Deborah E. Schuback

1.6k citations
30 papers · 1.3k · h-index 18

Impact in

  • Neurology top 2%
    • Neurological disorders and treatments
    • Botulinum Toxin and Related Neurological Disorders
    • Parkinson's Disease Mechanisms and Treatments
    • Genetic Neurodegenerative Diseases
    • Hereditary Neurological Disorders

Papers in

Deborah E. Schuback

30 papers receiving 1.3k citations

Peers

Deborah E. Schuback
Comparison fields: 5 of 75
  • Neurology 536
  • Cellular and Molecular Neuroscience 495
  • Genetics 412
  • Neurology 86
  • Epidemiology 247
Replace Rhys Roberts with:
Rhys Roberts United Kingdom
Lu‐Shiun Her Taiwan
Inês Martins United States
Yung‐Nien Chang United States
S.A. Rundle United Kingdom
Patrick D. Staber United States
Shoushu Jiao United States
Muriel Coulpier France
Janet Cunningham United States
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Citations per field
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Citations per year

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-authors

The 25 scholars most cited alongside Deborah E. Schuback, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Deborah E. Schuback Line = papers co-authored together Deborah E. Schuback links everyone, so they are left out of the graph.

All Works

20 of 20 papers shown

Showing the 20 most-cited of 30 papers — load more, or switch the sort, to bring in the rest.

#Work
1 1989186
2 2000122
3 1990109
4 1997108
5
Strong allelic association between the torsion dystonia gene (DYT1) andloci on chromosome 9q34 in Ashkenazi Jews.
199297
6 200393
7 199588
8 199571
9 198855
10 200441
11 200435
12 199233
13 200133
14
Identification of a highly polymorphic microsatellite VNTR within the argininosuccinate synthetase locus: exclusion of the dystonia gene on 9q32-34 as the cause of dopa-responsive dystonia in a large kindred.
199131
15 199925
16 199624
17
Torsion dystonia genes in two populations confined to a small region on chromosome 9q32-34.
199121
18 199920
19 199216
20 199215

About Deborah E. Schuback

Deborah E. Schuback is a scholar working on Genetics, Cellular and Molecular Neuroscience, Neurology, Molecular Biology and Epidemiology, having authored 30 papers that have together received 1.3k indexed citations. Recurring topics across this work include Neurological disorders and treatments (10 papers), Genetic Neurodegenerative Diseases (9 papers), Virus-based gene therapy research (8 papers), Hereditary Neurological Disorders (6 papers), Herpesvirus Infections and Treatments (5 papers), Genetics and Neurodevelopmental Disorders (4 papers), Animal Virus Infections Studies (3 papers) and Bacteriophages and microbial interactions (2 papers). The work is most often cited by research in Neurology (536 citations), Cellular and Molecular Neuroscience (495 citations), Genetics (412 citations), Neurology (86 citations) and Epidemiology (247 citations). Deborah E. Schuback has collaborated with scholars based in United States, Germany and Taiwan. Frequent co-authors include Laurie J. Ozelius, Xandra O. Breakefield, Xandra O. Breakefield, James F. Gusella, David J. Kwiatkowski, Robert E. Burke, Mitchell F. Brin, X. O. Breakefield, Susan Bressman and Neil Risch. Their work appears in journals such as Human Molecular Genetics, Cancer Gene Therapy, Nucleic Acids Research, Human Gene Therapy and Molecular Therapy.

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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