Yu Qi

1.2k total citations
62 papers, 856 citations indexed

About

Yu Qi is a scholar working on Molecular Biology, Genetics and Clinical Biochemistry. According to data from OpenAlex, Yu Qi has authored 62 papers receiving a total of 856 indexed citations (citations by other indexed papers that have themselves been cited), including 45 papers in Molecular Biology, 17 papers in Genetics and 14 papers in Clinical Biochemistry. Recurrent topics in Yu Qi's work include Mitochondrial Function and Pathology (14 papers), Metabolism and Genetic Disorders (14 papers) and ATP Synthase and ATPases Research (8 papers). Yu Qi is often cited by papers focused on Mitochondrial Function and Pathology (14 papers), Metabolism and Genetic Disorders (14 papers) and ATP Synthase and ATPases Research (8 papers). Yu Qi collaborates with scholars based in China, United States and Taiwan. Yu Qi's co-authors include Xiru Wu, Suiwen Hou, Wenqi Zhou, Xiaoping Gou, Jia Li, Chen Liang, Jiong Qin, Yuhe Liu, Yuehua Zhang and Songtao Wang and has published in prestigious journals such as SHILAP Revista de lepidopterología, PLoS ONE and New Phytologist.

In The Last Decade

Yu Qi

61 papers receiving 844 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Yu Qi China	17	537	198	150	129	87	62	856
Michaela Drögemüller Switzerland	17	243 0.5×	25 0.1×	171 1.1×	27 0.2×	27 0.3×	42	652
Sílvia Sisó United Kingdom	22	1.0k 1.9×	19 0.1×	57 0.4×	63 0.5×	51 0.6×	67	1.5k
Øivind Nilssen Norway	21	641 1.2×	17 0.1×	151 1.0×	66 0.5×	14 0.2×	47	1.2k
Oliver P. Forman United Kingdom	18	410 0.8×	53 0.3×	321 2.1×	17 0.1×	10 0.1×	37	805
Xin Wei China	18	256 0.5×	16 0.1×	111 0.7×	80 0.6×	25 0.3×	35	830
Minna Kujala Finland	18	589 1.1×	9 0.0×	152 1.0×	52 0.4×	120 1.4×	26	1.2k
Clare L. Chatot United States	11	967 1.8×	26 0.1×	451 3.0×	42 0.3×	36 0.4×	13	1.7k
L. Lü United States	13	460 0.9×	11 0.1×	305 2.0×	57 0.4×	8 0.1×	29	980
Ha Thi Thanh Tran Vietnam	21	810 1.5×	6 0.0×	195 1.3×	306 2.4×	135 1.6×	52	1.5k
Victor V. Chizhikov United States	24	1.3k 2.3×	25 0.1×	502 3.3×	57 0.4×	6 0.1×	47	2.0k

Countries citing papers authored by Yu Qi

Since Specialization

Citations

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

Fields of papers citing papers by Yu Qi

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Yu Qi

This figure shows the co-authorship network connecting the top 25 collaborators of Yu Qi. A scholar is included among the top collaborators of Yu Qi 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 Yu Qi. Yu Qi is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

Bai, Xiaoyong, Wenchao Wang, Yuebo Jin, et al.. (2024). TssL2 of T6SS2 is required for mobility, biofilm formation, wrinkly phenotype formation, and virulence of Vibrio parahaemolyticus SH112. Applied Microbiology and Biotechnology. 108(1). 537–537. 5 indexed citations

Pan, Hong, et al.. (2023). Reasons and Resolutions for Inconsistent Variant Interpretation. Human Mutation. 2023. 1–11. 1 indexed citations

Qi, Yu, et al.. (2023). Pathogenic bi‐allelic variants of meiotic ZMM complex gene SPO16 in premature ovarian insufficiency. Clinical Genetics. 104(4). 486–490. 4 indexed citations

Qi, Yu, et al.. (2023). Delayed progressive sensorineural hearing loss due to a novel compound heterozygous PTPRQ mutation in a Chinese patient. Journal of Clinical Laboratory Analysis. 37(7). e24886–e24886. 2 indexed citations

Zhou, Xintao, Jiaqi Fan, Yanyan Zhang, et al.. (2023). Evaluation of African Swine Fever Virus E111R Gene on Viral Replication and Porcine Virulence. Viruses. 15(4). 890–890. 7 indexed citations

Zhang, Ying, et al.. (2020). Clinical and genetic characteristics and prenatal diagnosis of patients presented GDD/ID with rare monogenic causes. Orphanet Journal of Rare Diseases. 15(1). 317–317. 9 indexed citations

Chen, Teng, Xintao Zhou, Yu Qi, et al.. (2019). Feline herpesvirus vectored-rabies vaccine in cats: A dual protection. Vaccine. 37(16). 2224–2231. 9 indexed citations

Zhu, Pinkuan, Qianwen Li, Yu Qi, et al.. (2018). Fungal Gene Mutation Analysis Elucidating Photoselective Enhancement of UV-C Disinfection Efficiency Toward Spoilage Agents on Fruit Surface. Frontiers in Microbiology. 9. 1141–1141. 7 indexed citations

Wang, Qi, et al.. (2016). Targeted Next-Generation Sequencing Successfully Detects Causative Genes in Chinese Patients with Hereditary Hearing Loss. Genetic Testing and Molecular Biomarkers. 20(11). 660–665. 28 indexed citations

10.

Li, Xiaotong, Yu Qi, Xiao Zhao, et al.. (2015). BmRobo2/3 is required for axon guidance in the silkworm Bombyx mori. Gene. 577(2). 174–179. 6 indexed citations

11.

Gao, Juanjuan, et al.. (2015). Whole Exome Sequencing Identified MCM2 as a Novel Causative Gene for Autosomal Dominant Nonsyndromic Deafness in a Chinese Family. PLoS ONE. 10(7). e0133522–e0133522. 26 indexed citations

12.

Qi, Yu, Xiaotong Li, Xiao Zhao, et al.. (2014). Coevolution of Axon Guidance Molecule Slit and Its Receptor Robo. PLoS ONE. 9(5). e94970–e94970. 4 indexed citations

13.

Qi, Yu, Xiaotong Li, Chun Liu, et al.. (2014). Evolutionarily Conserved Repulsive Guidance Role of Slit in the Silkworm Bombyx mori. PLoS ONE. 9(10). e109377–e109377. 8 indexed citations

14.

Liu, Hui, Fang Fang, Ying Zhang, et al.. (2013). Wild-Type Mitochondrial DNA Copy Number in Urinary Cells as a Useful Marker for Diagnosing Severity of the Mitochondrial Diseases. PLoS ONE. 8(6). e67146–e67146. 11 indexed citations

15.

Qi, Yu, et al.. (2012). Mutation Profile of the MUT Gene in Chinese Methylmalonic Aciduria Patients. JIMD Reports. 6. 55–64. 25 indexed citations

16.

Zhang, Yuehua, Xiaoyan Liu, Zhixian Yang, et al.. (2010). Analysis of SCN1A mutation and parental origin in patients with Dravet syndrome. Journal of Human Genetics. 55(7). 421–427. 32 indexed citations

17.

Fang, Fang, Yanling Yang, Li‐Ping Zou, et al.. (2009). The study of mitochondrial A3243G mutation in different samples. Mitochondrion. 9(2). 139–143. 30 indexed citations

18.

Zhang, Yuehua, Jianmin Liang, Xiaoyan Liu, et al.. (2008). SCN1A, SCN1B, and GABRG2 gene mutation analysis in Chinese families with generalized epilepsy with febrile seizures plus. Journal of Human Genetics. 53(8). 769–774. 56 indexed citations

19.

Qi, Yu, Ying Zhang, Zhaoxia Wang, et al.. (2006). Screening of common mitochondrial mutations in Chinese patients with mitochondrial encephalomyopathies. Mitochondrion. 7(1-2). 147–150. 20 indexed citations

20.

Qi, Yu, Zhiyue Chen, Jianjun Lu, et al.. (2004). Polymorphisms of casein kinase I gamma 2 gene associated with simple febrile seizures in Chinese Han population. Neuroscience Letters. 368(1). 2–6. 11 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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