Min-Chih Cheng

974 total citations
40 papers, 602 citations indexed

About

Min-Chih Cheng is a scholar working on Molecular Biology, Genetics and Cellular and Molecular Neuroscience. According to data from OpenAlex, Min-Chih Cheng has authored 40 papers receiving a total of 602 indexed citations (citations by other indexed papers that have themselves been cited), including 28 papers in Molecular Biology, 27 papers in Genetics and 10 papers in Cellular and Molecular Neuroscience. Recurrent topics in Min-Chih Cheng's work include Genetics and Neurodevelopmental Disorders (17 papers), Genomic variations and chromosomal abnormalities (10 papers) and Genetic Associations and Epidemiology (9 papers). Min-Chih Cheng is often cited by papers focused on Genetics and Neurodevelopmental Disorders (17 papers), Genomic variations and chromosomal abnormalities (10 papers) and Genetic Associations and Epidemiology (9 papers). Min-Chih Cheng collaborates with scholars based in Taiwan, United States and China. Min-Chih Cheng's co-authors include Chia‐Hsiang Chen, Ding‐Lieh Liao, Tsung‐Ming Hu, Chicheng Sun, Rosie Qin, Tzu-Ting Chen, Gong Chen, Carlos Castillo‐Chávez, S. Blythe and Jeffrey S. Palmer and has published in prestigious journals such as PLoS ONE, Brain Research and International Journal of Molecular Sciences.

In The Last Decade

Min-Chih Cheng

40 papers receiving 594 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Min-Chih Cheng Taiwan 14 310 234 194 117 46 40 602
Jean‐Bernard Dietrich France 12 434 1.4× 166 0.7× 170 0.9× 79 0.7× 36 0.8× 16 800
Ke-Sheng Wang United States 14 343 1.1× 224 1.0× 92 0.5× 45 0.4× 28 0.6× 23 708
Teresa F. Burke United States 15 299 1.0× 81 0.3× 204 1.1× 151 1.3× 110 2.4× 29 867
Yavuz Ayhan Türkiye 10 397 1.3× 148 0.6× 270 1.4× 95 0.8× 23 0.5× 32 815
Ayyappan Anitha Japan 17 492 1.6× 353 1.5× 112 0.6× 329 2.8× 44 1.0× 38 1.1k
Lorna M. Lopez Ireland 12 277 0.9× 343 1.5× 90 0.5× 77 0.7× 55 1.2× 34 882
Kimberly Bell United States 13 267 0.9× 183 0.8× 123 0.6× 108 0.9× 17 0.4× 30 720
Anabela Silva‐Fernandes Portugal 17 555 1.8× 175 0.7× 407 2.1× 93 0.8× 53 1.2× 26 803
Shunit Gal-Ben-Ari Israel 8 325 1.0× 72 0.3× 232 1.2× 87 0.7× 60 1.3× 9 611
Mark N. Ziats United States 16 617 2.0× 409 1.7× 91 0.5× 352 3.0× 24 0.5× 20 1.1k

Countries citing papers authored by Min-Chih Cheng

Since Specialization
Citations

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

Fields of papers citing papers by Min-Chih Cheng

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Min-Chih Cheng. 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 Min-Chih Cheng. The network helps show where Min-Chih Cheng may publish in the future.

Co-authorship network of co-authors of Min-Chih Cheng

This figure shows the co-authorship network connecting the top 25 collaborators of Min-Chih Cheng. A scholar is included among the top collaborators of Min-Chih Cheng 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 Min-Chih Cheng. Min-Chih Cheng 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.
Chien, Wei‐Hsien, Chia‐Hsiang Chen, Min-Chih Cheng, Yu‐Yu Wu, & Susan Shur‐Fen Gau. (2024). Neuregulin 2 Is a Candidate Gene for Autism Spectrum Disorder. International Journal of Molecular Sciences. 25(10). 5547–5547. 1 indexed citations
2.
Cheng, Min-Chih, et al.. (2023). Indicators of HSV1 Infection, ECM–Receptor Interaction, and Chromatin Modulation in a Nuclear Family with Schizophrenia. Journal of Personalized Medicine. 13(9). 1392–1392. 2 indexed citations
3.
Hu, Tsung‐Ming, et al.. (2020). Differential Expression of Multiple Disease-Related Protein Groups Induced by Valproic Acid in Human SH-SY5Y Neuroblastoma Cells. Brain Sciences. 10(8). 545–545. 6 indexed citations
4.
Chen, Chia‐Hsiang, et al.. (2020). Detection of Rare Methyl-CpG Binding Protein 2 Gene Missense Mutations in Patients With Schizophrenia. Frontiers in Genetics. 11. 476–476. 10 indexed citations
5.
Hu, Tsung‐Ming, et al.. (2019). Functional analyses and effect of DNA methylation on the EGR1 gene in patients with schizophrenia. Psychiatry Research. 275. 276–282. 16 indexed citations
6.
Hu, Tsung‐Ming, et al.. (2018). Mutation analysis of the WNT7A gene in patients with schizophrenia. Psychiatry Research. 265. 246–248. 2 indexed citations
7.
Chen, Chia‐Hsiang, et al.. (2017). Seroprevalence survey of selective anti-neuronal autoantibodies in patients with first-episode schizophrenia and chronic schizophrenia. Schizophrenia Research. 190. 28–31. 21 indexed citations
8.
Hu, Tsung‐Ming, et al.. (2016). Rare mutations and hypermethylation of the ARC gene associated with schizophrenia. Schizophrenia Research. 176(2-3). 106–113. 20 indexed citations
9.
Hu, Tsung‐Ming, et al.. (2015). Resequencing of early growth response 2 (EGR2) gene revealed a recurrent patient-specific mutation in schizophrenia. Psychiatry Research. 228(3). 958–960. 7 indexed citations
10.
11.
Chen, Chia‐Hsiang, Min-Chih Cheng, Yen‐Nan Chiu, et al.. (2014). Genetic analysis of GABRB3 as a candidate gene of autism spectrum disorders. Molecular Autism. 5(1). 36–36. 47 indexed citations
12.
Li, Junming, et al.. (2013). Exonic resequencing of the DLGAP3 gene as a candidate gene for schizophrenia. Psychiatry Research. 208(1). 84–87. 13 indexed citations
13.
Shen, Yu‐Chih, et al.. (2012). Genetic and functional analysis of the gene encoding neurogranin in schizophrenia. Schizophrenia Research. 137(1-3). 7–13. 12 indexed citations
14.
Shen, Yu‐Chih, et al.. (2011). Genetic and functional analysis of the gene encoding GAP-43 in schizophrenia. Schizophrenia Research. 134(2-3). 239–245. 7 indexed citations
15.
16.
Sun, Chicheng, Min-Chih Cheng, Rosie Qin, et al.. (2011). Identification and functional characterization of rare mutations of the neuroligin-2 gene ( NLGN2 ) associated with schizophrenia. Human Molecular Genetics. 20(15). 3042–3051. 98 indexed citations
17.
18.
Cheng, Min-Chih, et al.. (2010). Genetic and Functional Analysis of the DLG4 Gene Encoding the Post-Synaptic Density Protein 95 in Schizophrenia. PLoS ONE. 5(12). e15107–e15107. 41 indexed citations
19.
Cheng, Min-Chih, Ding‐Lieh Liao, Chao A. Hsiung, et al.. (2007). Chronic treatment with aripiprazole induces differential gene expression in the rat frontal cortex. The International Journal of Neuropsychopharmacology. 11(2). 207–16. 48 indexed citations
20.
Cheng, Min-Chih & Chia‐Hsiang Chen. (2006). Identification of rare mutations of synaptogyrin 1 gene in patients with schizophrenia. Journal of Psychiatric Research. 41(12). 1027–1031. 10 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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2026