Gabriele Schilling

4.1k total citations · 2 hit papers
25 papers, 3.3k citations indexed

About

Gabriele Schilling is a scholar working on Cellular and Molecular Neuroscience, Molecular Biology and Neurology. According to data from OpenAlex, Gabriele Schilling has authored 25 papers receiving a total of 3.3k indexed citations (citations by other indexed papers that have themselves been cited), including 22 papers in Cellular and Molecular Neuroscience, 21 papers in Molecular Biology and 7 papers in Neurology. Recurrent topics in Gabriele Schilling's work include Genetic Neurodegenerative Diseases (21 papers), Mitochondrial Function and Pathology (16 papers) and Muscle Physiology and Disorders (10 papers). Gabriele Schilling is often cited by papers focused on Genetic Neurodegenerative Diseases (21 papers), Mitochondrial Function and Pathology (16 papers) and Muscle Physiology and Disorders (10 papers). Gabriele Schilling collaborates with scholars based in United States, Germany and Japan. Gabriele Schilling's co-authors include Christopher A. Ross, Alan H. Sharp, Shihua Li, David Borchelt, Solomon H. Snyder, Frederick C. Nucifora, Molly V. Wagster, Xiao‐Jiang Li, Paul Worley and Anthony A. Lanahan and has published in prestigious journals such as Nature, Science and Proceedings of the National Academy of Sciences.

In The Last Decade

Gabriele Schilling

25 papers receiving 3.2k 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.

Intranuclear inclusions and neuritic aggregates in transgenic mice expressing a mutant N-terminal fragment of huntingtin [published erratum appears in Hum Mol Genet 1999 May;8(5):943]

1999 619 citations Gabriele Schilling Human Molecular Genetics profile →
A huntingtin-associated protein enriched in brain with implications for pathology

1995 512 citations Xiao‐Jiang Li, Shihua Li et al. Nature profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Gabriele Schilling United States	18	2.7k	2.6k	1.0k	258	196	25	3.3k
Michael A. Kalchman Canada	11	2.1k 0.8×	2.0k 0.7×	790 0.8×	208 0.8×	89 0.5×	11	2.5k
Ben Woodman United Kingdom	26	2.4k 0.9×	2.0k 0.8×	644 0.6×	361 1.4×	259 1.3×	29	3.0k
Jean‐Paul Vonsattel United States	18	2.2k 0.8×	2.6k 1.0×	1.6k 1.6×	283 1.1×	578 2.9×	37	3.7k
Juliette Gafni United States	19	1.9k 0.7×	1.7k 0.6×	483 0.5×	357 1.4×	221 1.1×	19	2.7k
Dorotea Rigamonti Italy	19	2.6k 1.0×	2.4k 0.9×	792 0.8×	257 1.0×	290 1.5×	25	3.7k
Georges Imbert France	11	2.3k 0.8×	2.2k 0.8×	860 0.8×	99 0.4×	246 1.3×	17	2.8k
J.-P. G. Vonsattel United States	16	2.6k 1.0×	3.2k 1.2×	2.0k 1.9×	307 1.2×	486 2.5×	22	4.4k
Tie-Shan Tang United States	21	2.3k 0.8×	1.5k 0.5×	456 0.5×	357 1.4×	199 1.0×	22	2.9k
Judit Pallos United States	13	2.2k 0.8×	1.8k 0.7×	503 0.5×	239 0.9×	287 1.5×	16	2.9k
H. Brent Clark United States	26	3.4k 1.3×	3.1k 1.2×	898 0.9×	274 1.1×	222 1.1×	40	4.1k

Countries citing papers authored by Gabriele Schilling

Since Specialization

Citations

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

Fields of papers citing papers by Gabriele Schilling

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Gabriele Schilling

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

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

Juenemann, Katrin, et al.. (2010). Modulation of Mutant Huntingtin N-Terminal Cleavage and Its Effect on Aggregation and Cell Death. Neurotoxicity Research. 20(2). 120–133. 26 indexed citations

Damian, Maxwell S., et al.. (2009). White matter lesions and cognitive deficits: relevance of lesion pattern?. Acta Neurologica Scandinavica. 90(6). 430–436. 16 indexed citations

Schilling, Gabriele, Alexandra M. Klevytska, Andrew T.N. Tebbenkamp, et al.. (2007). Characterization of Huntingtin Pathologic Fragments in Human Huntington Disease, Transgenic Mice, and Cell Models. Journal of Neuropathology & Experimental Neurology. 66(4). 313–320. 74 indexed citations

Schilling, Gabriele, et al.. (2004). Environmental, pharmacological, and genetic modulation of the HD phenotype in transgenic mice. Experimental Neurology. 187(1). 137–149. 67 indexed citations

Schilling, Gabriele, Alena Savonenko, Alexandra M. Klevytska, et al.. (2004). Nuclear-targeting of mutant huntingtin fragments produces Huntington's disease-like phenotypes in transgenic mice. Human Molecular Genetics. 13(15). 1599–1610. 78 indexed citations

Jankowsky, Joanna L., Alena Savonenko, Gabriele Schilling, et al.. (2002). Transgenic mouse models of neurodegenerative disease: Opportunities for therapeutic development. Current Neurology and Neuroscience Reports. 2(5). 457–464. 41 indexed citations

Schilling, Gabriele, Michael L. Coonfield, Christopher A. Ross, & David Borchelt. (2001). Coenzyme Q10 and remacemide hydrochloride ameliorate motor deficits in a Huntington's disease transgenic mouse model. Neuroscience Letters. 315(3). 149–153. 128 indexed citations

Andreassen, Ole A., Alpaslan Dedeoglu, Robert J. Ferrante, et al.. (2001). Creatine Increases Survival and Delays Motor Symptoms in a Transgenic Animal Model of Huntington's Disease. Neurobiology of Disease. 8(3). 479–491. 231 indexed citations

Schilling, Gabriele, Hyder A. Jinnah, Michael L. Coonfield, et al.. (2001). Distinct Behavioral and Neuropathological Abnormalities in Transgenic Mouse Models of HD and DRPLA. Neurobiology of Disease. 8(3). 405–418. 45 indexed citations

10.

Schilling, Gabriele, Jonathan Wood, Kui Duan, et al.. (1999). Nuclear Accumulation of Truncated Atrophin-1 Fragments in a Transgenic Mouse Model of DRPLA. Neuron. 24(1). 275–286. 143 indexed citations

11.

Schilling, Gabriele. (1999). Intranuclear inclusions and neuritic aggregates in transgenic mice expressing a mutant N-terminal fragment of huntingtin [published erratum appears in Hum Mol Genet 1999 May;8(5):943]. Human Molecular Genetics. 8(3). 397–407. 619 indexed citations breakdown →

12.

Ross, Christopher A., Jonathan Wood, Gabriele Schilling, et al.. (1999). Polyglutamine pathogenesis. Philosophical Transactions of the Royal Society B Biological Sciences. 354(1386). 1005–1011. 60 indexed citations

13.

Damian, Maxwell S., et al.. (1996). The clinical and genetic correlates of MRI findings in myotonic dystrophy. Neuroradiology. 38(7). 629–635. 58 indexed citations

14.

Sharp, Alan H., Gabriele Schilling, Shihua Li, et al.. (1995). Widespread expression of Huntington's disease gene (IT15) protein product. Neuron. 14(5). 1065–1074. 414 indexed citations

15.

Margolis, Russell L., W. Scott Young, Shihua Li, et al.. (1995). Cloning and expression of the rat atrophin-I (DRPLA disease gene) homologue. Neurobiology of Disease. 2(3). 129–138. 10 indexed citations

16.

Li, Xiao‐Jiang, Shihua Li, Alan H. Sharp, et al.. (1995). A huntingtin-associated protein enriched in brain with implications for pathology. Nature. 378(6555). 398–402. 512 indexed citations breakdown →

17.

Schilling, Gabriele, et al.. (1995). [Myotonic dystrophy: magnetic resonance tomography and clinico-genetic correlations].. PubMed. 66(6). 438–44. 3 indexed citations

18.

Schilling, Gabriele, et al.. (1994). Psychopathologie, Coping und Abwehr bei intensivmedizinisch behandelten Patienten. Fortschritte der Neurologie · Psychiatrie. 62(7). 233–240. 2 indexed citations

19.

Damian, Maxwell S., et al.. (1994). Brain disease and molecular analysis in myotonic dystrophy. Neuroreport. 5(18). 2549–2552. 17 indexed citations

20.

Li, S.-H., Gabriele Schilling, W. Scott Young, et al.. (1993). Huntington's disease gene (IT15) is widely expressed in human and rat tissues. Neuron. 11(5). 985–993. 268 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.

Explore authors with similar magnitude of impact