Brian C. Mansfield

4.1k total citations
84 papers, 3.0k citations indexed

About

Brian C. Mansfield is a scholar working on Rheumatology, Genetics and Molecular Biology. According to data from OpenAlex, Brian C. Mansfield has authored 84 papers receiving a total of 3.0k indexed citations (citations by other indexed papers that have themselves been cited), including 53 papers in Rheumatology, 37 papers in Genetics and 26 papers in Molecular Biology. Recurrent topics in Brian C. Mansfield's work include Glycogen Storage Diseases and Myoclonus (53 papers), Genetics and Neurodevelopmental Disorders (27 papers) and Lysosomal Storage Disorders Research (13 papers). Brian C. Mansfield is often cited by papers focused on Glycogen Storage Diseases and Myoclonus (53 papers), Genetics and Neurodevelopmental Disorders (27 papers) and Lysosomal Storage Disorders Research (13 papers). Brian C. Mansfield collaborates with scholars based in United States, New Zealand and Hungary. Brian C. Mansfield's co-authors include Janice Y. Chou, Hyun Sik Jun, Chi‐Jiunn Pan, Young‐Mock Lee, Yuan-Tsong Chen, Dietrich Matern, Yuk Yin Cheung, Jun‐Ho Cho, Jeng‐Jer Shieh and Wai Han Yiu and has published in prestigious journals such as Journal of Biological Chemistry, Journal of Clinical Investigation and Nature Genetics.

In The Last Decade

Brian C. Mansfield

82 papers receiving 2.9k citations

Peers

Brian C. Mansfield
S Lévy-Toledano France
Akihiro Imura Japan
Shoichi Iseki Japan
Songqing Na United States
Keiichi Morita Japan
Yoshiro Wada Japan
Holger Luthman Sweden
Jean Ruf France
Finian Martin Ireland
Hiroki Shima Japan
S Lévy-Toledano France
Brian C. Mansfield
Citations per year, relative to Brian C. Mansfield Brian C. Mansfield (= 1×) peers S Lévy-Toledano

Countries citing papers authored by Brian C. Mansfield

Since Specialization
Citations

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

Fields of papers citing papers by Brian C. Mansfield

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Brian C. Mansfield. 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 Brian C. Mansfield. The network helps show where Brian C. Mansfield may publish in the future.

Co-authorship network of co-authors of Brian C. Mansfield

This figure shows the co-authorship network connecting the top 25 collaborators of Brian C. Mansfield. A scholar is included among the top collaborators of Brian C. Mansfield 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 Brian C. Mansfield. Brian C. Mansfield 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.
Lee, Chul, Kunal Pratap, Sudeep Gautam, et al.. (2025). Persistent Activation of Renal Autophagy Contributes to Nephropathy in Murine Glycogen Storage Disease Type Ia. Journal of Inherited Metabolic Disease. 49(1). e70127–e70127.
2.
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Lee, Chul, Kunal Pratap, Lisa Zhang, et al.. (2023). Inhibition of Wnt/β-catenin signaling reduces renal fibrosis in murine glycogen storage disease type Ia. Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease. 1870(1). 166874–166874. 5 indexed citations
4.
Zhang, Lisa, Chul Lee, Irina Arnaoutova, et al.. (2020). Gene therapy using a novel G6PC-S298C variant enhances the long-term efficacy for treating glycogen storage disease type Ia. Biochemical and Biophysical Research Communications. 527(3). 824–830. 8 indexed citations
5.
Duncan, Jacque L., Karmen M Trzupek, Sari Tuupanen, et al.. (2019). Multiple copies of rhodopsin as a novel cause of autosomal dominant retinitis pigmentosa. Investigative Ophthalmology & Visual Science. 60(9). 2943–2943. 1 indexed citations
6.
Mansfield, Brian C., et al.. (2015). My Retina Tracker™: An On-line International Registry for People Affected with Inherited Orphan Retinal Degenerative Diseases and their Genetic Relatives - A New Resource. Advances in experimental medicine and biology. 854. 245–251. 7 indexed citations
7.
Chou, Janice Y. & Brian C. Mansfield. (2014). The SLC37 Family of Sugar-Phosphate/Phosphate Exchangers. Current topics in membranes. 73. 357–382. 42 indexed citations
8.
9.
Chou, Janice Y., Hyun Sik Jun, & Brian C. Mansfield. (2010). Glycogen storage disease type I and G6Pase-β deficiency: etiology and therapy. Nature Reviews Endocrinology. 6(12). 676–688. 160 indexed citations
10.
Chou, Janice Y., Hyun Sik Jun, & Brian C. Mansfield. (2009). Neutropenia in type Ib glycogen storage disease. Current Opinion in Hematology. 17(1). 36–42. 60 indexed citations
11.
Lecchi, Paolo, Jinghua Zhao, Greg P. Bertenshaw, et al.. (2009). A method for assessing and maintaining the reproducibility of mass spectrometric analyses of complex samples. Rapid Communications in Mass Spectrometry. 23(12). 1817–1824. 4 indexed citations
12.
Chou, Janice Y. & Brian C. Mansfield. (2008). Mutations in the glucose-6-phosphatase-α (G6PC) gene that cause type Ia glycogen storage disease. Human Mutation. 29(7). 921–930. 114 indexed citations
13.
Yiu, Wai Han, C J Pan, Wentao Peng, et al.. (2007). Angiotensin mediates renal fibrosis in the nephropathy of glycogen storage disease type Ia. Kidney International. 73(6). 716–723. 32 indexed citations
14.
Ghosh, Abhijit, et al.. (2005). Long-term correction of murine glycogen storage disease type Ia by recombinant adeno-associated virus-1-mediated gene transfer. Gene Therapy. 13(4). 321–329. 49 indexed citations
15.
Shieh, Jeng‐Jer, Chi‐Jiunn Pan, Brian C. Mansfield, & Janice Y. Chou. (2004). The islet‐specific glucose‐6‐phosphatase‐related protein, implicated in diabetes, is a glycoprotein embedded in the endoplasmic reticulum membrane. FEBS Letters. 562(1-3). 160–164. 17 indexed citations
16.
Shieh, Jeng‐Jer, Chi‐Jiunn Pan, Brian C. Mansfield, & Janice Y. Chou. (2003). A Glucose-6-phosphate Hydrolase, Widely Expressed Outside the Liver, Can Explain Age-dependent Resolution of Hypoglycemia in Glycogen Storage Disease Type Ia. Journal of Biological Chemistry. 278(47). 47098–47103. 82 indexed citations
17.
Chou, Janice Y. & Brian C. Mansfield. (1999). Molecular Genetics of Type 1 Glycogen Storage Diseases. Trends in Endocrinology and Metabolism. 10(3). 104–113. 51 indexed citations
18.
Annabi, Borhane, Brian C. Mansfield, Hisayuki Hiraiwa, et al.. (1998). The Gene for Glycogen-Storage Disease Type 1b Maps to Chromosome 11q23. The American Journal of Human Genetics. 62(2). 400–405. 91 indexed citations
19.
McLenachan, Patricia A., Peter J. Lockhart, H.R. Faber, & Brian C. Mansfield. (1996). Evolutionary analysis of the multigene pregnancy-specific β1-Glycoprotein family: Separation of historical and nonhistorical signals. Journal of Molecular Evolution. 42(2). 273–280. 11 indexed citations
20.
Brophy, Brigid, Rachel Macdonald, Patricia A. McLenachan, & Brian C. Mansfield. (1992). cDNA sequence of the pregnancy-specific β1-glycoprotein-11s (PSG-11s). Biochimica et Biophysica Acta (BBA) - Gene Structure and Expression. 1131(1). 119–121. 4 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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