Deborah E. Schuback

1.6k total citations
30 papers, 1.3k citations indexed

About

Deborah E. Schuback is a scholar working on Genetics, Cellular and Molecular Neuroscience and Neurology. According to data from OpenAlex, Deborah E. Schuback has authored 30 papers receiving a total of 1.3k indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Genetics, 11 papers in Cellular and Molecular Neuroscience and 11 papers in Neurology. Recurrent topics in Deborah E. Schuback's work include Neurological disorders and treatments (10 papers), Genetic Neurodegenerative Diseases (9 papers) and Virus-based gene therapy research (8 papers). Deborah E. Schuback is often cited by papers focused on Neurological disorders and treatments (10 papers), Genetic Neurodegenerative Diseases (9 papers) and Virus-based gene therapy research (8 papers). Deborah E. Schuback collaborates with scholars based in United States, Germany and United Kingdom. Deborah E. Schuback's co-authors include Laurie J. Ozelius, Xandra O. Breakefield, Xandra O. Breakefield, James F. Gusella, Robert E. Burke, Mitchell F. Brin, David J. Kwiatkowski, X. O. Breakefield, Susan Bressman and Neil Risch and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nucleic Acids Research and Neuron.

In The Last Decade

Deborah E. Schuback

30 papers receiving 1.3k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Deborah E. Schuback United States 18 536 495 446 412 247 30 1.3k
Rhys Roberts United Kingdom 18 195 0.4× 256 0.5× 729 1.6× 229 0.6× 115 0.5× 40 1.4k
Janet Cunningham United States 16 308 0.6× 516 1.0× 765 1.7× 746 1.8× 101 0.4× 17 1.4k
Yung‐Nien Chang United States 15 169 0.3× 517 1.0× 553 1.2× 392 1.0× 205 0.8× 19 1.2k
Tsuyoshi Inoshita Japan 17 356 0.7× 354 0.7× 490 1.1× 139 0.3× 351 1.4× 39 1.1k
Elvin Woodruff United States 18 211 0.4× 333 0.7× 879 2.0× 381 0.9× 86 0.3× 24 1.5k
Gerda Suchanek Austria 16 168 0.3× 249 0.5× 493 1.1× 98 0.2× 63 0.3× 20 1.5k
Shoushu Jiao United States 16 221 0.4× 520 1.1× 630 1.4× 404 1.0× 48 0.2× 19 1.3k
Pieter DeJong United States 12 353 0.7× 807 1.6× 1.3k 2.9× 428 1.0× 33 0.1× 14 1.7k
Inês Martins United States 15 252 0.5× 895 1.8× 2.3k 5.1× 1.2k 3.0× 243 1.0× 18 2.8k
E. Anne Buckmaster United Kingdom 9 71 0.1× 237 0.5× 256 0.6× 172 0.4× 353 1.4× 11 812

Countries citing papers authored by Deborah E. Schuback

Since Specialization
Citations

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

Fields of papers citing papers by Deborah E. Schuback

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Deborah E. Schuback. 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 Deborah E. Schuback. The network helps show where Deborah E. Schuback may publish in the future.

Co-authorship network of co-authors of Deborah E. Schuback

This figure shows the co-authorship network connecting the top 25 collaborators of Deborah E. Schuback. A scholar is included among the top collaborators of Deborah E. Schuback 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 Deborah E. Schuback. Deborah E. Schuback 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.
Grandi, Paola, Samuel Wang, Deborah E. Schuback, et al.. (2004). HSV-1 Virions Engineered for Specific Binding to Cell Surface Receptors. Molecular Therapy. 9(3). 419–427. 35 indexed citations
2.
Bragg, D. Cristopher, Sara M. Camp, Jeremy Wilbur, et al.. (2004). Perinuclear biogenesis of mutant torsin-a inclusions in cultured cells infected with tetracycline-regulated herpes simplex virus type 1 amplicon vectors. Neuroscience. 125(3). 651–661. 41 indexed citations
3.
Spear, Matthew A., Deborah E. Schuback, Kenichi Miyata, et al.. (2003). HSV-1 amplicon peptide display vector. Journal of Virological Methods. 107(1). 71–79. 12 indexed citations
4.
Herrlinger, Ulrich, Alice K. Jacobs, Manish K. Aghi, Deborah E. Schuback, & Xandra O. Breakefield. (2003). HSV-1 Vectors for Gene Therapy of Experimental CNS Tumors. Humana Press eBooks. 35. 287–312. 2 indexed citations
5.
Hewett, Jeffrey, Heather Boston, Damien Slater, et al.. (2003). TorsinA in PC12 cells: Localization in the endoplasmic reticulum and response to stress. Journal of Neuroscience Research. 72(2). 158–168. 93 indexed citations
6.
Spear, Matthew A., Xandra O. Breakefield, James Beltzer, et al.. (2001). Isolation, characterization, and recovery of small peptide phage display epitopes selected against viable malignant glioma cells. Cancer Gene Therapy. 8(7). 506–511. 33 indexed citations
7.
Bearer, Elaine L., Michelle L. Schlief, X. O. Breakefield, et al.. (1999). Squid Axoplasm Supports the Retrograde Axonal Transport of Herpes Simplex Virus. Biological Bulletin. 197(2). 257–258. 9 indexed citations
8.
Jacoby, David, Peter Pecháň, Cornel Fraefel, et al.. (1997). HSV/AAV Hybrid Amplicon Vectors Extend Transgene Expression in Human Glioma Cells. Human Gene Therapy. 8(3). 359–370. 108 indexed citations
9.
Tivol, Elizabeth, Christo Shalish, Deborah E. Schuback, Yun‐Pung P. Hsu, & Xandra O. Breakefield. (1996). Mutational analysis of the humanMAOA gene. American Journal of Medical Genetics. 67(1). 92–97. 24 indexed citations
10.
Hsu, Yun‐Pung P., Deborah E. Schuback, Elizabeth Tivol, et al.. (1995). Chapter 7 Analysis of MAOA mutations in humans. Progress in brain research. 106. 67–75. 5 indexed citations
11.
Schuback, Deborah E., et al.. (1995). Mutations in the Norrie disease gene. Human Mutation. 5(4). 285–292. 71 indexed citations
12.
Kramm, Christof M, Miguel Sena‐Esteves, Faith H. Barnett, et al.. (1995). Gene Therapy for Brain Tumors. Brain Pathology. 5(4). 345–381. 88 indexed citations
13.
Wahlström, J., Laurie J. Ozelius, P. L. Kramer, et al.. (1994). The gene for familial dystonia with myoclonic jerks responsive to alcohol is not located on the distal end of 9q. Clinical Genetics. 45(2). 88–92. 11 indexed citations
14.
Ozelius, Laurie J., David J. Kwiatkowski, Deborah E. Schuback, et al.. (1992). A genetic linkage map of human chromosome 9q. Genomics. 14(3). 715–720. 16 indexed citations
15.
Sims, Katherine B., R V Lebo, Gail V. Benson, et al.. (1992). The Norrie disease gene maps to a 150 kb region on chromosome Xp11.3. Human Molecular Genetics. 1(2). 83–89. 33 indexed citations
16.
Ozelius, Laurie J., et al.. (1992). Dinucleotide repeat polymorphism for the hexabrachion gene (HXB) on chromosome 9q32–34. Human Molecular Genetics. 1(2). 141–141. 15 indexed citations
17.
Schuback, Deborah E., Laurie J. Ozelius, Gösta Holmgren, et al.. (1991). Dopamine beta-hydroxylase gene excluded in four subtypes of hereditary dystonia. Human Genetics. 87(3). 311–316. 6 indexed citations
18.
Kramer, Patricia L., Deborah de Leon, Laurie J. Ozelius, et al.. (1990). Dystonia gene in Ashkenazi Jewish population is located on chromosome 9q32–34. Annals of Neurology. 27(2). 114–120. 109 indexed citations
19.
Ozelius, Laurie J., Patricia L. Kramer, Carol Moskowitz, et al.. (1989). Human gene for torsion dystonia located on chromosome 9q32-q34. Neuron. 2(5). 1427–1434. 186 indexed citations
20.
Kwiatkowski, D J, Laurie J. Ozelius, Deborah E. Schuback, James F. Gusella, & X. O. Breakefield. (1989). The gelsolin (GSN) cDNA clone, from 9q32-34, identifies Bell and StuI RFLPs. Nucleic Acids Research. 17(11). 4425–4425. 10 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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