Bryce L. Sopher

7.8k total citations
63 papers, 6.0k citations indexed

About

Bryce L. Sopher is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Physiology. According to data from OpenAlex, Bryce L. Sopher has authored 63 papers receiving a total of 6.0k indexed citations (citations by other indexed papers that have themselves been cited), including 42 papers in Molecular Biology, 32 papers in Cellular and Molecular Neuroscience and 17 papers in Physiology. Recurrent topics in Bryce L. Sopher's work include Genetic Neurodegenerative Diseases (25 papers), Mitochondrial Function and Pathology (17 papers) and Alzheimer's disease research and treatments (15 papers). Bryce L. Sopher is often cited by papers focused on Genetic Neurodegenerative Diseases (25 papers), Mitochondrial Function and Pathology (17 papers) and Alzheimer's disease research and treatments (15 papers). Bryce L. Sopher collaborates with scholars based in United States, United Kingdom and Canada. Bryce L. Sopher's co-authors include George M. Martin, Mark P. Mattson, Qing Guo, Albert R. La Spada, Katsutoshi Furukawa, Carol B. Ware, Miles W. Miller, Gwenn A. Garden, Randell T. Libby and Michael G. Katze and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Biological Chemistry and Nature Medicine.

In The Last Decade

Bryce L. Sopher

63 papers receiving 6.0k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Bryce L. Sopher United States 38 3.7k 2.3k 2.1k 1.0k 625 63 6.0k
Robert Siman United States 40 2.9k 0.8× 1.5k 0.7× 1.7k 0.8× 1.4k 1.4× 391 0.6× 63 5.4k
Adriana Ferreira United States 42 3.1k 0.8× 2.8k 1.2× 2.6k 1.2× 1.8k 1.7× 660 1.1× 76 6.4k
Carol M. Troy United States 32 2.8k 0.8× 1.3k 0.5× 1.2k 0.6× 663 0.7× 361 0.6× 65 4.6k
Katleen Craessaerts Belgium 28 4.7k 1.3× 1.4k 0.6× 4.6k 2.2× 1.4k 1.4× 1.3k 2.1× 39 7.9k
Laurent Pradier France 39 2.6k 0.7× 1.8k 0.8× 2.9k 1.4× 450 0.4× 815 1.3× 98 5.2k
Max Holzer Germany 35 2.3k 0.6× 1.6k 0.7× 3.1k 1.5× 720 0.7× 613 1.0× 89 5.0k
Lutgarde Serneels Belgium 37 3.4k 0.9× 1.2k 0.5× 3.3k 1.6× 882 0.9× 1.0k 1.7× 72 6.3k
Malcolm A. Leissring United States 36 2.4k 0.6× 1.1k 0.5× 3.1k 1.5× 827 0.8× 881 1.4× 65 5.0k
Inger Lauritzen France 33 2.7k 0.7× 1.6k 0.7× 1.2k 0.6× 545 0.5× 309 0.5× 47 4.5k
Ikuo Nishimoto Japan 50 5.5k 1.5× 1.9k 0.8× 3.1k 1.5× 2.3k 2.3× 597 1.0× 113 8.8k

Countries citing papers authored by Bryce L. Sopher

Since Specialization
Citations

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

Fields of papers citing papers by Bryce L. Sopher

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Bryce L. Sopher. 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 Bryce L. Sopher. The network helps show where Bryce L. Sopher may publish in the future.

Co-authorship network of co-authors of Bryce L. Sopher

This figure shows the co-authorship network connecting the top 25 collaborators of Bryce L. Sopher. A scholar is included among the top collaborators of Bryce L. Sopher 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 Bryce L. Sopher. Bryce L. Sopher 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
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Hsu, Cynthia L., Kohta Ohnishi, Jill Meisenhelder, et al.. (2023). MAP4K3 inhibits Sirtuin-1 to repress the LKB1–AMPK pathway to promote amino acid-dependent activation of the mTORC1 complex. Life Science Alliance. 6(8). e202201525–e202201525. 2 indexed citations
3.
Prater, Katherine E., et al.. (2021). The pro‐inflammatory microRNA miR‐155 influences fibrillar β‐Amyloid1‐42 catabolism by microglia. Glia. 69(7). 1736–1748. 33 indexed citations
4.
Fung, Susan, C. Smith, Katherine E. Prater, et al.. (2020). Early-Onset Familial Alzheimer Disease Variant PSEN2 N141I Heterozygosity is Associated with Altered Microglia Phenotype. Journal of Alzheimer s Disease. 77(2). 675–688. 23 indexed citations
5.
Wenzel, H. Jürgen, Karl D. Murray, Michael R. Hunsaker, et al.. (2019). Astroglial-targeted expression of the fragile X CGG repeat premutation in mice yields RAN translation, motor deficits and possible evidence for cell-to-cell propagation of FXTAS pathology. Acta Neuropathologica Communications. 7(1). 27–27. 15 indexed citations
6.
Su, Wei, Bryce L. Sopher, J. M. Gillespie, et al.. (2015). Recombinant adeno‐associated viral (rAAV) vectors mediate efficient gene transduction in cultured neonatal and adult microglia. Journal of Neurochemistry. 136(S1). 49–62. 23 indexed citations
7.
Wang, David B., Yoshito Kinoshita, C. Kinoshita, et al.. (2015). Loss of endophilin-B1 exacerbates Alzheimer’s disease pathology. Brain. 138(7). 2005–2019. 28 indexed citations
8.
Su, Wei, Stephanie Hopkins, Nicole K. Nesser, et al.. (2013). The p53 Transcription Factor Modulates Microglia Behavior through MicroRNA-Dependent Regulation of c-Maf. The Journal of Immunology. 192(1). 358–366. 73 indexed citations
9.
Wang, David B., Gwenn A. Garden, C. Kinoshita, et al.. (2013). Declines in Drp1 and Parkin Expression Underlie DNA Damage-Induced Changes in Mitochondrial Length and Neuronal Death. Journal of Neuroscience. 33(4). 1357–1365. 49 indexed citations
10.
Sopher, Bryce L., et al.. (2012). Reduction of mutant ataxin-7 expression restores motor function and prevents cerebellar synaptic reorganization in a conditional mouse model of SCA7. Human Molecular Genetics. 22(5). 890–903. 36 indexed citations
11.
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Wilburn, B., Dobrila D. Rudnicki, Jing Zhao, et al.. (2011). An Antisense CAG Repeat Transcript at JPH3 Locus Mediates Expanded Polyglutamine Protein Toxicity in Huntington's Disease-like 2 Mice. Neuron. 70(3). 427–440. 107 indexed citations
13.
Mookerjee, Shona A., Stephan J. Guyenet, Vanitha Sampath, et al.. (2009). Posttranslational Modification of Ataxin-7 at Lysine 257 Prevents Autophagy-Mediated Turnover of an N-Terminal Caspase-7 Cleavage Fragment. Journal of Neuroscience. 29(48). 15134–15144. 41 indexed citations
14.
Libby, Randell T., Katharine A. Hagerman, Victor V. Pineda, et al.. (2008). CTCF cis-Regulates Trinucleotide Repeat Instability in an Epigenetic Manner: A Novel Basis for Mutational Hot Spot Determination. PLoS Genetics. 4(11). e1000257–e1000257. 100 indexed citations
15.
Young, Jessica E., Launce Gouw, Stephanie Propp, et al.. (2007). Proteolytic Cleavage of Ataxin-7 by Caspase-7 Modulates Cellular Toxicity and Transcriptional Dysregulation. Journal of Biological Chemistry. 282(41). 30150–30160. 64 indexed citations
16.
Fan, Yuxin, Pornprot Limprasert, Ian Murray, et al.. (2006). β-synuclein modulates α-synuclein neurotoxicity by reducing α-synuclein protein expression. Human Molecular Genetics. 15(20). 3002–3011. 75 indexed citations
17.
Sopher, Bryce L., P. Thomas, Michelle LaFevre-Bernt, et al.. (2004). Androgen Receptor YAC Transgenic Mice Recapitulate SBMA Motor Neuronopathy and Implicate VEGF164 in the Motor Neuron Degeneration. Neuron. 41(5). 687–699. 144 indexed citations
18.
Garden, Gwenn A., Randell T. Libby, Ying‐Hui Fu, et al.. (2002). Polyglutamine-Expanded Ataxin-7 Promotes Non-Cell-Autonomous Purkinje Cell Degeneration and Displays Proteolytic Cleavage in Ataxic Transgenic Mice. Journal of Neuroscience. 22(12). 4897–4905. 125 indexed citations
19.
Furukawa, Katsutoshi, Bryce L. Sopher, Russell E. Rydel, et al.. (1996). Increased Activity‐Regulating and Neuroprotective Efficacy of α‐Secretase‐Derived Secreted Amyloid Precursor Protein Conferred by a C‐Terminal Heparin‐Binding Domain. Journal of Neurochemistry. 67(5). 1882–1896. 319 indexed citations
20.
Sopher, Bryce L., et al.. (1992). Purification and characterization of goat lysosomal beta-mannosidase using monoclonal and polyclonal antibodies.. Journal of Biological Chemistry. 267(9). 6178–6182. 14 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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