Michael Beck

503 total citations
12 papers, 363 citations indexed

About

Michael Beck is a scholar working on Cell Biology, Molecular Biology and Physiology. According to data from OpenAlex, Michael Beck has authored 12 papers receiving a total of 363 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Cell Biology, 4 papers in Molecular Biology and 4 papers in Physiology. Recurrent topics in Michael Beck's work include Connective tissue disorders research (3 papers), Lysosomal Storage Disorders Research (3 papers) and Proteoglycans and glycosaminoglycans research (3 papers). Michael Beck is often cited by papers focused on Connective tissue disorders research (3 papers), Lysosomal Storage Disorders Research (3 papers) and Proteoglycans and glycosaminoglycans research (3 papers). Michael Beck collaborates with scholars based in Germany, United States and Israel. Michael Beck's co-authors include Hans Kresse, Josef Glössl, Marie T. Vanier, Andreas Gal, Markus Ries, Frank Krummenauer, Eugen Mengel, John Rogers, Jürgen W. Spranger and Harold A. Taylor and has published in prestigious journals such as Journal of Biological Chemistry, SHILAP Revista de lepidopterología and Clinica Chimica Acta.

In The Last Decade

Michael Beck

12 papers receiving 351 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Michael Beck Germany	7	181	178	123	64	46	12	363
Kevin Brewer United States	5	149 0.8×	298 1.7×	244 2.0×	16 0.3×	52 1.1×	5	537
Tokiro Ishikawa Japan	13	302 1.7×	298 1.7×	47 0.4×	32 0.5×	110 2.4×	28	517
Dominick Amato Canada	10	150 0.8×	144 0.8×	200 1.6×	14 0.2×	52 1.1×	26	427
Luis Alejandro Barrera Colombia	11	79 0.4×	181 1.0×	357 2.9×	58 0.9×	163 3.5×	46	534
F X Arredondo-Vega United States	12	44 0.2×	284 1.6×	54 0.4×	136 2.1×	103 2.2×	16	478
C Peters Germany	9	131 0.7×	157 0.9×	363 3.0×	62 1.0×	177 3.8×	9	498
Y Fukuhara Japan	5	105 0.6×	123 0.7×	285 2.3×	37 0.6×	113 2.5×	5	341
Ingrid Kjos Norway	11	166 0.9×	211 1.2×	27 0.2×	20 0.3×	49 1.1×	12	339
Talita Giacomet de Carvalho Brazil	14	88 0.5×	199 1.1×	283 2.3×	57 0.9×	98 2.1×	21	474
Ida Eriksson Sweden	11	90 0.5×	174 1.0×	57 0.5×	10 0.2×	93 2.0×	18	377

Countries citing papers authored by Michael Beck

Since Specialization

Citations

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

Fields of papers citing papers by Michael Beck

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Michael Beck

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

All Works

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12 of 12 papers shown

Beck, Michael. (2021). Clinical Manifestation in Females with X-linked Metabolic Disorders: Genetic and Pathophysiological Considerations. SHILAP Revista de lepidopterología. 9. 1 indexed citations

Mitchell, John J., et al.. (2017). Farber disease: design of the first observational and cross-sectional cohort study capturing retrospective and prospective data on the natural history and phenotypic spectrum of patients, including novel methodologies for assessment of disease-specific symptoms. Molecular Genetics and Metabolism. 120(1-2). S125–S125. 2 indexed citations

Whybra, Catharina, et al.. (2010). Paraoxonase (PON1) Gene Polymorphisms in Fabry Disease: Correlation with Renal Disease. Nephron Clinical Practice. 116(4). c289–c293. 3 indexed citations

Cathey, Sara, Mariko Kudo, Stephan Tiede, et al.. (2008). Molecular order in mucolipidosis II and III nomenclature. American Journal of Medical Genetics Part A. 146A(4). 512–513. 44 indexed citations

Ries, Markus, Marie T. Vanier, Frank Krummenauer, et al.. (2006). Critical assessment of chitotriosidase analysis in the rational laboratory diagnosis of children with Gaucher disease and Niemann–Pick disease type A/B and C. Journal of Inherited Metabolic Disease. 29(5). 647–652. 77 indexed citations

Beck, Michael, Timothy M. Cox, & Marie T. Vanier. (2002). Foreword. Acta Paediatrica. 91(s439). 1–2. 1 indexed citations

Beck, Michael, Timothy M. Cox, & Marie T. Vanier. (2002). Foreword. Acta Paediatrica. 91(11). 1–2. 2 indexed citations

Beck, Michael, et al.. (1995). Inter‐ and intrafamilial variability in mucolipidosis II (I‐cell disease). Clinical Genetics. 47(4). 191–199. 24 indexed citations

Beck, Michael, et al.. (1984). Dyggve-Melchior-Clausen syndrome: Normal degradation of proteodermatan sulfate, proteokeratan sulfate and heparan sulfate. Clinica Chimica Acta. 141(1). 7–15. 13 indexed citations

10.

Glössl, Josef, Michael Beck, & Hans Kresse. (1984). Biosynthesis of proteodermatan sulfate in cultured human fibroblasts.. Journal of Biological Chemistry. 259(22). 14144–14150. 146 indexed citations

11.

Beck, Michael, et al.. (1983). Heterogeneity of metatropic dysplasia. European Journal of Pediatrics. 140(3). 231–237. 29 indexed citations

12.

Beck, Michael, et al.. (1983). ABNORMAL PROTEODERMATAN SULFATE IN THREE PATIENTS WITH COFFIN-LOWRY SYNDROME. Pediatric Research. 17(11). 926–929. 21 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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