Sabine Waltl

648 total citations
9 papers, 438 citations indexed

About

Sabine Waltl is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Physiology. According to data from OpenAlex, Sabine Waltl has authored 9 papers receiving a total of 438 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Molecular Biology, 6 papers in Cellular and Molecular Neuroscience and 2 papers in Physiology. Recurrent topics in Sabine Waltl's work include Genetic Neurodegenerative Diseases (5 papers), Mitochondrial Function and Pathology (4 papers) and Neutrophil, Myeloperoxidase and Oxidative Mechanisms (2 papers). Sabine Waltl is often cited by papers focused on Genetic Neurodegenerative Diseases (5 papers), Mitochondrial Function and Pathology (4 papers) and Neutrophil, Myeloperoxidase and Oxidative Mechanisms (2 papers). Sabine Waltl collaborates with scholars based in Canada, Austria and Singapore. Sabine Waltl's co-authors include Michael R. Hayden, Amber L. Southwell, Wolfgang Sattler, Ernst Malle, Erika B. Villanueva, Yuanyun Xie, Lisa M. Anderson, Eva Bernhart, Mahmoud A. Pouladi and Andrea Wintersperger and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Free Radical Biology and Medicine and Journal of Neurochemistry.

In The Last Decade

Sabine Waltl

9 papers receiving 431 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Sabine Waltl Canada 9 283 221 89 56 53 9 438
Kathleen Seyb United States 14 214 0.8× 183 0.8× 67 0.8× 146 2.6× 53 1.0× 19 546
Yongfang Zhao China 11 282 1.0× 164 0.7× 51 0.6× 43 0.8× 183 3.5× 15 523
Carla Lopes Portugal 13 434 1.5× 238 1.1× 79 0.9× 109 1.9× 46 0.9× 20 585
Mingshu Mo China 12 218 0.8× 100 0.5× 70 0.8× 38 0.7× 41 0.8× 14 376
Ryotaku Inoue Japan 8 165 0.6× 79 0.4× 103 1.2× 52 0.9× 48 0.9× 10 362
Takahiko Noro Japan 15 332 1.2× 101 0.5× 34 0.4× 55 1.0× 114 2.2× 34 642
Peter V. DiStefano United States 12 277 1.0× 190 0.9× 166 1.9× 56 1.0× 31 0.6× 17 640
Hariharan Saminathan United States 8 242 0.9× 142 0.6× 158 1.8× 99 1.8× 173 3.3× 11 500
Mibo Tang China 9 254 0.9× 75 0.3× 99 1.1× 73 1.3× 75 1.4× 20 403
Erika B. Villanueva Canada 15 636 2.2× 489 2.2× 187 2.1× 59 1.1× 69 1.3× 20 944

Countries citing papers authored by Sabine Waltl

Since Specialization
Citations

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

Fields of papers citing papers by Sabine Waltl

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Sabine Waltl

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

All Works

9 of 9 papers shown
1.
Bardile, Costanza Ferrari, Marta Garcia‐Miralles, Nicholas S. Caron, et al.. (2019). Intrinsic mutant HTT-mediated defects in oligodendroglia cause myelination deficits and behavioral abnormalities in Huntington disease. Proceedings of the National Academy of Sciences. 116(19). 9622–9627. 75 indexed citations
2.
Ehrnhoefer, Dagmar E., Amber L. Southwell, Xiaofan Qiu, et al.. (2017). HACE1 is essential for astrocyte mitochondrial function and influences Huntington disease phenotypes in vivo. Human Molecular Genetics. 27(2). 239–253. 29 indexed citations
3.
Sanders, Shaun S., Matthew P. Parsons, Amber L. Southwell, et al.. (2016). Sudden death due to paralysis and synaptic and behavioral deficits when Hip14/Zdhhc17 is deleted in adult mice. BMC Biology. 14(1). 108–108. 22 indexed citations
4.
Southwell, Amber L., Amy Smith-Dijak, Chris Kay, et al.. (2016). An enhanced Q175 knock-in mouse model of Huntington disease with higher mutant huntingtin levels and accelerated disease phenotypes. Human Molecular Genetics. 25(17). 3654–3675. 76 indexed citations
5.
Southwell, Amber L., Sonia Franciosi, Erika B. Villanueva, et al.. (2015). Anti-semaphorin 4D immunotherapy ameliorates neuropathology and some cognitive impairment in the YAC128 mouse model of Huntington disease. Neurobiology of Disease. 76. 46–56. 87 indexed citations
6.
Waltl, Sabine, Jay V. Patankar, Günter Fauler, et al.. (2013). 25-Hydroxycholesterol regulates cholesterol homeostasis in the murine CATH.a neuronal cell line. Neuroscience Letters. 539. 16–21. 22 indexed citations
7.
Fauler, Günter, Harald Köfeler, Sabine Waltl, et al.. (2010). Mouse brain plasmalogens are targets for hypochlorous acid-mediated modification in vitro and in vivo. Free Radical Biology and Medicine. 49(11). 1655–1665. 31 indexed citations
8.
Nusshold, Christoph, Manfred Kollroser, Harald Köfeler, et al.. (2010). Hypochlorite modification of sphingomyelin generates chlorinated lipid species that induce apoptosis and proteome alterations in dopaminergic PC12 neurons in vitro. Free Radical Biology and Medicine. 48(12). 1588–1600. 49 indexed citations
9.
Kratzer, Ingrid, Eva Bernhart, Andrea Wintersperger, et al.. (2008). Afamin is synthesized by cerebrovascular endothelial cells and mediates α‐tocopherol transport across an in vitro model of the blood–brain barrier. Journal of Neurochemistry. 108(3). 707–718. 47 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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