Yong‐hui Jiang

13.1k total citations · 3 hit papers
141 papers, 6.1k citations indexed

About

Yong‐hui Jiang is a scholar working on Genetics, Molecular Biology and Cognitive Neuroscience. According to data from OpenAlex, Yong‐hui Jiang has authored 141 papers receiving a total of 6.1k indexed citations (citations by other indexed papers that have themselves been cited), including 77 papers in Genetics, 68 papers in Molecular Biology and 45 papers in Cognitive Neuroscience. Recurrent topics in Yong‐hui Jiang's work include Genetics and Neurodevelopmental Disorders (52 papers), Autism Spectrum Disorder Research (41 papers) and Genetic Syndromes and Imprinting (25 papers). Yong‐hui Jiang is often cited by papers focused on Genetics and Neurodevelopmental Disorders (52 papers), Autism Spectrum Disorder Research (41 papers) and Genetic Syndromes and Imprinting (25 papers). Yong‐hui Jiang collaborates with scholars based in United States, China and France. Yong‐hui Jiang's co-authors include Arthur L. Beaudet, Michael Ehlers, J. David Sweatt, Jeffrey L. Noebels, Dawna Armstrong, Coleen M. Atkins, Urs Albrecht, Gregor Eichele, Ping Fang and Robert‐Jan H. Galjaard and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nature Medicine and Nature Communications.

In The Last Decade

Yong‐hui Jiang

131 papers receiving 5.9k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Mutation of the Angelman Ubiquitin Ligase in Mice Causes Increased Cytoplasmic p53 and Deficits of Contextual Learning and Long-Term Potentiation

1998 693 citations Yong‐hui Jiang, Arthur L. Beaudet et al. profile →
De novo truncating mutations in E6-AP ubiquitin-protein ligase gene (UBE3A) in Angelman syndrome

1997 662 citations Yong‐hui Jiang, Arthur L. Beaudet et al. profile →
Mutation of the E6-AP Ubiquitin Ligase Reduces Nuclear Inclusion Frequency While Accelerating Polyglutamine-Induced Pathology in SCA1 Mice

1999 409 citations Yong‐hui Jiang, Arthur L. Beaudet et al. profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Yong‐hui Jiang United States	39	3.5k	3.5k	1.5k	977	550	141	6.1k
Jonathan Sebat United States	32	4.3k 1.2×	4.7k 1.4×	1.4k 0.9×	570 0.6×	442 0.8×	62	7.7k
Vincent des Portes France	30	2.2k 0.6×	2.1k 0.6×	881 0.6×	780 0.8×	417 0.8×	91	4.1k
R. Frank Kooy Belgium	44	4.0k 1.1×	4.8k 1.4×	2.5k 1.7×	1.2k 1.2×	326 0.6×	170	6.8k
Sébastien Jacquemont United States	41	3.3k 0.9×	4.7k 1.3×	2.6k 1.8×	953 1.0×	252 0.5×	118	6.3k
Jamel Chelly France	38	3.3k 0.9×	3.3k 0.9×	1.0k 0.7×	955 1.0×	248 0.5×	110	5.3k
Yiping Shen United States	36	2.8k 0.8×	2.6k 0.8×	728 0.5×	582 0.6×	569 1.0×	195	5.6k
Gudrun Rappold Germany	53	5.9k 1.7×	5.1k 1.5×	652 0.4×	964 1.0×	431 0.8×	216	10.0k
Tjitske Kleefstra Netherlands	38	3.4k 0.9×	3.7k 1.1×	696 0.5×	483 0.5×	344 0.6×	131	5.7k
Jozef Gécz Australia	56	6.6k 1.9×	5.9k 1.7×	1.1k 0.7×	1.0k 1.0×	804 1.5×	232	10.5k
Shikshya Shrestha United States	7	3.4k 1.0×	1.9k 0.5×	1.4k 0.9×	1.9k 1.9×	258 0.5×	20	6.4k

Countries citing papers authored by Yong‐hui Jiang

Since Specialization

Citations

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

Fields of papers citing papers by Yong‐hui Jiang

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Yong‐hui Jiang. 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 Yong‐hui Jiang. The network helps show where Yong‐hui Jiang may publish in the future.

Co-authorship network of co-authors of Yong‐hui Jiang

This figure shows the co-authorship network connecting the top 25 collaborators of Yong‐hui Jiang. A scholar is included among the top collaborators of Yong‐hui Jiang 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 Yong‐hui Jiang. Yong‐hui Jiang 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

Wang, Sung Eun, Jaechul Lim, Mi‐Ae Jang, et al.. (2025). Mechanism of EHMT2-mediated genomic imprinting associated with Prader-Willi syndrome. Nature Communications. 16(1). 6125–6125. 1 indexed citations

Li, Yi, et al.. (2025). Autism-like atypical face processing in Shank3 mutant dogs. Science Advances. 11(14). eadu3793–eadu3793.

Wang, Sung Eun, et al.. (2025). Deficiency of Shank3 in the nucleus accumbens reveals a loss of social-specific motivation. Communications Biology. 8(1). 1569–1569.

Kim, Minseong, Yong‐hui Jiang, Esther Yang, et al.. (2025). Endothelial SHANK3 regulates tight junctions in the neonatal mouse blood-brain barrier through β-Catenin signaling. Nature Communications. 16(1). 1407–1407. 3 indexed citations

Abdelhamed, Zakia, et al.. (2024). P602: Genetic modifiers as a basis for phenotypic variability in mosaic trisomy 8. SHILAP Revista de lepidopterología. 2. 101508–101508.

Zhu, Feipeng, Qi Shi, Yong‐hui Jiang, Yongqing Zhang, & Hui Zhao. (2024). Impaired synaptic function and hyperexcitability of the pyramidal neurons in the prefrontal cortex of autism-associated Shank3 mutant dogs. Molecular Autism. 15(1). 9–9. 4 indexed citations

Gao, Yudong, Erik J. Soderblom, S. Alexandra Garcia-Moreno, et al.. (2024). Proximity analysis of native proteomes reveals phenotypic modifiers in a mouse model of autism and related neurodevelopmental conditions. Nature Communications. 15(1). 6801–6801. 13 indexed citations

Wang, Sung Eun & Yong‐hui Jiang. (2023). Novel epigenetic molecular therapies for imprinting disorders. Molecular Psychiatry. 28(8). 3182–3193. 13 indexed citations

Contestabile, Alessandro, Stefano Musardo, Federica Maltese, et al.. (2023). Shank3 deficits in the anteromedial bed nucleus of the stria terminalis trigger an anxiety phenotype in mice. European Journal of Neuroscience. 57(12). 1966–1979. 4 indexed citations

10.

Peng, Gang, Qinghua Zhou, Hongyan Chai, et al.. (2023). Estimation on risk of spontaneous abortions by genomic disorders from a meta‐analysis of microarray results on large case series of pregnancy losses. Molecular Genetics & Genomic Medicine. 11(8). e2181–e2181. 7 indexed citations

11.

Thaler, Roman, Farzaneh Khani, Ines Sturmlechner, et al.. (2022). Vitamin C epigenetically controls osteogenesis and bone mineralization. Nature Communications. 13(1). 5883–5883. 58 indexed citations

12.

Dai, Hongzheng, Wenmiao Zhu, Bo Yuan, et al.. (2022). A recurrent single‐exon deletion in TBCK might be under‐recognized in patients with infantile hypotonia and psychomotor delay. Human Mutation. 43(12). 1816–1823. 3 indexed citations

13.

Huang, Xiahe, Hui Zhao, Guodong Wang, et al.. (2022). Comparative Proteome and Cis-Regulatory Element Analysis Reveals Specific Molecular Pathways Conserved in Dog and Human Brains. Molecular & Cellular Proteomics. 21(8). 100261–100261. 7 indexed citations

14.

Tremblay, Martine, Andrew Aldridge, Jill A. Rosenfeld, et al.. (2021). Mutations of the histone linker H1–4 in neurodevelopmental disorders and functional characterization of neurons expressing C-terminus frameshift mutant H1.4. Human Molecular Genetics. 31(9). 1430–1442. 8 indexed citations

15.

Jiang, Yong‐hui, Aiqun Li, Linlin Xie, et al.. (2020). Development and Application of an Intelligent Modeling Method for Ancient Wooden Architecture. ISPRS International Journal of Geo-Information. 9(3). 167–167. 23 indexed citations

16.

Luo, Weijun, Chaolin Zhang, Yong‐hui Jiang, & Cory Brouwer. (2018). Systematic reconstruction of autism biology from massive genetic mutation profiles. Science Advances. 4(4). e1701799–e1701799. 35 indexed citations

17.

Wu, Song, Guangming Gan, Zhiping Zhang, et al.. (2017). A Presynaptic Function of Shank Protein inDrosophila. Journal of Neuroscience. 37(48). 11592–11604. 18 indexed citations

18.

Zhang, Wenhao, Weikun Xia, Q. Wang, et al.. (2016). Isoform Switch of TET1 Regulates DNA Demethylation and Mouse Development. Molecular Cell. 64(6). 1062–1073. 78 indexed citations

19.

Zhu, Li, Xiaoming Wang, Xinlei Li, et al.. (2013). Epigenetic dysregulation of SHANK3 in brain tissues from individuals with autism spectrum disorders. Human Molecular Genetics. 23(6). 1563–1578. 109 indexed citations

20.

Tsai, Ting‐Fen, Jan Bressler, Yong‐hui Jiang, & Arthur L. Beaudet. (2003). Disruption of the genomic imprint in trans with homologous recombination at Snrpn in ES cells. genesis. 37(4). 151–161. 13 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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