Christopher A. Ross

57.5k total citations · 13 hit papers
359 papers, 40.5k citations indexed

About

Christopher A. Ross is a scholar working on Cellular and Molecular Neuroscience, Molecular Biology and Neurology. According to data from OpenAlex, Christopher A. Ross has authored 359 papers receiving a total of 40.5k indexed citations (citations by other indexed papers that have themselves been cited), including 255 papers in Cellular and Molecular Neuroscience, 231 papers in Molecular Biology and 124 papers in Neurology. Recurrent topics in Christopher A. Ross's work include Genetic Neurodegenerative Diseases (218 papers), Mitochondrial Function and Pathology (135 papers) and Neurological disorders and treatments (85 papers). Christopher A. Ross is often cited by papers focused on Genetic Neurodegenerative Diseases (218 papers), Mitochondrial Function and Pathology (135 papers) and Neurological disorders and treatments (85 papers). Christopher A. Ross collaborates with scholars based in United States, Canada and United Kingdom. Christopher A. Ross's co-authors include Michelle A. Poirier, Sarah J. Tabrizi, Russell L. Margolis, David A. Ruggiero, Donald J. Reis, Ted M. Dawson, Alan H. Sharp, Valina L. Dawson, Solomon H. Snyder and Wanli W. Smith and has published in prestigious journals such as Nature, Science and Cell.

In The Last Decade

Christopher A. Ross

356 papers receiving 39.7k citations

Hit Papers

Protein aggregation and neurodegenerative dis... 1984 2026 1998 2012 2004 1997 2010 2015 2005 500 1000 1.5k 2.0k 2.5k

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Christopher A. Ross United States 105 24.7k 23.0k 12.4k 5.4k 3.7k 359 40.5k
James F. Gusella United States 96 22.3k 0.9× 14.1k 0.6× 10.4k 0.8× 7.1k 1.3× 3.0k 0.8× 462 41.2k
Allan I. Levey United States 118 24.0k 1.0× 26.2k 1.1× 7.0k 0.6× 11.8k 2.2× 3.0k 0.8× 507 52.1k
David Sulzer United States 94 10.4k 0.4× 14.8k 0.6× 10.7k 0.9× 4.4k 0.8× 4.2k 1.1× 248 28.9k
Stuart A. Lipton United States 125 26.9k 1.1× 18.7k 0.8× 4.1k 0.3× 12.3k 2.3× 3.2k 0.9× 386 52.8k
Patrik Brundin Sweden 97 14.5k 0.6× 17.7k 0.8× 15.5k 1.3× 5.6k 1.0× 1.6k 0.4× 363 35.5k
Olle Lindvall Sweden 107 15.9k 0.6× 23.9k 1.0× 7.5k 0.6× 3.9k 0.7× 1.3k 0.3× 362 42.7k
Valina L. Dawson United States 126 26.9k 1.1× 15.8k 0.7× 18.4k 1.5× 12.9k 2.4× 4.9k 1.3× 380 56.5k
Isidró Ferrer Spain 101 20.4k 0.8× 11.4k 0.5× 8.3k 0.7× 12.8k 2.4× 3.2k 0.9× 910 42.1k
Ted M. Dawson United States 133 28.9k 1.2× 19.4k 0.8× 20.6k 1.7× 15.3k 2.8× 5.3k 1.4× 433 61.8k
Stephen G. Waxman United States 110 23.7k 1.0× 22.1k 1.0× 6.4k 0.5× 18.5k 3.4× 1.7k 0.4× 684 46.5k

Countries citing papers authored by Christopher A. Ross

Since Specialization
Citations

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

Fields of papers citing papers by Christopher A. Ross

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Christopher A. Ross. 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 Christopher A. Ross. The network helps show where Christopher A. Ross may publish in the future.

Co-authorship network of co-authors of Christopher A. Ross

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

All Works

20 of 20 papers shown
1.
Ratovitski, Tamara, et al.. (2023). Arginine methylation of RNA-binding proteins is impaired in Huntington’s disease. Human Molecular Genetics. 32(20). 3006–3025. 1 indexed citations
2.
Younès, Laurent, Xuan Bu, J. Tilak Ratnanather, et al.. (2023). Mixed longitudinal and cross-sectional analyses of deep gray matter and white matter using diffusion weighted images in premanifest and manifest Huntington’s disease. NeuroImage Clinical. 39. 103493–103493. 1 indexed citations
3.
Feng, Hongxuan, Xin Hu, Xin Sun, et al.. (2021). A high-throughput screening to identify small molecules that suppress huntingtin promoter activity or activate huntingtin-antisense promoter activity. Scientific Reports. 11(1). 6157–6157. 7 indexed citations
4.
Ayhan, Fatma, B. Pérez, Hannah K. Shorrock, et al.. (2018). SCA 8 RAN polySer protein preferentially accumulates in white matter regions and is regulated by eIF 3F. The EMBO Journal. 37(19). 47 indexed citations
5.
Dickey, Audrey S., Weiwei Fan, Nicolas Arbez, et al.. (2017). PPARδ activation by bexarotene promotes neuroprotection by restoring bioenergetic and quality control homeostasis. Science Translational Medicine. 9(419). 47 indexed citations
6.
Nucifora, Leslie G., Brian J. Lee, Sha Li, et al.. (2016). A Mutation in NPAS3 That Segregates with Schizophrenia in a Small Family Leads to Protein Aggregation. PubMed. 2(3). 133–144. 19 indexed citations
7.
Ratovitski, Tamara, Xiaofang Wang, Mali Jiang, et al.. (2012). Transgenic Mouse Model Expressing the Caspase 6 Fragment of Mutant Huntingtin. Journal of Neuroscience. 32(1). 183–193. 45 indexed citations
8.
Juopperi, Tarja, Jason Chiang, Huimei Yu, et al.. (2012). Astrocytes generated from patient induced pluripotent stem cells recapitulate features of Huntington’s disease patient cells. Molecular Brain. 5(1). 17–17. 184 indexed citations
9.
Reading, Sarah, Kenichi Oishi, Graham W. Redgrave, et al.. (2011). Diffuse Abnormality of Low to Moderately Organized White Matter in Schizophrenia. Brain Connectivity. 1(6). 511–519. 8 indexed citations
11.
Liu, Zhong Wu, Ying Liang, Naoki Masuda, et al.. (2010). Synphilin-1 attenuates neuronal degeneration in the A53T  -synuclein transgenic mouse model. Human Molecular Genetics. 19(11). 2087–2098. 57 indexed citations
12.
Sawa, Akira, Eiichiro Nagata, Siobhan Sutcliffe, et al.. (2005). Huntingtin is cleaved by caspases in the cytoplasm and translocated to the nucleus via perinuclear sites in Huntington's disease patient lymphoblasts. Neurobiology of Disease. 20(2). 267–274. 35 indexed citations
13.
Smith, Wanli W., Haibing Jiang, Zhong Pei, et al.. (2005). Endoplasmic reticulum stress and mitochondrial cell death pathways mediate A53T mutant alpha-synuclein-induced toxicity. Human Molecular Genetics. 14(24). 3801–3811. 303 indexed citations
14.
Lim, Kah‐Leong, Katherine C. M. Chew, Jeanne M.M. Tan, et al.. (2005). Parkin Mediates Nonclassical, Proteasomal-Independent Ubiquitination of Synphilin-1: Implications for Lewy Body Formation. Journal of Neuroscience. 25(8). 2002–2009. 454 indexed citations
15.
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
16.
Holmes, Susan E., Melvin G. McInnis, Akira Sawa, et al.. (2003). Novel CAG/CTG repeat expansion mutations do not contribute to the genetic risk for most cases of bipolar disorder or schizophrenia. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 124B(1). 15–19. 7 indexed citations
17.
Nucifora, Frederick C., Lisa Ellerby, Cheryl L. Wellington, et al.. (2003). Nuclear Localization of a Non-caspase Truncation Product of Atrophin-1, with an Expanded Polyglutamine Repeat, Increases Cellular Toxicity. Journal of Biological Chemistry. 278(15). 13047–13055. 68 indexed citations
18.
Holbert, Sébastien, Adam Rosenblatt, Cheryl L. Wellington, et al.. (2001). The Gln-Ala repeat transcriptional activator CA150 interacts with huntingtin: Neuropathologic and genetic evidence for a role in Huntington's disease pathogenesis. Proceedings of the National Academy of Sciences. 98(4). 1811–1816. 143 indexed citations
19.
Ross, Christopher A.. (1997). Genes with triplet repeats. The FASEB Journal. 11(9). 3 indexed citations
20.
Wagster, Molly V., John C. Hedreen, Carol E. Peyser, Susan E. Folstein, & Christopher A. Ross. (1994). Selective Loss of [3H]Kainic Acid and [3H]AMPA Binding in Layer VI of Frontal Cortex in Huntington's Disease. Experimental Neurology. 127(1). 70–75. 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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