Irmgard Hölker

1.5k total citations
19 papers, 797 citations indexed

About

Irmgard Hölker is a scholar working on Molecular Biology, Genetics and Genetics. According to data from OpenAlex, Irmgard Hölker has authored 19 papers receiving a total of 797 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Molecular Biology, 11 papers in Genetics and 7 papers in Genetics. Recurrent topics in Irmgard Hölker's work include Neurogenetic and Muscular Disorders Research (11 papers), RNA modifications and cancer (6 papers) and RNA Research and Splicing (5 papers). Irmgard Hölker is often cited by papers focused on Neurogenetic and Muscular Disorders Research (11 papers), RNA modifications and cancer (6 papers) and RNA Research and Splicing (5 papers). Irmgard Hölker collaborates with scholars based in Germany, Poland and Italy. Irmgard Hölker's co-authors include Brunhilde Wirth, Lars Brichta, Walter Doerfler, Raoul Heller, Karsten Haug, Thomas Klockgether, Eric Hahnen, Ingmar Blümcke, Christian Tränkle and Markus Rießland and has published in prestigious journals such as Annals of Neurology, Journal of Virology and Biochemical and Biophysical Research Communications.

In The Last Decade

Irmgard Hölker

19 papers receiving 784 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Irmgard Hölker Germany 16 617 378 164 122 86 19 797
Deborah Y. Kwon United States 12 727 1.2× 287 0.8× 158 1.0× 90 0.7× 35 0.4× 14 849
María Inés Pérez‐Millán Argentina 17 347 0.6× 98 0.3× 175 1.1× 127 1.0× 34 0.4× 32 821
Judit Balog Netherlands 18 1.1k 1.8× 193 0.5× 197 1.2× 54 0.4× 120 1.4× 22 1.3k
Vasco Meneghini Italy 16 539 0.9× 210 0.6× 184 1.1× 27 0.2× 93 1.1× 22 847
Lucy E. Walmsley United Kingdom 7 499 0.8× 334 0.9× 237 1.4× 65 0.5× 195 2.3× 7 834
Susan Gribble United Kingdom 18 579 0.9× 96 0.3× 765 4.7× 53 0.4× 55 0.6× 29 1.2k
Fabiana Louise Motta Brazil 15 298 0.5× 134 0.4× 95 0.6× 35 0.3× 97 1.1× 37 589
Michał Milewski Poland 12 605 1.0× 141 0.4× 108 0.7× 167 1.4× 107 1.2× 34 1.1k
Jennifer A. Myers United States 13 777 1.3× 89 0.2× 91 0.6× 52 0.4× 69 0.8× 19 963
Françoise Piguet France 13 481 0.8× 50 0.1× 207 1.3× 85 0.7× 232 2.7× 28 743

Countries citing papers authored by Irmgard Hölker

Since Specialization
Citations

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

Fields of papers citing papers by Irmgard Hölker

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Irmgard Hölker

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

All Works

19 of 19 papers shown
1.
Hölker, Irmgard, Nikolai Tschernoster, Seyyedmohsen Hosseinibarkooie, et al.. (2023). Epigenetic regulation of plastin 3 expression by the macrosatellite DXZ4 and the transcriptional regulator CHD4. The American Journal of Human Genetics. 110(3). 442–459. 5 indexed citations
2.
Zanni, Ginevra, Matthias Eckenweiler, Markus Storbeck, et al.. (2022). CAPRIN1P512L causes aberrant protein aggregation and associates with early-onset ataxia. Cellular and Molecular Life Sciences. 79(10). 526–526. 9 indexed citations
3.
Gabriel, Elke, Irmgard Hölker, Aruljothi Mariappan, et al.. (2018). Novel insights into SMALED2: BICD2 mutations increase microtubule stability and cause defects in axonal and NMJ development. Human Molecular Genetics. 27(10). 1772–1784. 16 indexed citations
4.
Heilig, Juliane, Seyyedmohsen Hosseinibarkooie, Natalia Mendoza-Ferreira, et al.. (2018). Plastin 3 influences bone homeostasis through regulation of osteoclast activity. Human Molecular Genetics. 27(24). 4249–4262. 43 indexed citations
5.
Storbeck, Markus, Beate Horsberg Eriksen, Andreas Unger, et al.. (2017). Phenotypic extremes of BICD2-opathies: from lethal, congenital muscular atrophy with arthrogryposis to asymptomatic with subclinical features. European Journal of Human Genetics. 25(9). 1040–1048. 34 indexed citations
6.
Storbeck, Markus, Raoul Heller, Irmgard Hölker, et al.. (2016). Biallelic Loss of Proprioception-Related PIEZO2 Causes Muscular Atrophy with Perinatal Respiratory Distress, Arthrogryposis, and Scoliosis. The American Journal of Human Genetics. 99(5). 1206–1216. 72 indexed citations
7.
Heesen, Ludwig, Michael Peitz, Laura Torres‐Benito, et al.. (2015). Plastin 3 is upregulated in iPSC-derived motoneurons from asymptomatic SMN1-deleted individuals. Cellular and Molecular Life Sciences. 73(10). 2089–2104. 32 indexed citations
8.
Garbes, Lutz, Ludwig Heesen, Irmgard Hölker, et al.. (2012). VPA response in SMA is suppressed by the fatty acid translocase CD36. Human Molecular Genetics. 22(2). 398–407. 44 indexed citations
9.
Garbes, Lutz, Markus Rießland, Irmgard Hölker, et al.. (2009). LBH589 induces up to 10-fold SMN protein levels by several independent mechanisms and is effective even in cells from SMA patients non-responsive to valproate. Human Molecular Genetics. 18(19). 3645–3658. 87 indexed citations
10.
Brichta, Lars, Lutz Garbes, Maria Jędrzejowska, et al.. (2008). Nonsense-mediated messenger RNA decay of survival motor neuron 1 causes spinal muscular atrophy. Human Genetics. 123(2). 141–153. 26 indexed citations
11.
Brichta, Lars, Irmgard Hölker, Karsten Haug, Thomas Klockgether, & Brunhilde Wirth. (2006). In vivo activation of SMN in spinal muscular atrophy carriers and patients treated with valproate. Annals of Neurology. 59(6). 970–975. 116 indexed citations
12.
Hahnen, Eric, Ilker Y. Eyüpoglu, Lars Brichta, et al.. (2006). In vitro and ex vivo evaluation of second‐generation histone deacetylase inhibitors for the treatment of spinal muscular atrophy. Journal of Neurochemistry. 98(1). 193–202. 126 indexed citations
13.
Föcking, Melanie, Irmgard Hölker, & Thorsten Trapp. (2003). Chronic glucocorticoid receptor activation impairs CREB transcriptional activity in clonal neurons. Biochemical and Biophysical Research Communications. 304(4). 720–723. 23 indexed citations
14.
Trapp, Thorsten, László Oláh, Irmgard Hölker, et al.. (2001). GTPase RhoB: An Early Predictor of Neuronal Death after Transient Focal Ischemia in Mice. Molecular and Cellular Neuroscience. 17(5). 883–894. 62 indexed citations
16.
Munnes, Marc, Christian Schetter, Irmgard Hölker, & Walter Doerfler. (1995). A fully 5'-CG-3' but not a 5'-CCGG-3' methylated late frog virus 3 promoter retains activity. Journal of Virology. 69(4). 2240–2247. 18 indexed citations
17.
Schetter, Christian, et al.. (1993). Patterns of frog virus 3 DNA methylation and DNA methyltransferase activity in nuclei of infected cells. Journal of Virology. 67(12). 6973–6978. 15 indexed citations
18.
Behn-Krappa, Annett, et al.. (1991). Patterns of DNA methylation are indistinguishable in different individuals over a wide range of human DNA sequences. Genomics. 11(1). 1–7. 34 indexed citations
19.
Behn-Krappa, Annett, Manfred Jücker, Irmgard Hölker, et al.. (1991). Patterns of DNA methylation in selected human genes in different Hodgkin's lymphoma and leukemia cell lines and in normal human lymphocytes.. PubMed. 51(14). 3702–9. 17 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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