N. Miller
Impact in
- Genetics top 5%
- Neurogenetic and Muscular Disorders Research
- Virus-based gene therapy research
-
- Muscle Physiology and Disorders
- CRISPR and Genetic Engineering
- RNA Interference and Gene Delivery
- RNA modifications and cancer
Papers in
-
- Muscle Physiology and Disorders 21
- RNA Interference and Gene Delivery 3
- RNA modifications and cancer 3
- Genetics 14
- Neurogenetic and Muscular Disorders Research 13
- Virus-based gene therapy research 2
- Co-authors
- Linda Lowes (27 shared papers)Lindsay N. Alfano (21 shared papers)Jerry R. Mendell (13 shared papers)M. Iammarino (25 shared papers)Samiah Al-Zaidy (6 shared papers)Kathleen Church (8 shared papers)Louise R. Rodino‐Klapac (10 shared papers)Mark Hogan (4 shared papers)
- Journals
- Neuromuscular Disorders (14 papers)Neurology (6 papers)Neuropediatrics (2 papers)Human Gene Therapy (1 paper)Pediatric Neurology (1 paper)
- Partner nations
- United StatesFrance
In The Last Decade
N. Miller
25 papers receiving 568 citations
N. Miller's Hit Papers
Peers
Comparison fields: 5 of 57
- Genetics 168
- Molecular Biology 436
- Genetics 157
- Cardiology and Cardiovascular Medicine 72
- Aging 6
Countries citing papers authored by N. Miller
This map shows the geographic impact of N. Miller'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 N. Miller with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites N. Miller more than expected).
Fields of papers citing papers by N. Miller
This network shows the impact of papers produced by N. Miller. 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 N. Miller. The network helps show where N. Miller may publish in the future.
Co-authors
The 25 scholars most cited alongside N. Miller, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
Showing the 20 most-cited of 31 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Assessment of Systemic Delivery of rAAVrh74.MHCK7.micro-dystrophin in Children With Duchenne Muscular Dystrophy Hit paper breakdown → | 2020 | 279 |
| 2 | 2020 | 89 | |
| 3 | 2017 | 81 | |
| 4 | 2019 | 37 | |
| 5 | 2017 | 21 | |
| 6 | 2020 | 18 | |
| 7 | 2020 | 15 | |
| 8 | 2019 | 6 | |
| 9 | 2023 | 4 | |
| 10 | 2019 | 4 | |
| 11 | 2021 | 3 | |
| 12 | 2020 | 3 | |
| 13 | 2020 | 3 | |
| 14 | 2019 | 2 | |
| 15 | 2019 | 2 | |
| 16 | 2018 | 1 | |
| 17 | 2019 | 1 | |
| 18 | 2019 | 1 | |
| 19 | 2019 | 1 | |
| 20 | 2017 | 1 |
About N. Miller
N. Miller is a scholar working on Molecular Biology, Genetics, Psychiatry and Mental health, Developmental and Educational Psychology and Cellular and Molecular Neuroscience, having authored 31 papers that have together received 578 indexed citations. Recurring topics across this work include Muscle Physiology and Disorders (21 papers), Neurogenetic and Muscular Disorders Research (13 papers), Cerebral Palsy and Movement Disorders (5 papers), Children's Physical and Motor Development (4 papers), Genetic Neurodegenerative Diseases (3 papers), RNA Interference and Gene Delivery (3 papers), RNA modifications and cancer (3 papers) and Virus-based gene therapy research (2 papers). The work is most often cited by research in Genetics (168 citations), Molecular Biology (436 citations), Genetics (157 citations), Cardiology and Cardiovascular Medicine (72 citations) and Aging (6 citations). N. Miller has collaborated with scholars based in United States and France. Frequent co-authors include Linda Lowes, Lindsay N. Alfano, Jerry R. Mendell, M. Iammarino, Samiah Al-Zaidy, Kathleen Church, Louise R. Rodino‐Klapac, Mark Hogan, Sarah Lewis and Zarife Sahenk. Their work appears in journals such as Neuromuscular Disorders, Neurology, Neuropediatrics, Human Gene Therapy 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.