Jutta Gärtner

1.5k total citations
19 papers, 650 citations indexed

About

Jutta Gärtner is a scholar working on Molecular Biology, Clinical Biochemistry and Genetics. According to data from OpenAlex, Jutta Gärtner has authored 19 papers receiving a total of 650 indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Molecular Biology, 5 papers in Clinical Biochemistry and 3 papers in Genetics. Recurrent topics in Jutta Gärtner's work include Peroxisome Proliferator-Activated Receptors (11 papers), Metabolism and Genetic Disorders (5 papers) and RNA modifications and cancer (5 papers). Jutta Gärtner is often cited by papers focused on Peroxisome Proliferator-Activated Receptors (11 papers), Metabolism and Genetic Disorders (5 papers) and RNA modifications and cancer (5 papers). Jutta Gärtner collaborates with scholars based in Germany, Israel and United Kingdom. Jutta Gärtner's co-authors include Sven Thoms, Bernd Krone, Kevin Rostásy, Elke Kahler, Daniela Pohl, Edgar Brunner, M. Lehnert, Hans‐Joachim Wagner, F. Hanefeld and Peter Huppke and has published in prestigious journals such as Journal of Biological Chemistry, PLoS ONE and Neurology.

In The Last Decade

Jutta Gärtner

19 papers receiving 629 citations

Peers

Jutta Gärtner

PFM

GENET

ONCOL

IMMUN

Tomoko Tsuruta Japan

Andreas Lipski Germany

Aleksandra Jezela‐Stanek Poland

Eric Bareke Canada

Jong-Yeon Shin South Korea

Jorge Urresti United States

Martin Wolkersdorfer Austria

George Kitsos Greece

Chee‐Seng Ku Singapore

Tomoko Tsuruta Japan

Jutta Gärtner

343 ×0.9

55 ×0.3

PFM

50 ×0.5

GENET

195 ×1.9

ONCOL

52 ×0.7

IMMUN

Citations per year, relative to Jutta Gärtner Jutta Gärtner (= 1×) peers Tomoko Tsuruta

Countries citing papers authored by Jutta Gärtner

Since Specialization

Citations

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

Fields of papers citing papers by Jutta Gärtner

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Jutta Gärtner

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

All Works

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19 of 19 papers shown

Sahoo, Prativa, et al.. (2024). Atlas‐based assessment of hypomyelination: Quantitative MRI in Pelizaeus‐Merzbacher disease. Human Brain Mapping. 45(13). e70014–e70014. 2 indexed citations

Gärtner, Jutta, Reinhard Berner, Klaus‐Michael Debatin, et al.. (2024). Deutsches Zentrum für Kinder- und Jugendgesundheit. Monatsschrift Kinderheilkunde. 172(8). 704–710. 1 indexed citations

Rosewich, Hendrik, Stefan Nessler, Wolfgang Brück, & Jutta Gärtner. (2019). B cell depletion can be effective in multiple sclerosis but failed in a patient with advanced childhood cerebral X-linked adrenoleukodystrophy. Therapeutic Advances in Neurological Disorders. 12. 1278089701–1278089701. 1 indexed citations

Buentzel, Judith, Fabio Vilardi, Amelie S. Lotz‐Havla, Jutta Gärtner, & Sven Thoms. (2015). Conserved targeting information in mammalian and fungal peroxisomal tail-anchored proteins. Scientific Reports. 5(1). 17420–17420. 13 indexed citations

Huppke, Peter, Eike Wegener, Hanno J. Bolz, et al.. (2014). Tectonic gene mutations in patients with Joubert syndrome. European Journal of Human Genetics. 23(5). 616–620. 28 indexed citations

Wegener, Eike, Cornelia Brendel, André Fischer, et al.. (2014). Characterization of the MeCP2R168X Knockin Mouse Model for Rett Syndrome. PLoS ONE. 9(12). e115444–e115444. 26 indexed citations

Schultz, Verena, Hendrik Rosewich, Stefan Nessler, et al.. (2012). MicroRNA regulation in experimental autoimmune encephalomyelitis in mice and marmosets resembles regulation in human multiple sclerosis lesions. Journal of Neuroimmunology. 246(1-2). 27–33. 44 indexed citations

Hillebrand, Merle, Søren W. Gersting, Amelie S. Lotz‐Havla, et al.. (2011). Identification of a New Fatty Acid Synthesis-Transport Machinery at the Peroxisomal Membrane. Journal of Biological Chemistry. 287(1). 210–221. 28 indexed citations

Thoms, Sven, et al.. (2011). Peroxisome Formation Requires the Endoplasmic Reticulum Channel Protein Sec61. Traffic. 13(4). 599–609. 39 indexed citations

10.

Brendel, Cornelia, Valery Belakhov, Hauke Werner, et al.. (2010). Readthrough of nonsense mutations in Rett syndrome: evaluation of novel aminoglycosides and generation of a new mouse model. Journal of Molecular Medicine. 89(4). 389–398. 79 indexed citations

11.

Thoms, Sven, Sabine Grønborg, & Jutta Gärtner. (2009). Organelle interplay in peroxisomal disorders. Trends in Molecular Medicine. 15(7). 293–302. 46 indexed citations

12.

Schönberger, Stefan, Peter Roerig, Dominik T. Schneider, et al.. (2007). Genotype and Protein Expression After Bone Marrow Transplantation for Adrenoleukodystrophy. Archives of Neurology. 64(5). 651–651. 12 indexed citations

13.

Krone, Bernd, Daniela Pohl, Kevin Rostásy, et al.. (2007). Common infectious agents in multiple sclerosis: a case—control study in children. Multiple Sclerosis Journal. 14(1). 136–139. 39 indexed citations

14.

Pohl, Daniela, Bernd Krone, Kevin Rostásy, et al.. (2006). High seroprevalence of Epstein–Barr virus in children with multiple sclerosis. Neurology. 67(11). 2063–2065. 169 indexed citations

15.

Gärtner, Jutta. (2003). Is there a Phenotype/Genotype Correlation in Peroxisome Biogenesis Disorders (PBDs)?. Advances in experimental medicine and biology. 544. 59–65. 2 indexed citations

16.

Gärtner, Jutta, et al.. (2002). Human Genome and Diseases:¶Cellular and molecular aspects of Zellweger syndrome and other peroxisome biogenesis disorders. Cellular and Molecular Life Sciences. 59(6). 1058–1069. 34 indexed citations

17.

Gärtner, Jutta, et al.. (2001). Targeting Elements in the Amino-Terminal Part Direct the Human 70-kDa Peroxisomal Integral Membrane Protein (PMP70) to Peroxisomes. Biochemical and Biophysical Research Communications. 285(3). 649–655. 25 indexed citations

18.

Roerig, Peter, Peter Mayerhofer, Andreas Holzinger, & Jutta Gärtner. (2001). Characterization and functional analysis of the nucleotide binding fold in human peroxisomal ATP binding cassette transporters. FEBS Letters. 492(1-2). 66–72. 31 indexed citations

19.

Gärtner, Jutta, et al.. (1998). Clinical and Genetic Aspects of X-Linked Adrenoleukodystrophy. Neuropediatrics. 29(1). 3–13. 31 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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