Xiangbin Jia

441 total citations
7 papers, 60 citations indexed

About

Xiangbin Jia is a scholar working on Molecular Biology, Genetics and Cognitive Neuroscience. According to data from OpenAlex, Xiangbin Jia has authored 7 papers receiving a total of 60 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Molecular Biology, 6 papers in Genetics and 2 papers in Cognitive Neuroscience. Recurrent topics in Xiangbin Jia's work include Genetics and Neurodevelopmental Disorders (6 papers), Congenital heart defects research (4 papers) and Genomic variations and chromosomal abnormalities (2 papers). Xiangbin Jia is often cited by papers focused on Genetics and Neurodevelopmental Disorders (6 papers), Congenital heart defects research (4 papers) and Genomic variations and chromosomal abnormalities (2 papers). Xiangbin Jia collaborates with scholars based in China, Netherlands and Germany. Xiangbin Jia's co-authors include Hui Guo, Zhengmao Hu, Huidan Wu, Ying Li, Qiumeng Zhang, Jianjun Ou, Honghui Li, Ting Bai, Guanglei Xun and Lin Han and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Molecular Neurobiology and Genetics in Medicine.

In The Last Decade

Xiangbin Jia

6 papers receiving 58 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Xiangbin Jia China	4	31	31	14	6	5	7	60
Cailyn H. Spurrell United States	6	63 2.0×	40 1.3×	18 1.3×	9 1.5×	3 0.6×	7	115
Huidan Wu China	8	65 2.1×	68 2.2×	28 2.0×	11 1.8×	8 1.6×	13	126
J. Russell Moore United States	2	75 2.4×	53 1.7×	15 1.1×	4 0.7×	3 0.6×	3	84
Ryan D. Risgaard United States	5	72 2.3×	46 1.5×	21 1.5×	6 1.0×	3 0.6×	8	92
Ed Scolnick United States	2	29 0.9×	26 0.8×	6 0.4×	5 0.8×	4 0.8×	3	47
Jennifer Grundman United States	3	40 1.3×	19 0.6×	16 1.1×	4 0.7×	5 1.0×	3	64
Natalie Bir United States	4	47 1.5×	38 1.2×	21 1.5×	7 1.2×	8 1.6×	4	79
Adrian Camarena United States	4	48 1.5×	19 0.6×	5 0.4×	7 1.2×	4 0.8×	7	77
Chontelle King New Zealand	6	48 1.5×	51 1.6×	9 0.6×	4 0.7×	5 1.0×	6	109
Sarah Grotto France	5	51 1.6×	26 0.8×	8 0.6×	17 2.8×	3 0.6×	12	79

Countries citing papers authored by Xiangbin Jia

Since Specialization

Citations

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

Fields of papers citing papers by Xiangbin Jia

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Xiangbin Jia

This figure shows the co-authorship network connecting the top 25 collaborators of Xiangbin Jia. A scholar is included among the top collaborators of Xiangbin 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 Xiangbin Jia. Xiangbin Jia 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:

7 of 7 papers shown

1.

Du, Bing, et al.. (2025). Naa15 Haploinsufficiency and De Novo Missense Variants Associate With Neurodevelopmental Disorders and Interfere With Neurogenesis and Neuron Development. Autism Research. 18(5). 954–965. 1 indexed citations

2.

Jia, Xiangbin, et al.. (2024). CELF2 Deficiency Demonstrates Autism-Like Behaviors and Interferes with Late Development of Cortical Neurons in Mice. Molecular Neurobiology. 62(1). 156–168. 3 indexed citations

3.

Cheng, Jianbo, Zhen Wang, Guozhong Li, et al.. (2024). KCTD10 regulates brain development by destabilizing brain disorder–associated protein KCTD13. Proceedings of the National Academy of Sciences. 121(12). e2315707121–e2315707121. 2 indexed citations

4.

Han, Lin, Xiangbin Jia, Huidan Wu, et al.. (2022). Loss-of-function of KMT5B leads to neurodevelopmental disorder and impairs neuronal development and neurogenesis. Journal of genetics and genomics. 49(9). 881–890. 10 indexed citations

5.

Jia, Xiangbin, Mariëlle Alders, Arjan Bouman, et al.. (2022). De novo variants in the PABP domain of PABPC1 lead to developmental delay. Genetics in Medicine. 24(8). 1761–1773. 4 indexed citations

6.

Zhao, Wenjing, Jieqiong Tan, Tengfei Zhu, et al.. (2019). Rare inherited missense variants of POGZ associate with autism risk and disrupt neuronal development. Journal of genetics and genomics. 46(5). 247–257. 16 indexed citations

7.

Li, Ying, Xiangbin Jia, Huidan Wu, et al.. (2018). Genotype and phenotype correlations for SHANK3 de novo mutations in neurodevelopmental disorders. American Journal of Medical Genetics Part A. 176(12). 2668–2676. 24 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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