Xiaohua Jin

424 total citations
21 papers, 340 citations indexed

About

Xiaohua Jin is a scholar working on Molecular Biology, Cancer Research and Genetics. According to data from OpenAlex, Xiaohua Jin has authored 21 papers receiving a total of 340 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Molecular Biology, 6 papers in Cancer Research and 4 papers in Genetics. Recurrent topics in Xiaohua Jin's work include CRISPR and Genetic Engineering (4 papers), Hearing, Cochlea, Tinnitus, Genetics (3 papers) and Metabolism and Genetic Disorders (3 papers). Xiaohua Jin is often cited by papers focused on CRISPR and Genetic Engineering (4 papers), Hearing, Cochlea, Tinnitus, Genetics (3 papers) and Metabolism and Genetic Disorders (3 papers). Xiaohua Jin collaborates with scholars based in China, Japan and United States. Xiaohua Jin's co-authors include Peipei Song, Yi Cui, Xu Ma, Chunmei Liu, Hong-Fei Xia, Xu Ma, Hong‐Fei Xia, Huafang Gao, Xiangdong Gao and Qian Liu and has published in prestigious journals such as Cancer Research, Molecular Therapy and Biochimica et Biophysica Acta (BBA) - General Subjects.

In The Last Decade

Xiaohua Jin

21 papers receiving 337 citations

Peers

Xiaohua Jin

IMMUN

GENET

Anne Zirkel Germany

Shiyue Mei China

Charles Ashton United States

Enzo Tedone United States

Davood Zare‐Abdollahi Iran

Mehran Piran Iran

Jinmi Choi South Korea

Benjamin Philipson United States

Yingying Wen China

Kyster K. Nanan United States

Anne Zirkel Germany

Xiaohua Jin

436 ×1.8

139 ×0.8

57 ×1.0

IMMUN

33 ×0.9

GENET

34 ×1.3

GENET

Citations per year, relative to Xiaohua Jin Xiaohua Jin (= 1×) peers Anne Zirkel

Countries citing papers authored by Xiaohua Jin

Since Specialization

Citations

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

Fields of papers citing papers by Xiaohua Jin

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Xiaohua Jin

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

All Works

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20 of 20 papers shown

Jia, Jinlin, et al.. (2025). Development and validation of optimized lentivirus-like particles for gene editing tool delivery with Gag-Only strategy. European journal of medical research. 30(1). 242–242. 5 indexed citations

Liu, Zhiwei, et al.. (2024). Restoring T and B cell generation in X-linked severe combined immunodeficiency mice through hematopoietic stem cells adenine base editing. Molecular Therapy. 32(6). 1658–1671. 1 indexed citations

Yang, Yi, Xia Wang, Chunyan Niu, et al.. (2024). Establishment of genomic RNA reference materials for BCR-ABL1 P210 measurement. Analytical and Bioanalytical Chemistry. 416(26). 5733–5742. 1 indexed citations

Huang, Shisheng, Wenxia Yu, Guanglei Li, et al.. (2022). Engineering of near-PAMless adenine base editor with enhanced editing activity and reduced off-target. Molecular Therapy — Nucleic Acids. 28. 732–742. 15 indexed citations

Jin, Xiaohua, Shasha Huang, Chuan Zhang, et al.. (2022). Variant analysis of 92 Chinese Han families with hearing loss. BMC Medical Genomics. 15(1). 12–12. 9 indexed citations

Wang, Xia, Yongzhuo Zhang, Chunyan Niu, et al.. (2021). Establishment of primary reference measurement procedures and reference materials for EGFR variant detection in non-small cell lung cancer. Analytical Methods. 13(18). 2114–2123. 10 indexed citations

Jin, Xiaohua, Xinjie Wang, Shasha Huang, et al.. (2021). Novel CRISPR/Cas12a-based genetic diagnostic approach for SLC26A4 mutation-related hereditary hearing loss. European Journal of Medical Genetics. 65(2). 104406–104406. 5 indexed citations

Jin, Xiaohua, Yousheng Yan, Chuan Zhang, et al.. (2021). Identification of novel deep intronic PAH gene variants in patients diagnosed with phenylketonuria. Human Mutation. 43(1). 56–66. 10 indexed citations

Jin, Xiaohua, Qian Liu, Qinhua Zhang, et al.. (2020). Compound heterozygous variants of the FBXO7 gene resulting in infantile‐onset Parkinsonian‐pyramidal syndrome in siblings of a Chinese family. Journal of Clinical Laboratory Analysis. 34(8). 6 indexed citations

10.

Zhang, Chuan, Yousheng Yan, Qinghua Zhang, et al.. (2020). Mutation analysis of TCOF1 gene in Chinese Treacher Collins syndrome patients. Journal of Clinical Laboratory Analysis. 35(1). e23567–e23567. 8 indexed citations

11.

Yan, Yousheng, Xiaohua Jin, Xing Wang, et al.. (2020). Screening of PAH Common Mutations in Chinese Phenylketonuria Patients Using iPLEX MALDI-TOF MS. ACS Omega. 5(4). 1805–1812. 4 indexed citations

12.

Yan, Yousheng, Chuan Zhang, Xiaohua Jin, et al.. (2019). Mutation spectrum of PAH gene in phenylketonuria patients in Northwest China: identification of twenty novel variants. Metabolic Brain Disease. 34(3). 733–745. 13 indexed citations

13.

Yan, Yousheng, Fang Wang, Chuan Zhang, et al.. (2019). Evaluation of droplet digital PCR for non-invasive prenatal diagnosis of phenylketonuria. Analytical and Bioanalytical Chemistry. 411(27). 7115–7126. 9 indexed citations

14.

Jiang, Yue, et al.. (2019). Abstract P2-08-33: A novel seven-gene signature predicts prognosis in early-stage triple-negative breast cancer. Cancer Research. 79(4_Supplement). P2–8. 2 indexed citations

15.

Yan, Yousheng, et al.. (2018). Five Novel COL7A1 Gene Mutations in Three Chinese Patients with Recessive Dystrophic Epidermolysis Bullosa.. PubMed. 48(1). 100–105. 6 indexed citations

16.

Jiang, Yi, Song Gao, Xiaohua Jin, et al.. (2017). Mutation spectra and founder effect of TMC1 in patients with non‐syndromic deafness in Xiamen area, China. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 177(3). 301–307. 6 indexed citations

17.

Wang, Xuan, Xiaohua Jin, Qian Liu, et al.. (2015). NF-κB inhibitor reverses temozolomide resistance in human glioma TR/U251 cells. Oncology Letters. 9(6). 2586–2590. 48 indexed citations

18.

Shi, Tian, Xing Su, Lu Qi, et al.. (2014). MiR-143 and rat embryo implantation. Biochimica et Biophysica Acta (BBA) - General Subjects. 1850(4). 708–721. 15 indexed citations

19.

Xia, Hong-Fei, Chunmei Liu, Yi Cui, et al.. (2009). <i>MiR-125b</i> Expression Affects the Proliferation and Apoptosis of Human Glioma Cells by Targeting <i>Bmf</i>. Cellular Physiology and Biochemistry. 23(4-6). 347–358. 134 indexed citations

20.

Zhang, Meng, et al.. (2007). [EXT1 and EXT2 mutation identified by denaturing high performance liquid chromatograph in three families with hereditary multiple exostoses].. PubMed. 24(6). 646–51. 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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