Jiani Yin

3.4k total citations
13 papers, 440 citations indexed

About

Jiani Yin is a scholar working on Genetics, Molecular Biology and Cognitive Neuroscience. According to data from OpenAlex, Jiani Yin has authored 13 papers receiving a total of 440 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Genetics, 9 papers in Molecular Biology and 5 papers in Cognitive Neuroscience. Recurrent topics in Jiani Yin's work include Genetics and Neurodevelopmental Disorders (8 papers), Autism Spectrum Disorder Research (5 papers) and Genetic Syndromes and Imprinting (3 papers). Jiani Yin is often cited by papers focused on Genetics and Neurodevelopmental Disorders (8 papers), Autism Spectrum Disorder Research (5 papers) and Genetic Syndromes and Imprinting (3 papers). Jiani Yin collaborates with scholars based in United States, Germany and China. Jiani Yin's co-authors include Christian P. Schaaf, Guangfeng Wei, Lingzhi Zhao, Chengzhong Yu, Yunhua Wang, Jie Yang, Liang Zhou, Kun Qian, Hongwei Zhang and Wu Chen and has published in prestigious journals such as Scientific Reports, Journal of Materials Chemistry and The American Journal of Human Genetics.

In The Last Decade

Jiani Yin

13 papers receiving 434 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Jiani Yin United States 11 199 189 108 93 86 13 440
Hyun-Taek Kim South Korea 10 104 0.5× 381 2.0× 15 0.1× 10 0.1× 10 0.1× 11 581
Zeyuan Liu China 12 33 0.2× 319 1.7× 12 0.1× 11 0.1× 26 0.3× 26 592
Xiaomei Liao China 14 17 0.1× 152 0.8× 9 0.1× 41 0.4× 57 0.7× 23 574
Lucia Schoderboeck New Zealand 12 109 0.5× 317 1.7× 12 0.1× 6 0.1× 11 0.1× 14 548
Nguyêñ Quôć Thǎńg Vietnam 12 39 0.2× 82 0.4× 10 0.1× 87 0.9× 9 0.1× 80 640
Xinyu Du China 13 19 0.1× 234 1.2× 22 0.2× 16 0.2× 9 0.1× 50 551
Inmaculada Crespo Spain 12 47 0.2× 119 0.6× 8 0.1× 112 1.2× 3 0.0× 16 392
Xin Yi Yeo Singapore 11 33 0.2× 125 0.7× 41 0.4× 38 0.4× 2 0.0× 23 347
Haoqi Pan China 11 28 0.1× 147 0.8× 5 0.0× 39 0.4× 9 0.1× 21 430
Tingfeng Guo United States 5 30 0.2× 374 2.0× 20 0.2× 22 0.2× 6 0.1× 5 504

Countries citing papers authored by Jiani Yin

Since Specialization
Citations

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

Fields of papers citing papers by Jiani Yin

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Jiani Yin

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

All Works

13 of 13 papers shown
1.
Chen, Chun‐An, Rituraj Pal, Jiani Yin, et al.. (2020). Combination of whole exome sequencing and animal modeling identifies TMPRSS9 as a candidate gene for autism spectrum disorder. Human Molecular Genetics. 29(3). 459–470. 4 indexed citations
2.
Yin, Jiani, Н. Н. Заваденко, Oxana Yu. Naumova, et al.. (2020). Next Generation Sequencing of 134 Children with Autism Spectrum Disorder and Regression. Genes. 11(8). 853–853. 16 indexed citations
3.
Chen, Chun‐An, Wei Wang, Steen E. Pedersen, et al.. (2019). Nr2f1 heterozygous knockout mice recapitulate neurological phenotypes of Bosch-Boonstra-Schaaf optic atrophy syndrome and show impaired hippocampal synaptic plasticity. Human Molecular Genetics. 29(5). 705–715. 12 indexed citations
4.
Gillentine, Madelyn A., Jiani Yin, Christopher M. Grochowski, et al.. (2018). CHRNA7 copy number gains are enriched in adolescents with major depressive and anxiety disorders. Journal of Affective Disorders. 239. 247–252. 12 indexed citations
5.
Yin, Jiani, Wu Chen, Sirena Soriano, et al.. (2018). Otud7a Knockout Mice Recapitulate Many Neurological Features of 15q13.3 Microdeletion Syndrome. The American Journal of Human Genetics. 102(2). 296–308. 53 indexed citations
6.
McCarthy, John, Jiani Yin, Chun‐An Chen, et al.. (2018). Hormonal, metabolic and skeletal phenotype of Schaaf-Yang syndrome: a comparison to Prader-Willi syndrome. Journal of Medical Genetics. 55(5). 307–315. 29 indexed citations
7.
Yin, Jiani, et al.. (2018). Next Generation Sequencing in Autism Spectrum Disorder. 2(1). 1–5. 2 indexed citations
8.
Yin, Jiani, Wu Chen, Hongxing Yang, Mingshan Xue, & Christian P. Schaaf. (2017). Chrna7 deficient mice manifest no consistent neuropsychiatric and behavioral phenotypes. Scientific Reports. 7(1). 39941–39941. 36 indexed citations
9.
Gillentine, Madelyn A., Jiani Yin, Aleksandar Bajić, et al.. (2017). Functional Consequences of CHRNA7 Copy-Number Alterations in Induced Pluripotent Stem Cells and Neural Progenitor Cells. The American Journal of Human Genetics. 101(6). 874–887. 40 indexed citations
10.
Fountain, Michael D., Tao Huang, Chi‐An Chen, Jiani Yin, & Christian P. Schaaf. (2017). Magel2 knockout mice manifest altered social phenotypes and a deficit in preference for social novelty. Genes Brain & Behavior. 16(6). 592–600. 37 indexed citations
11.
Chen, Chun‐An, Jiani Yin, Richard A. Lewis, & Christian P. Schaaf. (2017). Genetic causes of optic nerve hypoplasia. Journal of Medical Genetics. 54(7). 441–449. 23 indexed citations
12.
Yin, Jiani & Christian P. Schaaf. (2016). Autism genetics – an overview. Prenatal Diagnosis. 37(1). 14–30. 48 indexed citations
13.
Yang, Jie, Liang Zhou, Lingzhi Zhao, et al.. (2011). A designed nanoporous material for phosphate removal with high efficiency. Journal of Materials Chemistry. 21(8). 2489–2489. 128 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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