Shu Pei Wang

1.6k total citations
26 papers, 1.3k citations indexed

About

Shu Pei Wang is a scholar working on Biochemistry, Physiology and Surgery. According to data from OpenAlex, Shu Pei Wang has authored 26 papers receiving a total of 1.3k indexed citations (citations by other indexed papers that have themselves been cited), including 19 papers in Biochemistry, 16 papers in Physiology and 15 papers in Surgery. Recurrent topics in Shu Pei Wang's work include Lipid metabolism and biosynthesis (18 papers), Pancreatic function and diabetes (15 papers) and Adipose Tissue and Metabolism (13 papers). Shu Pei Wang is often cited by papers focused on Lipid metabolism and biosynthesis (18 papers), Pancreatic function and diabetes (15 papers) and Adipose Tissue and Metabolism (13 papers). Shu Pei Wang collaborates with scholars based in Canada, China and United States. Shu Pei Wang's co-authors include Grant A. Mitchell, Jiang Wei Wu, Krishnakant G. Soni, Nicolas Gauthier, Nancy Laurin, Marc Prentki, Jacquetta M. Trasler, Gongshe Yang, Fernando Alvarez and Louis Hermo and has published in prestigious journals such as PLoS ONE, Hepatology and Diabetes.

In The Last Decade

Shu Pei Wang

25 papers receiving 1.3k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Shu Pei Wang Canada 20 709 688 474 427 223 26 1.3k
Sarah M. Turpin-Nolan Australia 11 687 1.0× 312 0.5× 1.0k 2.1× 263 0.6× 464 2.1× 16 1.7k
Sheene Kim United States 10 862 1.2× 202 0.3× 879 1.9× 248 0.6× 427 1.9× 11 1.5k
Susumu Taniguchi Japan 11 315 0.4× 374 0.5× 465 1.0× 178 0.4× 167 0.7× 16 1.1k
Abudukadier Abulizi United States 15 573 0.8× 124 0.2× 640 1.4× 289 0.7× 431 1.9× 17 1.3k
Angela M. Siesky United States 8 531 0.7× 172 0.3× 816 1.7× 225 0.5× 326 1.5× 8 1.3k
Karina Preiss-Landl Austria 11 443 0.6× 469 0.7× 434 0.9× 211 0.5× 121 0.5× 11 1.0k
Hong-Ping Guan United States 13 604 0.9× 221 0.3× 725 1.5× 204 0.5× 274 1.2× 13 1.2k
Xian‐Man Zhang United States 14 722 1.0× 166 0.2× 646 1.4× 373 0.9× 809 3.6× 16 1.8k
Marie Daval United States 11 565 0.8× 109 0.2× 585 1.2× 429 1.0× 306 1.4× 12 1.2k
Sarah Hummasti United States 8 309 0.4× 127 0.2× 564 1.2× 577 1.4× 314 1.4× 8 1.3k

Countries citing papers authored by Shu Pei Wang

Since Specialization
Citations

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

Fields of papers citing papers by Shu Pei Wang

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Shu Pei Wang. 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 Shu Pei Wang. The network helps show where Shu Pei Wang may publish in the future.

Co-authorship network of co-authors of Shu Pei Wang

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

All Works

20 of 20 papers shown
1.
Zhang, Xiao, Hao Yang, Krishnakant G. Soni, et al.. (2019). An Epistatic Interaction between Pnpla2 and Lipe Reveals New Pathways of Adipose Tissue Lipolysis. Cells. 8(5). 395–395. 27 indexed citations
2.
Yang, Hao, Chen Zhao, Youlin Wang, et al.. (2019). Inborn errors of mitochondrial acyl-coenzyme a metabolism: acyl-CoA biology meets the clinic. Molecular Genetics and Metabolism. 128(1-2). 30–44. 12 indexed citations
3.
Yang, Hao, Francis Rossignol, Denis Cyr, et al.. (2017). Mildly elevated succinylacetone and normal liver function in compound heterozygotes with pathogenic and pseudodeficient FAH alleles. Molecular Genetics and Metabolism Reports. 14. 55–58. 7 indexed citations
4.
Wu, Jiang Wei, Christoph Preuß, Shu Pei Wang, et al.. (2017). Epistatic interaction between the lipase-encoding genes Pnpla2 and Lipe causes liposarcoma in mice. PLoS Genetics. 13(5). e1006716–e1006716. 37 indexed citations
5.
Xia, Bo, et al.. (2017). Adipose tissue deficiency of hormone-sensitive lipase causes fatty liver in mice. PLoS Genetics. 13(12). e1007110–e1007110. 73 indexed citations
6.
Yang, Hao, Walla Al‐Hertani, Denis Cyr, et al.. (2016). Hypersuccinylacetonaemia and normal liver function in maleylacetoacetate isomerase deficiency. Journal of Medical Genetics. 54(4). 241–247. 21 indexed citations
7.
Wang, Shu Pei, Jiang Wei Wu, J Lefebvre, et al.. (2014). The Catalytic Function of Hormone-Sensitive Lipase is Essential for Fertility in Male Mice. Endocrinology. 155(8). 3047–3053. 13 indexed citations
8.
Wang, Shu Pei, et al.. (2014). Metabolism as a tool for understanding human brain evolution: Lipid energy metabolism as an example. Journal of Human Evolution. 77. 41–49. 38 indexed citations
9.
Wu, Jiang Wei, Hao Yang, Shu Pei Wang, et al.. (2014). Inborn errors of cytoplasmic triglyceride metabolism. Journal of Inherited Metabolic Disease. 38(1). 85–98. 27 indexed citations
10.
Gauthier, Nicolas, Jiang Wei Wu, Shu Pei Wang, et al.. (2013). A Liver-Specific Defect of Acyl-CoA Degradation Produces Hyperammonemia, Hypoglycemia and a Distinct Hepatic Acyl-CoA Pattern. PLoS ONE. 8(7). e60581–e60581. 12 indexed citations
11.
Lian, Jihong, En‐Hui Wei, Shu Pei Wang, et al.. (2012). Liver specific inactivation of carboxylesterase 3/triacylglycerol hydrolase decreases blood lipids without causing severe steatosis in mice. Hepatology. 56(6). 2154–2162. 55 indexed citations
12.
Wu, Jiang Wei, Shu Pei Wang, Fernando Alvarez, et al.. (2011). Deficiency of liver adipose triglyceride lipase in mice causes progressive hepatic steatosis. Hepatology. 54(1). 122–132. 198 indexed citations
13.
Hermo, Louis, Mary Gregory, Charles E. Smith, et al.. (2007). Alterations in the testis of hormone sensitive lipase‐deficient mice is associated with decreased sperm counts, sperm motility, and fertility. Molecular Reproduction and Development. 75(4). 565–577. 28 indexed citations
14.
Fortier, Mélanie, Krishnakant G. Soni, Nancy Laurin, et al.. (2005). Human hormone-sensitive lipase (HSL): expression in white fat corrects the white adipose phenotype of HSL-deficient mice. Journal of Lipid Research. 46(9). 1860–1867. 28 indexed citations
15.
Fortier, Mélanie, Shu Pei Wang, Pascale Mauriège, et al.. (2004). Hormone-sensitive lipase-independent adipocyte lipolysis during β-adrenergic stimulation, fasting, and dietary fat loading. American Journal of Physiology-Endocrinology and Metabolism. 287(2). E282–E288. 49 indexed citations
16.
Wang, Shu Pei, et al.. (2004). Expression of Human Hormone-Sensitive Lipase (HSL) in Postmeiotic Germ Cells Confers Normal Fertility to HSL-Deficient Mice. Endocrinology. 145(12). 5688–5693. 29 indexed citations
17.
18.
Wang, Shu Pei, Nancy Laurin, Jean Himms‐Hagen, et al.. (2001). The Adipose Tissue Phenotype of Hormone‐Sensitive Lipase Deficiency in Mice. Obesity Research. 9(2). 119–128. 185 indexed citations
19.
Wang, Shu Pei, et al.. (2001). Infertility and Testicular Defects in Hormone-Sensitive Lipase-Deficient Mice. Endocrinology. 142(10). 4272–4281. 80 indexed citations
20.
Laurin, Nancy, Shu Pei Wang, & Grant A. Mitchell. (2000). The hormone-sensitive lipase gene is transcribed from at least five alternative first exons in mouse adipose tissue. Mammalian Genome. 11(11). 972–978. 25 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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