Zhengjun Jia

400 total citations
23 papers, 262 citations indexed

About

Zhengjun Jia is a scholar working on Molecular Biology, Pediatrics, Perinatology and Child Health and Genetics. According to data from OpenAlex, Zhengjun Jia has authored 23 papers receiving a total of 262 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Molecular Biology, 9 papers in Pediatrics, Perinatology and Child Health and 9 papers in Genetics. Recurrent topics in Zhengjun Jia's work include Prenatal Screening and Diagnostics (8 papers), Genomic variations and chromosomal abnormalities (5 papers) and Mitochondrial Function and Pathology (3 papers). Zhengjun Jia is often cited by papers focused on Prenatal Screening and Diagnostics (8 papers), Genomic variations and chromosomal abnormalities (5 papers) and Mitochondrial Function and Pathology (3 papers). Zhengjun Jia collaborates with scholars based in China, United States and France. Zhengjun Jia's co-authors include Hui Xi, Jing Liu, Xiao Mao, Laurent Aniksztejn, Ying Peng, Hua Wang, Nadine Bruneau, Pierre Szepetowski, Hélène Becq and Hua Wang and has published in prestigious journals such as Human Molecular Genetics, Medicine and Frontiers in Cellular Neuroscience.

In The Last Decade

Zhengjun Jia

22 papers receiving 255 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Zhengjun Jia China 9 112 106 86 36 30 23 262
Renske Oegema Netherlands 13 217 1.9× 245 2.3× 147 1.7× 26 0.7× 23 0.8× 21 534
Filip Roelens Belgium 10 141 1.3× 160 1.5× 46 0.5× 18 0.5× 22 0.7× 17 346
Luigina Spaccini Italy 13 159 1.4× 208 2.0× 104 1.2× 39 1.1× 15 0.5× 47 455
Mathilde Nizon France 13 153 1.4× 239 2.3× 41 0.5× 70 1.9× 15 0.5× 26 387
Bird Td United States 6 90 0.8× 162 1.5× 20 0.2× 51 1.4× 23 0.8× 244 342
Michèle Mathieu‐Dramard France 9 170 1.5× 200 1.9× 44 0.5× 27 0.8× 31 1.0× 15 363
Mefford Hc 6 90 0.8× 163 1.5× 19 0.2× 51 1.4× 21 0.7× 239 337
Emmanuelle Ranza Switzerland 12 103 0.9× 137 1.3× 20 0.2× 19 0.5× 27 0.9× 22 295
Audrey Putoux France 11 215 1.9× 236 2.2× 72 0.8× 12 0.3× 21 0.7× 32 369
Cristina Dias United Kingdom 11 143 1.3× 172 1.6× 23 0.3× 24 0.7× 26 0.9× 16 359

Countries citing papers authored by Zhengjun Jia

Since Specialization
Citations

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

Fields of papers citing papers by Zhengjun Jia

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Zhengjun Jia

This figure shows the co-authorship network connecting the top 25 collaborators of Zhengjun Jia. A scholar is included among the top collaborators of Zhengjun Jia 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 Zhengjun Jia. Zhengjun Jia 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.
Liu, Qin, Jing Liu, Zhengjun Jia, et al.. (2023). Identification of rare thalassemia variants using third-generation sequencing. Frontiers in Genetics. 13. 1076035–1076035. 11 indexed citations
2.
Sheng, Xiaoqi, et al.. (2021). Clinical significance of S100B protein in pregnant woman with early- onset severe preeclampsia. Ginekologia Polska. 95(9). 711–717. 2 indexed citations
3.
Liu, Zhimei, Bei Cao, Victor Wei Zhang, et al.. (2021). Novel Mutations in the GTPBP3 Gene for Mitochondrial Disease and Characteristics of Related Phenotypic Spectrum: The First Three Cases From China. Frontiers in Genetics. 12. 611226–611226. 7 indexed citations
4.
Ma, Na, Hui Xi, Jing Chen, et al.. (2021). Integrated CNV-seq, karyotyping and SNP-array analyses for effective prenatal diagnosis of chromosomal mosaicism. BMC Medical Genomics. 14(1). 56–56. 31 indexed citations
5.
Ma, Na, Zhenhua Zhu, Jing Liu, et al.. (2021). Clinical and genetic analysis of classical Ehlers‐Danlos syndrome patient caused by synonymous mutation in COL5A2. Molecular Genetics & Genomic Medicine. 9(5). e1632–e1632. 5 indexed citations
6.
Liu, Jing, Qin Liu, Na Ma, et al.. (2021). Prenatal case of Simpson–Golabi–Behmel syndrome with a de novo 370Kb‐sized microdeletion of Xq26.2 compassing partial GPC3 gene and review. Molecular Genetics & Genomic Medicine. 9(8). e1750–e1750. 4 indexed citations
7.
8.
Liu, Jing, Hui Xi, Ying Peng, et al.. (2020). [Genetic analysis of a pedigree with MECP duplication syndrome].. PubMed. 37(10). 1146–1149. 1 indexed citations
9.
Xi, Hui, Jing Chen, Dan Wang, et al.. (2020). Prenatal genetic analysis and differential pregnancy outcomes of two de novo cases showing mosaic isodicentric Y chromosome. Molecular Cytogenetics. 13(1). 7–7. 6 indexed citations
10.
Wang, Hui, Zhengjun Jia, Aiping Mao, et al.. (2020). Analysis of balanced reciprocal translocations in patients with subfertility using single-molecule optical mapping. Journal of Assisted Reproduction and Genetics. 37(3). 509–516. 31 indexed citations
11.
Liu, Jing, Zhengjun Jia, Ying Peng, et al.. (2020). Identification of a novel gross deletion of TCOF1 in a Chinese prenatal case with Treacher Collins syndrome. Molecular Genetics & Genomic Medicine. 8(8). e1313–e1313. 8 indexed citations
12.
Huang, Yan, Xiao Mao, Richard H. van Jaarsveld, et al.. (2020). Variants in CAPZA2, a member of an F-actin capping complex, cause intellectual disability and developmental delay. Human Molecular Genetics. 29(9). 1537–1546. 21 indexed citations
13.
Liu, Qin, Zhengjun Jia, Hui Xi, et al.. (2019). [Analysis on the Genotype of 5018 Cases of Thalassemia in Hunan Area].. PubMed. 27(6). 1938–1942. 9 indexed citations
14.
15.
Li, Haoxian, Jing Liu, Qin Liu, et al.. (2019). Molecular investigation in Chinese patients with primary carnitine deficiency. Molecular Genetics & Genomic Medicine. 7(9). e901–e901. 9 indexed citations
16.
Hu, Hao, et al.. (2017). Carnitine-acylcarnitine translocase deficiency with c.199-10 T>G and novel c.1A>G mutation. Medicine. 96(45). e8549–e8549. 23 indexed citations
17.
Liu, Jing, Hao Hu, Na Ma, et al.. (2016). A de novo duplication of chromosome 9q34.13-qter in a fetus with Tetralogy of Fallot Syndrome. Molecular Cytogenetics. 9(1). 54–54. 7 indexed citations
18.
Wang, Hua, et al.. (2016). [Genetic analysis for 2 females carrying idic(Y)(p) and with sex development disorders].. PubMed. 33(3). 335–9. 1 indexed citations
19.
Liu, Jing, Hua Wang, Hui Xi, et al.. (2015). [Application of next-generation DNA sequencing for prenatal testing of fetal chromosomal aneuploidies].. PubMed. 32(4). 533–7. 3 indexed citations
20.
Hu, Hao, et al.. (2014). [Prenatal genetic diagnosis for two Chinese families affected with oculocutaneous albinism type Ⅱ].. PubMed. 31(4). 424–7. 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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