Yuting Lou

449 total citations
24 papers, 300 citations indexed

About

Yuting Lou is a scholar working on Cognitive Neuroscience, Molecular Biology and Clinical Psychology. According to data from OpenAlex, Yuting Lou has authored 24 papers receiving a total of 300 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Cognitive Neuroscience, 8 papers in Molecular Biology and 7 papers in Clinical Psychology. Recurrent topics in Yuting Lou's work include Obsessive-Compulsive Spectrum Disorders (7 papers), Genetics and Neurodevelopmental Disorders (5 papers) and Epilepsy research and treatment (4 papers). Yuting Lou is often cited by papers focused on Obsessive-Compulsive Spectrum Disorders (7 papers), Genetics and Neurodevelopmental Disorders (5 papers) and Epilepsy research and treatment (4 papers). Yuting Lou collaborates with scholars based in China and United States. Yuting Lou's co-authors include Wei Luo, Zhidong Cen, Min Xuan, Minming Zhang, Peiyu Huang, Jianhua Feng, Dan Li, Quanquan Gu, Yufan Guo and Zhiyuan Ouyang and has published in prestigious journals such as Movement Disorders, Clinical Neurophysiology and Journal of Psychiatric Research.

In The Last Decade

Yuting Lou

23 papers receiving 300 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Yuting Lou China	10	158	133	58	56	38	24	300
Nicholas D. Child New Zealand	8	147 0.9×	135 1.0×	138 2.4×	40 0.7×	74 1.9×	14	318
Julieta Arena Argentina	9	229 1.4×	108 0.8×	111 1.9×	36 0.6×	87 2.3×	17	391
Carina Soemmer Germany	5	190 1.2×	48 0.4×	64 1.1×	46 0.8×	65 1.7×	5	327
Jue Zhao China	14	287 1.8×	76 0.6×	99 1.7×	37 0.7×	30 0.8×	31	413
Olga Ulmanová Czechia	12	239 1.5×	50 0.4×	108 1.9×	30 0.5×	13 0.3×	32	368
Pierre Kolber Germany	9	131 0.8×	96 0.7×	30 0.5×	124 2.2×	14 0.4×	9	351
Téodor Danaila France	11	238 1.5×	58 0.4×	66 1.1×	29 0.5×	45 1.2×	27	342
Jérôme Aupy France	8	127 0.8×	118 0.9×	95 1.6×	14 0.3×	91 2.4×	29	323
Mayako Takanashi Japan	11	229 1.4×	111 0.8×	74 1.3×	85 1.5×	58 1.5×	12	433
Jong Woo Han South Korea	10	122 0.8×	88 0.7×	48 0.8×	51 0.9×	14 0.4×	18	350

Countries citing papers authored by Yuting Lou

Since Specialization

Citations

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

Fields of papers citing papers by Yuting Lou

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Yuting Lou

This figure shows the co-authorship network connecting the top 25 collaborators of Yuting Lou. A scholar is included among the top collaborators of Yuting Lou 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 Yuting Lou. Yuting Lou 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, Jue, Ye Wang, Xiaolong Li, et al.. (2025). Function‐Specific Localization in the Supplementary Motor Area: A Potential Effective Target for Tourette Syndrome. CNS Neuroscience & Therapeutics. 31(2). e70280–e70280. 1 indexed citations

Lou, Yuting, et al.. (2024). Hemizygous splicing variant in CNKSR2 results in X‐linked intellectual developmental disorder. Molecular Genetics & Genomic Medicine. 12(2). e2389–e2389. 1 indexed citations

Wang, Ye, et al.. (2024). Abnormal individualized functional connectivity: A potential stimulation target for pediatric tourette syndrome. Clinical Neurophysiology. 168. 25–33. 1 indexed citations

Zhou, Tianshu, Yufan Guo, Yu Tian, et al.. (2023). Video-based evaluation system for tic action in Tourette syndrome: modeling, detection, and evaluation. Health Information Science and Systems. 11(1). 39–39. 2 indexed citations

Chen, Xiaoquan, Yuting Lou, Zheng Wan, et al.. (2023). A heterozygous pathogenic variant in the ATP6V1A gene triggering epilepsy in a large Chinese pedigree. Clinical Neurology and Neurosurgery. 233. 107956–107956. 3 indexed citations

Lou, Yuting, et al.. (2023). Abnormal dynamics of brain functional networks in children with Tourette syndrome. Journal of Psychiatric Research. 159. 249–257. 3 indexed citations

Cheng, Hai‐Ying Mary, Ye Wang, Yuting Lou, et al.. (2023). A Heterozygous Variant of FGF13 Caused X-Linked Developmental and Epileptic Encephalopathy 90 in a Chinese Family. Cytogenetic and Genome Research. 163(1-2). 36–41.

Zang, Yu‐Feng, et al.. (2022). Multivariate Classification of Brain Blood-Oxygen Signal Complexity for the Diagnosis of Children with Tourette Syndrome. Molecular Neurobiology. 59(2). 1249–1261. 1 indexed citations

Zhou, Tianshu, Yufan Guo, Yu Tian, et al.. (2021). Tic Detection in Tourette Syndrome Patients Based on Unsupervised Visual Feature Learning. Journal of Healthcare Engineering. 2021. 1–10. 10 indexed citations

10.

Guo, Yufan, Xueying Zhu, Jianda Wang, et al.. (2021). Giant axonal neuropathy (GAN) in an 8‐year‐old girl caused by a homozygous pathogenic splicing variant in GAN gene. American Journal of Medical Genetics Part A. 188(3). 836–846. 6 indexed citations

11.

Guo, Yufan, Jianda Wang, Zhiliang Wang, et al.. (2021). Establishment of an induced pluripotent stem cell line (ZJSHi001-A) from a patient with epileptic encephalopathy carrying KCNB1 Glu330Asp mutation. Stem Cell Research. 52. 102224–102224. 2 indexed citations

12.

Wang, Jianda, Lin Han, Yufan Guo, et al.. (2020). Autosomal dominant hereditary spastic paraplegia caused by mutation of UBAP1. Neurogenetics. 21(3). 169–177. 7 indexed citations

13.

Lou, Yuting, Xiaolong Li, Ye Wang, et al.. (2020). Frequency-Specific Regional Homogeneity Alterations in Tourette Syndrome. Frontiers in Psychiatry. 11. 543049–543049. 8 indexed citations

14.

Cen, Zhidong, Yufan Guo, Yuting Lou, et al.. (2017). De novo mutation in DEPDC5 associated with unilateral pachygyria and intractable epilepsy. Seizure. 50. 1–3. 9 indexed citations

15.

Cen, Zhidong, Yuting Lou, Yufan Guo, Jianda Wang, & Jianhua Feng. (2017). Q10R mutation in SCN9A gene is associated with generalized epilepsy with febrile seizures plus. Seizure. 50. 186–188. 11 indexed citations

16.

Ye, Xiaoyun, Yuting Lou, Zhidong Cen, et al.. (2017). A clinical study of the coronal plane deformity in Parkinson disease. European Spine Journal. 26(7). 1862–1870. 17 indexed citations

17.

Huang, Peiyu, Yuting Lou, Min Xuan, et al.. (2016). Cortical abnormalities in Parkinson’s disease patients and relationship to depression: A surface-based morphometry study. Psychiatry Research Neuroimaging. 250. 24–28. 38 indexed citations

18.

Cen, Zhidong, Fei Xie, Zhiyuan Ouyang, et al.. (2016). Clinical and neurophysiological features of familial cortical myoclonic tremor with epilepsy. Movement Disorders. 31(11). 1704–1710. 14 indexed citations

19.

Lou, Yuting, Peiyu Huang, Dan Li, et al.. (2015). Altered brain network centrality in depressed Parkinson's disease patients. Movement Disorders. 30(13). 1777–1784. 85 indexed citations

20.

Yin, Lijun, Yuting Lou, Mingxia Fan, Zhaoxin Wang, & Yi Hu. (2015). Neural evidence for the use of digit-image mnemonic in a superior memorist: an fMRI study. Frontiers in Human Neuroscience. 9. 109–109. 9 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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