Min-Chih Cheng
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Explore the profile of Min-Chih Cheng including associated specialties, affiliations and a list of published articles.
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39
Citations
362
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Recent Articles
1.
Chien W, Chen C, Cheng M, Wu Y, Gau S
Int J Mol Sci
. 2024 May;
25(10).
PMID: 38791584
Autism spectrum disorder (ASD) is a complex neurodevelopmental disorder with heterogeneous and complex genetic underpinnings. Our previous microarray gene expression profiling identified significantly different neuregulin-2 gene (NRG2) expression between ASD...
2.
Huang Y, Ping L, Hsu S, Tsai H, Cheng M
J Pers Med
. 2023 Sep;
13(9).
PMID: 37763159
Schizophrenia (SCZ) is a complex psychiatric disorder with high heritability; identifying risk genes is essential for deciphering the disorder's pathogenesis and developing novel treatments. Using whole-exome sequencing, we screened for...
3.
Lin K, Hu T, Hsu S, Tsai H, Cheng M
Psychiatr Genet
. 2023 Jan;
33(1):20-25.
PMID: 36617743
Objective: The alpha-amino-3-hydroxy-5-methyl-4-isoxazole propionate (AMPA) receptors significantly regulate the synaptic transmission and functions of various synaptic receptors. This study aimed to identify single nucleotide mutations in the glutamate receptor, ionotropic,...
4.
Hu T, Wu C, Hsu S, Tsai H, Cheng F, Cheng M
J Pers Med
. 2022 May;
12(5).
PMID: 35629206
Schizophrenia is a complex mental disorder with a genetic component. The GRIK gene family encodes ionotropic glutamate receptors of the kainate subtype, which are considered candidate genes for schizophrenia. We...
5.
Wang Y, Hsu S, Tsai H, Cheng F, Cheng M
Int J Mol Sci
. 2022 May;
23(9).
PMID: 35562887
Arc/Arg3.1 (activity-regulated cytoskeletal-associated protein (ARC)) is a critical regulator of long-term synaptic plasticity and is involved in the pathophysiology of schizophrenia. The functions and mechanisms of human ARC action are...
6.
Chen C, Cheng M, Hu T, Ping L, Kushima I, Aleksic B
Psychiatr Genet
. 2022 Mar;
32(3):125-130.
PMID: 35353798
Objective: Studies showed that rare copy number variations (CNVs) encompassing the vasoactive intestinal peptide receptor 2 gene (VIPR2) were associated with schizophrenia, indicating VIPR2 is a risk gene for schizophrenia....
7.
Cheng M, Chien W, Huang Y, Fang T, Chen C
Int J Mol Sci
. 2022 Jan;
23(1).
PMID: 35008879
Rare copy number variations (CNVs) are part of the genetics of schizophrenia; they are highly heterogeneous and personalized. The CNV Analysis Group of the Psychiatric Genomic Consortium (PGC) conducted a...
8.
Chen C, Cheng M, Hu T, Ping L
Front Genet
. 2021 Oct;
12:620496.
PMID: 34659328
Schizophrenia is a chronic, devastating mental disorder with complex genetic components. Given the advancements in the molecular genetic research of schizophrenia in recent years, there is still a lack of...
9.
Wang Y, Chen C, Chen S, Cheng F, Hsu S, Tsai H, et al.
Schizophr Res
. 2021 Jul;
235:60-62.
PMID: 34325211
No abstract available.
10.
Wang Y, Hsu S, Tsai H, Cheng M
Psychiatry Res
. 2021 May;
300:113943.
PMID: 33932639
GNB1L haploinsufficiency caused by 22q11.2 deletion syndrome may contribute to schizophrenia pathophysiology. We resequenced the protein-coding sequences of GNB1L in 553 patients with schizophrenia and 535 controls from Taiwan. Four...