Fengqing Xiang

1.4k total citations
18 papers, 1.0k citations indexed

About

Fengqing Xiang is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Cardiology and Cardiovascular Medicine. According to data from OpenAlex, Fengqing Xiang has authored 18 papers receiving a total of 1.0k indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Molecular Biology, 4 papers in Cellular and Molecular Neuroscience and 4 papers in Cardiology and Cardiovascular Medicine. Recurrent topics in Fengqing Xiang's work include Cardiomyopathy and Myosin Studies (4 papers), RNA regulation and disease (3 papers) and Muscle Physiology and Disorders (3 papers). Fengqing Xiang is often cited by papers focused on Cardiomyopathy and Myosin Studies (4 papers), RNA regulation and disease (3 papers) and Muscle Physiology and Disorders (3 papers). Fengqing Xiang collaborates with scholars based in Sweden, United States and United Kingdom. Fengqing Xiang's co-authors include Lars Edström, Maria Anvret, Elena Rostkova, Thomas Sejersen, Mathias Gautel, Stephan Lange, Lars Gunnarsson, Anna Vihola, Jakob Kristensen and Bjarne Udd and has published in prestigious journals such as Science, The American Journal of Human Genetics and Neurobiology of Aging.

In The Last Decade

Fengqing Xiang

17 papers receiving 982 citations

Peers

Fengqing Xiang
Harold G. Marks United States
Brett Simms Canada
Anthony Simone United States
Valeswara‐Rao Gazula United States
Namita Ravi United States
Kenzo Hamano Japan
María Dolores Rubio Spain
Ulrike B. S. Hedrich Germany
Cassia N. Cearley United States
Waldy San Sebastián United States
Harold G. Marks United States
Fengqing Xiang
Citations per year, relative to Fengqing Xiang Fengqing Xiang (= 1×) peers Harold G. Marks

Countries citing papers authored by Fengqing Xiang

Since Specialization
Citations

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

Fields of papers citing papers by Fengqing Xiang

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Fengqing Xiang

This figure shows the co-authorship network connecting the top 25 collaborators of Fengqing Xiang. A scholar is included among the top collaborators of Fengqing Xiang 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 Fengqing Xiang. Fengqing Xiang is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

18 of 18 papers shown
1.
Ran, Caroline, Karin Wirdefeldt, Marie Westerlund, et al.. (2017). Genetic Variations and mRNA Expression of NRF2 in Parkinson’s Disease. Parkinson s Disease. 2017. 1–7. 18 indexed citations
2.
Ran, Caroline, Lars Forsgren, Marie Westerlund, et al.. (2016). Strong association between glucocerebrosidase mutations and Parkinson's disease in Sweden. Neurobiology of Aging. 45. 212.e5–212.e11. 39 indexed citations
3.
Ran, Caroline, Fengqing Xiang, Hans Nissbrandt, et al.. (2016). No Association Between rs7077361 in ITGA8 and Parkinson’s Disease in Sweden. The Open Neurology Journal. 10(1). 25–29. 2 indexed citations
4.
Vihola, Anna, Johanna Palmio, Giorgio Tasca, et al.. (2014). A.P.4. Neuromuscular Disorders. 24(9-10). 831–832.
5.
Paucar, Martin, et al.. (2013). Genotype-phenotype analysis in inherited prion disease with eight octapeptide repeat insertional mutation. Prion. 7(6). 501–510. 15 indexed citations
6.
Meng, Zhongji, Xinghuan Wang, Zhonghua Yang, & Fengqing Xiang. (2012). Expression of Transient Receptor Potential Melastatin 7 Up-regulated in the Early Stage of Renal Ischemia-Reperfusion. Transplantation Proceedings. 44(5). 1206–1210. 15 indexed citations
7.
Xiang, Fengqing, et al.. (2012). Gene mapping and mutation screeneng in candidate genes in a Chinese family of autosomal dominant retinitis pigmentosa. Russian Journal of Genetics. 48(1). 113–117. 1 indexed citations
8.
Lange, Stephan, Fengqing Xiang, Anna Vihola, et al.. (2005). The Kinase Domain of Titin Controls Muscle Gene Expression and Protein Turnover. Science. 308(5728). 1599–1603. 454 indexed citations
9.
10.
Moore, Richard C., Fengqing Xiang, Dong Han, et al.. (2001). Huntington Disease Phenocopy Is a Familial Prion Disease. The American Journal of Human Genetics. 69(6). 1385–1388. 95 indexed citations
11.
Xiang, Fengqing, et al.. (2001). Closely Related Swedish Rett Syndrome Females - None with MECP2 Mutation Revealed. Neuropediatrics. 32(4). 217–218. 4 indexed citations
12.
Buervenich, Silvia, Andrea Carmine, Fengqing Xiang, et al.. (2000). NURR1 Mutations in cases of schizophrenia and manic-depressive disorder. American Journal of Medical Genetics. 96(6). 808–813. 130 indexed citations
13.
Xiang, Fengqing, et al.. (2000). Mutation screening in Rett syndrome patients. Journal of Medical Genetics. 37(4). 250–255. 84 indexed citations
14.
Lin, Shuei‐Liong, et al.. (2000). [Changes of glucocorticoid receptor in cerebral and hepatic cytosol during decompression stress injury in rats].. PubMed. 13(5). 374–7. 1 indexed citations
15.
16.
Xiang, Fengqing, Lars‐Gunnar Gunnarsson, Bruno Giometto, et al.. (1999). Autosomal Dominant Myopathy with Proximal Weakness and Early Respiratory Muscle Involvement Maps to Chromosome 2q. The American Journal of Human Genetics. 64(3). 788–792. 34 indexed citations
17.
Xiang, Fengqing, E. Almqvist, Anders Lundin, et al.. (1998). A Huntington Disease–Like Neurodegenerative Disorder Maps to Chromosome 20p. The American Journal of Human Genetics. 63(5). 1431–1438. 41 indexed citations
18.
Xiang, Fengqing, Zhengxiao Zhang, Angus Clarke, et al.. (1998). Chromosome mapping of Rett syndrome: a likely candidate region on the telomere of Xq.. Journal of Medical Genetics. 35(4). 297–300. 32 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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