Laura E. Warner
Impact in
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- Hereditary Neurological Disorders
- Genetic Neurodegenerative Diseases
- Nerve injury and regeneration
- Neurology top 2%
- Neurological diseases and metabolism
- Botulinum Toxin and Related Neurological Disorders
- Peripheral Neuropathies and Disorders
Papers in
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- Hereditary Neurological Disorders 17
- Genetic Neurodegenerative Diseases 4
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- RNA regulation and disease 5
- RNA Research and Splicing 5
- Co-authors
- James R. Lupski (14 shared papers)Pedro Mancías (1 shared paper)Laura Davis Keppen (1 shared paper)Ian J. Butler (1 shared paper)Craig M. McDonald (1 shared paper)Christine Van Broeckhoven (3 shared papers)Eva Nelis (2 shared papers)Carlos García (2 shared papers)
- Journals
- Human Mutation (6 papers)Human Molecular Genetics (2 papers)Annual Review of Medicine (1 paper)Cold Spring Harbor Symposia on Quantitative Biology (1 paper)Pediatric Neurology (1 paper)
- Partner nations
- United StatesBelgiumIsrael
In The Last Decade
Laura E. Warner
19 papers receiving 1.3k citations
Peers
Comparison fields: 5 of 56
- Cellular and Molecular Neuroscience 1.0k
- Neurology 331
- Neurology 279
- Cell Biology 224
- Genetics 75
Countries citing papers authored by Laura E. Warner
This map shows the geographic impact of Laura E. Warner'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 Laura E. Warner with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Laura E. Warner more than expected).
Fields of papers citing papers by Laura E. Warner
This network shows the impact of papers produced by Laura E. Warner. 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 Laura E. Warner. The network helps show where Laura E. Warner may publish in the future.
Co-authors
The 25 scholars most cited alongside Laura E. Warner, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
| # | Work | ||
|---|---|---|---|
| 1 | 1998 | 374 | |
| 2 | 1996 | 287 | |
| 3 | 1999 | 121 | |
| 4 | 1999 | 103 | |
| 5 | 2000 | 68 | |
| 6 | 1999 | 66 | |
| 7 | 2002 | 64 | |
| 8 | 1996 | 57 | |
| 9 | 1999 | 34 | |
| 10 | 1999 | 33 | |
| 11 | 1996 | 31 | |
| 12 | 1996 | 28 | |
| 13 | 1997 | 21 | |
| 14 | 1996 | 6 | |
| 15 | 1996 | 4 | |
| 16 | 1996 | 4 | |
| 17 | 1996 | 3 | |
| 18 | Mutational analysis of the myelin protein zero (MPZ) gene associated with Charcot-Marie-Tooth neuropathy type 1B | 1994 | 1 |
| 19 | 1997 | 1 |
About Laura E. Warner
Laura E. Warner is a scholar working on Cellular and Molecular Neuroscience, Molecular Biology, Cell Biology, Genetics and Neurology, having authored 19 papers that have together received 1.3k indexed citations. Recurring topics across this work include Hereditary Neurological Disorders (17 papers), RNA regulation and disease (5 papers), RNA Research and Splicing (5 papers), Genetic Neurodegenerative Diseases (4 papers), Cellular Mechanics and Interactions (3 papers), Neurogenetic and Muscular Disorders Research (2 papers), Endoplasmic Reticulum Stress and Disease (2 papers) and Caveolin-1 and cellular processes (2 papers). The work is most often cited by research in Cellular and Molecular Neuroscience (1.0k citations), Neurology (331 citations), Neurology (279 citations), Cell Biology (224 citations) and Genetics (75 citations). Laura E. Warner has collaborated with scholars based in United States, Belgium and Israel. Frequent co-authors include James R. Lupski, Pedro Mancías, Laura Davis Keppen, Ian J. Butler, Craig M. McDonald, Christine Van Broeckhoven, Eva Nelis, Carlos García, David R. Witt and Adria Bodell. Their work appears in journals such as Human Mutation, Human Molecular Genetics, Annual Review of Medicine, Cold Spring Harbor Symposia on Quantitative Biology and Pediatric Neurology.
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.