.

In The Last Decade

Xiaolan Gao

64 papers receiving 559 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Xiaolan Gao China 14 252 214 146 115 104 69 572
Csilla Putz‐Bankuti Austria 14 59 0.2× 133 0.6× 26 0.2× 65 0.6× 49 0.5× 24 783
Barry C. Herzlich United States 14 46 0.2× 68 0.3× 179 1.2× 63 0.5× 21 0.2× 23 427
Isidor Minović Netherlands 13 46 0.2× 85 0.4× 89 0.6× 70 0.6× 38 0.4× 39 439
Jean-Pierre Fulgencio France 11 32 0.1× 162 0.8× 15 0.1× 54 0.5× 13 0.1× 23 453
Daan Kremer Netherlands 12 13 0.1× 92 0.4× 34 0.2× 72 0.6× 45 0.4× 70 671
Ben-Ami Sela Israel 13 36 0.1× 199 0.9× 85 0.6× 87 0.8× 21 0.2× 27 580
Kari Hortos United States 8 56 0.2× 61 0.3× 8 0.1× 267 2.3× 71 0.7× 11 800
Cinzia Lombardi Italy 16 27 0.1× 119 0.6× 83 0.6× 104 0.9× 48 0.5× 34 677
İlyas Çapoğlu Türkiye 13 54 0.2× 104 0.5× 41 0.3× 60 0.5× 16 0.2× 28 455
Kenzo Oba Japan 14 36 0.1× 137 0.6× 18 0.1× 119 1.0× 26 0.3× 56 761

Countries citing papers authored by Xiaolan Gao

Since Specialization
Citations

This map shows the geographic impact of Xiaolan Gao's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Xiaolan Gao with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Xiaolan Gao more than expected).

Fields of papers citing papers by Xiaolan Gao

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Xiaolan Gao. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Xiaolan Gao. The network helps show where Xiaolan Gao may publish in the future.

Co-authorship network of co-authors of Xiaolan Gao

This figure shows the co-authorship network connecting the top 25 collaborators of Xiaolan Gao. A scholar is included among the top collaborators of Xiaolan Gao based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Xiaolan Gao. Xiaolan Gao is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
2.
Zhong, Lin, Xiaolan Gao, Yu Wang, et al.. (2023). Clinical characteristics and genotypes of 201 patients with mucopolysaccharidosis type II in China: A retrospective, observational study. Clinical Genetics. 103(6). 655–662. 2 indexed citations
3.
Li, Miao, Jian Li, Wei Liu, et al.. (2023). A high-quality assembled genome of a representative peach landrace, ‘Feichenghongli’, and analysis of distinct late florescence and narrow leaf traits. BMC Plant Biology. 23(1). 230–230. 1 indexed citations
4.
Xu, Feng, Wenjun Ji, Xia Zhan, et al.. (2023). Newborn screening of maple syrup urine disease and the effect of early diagnosis. Clinica Chimica Acta. 548. 117483–117483. 12 indexed citations
5.
Liu, Xinyan, Erin F. Barreto, Yue Dong, et al.. (2023). Discrepancy between perceptions and acceptance of clinical decision support Systems: implementation of artificial intelligence for vancomycin dosing. BMC Medical Informatics and Decision Making. 23(1). 157–157. 9 indexed citations
6.
Hao, Lili, Lili Liang, Xiaolan Gao, et al.. (2023). Screening of 1.17 million newborns for inborn errors of metabolism using tandem mass spectrometry in Shanghai, China: A 19-year report. Molecular Genetics and Metabolism. 141(1). 108098–108098. 4 indexed citations
7.
Gao, Xiaolan, J. Kyle Bohman, Jason K. Viehman, et al.. (2023). Extracorporeal membrane oxygenation and acute kidney injury: a single-center retrospective cohort. Scientific Reports. 13(1). 15112–15112. 9 indexed citations
8.
Wang, Yu, Xiaolan Gao, Lianshu Han, et al.. (2022). Investigation of GALNS variants and genotype–phenotype correlations in a large cohort of patients with mucopolysaccharidosis type IVA. Journal of Inherited Metabolic Disease. 45(3). 593–604. 6 indexed citations
9.
Hu, Jiayue, Gustavo Maegawa, Xia Zhan, et al.. (2021). Clinical, biochemical, and genotype‐phenotype correlations of 118 patients with Niemann‐Pick disease Types A/B. Human Mutation. 42(5). 614–625. 20 indexed citations
10.
Song, Xuan, Xinyan Liu, Ryan D. Frank, et al.. (2021). The order of vasopressor discontinuation and incidence of hypotension: a retrospective cohort analysis. Scientific Reports. 11(1). 16680–16680. 3 indexed citations
11.
Gao, Xiaolan, et al.. (2018). Factors associated with unplanned extubation in the Intensive Care Unit for adult patients: A systematic review and meta-analysis. Intensive and Critical Care Nursing. 47. 62–68. 45 indexed citations
12.
Wang, Yu, Jun Ye, Wenjuan Qiu, et al.. (2018). Identification of predominant GNPTAB gene mutations in Eastern Chinese patients with mucolipidosis II/III and a prenatal diagnosis of mucolipidosis II. Acta Pharmacologica Sinica. 40(2). 279–287. 13 indexed citations
13.
Wang, Yu, Xiaolan Gao, Wenjuan Qiu, et al.. (2018). Genotypes and phenotypes in 20 Chinese patients with type 2 Gaucher disease. Brain and Development. 40(10). 876–883. 5 indexed citations
14.
Huang, Zhuo, Lianshu Han, Jun Ye, et al.. (2014). Analysis of clinical data in 143 patients with methylmalonic acidemia. Zhonghua neifenmi daixie zazhi. 30(6). 490–494.
15.
Wang, Fei, Yu Wang, Jun Ye, et al.. (2014). Analysis of genetic mutations in Chinese patients with systemic primary carnitine deficiency. European Journal of Medical Genetics. 57(10). 571–575. 26 indexed citations
16.
Han, Lianshu, Jun Ye, Wenjuan Qiu, et al.. (2013). A disease spectrum analysis of 564 cases of inherited metabolic diseases tested by gas chromatography-mass spectrometry. Zhonghua neifenmi daixie zazhi. 29(8). 693–695.
17.
Zhang, Huiwen, Jing Li, Xinshun Zhang, et al.. (2011). 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. PLoS ONE. 6(8). e22951–e22951. 38 indexed citations
18.
Liu, Bitao, et al.. (2010). 加熱処理時のBaMgAl 10 O 17 :Eu 2+ の光ルミネセンス特性および劣化機構. Electrochemical and Solid-State Letters. 13(3). 15–17. 3 indexed citations
19.
Han, Lianshu, Fei Wang, Yuhui Hu, et al.. (2009). Clinical and gene mutation analysis in patients with methylmalonic acidemia and homocystelnemia. Zhonghua neifenmi daixie zazhi. 25(4). 405–408. 1 indexed citations
20.
Ye, Jun, Xuefan Gu, Yafen Zhang, Xiaodong Huang, & Xiaolan Gao. (2002). Diagnosis, treatment and gene detection in 769 cases with hyperphenylalaninemia. 40(4). 210–213. 1 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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