Chih‐Ya Cheng

926 total citations
24 papers, 779 citations indexed

About

Chih‐Ya Cheng is a scholar working on Cellular and Molecular Neuroscience, Cognitive Neuroscience and Physiology. According to data from OpenAlex, Chih‐Ya Cheng has authored 24 papers receiving a total of 779 indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Cellular and Molecular Neuroscience, 7 papers in Cognitive Neuroscience and 7 papers in Physiology. Recurrent topics in Chih‐Ya Cheng's work include Neurotransmitter Receptor Influence on Behavior (7 papers), Nerve injury and regeneration (6 papers) and Autism Spectrum Disorder Research (6 papers). Chih‐Ya Cheng is often cited by papers focused on Neurotransmitter Receptor Influence on Behavior (7 papers), Nerve injury and regeneration (6 papers) and Autism Spectrum Disorder Research (6 papers). Chih‐Ya Cheng collaborates with scholars based in Taiwan, United States and Japan. Chih‐Ya Cheng's co-authors include Shih‐Jen Tsai, Chen‐Jee Hong, Tai‐Jui Chen, Younger W.‐Y. Yu, Chen‐Jee Hong, Hsiu-Chih Liu, Tsung‐Yun Liu, Ching‐Hua Lin, Hung‐Chi Wu and Ching‐Chi Hsu and has published in prestigious journals such as Scientific Reports, Life Sciences and Psychiatry Research.

In The Last Decade

Chih‐Ya Cheng

23 papers receiving 760 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Chih‐Ya Cheng Taiwan	15	463	216	174	146	108	24	779
Shuken Boku Japan	13	275 0.6×	144 0.7×	215 1.2×	133 0.9×	92 0.9×	19	943
Anna Schuhmacher Germany	18	215 0.5×	192 0.9×	171 1.0×	161 1.1×	135 1.3×	26	731
Henriette Husum Denmark	19	615 1.3×	97 0.4×	297 1.7×	191 1.3×	37 0.3×	24	991
Patricia Jiménez-Vasquez Sweden	12	394 0.9×	72 0.3×	144 0.8×	113 0.8×	40 0.4×	12	629
Rachel L. Navarra United States	10	426 0.9×	229 1.1×	379 2.2×	168 1.2×	223 2.1×	16	1.0k
Fabien Boulle Netherlands	10	269 0.6×	119 0.6×	185 1.1×	61 0.4×	60 0.6×	13	854
Alice Borella United States	8	320 0.7×	162 0.8×	173 1.0×	61 0.4×	56 0.5×	9	651
Feng-Chang Yen Taiwan	10	215 0.5×	124 0.6×	87 0.5×	109 0.7×	72 0.7×	11	446
Taisuke Yoshida Japan	12	234 0.5×	132 0.6×	215 1.2×	134 0.9×	30 0.3×	14	631
Chan Hong Lee South Korea	15	341 0.7×	94 0.4×	219 1.3×	83 0.6×	51 0.5×	18	732

Countries citing papers authored by Chih‐Ya Cheng

Since Specialization

Citations

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

Fields of papers citing papers by Chih‐Ya Cheng

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Chih‐Ya Cheng

This figure shows the co-authorship network connecting the top 25 collaborators of Chih‐Ya Cheng. A scholar is included among the top collaborators of Chih‐Ya 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 Chih‐Ya Cheng. Chih‐Ya Cheng 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

Liang, Kung‐Hao, Yun‐Ru Chen, Chih‐Ya Cheng, et al.. (2020). The Fabry disease-causing mutation, GLA IVS4+919G>A, originated in Mainland China more than 800 years ago. Journal of Human Genetics. 65(7). 619–625. 11 indexed citations

Lin, Yung‐Shuan, Chih‐Ya Cheng, Yi‐Chu Liao, Chen‐Jee Hong, & Jong‐Ling Fuh. (2020). Mutational analysis in familial Alzheimer’s disease of Han Chinese in Taiwan with a predominant mutation PSEN1 p.Met146Ile. Scientific Reports. 10(1). 19769–19769. 6 indexed citations

Niu, Dau‐Ming, et al.. (2020). Early detection of the irreversible cardiac damages in the adults with late onset Fabry disease in a large cohort study via newborn screening. Molecular Genetics and Metabolism. 129(2). S117–S117. 1 indexed citations

Cheng, Chih‐Ya, et al.. (2017). AB049. Diagnosis and treatment of phenylketonuria in Taiwan- experience from a national newborn screening confirmatory center. Annals of Translational Medicine. 5(S2). AB049–AB049.

Chen, Wei‐Ting, Chen‐Jee Hong, Wenhan Chang, et al.. (2012). Amyloid-Beta (Ab) D7H Mutation Increases Oligomeric Ab42 and Alters Properties of Ab-Zinc/Copper Assemblies. 3 indexed citations

Cheng, Chih‐Ya, Chen‐Jee Hong, Younger W.‐Y. Yu, et al.. (2005). Brain-derived neurotrophic factor (Val66Met) genetic polymorphism is associated with substance abuse in males. Molecular Brain Research. 140(1-2). 86–90. 99 indexed citations

Cheng, Chih‐Ya, Chen‐Jee Hong, & Shih‐Jen Tsai. (2005). Effects of subchronic clozapine administration on serum glucose, cholesterol and triglyceride levels, and body weight in male BALB/c mice. Life Sciences. 76(19). 2269–2273. 14 indexed citations

Tsai, Shih‐Jen, Ding‐Lieh Liao, Younger W.‐Y. Yu, et al.. (2005). A study of the association of (Val66Met) polymorphism in the Brain-derived Neurotrophic Factor gene with alcohol dependence and extreme violence in Chinese males. Neuroscience Letters. 381(3). 340–343. 37 indexed citations

Cheng, Chih‐Ya, et al.. (2004). Expression of c-Fos-like immunoreactivity in the brain of mice with learned helplessness. Neuroscience Letters. 363(3). 280–283. 25 indexed citations

10.

Yen, Feng-Chang, et al.. (2004). X-box binding protein 1 (XBP1) C−116G polymorphisms in bipolar disorders and age of onset. Neuroscience Letters. 367(2). 232–234. 30 indexed citations

11.

Cheng, Chih‐Ya, et al.. (2004). Association Study of a Brain-Derived Neurotrophic Factor (Val66Met) Genetic Polymorphism and Panic Disorder. Neuropsychobiology. 49(4). 178–181. 39 indexed citations

12.

Tsai, Shih‐Jen, et al.. (2003). Association study of a brain‐derived neurotrophic‐factor genetic polymorphism and major depressive disorders, symptomatology, and antidepressant response. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 123B(1). 19–22. 187 indexed citations

13.

Hong, Chen‐Jee, Hsiu-Chih Liu, Tsung‐Yun Liu, et al.. (2003). Brain-derived neurotrophic factor (BDNF) Val66Met polymorphisms in Parkinson's disease and age of onset. Neuroscience Letters. 353(1). 75–77. 48 indexed citations

14.

Tsai, Shih‐Jen, et al.. (2002). No association for D2 and D4 dopamine receptor polymorphisms and methamphetamine abuse in Chinese males. Psychiatric Genetics. 12(1). 29–33. 25 indexed citations

15.

Tsai, Shih‐Jen, Chen‐Jee Hong, & Chih‐Ya Cheng. (2002). Serotonin transporter genetic polymorphisms and harm avoidance in the Chinese. Psychiatric Genetics. 12(3). 165–168. 36 indexed citations

16.

Cheng, Chih‐Ya, Chen‐Jee Hong, Hsiu-Chih Liu, Tsung‐Yun Liu, & Shih‐Jen Tsai. (2002). Study of the Association between Alzheimer’s Disease and Angiotensin-Converting Enzyme Gene Polymorphism Using DNA from Lymphocytes. European Neurology. 47(1). 26–29. 49 indexed citations

17.

Tsai, Shih‐Jen, Hsiu-Chih Liu, Tsung‐Yun Liu, Chih‐Ya Cheng, & Chen‐Jee Hong. (2002). Association Analysis for the Genetic Variants of the NMDA Receptor Subunit 2b and Alzheimer’s Disease. Dementia and Geriatric Cognitive Disorders. 13(2). 91–94. 12 indexed citations

18.

Tsai, Shih‐Jen, Chen‐Jee Hong, Tsung‐Yun Liu, Chih‐Ya Cheng, & Hsiu-Chih Liu. (2001). Association Study for a Functional Serotonin Transporter Gene Polymorphism and Late-Onset Alzheimer’s Disease for Chinese Patients. Neuropsychobiology. 44(1). 27–30. 15 indexed citations

19.

Hong, Chen‐Jee, Younger W.‐Y. Yu, Ching‐Hua Lin, Chih‐Ya Cheng, & Shih‐Jen Tsai. (2001). Association analysis for NMDA receptor subunit 2B (GRIN2B) genetic variants and psychopathology and clozapine response in schizophrenia. Psychiatric Genetics. 11(4). 219–222. 48 indexed citations

20.

Ouyang, Wen‐Chen, et al.. (2001). Association Study of Angiotensin-Converting Enzyme Gene Polymorphism with Schizophrenia and Polydipsia. Neuropsychobiology. 44(1). 31–35. 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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