Xin‐Ming Shen

3.8k citations

79 papers · 2.6k indexed · 1 hit paper · h-index 31

Impact in

Neurology top 0.5%
- Myasthenia Gravis and Thymoma
- Neuroblastoma Research and Treatments
- Peripheral Neuropathies and Disorders
Cell Biology top 1%
- Cellular transport and secretion

Papers in

Neurology 43
- Myasthenia Gravis and Thymoma 40
Cell Biology 32
- Cellular transport and secretion 27
- Biotin and Related Studies 4

Co-authors: Andrew G. Engel Duygu Selcen Steven M. Sine Kinji Ohno Joan M. Brengman Margherita Milone Akira Tsujino Taku Fukuda
Journals: Neurology (13 papers)Neuromuscular Disorders (8 papers)Annals of the New York Academy of Sciences (6 papers)Journal of Clinical Investigation (4 papers)Annals of Clinical and Translational Neurology (4 papers)
Partner nations: United States China Japan

In The Last Decade

Xin‐Ming Shen

75 papers receiving 2.6k citations

Hit Papers

align trajectories log scale

Congenital myasthenic syndromes: pathogenesis, diagnosis, and treatment 2015 · 361 citations

Peers

Countries citing papers authored by Xin‐Ming Shen

Since Specialization

Citations

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

Fields of papers citing papers by Xin‐Ming Shen

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Xin‐Ming Shen. 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 Xin‐Ming Shen. The network helps show where Xin‐Ming Shen may publish in the future.

Co-authors

The 25 scholars most cited alongside Xin‐Ming Shen, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Xin‐Ming Shen Line = papers co-authored together Xin‐Ming Shen links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	Per- and polyfluoroalkyl substances on the surface of children's feeding smocks: High-throughput characterization and implications for exposure assessment Environmental Chemistry and Ecotoxicology ·Yatai Li, Yong Zhao, Xin‐Ming Shen, Yuan Xue, Ling‐Yan He, Shoucong Xu, Lizhong Yang, Jun Yi, Jia Zhang, Guangtao Fan, Qihong Deng	2025	0
2	Short-term and long-term prognoses in AChR-Ab positive very-late-onset myasthenia gravis patients Therapeutic Advances in Neurological Disorders ·Nairong Xie, Qing Liu, Qi Wen, Yaye Wang, Haoran Liu, Yuting Jiang, Yan Lü, Li Di, Min Wang, Wenjia Zhu, Xinmei Wen, Xuxiang Zhang, Xin‐Ming Shen, Yuwei Da	2025	4
3	A rare complex structural variant of novel intragenic inversion combined with reciprocal translocation t(X;1)(p21.2;p13.3) in Duchenne muscular dystrophy Neuromuscular Disorders ·Yaye Wang, Xinmei Wen, Xin‐Ming Shen, Li Di, Yanan Sun, Yun Li, Shu Zhang, Qi Wen, Jingsi Wang, Jianying Duo, Yue Huang, Yan Lü, Min Xu, Min Wang, Hailan Chen, Wenjia Zhu, Yuwei Da	2024	1
4	Comparison between mono‐tacrolimus and mono‐glucocorticoid in the treatment of myasthenia gravis Annals of Clinical and Translational Neurology ·Zhirong Fan, Lin Lei, Shengyao Su, Shu Zhang, Nairong Xie, Ling Li, Yan Lü, Li Di, Min Wang, Min Xu, Xin‐Ming Shen, Yuwei Da	2023	1
5	Clinical and Pathologic Features of Congenital Myasthenic Syndromes Caused by 35 Genes—A Comprehensive Review International Journal of Molecular Sciences ·Kinji Ohno, Bisei Ohkawara, Xin‐Ming Shen, Duygu Selcen, Andrew G. Engel	2023	52
6	Missense Mutations of Codon 116 in the SOD1 Gene Cause Rapid Progressive Familial ALS and Predict Short Viability With PMA Phenotype Frontiers in Genetics ·Xinmei Wen, Wenjia Zhu, Nan Xia, Qianwen Li, Li Di, Shu Zhang, Hai Chen, Yan Lü, Min Wang, Min Xu, Suobin Wang, Xin‐Ming Shen, Jie Lu, Yuwei Da	2021	2
7	Presence of antibodies against low-density lipoprotein receptor-related protein 4 and impairment of neuromuscular junction in a Chinese cohort of amyotrophic lateral sclerosis Chinese Medical Journal ·Lin Lei, Xin‐Ming Shen, Shuyan Wang, Yan Lü, Suo-Bin Wang, Hai Chen, Zheng Liu, Ya-Sheng Ouyang, Jianying Duo, Yuwei Da, Zhiguo Chen	2019	3
8	Low-dose PCB126 compromises circadian rhythms associated with disordered glucose and lipid metabolism in mice Environment International ·Xin‐Ming Shen, Yongjiu Chen, J. X. Zhang, Yan Xu, Wei Liu, Yifan Guo, Qiuli Shan, Sijin Liu	2019	29
9	Limb girdle muscular dystrophy D3 HNRNPDL related in a Chinese family with distal muscle weakness caused by a mutation in the prion-like domain Journal of Neurology ·Yanan Sun, Hailan Chen, Yan Lü, Jianying Duo, Lin Lei, Ya-Sheng Ouyang, Yifeng Hao, Yuwei Da, Xin‐Ming Shen	2019	16
10	Atypical familial amyotrophic lateral sclerosis with initial symptoms of pain or tremor in a Chinese family harboring VAPB-P56S mutation Journal of Neurology ·Di Li, Hai Chen, Yuwei Da, Suobing Wang, Xin‐Ming Shen	2015	19
11	Congenital myasthenic syndrome in Japan: Ethnically unique mutations in muscle nicotinic acetylcholine receptor subunits Neuromuscular Disorders ·Yoshiteru Azuma, Tomohiko Nakata, Motoki Tanaka, Xin‐Ming Shen, Mikako Ito, Satoshi Iwata, Tatsuya Okuno, Yoshiko Nomura, N Ando, Keiko Ishigaki, Bisei Ohkawara, Akio Masuda, Jun Natsume, Seiji Kojima, Masahiro Sokabe, Kinji Ohno	2014	19
12	New horizons for congenital myasthenic syndromes Annals of the New York Academy of Sciences ·Andrew G. Engel, Xin‐Ming Shen, Duygu Selcen, Steven M. Sine	2012	23
13	Endplate structure and parameters of neuromuscular transmission in sporadic centronuclear myopathy associated with myasthenia Neuromuscular Disorders ·Teerin Liewluck, Xin‐Ming Shen, Margherita Milone, Andrew G. Engel	2011	33
14	Functional consequences and structural interpretation of mutations of human choline acetyltransferase Human Mutation ·Xin‐Ming Shen, Thomas O. Crawford, Joan M. Brengman, Gyula Acsádi, Susan Iannaconne, Emin Karaca, Chaouky Khoury, Jean K. Mah, Simon Edvardson, Željko Bajzer, David W. Rodgers, Andrew G. Engel	2011	30
15	What Have We Learned from the Congenital Myasthenic Syndromes Journal of Molecular Neuroscience ·Andrew G. Engel, Xin‐Ming Shen, Duygu Selcen, Steven M. Sine	2009	55
16	Dok‐7 myasthenia: Phenotypic and molecular genetic studies in 16 patients Annals of Neurology ·Duygu Selcen, Margherita Milone, Xin‐Ming Shen, C. Michel Harper, Anthony A. Stans, Eric D. Wieben, Andrew G. Engel	2008	89
17	Further Observations in Congenital Myasthenic Syndromes Annals of the New York Academy of Sciences ·Andrew G. Engel, Xin‐Ming Shen, Duygu Selcen, Steven M. Sine	2008	22
18	Congenital myasthenia–related AChR δ subunit mutation interferes with intersubunit communication essential for channel gating Journal of Clinical Investigation ·Xin‐Ming Shen, Taku Fukuda, Kinji Ohno, Steven M. Sine, Andrew G. Engel	2008	41
19	Mutation causing severe myasthenia reveals functional asymmetry of AChR signature cystine loops in agonist binding and gating Journal of Clinical Investigation ·Xin‐Ming Shen, Kinji Ohno, Akira Tsujino, Joan M. Brengman, Monique Gingold, Steven M. Sine, Andrew G. Engel	2003	60
20	Rapsyn Mutations in Humans Cause Endplate Acetylcholine-Receptor Deficiency and Myasthenic Syndrome The American Journal of Human Genetics ·Kinji Ohno, Andrew G. Engel, Xin‐Ming Shen, Duygu Selcen, Joan M. Brengman, C. Michel Harper, Akira Tsujino, Margherita Milone	2002	170

About Xin‐Ming Shen

Xin‐Ming Shen is a scholar working on Neurology, Cell Biology, Molecular Biology, Genetics and Cellular and Molecular Neuroscience, having authored 79 papers that have together received 2.6k indexed citations. Recurring topics across this work include Myasthenia Gravis and Thymoma (40 papers), Ion channel regulation and function (29 papers), Cellular transport and secretion (27 papers), Cancer Treatment and Pharmacology (8 papers), Nicotinic Acetylcholine Receptors Study (6 papers), Receptor Mechanisms and Signaling (5 papers), Neurogenetic and Muscular Disorders Research (5 papers) and Biotin and Related Studies (4 papers). The work is most often cited by research in Neurology (1.5k citations), Cell Biology (907 citations), Cellular and Molecular Neuroscience (387 citations), Molecular Biology (1.3k citations) and Genetics (196 citations). Xin‐Ming Shen has collaborated with scholars based in United States, China and Japan. Frequent co-authors include Andrew G. Engel, Duygu Selcen, Steven M. Sine, Kinji Ohno, Joan M. Brengman, Margherita Milone, Akira Tsujino, Taku Fukuda, C. Michel Harper and Charles M. Harper. Their work appears in journals such as Neurology, Neuromuscular Disorders, Annals of the New York Academy of Sciences, Journal of Clinical Investigation and Annals of Clinical and Translational Neurology.

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