Ruolan Guo

574 total citations
41 papers, 332 citations indexed

About

Ruolan Guo is a scholar working on Molecular Biology, Genetics and Cardiology and Cardiovascular Medicine. According to data from OpenAlex, Ruolan Guo has authored 41 papers receiving a total of 332 indexed citations (citations by other indexed papers that have themselves been cited), including 21 papers in Molecular Biology, 20 papers in Genetics and 6 papers in Cardiology and Cardiovascular Medicine. Recurrent topics in Ruolan Guo's work include Genomic variations and chromosomal abnormalities (11 papers), Genomics and Rare Diseases (7 papers) and Congenital heart defects research (5 papers). Ruolan Guo is often cited by papers focused on Genomic variations and chromosomal abnormalities (11 papers), Genomics and Rare Diseases (7 papers) and Congenital heart defects research (5 papers). Ruolan Guo collaborates with scholars based in China, United States and Canada. Ruolan Guo's co-authors include Chanjuan Hao, Lingqian Wu, Desheng Liang, Jun Guo, Xuyun Hu, Wei Li, Haoxian Li, Ying Peng, Weigang Lv and Ting Bai and has published in prestigious journals such as Scientific Reports, Clinical Chemistry and Frontiers in Immunology.

In The Last Decade

Ruolan Guo

37 papers receiving 329 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Ruolan Guo China 11 158 120 62 50 48 41 332
Tracy Brandt United States 10 286 1.8× 399 3.3× 82 1.3× 23 0.5× 42 0.9× 14 581
Ho‐Ming Luk China 13 249 1.6× 267 2.2× 100 1.6× 14 0.3× 24 0.5× 67 471
Luis Rohena United States 12 192 1.2× 154 1.3× 46 0.7× 29 0.6× 15 0.3× 27 383
Alina Kurolap Israel 12 150 0.9× 118 1.0× 61 1.0× 22 0.4× 12 0.3× 42 399
Alicia S. Martínez Argentina 10 238 1.5× 256 2.1× 75 1.2× 64 1.3× 25 0.5× 16 582
Angeline Lai Singapore 10 152 1.0× 133 1.1× 23 0.4× 12 0.2× 28 0.6× 31 349
Kristbjorn O. Gudmundsson United States 13 195 1.2× 69 0.6× 18 0.3× 18 0.4× 42 0.9× 23 400
Fong Ct United States 6 141 0.9× 74 0.6× 16 0.3× 23 0.5× 30 0.6× 186 296
Majdi Nagara Tunisia 10 161 1.0× 140 1.2× 19 0.3× 18 0.4× 26 0.5× 25 343
Güven Toksoy Türkiye 12 185 1.2× 116 1.0× 57 0.9× 12 0.2× 23 0.5× 51 353

Countries citing papers authored by Ruolan Guo

Since Specialization
Citations

This map shows the geographic impact of Ruolan Guo'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 Ruolan Guo with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Ruolan Guo more than expected).

Fields of papers citing papers by Ruolan Guo

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Ruolan Guo. 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 Ruolan Guo. The network helps show where Ruolan Guo may publish in the future.

Co-authorship network of co-authors of Ruolan Guo

This figure shows the co-authorship network connecting the top 25 collaborators of Ruolan Guo. A scholar is included among the top collaborators of Ruolan Guo 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 Ruolan Guo. Ruolan Guo 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.
Hao, Chanjuan, Xuyun Hu, Ruolan Guo, et al.. (2024). Targeted gene sequencing and hearing follow-up in 7501 newborns reveals an improved strategy for newborn hearing screening. European Journal of Human Genetics. 33(4). 468–475.
3.
Hu, Xuyun, et al.. (2024). Genetic screening reveals hotspot variants and prevalence rates of Hermansky-Pudlak syndrome in the Chinese population. Clinica Chimica Acta. 561. 119813–119813. 1 indexed citations
4.
Leng, Fei, Song Mei, Xiaolin Zhou, et al.. (2023). DVsc: An Automated Framework for Efficiently Detecting Viral Infection from Single-cell Transcriptomics Data. Genomics Proteomics & Bioinformatics. 22(2).
5.
Liu, Xuanshi, Wenjian Xu, Fei Leng, et al.. (2023). NeuroCNVscore: a tissue-specific framework to prioritise the pathogenicity of CNVs in neurodevelopmental disorders. BMJ Paediatrics Open. 7(1). e001966–e001966. 3 indexed citations
6.
Zhang, Yue, Ying Li, Ruolan Guo, et al.. (2023). Genetic diagnostic yields of 354 Chinese ASD children with rare mutations by a pipeline of genomic tests. Frontiers in Genetics. 14. 1108440–1108440. 3 indexed citations
7.
Zhang, Wenyan, Ruolan Guo, Zhan Qi, et al.. (2022). Newborn Genetic Screening Revealed Increased Levels of Biochemical Indicators in Carriers of Heterozygous Variants. Genetic Testing and Molecular Biomarkers. 26(12). 573–581.
8.
Chen, Yuanying, Qiqing Sun, Chanjuan Hao, et al.. (2022). Identification of a novel variant in N-cadherin associated with dilated cardiomyopathy. Frontiers in Medicine. 9. 944950–944950. 3 indexed citations
9.
Zhang, Wenyan, Ruolan Guo, Shuang Zhao, et al.. (2022). Molecular identification of T-box transcription factor 6 and prognostic assessment in patients with congenital scoliosis: A single-center study. Frontiers in Medicine. 9. 941468–941468.
10.
Hao, Chanjuan, Ruolan Guo, Jun Liu, et al.. (2021). Exome sequencing as the first‐tier test for pediatric respiratory diseases: A single‐center study. Human Mutation. 42(7). 891–900. 2 indexed citations
11.
Mou, Wenjun, Yang Shen, Ruolan Guo, et al.. (2021). A Novel Homozygous TTC7A Missense Mutation Results in Familial Multiple Intestinal Atresia and Combined Immunodeficiency. Frontiers in Immunology. 12. 759308–759308. 14 indexed citations
12.
Hao, Chanjuan, Xuyun Hu, Ruolan Guo, et al.. (2021). Clinical Application of Whole Exome Sequencing for Monogenic Disorders in PICU of China. Frontiers in Genetics. 12. 677699–677699. 8 indexed citations
13.
Hu, Xuyun, Ruolan Guo, Jun Guo, et al.. (2020). Parallel Tests of Whole Exome Sequencing and Copy Number Variant Sequencing Increase the Diagnosis Yields of Rare Pediatric Disorders. Frontiers in Genetics. 11. 473–473. 12 indexed citations
14.
Liu, Jun, Xuyun Hu, Ruolan Guo, et al.. (2019). Compound heterozygous LPIN2 pathogenic variants in a patient with Majeed syndrome with recurrent fever and severe neutropenia: case report. BMC Medical Genetics. 20(1). 11 indexed citations
15.
Guo, Jun, Zheng Li, Chanjuan Hao, et al.. (2019). A novel de novo CASZ1 heterozygous frameshift variant causes dilated cardiomyopathy and left ventricular noncompaction cardiomyopathy. Molecular Genetics & Genomic Medicine. 7(8). e828–e828. 20 indexed citations
16.
Chen, Jiang, Nan Pan, Ying Peng, et al.. (2019). [Molecular diagnosis and functional study of a pedigree affected with Lubs X-linked mental retardation syndrome].. PubMed. 36(4). 340–343. 1 indexed citations
17.
Hu, Xuyun, Jun Liu, Ruolan Guo, et al.. (2019). A novel 14q13.1–21.1 deletion identified by CNV-Seq in a patient with brain-lung-thyroid syndrome, tooth agenesis and immunodeficiency. Molecular Cytogenetics. 12(1). 51–51. 5 indexed citations
18.
Kang, Huiying, Miao Zhang, Minhui Ouyang, et al.. (2018). Brain white matter microstructural alterations in children of type I Gaucher disease characterized with diffusion tensor MR imaging. European Journal of Radiology. 102. 22–29. 10 indexed citations
19.
20.
Zhao, Lijuan, Chen Chen, Ying Peng, et al.. (2015). Pachygyria, seizures, hypotonia, and growth retardation in a patient with an atypical 1.33Mb inherited microduplication at 22q11.23. Gene. 569(1). 46–50. 7 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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