Ernst Conzelmann

5.5k total citations · 1 hit paper
72 papers, 4.3k citations indexed

About

Ernst Conzelmann is a scholar working on Molecular Biology, Physiology and Clinical Biochemistry. According to data from OpenAlex, Ernst Conzelmann has authored 72 papers receiving a total of 4.3k indexed citations (citations by other indexed papers that have themselves been cited), including 57 papers in Molecular Biology, 43 papers in Physiology and 15 papers in Clinical Biochemistry. Recurrent topics in Ernst Conzelmann's work include Lysosomal Storage Disorders Research (34 papers), Glycosylation and Glycoproteins Research (23 papers) and Peroxisome Proliferator-Activated Receptors (15 papers). Ernst Conzelmann is often cited by papers focused on Lysosomal Storage Disorders Research (34 papers), Glycosylation and Glycoproteins Research (23 papers) and Peroxisome Proliferator-Activated Receptors (15 papers). Ernst Conzelmann collaborates with scholars based in Germany, Finland and United States. Ernst Conzelmann's co-authors include Konrad Sandhoff, Werner Schmitz, Ralph Fingerhut, Josef Burg, Heidi NEHRKORN, Vytautas Ivaškevičius, Edward G. D. Tuddenham, Hans‐Joachim Pelz, Andreas Fregin and Simone Rost and has published in prestigious journals such as Nature, Proceedings of the National Academy of Sciences and Journal of Biological Chemistry.

In The Last Decade

Ernst Conzelmann

71 papers receiving 4.2k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Mutations in VKORC1 cause warfarin resistance and multiple coagulation factor deficiency type 2

2004 857 citations Ernst Conzelmann et al. profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Ernst Conzelmann Germany	36	2.4k	1.7k	763	617	503	72	4.3k
Maurice Wibo Belgium	27	2.3k 1.0×	654 0.4×	670 0.9×	281 0.5×	255 0.5×	67	3.9k
G S Tint United States	32	2.6k 1.1×	1.3k 0.8×	324 0.4×	142 0.2×	219 0.4×	100	5.4k
Chieko Yokoyama Japan	35	2.8k 1.2×	690 0.4×	351 0.5×	335 0.5×	324 0.6×	80	6.1k
Roelof Ottenhoff Netherlands	36	1.6k 0.7×	1.3k 0.8×	550 0.7×	104 0.2×	912 1.8×	77	4.0k
D J Hanahan United States	34	1.5k 0.6×	900 0.5×	233 0.3×	163 0.3×	393 0.8×	58	4.5k
Robert L. Wykle United States	49	3.4k 1.4×	1.1k 0.7×	444 0.6×	131 0.2×	268 0.5×	110	5.9k
Derek J. Parks United States	29	4.4k 1.8×	1.1k 0.7×	312 0.4×	1.3k 2.2×	1.2k 2.5×	42	9.5k
Werner Kramer Germany	42	1.7k 0.7×	480 0.3×	222 0.3×	297 0.5×	487 1.0×	115	4.8k
Jeffrey T. Billheimer United States	46	3.8k 1.6×	695 0.4×	598 0.8×	150 0.2×	595 1.2×	121	6.9k
James D. Bergstrom United States	27	3.1k 1.3×	599 0.3×	512 0.7×	106 0.2×	209 0.4×	61	4.5k

Countries citing papers authored by Ernst Conzelmann

Since Specialization

Citations

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

Fields of papers citing papers by Ernst Conzelmann

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Ernst Conzelmann

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

All Works

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20 of 20 papers shown

Salonurmi, Tuire, Markku J. Savolainen, Matti Jauhiainen, et al.. (2013). Metabolic adaptation allows Amacr-deficient mice to remain symptom-free despite low levels of mature bile acids. Biochimica et Biophysica Acta (BBA) - Molecular and Cell Biology of Lipids. 1831(8). 1335–1343. 10 indexed citations

Bhaumik, Prasenjit, Werner Schmitz, Antti Hassinen, et al.. (2007). The Catalysis of the 1,1-Proton Transfer by α-Methyl-acyl-CoA Racemase Is Coupled to a Movement of the Fatty Acyl Moiety Over a Hydrophobic, Methionine-rich Surface. Journal of Molecular Biology. 367(4). 1145–1161. 38 indexed citations

Bhaumik, Prasenjit, Werner Schmitz, Tiina Kotti, et al.. (2005). α-Methylacyl-CoA Racemase from Mycobacterium tuberculosis. Journal of Biological Chemistry. 280(13). 12611–12620. 41 indexed citations

Bhaumik, Prasenjit, Petri Kursula, Ernst Conzelmann, et al.. (2003). Crystallization and preliminary X-ray diffraction studies of an α-methylacyl-CoA racemase fromMycobacterium tuberculosis. Acta Crystallographica Section D Biological Crystallography. 59(2). 353–355. 15 indexed citations

Cuebas, D, et al.. (2002). The role of α-methylacyl-CoA racemase in bile acid synthesis. Biochemical Journal. 363(3). 801–801. 32 indexed citations

Asfaw, Befekadu, J. Ledvinová, Robert Dobrovolný, et al.. (2002). Defects in degradation of blood group A and B glycosphingolipids in Schindler and Fabry diseases. Journal of Lipid Research. 43(7). 1096–1104. 24 indexed citations

Muntau, Ania C., et al.. (2002). PEX1 Mutations in Complementation Group 1 of Zellweger Spectrum Patients Correlate with Severity of Disease. Pediatric Research. 51(6). 706–714. 49 indexed citations

Kotti, Tiina, Heli Helander, Ahmed Yagi, et al.. (2000). In Mouse α-Methylacyl-CoA Racemase, the Same Gene Product Is Simultaneously Located in Mitochondria and Peroxisomes. Journal of Biological Chemistry. 275(27). 20887–20895. 53 indexed citations

Berná, Linda, et al.. (1999). Determination of Urinary Sulfatides and Other Lipids by Combination of Reversed-Phase and Thin-Layer Chromatographies. Analytical Biochemistry. 269(2). 304–311. 29 indexed citations

10.

Galle, Jan, Reinhard Schneider, Alexandra N. Heinloth, et al.. (1999). Lp(a) and LDL induce apoptosis in human endothelial cells and in rabbit aorta: Role of oxidative stress. Kidney International. 55(4). 1450–1461. 111 indexed citations

11.

Galle, Jan, Reinhard Schneider, Beate Winner, et al.. (1998). Glyc-oxidized LDL impair endothelial function more potently than oxidized LDL: role of enhanced oxidative stress. Atherosclerosis. 138(1). 65–77. 44 indexed citations

12.

Schmitz, Werner, Ralph Fingerhut, & Ernst Conzelmann. (1994). Purification and properties of an α‐methylacyl‐CoA racemase from rat liver. European Journal of Biochemistry. 222(2). 313–323. 105 indexed citations

13.

Michel, Sylvie, et al.. (1992). Quantitative correlation between the residual activity of β-hexosaminidase A and arylsulfatase A and the severity of the resulting lysosomal storage disease. Human Genetics. 88(5). 513–523. 256 indexed citations

14.

Kappler, Joachim, et al.. (1991). Genotype-phenotype relationship in various degrees of arylsulfatase A deficiency. Human Genetics. 86(5). 463–70. 36 indexed citations

15.

Klemm, E. & Ernst Conzelmann. (1989). Adult-onset metachromatic leucodystrophy presenting without psychiatric symptoms. Journal of Neurology. 236(7). 427–429. 7 indexed citations

16.

Friedl, Waltraut, et al.. (1989). Pseudodeficiency of arylsulfatase A: a common genetic polymorphism with possible disease implications. Human Genetics. 82(1). 45–48. 55 indexed citations

17.

Friedl, Waltraut, Abdül Waheed, Ernst Conzelmann, et al.. (1988). Probable metachromatic leukodystrophy/pseudodeficiency compound heterozygote at the arylsulfatase A locus with neurological and psychiatric symptomatology. American Journal of Medical Genetics. 31(1). 169–175. 25 indexed citations

18.

Fürst, Werner, et al.. (1987). Identity of the activator proteins for the enzymatic hydrolysis of sulfatide, ganglioside GM1, and globotriaosylceramide. Archives of Biochemistry and Biophysics. 259(2). 627–638. 32 indexed citations

19.

Conzelmann, Ernst, et al.. (1987). Assay for cerebroside sulfate (sulfatide) sulfatase in cultured skin fibroblasts with the natural activator protein. Clinica Chimica Acta. 168(1). 55–68. 8 indexed citations

20.

Schwarzmann, Günter, et al.. (1984). Insertion into cultured cells and metabolism and intracellular transport of exogenous gangliosides.. MPG.PuRe (Max Planck Society). 195–210. 1 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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