Joan Keutzer

3.9k total citations
50 papers, 2.7k citations indexed

About

Joan Keutzer is a scholar working on Physiology, Rheumatology and Epidemiology. According to data from OpenAlex, Joan Keutzer has authored 50 papers receiving a total of 2.7k indexed citations (citations by other indexed papers that have themselves been cited), including 48 papers in Physiology, 15 papers in Rheumatology and 13 papers in Epidemiology. Recurrent topics in Joan Keutzer's work include Lysosomal Storage Disorders Research (47 papers), Glycogen Storage Diseases and Myoclonus (15 papers) and Trypanosoma species research and implications (11 papers). Joan Keutzer is often cited by papers focused on Lysosomal Storage Disorders Research (47 papers), Glycogen Storage Diseases and Myoclonus (15 papers) and Trypanosoma species research and implications (11 papers). Joan Keutzer collaborates with scholars based in United States, Taiwan and Canada. Joan Keutzer's co-authors include Wei‐Lien Chuang, Wuh‐Liang Hwu, Yin‐Hsiu Chien, Ni‐Chung Lee, Pramod K. Mistry, Xiaokui Zhang, Samantha Cooper, Carole Elbin, Joshua Pacheco and Ai-Chu Huang and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Neuroscience and SHILAP Revista de lepidopterología.

In The Last Decade

Joan Keutzer

47 papers receiving 2.6k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Joan Keutzer United States 29 2.3k 673 662 598 561 50 2.7k
Guillem Pintos‐Morell Spain 25 1.3k 0.6× 558 0.8× 526 0.8× 317 0.5× 322 0.6× 94 2.2k
Helen Michelakakis Greece 27 1.3k 0.6× 387 0.6× 330 0.5× 469 0.8× 322 0.6× 101 2.1k
Manisha Balwani United States 28 1.1k 0.5× 320 0.5× 377 0.6× 560 0.9× 332 0.6× 114 2.6k
J. Ledvinová Czechia 20 1.4k 0.6× 616 0.9× 266 0.4× 447 0.7× 325 0.6× 53 1.7k
Irène Maire France 21 950 0.4× 387 0.6× 379 0.6× 358 0.6× 285 0.5× 42 1.5k
Anaïs Brassier France 19 714 0.3× 230 0.3× 168 0.3× 294 0.5× 168 0.3× 84 1.7k
Julian Raiman Canada 24 738 0.3× 331 0.5× 439 0.7× 127 0.2× 181 0.3× 58 1.5k
Mina Mirzaian Netherlands 20 1.3k 0.6× 577 0.9× 163 0.2× 533 0.9× 451 0.8× 35 1.6k
Laura Gort Spain 24 758 0.3× 221 0.3× 226 0.3× 282 0.5× 275 0.5× 67 1.3k
Francyne Kubaski United States 24 1.2k 0.5× 522 0.8× 268 0.4× 297 0.5× 307 0.5× 79 1.5k

Countries citing papers authored by Joan Keutzer

Since Specialization
Citations

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

Fields of papers citing papers by Joan Keutzer

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Joan Keutzer

This figure shows the co-authorship network connecting the top 25 collaborators of Joan Keutzer. A scholar is included among the top collaborators of Joan Keutzer 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 Joan Keutzer. Joan Keutzer 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.
Oliva, Petra, Markus Schwarz, Thomas P. Mechtler, et al.. (2023). Importance to include differential diagnostics for acid sphingomyelinase deficiency (ASMD) in patients suspected to have to Gaucher disease. Molecular Genetics and Metabolism. 139(1). 107563–107563. 4 indexed citations
2.
Taguchi, Yumiko, Jun Liu, Jiapeng Ruan, et al.. (2017). Glucosylsphingosine Promotes α-Synuclein Pathology in Mutant GBA-Associated Parkinson's Disease. Journal of Neuroscience. 37(40). 9617–9631. 186 indexed citations
3.
Lévesque, Sébastien, Christiane Auray‐Blais, Michel Boutin, et al.. (2016). Diagnosis of late-onset Pompe disease and other muscle disorders by next-generation sequencing. Orphanet Journal of Rare Diseases. 11(1). 8–8. 43 indexed citations
4.
Chuang, Wei‐Lien, Joshua Pacheco, Samantha Cooper, et al.. (2015). Improved sensitivity of an acid sphingomyelinase activity assay using a C6:0 sphingomyelin substrate. SHILAP Revista de lepidopterología. 3. 55–57. 5 indexed citations
5.
Chuang, Wei‐Lien, Joshua Pacheco, Samantha Cooper, et al.. (2013). Lyso-sphingomyelin is elevated in dried blood spots of Niemann–Pick B patients. Molecular Genetics and Metabolism. 111(2). 209–211. 66 indexed citations
6.
Wang, Zhaohui, Patricia M. Okamoto, & Joan Keutzer. (2013). A new assay for fast, reliable CRIM status determination in infantile-onset Pompe disease. Molecular Genetics and Metabolism. 111(2). 92–100. 21 indexed citations
7.
Elbin, Carole, et al.. (2011). The effect of preparation, storage and shipping of dried blood spots on the activity of five lysosomal enzymes. Clinica Chimica Acta. 412(13-14). 1207–1212. 29 indexed citations
8.
Reuser, Arnold, Frans W. Verheijen, Deeksha Bali, et al.. (2011). The use of dried blood spot samples in the diagnosis of lysosomal storage disorders — Current status and perspectives. Molecular Genetics and Metabolism. 104(1-2). 144–148. 60 indexed citations
9.
Chien, Yin‐Hsiu, Petra Olivova, Shu-Chuan Chiang, et al.. (2010). Elevation of urinary globotriaosylceramide (GL3) in infants with Fabry disease. Molecular Genetics and Metabolism. 102(1). 57–60. 9 indexed citations
10.
Auray‐Blais, Christiane, Joe T.R. Clarke, David G. Warnock, et al.. (2010). How well does urinary lyso-Gb3 function as a biomarker in Fabry disease?. Clinica Chimica Acta. 411(23-24). 1906–1914. 92 indexed citations
11.
Dajnoki, Angéla, György Fekete, Joan Keutzer, et al.. (2010). Newborn screening for Fabry disease by measuring GLA activity using tandem mass spectrometry. Clinica Chimica Acta. 411(19-20). 1428–1431. 44 indexed citations
12.
Orsini, Joseph J., Mark A. Morrissey, Monica Martin, et al.. (2009). Implementation of newborn screening for Krabbe disease: Population study and cutoff determination. Clinical Biochemistry. 42(9). 877–884. 45 indexed citations
13.
Elbin, Carole, et al.. (2009). Multiplex Lysosomal Enzyme Activity Assay on Dried Blood Spots Using Tandem Mass Spectrometry. Methods in molecular biology. 603. 339–350. 22 indexed citations
14.
Olivova, Petra, et al.. (2009). Effect of sample collection on α-galactosidase A enzyme activity measurements in dried blood spots on filter paper. Clinica Chimica Acta. 403(1-2). 159–162. 28 indexed citations
15.
Tomanin, Rosella, Anna Chiara Frigo, Gabriela Niizawa, et al.. (2008). Rapid diagnostic testing procedures for lysosomal storage disorders: α-glucosidase and β-galactosidase assays on dried blood spots. Clinica Chimica Acta. 402(1-2). 38–41. 26 indexed citations
16.
Elbin, Carole, et al.. (2008). Multiplex Enzyme Assay Screening of Dried Blood Spots for Lysosomal Storage Disorders by Using Tandem Mass Spectrometry. Clinical Chemistry. 54(10). 1725–1728. 135 indexed citations
17.
Yoon, Hye‐Ran, Kyunghee Cho, Han‐Wook Yoo, et al.. (2007). Determination of plasma C16-C24 globotriaosylceramide (Gb3) isoforms by tandem mass spectrometry for diagnosis of Fabry disease. 4(1). 45–52.
18.
Kallwass, Helmut, Robert J. Pomponio, Deeksha Bali, et al.. (2007). Rapid diagnosis of late-onset Pompe disease by fluorometric assay of α-glucosidase activities in dried blood spots. Molecular Genetics and Metabolism. 90(4). 449–452. 46 indexed citations
19.
Zhang, Haoyue, Helmut Kallwass, Sarah P. Young, et al.. (2006). Comparison of maltose and acarbose as inhibitors of maltase-glucoamylase activity in assaying acid α-glucosidase activity in dried blood spots for the diagnosis of infantile Pompe disease. Genetics in Medicine. 8(5). 302–306. 63 indexed citations
20.
Kitagawa, Teruo, Nobuyuki Ishige, Ken Suzuki, et al.. (2005). Non-invasive screening method for Fabry disease by measuring globotriaosylceramide in whole urine samples using tandem mass spectrometry. Molecular Genetics and Metabolism. 85(3). 196–202. 48 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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